Gene Details



SLC12A6 and homologs in 5 species are found in 537 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse MP 24 Genes GS163456: MP:0006390 abnormal cochlear endolymph
Expand Tier I Mouse GO 782 Genes GS192507: GO:0006812 cation transport
Expand Tier I Human 83 Genes GS172224: HP:0001770 Toe syndactyly
Expand Tier I Human GO 146 Genes GS208908: GO:0071214 cellular response to abiotic stimulus
Expand Tier I Human CTD 382 Genes GS122940: Dimethylnitrosamine interacting genes (MeSH:D004128) in CTD
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human GO 1 Genes GS204057: GO:0071477 cellular hypotonic salinity response
Expand Tier I Mouse 690 Genes GS136114: body length 1 (Lgth1, Published QTL Chr 2)
Expand Tier I Mouse MP 3631 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Mouse MP 23 Genes GS170689: MP:0002690 akinesia
Expand Tier I Mouse MP 18 Genes GS166116: MP:0004411 decreased endocochlear potential
Expand Tier I Mouse MP 58 Genes GS165022: MP:0002857 cochlear ganglion degeneration
Expand Tier I Mouse MP 78 Genes GS164564: MP:0003871 abnormal myelin sheath morphology
Expand Tier I Human 17 Genes GS171507: HP:0002922 Increased CSF protein
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier I Human 10 Genes GS174464: HP:0002410 Aqueductal stenosis
Expand Tier I Mouse MP 30 Genes GS170350: MP:0004740 sensorineural hearing loss
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Mouse MP 214 Genes GS167898: MP:0009357 abnormal seizure response to inducing agent
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Mouse GO 774 Genes GS181423: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Mouse MP 129 Genes GS166186: MP:0009939 abnormal hippocampus neuron morphology
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human GO 433 Genes GS203054: GO:0048514 blood vessel morphogenesis
Expand Tier I Human 58 Genes GS171880: HP:0003134 Abnormality of peripheral nerve conduction
Expand Tier I Human GO 246 Genes GS195413: GO:0008509 anion transmembrane transporter activity
Expand Tier I Mouse 448 Genes GS135237: activity response to ethanol 4 (Actre4, Published QTL Chr 2)
Expand Tier I Mouse MP 175 Genes GS169585: MP:0001413 abnormal response to new environment
Expand Tier I Mouse 469 Genes GS136403: organ weight QTL 3 (Orgwq3, Published QTL Chr 2)
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
Expand Tier I Mouse MP 205 Genes GS163837: MP:0008026 abnormal brain white matter morphology
Expand Tier I Mouse MP 245 Genes GS170569: MP:0005404 abnormal axon morphology
Expand Tier I Mouse MP 173 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier I Mouse GO 1106 Genes GS192508: GO:0006811 ion transport
Expand Tier I Human 46 Genes GS172570: HP:0000341 Narrow forehead
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Mouse 552 Genes GS136115: body length 2 (Lgth2, Published QTL Chr 2)
Expand Tier I Mouse MP 72 Genes GS163843: MP:0000231 hypertension
Expand Tier I Mouse MP 202 Genes GS166905: MP:0001486 abnormal startle reflex
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 63 Genes GS171802: HP:0009553 Abnormality of the hairline
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Mouse GO 119 Genes GS190516: GO:0015293 symporter activity
Expand Tier I Human GO 192 Genes GS207409: GO:0015291 secondary active transmembrane transporter activity
Expand Tier I Mouse MP 57 Genes GS169512: MP:0002651 abnormal sciatic nerve morphology
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse 568 Genes GS136872: T cell ratio modifier QTL 2 (Trmq2, Published QTL Chr 2)
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse GO 888 Genes GS192671: GO:0055085 transmembrane transport
Expand Tier I Human 28 Genes GS172164: HP:0001182 Tapered finger
Expand Tier I Mouse MP 49 Genes GS165732: MP:0002735 abnormal chemical nociception
Expand Tier I Human GO 786 Genes GS195226: GO:0015075 ion transmembrane transporter activity
Expand Tier I Human 179 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Mouse MP 380 Genes GS165261: MP:0001393 ataxia
Expand Tier I Human 53 Genes GS173697: HP:0001319 Neonatal hypotonia
Expand Tier I Mouse GO 1064 Genes GS179401: GO:0005215 transporter activity
Expand Tier I Human 202 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Mouse GO 19 Genes GS187194: GO:0071472 cellular response to salt stress
Expand Tier I Mouse GO 4 Genes GS177562: GO:0006971 hypotonic response
Expand Tier I Human 48 Genes GS174921: HP:0000763 Sensory neuropathy
Expand Tier I Mouse MP 13 Genes GS168413: MP:0004292 abnormal spiral ligament fibrocyte morphology
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 1914 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human 10 Genes GS172524: HP:0001349 Facial diplegia
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier II Mouse 34 Genes GS36234: Striatum Gene expression correlates of Novel environment locomotion (activity beam breaks) 45-60 min in the center in Males BXD
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier II Mouse 55 Genes GS36264: Striatum Gene expression correlates of Novel environment locomotion (cm) 30-45 min in the center in Males BXD
Expand Tier I Mouse 451 Genes GS135918: graft-versus host disease 3 (Gvhd3, Published QTL Chr 2)
Expand Tier I Mouse GO 366 Genes GS179009: GO:0015672 monovalent inorganic cation transport
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Human GO 22 Genes GS202193: GO:0009651 response to salt stress
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Mouse MP 482 Genes GS163429: MP:0000849 abnormal cerebellum morphology
Expand Tier I Mouse MP 268 Genes GS164346: MP:0006335 abnormal hearing electrophysiology
Expand Tier I Mouse MP 1966 Genes GS166590: MP:0002873 normal phenotype
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Mouse 3115 Genes GS128575: Ethanol induced LORR Chr# 2
Expand Tier I Mouse MP 185 Genes GS165208: MP:0002842 increased systemic arterial blood pressure
Expand Tier I Human CTD 765 Genes GS123769: 2-(1'H-indolo-3'-carbonyl)thiazole-4-carboxylic acid methyl ester interacting genes (MeSH:C548651) in CTD
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 54 Genes GS175935: HP:0000248 Brachycephaly
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Mouse 742 Genes GS129195: Tmc1 modifier 1 (Tmc1m1 Published QTL Chr 2)
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 11 Genes GS167923: MP:0000958 peripheral nervous system degeneration
Expand Tier I Mouse 560 Genes GS136160: leishmaniasis resistance 14 (Lmr14, Published QTL Chr 2)
Expand Tier I Mouse MP 648 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier II Mouse 22 Genes GS35223: Striatum Gene expression correlates of Open field locomotion - Saline- (cm) 45-60 min in Females BXD
Expand Tier I Mouse MP 111 Genes GS169367: MP:0005405 axon degeneration
Expand Tier I Human 19 Genes GS171721: HP:0003445 EMG: neuropathic changes
Expand Tier I Mouse MP 189 Genes GS168606: MP:0000778 abnormal nervous system tract morphology
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 188 Genes GS171167: HP:0000235 Abnormality of the fontanelles and cranial sutures
Expand Tier I Mouse MP 86 Genes GS169944: MP:0004142 abnormal muscle tone
Expand Tier I Human 4 Genes GS171307: HP:0003444 EMG: chronic denervation signs
Expand Tier I Human 236 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Mouse 559 Genes GS136595: rotarod performance 2 (Rrodp2, Published QTL Chr 2)
Expand Tier II Mouse 32 Genes GS34256: Striatum Gene expression correlates of Suppression of activity in altered context in Females BXD
Expand Tier I Mouse 736 Genes GS136914: vertebral morphology and mechanical traits 2 (Vmmt2, Published QTL Chr 2)
Expand Tier I Mouse 501 Genes GS136873: T cell ratio modifier QTL 3 (Trmq3, Published QTL Chr 2)
Expand Tier I Mouse MP 30 Genes GS164066: MP:0006329 sensorineural hearing impairment
Expand Tier II Mouse 389 Genes GS36133: Hippocampus Gene expression correlates of Activity during 1st tone shock pairing in Males BXD
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 497 Genes GS196432: GO:0030001 metal ion transport
Expand Tier I Mouse 555 Genes GS136360: Neuroadapted Sindbis viral RNA level 1 (Nsv1, Published QTL Chr 2)
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 27 Genes GS172613: HP:0003477 Peripheral axonal neuropathy
Expand Tier I Human 56 Genes GS174922: HP:0000762 Decreased nerve conduction velocity
Expand Tier II Mouse 613 Genes GS84132: ethanol induced locomotor activity (Published QTL, Chr 2)
Expand Tier I Mouse 631 Genes GS136010: hemotopoietic response to early cytokines (Hrec, Published QTL Chr 2)
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Human 7 Genes GS172458: HP:0003448 Decreased sensory nerve conduction velocity
Expand Tier I Mouse MP 1615 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Mouse GO 886 Genes GS181425: GO:0022892 substrate-specific transporter activity
Expand Tier I Mouse 450 Genes GS136055: IgA nephropathy QTL 1 (Ignpq1, Published QTL Chr 2)
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Mouse MP 35 Genes GS164265: MP:0000811 hippocampal neuron degeneration
Expand Tier I Mouse MP 1989 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Mouse MP 29 Genes GS165132: MP:0004885 abnormal endolymph
Expand Tier I Mouse MP 41 Genes GS167029: MP:0002176 increased brain weight
Expand Tier I Mouse MP 476 Genes GS169227: MP:0001405 impaired coordination
Expand Tier I Mouse GO 621 Genes GS180679: GO:0009628 response to abiotic stimulus
Expand Tier I Mouse MP 438 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier I Human 70 Genes GS171543: HP:0000276 Long face
Expand Tier I Mouse MP 2199 Genes GS165244: MP:0010771 integument phenotype
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 128 Genes GS207410: GO:0015293 symporter activity
Expand Tier I Mouse MP 661 Genes GS169386: MP:0002063 abnormal learning/memory/conditioning
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Mouse MP 72 Genes GS164745: MP:0005238 increased brain size
Expand Tier I Mouse MP 41 Genes GS167754: MP:0000781 decreased corpus callosum size
Expand Tier I Mouse GO 112 Genes GS191967: GO:0071214 cellular response to abiotic stimulus
Expand Tier I Mouse MP 68 Genes GS165873: MP:0004404 cochlear outer hair cell degeneration
Expand Tier I Mouse MP 71 Genes GS167541: MP:0009142 decreased prepulse inhibition
Expand Tier I Human GO 761 Genes GS209613: GO:0055085 transmembrane transport
Expand Tier I Mouse 451 Genes GS135858: femur breaking strength 1 (Fembrs1, Published QTL Chr 2)
Expand Tier I Mouse 467 Genes GS136105: lymph node cytotoxic T lymphocyte percentage 1 (Lctlp1, Published QTL Chr 2)
Expand Tier I Mouse 451 Genes GS136797: total body bone mineral density 2 (Tbbmd2, Published QTL Chr 2)
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse MP 113 Genes GS168215: MP:0001967 deafness
Expand Tier I Human GO 311 Genes GS209586: GO:0022804 active transmembrane transporter activity
Expand Tier I Mouse MP 110 Genes GS169363: MP:0000921 demyelination
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Mouse MP 865 Genes GS167759: MP:0000787 abnormal telencephalon morphology
Expand Tier II Mouse 554 Genes GS84133: activity response to ethanol (Published QTL, Chr 2)
Expand Tier I Human 81 Genes GS175456: HP:0100037 Abnormality of the scalp hair
Expand Tier I Mouse MP 23 Genes GS166279: MP:0004268 abnormal optic stalk morphology
Expand Tier I Mouse MP 181 Genes GS163498: MP:0003308 abnormal cochlear sensory epithelium morphology
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier II Mouse 39 Genes GS36279: Striatum Gene expression correlates of Novel environment locomotion (cm) 45-60 min in the center in Males BXD
Expand Tier I Mouse MP 298 Genes GS164949: MP:0001504 abnormal posture
Expand Tier I Mouse GO 1 Genes GS180955: GO:0042539 hypotonic salinity response
Expand Tier I Mouse MP 677 Genes GS165538: MP:0005377 hearing/vestibular/ear phenotype
Expand Tier I Mouse MP 574 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Mouse MP 3494 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Mouse MP 400 Genes GS164570: MP:0003878 abnormal ear physiology
Expand Tier I Mouse MP 1963 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Mouse MP 633 Genes GS163101: MP:0008540 abnormal cerebrum morphology
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Mouse MP 39 Genes GS166455: MP:0009434 paraparesis
Expand Tier I Mouse DRG 514 Genes provisional GS87011: Table S2: List of Cocaine-Treated HDAC5 KO vs. Cocaine-Treated WT Significantly Regulated Genes. [DRG]
Expand Tier I Mouse 690 Genes GS136090: lean body mass 2 (Lbm2, Published QTL Chr 2)
Expand Tier I Mouse GO 1440 Genes GS181988: GO:0044459 plasma membrane part
Expand Tier I Human 25 Genes GS171767: HP:0003431 Decreased motor nerve conduction velocity
Expand Tier I Mouse MP 12 Genes GS164654: MP:0003063 increased coping response
Expand Tier I Mouse MP 379 Genes GS164530: MP:0000801 abnormal temporal lobe morphology
Expand Tier I Mouse MP 582 Genes GS169658: MP:0002572 abnormal emotion/affect behavior
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier II Mouse 580 Genes GS84131: ethanol consumption (Published QTL, Chr 2)
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse MP 1130 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Human GO 357 Genes GS209923: GO:0001525 angiogenesis
Expand Tier I Human 202 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human 197 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Mouse GO 158 Genes GS193353: GO:0016323 basolateral plasma membrane
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Mouse GO 7 Genes GS184183: GO:0015377 cation:chloride symporter activity
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse GO 725 Genes GS178474: GO:0015075 ion transmembrane transporter activity
Expand Tier I Human GO 925 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Mouse GO 4 Genes GS181538: GO:0015379 potassium:chloride symporter activity
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Mouse MP 291 Genes GS164046: MP:0001968 abnormal touch/ nociception
Expand Tier I Mouse MP 124 Genes GS167753: MP:0000780 abnormal corpus callosum morphology
Expand Tier I Human 2 Genes GS173902: HP:0006125 Long tapered fingers
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse 1157 Genes GS129156: multigenic obesity QTL 5 (Mobq5 Published QTL Chr 2)
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Mouse GO 852 Genes GS180817: GO:0022857 transmembrane transporter activity
Expand Tier I Mouse 450 Genes GS135855: femoral bone morphometry 4 (Fembm4, Published QTL Chr 2)
Expand Tier I Mouse MP 249 Genes GS163316: MP:0000035 abnormal membranous labyrinth morphology
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
Expand Tier I Human 39 Genes GS173054: HP:0000327 Hypoplasia of the maxilla
Expand Tier I Human GO 1189 Genes GS197275: GO:0033554 cellular response to stress
Expand Tier I Human 183 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Mouse MP 209 Genes GS167140: MP:0003169 abnormal scala media morphology
Expand Tier II Mouse 240 Genes GS36123: Hippocampus Gene expression correlates of Activity during 1st tone shock pairing in Females & Males BXD
Expand Tier I Mouse MP 19 Genes GS164653: MP:0003062 abnormal coping response
Expand Tier I Mouse MP 1 Genes GS168420: MP:0004295 abnormal type III spiral ligament fibrocytes
Expand Tier I Mouse MP 95 Genes GS164539: MP:0003360 abnormal depression-related behavior
Expand Tier I Mouse MP 462 Genes GS169393: MP:0002064 seizures
Expand Tier I Mouse 450 Genes GS135892: failure of ureteric bud invasion 1 (Fubi1, Published QTL Chr 2)
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse GO 3 Genes GS187197: GO:0071476 cellular hypotonic response
Expand Tier I Mouse GO 56 Genes GS177560: GO:0006970 response to osmotic stress
Expand Tier I Human 43 Genes GS173055: HP:0000326 Abnormality of the maxilla
Expand Tier I Mouse 556 Genes GS135584: cholesterol absorption 1 (Chab1, Published QTL Chr 2)
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 3 Genes GS204055: GO:0071472 cellular response to salt stress
Expand Tier I Human GO 980 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Tier I Human 49 Genes GS171306: HP:0003130 Abnormal peripheral myelination
Expand Tier I Mouse MP 562 Genes GS163436: MP:0000841 abnormal hindbrain morphology
Expand Tier I Mouse MP 300 Genes GS163842: MP:0000230 abnormal systemic arterial blood pressure
Expand Tier I Human GO 1 Genes GS197747: GO:0042539 hypotonic salinity response
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 12 Genes GS204056: GO:0071470 cellular response to osmotic stress
Expand Tier I Mouse MP 2644 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier I Human GO 1588 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Mouse MP 255 Genes GS166583: MP:0001513 limb grasping
Expand Tier I Mouse GO 935 Genes GS180482: GO:0033554 cellular response to stress
Expand Tier I Mouse 617 Genes GS136527: prion disease incubation time 1 (Prdt1, Published QTL Chr 2)
Expand Tier I Human 250 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Mouse MP 61 Genes GS167666: MP:0000032 cochlear degeneration
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Mouse GO 3268 Genes GS177721: GO:0051234 establishment of localization
Expand Tier II Mouse 27 Genes GS35180: Striatum Gene expression correlates of Open Field - locomotion (activity beam breaks) 30-45 min post saline in Males BXD
Expand Tier I Mouse GO 30 Genes GS185371: GO:0009651 response to salt stress
Expand Tier II Mouse 49 Genes GS36274: Striatum Gene expression correlates of Novel environment locomotion (cm) 45-60 min in the center in Females BXD
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Mouse GO 66 Genes GS190512: GO:0015294 solute:cation symporter activity
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Mouse GO 22 Genes GS190514: GO:0015296 anion:cation symporter activity
Expand Tier I Mouse GO 2101 Genes GS193563: GO:0006950 response to stress
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier II Mouse 61 Genes GS36224: Striatum Gene expression correlates of Novel environment locomotion (activity beam breaks) 45-60 min in the center in Females & Males BXD
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse MP 389 Genes GS167918: MP:0000955 abnormal spinal cord morphology
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse MP 5 Genes GS168414: MP:0004293 abnormal type I spiral ligament fibrocytes
Expand Tier I Mouse MP 281 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier I Mouse 643 Genes GS135594: mean cell hemoglobin concentration QTL 1 (Chcmq1, Published QTL Chr 2)
Expand Tier I Mouse MP 1055 Genes GS166120: MP:0002106 abnormal muscle physiology
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier II Mouse 171 Genes GS33995: Neocortex Gene expression correlates of blood ethanol concentration in mg/dl in Females & Males BXD
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Mouse 451 Genes GS135564: cytokine deficiency colitis susceptibility 3 (Cdcs3, Published QTL Chr 2)
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human GO 8 Genes GS200987: GO:0015377 cation:chloride symporter activity
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 109 Genes GS176899: HP:0002353 EEG abnormality
Expand Tier I Human 17 Genes GS176999: HP:0001290 Generalized hypotonia
Expand Tier I Human GO 2940 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Mouse MP 466 Genes GS165253: MP:0001399 hyperactivity
Expand Tier I Mouse MP 246 Genes GS167941: MP:0001970 abnormal pain threshold
Expand Tier I Mouse 1196 Genes GS129192: type 2 diabetes mellitus 2 in SMXA RI mice (T2dm2sa Published QTL Chr 2)
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier II Mouse 67 Genes GS36269: Striatum Gene expression correlates of Novel environment locomotion (cm) 45-60 min in the center in Females & Males BXD
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Mouse MP 3 Genes GS168047: MP:0004487 type I spiral ligament fibrocyte degeneration
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Mouse MP 1628 Genes GS163852: MP:0001544 abnormal cardiovascular system physiology
Expand Tier I Mouse MP 24 Genes GS167781: MP:0002630 abnormal endocochlear potential
Expand Tier I Human 18 Genes GS173678: HP:0003383 Onion bulb formation
Expand Tier I Human 119 Genes GS172170: HP:0003196 Short nose
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human GO 4 Genes GS198329: GO:0015379 potassium:chloride symporter activity
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Rat DRG 4920 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Mouse MP 230 Genes GS163320: MP:0000031 abnormal cochlea morphology
Expand Tier I Mouse MP 70 Genes GS170583: MP:0005407 hyperalgesia
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 2057 Genes GS169835: MP:0005389 reproductive system phenotype
Expand Tier I Mouse MP 471 Genes GS169228: MP:0001406 abnormal gait
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 517 Genes GS194493: GO:0001944 vasculature development
Expand Tier I Mouse MP 332 Genes GS164681: MP:0004262 abnormal physical strength
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse GO 118 Genes GS192880: GO:0015698 inorganic anion transport
Expand Tier I Human 69 Genes GS170981: HP:0011361 Congenital abnormal hair pattern
Expand Tier I Mouse 559 Genes GS135670: circadian period of locomotor activity 7 (Cplaq7, Published QTL Chr 2)
Expand Tier I Human GO 278 Genes GS195770: GO:0015672 monovalent inorganic cation transport
Expand Tier I Mouse 621 Genes GS136639: salmonella enteritidis susceptibility 7 (Ses7, Published QTL Chr 2)
Expand Tier I Mouse MP 46 Genes GS165617: MP:0004398 cochlear inner hair cell degeneration
Expand Tier I Mouse 708 Genes GS136735: segregation of mitochondrial DNA QTL 2 (Smdq2, Published QTL Chr 2)
Expand Tier I Mouse 482 Genes GS135219: aberrant activation of B cell proliferation (Aabpr, Published QTL Chr 2)
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Human GO 4 Genes GS194299: GO:0006971 hypotonic response
Expand Tier I Mouse MP 814 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human 79 Genes GS171959: HP:0000400 Macrotia
Expand Tier I Mouse MP 695 Genes GS168579: MP:0003635 abnormal synaptic transmission
Expand Tier I Mouse MP 306 Genes GS169962: MP:0001286 abnormal eye development
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Mouse MP 49 Genes GS166245: MP:0004263 abnormal limb posture
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 23 Genes GS175301: HP:0000294 Low anterior hairline
Expand Tier I Mouse GO 160 Genes GS192506: GO:0006813 potassium ion transport
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier II Mouse 21 Genes GS34413: Striatum Gene expression correlates of Novel environment rears 45-60 min in the center in Females & Males BXD
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Mouse MP 180 Genes GS163068: MP:0000045 abnormal hair cell morphology
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Mouse 585 Genes GS136377: obesity QTL 3 (Obq3, Published QTL Chr 2)
Expand Tier I Human GO 83 Genes GS195882: GO:0015108 chloride transmembrane transporter activity
Expand Tier I Human GO 806 Genes GS197478: GO:0009628 response to abiotic stimulus
Expand Tier I Human 14 Genes GS173755: HP:0004691 2-3 toe syndactyly
Expand Tier I Mouse MP 21 Genes GS165395: MP:0003225 axonal dystrophy
Expand Tier I Human 72 Genes GS176488: HP:0010720 Abnormal hair pattern
Expand Tier I Mouse MP 184 Genes GS164059: MP:0006325 impaired hearing
Expand Tier I Human GO 82 Genes GS207406: GO:0015294 solute:cation symporter activity
Expand Tier I Human GO 32 Genes GS207408: GO:0015296 anion:cation symporter activity
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Human 154 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Mouse GO 1 Genes GS187196: GO:0071477 cellular hypotonic salinity response
Expand Tier I Human 62 Genes GS171488: HP:0002921 Abnormality of the cerebrospinal fluid
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Mouse MP 1083 Genes GS167755: MP:0000783 abnormal forebrain morphology
Expand Tier I Human GO 754 Genes GS204108: GO:0072358 cardiovascular system development
Expand Tier I Human 123 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human 66 Genes GS175643: HP:0006989 Dysplastic corpus callosum
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Mouse MP 425 Genes GS169631: MP:0004166 abnormal limbic system morphology
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse MP 1856 Genes GS165386: MP:0001262 decreased body weight
Expand Tier I Mouse GO 5654 Genes GS182325: GO:0051716 cellular response to stimulus
Expand Tier I Mouse 552 Genes GS136011: heart rate quantitative locus 1 (Hrq1, Published QTL Chr 2)
Expand Tier I Mouse GO 281 Genes GS192646: GO:0022804 active transmembrane transporter activity
Expand Tier I Mouse MP 88 Genes GS164962: MP:0002855 abnormal cochlear ganglion morphology
Expand Tier I Mouse MP 17 Genes GS168692: MP:0004288 abnormal spiral ligament morphology
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier II Mouse 28 Genes GS35218: Striatum Gene expression correlates of Open Field - Total horizontal distance (cm) 30-45 min post saline (10 ml/kg) in Males BXD
Expand Tier I Mouse MP 898 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Mouse 552 Genes GS136600: serum alkaline phosphatase activity 1 (Salpa1, Published QTL Chr 2)
Expand Tier I Human GO 128 Genes GS196999: GO:0015103 inorganic anion transmembrane transporter activity
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Mouse MP 128 Genes GS169004: MP:0008219 abnormal dorsal telencephalic commissure morphology
Expand Tier I Mouse 547 Genes GS136364: obesity QTL 10 (Obq10, Published QTL Chr 2)
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Mouse 625 Genes GS135837: total fat pad mass QTL 1 (Fatmq1, Published QTL Chr 2)
Expand Tier I Human GO 754 Genes GS204107: GO:0072359 circulatory system development
Expand Tier I Mouse MP 495 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier I Human 207 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human GO 166 Genes GS210294: GO:0016323 basolateral plasma membrane
Expand Tier I Mouse 791 Genes GS129169: plasma plant sterol 2b (Plast2b Published QTL Chr 2)
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier I Mouse MP 1485 Genes GS166712: MP:0002161 abnormal fertility/fecundity
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Mouse GO 600 Genes GS179671: GO:0030001 metal ion transport
Expand Tier I Mouse MP 373 Genes GS164526: MP:0000807 abnormal hippocampus morphology
Expand Tier I Mouse GO 175 Genes GS190515: GO:0015291 secondary active transmembrane transporter activity
Expand Tier I Mouse MP 248 Genes GS166029: MP:0000960 abnormal sensory ganglion morphology
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse 534 Genes GS135235: activity response to ethanol 2 (Actre2, Published QTL Chr 2)
Expand Tier I Mouse GO 549 Genes GS180083: GO:0034220 ion transmembrane transport
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Mouse MP 51 Genes GS164273: MP:0000043 organ of Corti degeneration
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Mouse MP 157 Genes GS168746: MP:0002199 abnormal brain commissure morphology
Expand Tier II Mouse 19 Genes GS35184: Striatum Gene expression correlates of Open Field - locomotion (activity beam breaks) 45-60 min post saline in Females BXD
Expand Tier I Mouse GO 509 Genes GS192789: GO:0008324 cation transmembrane transporter activity
Expand Tier I Mouse GO 792 Genes GS190899: GO:0043005 neuron projection
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Mouse GO 80 Genes GS179117: GO:0015108 chloride transmembrane transporter activity
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 1817 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Human 4 Genes GS174621: HP:0002111 Restrictive respiratory insufficiency
Expand Tier I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 132 Genes GS171835: HP:0011329 Abnormality of cranial sutures
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Mouse MP 143 Genes GS169847: MP:0004399 abnormal cochlear outer hair cell morphology
Expand Tier I Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Human 65 Genes GS176590: HP:0001274 Agenesis of corpus callosum
Expand Tier I Mouse MP 903 Genes GS167075: MP:0001924 infertility
Expand Tier I Mouse GO 326 Genes GS185304: GO:0030424 axon
Expand Tier I Human GO 491 Genes GS202261: GO:0001568 blood vessel development
Expand Tier I Mouse MP 105 Genes GS162819: MP:0002906 increased susceptibility to pharmacologically induced seizures
Expand Tier I Mouse MP 1 Genes GS168045: MP:0004489 type III spiral ligament fibrocyte degeneration
Expand Tier II Mouse 23 Genes GS34246: Striatum Gene expression correlates of Activity in altered context during presentation of cue in Females BXD
Expand Tier I Mouse MP 220 Genes GS168838: MP:0003107 abnormal response to novelty
Expand Tier I Human GO 845 Genes GS198212: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Mouse MP 162 Genes GS169277: MP:0001081 abnormal cranial ganglia morphology
Expand Tier I Human GO 118 Genes GS209449: GO:0006813 potassium ion transport
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse MP 605 Genes GS167357: MP:0002206 abnormal CNS synaptic transmission
Expand Tier I Human 18 Genes GS175821: HP:0002091 Restrictive lung disease
Expand Tier I Human GO 569 Genes GS209735: GO:0008324 cation transmembrane transporter activity
Expand Tier II Mouse 148 Genes GS34251: Striatum Gene expression correlates of Activity in altered context during presentation of cue in Males BXD
Expand Tier I Mouse 610 Genes GS135704: diabetes mRNA cluster 1 (Dbmc1, Published QTL Chr 2)
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Mouse MP 278 Genes GS168600: MP:0000771 abnormal brain size
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Mouse MP 22 Genes GS169052: MP:0004143 hypertonia
Expand Tier I Human 44 Genes GS174918: HP:0000764 Peripheral axonal degeneration
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Mouse GO 356 Genes GS179592: GO:0006820 anion transport
Expand Tier I Human GO 4 Genes GS204058: GO:0071476 cellular hypotonic response
Expand Tier I Human GO 57 Genes GS194296: GO:0006970 response to osmotic stress
Expand Tier I Mouse MP 221 Genes GS169362: MP:0000920 abnormal myelination
Expand Tier I Mouse MP 12 Genes GS166877: MP:0008532 decreased chemical nociceptive threshold
Expand Tier I Mouse 683 Genes GS135418: bitterness sensitivity 1 (Bits1, Published QTL Chr 2)
Expand Tier I Mouse 622 Genes GS135708: diabetes susceptibility QTL 5 (Dbsq5, Published QTL Chr 2)
Expand Tier I Mouse 736 Genes GS135554: CD8 memory T cell subset 3 (Cd8mts3, Published QTL Chr 2)
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Mouse 28 Genes GS35507: Striatum Gene expression correlates of Neurogenesis- BrdU labeled new neurons in Adult Rostral Migratory Stream 1 hr post BrdU in Males BXD
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Mouse MP 43 Genes GS168157: MP:0005504 abnormal ligament morphology
Expand Tier I Human 215 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Mouse MP 1672 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Mouse MP 115 Genes GS169841: MP:0004393 abnormal cochlear inner hair cell morphology
Expand Tier I Mouse DRG 867 Genes provisional GS86789: Table S1: Cocaine Regulation of H3 Acetylation. [DRG]
Expand Tier I Mouse GO 112 Genes GS180219: GO:0015103 inorganic anion transmembrane transporter activity
Expand Tier I Mouse GO 228 Genes GS178656: GO:0008509 anion transmembrane transporter activity
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Mouse 471 Genes GS135685: C. trachomatis resistance QTL 1 (Ctrq1, Published QTL Chr 2)
Expand Tier I Mouse 622 Genes GS136950: weight gain in high growth mice 5 (Wg5, Published QTL Chr 2)
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier I Mouse MP 144 Genes GS167915: MP:0000950 abnormal seizure response to pharmacological agent
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 344 Genes GS168218: MP:0001963 abnormal hearing physiology
Expand Tier I Mouse MP 486 Genes GS163438: MP:0000847 abnormal metencephalon morphology
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 153 Genes GS175067: HP:0001159 Syndactyly
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse GO 84 Genes GS179593: GO:0006821 chloride transport
Expand Tier I Mouse MP 1848 Genes GS167622: MP:0002152 abnormal brain morphology
Expand Tier I Mouse MP 106 Genes GS167585: MP:0001417 decreased exploration in new environment
Expand Tier I Mouse MP 182 Genes GS163063: MP:0000042 abnormal organ of Corti morphology
Expand Tier I Mouse MP 875 Genes GS168958: MP:0003492 abnormal involuntary movement
Expand Tier I Mouse 559 Genes GS135694: directional asymmetry QTL 18 (Daq18, Published QTL Chr 2)
Expand Tier I Mouse MP 397 Genes GS166531: MP:0009745 abnormal behavioral response to xenobiotic
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Mouse 552 Genes GS135795: ethanol induced low dose activation 3 (Elda3, Published QTL Chr 2)