Gene Details



VPS13A and homologs in 6 species are found in 338 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 GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Human 41 Genes GS171926: HP:0007018 Attention deficit hyperactivity disorder
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse 645 Genes GS136227: mandible length 19 (Manln19, Published QTL Chr 19)
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 11 Genes GS173817: HP:0000734 Disinhibition
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 111 Genes GS171784: HP:0001399 Hepatic failure
Expand Tier III Human 735 Genes GS1229: Differential gene expression among both the Heroin and Cocaine Abusers
Expand Tier I Mouse 522 Genes GS136295: modifier of p53-deficiency 1 (Mp53d1, Published QTL Chr 19)
Expand Tier I Human CTD 2780 Genes GS123332: 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide interacting genes (MeSH:D015123) in CTD
Expand Tier I Mouse 440 Genes GS135479: bone response to mechanical loading 12 (Brml12, Published QTL Chr 19)
Expand Tier I Mouse 648 Genes GS136241: macrophage-associated risk inflammatory factor 3 (Marif3, Published QTL Chr 19)
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Mouse 427 Genes GS135338: atherosclerosis 16 (Ath16, Published QTL Chr 19)
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Mouse 645 Genes GS135445: bone length and organs 11 (Bod11, Published QTL Chr 19)
Expand Tier II Mouse 786 Genes GS84315: METH responses for body temperature (Published QTL, Chr 19)
Expand Tier I Human 187 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier II Mouse 466 Genes GS35708: Hippocampus Gene expression correlates of Open Field locomotion 0-15 min post cocaine in Females & Males BXD
Expand Tier I Human 123 Genes GS173242: HP:0001337 Tremor
Expand Tier II Mouse 685 Genes GS84317: alcohol preference locus (Published QTL, Chr 19)
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier III Mouse 81 Genes GS34311: Striatum Gene expression correlates of Cue Conditioning - Activity suppression after 3rd tone/shock pairing [Basal Behavior] in Males BXD
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 6 Genes GS173047: HP:0002310 Orofacial dyskinesia
Expand Tier I Human 197 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human DRG 911 Genes provisional GS86977: Table S1: All transcripts significantly different in abundance between the majority of heroin subjects and their matched controls [DRG]
Expand Tier I Human 202 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 102 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human 48 Genes GS174921: HP:0000763 Sensory neuropathy
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse GO 560 Genes GS189224: GO:0007610 behavior
Expand Tier II Mouse 119 Genes GS36775: Hippocampus Gene expression correlates of Zero Maze - Percentage open time in Males BXD
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 123 Genes GS176672: HP:0000980 Pallor
Expand Tier I Mouse MP 1083 Genes GS167755: MP:0000783 abnormal forebrain morphology
Expand Tier I Human 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier I Human GO 1972 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human 74 Genes GS175265: HP:0002733 Abnormality of the lymph nodes
Expand Tier II Mouse 632 Genes GS84314: METH responses for body temperature (Published QTL, Chr 19)
Expand Tier II Mouse 134 Genes GS36790: Hippocampus Gene expression correlates of Zero Maze - Time in Closed Arms in Males BXD
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier II Mouse 465 Genes GS35733: Hippocampus Gene expression correlates of Open Field locomotion (cm) 0-15 min post cocaine in Males BXD
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 246 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier II Mouse 48 Genes GS35199: Striatum Gene expression correlates of Open Field - Total horizontal distance (cm) 0-15 min post saline in Males BXD
Expand Tier II Mouse 464 Genes GS35718: Hippocampus Gene expression correlates of Open Field locomotion 0-15 min post cocaine in Males BXD
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
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 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Human 106 Genes GS173246: HP:0001332 Dystonia
Expand Tier III Mouse 5726 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 130 Genes GS174137: HP:0002017 Nausea and vomiting
Expand Tier I Mouse GO 777 Genes GS186645: GO:0051704 multi-organism process
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 61 Genes GS174375: HP:0002027 Abdominal pain
Expand Tier I Human 36 Genes GS171175: HP:0001541 Ascites
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier II Mouse 67 Genes GS35502: Striatum Gene expression correlates of Neurogenesis- BrdU labeled new neurons in Adult Rostral Migratory Stream 1 hr post BrdU in Females BXD
Expand Tier I Mouse MP 81 Genes GS169229: MP:0001407 short stride length
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier II Mouse 466 Genes GS35723: Hippocampus Gene expression correlates of Open Field locomotion (cm) 0-15 min post cocaine in Females & Males BXD
Expand Tier I Mouse 522 Genes GS135752: experimental allergic encephalomyelitis susceptibility 19 (Eae19, Published QTL Chr 19)
Expand Tier II Mouse 55 Genes GS35161: Striatum Gene expression correlates of Open Field - locomotion (activity beam breaks) 0-15 min in Males BXD
Expand Tier I Mouse 552 Genes GS135277: "alcohol preference locus 23, male specific" (Alcp23, Published QTL Chr 19)
Expand Tier I Human 271 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 96 Genes GS174135: HP:0002015 Dysphagia
Expand Tier I Human 161 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human 207 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human 35 Genes GS176798: HP:0001266 Choreoathetosis
Expand Tier III Mouse 8392 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse MP 3 Genes GS167487: MP:0003242 loss of basal ganglia neurons
Expand Tier I Mouse MP 2754 Genes GS169767: MP:0002396 abnormal hematopoietic system morphology/development
Expand Tier I Mouse 552 Genes GS135278: "alcohol preference locus 24, female specific" (Alcp24, Published QTL Chr 19)
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 2 Genes GS173420: HP:0100033 Tics
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 58 Genes GS203493: GO:0051705 multi-organism behavior
Expand Tier I Mouse GO 1598 Genes GS188957: GO:0033036 macromolecule localization
Expand Tier I Human 108 Genes GS176797: HP:0001268 Mental deterioration
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 53 Genes GS175407: HP:0002072 Chorea
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human 62 Genes GS174055: HP:0000726 Dementia
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier II Mouse 48 Genes GS35321: Striatum Gene expression correlates of Open Field rears 0-15 min post saline in Females & Males BXD
Expand Tier II Mouse 18 Genes GS34235: Cerebellum Gene expression correlates of Light-Dark Box Percentage of distance traveled in light compartment in Males BXD
Expand Tier II Mouse 452 Genes GS34322: Hippocampus Gene expression correlates of Cocaine TOTAL locomotion (activity beam breaks) in Males BXD
Expand Tier I Human GO 333 Genes GS204027: GO:0044708 single-organism behavior
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse GO 1686 Genes GS184220: GO:0071702 organic substance transport
Expand Tier I Mouse 522 Genes GS136110: long free running period 2 (Lfp2, Published QTL Chr 19)
Expand Tier I Mouse MP 724 Genes GS170366: MP:0000245 abnormal erythropoiesis
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse 405 Genes GS135830: exploratory and excitability QTL 4 (Exq4, Published QTL Chr 19)
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 1699 Genes GS203755: GO:0016265 death
Expand Tier I Mouse MP 2821 Genes GS169535: MP:0005397 hematopoietic system phenotype
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier II Mouse 219 Genes GS36477: Whole Brain Gene expression correlates of Morphine - Severity of ptosis in Males BXD
Expand Tier I Mouse 645 Genes GS135421: bitterness sensitivity 4 (Bits4, Published QTL Chr 19)
Expand Tier I Human 7 Genes GS177041: HP:0001927 Acanthocytosis
Expand Tier I Human 49 Genes GS173815: HP:0000736 Short attention span
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 30 Genes GS176897: HP:0002354 Memory impairment
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse 705 Genes GS136848: thymic lymphoma resistance 1 (Tlyr1, Published QTL Chr 19)
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Mouse MP 476 Genes GS169227: MP:0001405 impaired coordination
Expand Tier I Human 1 Genes GS175493: HP:0008767 Self-mutilation of tongue and lips due to involuntary movements
Expand Tier I Human 160 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 3 Genes GS172145: HP:0010994 Abnormality of the striatum
Expand Tier I Human GO 1127 Genes GS196794: GO:0046907 intracellular transport
Expand Tier I Human 3 Genes GS171052: HP:0002340 Caudate atrophy
Expand Tier I Human 4 Genes GS171814: HP:0001575 Mood changes
Expand Tier I Mouse 705 Genes GS136033: induction of brown adipocytes 4 (Iba4, Published QTL Chr 19)
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
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 471 Genes GS136359: nerve sheath tumor resistance QTL 1 (Nstr1, Published QTL Chr 19)
Expand Tier I Mouse MP 87 Genes GS164854: MP:0001360 abnormal social investigation
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 68 Genes GS175906: HP:0002910 Elevated hepatic transaminases
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Mouse MP 2404 Genes GS165615: MP:0002123 abnormal hematopoiesis
Expand Tier I Human 20 Genes GS176236: HP:0002307 Drooling
Expand Tier I Mouse 609 Genes GS135586: cholesterol absorption 5 (Chab5, Published QTL Chr 19)
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 1269 Genes GS197769: GO:0045184 establishment of protein localization
Expand Tier I Mouse MP 412 Genes GS163851: MP:0001545 abnormal hematopoietic system physiology
Expand Tier I Human 114 Genes GS172283: HP:0000820 Abnormality of the thyroid gland
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 192 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Mouse MP 2419 Genes GS168551: MP:0002429 abnormal blood cell morphology/development
Expand Tier I Human GO 182 Genes GS196459: GO:0048193 Golgi vesicle transport
Expand Tier I Human 67 Genes GS174328: HP:0002716 Lymphadenopathy
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 123 Genes GS176799: HP:0001265 Hyporeflexia
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human GO 136 Genes GS202323: GO:0007626 locomotory behavior
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse GO 1081 Genes GS180977: GO:0045184 establishment of protein localization
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Mouse 705 Genes GS136958: weight 6 (Wght6, Published QTL Chr 19)
Expand Tier I Human GO 9 Genes GS196054: GO:0006895 Golgi to endosome transport
Expand Tier II Mouse 685 Genes GS84316: alcohol preference locus (Published QTL, Chr 19)
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
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 Human 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
Expand Tier I Mouse MP 865 Genes GS167759: MP:0000787 abnormal telencephalon morphology
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse GO 165 Genes GS185499: GO:0007626 locomotory behavior
Expand Tier I Human GO 36 Genes GS198040: GO:0035176 social behavior
Expand Tier I Mouse 465 Genes GS136458: postnatal body weight growth 20 (Pbwg20, Published QTL Chr 19)
Expand Tier I Human 33 Genes GS174504: HP:0000709 Psychosis
Expand Tier I Human GO 142 Genes GS195505: GO:0016197 endosomal transport
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human 16 Genes GS174301: HP:0000719 Inappropriate behavior
Expand Tier I Mouse MP 661 Genes GS169421: MP:0002447 abnormal erythrocyte morphology
Expand Tier I Mouse MP 26 Genes GS169813: MP:0002641 anisopoikilocytosis
Expand Tier I Mouse MP 380 Genes GS163569: MP:0002557 abnormal social/conspecific interaction
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Mouse 400 Genes GS135869: fat induced diabetes 1 (Find1, Published QTL Chr 19)
Expand Tier II Mouse 446 Genes GS34054: Hippocampus Gene expression correlates of Open Field locomotion (cm) 45-60 min post cocaine in Males BXD
Expand Tier I Human GO 1825 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human 3 Genes GS175884: HP:0007374 Atrophy/Degeneration involving the caudate nucleus
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Mouse MP 156 Genes GS169677: MP:0006007 abnormal basal ganglion morphology
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Mouse MP 10 Genes GS169337: MP:0010177 acanthocytosis
Expand Tier I Human GO 1751 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse MP 1848 Genes GS167622: MP:0002152 abnormal brain morphology
Expand Tier I Human 21 Genes GS176207: HP:0003781 Excessive salivation
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human CTD 3171 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Human 83 Genes GS174968: HP:0003236 Elevated serum creatine phosphokinase
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 24 Genes GS174509: HP:0100716 Autoagression
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 II Mouse 452 Genes GS34332: Hippocampus Gene expression correlates of Cocaine TOTAL locomotion ( cm in 1 hr) in Males BXD
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse 511 Genes GS136187: lipoprotein QTL 2 (Lprq2, Published QTL Chr 19)
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human GO 507 Genes GS206091: GO:0007610 behavior
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Mouse MP 506 Genes GS168592: MP:0003634 abnormal glial cell morphology
Expand Tier I Human 111 Genes GS177023: HP:0010876 Abnormality of circulating protein level
Expand Tier II Mouse 134 Genes GS36805: Hippocampus Gene expression correlates of Zero Maze - total time in open quadrants in Males BXD
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Mouse MP 1013 Genes GS164724: MP:0001516 abnormal motor coordination/ balance
Expand Tier I Mouse GO 3211 Genes GS192509: GO:0006810 transport
Expand Tier II Mouse 81 Genes GS34306: Striatum Gene expression correlates of Cue Conditioning - Activity suppression after 3rd tone/shock pairing in Males BXD
Expand Tier I Human 31 Genes GS175341: HP:0100755 Abnormality of salivation
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier II Mouse 519 Genes GS84313: METH responses for body temperature (Published QTL, Chr 19)
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 940 Genes GS194065: GO:0016192 vesicle-mediated transport
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Mouse MP 283 Genes GS168473: MP:0002183 gliosis
Expand Tier I Mouse 510 Genes GS135495: brain volume 2 (Brnvl2, Published QTL Chr 19)
Expand Tier I Human 228 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 77 Genes GS171254: HP:0002360 Sleep disturbance
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human GO 1231 Genes GS199113: GO:0015031 protein transport
Expand Tier I Mouse MP 461 Genes GS169957: MP:0001402 hypoactivity
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 GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Mouse 645 Genes GS136687: skull morphology 26 (Skull26, Published QTL Chr 19)
Expand Tier I Mouse GO 379 Genes GS187166: GO:0044708 single-organism behavior
Expand Tier I Human GO 1929 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human GO 73 Genes GS196048: GO:0006892 post-Golgi vesicle-mediated transport
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Mouse 645 Genes GS136430: pulmonary adenoma susceptibility 3 (Pas3, Published QTL Chr 19)
Expand Tier I Human 27 Genes GS175840: HP:0000739 Anxiety
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human CTD 157 Genes GS125949: Clorgyline interacting genes (MeSH:D003010) in CTD
Expand Tier I Human GO 1697 Genes GS194905: GO:0008219 cell death
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Mouse MP 112 Genes GS169126: MP:0004077 abnormal striatum morphology
Expand Tier I Human 19 Genes GS174934: HP:0004447 Poikilocytosis
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 83 Genes GS175811: HP:0011021 Abnormality of circulating enzyme level
Expand Tier I Human 58 Genes GS172829: HP:0001824 Weight loss
Expand Tier I Human 200 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 38 Genes GS173459: HP:0001300 Parkinsonism
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 19 Genes GS171265: HP:0002633 Vasculitis
Expand Tier I Human 48 Genes GS172577: HP:0003690 Limb muscle weakness
Expand Tier I Mouse 440 Genes GS136111: long free running period 3 (Lfp3, Published QTL Chr 19)
Expand Tier I Mouse GO 1034 Genes GS182314: GO:0015031 protein transport
Expand Tier I Mouse GO 28 Genes GS181251: GO:0035176 social behavior
Expand Tier I Mouse GO 57 Genes GS186644: GO:0051705 multi-organism behavior
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 73 Genes GS175408: HP:0002071 Abnormality of extrapyramidal motor function
Expand Tier I Mouse GO 3268 Genes GS177721: GO:0051234 establishment of localization
Expand Tier II Mouse 507 Genes GS84312: METH responses for body temperature (Published QTL, Chr 19)
Expand Tier I Human 10 Genes GS176326: HP:0006554 Acute hepatic failure
Expand Tier I Mouse 465 Genes GS136282: modifier of engrailed QTL 2 (Moen2, Published QTL Chr 19)
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier I Human 3 Genes GS174667: HP:0002339 Abnormality of the caudate nucleus
Expand Tier I Human 11 Genes GS172496: HP:0000742 Self-mutilation
Expand Tier II Mouse 450 Genes GS34024: Hippocampus Gene expression correlates of Open Field locomotion 45-60 min post cocaine in Males BXD
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 71 Genes GS170917: HP:0100852 Abnormal fear/anxiety-related behavior
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 10 Genes GS173117: HP:0100660 Dyskinesia
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 103 Genes GS174372: HP:0002024 Malabsorption
Expand Tier III Mouse 80 Genes GS1069: ZM_ACTIVITY_Chr19_12.000000-17.000000
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 I Mouse 645 Genes GS135832: fluctuating asymmetry QTL 10 (Faq10, Published QTL Chr 19)
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Mouse 558 Genes GS136805: tibia bone quality traits 7 (Tbqt7, Published QTL Chr 19)
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 III Human 15 Genes GS26287: Positional candidates from genome-wide association study for nicotine dependence
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human GO 1559 Genes GS201869: GO:0008104 protein localization
Expand Tier I Human 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human 189 Genes GS172471: HP:0001744 Splenomegaly
Expand Tier I Human 125 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
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 1 Genes GS173730: HP:0007326 Progressive choreoathetosis
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier III Human 36 Genes GS26305: Nicotine dependence Candidate Genes combined from GWAS and SNP association methods
Expand Tier I Human 84 Genes GS174760: HP:0002376 Developmental regression
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Mouse GO 1380 Genes GS185054: GO:0008104 protein localization
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Mouse MP 814 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human 26 Genes GS176059: HP:0002134 Abnormality of the basal ganglia
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 1374 Genes GS203494: GO:0051704 multi-organism process
Expand Tier I Human 15 Genes GS171130: HP:0000751 Personality changes