Gene Details



GJB2 and homologs in 3 species are found in 528 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 Mouse MP 24 Genes GS163456: MP:0006390 abnormal cochlear endolymph
Expand Tier I Human 131 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier I Human GO 408 Genes GS199582: GO:0016044 cellular membrane organization
Expand Tier I Human 146 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
Expand Tier I Mouse 573 Genes GS136327: non-insulin-dependent diabetes mellitus 2 in NSY (Nidd2n, Published QTL Chr 14)
Expand Tier I Mouse 576 Genes GS135493: behavioral response to methamphetamines 9 (Brmth9, Published QTL Chr 14)
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse 561 Genes GS136598: resistance to thymic deletion 4 (Rthyd4, Published QTL Chr 14)
Expand Tier I Human 38 Genes GS175272: HP:0200020 Corneal erosions
Expand Tier I Mouse MP 599 Genes GS164506: MP:0001698 decreased embryo size
Expand Tier I Mouse MP 88 Genes GS167649: MP:0004201 fetal growth retardation
Expand Tier I Mouse MP 3631 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human 154 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Mouse MP 18 Genes GS166116: MP:0004411 decreased endocochlear potential
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human CTD 2424 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Human GO 412 Genes GS201052: GO:0061024 membrane organization
Expand Tier I Mouse 572 Genes GS136342: nicotine induced locomotor activity 8 (Nilac8, Published QTL Chr 14)
Expand Tier I Mouse 468 Genes GS136307: myocardial infarction 2 (Myci2, Published QTL Chr 14)
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 124 Genes GS210482: GO:0007605 sensory perception of sound
Expand Tier I Human GO 1099 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human 2 Genes GS172169: HP:0011859 Punctate keratitis
Expand Tier I Human 198 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 150 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 12 Genes GS176566: HP:0001019 Erythroderma
Expand Tier I Mouse MP 205 Genes GS165218: MP:0001240 abnormal epidermis stratum corneum morphology
Expand Tier I Mouse MP 254 Genes GS165859: MP:0000351 increased cell proliferation
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 149 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Mouse MP 54 Genes GS166643: MP:0010055 abnormal sensory neuron physiology
Expand Tier I Mouse MP 39 Genes GS164569: MP:0003879 abnormal hair cell physiology
Expand Tier I Human 53 Genes GS171286: HP:0002996 Limited elbow movement
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse MP 792 Genes GS170024: MP:0011086 partial postnatal lethality
Expand Tier I Mouse MP 173 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier I Mouse MP 49 Genes GS164674: MP:0000579 abnormal nail morphology
Expand Tier I Mouse MP 876 Genes GS165866: MP:0000350 abnormal cell proliferation
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Mouse 573 Genes GS136682: skull morphology 21 (Skull21, Published QTL Chr 14)
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Mouse MP 91 Genes GS165849: MP:0008803 abnormal placental labyrinth vasculature morphology
Expand Tier I Human GO 61 Genes GS201080: GO:0005793 endoplasmic reticulum-Golgi intermediate compartment
Expand Tier I Mouse MP 197 Genes GS167660: MP:0004200 decreased fetal size
Expand Tier I Human 41 Genes GS176789: HP:0100872 Abnormality of the plantar skin of foot
Expand Tier I Mouse MP 39 Genes GS168119: MP:0001196 shiny skin
Expand Tier I Human 47 Genes GS171564: HP:0000383 Abnormality of periauricular region
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse 3319 Genes GS127931: Olfactory bulb - Allen Mouse Brain Atlas
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 4 Genes GS174838: HP:0001096 Keratoconjunctivitis
Expand Tier I Human 7 Genes GS174748: HP:0008404 Nail dystrophy
Expand Tier I Human 202 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Mouse MP 207 Genes GS169118: MP:0004198 abnormal fetal size
Expand Tier I Human 28 Genes GS176707: HP:0007556 Plantar hyperkeratosis
Expand Tier I Human 157 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human GO 1914 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human 212 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier I Human 28 Genes GS172665: HP:0001025 Urticaria
Expand Tier I Mouse MP 96 Genes GS168115: MP:0001192 scaly skin
Expand Tier I Human 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier I Mouse 2963 Genes GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Human 9 Genes GS173080: HP:0000495 Recurrent corneal erosions
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
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 Human CTD 36 Genes GS123519: 1,3-dimethylthiourea interacting genes (MeSH:C038983) in CTD
Expand Tier I Human 68 Genes GS176572: HP:0008064 Ichthyosiform abnormality of the skin
Expand Tier I Mouse 572 Genes GS135363: B.burgdorferi-associated arthritis 21 (Bbaa21, Published QTL Chr 14)
Expand Tier I Mouse MP 268 Genes GS164346: MP:0006335 abnormal hearing electrophysiology
Expand Tier I Human 32 Genes GS175414: HP:0008619 Bilateral sensorineural hearing impairment
Expand Tier I Human CTD 729 Genes GS127012: Raloxifene interacting genes (MeSH:D020849) in CTD
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human DRG 53 Genes provisional GS87259: Table 2: Mean p-value and z-ratio scores for 65 selected transcripts (Whole Table) [DRG]
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 47 Genes GS200110: GO:0048806 genitalia development
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
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 11 Genes GS172426: HP:0001218 Autoamputation
Expand Tier I Mouse MP 75 Genes GS167468: MP:0002796 impaired skin barrier function
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 23 Genes GS173296: HP:0011830 Abnormality of oral mucosa
Expand Tier I Mouse MP 1104 Genes GS169389: MP:0002060 abnormal skin morphology
Expand Tier I Mouse MP 1460 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 183 Genes GS170137: MP:0001712 abnormal placenta development
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 GO 271 Genes GS202998: GO:0061458 reproductive system development
Expand Tier I Mouse 462 Genes GS136025: heart weight quantitative locus 1 (Hwq1, Published QTL Chr 14)
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse 3267 Genes GS127938: Striatum - Allen Mouse Brain Atlas
Expand Tier I Human 94 Genes GS174190: HP:0001596 Alopecia
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human GO 230 Genes GS209107: GO:0045137 development of primary sexual characteristics
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 III Mouse 1964 Genes GS865: Sey_Pax6_Age_Reduced_Linear_Incr
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse GO 133 Genes GS193043: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Mouse MP 352 Genes GS168152: MP:0005501 abnormal skin physiology
Expand Tier I Human 34 Genes GS172732: HP:0001751 Vestibular dysfunction
Expand Tier I Mouse MP 549 Genes GS166194: MP:0009931 abnormal skin appearance
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse MP 1302 Genes GS166719: MP:0010678 abnormal skin adnexa morphology
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 16 Genes GS173084: HP:0000491 Keratitis
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human 49 Genes GS174713: HP:0002213 Fine hair
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 1692 Genes GS169833: MP:0005380 embryogenesis phenotype
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Mouse MP 165 Genes GS169953: MP:0001242 hyperkeratosis
Expand Tier I Mouse MP 14 Genes GS168613: MP:0004465 degeneration of organ of Corti supporting cells
Expand Tier I Mouse 3096 Genes GS127928: Lateral septal complex - Allen Mouse Brain Atlas
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse MP 29 Genes GS165132: MP:0004885 abnormal endolymph
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Mouse 2918 Genes GS127935: Striatum dorsal region - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 290 Genes GS192254: GO:0005911 cell-cell junction
Expand Tier I Mouse MP 438 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier I Human 12 Genes GS175320: HP:0000561 Absent eyelashes
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
Expand Tier I Human 81 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier I Mouse MP 44 Genes GS167233: MP:0004300 abnormal organ of Corti supporting cell morphology
Expand Tier I Human 132 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Mouse MP 2199 Genes GS165244: MP:0010771 integument phenotype
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse MP 9 Genes GS168702: MP:0004287 abnormal spiral limbus morphology
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 Human GO 124 Genes GS201317: GO:0045216 cell-cell junction organization
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Mouse MP 68 Genes GS165873: MP:0004404 cochlear outer hair cell degeneration
Expand Tier I Mouse GO 119 Genes GS193537: GO:0007605 sensory perception of sound
Expand Tier I Mouse MP 396 Genes GS165214: MP:0001711 abnormal placenta morphology
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 50 Genes GS174380: HP:0010624 Aplastic/hypoplastic toenails
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 4 Genes GS163193: MP:0004482 abnormal interdental cell morphology
Expand Tier I Human GO 419 Genes GS195569: GO:0015267 channel activity
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 20 Genes GS205640: GO:0022829 wide pore channel activity
Expand Tier I Human 189 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human CTD 175 Genes GS121386: Zearalenone interacting genes (MeSH:D015025) in CTD
Expand Tier I Mouse MP 346 Genes GS167073: MP:0001926 female infertility
Expand Tier I Mouse MP 1307 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier I Mouse MP 692 Genes GS163620: MP:0002086 abnormal extraembryonic tissue morphology
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 71 Genes GS171136: HP:0100840 Aplasia/Hypoplasia of the eyebrow
Expand Tier I Human 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Human GO 119 Genes GS195315: GO:0046546 development of primary male sexual characteristics
Expand Tier I Mouse MP 1692 Genes GS169603: MP:0001672 abnormal embryogenesis/ development
Expand Tier I Human 15 Genes GS174120: HP:0002860 Squamous cell carcinoma
Expand Tier I Mouse MP 418 Genes GS164482: MP:0001216 abnormal epidermal layer morphology
Expand Tier I Mouse MP 267 Genes GS169111: MP:0004197 abnormal fetal growth/weight/body size
Expand Tier I Mouse MP 181 Genes GS163498: MP:0003308 abnormal cochlear sensory epithelium morphology
Expand Tier I Human 81 Genes GS173031: HP:0004362 Abnormality of the enteric ganglia
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human GO 31 Genes GS196135: GO:0005921 gap junction
Expand Tier I Mouse MP 639 Genes GS164032: MP:0004811 abnormal neuron physiology
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 400 Genes GS164570: MP:0003878 abnormal ear physiology
Expand Tier I Human 90 Genes GS173087: HP:0000499 Abnormality of the eyelashes
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 Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 271 Genes GS196165: GO:0048608 reproductive structure development
Expand Tier I Human 41 Genes GS172655: HP:0001792 Small nail
Expand Tier I Mouse GO 1440 Genes GS181988: GO:0044459 plasma membrane part
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 1597 Genes GS207991: GO:0000003 reproduction
Expand Tier I Mouse 557 Genes GS135791: epilepsy 5 (El5, Published QTL Chr 14)
Expand Tier I Human 30 Genes GS174237: HP:0000535 Sparse eyebrow
Expand Tier I Human CTD 3171 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Mouse MP 69 Genes GS166271: MP:0009582 abnormal keratinocyte proliferation
Expand Tier I Mouse MP 544 Genes GS166405: MP:0002111 abnormal tail morphology
Expand Tier I Mouse GO 32 Genes GS179368: GO:0005921 gap junction
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Human CTD 185 Genes GS125836: coumarin interacting genes (MeSH:C030123) in CTD
Expand Tier I Mouse 3289 Genes GS127924: Cerebral cortex - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 114 Genes GS168370: MP:0003453 abnormal keratinocyte physiology
Expand Tier I Mouse 3384 Genes GS127925: Hippocampal formation - Allen Mouse Brain Atlas
Expand Tier I Human 16 Genes GS175398: HP:0002298 Absent hair
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 Human GO 1592 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Human GO 419 Genes GS202908: GO:0022803 passive transmembrane transporter activity
Expand Tier I Human 77 Genes GS175692: HP:0200042 Skin ulcer
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 288 Genes GS209188: GO:0005911 cell-cell junction
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human 67 Genes GS173029: HP:0000684 Delayed eruption of teeth
Expand Tier I Human 38 Genes GS173880: HP:0005750 Contractures of the joints of the lower limbs
Expand Tier I Human 111 Genes GS175068: HP:0000971 Abnormality of the sweat gland
Expand Tier I Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Mouse 583 Genes GS136712: susceptibility to lung cancer 13 (Sluc13, Published QTL Chr 14)
Expand Tier I Mouse MP 585 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Mouse MP 211 Genes GS165114: MP:0004426 abnormal cochlear labyrinth morphology
Expand Tier I Mouse MP 50 Genes GS166270: MP:0009583 increased keratinocyte proliferation
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 22 Genes GS172271: HP:0001194 Abnormalities of placenta and umbilical cord
Expand Tier I Human GO 1126 Genes GS195108: GO:0071844 cellular component assembly at cellular level
Expand Tier I Human GO 925 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human GO 424 Genes GS209955: GO:0003006 developmental process involved in reproduction
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Mouse 2944 Genes GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
Expand Tier I Human 57 Genes GS174337: HP:0002718 Recurrent bacterial infections
Expand Tier I Mouse MP 87 Genes GS165544: MP:0004362 cochlear hair cell degeneration
Expand Tier I Human GO 195 Genes GS208290: GO:0034330 cell junction organization
Expand Tier I Mouse GO 20 Genes GS179366: GO:0005922 connexon complex
Expand Tier I Human GO 32 Genes GS210288: GO:0016328 lateral plasma membrane
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Mouse 2962 Genes GS127936: Striatum ventral region - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 206 Genes GS165391: MP:0000972 abnormal mechanoreceptor morphology
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 1685 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Human 8 Genes GS171046: HP:0011409 Abnormality of placental membranes
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse MP 3924 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 144 Genes GS175128: HP:0011123 Inflammatory abnormality of the skin
Expand Tier I Human 29 Genes GS171563: HP:0000384 Preauricular skin tag
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Mouse MP 750 Genes GS170442: MP:0010866 abnormal prenatal body size
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Mouse MP 175 Genes GS170151: MP:0001716 abnormal placenta labyrinth morphology
Expand Tier I Human CTD 130 Genes GS122250: Hexachlorobenzene interacting genes (MeSH:D006581) in CTD
Expand Tier I Mouse MP 1688 Genes GS168174: MP:0001919 abnormal reproductive system physiology
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Mouse MP 249 Genes GS163316: MP:0000035 abnormal membranous labyrinth morphology
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Mouse MP 463 Genes GS168567: MP:0011091 complete prenatal lethality
Expand Tier I Mouse GO 731 Genes GS179748: GO:0030054 cell junction
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 198 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human 177 Genes GS175431: HP:0011122 Abnormality of skin physiology
Expand Tier I Human CTD 1291 Genes GS125402: Diethylnitrosamine interacting genes (MeSH:D004052) in CTD
Expand Tier I Mouse MP 4772 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Mouse 484 Genes GS136088: lean body mass 10 (Lbm10, Published QTL Chr 14)
Expand Tier I Mouse MP 209 Genes GS167140: MP:0003169 abnormal scala media morphology
Expand Tier I Human CTD 1398 Genes GS124312: sodium arsenite interacting genes (MeSH:C017947) in CTD
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 86 Genes GS175086: HP:0008388 Abnormality of the toenails
Expand Tier I Human 120 Genes GS171657: HP:0000613 Photophobia
Expand Tier I Mouse MP 3815 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Mouse MP 568 Genes GS166535: MP:0010865 prenatal growth retardation
Expand Tier I Human GO 170 Genes GS203936: GO:0034329 cell junction assembly
Expand Tier I Human CTD 746 Genes GS125403: Diethylstilbestrol interacting genes (MeSH:D004054) in CTD
Expand Tier II Mouse 511 Genes GS84277: METH responses for home cage activity (Published QTL, Chr 14)
Expand Tier I Human CTD 36 Genes GS124531: limonene interacting genes (MeSH:C008281) in CTD
Expand Tier I Mouse 3315 Genes GS127939: Thalamus - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Human CTD 766 Genes GS124457: Mustard Gas interacting genes (MeSH:D009151) in CTD
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 127 Genes GS206630: GO:0046661 male sex differentiation
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 34 Genes GS173962: HP:0001581 Recurrent skin infections
Expand Tier I Mouse MP 413 Genes GS164004: MP:0011101 partial prenatal lethality
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
Expand Tier I Mouse MP 1628 Genes GS167505: MP:0008762 embryonic lethality
Expand Tier I Mouse MP 2644 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 22 Genes GS174536: HP:0000972 Palmoplantar hyperkeratosis
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Human GO 67 Genes GS201945: GO:0007043 cell-cell junction assembly
Expand Tier I Human CTD 1760 Genes GS123048: Tretinoin interacting genes (MeSH:D014212) in CTD
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 3343 Genes GS127930: Midbrain - Allen Mouse Brain Atlas
Expand Tier I Mouse 3329 Genes GS127933: Pons - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 2263 Genes GS164262: MP:0002080 prenatal lethality
Expand Tier I Mouse MP 7 Genes GS167000: MP:0004562 abnormal inner hair cell synaptic ribbon morphology
Expand Tier I Mouse MP 68 Genes GS168762: MP:0005423 abnormal somatic nervous system physiology
Expand Tier I Mouse MP 610 Genes GS164511: MP:0001697 abnormal embryo size
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Mouse MP 141 Genes GS169966: MP:0001219 thick epidermis
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse 576 Genes GS136852: Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 3 (Tmevd3, Published QTL Chr 14)
Expand Tier I Mouse MP 281 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Mouse MP 762 Genes GS166154: MP:0011098 complete embryonic lethality during organogenesis
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human CTD 37 Genes GS122337: Iron, Dietary interacting genes (MeSH:D019266) in CTD
Expand Tier I Mouse 573 Genes GS135405: body growth late QTL 15 (Bglq15, Published QTL Chr 14)
Expand Tier I Human 8 Genes GS175235: HP:0009775 Amniotic constriction ring
Expand Tier I Human 125 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 138 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier I Human 20 Genes GS173940: HP:0007431 Congenital ichthyosiform erythroderma
Expand Tier I Mouse 3109 Genes GS127923: Cerebellum - Allen Mouse Brain Atlas
Expand Tier I Human CTD 18 Genes GS121651: Sodium Dodecyl Sulfate interacting genes (MeSH:D012967) in CTD
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 12 Genes GS174659: HP:0001426 Multifactorial inheritance
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Mouse MP 24 Genes GS167781: MP:0002630 abnormal endocochlear potential
Expand Tier II Mouse 500 Genes GS84278: chronic alcohol withdrawal severity (Published QTL, Chr 14)
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human CTD 1201 Genes GS123595: Progesterone interacting genes (MeSH:D011374) in CTD
Expand Tier I Human 88 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Mouse MP 230 Genes GS163320: MP:0000031 abnormal cochlea morphology
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 Human 34 Genes GS172053: HP:0000966 Hypohidrosis
Expand Tier I Mouse 569 Genes GS136040: insulin dependent diabetes susceptibility 12 (Idd12, Published QTL Chr 14)
Expand Tier I Mouse MP 190 Genes GS169758: MP:0004765 decreased brainstem auditory evoked potential
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 137 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Mouse MP 870 Genes GS168593: MP:0002088 abnormal embryonic growth/weight/body size
Expand Tier I Human 165 Genes GS171654: HP:0003121 Limb joint contracture
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human GO 21 Genes GS196133: GO:0005922 connexon complex
Expand Tier I Mouse 572 Genes GS136293: modifier of obesity related sterility 3 (Mors3, Published QTL Chr 14)
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse 498 Genes GS129081: atherosclerosis 13 (Ath13 Published QTL Chr 14)
Expand Tier I Mouse MP 10 Genes GS164678: MP:0004265 abnormal placental transport
Expand Tier I Human 104 Genes GS175835: HP:0007759 Opacification of the corneal stroma
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Mouse MP 749 Genes GS167833: MP:0001784 abnormal fluid regulation
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Mouse MP 1038 Genes GS169114: MP:0004196 abnormal prenatal growth/weight/body size
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 28 Genes GS173589: HP:0008513 Bilateral conductive hearing impairment
Expand Tier I Human 27 Genes GS172114: HP:0002987 Elbow flexion contracture
Expand Tier I Mouse MP 180 Genes GS163068: MP:0000045 abnormal hair cell morphology
Expand Tier I Mouse 503 Genes GS136456: postnatal body weight growth 18 (Pbwg18, Published QTL Chr 14)
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Mouse GO 33 Genes GS193346: GO:0016328 lateral plasma membrane
Expand Tier I Human GO 1165 Genes GS206696: GO:0044702 single organism reproductive process
Expand Tier I Mouse 379 Genes GS135853: femoral bone morphometry 2 (Fembm2, Published QTL Chr 14)
Expand Tier I Human 49 Genes GS173990: HP:0000502 Abnormality of the conjunctiva
Expand Tier I Mouse MP 184 Genes GS164059: MP:0006325 impaired hearing
Expand Tier II Mouse 426 Genes GS84279: METH responses for climbing (Published QTL, Chr 14)
Expand Tier I Human GO 7 Genes GS203756: GO:0016264 gap junction assembly
Expand Tier I Mouse 3136 Genes GS127926: Hippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human CTD 395 Genes GS125893: Tetradecanoylphorbol Acetate interacting genes (MeSH:D013755) in CTD
Expand Tier I Human 3 Genes GS175720: HP:0001097 Keratoconjunctivitis sicca
Expand Tier I Mouse 3289 Genes GS127932: Pallidum - Allen Mouse Brain Atlas
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 Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 26 Genes GS172624: HP:0000653 Sparse eyelashes
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 177 Genes GS173540: HP:0002115 Sparse or absent hair
Expand Tier I Human CTD 148 Genes GS127114: Methylnitronitrosoguanidine interacting genes (MeSH:D008769) in CTD
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 CTD 14 Genes GS124619: Heptachlor Epoxide interacting genes (MeSH:D006534) in CTD
Expand Tier I Mouse 583 Genes GS135777: epistatic circling SWR/J (ecs, Published QTL Chr 14)
Expand Tier I Human 80 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 23 Genes GS173301: HP:0001800 Hypoplastic toenails
Expand Tier III Mouse 167 Genes GS35878: Hippocampus Gene expression correlates of Number of entries into closed arms of plus maze [Ethanol] in Females BXD
Expand Tier I Human 5 Genes GS171357: HP:0010984 Digenic inheritance
Expand Tier I Human 36 Genes GS176036: HP:0002797 Osteolysis
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 32 Genes GS172593: HP:0010609 Skin tags
Expand Tier I Human 79 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Mouse MP 176 Genes GS168687: MP:0000592 short tail
Expand Tier I Mouse 461 Genes GS129121: cocaine seizure 2 (Cosz2 Published QTL Chr 14)
Expand Tier II Mouse 718 Genes GS84276: nicotine sensitivity (Published QTL, Chr 14)
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse 3395 Genes GS127929: Medulla - Allen Mouse Brain Atlas
Expand Tier I Human 123 Genes GS176695: HP:0009811 Abnormality of the elbow
Expand Tier III Rat 3441 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Human 3 Genes GS172827: HP:0001820 Leukonychia
Expand Tier I Mouse MP 495 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Human CTD 73 Genes GS122944: Dimethyl Sulfoxide interacting genes (MeSH:D004121) in CTD
Expand Tier I Human CTD 999 Genes GS124711: Genistein interacting genes (MeSH:D019833) in CTD
Expand Tier III Rat 3441 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Mouse MP 1485 Genes GS166712: MP:0002161 abnormal fertility/fecundity
Expand Tier I Human GO 24 Genes GS195491: GO:0030539 male genitalia development
Expand Tier I Human CTD 137 Genes GS124810: Urethane interacting genes (MeSH:D014520) in CTD
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier II Mouse 515 Genes GS83995: cocaine seizure 2 (Cosz2, Published QTL, Chr 14)
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human CTD 150 Genes GS121939: Dieldrin interacting genes (MeSH:D004026) in CTD
Expand Tier I Human 51 Genes GS174243: HP:0011495 Abnormality of corneal epithelium
Expand Tier I Mouse MP 51 Genes GS164273: MP:0000043 organ of Corti degeneration
Expand Tier I Human 10 Genes GS171595: HP:0005406 Recurrent bacterial skin infections
Expand Tier I Human 19 Genes GS172735: HP:0006380 Knee flexion contracture
Expand Tier I Human 96 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human CTD 1601 Genes GS123916: Aflatoxin B1 interacting genes (MeSH:D016604) in CTD
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 9 Genes GS173616: HP:0002745 Oral leukoplakia
Expand Tier I Human GO 1544 Genes GS195733: GO:0022607 cellular component assembly
Expand Tier I Mouse MP 743 Genes GS168294: MP:0003699 abnormal female reproductive system physiology
Expand Tier I Human 23 Genes GS170988: HP:0010765 Palmar hyperkeratosis
Expand Tier I Mouse MP 2099 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Human GO 735 Genes GS196511: GO:0030054 cell junction
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human CTD 239 Genes GS122047: Ethylnitrosourea interacting genes (MeSH:D005038) in CTD
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Mouse 459 Genes GS136280: modifier of ocular retardation 3 (Modor3, Published QTL Chr 14)
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 134 Genes GS167388: MP:0003231 abnormal placenta vasculature
Expand Tier I Mouse MP 2485 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Human 114 Genes GS176227: HP:0010719 Abnormality of hair texture
Expand Tier I Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Mouse MP 903 Genes GS167075: MP:0001924 infertility
Expand Tier I Human GO 132 Genes GS209984: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Mouse 569 Genes GS136627: Stem cell proliferation 9 (Scpro9, Published QTL Chr 14)
Expand Tier I Mouse MP 34 Genes GS164679: MP:0004264 abnormal extraembryonic tissue physiology
Expand Tier I Human GO 260 Genes GS195560: GO:0007548 sex differentiation
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse 573 Genes GS135518: body weight 1 (Bwt1, Published QTL Chr 14)
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human 30 Genes GS173994: HP:0000509 Conjunctivitis
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Human 115 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Mouse MP 498 Genes GS162897: MP:0003984 embryonic growth retardation
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 1 Genes GS177011: HP:0001128 Trichiasis
Expand Tier I Human 9 Genes GS176218: HP:0100643 Abnormality of nail color
Expand Tier I Human 107 Genes GS176569: HP:0008069 Neoplasm of the skin
Expand Tier I Human 80 Genes GS172887: HP:0100533 Inflammatory abnormality of the eye
Expand Tier I Human 7 Genes GS174272: HP:0007460 Autoamputation of digits
Expand Tier I Human 84 Genes GS175244: HP:0006292 Abnormality of dental eruption
Expand Tier I Mouse 809 Genes GS129166: plasma plant sterol 1 (Plast1 Published QTL Chr 14)
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse MP 953 Genes GS165160: MP:0006207 embryonic lethality during organogenesis
Expand Tier I Mouse MP 24 Genes GS168400: MP:0010038 abnormal placenta physiology
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand