Gene Details



GJB2 and homologs in 1 species are found in 322 GeneSets:


- Entrez   - GeneNetwork   - 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 Human 10 Genes GS171595: HP:0005406 Recurrent bacterial skin infections
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 131 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier I Human 19 Genes GS172735: HP:0006380 Knee flexion contracture
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human GO 408 Genes GS199582: GO:0016044 cellular membrane organization
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 146 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
Expand Tier I Human 34 Genes GS172732: HP:0001751 Vestibular dysfunction
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
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 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 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
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 49 Genes GS174713: HP:0002213 Fine hair
Expand Tier I Human GO 1544 Genes GS195733: GO:0022607 cellular component assembly
Expand Tier I Human 38 Genes GS175272: HP:0200020 Corneal erosions
Expand Tier I Human 23 Genes GS170988: HP:0010765 Palmar hyperkeratosis
Expand Tier I Human GO 735 Genes GS196511: GO:0030054 cell junction
Expand Tier I Human CTD 37 Genes GS122337: Iron, Dietary interacting genes (MeSH:D019266) in CTD
Expand Tier I Human 8 Genes GS175235: HP:0009775 Amniotic constriction ring
Expand Tier I Human CTD 239 Genes GS122047: Ethylnitrosourea interacting genes (MeSH:D005038) in CTD
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 125 Genes GS173384: HP:0002750 Delayed skeletal maturation
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 Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
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 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
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 114 Genes GS176227: HP:0010719 Abnormality of hair texture
Expand Tier I Human GO 412 Genes GS201052: GO:0061024 membrane organization
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 138 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier I Human GO 132 Genes GS209984: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Human 20 Genes GS173940: HP:0007431 Congenital ichthyosiform erythroderma
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 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 81 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier I Human GO 124 Genes GS210482: GO:0007605 sensory perception of sound
Expand Tier I Human CTD 18 Genes GS121651: Sodium Dodecyl Sulfate interacting genes (MeSH:D012967) in CTD
Expand Tier I Human GO 1099 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
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 132 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human GO 260 Genes GS195560: GO:0007548 sex differentiation
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 150 Genes GS175411: HP:0100871 Abnormality of the palm
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 Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Human 12 Genes GS176566: HP:0001019 Erythroderma
Expand Tier I Human 30 Genes GS173994: HP:0000509 Conjunctivitis
Expand Tier I Human CTD 1201 Genes GS123595: Progesterone interacting genes (MeSH:D011374) in CTD
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
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 88 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Human 115 Genes GS172500: HP:0007400 Irregular hyperpigmentation
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 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 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 149 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human 34 Genes GS172053: HP:0000966 Hypohidrosis
Expand Tier I Human 107 Genes GS176569: HP:0008069 Neoplasm of the skin
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 Human 80 Genes GS172887: HP:0100533 Inflammatory abnormality of the eye
Expand Tier I Human 53 Genes GS171286: HP:0002996 Limited elbow movement
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 7 Genes GS174272: HP:0007460 Autoamputation of digits
Expand Tier I Human 137 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier I Human 84 Genes GS175244: HP:0006292 Abnormality of dental eruption
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
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 50 Genes GS174380: HP:0010624 Aplastic/hypoplastic toenails
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 419 Genes GS195569: GO:0015267 channel activity
Expand Tier I Human GO 21 Genes GS196133: GO:0005922 connexon complex
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 Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human CTD 999 Genes GS124711: Genistein interacting genes (MeSH:D019833) in CTD
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Human GO 271 Genes GS202998: GO:0061458 reproductive system development
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
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 Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 170 Genes GS203936: GO:0034329 cell junction assembly
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 237 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human 104 Genes GS175835: HP:0007759 Opacification of the corneal stroma
Expand Tier I Human CTD 746 Genes GS125403: Diethylstilbestrol interacting genes (MeSH:D004054) in CTD
Expand Tier I Human GO 61 Genes GS201080: GO:0005793 endoplasmic reticulum-Golgi intermediate compartment
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 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human CTD 36 Genes GS124531: limonene interacting genes (MeSH:C008281) in CTD
Expand Tier I Human 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human GO 13 Genes GS201112: GO:0005243 gap junction channel activity
Expand Tier I Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human GO 119 Genes GS195315: GO:0046546 development of primary male sexual characteristics
Expand Tier I Human 15 Genes GS174120: HP:0002860 Squamous cell carcinoma
Expand Tier I Human 94 Genes GS174190: HP:0001596 Alopecia
Expand Tier I Human 81 Genes GS173031: HP:0004362 Abnormality of the enteric ganglia
Expand Tier I Human CTD 766 Genes GS124457: Mustard Gas interacting genes (MeSH:D009151) in CTD
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
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 Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
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 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 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 Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
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 Human GO 67 Genes GS201945: GO:0007043 cell-cell junction assembly
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
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 41 Genes GS176789: HP:0100872 Abnormality of the plantar skin of foot
Expand Tier I Human GO 31 Genes GS196135: GO:0005921 gap junction
Expand Tier I Human CTD 1760 Genes GS123048: Tretinoin interacting genes (MeSH:D014212) in CTD
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 250 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 28 Genes GS173589: HP:0008513 Bilateral conductive hearing impairment
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 27 Genes GS172114: HP:0002987 Elbow flexion contracture
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human CTD 150 Genes GS121939: Dieldrin interacting genes (MeSH:D004026) in CTD
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 Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 90 Genes GS173087: HP:0000499 Abnormality of the eyelashes
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 1165 Genes GS206696: GO:0044702 single organism reproductive process
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 51 Genes GS174243: HP:0011495 Abnormality of corneal epithelium
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 49 Genes GS173990: HP:0000502 Abnormality of the conjunctiva
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
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 20 Genes GS172391: HP:0000221 Furrowed tongue
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
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 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 41 Genes GS172655: HP:0001792 Small nail
Expand Tier I Human 202 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human GO 7 Genes GS203756: GO:0016264 gap junction assembly
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 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 1914 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 212 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier I Human GO 1597 Genes GS207991: GO:0000003 reproduction
Expand Tier I Human 30 Genes GS174237: HP:0000535 Sparse eyebrow
Expand Tier I Human CTD 395 Genes GS125893: Tetradecanoylphorbol Acetate interacting genes (MeSH:D013755) in CTD
Expand Tier I Human CTD 3171 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Human 28 Genes GS172665: HP:0001025 Urticaria
Expand Tier I Human 3 Genes GS175720: HP:0001097 Keratoconjunctivitis sicca
Expand Tier I Human CTD 185 Genes GS125836: coumarin interacting genes (MeSH:C030123) in CTD
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
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 GO 9128 Genes GS194133: GO:0005737 cytoplasm
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 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier I Human 77 Genes GS175692: HP:0200042 Skin ulcer
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 26 Genes GS172624: HP:0000653 Sparse eyelashes
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
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 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 177 Genes GS173540: HP:0002115 Sparse or absent hair
Expand Tier I Human 9 Genes GS173080: HP:0000495 Recurrent corneal erosions
Expand Tier I Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human CTD 148 Genes GS127114: Methylnitronitrosoguanidine interacting genes (MeSH:D008769) in CTD
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
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 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
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 CTD 36 Genes GS123519: 1,3-dimethylthiourea interacting genes (MeSH:C038983) in CTD
Expand Tier I Human CTD 14 Genes GS124619: Heptachlor Epoxide interacting genes (MeSH:D006534) in CTD
Expand Tier I Human 68 Genes GS176572: HP:0008064 Ichthyosiform abnormality of the skin
Expand Tier I Human GO 424 Genes GS209955: GO:0003006 developmental process involved in reproduction
Expand Tier I Human 80 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier I Human 32 Genes GS175414: HP:0008619 Bilateral sensorineural hearing impairment
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 Human CTD 729 Genes GS127012: Raloxifene interacting genes (MeSH:D020849) in CTD
Expand Tier I Human 57 Genes GS174337: HP:0002718 Recurrent bacterial infections
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 195 Genes GS208290: GO:0034330 cell junction organization
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 23 Genes GS173301: HP:0001800 Hypoplastic toenails
Expand Tier I Human 5 Genes GS171357: HP:0010984 Digenic inheritance
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 36 Genes GS176036: HP:0002797 Osteolysis
Expand Tier I Human GO 47 Genes GS200110: GO:0048806 genitalia development
Expand Tier I Human GO 32 Genes GS210288: GO:0016328 lateral plasma membrane
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
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 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 1685 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 32 Genes GS172593: HP:0010609 Skin tags
Expand Tier I Human 11 Genes GS172426: HP:0001218 Autoamputation
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 GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
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 Human 79 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
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 Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human CTD 130 Genes GS122250: Hexachlorobenzene interacting genes (MeSH:D006581) in CTD
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 123 Genes GS176695: HP:0009811 Abnormality of the elbow
Expand Tier I Human 3 Genes GS172827: HP:0001820 Leukonychia
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 Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human CTD 73 Genes GS122944: Dimethyl Sulfoxide interacting genes (MeSH:D004121) in CTD
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