Gene Details



ABCC9 and homologs in 1 species are found in 352 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 Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Human 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 203 Genes GS198194: GO:0034702 ion channel complex
Expand Tier I Human GO 108 Genes GS209137: GO:0015399 primary active transmembrane transporter activity
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier I Human GO 1496 Genes GS201792: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Human 1 Genes GS172552: HP:0004634 Cuboid-shaped vertebral bodies
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 497 Genes GS196432: GO:0030001 metal ion transport
Expand Tier I Human GO 1821 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier I Human 13 Genes GS172154: HP:0002679 Abnormality of the sella turcica
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 12 Genes GS173691: HP:0001647 Bicuspid aortic valve
Expand Tier I Human CTD 4424 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 274 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human 44 Genes GS174915: HP:0003016 Metaphyseal widening
Expand Tier I Human 95 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Tier I Human 26 Genes GS173686: HP:0001640 Cardiomegaly
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 4 Genes GS174459: HP:0010174 Broad phalanx of the toes
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 354 Genes GS208384: GO:0016887 ATPase activity
Expand Tier I Human CTD 420 Genes GS121514: Paraquat interacting genes (MeSH:D010269) in CTD
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 76 Genes GS172300: HP:0001991 Aplasia/Hypoplasia of the toes
Expand Tier I Human 100 Genes GS175101: HP:0000280 Coarse facial features
Expand Tier I Human 5 Genes GS177024: HP:0000215 Thick upper lip vermilion
Expand Tier I Human GO 576 Genes GS203491: GO:0051707 response to other organism
Expand Tier I Human 141 Genes GS174721: HP:0000772 Abnormality of the ribs
Expand Tier I Human GO 70 Genes GS198193: GO:0034705 potassium channel complex
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Human 49 Genes GS174071: HP:0009125 Lipodystrophy
Expand Tier I Human 13 Genes GS175505: HP:0010057 Abnormality of the phalanges of the hallux
Expand Tier I Human 174 Genes GS172015: HP:0000969 Edema
Expand Tier I Human 201 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier I Human GO 70 Genes GS204008: GO:0008076 voltage-gated potassium channel complex
Expand Tier I Human 60 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 2921 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 122 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 2 Genes GS173630: HP:0002690 Large sella turcica
Expand Tier I Human GO 1832 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human GO 25 Genes GS194489: GO:0071805 potassium ion transmembrane transport
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 176 Genes GS175103: HP:0000288 Abnormality of the philtrum
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Human 112 Genes GS172569: HP:0000343 Long philtrum
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 5 Genes GS175506: HP:0010054 Abnormality of the first metatarsal
Expand Tier I Human 158 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human GO 29 Genes GS204171: GO:0015459 potassium channel regulator activity
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Human 20 Genes GS175507: HP:0010055 Broad hallux
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human GO 1098 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human GO 74 Genes GS195655: GO:0016247 channel regulator activity
Expand Tier I Human 107 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 282 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 51 Genes GS175893: HP:0000932 Abnormality of the posterior cranial fossa
Expand Tier I Human 45 Genes GS176166: HP:0001256 Intellectual disability, mild
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 1822 Genes GS197443: GO:0032549 ribonucleoside binding
Expand Tier I Human GO 118 Genes GS209449: GO:0006813 potassium ion transport
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 1 Genes GS175249: HP:0008822 Hypoplastic ischiopubic rami
Expand Tier I Human GO 128 Genes GS208922: GO:0030017 sarcomere
Expand Tier I Human 119 Genes GS172170: HP:0003196 Short nose
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 110 Genes GS176907: HP:0009804 Reduced number of teeth
Expand Tier I Human 118 Genes GS170783: HP:0010974 Abnormality of myeloid leukocytes
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 461 Genes GS201730: GO:0002252 immune effector process
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human 148 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human GO 606 Genes GS208107: GO:0009607 response to biotic stimulus
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human CTD 2014 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human GO 1500 Genes GS203649: GO:0030554 adenyl nucleotide binding
Expand Tier I Human 2 Genes GS176154: HP:0010068 Broad first metatarsal
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 60 Genes GS171207: HP:0000098 Tall stature
Expand Tier I Human 3 Genes GS173234: HP:0004975 Erlenmeyer flask deformity of the femurs
Expand Tier I Human 74 Genes GS174070: HP:0009124 Abnormality of adipose tissue
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human GO 273 Genes GS196857: GO:0034220 ion transmembrane transport
Expand Tier I Human GO 761 Genes GS209613: GO:0055085 transmembrane transport
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 786 Genes GS210137: GO:0016462 pyrophosphatase activity
Expand Tier I Human GO 100 Genes GS210132: GO:0043492 ATPase activity, coupled to movement of substances
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 278 Genes GS195770: GO:0015672 monovalent inorganic cation transport
Expand Tier I Human 32 Genes GS171753: HP:0001712 Left ventricular hypertrophy
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 20 Genes GS172151: HP:0002673 Coxa valga
Expand Tier I Human 1 Genes GS174549: HP:0005129 Congenital hypertrophy of left ventricle
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 238 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 102 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Human 54 Genes GS176099: HP:0000926 Platyspondyly
Expand Tier I Human 112 Genes GS176840: HP:0001911 Abnormality of granulocytes
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human 307 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Human GO 311 Genes GS209586: GO:0022804 active transmembrane transporter activity
Expand Tier I Human 7 Genes GS172547: HP:0001520 Large for gestational age
Expand Tier I Human 178 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human CTD 453 Genes GS125669: Phenylephrine interacting genes (MeSH:D010656) in CTD
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 182 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 7 Genes GS172525: HP:0001698 Pericardial effusion
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human CTD 1001 Genes GS124711: Genistein interacting genes (MeSH:D019833) in CTD
Expand Tier I Human 28 Genes GS171409: HP:0011306 Aplasia of the toes
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 108 Genes GS200456: GO:0015405 P-P-bond-hydrolysis-driven transmembrane transporter activity
Expand Tier I Human GO 278 Genes GS207263: GO:0042623 ATPase activity, coupled
Expand Tier I Human GO 3310 Genes GS209452: GO:0006810 transport
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human GO 736 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier I Human 47 Genes GS174089: HP:0003367 Abnormality of the femoral neck
Expand Tier I Human 200 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 17 Genes GS173343: HP:0001548 Overgrowth
Expand Tier I Human 222 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human GO 2 Genes GS209491: GO:0008281 sulfonylurea receptor activity
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 25 Genes GS194488: GO:0071804 cellular potassium ion transport
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 2410 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human 13 Genes GS176189: HP:0009103 Aplasia/Hypoplasia involving the pelvis
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 200 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 38 Genes GS171754: HP:0001711 Abnormality of the left ventricle
Expand Tier I Human 24 Genes GS172590: HP:0001837 Broad toe
Expand Tier I Human 148 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier I Human 41 Genes GS175113: HP:0000574 Thick eyebrow
Expand Tier I Human 194 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human GO 1362 Genes GS203494: GO:0051704 multi-organism process
Expand Tier III Human 2161 Genes GS216491: Genes that are binding sites for CREB and zif268,transcription factors mediating nieuronal activity and plasticity, in Homo sapiens.
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 62 Genes GS173367: HP:0005257 Thoracic hypoplasia
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 49 Genes GS174245: HP:0001844 Abnormality of the hallux
Expand Tier I Human 198 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human GO 3364 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human 93 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier I Human GO 1466 Genes GS205179: GO:0005524 ATP binding
Expand Tier I Human 19 Genes GS172514: HP:0001697 Abnormality of the pericardium
Expand Tier I Human 41 Genes GS171758: HP:0001714 Ventricular hypertrophy
Expand Tier I Human 8 Genes GS171020: HP:0003174 Abnormality of the ischium
Expand Tier I Human GO 1619 Genes GS204106: GO:0060089 molecular transducer activity
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human GO 1619 Genes GS202760: GO:0004871 signal transducer activity
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 8 Genes GS176246: HP:0001783 Broad metatarsal
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human 5 Genes GS171235: HP:0010184 Abnormality of the proximal phalanges of the toes
Expand Tier I Human 9 Genes GS173361: HP:0004540 Congenital, generalized hypertrichosis
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 8 Genes GS176251: HP:0009104 Aplasia/Hypoplasia of the pubic bone
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human CTD 117 Genes GS124346: dicyclanil interacting genes (MeSH:C121718) in CTD
Expand Tier I Human 218 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human GO 1818 Genes GS201799: GO:0032550 purine ribonucleoside binding
Expand Tier I Human GO 1859 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier I Human GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 88 Genes GS173087: HP:0000499 Abnormality of the eyelashes
Expand Tier I Human 4 Genes GS175509: HP:0010059 Broad phalanges of the hallux
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human CTD 629 Genes GS122305: resveratrol interacting genes (MeSH:C059514) in CTD
Expand Tier I Human 286 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 33 Genes GS176924: HP:0000212 Gingival overgrowth
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Human 56 Genes GS176885: HP:0002693 Abnormality of the skull base
Expand Tier I Human GO 1809 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human GO 182 Genes GS209993: GO:0051607 defense response to virus
Expand Tier I Human GO 1521 Genes GS202759: GO:0004872 receptor activity
Expand Tier I Human 208 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human GO 789 Genes GS202822: GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 173 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 278 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 754 Genes GS195665: GO:0017111 nucleoside-triphosphatase activity
Expand Tier I Human 6 Genes GS171018: HP:0003173 Hypoplastic pubic bones
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 47 Genes GS172604: HP:0005445 Widened posterior fossa
Expand Tier I Human 60 Genes GS174088: HP:0003366 Abnormality of the femoral neck and head region
Expand Tier I Human 177 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human GO 3116 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human GO 1851 Genes GS200446: GO:0017076 purine nucleotide binding
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 228 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human 3 Genes GS174998: HP:0007665 Curly eyelashes
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 1775 Genes GS194586: GO:0002376 immune system process
Expand Tier I Human GO 1320 Genes GS209622: GO:0038023 signaling receptor activity
Expand Tier I Human 127 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human GO 5623 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 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 1905 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 145 Genes GS206312: GO:0044449 contractile fiber part
Expand Tier I Human GO 752 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Human 184 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Human 123 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier I Human GO 162 Genes GS206183: GO:0043292 contractile fiber
Expand Tier I Human 12 Genes GS171019: HP:0003172 Abnormality of the pubic bones
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human CTD 1122 Genes GS127166: bisphenol A interacting genes (MeSH:C006780) in CTD
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human 66 Genes GS172588: HP:0001831 Short toe
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human GO 3 Genes GS208663: GO:0008282 ATP-sensitive potassium channel complex
Expand Tier I Human 122 Genes GS171390: HP:0000178 Abnormality of lower lip
Expand Tier I Human GO 4 Genes GS194001: GO:0010107 potassium ion import
Expand Tier I Human 282 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human GO 99 Genes GS207260: GO:0042626 ATPase activity, coupled to transmembrane movement of substances
Expand Tier I Human 193 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human GO 1254 Genes GS199199: GO:0031226 intrinsic to plasma membrane
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 2411 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 924 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human 16 Genes GS174486: HP:0000527 Long eyelashes
Expand Tier I Human GO 794 Genes GS202828: GO:0016817 hydrolase activity, acting on acid anhydrides
Expand Tier I Human 7 Genes GS176082: HP:0003175 Hypoplastic ischia
Expand Tier I Human GO 1226 Genes GS204740: GO:0004888 transmembrane signaling receptor activity
Expand Tier I Human 70 Genes GS171600: HP:0000168 Abnormality of the gingiva
Expand Tier I Human GO 260 Genes GS204130: GO:0009615 response to virus
Expand Tier I Human GO 39 Genes GS208574: GO:0044325 ion channel binding
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 147 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human GO 652 Genes GS195082: GO:0007268 synaptic transmission
Expand Tier I Human 44 Genes GS171924: HP:0100578 Lipoatrophy
Expand Tier I Human CTD 18 Genes GS123803: Glyburide interacting genes (MeSH:D005905) in CTD
Expand Tier I Human CTD 71 Genes GS126830: Potassium interacting genes (MeSH:D011188) in CTD
Expand Tier I Human 120 Genes GS170890: HP:0006483 Abnormal number of teeth
Expand Tier I Human 146 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human GO 132 Genes GS198195: GO:0034703 cation channel complex
Expand Tier I Human 261 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 26 Genes GS176727: HP:0003043 Abnormality of the shoulder
Expand Tier I Human GO 1091 Genes GS206909: GO:0006952 defense response
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 153 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Human 69 Genes GS172585: HP:0001832 Abnormality of the metatarsal bones
Expand Tier I Human 52 Genes GS174719: HP:0000774 Narrow chest
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 96 Genes GS174851: HP:0000944 Abnormality of the metaphyses
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 1210 Genes GS197008: GO:0005887 integral to plasma membrane
Expand Tier I Human 14 Genes GS174014: HP:0010109 Small hallux
Expand Tier I Human 184 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Human GO 152 Genes GS208921: GO:0030016 myofibril
Expand Tier I Human 48 Genes GS174251: HP:0010161 Abnormality of the phalanges of the toes
Expand Tier I Human GO 632 Genes GS209450: GO:0006812 cation transport
Expand Tier I Human 134 Genes GS171627: HP:0000470 Short neck
Expand Tier I Human 220 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 14 Genes GS171862: HP:0008362 Aplasia/Hypoplasia of the hallux
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 35 Genes GS176775: HP:0001004 Lymphedema
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 138 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Human GO 102 Genes GS199048: GO:0016820 hydrolase activity, acting on acid anhydrides, catalyzing transmembrane movement of substances
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Human 19 Genes GS172681: HP:0003300 Ovoid vertebral bodies
Expand Tier I Human GO 1844 Genes GS201794: GO:0032555 purine ribonucleotide binding
Expand Tier I Human GO 1193 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human 74 Genes GS171391: HP:0000179 Thick lower lip vermilion
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear