Gene Details



SRCAP and homologs in 1 species are found in 310 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 GO 718 Genes GS206695: GO:0044703 multi-organism reproductive process
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 112 Genes GS171810: HP:0005651 Flexion contracture of finger
Expand Tier I Human GO 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 130 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier I Human GO 3714 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human 145 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
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 21 Genes GS174254: HP:0005920 Abnormality of the epiphyses of the phalanges of the hand
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 260 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human GO 1821 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 39 Genes GS174330: HP:0002714 Downturned corners of mouth
Expand Tier I Human 41 Genes GS171926: HP:0007018 Attention deficit hyperactivity disorder
Expand Tier I Human 274 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 130 Genes GS200930: GO:0006473 protein acetylation
Expand Tier I Human 51 Genes GS173085: HP:0000490 Deeply set eye
Expand Tier I Human 104 Genes GS171247: HP:0002019 Constipation
Expand Tier I Human GO 3304 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 3334 Genes GS205622: GO:0009889 regulation of biosynthetic process
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 GO 1832 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 49 Genes GS173815: HP:0000736 Short attention span
Expand Tier I Human 100 Genes GS174372: HP:0002024 Malabsorption
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 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 23 Genes GS174376: HP:0005924 Abnormality of the epiphyses of the hand
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 148 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier I Human 15 Genes GS175386: HP:0010230 Cone-shaped epiphyses of the phalanges of the hand
Expand Tier I Human 176 Genes GS175103: HP:0000288 Abnormality of the philtrum
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 143 Genes GS208190: GO:0018205 peptidyl-lysine modification
Expand Tier I Human GO 3180 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 147 Genes GS204642: GO:0043543 protein acylation
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
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 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 49 Genes GS173059: HP:0000322 Short philtrum
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 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 263 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 243 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human GO 4354 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human 148 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
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 60 Genes GS170970: HP:0000154 Wide mouth
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Tier I Human GO 92 Genes GS197582: GO:0016410 N-acyltransferase activity
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
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 2455 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human GO 1500 Genes GS203649: GO:0030554 adenyl nucleotide binding
Expand Tier I Human GO 2878 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human 472 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
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 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 1844 Genes GS201794: GO:0032555 purine ribonucleotide binding
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human GO 4292 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 786 Genes GS210137: GO:0016462 pyrophosphatase activity
Expand Tier I Human 2 Genes GS172668: HP:0002474 Expressive language delay
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 4138 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human 69 Genes GS170981: HP:0011361 Congenital abnormal hair pattern
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human GO 447 Genes GS209385: GO:0044403 symbiosis, encompassing mutualism through parasitism
Expand Tier I Human GO 3300 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 164 Genes GS171654: HP:0003121 Limb joint contracture
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 3603 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human GO 3891 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 4787 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human 120 Genes GS171607: HP:0011337 Abnormality of mouth size
Expand Tier I Human 300 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 21 Genes GS173291: HP:0000319 Smooth philtrum
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 309 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 54 Genes GS171548: HP:0001388 Joint laxity
Expand Tier I Human 46 Genes GS170867: HP:0100736 Abnormality of the soft palate
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 2939 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 187 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human GO 3277 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human 296 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human GO 540 Genes GS196195: GO:0022415 viral reproductive process
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
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 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human 59 Genes GS172412: HP:0002244 Abnormality of the small intestine
Expand Tier I Human GO 3264 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 130 Genes GS173970: HP:0009473 Joint contracture of the hand
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 200 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human GO 174 Genes GS208737: GO:0016747 transferase activity, transferring acyl groups other than amino-acyl groups
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
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 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
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 524 Genes GS194524: GO:0006325 chromatin organization
Expand Tier I Human GO 2410 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human GO 267 Genes GS200351: GO:0016569 covalent chromatin modification
Expand Tier I Human 63 Genes GS171802: HP:0009553 Abnormality of the hairline
Expand Tier I Human 200 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 50 Genes GS173052: HP:0000325 Triangular face
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 148 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 62 Genes GS173993: HP:0000506 Telecanthus
Expand Tier I Human 57 Genes GS173426: HP:0000889 Abnormality of the clavicles
Expand Tier I Human GO 3550 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human 80 Genes GS175456: HP:0100037 Abnormality of the scalp hair
Expand Tier I Human GO 3617 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human GO 3468 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 369 Genes GS199224: GO:0019048 virus-host interaction
Expand Tier I Human 39 Genes GS170829: HP:0002162 Low posterior hairline
Expand Tier I Human GO 688 Genes GS193888: GO:0051276 chromosome organization
Expand Tier I Human GO 427 Genes GS200350: GO:0016568 chromatin modification
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Human GO 1362 Genes GS203494: GO:0051704 multi-organism process
Expand Tier I Human GO 229 Genes GS208736: GO:0016746 transferase activity, transferring acyl groups
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human 10 Genes GS174585: HP:0009929 Abnormality of the columella
Expand Tier I Human 1 Genes GS171468: HP:0002608 Celiac disease
Expand Tier I Human 147 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier I Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human GO 1466 Genes GS205179: GO:0005524 ATP binding
Expand Tier I Human GO 113 Genes GS203092: GO:0018394 peptidyl-lysine acetylation
Expand Tier I Human GO 480 Genes GS209023: GO:0000989 transcription factor binding transcription factor activity
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 146 Genes GS208180: GO:0004386 helicase activity
Expand Tier I Human GO 636 Genes GS199538: GO:0018193 peptidyl-amino acid modification
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human GO 90 Genes GS201970: GO:0016407 acetyltransferase activity
Expand Tier I Human 4 Genes GS170986: HP:0010761 Broad columella
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 4245 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human 249 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human 80 Genes GS172248: HP:0001373 Joint dislocation
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 40 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 2857 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human GO 261 Genes GS204656: GO:0016570 histone modification
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 3325 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 38 Genes GS176960: HP:0000430 Hypoplastic nasal alae
Expand Tier I Human 88 Genes GS173087: HP:0000499 Abnormality of the eyelashes
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 52 Genes GS174577: HP:0009924 Aplasia/Hypoplasia involving the nose
Expand Tier I Human 256 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human GO 3239 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human GO 1166 Genes GS201075: GO:0005794 Golgi apparatus
Expand Tier I Human GO 1809 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human 53 Genes GS176772: HP:0001007 Hirsutism
Expand Tier I Human 117 Genes GS170853: HP:0006261 Abnormality of phalangeal joints of the hand
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 GO 268 Genes GS200080: GO:0003713 transcription coactivator activity
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 1391 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
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 72 Genes GS176488: HP:0010720 Abnormal hair pattern
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 4682 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 1718 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 177 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human GO 1851 Genes GS200446: GO:0017076 purine nucleotide binding
Expand Tier I Human GO 689 Genes GS203305: GO:0016032 viral reproduction
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 GO 411 Genes GS203490: GO:0051701 interaction with host
Expand Tier I Human GO 2310 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 40 Genes GS172205: HP:0100326 Immunologic hypersensitivity
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human GO 2104 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 108 Genes GS204657: GO:0016573 histone acetylation
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 211 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier I Human GO 1596 Genes GS207991: GO:0000003 reproduction
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 184 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Human GO 3099 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 465 Genes GS197319: GO:0003712 transcription cofactor activity
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 GO 76 Genes GS207098: GO:0008080 N-acetyltransferase activity
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
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 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 1214 Genes GS198360: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 1591 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Human 82 Genes GS171602: HP:0001965 Abnormality of the scalp
Expand Tier I Human 15 Genes GS176404: HP:0000448 Prominent nose
Expand Tier I Human 24 Genes GS171675: HP:0003839 Abnormality involving the epiphyses of the upper limbs
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 GO 51 Genes GS202937: GO:0004402 histone acetyltransferase activity
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
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 4129 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human 194 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human GO 2549 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
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 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
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 65 Genes GS171085: HP:0009602 Abnormality of the phalanges of the thumb
Expand Tier I Human GO 496 Genes GS209024: GO:0000988 protein binding transcription factor activity
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 447 Genes GS196889: GO:0044419 interspecies interaction between organisms
Expand Tier I Human 146 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human 12 Genes GS175927: HP:0000243 Trigonocephaly
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human GO 116 Genes GS202813: GO:0006475 internal protein amino acid acetylation
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 110 Genes GS200950: GO:0018393 internal peptidyl-lysine acetylation
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3383 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Human 46 Genes GS175664: HP:0006505 Abnormality involving the epiphyses of the limbs
Expand Tier I Human 161 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 134 Genes GS171627: HP:0000470 Short neck
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 112 Genes GS171616: HP:0100490 Camptodactyly of finger
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 75 Genes GS171608: HP:0011338 Abnormality of mouth shape
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 3178 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis