Gene Details



KIAA1267 and homologs in 2 species are found in 487 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 GO 9 Genes GS196804: GO:0043996 histone acetyltransferase activity (H4-K8 specific)
Expand Tier I Human 32 Genes GS173773: HP:0000194 Open mouth
Expand Tier I Mouse 1061 Genes GS136647: serum IGFBP-5 level QTL 6 (Si5lq6, Published QTL Chr 11)
Expand Tier I Human 58 Genes GS172176: HP:0000232 Everted lower lip vermilion
Expand Tier I Mouse 579 Genes GS129172: pregnancy QTL 2 (Pregq2 Published QTL Chr 11)
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 100 Genes GS175101: HP:0000280 Coarse facial features
Expand Tier I Mouse 996 Genes GS136853: Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 5 (Tmevd5, Published QTL Chr 11)
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
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 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse 692 Genes GS135389: body growth early QTL 10 (Bgeq10, Published QTL Chr 11)
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 147 Genes GS204642: GO:0043543 protein acylation
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 150 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 177 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Mouse 1003 Genes GS135818: ethanol induced thermoregulation 4 (Ethm4, Published QTL Chr 11)
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse 1046 Genes GS135496: brain weight QTL 1 (Brwq1, Published QTL Chr 11)
Expand Tier I Human GO 93 Genes GS197582: GO:0016410 N-acyltransferase activity
Expand Tier I Human GO 60 Genes GS200520: GO:0035097 histone methyltransferase complex
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human 66 Genes GS176033: HP:0011039 Abnormality of the helix
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 1046 Genes GS135528: castaneus 10 week body weight 3 (C10bw3, Published QTL Chr 11)
Expand Tier I Human 283 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Mouse 1008 Genes GS136767: streptozotocin induced diabetes susceptibility (Stzid, Published QTL Chr 11)
Expand Tier I Human 19 Genes GS176247: HP:0002948 Vertebral fusion
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Human GO 2098 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Mouse 988 Genes GS136696: systematic lupus erythematosus susceptibility 13 (Sle13, Published QTL Chr 11)
Expand Tier I Mouse 988 Genes GS136481: plasmacytoma susceptibility 3 (Pcyts3, Published QTL Chr 11)
Expand Tier I Mouse 801 Genes GS136780: seizure susceptibility 3 (Szs3, Published QTL Chr 11)
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier I Human 17 Genes GS174162: HP:0000960 Sacral dimple
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human GO 688 Genes GS193888: GO:0051276 chromosome organization
Expand Tier I Human GO 230 Genes GS208736: GO:0016746 transferase activity, transferring acyl groups
Expand Tier I Human 51 Genes GS172933: HP:0003745 Sporadic
Expand Tier I Human 210 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse 1060 Genes GS135973: wound healing/regeneration 10 (Heal10, Published QTL Chr 11)
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 179 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 157 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 47 Genes GS175737: HP:0001238 Slender finger
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 2 Genes GS172663: HP:0100024 Conspicuously happy disposition
Expand Tier I Mouse GO 27 Genes GS185595: GO:0071339 MLL1 complex
Expand Tier I Mouse 2963 Genes GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 152 Genes GS191271: GO:0018205 peptidyl-lysine modification
Expand Tier II Mouse 86 Genes GS36755: Hippocampus Gene expression correlates of Vocalization Threshold - shock intensity (mA) in Females BXD
Expand Tier I Mouse 767 Genes GS135792: epilepsy 6 (El6, Published QTL Chr 11)
Expand Tier II Mouse 792 Genes GS84255: alcohol preference locus (Published QTL, Chr 11)
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier II Mouse 40 Genes GS36136: Cerebellum Gene expression correlates of Activity during 1st tone shock pairing in Males BXD
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 68 Genes GS176572: HP:0008064 Ichthyosiform abnormality of the skin
Expand Tier I Mouse GO 147 Genes GS187783: GO:0043543 protein acylation
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 1477 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human GO 9 Genes GS201038: GO:0046972 histone acetyltransferase activity (H4-K16 specific)
Expand Tier I Mouse 705 Genes GS136357: novelty/stress induced locomotor activation 8 (Nsila8, Published QTL Chr 11)
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human GO 110 Genes GS200950: GO:0018393 internal peptidyl-lysine acetylation
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Human 79 Genes GS171553: HP:0001384 Abnormality of the hip joint
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Mouse 1281 Genes GS129115: collagen induced arthritis 40 (Cia40 Published QTL Chr 11)
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 53 Genes GS173835: HP:0003422 Vertebral segmentation defect
Expand Tier I Human 84 Genes GS176462: HP:0100240 Synostosis of joints
Expand Tier I Mouse 792 Genes GS136831: TNF-induced lethal shock susceptibility 2 (Tilss2, Published QTL Chr 11)
Expand Tier I Human 57 Genes GS171029: HP:0010944 Abnormality of the renal pelvis
Expand Tier I Mouse GO 276 Genes GS187797: GO:0016570 histone modification
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
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 188 Genes GS171167: HP:0000235 Abnormality of the fontanelles and cranial sutures
Expand Tier I Mouse 1061 Genes GS136477: periosteal circumference 2 (Pcir2, Published QTL Chr 11)
Expand Tier I Human GO 267 Genes GS200351: GO:0016569 covalent chromatin modification
Expand Tier I Mouse 735 Genes GS135274: "alcohol preference locus 18, male specific" (Alcp18, Published QTL Chr 11)
Expand Tier I Mouse GO 2303 Genes GS177598: GO:0043412 macromolecule modification
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 89 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier I Human GO 637 Genes GS199538: GO:0018193 peptidyl-amino acid modification
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse DRG 2693 Genes GS87380: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
Expand Tier I Human 27 Genes GS171447: HP:0000601 Hypotelorism
Expand Tier I Mouse 1004 Genes GS135766: experimental allergic encephalomyelitis susceptibility 7 (Eae7, Published QTL Chr 11)
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 9 Genes GS175324: HP:0001211 Abnormality of the fingertips
Expand Tier I Human 72 Genes GS176835: HP:0000426 Prominent nasal bridge
Expand Tier I Human GO 13 Genes GS197819: GO:0010485 H4 histone acetyltransferase activity
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse 998 Genes GS136543: periosteal circumference 2 (Pstc2, Published QTL Chr 11)
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
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 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 GO 5247 Genes GS178448: GO:0005634 nucleus
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 Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier II Mouse 319 Genes GS36750: Hippocampus Gene expression correlates of Vocalization Threshold - shock intensity (mA) in Females & Males BXD
Expand Tier I Human GO 15 Genes GS209300: GO:0043982 histone H4-K8 acetylation
Expand Tier I Mouse 710 Genes GS136328: non-insulin-dependent diabetes mellitus 4 (Nidd4, Published QTL Chr 11)
Expand Tier I Human CTD 1148 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier I Human 70 Genes GS171543: HP:0000276 Long face
Expand Tier I Human 25 Genes GS175426: HP:0010767 Sacrococcygeal pilonidal abnormality
Expand Tier I Human 55 Genes GS173685: HP:0001641 Abnormality of the pulmonary valve
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 189 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human 81 Genes GS174550: HP:0000958 Dry skin
Expand Tier I Human 50 Genes GS173561: HP:0000691 Microdontia
Expand Tier I Human 111 Genes GS176907: HP:0009804 Reduced number of teeth
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse 988 Genes GS136337: nicotine induced locomotor activity 2 (Nilac2, Published QTL Chr 11)
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse 1039 Genes GS136708: semilethal sex-restricted (Slthsr, Published QTL Chr 11)
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 52 Genes GS177055: HP:0005599 Hypopigmentation of hair
Expand Tier I Mouse 792 Genes GS136514: protein kinase C content in lungs (Pkccl, Published QTL Chr 11)
Expand Tier I Mouse 1061 Genes GS136560: QTL for body weight independent of sex 3 (Qbis3, Published QTL Chr 11)
Expand Tier I Human 81 Genes GS173600: HP:0002926 Abnormality of thyroid physiology
Expand Tier I Mouse 1061 Genes GS136086: kidney weight QTL 15 (Kwq15, Published QTL Chr 11)
Expand Tier I Mouse GO 610 Genes GS177169: GO:0051276 chromosome organization
Expand Tier I Human 114 Genes GS172283: HP:0000820 Abnormality of the thyroid gland
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 98 Genes GS171910: HP:0003828 Variable expressivity
Expand Tier I Human 17 Genes GS174402: HP:0001611 Nasal speech
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human 54 Genes GS172298: HP:0001518 Small for gestational age
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 50 Genes GS175148: HP:0010511 Long toe
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 180 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Mouse 1077 Genes GS135507: body weight QTL 4 (Bw4, Published QTL Chr 11)
Expand Tier I Human 237 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 160 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 524 Genes GS194524: GO:0006325 chromatin organization
Expand Tier III Mouse 3192 Genes GS213073: Genes with suggestive difference in (PB6F1) vs (B6PF1 + B6 + PWD) comparison
Expand Tier I Human 215 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse 988 Genes GS136566: retinoic acid induced forelimb autopod reduction (Rafar, Published QTL Chr 11)
Expand Tier I Human 17 Genes GS174660: HP:0001421 Abnormality of the musculature of the hand
Expand Tier I Mouse GO 412 Genes GS183552: GO:0016568 chromatin modification
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier I Human GO 427 Genes GS200350: GO:0016568 chromatin modification
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human GO 15 Genes GS209302: GO:0043981 histone H4-K5 acetylation
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier I Mouse 697 Genes GS135386: berghei resistance locus 2 (Berr2, Published QTL Chr 11)
Expand Tier I Human 148 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier III Human 2403 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human GO 91 Genes GS201970: GO:0016407 acetyltransferase activity
Expand Tier I Human 81 Genes GS172248: HP:0001373 Joint dislocation
Expand Tier I Human 6 Genes GS175322: HP:0001212 Prominent fingertip pads
Expand Tier I Human 27 Genes GS173688: HP:0001642 Pulmonic stenosis
Expand Tier I Mouse 1077 Genes GS135366: B.burgdorferi-associated arthritis 4 (Bbaa4, Published QTL Chr 11)
Expand Tier I Human 53 Genes GS172660: HP:0002021 Pyloric stenosis
Expand Tier I Mouse GO 27 Genes GS187085: GO:0044665 MLL1/2 complex
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human 78 Genes GS175969: HP:0000069 Abnormality of the ureter
Expand Tier I Mouse 1060 Genes GS135353: Alzheimer's disease modifier 5 (Azdm5, Published QTL Chr 11)
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 Mouse 1142 Genes GS129196: Tmc1 modifier 2 (Tmc1m2 Published QTL Chr 11)
Expand Tier II Mouse 1002 Genes GS84253: alcohol preference locus (Published QTL, Chr 11)
Expand Tier I Human 24 Genes GS173416: HP:0000414 Bulbous nose
Expand Tier I Mouse 3375 Genes GS127927: Hypothalamus - Allen Mouse Brain Atlas
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 Mouse 735 Genes GS135276: "alcohol preference locus 20, female specific" (Alcp20, Published QTL Chr 11)
Expand Tier I Human 51 Genes GS177034: HP:0000436 Abnormality of the nasal tip
Expand Tier I Human GO 1736 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human 2 Genes GS176409: HP:0000447 Pear-shaped nose
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier III Mouse 1654 Genes GS37188: Positional candidate on Chromosome 11 (30-110 Mb) for dominant deviation measuring EtOH consumption during DID, 24 hour access and BEC.
Expand Tier I Human GO 108 Genes GS204657: GO:0016573 histone acetylation
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 700 Genes GS136632: small effect CIA locus 6 (Secia6, Published QTL Chr 11)
Expand Tier I Mouse 714 Genes GS135555: CD8 memory T cell subset 4 (Cd8mts4, Published QTL Chr 11)
Expand Tier I Mouse 990 Genes GS136439: peak bone density 1 (Pbd1, Published QTL Chr 11)
Expand Tier I Human 114 Genes GS174643: HP:0005120 Abnormality of cardiac atrium
Expand Tier I Mouse 792 Genes GS136220: mandible length 12 (Manln12, Published QTL Chr 11)
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Mouse 3289 Genes GS127924: Cerebral cortex - Allen Mouse Brain Atlas
Expand Tier I Human GO 77 Genes GS207098: GO:0008080 N-acetyltransferase activity
Expand Tier I Mouse 3384 Genes GS127925: Hippocampal formation - Allen Mouse Brain Atlas
Expand Tier I Human 1495 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 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 GO 14 Genes GS201671: GO:0043984 histone H4-K16 acetylation
Expand Tier I Human 251 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 51 Genes GS202937: GO:0004402 histone acetyltransferase activity
Expand Tier I Mouse 996 Genes GS135295: acute lung injury QTL 1 (Aliq1, Published QTL Chr 11)
Expand Tier I Human GO 2464 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 123 Genes GS171390: HP:0000178 Abnormality of lower lip
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Mouse GO 61 Genes GS183716: GO:0035097 histone methyltransferase complex
Expand Tier I Mouse 1003 Genes GS135678: compensatory renal hypertrophy QTL 1 (Crhq1, Published QTL Chr 11)
Expand Tier I Human 197 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Human 5 Genes GS171673: HP:0004283 Narrow palm
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse GO 282 Genes GS183553: GO:0016569 covalent chromatin modification
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Mouse GO 62 Genes GS186444: GO:0034708 methyltransferase complex
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse GO 690 Genes GS180673: GO:0044451 nucleoplasm part
Expand Tier I Mouse GO 561 Genes GS182740: GO:0018193 peptidyl-amino acid modification
Expand Tier II Mouse 730 Genes GS83981: cocaine related behavior 12 (Cocrb12, Published QTL, Chr 11)
Expand Tier II Mouse 1017 Genes GS84254: nicotine sensitivity (Published QTL,Chr 11)
Expand Tier I Mouse 1004 Genes GS136517: platelet count 2 (Pltct2, Published QTL Chr 11)
Expand Tier I Mouse 2944 Genes GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
Expand Tier I Mouse 692 Genes GS136896: visual placing (Vispl, Published QTL Chr 11)
Expand Tier I Human 136 Genes GS175524: HP:0000009 Functional abnormality of the bladder
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse 2962 Genes GS127936: Striatum ventral region - Allen Mouse Brain Atlas
Expand Tier I Human GO 116 Genes GS202813: GO:0006475 internal protein amino acid acetylation
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier I Human 51 Genes GS174123: HP:0100807 Long fingers
Expand Tier I Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 138 Genes GS174289: HP:0002577 Abnormality of the stomach
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
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 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human 49 Genes GS171726: HP:0005107 Abnormality of the sacrum
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 GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 20 Genes GS171369: HP:0000396 Overfolded helix
Expand Tier I Mouse 996 Genes GS135461: bone mineral density 7 (Bomd7, Published QTL Chr 11)
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Mouse DRG 2537 Genes provisional GS86906: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). Lists of probe sets and gene names altered by strain (3457). [DRG]
Expand Tier I Human 121 Genes GS175023: HP:0001629 Ventricular septal defect
Expand Tier I Mouse 697 Genes GS136244: methamphetamine response QTL 3 (Marq3, Published QTL Chr 11)
Expand Tier I Human 41 Genes GS176115: HP:0000540 Hypermetropia
Expand Tier I Human 111 Genes GS174806: HP:0001631 Defect in the atrial septum
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Mouse 981 Genes GS135755: experimental allergic encephalomyelitis susceptibility 22 (Eae22, Published QTL Chr 11)
Expand Tier I Mouse GO 46 Genes GS184574: GO:0043967 histone H4 acetylation
Expand Tier I Human 56 Genes GS171290: HP:0000126 Hydronephrosis
Expand Tier I Human 177 Genes GS175431: HP:0011122 Abnormality of skin physiology
Expand Tier I Human 183 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human 2 Genes GS176260: HP:0006006 Hypotrophy of the small hand muscles
Expand Tier I Mouse 792 Genes GS135341: atherosclerosis 19 (Ath19, Published QTL Chr 11)
Expand Tier I Human 16 Genes GS173551: HP:0005487 Prominent metopic ridge
Expand Tier I Human 129 Genes GS174925: HP:0000769 Abnormality of the breast
Expand Tier I Human GO 175 Genes GS208737: GO:0016747 transferase activity, transferring acyl groups other than amino-acyl groups
Expand Tier I Human 79 Genes GS172284: HP:0000821 Hypothyroidism
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse GO 471 Genes GS177784: GO:0006325 chromatin organization
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse 3315 Genes GS127939: Thalamus - Allen Mouse Brain Atlas
Expand Tier II Mouse 193 Genes GS36157: Hippocampus Gene expression correlates of Locomotor response of 10 mg/kg MDMA injected on Day 2 in Females BXD
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Human GO 27 Genes GS202425: GO:0071339 MLL1 complex
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 10 Genes GS171554: HP:0001385 Hip dysplasia
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Human 6 Genes GS173312: HP:0011298 Prominent digit pad
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 Human CTD 513 Genes GS122168: irinotecan interacting genes (MeSH:C051890) in CTD
Expand Tier I Human 59 Genes GS175262: HP:0000964 Eczema
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Mouse GO 1628 Genes GS177813: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Human 52 Genes GS174577: HP:0009924 Aplasia/Hypoplasia involving the nose
Expand Tier I Mouse GO 1381 Genes GS192610: GO:0031981 nuclear lumen
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse 1003 Genes GS136433: pulmonary adenoma susceptibility 5a (Pas5a, Published QTL Chr 11)
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 Human 22 Genes GS173583: HP:0008544 Abnormally folded helix
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Mouse GO 778 Genes GS186526: GO:0005654 nucleoplasm
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 203 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human 17 Genes GS176999: HP:0001290 Generalized hypotonia
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Mouse 990 Genes GS136605: spinal bone mineral density 4 (Sbmd4, Published QTL Chr 11)
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Mouse GO 2223 Genes GS179830: GO:0006464 cellular protein modification process
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse GO 113 Genes GS186246: GO:0018394 peptidyl-lysine acetylation
Expand Tier I Mouse 3109 Genes GS127923: Cerebellum - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 110 Genes GS184149: GO:0018393 internal peptidyl-lysine acetylation
Expand Tier I Mouse 1061 Genes GS136798: total body bone mineral density 5 (Tbbmd5, Published QTL Chr 11)
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 Mouse 1061 Genes GS136208: liver weight QTL 9 (Lwq9, Published QTL Chr 11)
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Mouse GO 1870 Genes GS192986: GO:0006996 organelle organization
Expand Tier I Human GO 62 Genes GS203291: GO:0034708 methyltransferase complex
Expand Tier I Human GO 75 Genes GS209724: GO:0000123 histone acetyltransferase complex
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human GO 27 Genes GS203944: GO:0044665 MLL1/2 complex
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Mouse GO 3548 Genes GS184566: GO:0019538 protein metabolic process
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
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 Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Human 42 Genes GS174226: HP:0001446 Abnormality of the musculature of the upper limbs
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier I Human 44 Genes GS176179: HP:0000076 Vesicoureteral reflux
Expand Tier I Human 70 Genes GS172568: HP:0000348 High forehead
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 79 Genes GS171959: HP:0000400 Macrotia
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 46 Genes GS201376: GO:0043967 histone H4 acetylation
Expand Tier I Human 111 Genes GS173580: HP:0011994 Abnormality of the atrial septum
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 71 Genes GS174073: HP:0009127 Abnormality of the musculature of the limbs
Expand Tier I Human 57 Genes GS171460: HP:0002827 Hip dislocation
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 56 Genes GS175220: HP:0009887 Abnormality of hair pigmentation
Expand Tier I Human 38 Genes GS176960: HP:0000430 Hypoplastic nasal alae
Expand Tier I Mouse 715 Genes GS135815: ethanol induced ataxia 10 (Etax10, Published QTL Chr 11)
Expand Tier I Mouse GO 13 Genes GS184858: GO:0043984 histone H4-K16 acetylation
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 151 Genes GS174920: HP:0000766 Abnormality of the sternum
Expand Tier I Human GO 2108 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Mouse 3136 Genes GS127926: Hippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human 154 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Mouse GO 15 Genes GS192364: GO:0043982 histone H4-K8 acetylation
Expand Tier I Mouse 1046 Genes GS136952: weight gain in high growth mice 7 (Wg7, Published QTL Chr 11)
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 97 Genes GS174919: HP:0000767 Pectus excavatum
Expand Tier I Mouse 1046 Genes GS135812: estradiol regulated response QTL 3 (Estq3, Published QTL Chr 11)
Expand Tier I Mouse GO 108 Genes GS187798: GO:0016573 histone acetylation
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
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 Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
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 Mouse GO 127 Genes GS184130: GO:0006473 protein acetylation
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Mouse 705 Genes GS135906: gonadal fat pad weight QTL 1 (Gfpq1, Published QTL Chr 11)
Expand Tier I Human 121 Genes GS170890: HP:0006483 Abnormal number of teeth
Expand Tier I Mouse 1061 Genes GS136119: body length 6 (Lgth6, Published QTL Chr 11)
Expand Tier I Mouse 1061 Genes GS136528: prion disease incubation time 3 (Prdt3, Published QTL Chr 11)
Expand Tier I Human 68 Genes GS170896: HP:0004404 Abnormality of the nipple
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 19 Genes GS172450: HP:0006610 Wide intermamillary distance
Expand Tier I Mouse 1068 Genes GS136388: autoimmune orchitis resistance 3 (Orch3, Published QTL Chr 11)
Expand Tier I Mouse 697 Genes GS136957: weight 5 (Wght5, Published QTL Chr 11)
Expand Tier I Human 76 Genes GS171608: HP:0011338 Abnormality of mouth shape
Expand Tier I Mouse GO 114 Genes GS185975: GO:0006475 internal protein amino acid acetylation
Expand Tier I Human 56 Genes GS171030: HP:0010946 Dilatation of the renal pelvis
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 8 Genes GS172680: HP:0003302 Spondylolisthesis
Expand Tier I Mouse GO 15 Genes GS192366: GO:0043981 histone H4-K5 acetylation
Expand Tier I Mouse 981 Genes GS136789: tail length QTL 8 (Tailq8, Published QTL Chr 11)
Expand Tier I Human 19 Genes GS172292: HP:0010781 Skin dimples
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Mouse 3395 Genes GS127929: Medulla - Allen Mouse Brain Atlas
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse GO 1582 Genes GS188684: GO:0070013 intracellular organelle lumen
Expand Tier I Human 46 Genes GS175267: HP:0001166 Arachnodactyly
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 17 Genes GS173127: HP:0005556 Abnormality of the metopic suture
Expand Tier I Human GO 113 Genes GS203092: GO:0018394 peptidyl-lysine acetylation
Expand Tier I Human GO 9 Genes GS196802: GO:0043995 histone acetyltransferase activity (H4-K5 specific)
Expand Tier I Human 39 Genes GS172815: HP:0000337 Broad forehead
Expand Tier I Mouse GO 1587 Genes GS182475: GO:0043233 organelle lumen
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Mouse GO 2223 Genes GS182234: GO:0036211 protein modification process
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 261 Genes GS204656: GO:0016570 histone modification
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human 123 Genes GS175583: HP:0010438 Abnormality of the ventricular septum
Expand Tier I Human 53 Genes GS170905: HP:0004400 Abnormality of the pylorus
Expand Tier I Human 12 Genes GS173691: HP:0001647 Bicuspid aortic valve
Expand Tier I Mouse GO 2926 Genes GS183803: GO:0044267 cellular protein metabolic process
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Mouse GO 73 Genes GS192778: GO:0000123 histone acetyltransferase complex
Expand Tier I Human 83 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 130 Genes GS200930: GO:0006473 protein acetylation
Expand Tier I Mouse 1003 Genes GS136677: skull morphology 16 (Skull16, Published QTL Chr 11)
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 132 Genes GS171835: HP:0011329 Abnormality of cranial sutures
Expand Tier I Mouse 1038 Genes GS136434: pulmonary adenoma susceptibility 5b (Pas5b, Published QTL Chr 11)
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 114 Genes GS176227: HP:0010719 Abnormality of hair texture
Expand Tier I Human GO 143 Genes GS208190: GO:0018205 peptidyl-lysine modification