Gene Details



SRCAP and homologs in 3 species are found in 386 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 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse 786 Genes GS135979: wound healing/regeneration 6 (Heal6, Published QTL Chr 7)
Expand Tier I Human 131 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier II Mouse 25 Genes GS26255: Striatum Gene expression correlates of Thermal Nociception Tail Withdrawal Test in Females BXD
Expand Tier I Human 146 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
Expand Tier I Human GO 1839 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 41 Genes GS171926: HP:0007018 Attention deficit hyperactivity disorder
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier II Mouse 64 Genes GS36349: Striatum Gene expression correlates of Naloxone induced Morphine Withdrawal - TOTAL vertical activity counts in 15 minutes in Females BXD
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse 874 Genes GS136784: seizure severity 2 (Szv2, Published QTL Chr 7)
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 Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human 125 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 269 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 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 103 Genes GS174372: HP:0002024 Malabsorption
Expand Tier I Mouse 874 Genes GS136339: nicotine induced locomotor activity 4 (Nilac4, Published QTL Chr 7)
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 150 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier I Human 176 Genes GS175103: HP:0000288 Abnormality of the philtrum
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse 454 Genes GS136306: myocardial infarction 1 (Myci1, Published QTL Chr 7)
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 147 Genes GS204642: GO:0043543 protein acylation
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 1840 Genes GS197443: GO:0032549 ribonucleoside binding
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
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 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 427 Genes GS136460: postnatal body weight growth 3 (Pbwg3, Published QTL Chr 7)
Expand Tier I Human 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Tier I Human GO 93 Genes GS197582: GO:0016410 N-acyltransferase activity
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human CTD 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human 149 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human GO 2896 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier II Mouse 256 Genes GS34191: Hippocampus Gene expression correlates of Number of entries into closed arms of plus maze in Males BXD
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human GO 790 Genes GS210137: GO:0016462 pyrophosphatase activity
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Mouse 501 Genes GS136843: thymic lymphoma susceptible 1 (Tlsm1, Published QTL Chr 7)
Expand Tier I Human 69 Genes GS170981: HP:0011361 Congenital abnormal hair pattern
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 165 Genes GS171654: HP:0003121 Limb joint contracture
Expand Tier I Human GO 3917 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human GO 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 21 Genes GS173291: HP:0000319 Smooth philtrum
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 2957 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 189 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Mouse 796 Genes GS136153: limb length QTL 3 (Lmblgq3, Published QTL Chr 7)
Expand Tier I Human GO 540 Genes GS196195: GO:0022415 viral reproductive process
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 59 Genes GS172412: HP:0002244 Abnormality of the small intestine
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier II Mouse 256 Genes GS36850: Hippocampus Gene expression correlates of Percentage of entries into closed arms of plus maze in Males BXD
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Mouse 757 Genes GS135942: HDL cholesterol level 1 (Hdlcl1, Published QTL Chr 7)
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 524 Genes GS194524: GO:0006325 chromatin organization
Expand Tier I Human GO 2432 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 63 Genes GS171802: HP:0009553 Abnormality of the hairline
Expand Tier I Mouse 756 Genes GS136671: skull morphology 10 (Skull10, Published QTL Chr 7)
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse 716 Genes GS135273: "alcohol preference locus 14, female specific" (Alcp14, Published QTL Chr 7)
Expand Tier I Human 150 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 63 Genes GS173993: HP:0000506 Telecanthus
Expand Tier I Human 58 Genes GS173426: HP:0000889 Abnormality of the clavicles
Expand Tier I Human GO 3573 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human 81 Genes GS175456: HP:0100037 Abnormality of the scalp hair
Expand Tier I Human GO 369 Genes GS199224: GO:0019048 virus-host interaction
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 GO 1374 Genes GS203494: GO:0051704 multi-organism process
Expand Tier I Human GO 230 Genes GS208736: GO:0016746 transferase activity, transferring acyl groups
Expand Tier I Mouse 426 Genes GS135396: body growth early QTL 6 (Bgeq6, Published QTL Chr 7)
Expand Tier I Human 10 Genes GS174585: HP:0009929 Abnormality of the columella
Expand Tier I Mouse 673 Genes GS135720: determination of interleukin 4 commitment 2 (Dice2, Published QTL Chr 7)
Expand Tier I Human 148 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier I Human GO 91 Genes GS201970: GO:0016407 acetyltransferase activity
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 81 Genes GS172248: HP:0001373 Joint dislocation
Expand Tier I Human 41 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier II Mouse 880 Genes GS84196: alcohol preference locus (Published QTL, Chr 7)
Expand Tier I Human GO 1836 Genes GS201799: GO:0032550 purine ribonucleoside binding
Expand Tier I Human GO 1877 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 38 Genes GS176960: HP:0000430 Hypoplastic nasal alae
Expand Tier I Human 90 Genes GS173087: HP:0000499 Abnormality of the eyelashes
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human GO 1178 Genes GS201075: GO:0005794 Golgi apparatus
Expand Tier I Human GO 1827 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
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 577 Genes GS136899: ventral midbrain iron content 3 (Vmbic3, Published QTL Chr 7)
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 1393 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Human 281 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 758 Genes GS195665: GO:0017111 nucleoside-triphosphatase activity
Expand Tier I Human 72 Genes GS176488: HP:0010720 Abnormal hair pattern
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 1736 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 179 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human GO 1869 Genes GS200446: GO:0017076 purine nucleotide binding
Expand Tier I Human GO 694 Genes GS203305: GO:0016032 viral reproduction
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier III Mouse 398 Genes GS1140: Differential expression in brain of 22TNJ, a high alcohol-induced locomotor activation mutant
Expand Tier I Human GO 411 Genes GS203490: GO:0051701 interaction with host
Expand Tier I Human GO 2332 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 40 Genes GS172205: HP:0100326 Immunologic hypersensitivity
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse 2121 Genes GS128593: Average rotarod training latency Chr# 7
Expand Tier I Human GO 2108 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Mouse 757 Genes GS135758: experimental allergic encephalomyelitis susceptibility 26 (Eae26, Published QTL Chr 7)
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 108 Genes GS204657: GO:0016573 histone acetylation
Expand Tier I Human 179 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 212 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier I Human GO 1597 Genes GS207991: GO:0000003 reproduction
Expand Tier II Mouse 657 Genes GS84199: METH responses for body temperature (Published QTL, Chr 7)
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Human 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Mouse 716 Genes GS135272: "alcohol preference locus 12, male specific" (Alcp12, Published QTL Chr 7)
Expand Tier I Human GO 3118 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Mouse 852 Genes GS135542: cerebellar cAMP 5 (Ccmp5, Published QTL Chr 7)
Expand Tier I Human GO 465 Genes GS197319: GO:0003712 transcription cofactor activity
Expand Tier I Mouse 577 Genes GS135632: collagen induced arthritis 42 (Cia42, Published QTL Chr 7)
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Mouse 491 Genes GS136763: soft tissue heal 7 (Stheal7, Published QTL Chr 7)
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 77 Genes GS207098: GO:0008080 N-acetyltransferase activity
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 281 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 1592 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Human 83 Genes GS171602: HP:0001965 Abnormality of the scalp
Expand Tier I Human 16 Genes GS176404: HP:0000448 Prominent nose
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human 25 Genes GS171675: HP:0003839 Abnormality involving the epiphyses of the upper limbs
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 51 Genes GS202937: GO:0004402 histone acetyltransferase activity
Expand Tier I Mouse 870 Genes GS136924: VPA induced neural tube defect (Vpantd, Published QTL Chr 7)
Expand Tier I Human GO 2464 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier III Mouse 264 Genes GS800: UCSD_CEREBELLUM_Additive_Time_Pattern_4th
Expand Tier II Mouse 54 Genes GS35257: Hippocampus Gene expression correlates of Maximum startle response to 70 db in Males BXD
Expand Tier I Human GO 4151 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Mouse 786 Genes GS136762: soft tissue heal 6 (Stheal6, Published QTL Chr 7)
Expand Tier I Human 196 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Mouse 868 Genes GS136937: vertebral trabecular bone trait 4 (Vtbt4, Published QTL Chr 7)
Expand Tier I Human GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 2433 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Mouse GO 1006 Genes GS184267: GO:0005794 Golgi apparatus
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 16 Genes GS174486: HP:0000527 Long eyelashes
Expand Tier I Human GO 798 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 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human GO 447 Genes GS196889: GO:0044419 interspecies interaction between organisms
Expand Tier I Human 148 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human 12 Genes GS175927: HP:0000243 Trigonocephaly
Expand Tier I Mouse 852 Genes GS135817: ethanol induced thermoregulation 3 (Ethm3, Published QTL Chr 7)
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 426 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 Mouse 753 Genes GS136748: susceptibility to sialadenitis 3 (Ssial3, Published QTL Chr 7)
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 472 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 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3401 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Human 47 Genes GS175664: HP:0006505 Abnormality involving the epiphyses of the limbs
Expand Tier I Mouse 491 Genes GS136142: lithogenic gene 22 (Lith22, Published QTL Chr 7)
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 136 Genes GS171627: HP:0000470 Short neck
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 112 Genes GS171616: HP:0100490 Camptodactyly of finger
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 76 Genes GS171608: HP:0011338 Abnormality of mouth shape
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse 868 Genes GS135577: cystic fibrosis lung disease 4 (Cfld4, Published QTL Chr 7)
Expand Tier I Human GO 3201 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier II Mouse 760 Genes GS84195: nicotine sensitivity (Published QTL, Chr 7)
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 1862 Genes GS201794: GO:0032555 purine ribonucleotide binding
Expand Tier I Human GO 4314 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human 2 Genes GS172668: HP:0002474 Expressive language delay
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 5379 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 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 3626 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier III Mouse 936 Genes GS863: Differential expression across development in Sey Pax6 mutants and controls in an inverted-U (downward parabola).
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Mouse 727 Genes GS136609: colon tumor susceptibility 12 (Scc12, Published QTL Chr 7)
Expand Tier I Human 120 Genes GS171607: HP:0011337 Abnormality of mouth size
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 55 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 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 3310 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Mouse 523 Genes GS135440: bone mineral density 9 (Bmd9, Published QTL Chr 7)
Expand Tier I Mouse 426 Genes GS136732: susceptibility to lung cancer 8 (Sluc8, Published QTL Chr 7)
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
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 GO 2353 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 3287 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human 130 Genes GS173970: HP:0009473 Joint contracture of the hand
Expand Tier I Human GO 175 Genes GS208737: GO:0016747 transferase activity, transferring acyl groups other than amino-acyl groups
Expand Tier I Mouse 868 Genes GS135571: cystic fibrosis body weight 3 (Cfbw3, Published QTL Chr 7)
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human GO 267 Genes GS200351: GO:0016569 covalent chromatin modification
Expand Tier I Human 202 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 50 Genes GS173052: HP:0000325 Triangular face
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Human GO 3640 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Mouse 627 Genes GS136663: skin tumor susceptibility 2 (Skts2, Published QTL Chr 7)
Expand Tier I Human GO 3487 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human 39 Genes GS170829: HP:0002162 Low posterior hairline
Expand Tier I Human 201 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human GO 3721 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Mouse 755 Genes GS136368: obesity QTL 15 (Obq15, Published QTL Chr 7)
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 1 Genes GS171468: HP:0002608 Celiac disease
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human GO 1480 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 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 Mouse 757 Genes GS135985: hematocrit QTL 3 (Hemq3, Published QTL Chr 7)
Expand Tier I Human GO 146 Genes GS208180: GO:0004386 helicase activity
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 Mouse 127 Genes GS129150: IL-4 producing potential QTL (Il4ppq Published QTL Chr 7)
Expand Tier I Human 4 Genes GS170986: HP:0010761 Broad columella
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 4276 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human 250 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 2875 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 261 Genes GS204656: GO:0016570 histone modification
Expand Tier I Human 220 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human GO 3344 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 52 Genes GS174577: HP:0009924 Aplasia/Hypoplasia involving the nose
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
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 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human GO 793 Genes GS202822: GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides
Expand Tier I Mouse 612 Genes GS135999: hepatic lipase activity in BSB 1 (Hlbsb1, Published QTL Chr 7)
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 II Mouse 76 Genes GS35247: Hippocampus Gene expression correlates of Maximum startle to 120 db in Males BXD
Expand Tier I Human GO 718 Genes GS206695: GO:0044703 multi-organism reproductive process
Expand Tier I Human 112 Genes GS171810: HP:0005651 Flexion contracture of finger
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier II Mouse 155 Genes GS34262: Hippocampus Gene expression correlates of Suppression of activity in altered context in Males BXD
Expand Tier I Mouse 868 Genes GS136272: multigenic obesity QTL 1 (Mobq1, Published QTL Chr 7)
Expand Tier I Human GO 3737 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier I Human GO 1510 Genes GS201792: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Human 22 Genes GS174254: HP:0005920 Abnormality of the epiphyses of the phalanges of the hand
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 262 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human 40 Genes GS174330: HP:0002714 Downturned corners of mouth
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 130 Genes GS200930: GO:0006473 protein acetylation
Expand Tier II Mouse 875 Genes GS84197: alcohol preference locus 14, female specific (Alcp14, Published QTL, Chr 7)
Expand Tier I Human GO 3324 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Mouse 491 Genes GS135492: behavioral response to methamphetamines 6 (Brmth6, Published QTL Chr 7)
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 3354 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human GO 1850 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human 49 Genes GS173815: HP:0000736 Short attention span
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 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Mouse 716 Genes GS136716: susceptibility to lung cancer 19 (Sluc19, Published QTL Chr 7)
Expand Tier I Human 24 Genes GS174376: HP:0005924 Abnormality of the epiphyses of the hand
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier II Mouse 882 Genes GS84198: METH responses for home cage activity (Published QTL, Chr 7)
Expand Tier I Human 16 Genes GS175386: HP:0010230 Cone-shaped epiphyses of the phalanges of the hand
Expand Tier I Mouse 852 Genes GS135854: femoral bone morphometry 3 (Fembm3, Published QTL Chr 7)
Expand Tier I Human GO 143 Genes GS208190: GO:0018205 peptidyl-lysine modification
Expand Tier I Human GO 3199 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 211 Genes GS173206: HP:0003241 Genital hypoplasia
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 49 Genes GS173059: HP:0000322 Short philtrum
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Mouse 812 Genes GS136596: resistance to thymic deletion 1 (Rthyd1, Published QTL Chr 7)
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 4377 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human 150 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
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 60 Genes GS170970: HP:0000154 Wide mouth
Expand Tier I Mouse 432 Genes GS136261: "murine leukemia virus infection QTL, 1" (Mlviq1, Published QTL Chr 7)
Expand Tier I Human GO 1514 Genes GS203649: GO:0030554 adenyl nucleotide binding
Expand Tier I Mouse 2087 Genes GS128573: Ethanol Induced Hypothermia Chr# 7