Gene Details



COLQ and homologs in 4 species are found in 239 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 Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Mouse GO 335 Genes GS193273: GO:0005578 proteinaceous extracellular matrix
Expand Tier III Mouse 2551 Genes GS866: Linear decrease in expression in both Pax6 (Sey) mutants and controls.
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse 576 Genes GS136852: Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 3 (Tmevd3, Published QTL Chr 14)
Expand Tier I Mouse 393 Genes GS136223: mandible length 15 (Manln15, Published QTL Chr 14)
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Mouse 576 Genes GS135493: behavioral response to methamphetamines 9 (Brmth9, Published QTL Chr 14)
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Mouse GO 2260 Genes GS189855: GO:0043168 anion binding
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse MP 376 Genes GS168021: MP:0000745 tremors
Expand Tier I Human 10 Genes GS175458: HP:0003554 Type 2 muscle fiber atrophy
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human GO 22 Genes GS207578: GO:0007271 synaptic transmission, cholinergic
Expand Tier I Mouse MP 114 Genes GS167664: MP:0008569 lethality at weaning
Expand Tier I Human GO 89 Genes GS208328: GO:0005604 basement membrane
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
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 Human 36 Genes GS173618: HP:0002747 Respiratory insufficiency due to muscle weakness
Expand Tier I Rat 362 Genes GS127683: Alcohol consumption QTL 7 (Alc7, Published QTL, Chr 16)
Expand Tier I Mouse GO 116 Genes GS184926: GO:0001505 regulation of neurotransmitter levels
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Mouse MP 304 Genes GS168013: MP:0010831 partial lethality
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human GO 131 Genes GS207420: GO:0008201 heparin binding
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Mouse GO 5111 Genes GS187146: GO:0044700 single organism signaling
Expand Tier I Mouse 569 Genes GS136627: Stem cell proliferation 9 (Scpro9, Published QTL Chr 14)
Expand Tier I Human GO 1099 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human 14 Genes GS175354: HP:0003473 Fatigable weakness
Expand Human 89 Genes GS219923: http://www.broadinstitute.org/gsea/msigdb/cards/PROTEINACEOUS_EXTRACELLULAR_MATRIX
Expand Tier I Human GO 173 Genes GS209592: GO:0005539 glycosaminoglycan binding
Expand Tier I Mouse 393 Genes GS136961: weight adult 3 (Wta3, Published QTL Chr 14)
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
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 Human 236 Genes GS219934: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_SPACE
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Human 91 Genes GS219707: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_MATRIX
Expand Tier I Human GO 1668 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human GO 1559 Genes GS201869: GO:0008104 protein localization
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Mouse MP 126 Genes GS170610: MP:0001051 abnormal somatic motor system morphology
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 854 Genes GS203972: GO:0005615 extracellular space
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse GO 734 Genes GS178334: GO:0007267 cell-cell signaling
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Mouse 569 Genes GS136040: insulin dependent diabetes susceptibility 12 (Idd12, Published QTL Chr 14)
Expand Tier I Human CTD 291 Genes GS124722: kojic acid interacting genes (MeSH:C011890) in CTD
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Mouse GO 87 Genes GS181440: GO:0005581 collagen
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Human 48 Genes GS219897: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_MATRIX_PART
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 192 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Human 15 Genes GS219761: http://www.broadinstitute.org/gsea/msigdb/cards/AMINO_ACID_DERIVATIVE_METABOLIC_PROCESS
Expand Tier I Mouse MP 273 Genes GS167796: MP:0008770 decreased survivor rate
Expand Tier I Mouse GO 10 Genes GS188692: GO:0042135 neurotransmitter catabolic process
Expand Tier I Mouse 809 Genes GS129166: plasma plant sterol 1 (Plast1 Published QTL Chr 14)
Expand Tier I Human GO 1097 Genes GS201255: GO:0044421 extracellular region part
Expand Tier II Mouse 582 Genes GS84271: METH responses for chewing (Published QTL, Chr 14)
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Mouse 323 Genes GS136949: white blood cell quantitative locus 6 (Wbcq6, Published QTL Chr 14)
Expand Tier I Mouse MP 1082 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 735 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Mouse 354 Genes GS129167: plasma plant sterol 1a (Plast1a Published QTL Chr 14)
Expand Human 438 Genes GS219938: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Human 89 Genes GS219706: http://www.broadinstitute.org/gsea/msigdb/cards/PROTEINACEOUS_EXTRACELLULAR_MATRIX
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 188 Genes GS201611: GO:0097367 carbohydrate derivative binding
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human 14 Genes GS174744: HP:0003398 Abnormality of the neuromuscular junction
Expand Tier I Human CTD 480 Genes GS122634: Ketone Bodies interacting genes (MeSH:D007657) in CTD
Expand Tier I Mouse GO 151 Genes GS192650: GO:0005539 glycosaminoglycan binding
Expand Tier II Mouse 559 Genes GS84274: METH responses for home cage activity (Published QTL, Chr 14)
Expand Tier I Mouse GO 5221 Genes GS179211: GO:0007154 cell communication
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Mouse GO 22 Genes GS188690: GO:0042133 neurotransmitter metabolic process
Expand Tier I Human 78 Genes GS172684: HP:0003307 Hyperlordosis
Expand Tier I Human GO 5 Genes GS207645: GO:1900619 acetate ester metabolic process
Expand Tier II Mouse 661 Genes GS84275: cocaine seizure (Published QTL, Chr 14)
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse GO 1395 Genes GS185366: GO:0044248 cellular catabolic process
Expand Tier I Mouse 428 Genes GS136279: modifier of ocular retardation 2 (Modor2, Published QTL Chr 14)
Expand Human 20 Genes GS219822: http://www.broadinstitute.org/gsea/msigdb/cards/NITROGEN_COMPOUND_CATABOLIC_PROCESS
Expand Tier II Mouse 532 Genes GS84273: METH responses for home cage activity (Published QTL, Chr 14)
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Human 18 Genes GS219845: http://www.broadinstitute.org/gsea/msigdb/cards/AMINE_CATABOLIC_PROCESS
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human GO 20 Genes GS208327: GO:0005605 basal lamina
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 89 Genes GS198230: GO:0005581 collagen
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Mouse MP 52 Genes GS166453: MP:0011084 partial lethality at weaning
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human GO 1825 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human 34 Genes GS171944: HP:0003324 Generalized muscle weakness
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
Expand Tier I Human 58 Genes GS172853: HP:0004303 Abnormality of muscle fibers
Expand Tier I Mouse 305 Genes GS136597: resistance to thymic deletion 3 (Rthyd3, Published QTL Chr 14)
Expand Human 91 Genes GS219924: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_MATRIX
Expand Human 236 Genes GS219717: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_SPACE
Expand Tier I Human GO 2139 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Mouse GO 377 Genes GS179537: GO:0031012 extracellular matrix
Expand Tier I Human GO 2 Genes GS207510: GO:0001507 acetylcholine catabolic process in synaptic cleft
Expand Tier I Mouse GO 2172 Genes GS180156: GO:0065008 regulation of biological quality
Expand Tier I Mouse GO 5111 Genes GS189484: GO:0023052 signaling
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 370 Genes GS197471: GO:0044456 synapse part
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 751 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse MP 875 Genes GS168958: MP:0003492 abnormal involuntary movement
Expand Tier I Mouse GO 188 Genes GS184450: GO:0044420 extracellular matrix part
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Mouse MP 1007 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human 10 Genes GS173673: HP:0100295 Muscle fiber atrophy
Expand Human 438 Genes GS219721: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 360 Genes GS210217: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human GO 185 Genes GS201254: GO:0044420 extracellular matrix part
Expand Tier I Rat 136 Genes GS128035: Alcohol consumption QTL 13 (Alc13, Published QTL, Chr 16)
Expand Tier I Human 12 Genes GS174326: HP:0003199 Decreased muscle mass
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Human 15 Genes GS174533: HP:0003388 Easy fatigability
Expand Tier I Human GO 5 Genes GS196213: GO:0008291 acetylcholine metabolic process
Expand Tier I Human GO 7 Genes GS209040: GO:0043083 synaptic cleft
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Mouse GO 563 Genes GS187747: GO:0019226 transmission of nerve impulse
Expand Tier I Mouse 583 Genes GS136712: susceptibility to lung cancer 13 (Sluc13, Published QTL Chr 14)
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Rat 568 Genes GS128036: Alcohol consumption QTL 11 (Alc11, Published QTL, Chr 16)
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Human 132 Genes GS219791: http://www.broadinstitute.org/gsea/msigdb/cards/AMINE_METABOLIC_PROCESS
Expand Tier I Mouse 583 Genes GS135777: epistatic circling SWR/J (ecs, Published QTL Chr 14)
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Human 28 Genes GS219894: http://www.broadinstitute.org/gsea/msigdb/cards/BASEMENT_MEMBRANE
Expand Human 28 Genes GS219677: http://www.broadinstitute.org/gsea/msigdb/cards/BASEMENT_MEMBRANE
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human GO 651 Genes GS195082: GO:0007268 synaptic transmission
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human 7 Genes GS177009: HP:0003403 EMG: decremental response of compound muscle action potential (CMAP) to repetitive nerve stimulation
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 266 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 39 Genes GS174455: HP:0004347 Weakness of muscles of respiration
Expand Tier III Mouse 5726 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Human GO 137 Genes GS201740: GO:0001505 regulation of neurotransmitter levels
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 587 Genes GS185880: GO:0035637 multicellular organismal signaling
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier II Mouse 718 Genes GS84276: nicotine sensitivity (Published QTL, Chr 14)
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Mouse GO 448 Genes GS178333: GO:0007268 synaptic transmission
Expand Tier II Mouse 527 Genes GS84272: METH responses for body temperature (Published QTL, Chr 14)
Expand Tier I Mouse GO 731 Genes GS179748: GO:0030054 cell junction
Expand Tier I Human 5 Genes GS173852: HP:0003436 Prolonged miniature endplate currents
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Mouse GO 1041 Genes GS184451: GO:0044421 extracellular region part
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Mouse GO 1825 Genes GS193270: GO:0005576 extracellular region
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Mouse GO 118 Genes GS190528: GO:0008201 heparin binding
Expand Human 48 Genes GS219680: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_MATRIX_PART
Expand Tier I Human 7 Genes GS171703: HP:0003443 Decreased size of nerve terminals
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 4772 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human 96 Genes GS174135: HP:0002015 Dysphagia
Expand Tier I Human 161 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 2 Genes GS200023: GO:0006581 acetylcholine catabolic process
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Mouse GO 554 Genes GS188813: GO:0045202 synapse
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human CTD 323 Genes GS121837: bexarotene interacting genes (MeSH:C095105) in CTD
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Mouse 393 Genes GS135452: bone length and organs 8 (Bod8, Published QTL Chr 14)
Expand Tier I Human GO 488 Genes GS205674: GO:0045202 synapse
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 17 Genes GS201868: GO:0008105 asymmetric protein localization
Expand Human 329 Genes GS219927: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse 393 Genes GS136049: insulin dependent diabetes susceptibility 8 (Idd8, Published QTL Chr 14)
Expand Tier I Human GO 26 Genes GS205549: GO:0042133 neurotransmitter metabolic process
Expand Tier I Mouse MP 99 Genes GS170608: MP:0001053 abnormal neuromuscular synapse morphology
Expand Tier I Human 48 Genes GS172577: HP:0003690 Limb muscle weakness
Expand Tier I Human GO 9 Genes GS205551: GO:0042135 neurotransmitter catabolic process
Expand Tier I Human 16 Genes GS174400: HP:0001612 Weak cry
Expand Tier I Mouse GO 168 Genes GS184799: GO:0097367 carbohydrate derivative binding
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Human 92 Genes GS219805: http://www.broadinstitute.org/gsea/msigdb/cards/AMINO_ACID_AND_DERIVATIVE_METABOLIC_PROCESS
Expand Tier I Mouse GO 1648 Genes GS190954: GO:0009056 catabolic process
Expand Tier I Mouse 393 Genes GS136224: mandible length 16 (Manln16, Published QTL Chr 14)
Expand Human 329 Genes GS219710: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Mouse MP 163 Genes GS164491: MP:0009538 abnormal synapse morphology
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse 504 Genes GS135743: dystrophic cardiac calcinosis 4 (Dyscalc4, Published QTL Chr 14)
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 1777 Genes GS164263: MP:0002083 premature death
Expand Tier I Human GO 735 Genes GS196511: GO:0030054 cell junction