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GENE - TERM ANNOTATION REPORT

RGD ID: 14128523
Species: Sus scrofa
RGD Object: Gene
Symbol: LOC100623720
Name: collagen alpha-1(VI) chain
Acc ID: DOID:0050663
Term: Bethlem myopathy
Definition: A congenital muscular dystrophy that is characterized by myopathy and joint contractures that progresses slowly, has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the COL6A1 gene, the COL6A2 gene, or the COL6A3 gene. (DO)
Definition Source(s): https://rarediseases.info.nih.gov/diseases/873/bethlem-myopathy "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
LOC100623720 ISOCOL6A1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Myopathy, benign congenital, with contracturesPMID:10419498 PMID:11707460 PMID:12840783 PMID:15689448 PMID:15955946 PMID:16088929 PMID:16130093 PMID:16199547 PMID:17015493 PMID:17576681 PMID:17785673 PMID:17785674 PMID:17886299 PMID:18366090 PMID:18414213 PMID:18642359 PMID:18825676 PMID:19204719 PMID:19344236 PMID:19564581 PMID:20301676 PMID:20302629 PMID:20882040 PMID:20976770 PMID:20981092 PMID:21280092 PMID:22075033 PMID:22789865 PMID:22975586 PMID:23040494 PMID:23572247 PMID:23757202 PMID:24033266 PMID:24038877 PMID:24223098 PMID:24271325 PMID:24801232 PMID:24959844 PMID:25741868 PMID:25749816 PMID:26467025 PMID:26867126 PMID:27363342 PMID:27708273 PMID:27854213 PMID:27884173 PMID:28182637 PMID:28492532 PMID:29419890 PMID:30564623 PMID:32154989 PMID:34008892 PMID:34167565 PMID:7551830 PMID:7695699 PMID:8218237 PMID:8730294 PMID:9536098 PMID:9724608
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