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GENE - TERM ANNOTATION REPORT

RGD ID: 731562
Species: Homo sapiens
RGD Object: Gene
Symbol: MSX1
Name: msh homeobox 1
Acc ID: DOID:0050567
Term: orofacial cleft
Definition: A physical disorder that is characterized by cleft lip and/or cleft palate that result in feeding, speech and hearing problems caused by failures during development. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/Cleft_lip_and_cleft_palate "DO" "DO", https://www.cdc.gov/ncbddd/birthdefects/surveillancemanual/chapters/chapter-4/chapter4-6.html "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)
MSX1 ISSMsx1 (Mus musculus)13592920MouseDOOMIM:119530 | OMIM:600625 | OMIM:600757 | OMIM:602966 | OMIM:608371 | OMIM:608864 | OMIM:608874 | OMIM:610361 | OMIM:612858 | OMIM:613705 | OMIM:613857 | OMIM:615892 
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