full name
myosin VIIA

synonyms
DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B, MYO7A, ENSG00000137474

HGNC
HGNC:7606

Entrez Gene
Gene:4647

ENSEMBL
ENSG00000137474
ENSG00000261910

location
chr: 11
start: 76839302
stop: 76926286
strand: +

OMIM
OMIM:276903: MYO7A (Autosomal dominant inheritance)
OMIM:601317: Deafness, autosomal dominant 11
OMIM:600060: Deafness, autosomal recessive 2
OMIM:276900: Usher syndrome, type 1B

transcripts
NM_000260.3
NM_001127179.2
NM_001127180.1

pathways
Signal Transduction [NCBI:1269379] [REACTOME:R-HSA-162582] [PUBMED:17604717] [PUBMED:19648010] [PUBMED:16260143] [PUBMED:11742412] [PUBMED:19536106] [PUBMED:15863030] [PUBMED:19379690] [PUBMED:19458711] [PUBMED:19935667] [PUBMED:21252999] [PUBMED:15520807] [PUBMED:17496910] [PUBMED:15450248] [PUBMED:18043707] [PUBMED:16939974] [PUBMED:19762341] [PUBMED:18483217] [PUBMED:17084981] [PUBMED:21781017] [PUBMED:19619488]
The canonical retinoid cycle in rods (twilight vision) [NCBI:1269625] [REACTOME:R-HSA-2453902] [PUBMED:20188572] [PUBMED:16688755] [PUBMED:22074927] [PUBMED:21350678]
Visual phototransduction [NCBI:1269623] [REACTOME:R-HSA-2187338] [PUBMED:15384919] [PUBMED:22074928] [PUBMED:20188572] [PUBMED:21111842] [PUBMED:16688755] [PUBMED:8382952] [PUBMED:22658984] [PUBMED:20430952] [PUBMED:21350678] [PUBMED:22074927] [PUBMED:16011460] [PUBMED:11340090]