| kinesin family member 21A | OKDB#: 5498 |
| Symbols: | KIF21A | Species: | human | ||
| Synonyms: | FEOM1, CFEOM1, FEOM3A | Locus: | 12q12 in Homo sapiens |
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OMIM
Entrez Gene
Mammalian Reproductive Genetics Endometrium Database Resource Orthologous Genes UCSC Genome Browser GEO Profiles new! Amazonia (transcriptome data) new! R-L INTERACTIONS MGI |
| General Comment | NCBI Summary: This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010] | ||||
| General function | Microtubule binding | ||||
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| Cellular localization | microtubule | ||||
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| Ovarian localization | Oocyte, Granulosa | ||||
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| Mutations | 0 mutations | ||||
| Genomic Region | show genomic region | ||||
| Phenotypes and GWAS | show phenotypes and GWAS | ||||
| Links |
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| created: | Sept. 12, 2017, 10:30 a.m. | by: |
system email:
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| last update: | Sept. 12, 2017, 10:32 a.m. | by: | hsueh email: |
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