SNX21
From Infogalactic: the planetary knowledge core
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| Sorting nexin family member 21 | |||||||||||||
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| Identifiers | |||||||||||||
| Symbols | SNX21 ; C20orf161; PP3993; SNX-L; dJ337O18.4 | ||||||||||||
| External IDs | MGI: 1917729 HomoloGene: 43132 GeneCards: SNX21 Gene | ||||||||||||
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| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 90203 | 101113 | |||||||||||
| Ensembl | ENSG00000124104 | ENSMUSG00000050373 | |||||||||||
| UniProt | Q969T3 | Q149Q9 | |||||||||||
| RefSeq (mRNA) | NM_001042632 | NM_133924 | |||||||||||
| RefSeq (protein) | NP_001036097 | NP_598685 | |||||||||||
| Location (UCSC) | Chr 20: 45.83 – 45.84 Mb |
Chr 2: 164.79 – 164.79 Mb |
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| PubMed search | [1] | [2] | |||||||||||
Sorting nexin-21 is a protein that in humans is encoded by the SNX21 gene.[1][2][3]
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. The specific function of this protein has not been determined. Multiple transcript variants encoding distinct isoforms have been identified for this gene.[3]
References
Further reading
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