SLC35C2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Solute carrier family 35 member C2 is a protein that in humans is encoded by the SLC35C2 gene.[5][6][7]

AliasesSLC35C2, BA394O2.1, C20orf5, CGI-15, OVCOV1, solute carrier family 35 member C2
End46,364,458 bp[1]
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SLC35C2
Identifiers
AliasesSLC35C2, BA394O2.1, C20orf5, CGI-15, OVCOV1, solute carrier family 35 member C2
External IDsMGI: 2385166; HomoloGene: 6581; GeneCards: SLC35C2; OMA:SLC35C2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)
RefSeq (protein)
Location (UCSC)Chr 20: 46.35 – 46.36 MbChr 2: 165.12 – 165.13 Mb
PubMed search[3][4]
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Oxygenation levels play an important role in the regulation of cellular invasiveness which occurs during early implantation when the trophoblast cells invade the uterus as well as during tumour progression and metastasis. This gene, which is regulated by oxygen tension, is induced in hypoxic trophoblast cells and is overexpressed in ovarian cancer. Two protein isoforms are encoded by transcript variants of this gene.[7]

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