Homo sapiens Gene: SLC35C2 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Gene | IDBG-79031.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | SLC35C2 | ||||||||||||||||||
Gene Name | solute carrier family 35, member C2 | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Gene | ENSG00000080189 | ||||||||||||||||||
Encoded Proteins |
solute carrier family 35, member C2
solute carrier family 35, member C2
solute carrier family 35, member C2
solute carrier family 35, member C2
solute carrier family 35, member C2
solute carrier family 35, member C2
solute carrier family 35, member C2
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Protein Structure |
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Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
Entrez Gene | |||||||||||||||||||
Summary |
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. [provided by RefSeq, Jul 2008] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome 20:46345980-46364458 | ||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||
Band | q13.12 | ||||||||||||||||||
Transcripts | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Cross-References | |||||||||||||||||||
SwissProt | Q9NQQ7 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 51006 | ||||||||||||||||||
UniGene | Hs.742147 | ||||||||||||||||||
RefSeq | NM_173179 NM_001281457 NM_001281458 NM_001281459 NM_001281460 NM_015945 NM_173073 XM_005260414 | ||||||||||||||||||
HUGO | HGNC:17117 | ||||||||||||||||||
OMIM | |||||||||||||||||||
CCDS | CCDS13396 CCDS13397 CCDS63292 | ||||||||||||||||||
HPRD | 15371 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AF132949 AF455052 AL133227 BC014191 BC021138 BC025277 CH471077 | ||||||||||||||||||
GenPept | AAD27724 AAH14191 AAH21138 AAH25277 AAL59605 CAC00659 CAI40552 EAW75747 EAW75748 EAW75750 EAW75751 EAW75752 | ||||||||||||||||||
RNA Seq Atlas | 51006 | ||||||||||||||||||