Homo sapiens Protein: SLC35A1 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-94140.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | SLC35A1 | ||||||||||||||||||
Protein Name | solute carrier family 35 (CMP-sialic acid transporter), member A1 | ||||||||||||||||||
Synonyms | CDG2F; CMPST; CST; hCST; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000358565 | ||||||||||||||||||
InnateDB Gene | IDBG-94128 (SLC35A1) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Transports CMP-sialic acid from the cytosol into Golgi vesicles where glycosyltransferases function. | ||||||||||||||||||
Subcellular Localization | Golgi apparatus membrane; Multi-pass membrane protein. | ||||||||||||||||||
Disease Associations | Congenital disorder of glycosylation 2F (CDG2F) [MIM:603585]: CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. {ECO:0000269PubMed:15576474}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | |||||||||||||||||||
Comments | |||||||||||||||||||
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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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR004689
UDP-galactose transporter IPR007271 Nucleotide-sugar transporter IPR013657 UAA transporter IPR021189 UDP/CMP-sugar transporter |
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PFAM |
PF04142
PF08449 |
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PRINTS | |||||||||||||||||||
PIRSF |
PIRSF005799
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SMART | |||||||||||||||||||
TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | P78382 | ||||||||||||||||||
PhosphoSite | PhosphoSite- | ||||||||||||||||||
TrEMBL | Q5W1L6 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 10559 | ||||||||||||||||||
UniGene | Hs.713287 | ||||||||||||||||||
RefSeq | NP_006407 | ||||||||||||||||||
HUGO | HGNC:11021 | ||||||||||||||||||
OMIM | 605634 | ||||||||||||||||||
CCDS | CCDS5010 | ||||||||||||||||||
HPRD | 09290 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AJ851888 AJ851890 AK293696 AL049697 BC017807 D87969 | ||||||||||||||||||
GenPept | AAH17807 BAA13522 BAG57132 CAB76857 CAH65468 CAH65470 | ||||||||||||||||||