Homo sapiens Protein: SLC35A2 | |||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Summary | |||||||||||||||||||
InnateDB Protein | IDBP-64577.7 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | SLC35A2 | ||||||||||||||||||
Protein Name | solute carrier family 35 (UDP-galactose transporter), member A2 | ||||||||||||||||||
Synonyms | CDG2M; CDGX; UDP-Gal-Tr; UGALT; UGAT; UGT; UGT1; UGT2; UGTL; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000365704 | ||||||||||||||||||
InnateDB Gene | IDBG-64571 (SLC35A2) | ||||||||||||||||||
Protein Structure |
![]() |
||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Transports nucleotide sugars from the cytosol into Golgi vesicles where glycosyltransferases function. | ||||||||||||||||||
Subcellular Localization | Golgi apparatus membrane; Multi-pass membrane protein. | ||||||||||||||||||
Disease Associations | Congenital disorder of glycosylation 2M (CDG2M) [MIM:300896]: A disorder characterized by developmental delay, hypotonia, ocular anomalies, and brain malformations. Othere more variable clinical features included seizures, hypsarrhythmia, poor feeding, microcephaly, recurrent infections, dysmorphic features, shortened limbs, and coagulation defects. Congenital disorders of glycosylation are caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins and a wide variety of clinical features. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. {ECO:0000269PubMed:23561849}. 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 3 experimentally validated interaction(s) in this database.
|
||||||||||||||||||
Gene Ontology | |||||||||||||||||||
Molecular Function |
|
||||||||||||||||||
Biological Process |
|
||||||||||||||||||
Cellular Component |
|
||||||||||||||||||
Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR000620
Drug/metabolite transporter IPR004689 UDP-galactose transporter IPR007271 Nucleotide-sugar transporter IPR013657 UAA transporter IPR021189 UDP/CMP-sugar transporter |
||||||||||||||||||
PFAM |
PF00892
PF04142 PF08449 |
||||||||||||||||||
PRINTS | |||||||||||||||||||
PIRSF |
PIRSF005799
|
||||||||||||||||||
SMART | |||||||||||||||||||
TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | P78381 | ||||||||||||||||||
PhosphoSite | PhosphoSite-P78381 | ||||||||||||||||||
TrEMBL | C9JCV5 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 7355 | ||||||||||||||||||
UniGene | Hs.733341 | ||||||||||||||||||
RefSeq | NP_001035963 | ||||||||||||||||||
HUGO | HGNC:11022 | ||||||||||||||||||
OMIM | 314375 | ||||||||||||||||||
CCDS | CCDS43937 | ||||||||||||||||||
HPRD | 02441 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB042425 AF207550 AK290284 AK292816 AK293415 AK298484 BC035747 CH471224 D84454 D88146 | ||||||||||||||||||
GenPept | AAH35747 BAA12673 BAA13545 BAA95614 BAA95615 BAF82973 BAF85505 BAG56922 BAG60694 EAW50733 EAW50734 | ||||||||||||||||||