QuickView for STT3B (gene)

Gene Symbol:

STT3B Homo sapiens

Full name:

STT3B, catalytic subunit of the oligosaccharyltransferase complex

Synonyms:

CDG1X, SIMP, STT3-B, dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, STT3, subunit of the oligosaccharyltransferase complex, homolog B, STT3B, subunit of the oligosaccharyltransferase complex (catalytic), dolichyl-diphosphooligosaccharide protein glycotransferase, homolog of yeast STT3, oligosaccharyl transferase subunit STT3B, source of immunodominant MHC-associated peptides homolog

Genomic Location:

Chr 3: 31549495-31652560

Description:

The protein encoded by this gene is a catalytic subunit of a protein complex that transfers oligosaccharides onto asparagine residues. Defects in this gene are a cause of congenital disorder of glycosylation Ix (CDG1X).

The protein encoded by this gene is a catalytic subunit of a protein complex that transfers oligosaccharides onto asparagine residues. Defects in this gene are a cause of congenital disorder of glycosylation Ix (CDG1X).

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  D. melanogaster ,  C. elegans ,  Saccharomyces cerevisiae ,  Macaca mulatta ,  Schizosaccharomyces pombe ,  Danio rerio ,  Gallus gallus ,  Canis lupus familiaris ,  Bos taurus ,  Pan troglodytes

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

CMYB_01 ,  USF_Q6 ,  TCANNTGAY_SREBP1_01 ,  E2F1_Q4_01 ,  CACGTG_MYC_Q2 ,  E2F4DP1_01 ,  E2F_Q6_01 ,  PBX1_01 ,  MYB_Q5_01 ,  WHN_B ,  HNF4_01 ,  E2F_Q6 ,  E2F1_Q6_01 ,  E2F_Q4 ,  GGGCGGR_SP1_Q6 ,  E2F1DP2_01 ,  IRF_Q6 ,  MEIS1_01 ,  E2F_03 ,  E2F1DP1_01 ,  E2F_Q4_01 ,  USF_Q6_01 ,  E2F1DP1RB_01 ,  E2F_02 ,  E2F1_Q3 ,  TGACAGNY_MEIS1_01 ,  E2F4DP2_01 ,  RCGCANGCGY_NRF1_Q6 ,  E2F_Q3 ,  TGACATY_UNKNOWN ,  E2F_Q3_01 ,  E2F1_Q6 ,  SGCGSSAAA_E2F1DP2_01 ,  MYB_Q3

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Cytogenetic Map:

3p23

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