ALG11

Asparagine-linked glycosylation protein 11 is an enzyme encoded by the ALG11 gene.[5]

ALG11
Identifiers
AliasesALG11, CDG1P, GT8, alpha-1,2-mannosyltransferase, ALG11 alpha-1,2-mannosyltransferase
External IDsOMIM: 613666 MGI: 2142632 HomoloGene: 68893 GeneCards: ALG11
Gene location (Human)
Chr.Chromosome 13 (human)[1]
Band13q14.3Start52,012,398 bp[1]
End52,033,600 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

440138

207958

Ensembl

ENSG00000253710

ENSMUSG00000063362

UniProt

Q2TAA5

Q3TZM9

RefSeq (mRNA)

NM_001004127

NM_001243161
NM_183142

RefSeq (protein)

NP_001004127

NP_001230090
NP_898965

Location (UCSC)Chr 13: 52.01 – 52.03 MbChr 8: 22.06 – 22.07 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

See also

[6]

[7]

References

  1. GRCh38: Ensembl release 89: ENSG00000253710 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000063362 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: asparagine-linked glycosylation 11".
  6. Cipollo, JF; Trimble, RB; Chi, JH; Yan, Q; Dean, N (2001). "The yeast ALG11 gene specifies addition of the terminal alpha 1,2-Man to the Man5GlcNAc2-PP-dolichol N-glycosylation intermediate formed on the cytosolic side of the endoplasmic reticulum". J. Biol. Chem. 276 (24): 21828–40. doi:10.1074/jbc.m010896200. PMID 11278778.
  7. Gao, XD; Nishikawa, A; Dean, N. (Jun 2004). "Physical interactions between the Alg1, Alg2, and Alg11 mannosyltransferases of the endoplasmic reticulum. 2004". Glycobiology. 14 (6): 559–70. CiteSeerX 10.1.1.572.6611. doi:10.1093/glycob/cwh072. PMID 15044395.

Further reading

  • Rohozinski J, Lamb DJ, Bishop CE (2006). "UTP14c is a recently acquired retrogene associated with spermatogenesis and fertility in man". Biol. Reprod. 74 (4): 644–51. doi:10.1095/biolreprod.105.046698. PMID 16354793.
  • Rind N, Schmeiser V, Thiel C, et al. (2010). "A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip". Hum. Mol. Genet. 19 (8): 1413–24. doi:10.1093/hmg/ddq016. PMID 20080937.
  • Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Mol. Syst. Biol. 3 (1): 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.
  • Cipollo JF, Trimble RB, Chi JH, Yan Q, Dean N (June 2001). "The yeast ALG11 gene specifies addition of the terminal alpha 1,2-Man to the Man5GlcNAc2-PP-dolichol N-glycosylation intermediate formed on the cytosolic side of the endoplasmic reticulum". J. Biol. Chem. 276 (24): 21828–40. doi:10.1074/jbc.M010896200. PMID 11278778.


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