SAR1B

From Wikipedia, the free encyclopedia

SAR1 gene homolog B (S. cerevisiae)

PDB rendering based on 1f6b.

Available structures: 1f6b, 2fa9, 2fmx

Identifiers

Symbol(s)

SAR1B; CMRD; GTBPB; SARA2

External IDs

OMIM: 607690 MGI: 1913647 HomoloGene: 7064

Gene ontology
Molecular Function:	• nucleotide binding • magnesium ion binding • GTP binding
Cellular Component:	• intracellular • endoplasmic reticulum • membrane
Biological Process:	• intracellular protein transport • ER to Golgi vesicle-mediated transport • small GTPase mediated signal transduction

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_001033503 (mRNA)
NP_001028675 (protein)

NM_025535 (mRNA)
NP_079811 (protein)

Location

Chr 5: 133.97 - 134 Mb

Chr 11: 51.61 - 51.64 Mb

Pubmed search

[1]

[2]

SAR1 gene homolog B (S. cerevisiae), also known as SAR1B, is a human gene.^[1]

[edit] References

^ Entrez Gene: SAR1B SAR1 gene homolog B (S. cerevisiae).

[edit] Further reading

Jardim DL, da Cunha AF, Duarte Ada S, et al. (2005). "Expression of Sara2 human gene in erythroid progenitors.". J. Biochem. Mol. Biol. 38 (3): 328-33. PMID 15943909.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40-5. doi:10.1038/ng1285. PMID 14702039.
Jones B, Jones EL, Bonney SA, et al. (2003). "Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders.". Nat. Genet. 34 (1): 29-31. doi:10.1038/ng1145. PMID 12692552.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932.
Aguglia U, Annesi G, Pasquinelli G, et al. (2000). "Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjögren syndrome.". Ann. Neurol. 47 (2): 260-4. PMID 10665502.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 149-56. PMID 9373149.
Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 171-4. PMID 8125298.