GBAS (gene)

NIPSNAP2
Identifiers
Aliases	NIPSNAP2, GBAS, glioblastoma amplified sequence, nipsnap homolog 2
External IDs	OMIM: 603004; MGI: 1278343; HomoloGene: 1137; GeneCards: NIPSNAP2; OMA:NIPSNAP2 - orthologs
Gene location (Human)
Chr.	Chromosome 7 (human)
End	56,000,181 bp
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)
End	129,835,391 bp
RNA expression pattern
	Top expressed in
	biceps brachii; ; Skeletal muscle tissue of biceps brachii; ; vastus lateralis muscle; ; right ventricle; ; Skeletal muscle tissue of rectus abdominis; ; thoracic diaphragm; ; gastrocnemius muscle; ; deltoid muscle; ; muscle of thigh; ; triceps brachii muscle;
	Top expressed in
	cardiac muscle tissue of left ventricle; ; muscle of thigh; ; choroid plexus of fourth ventricle; ; aortic valve; ; atrioventricular valve; ; skeletal muscle tissue; ; plantaris muscle; ; lip; ; superior surface of tongue; ; interventricular septum;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	protein binding;
Cellular component	integral component of plasma membrane; membrane; mitochondrion; cytoplasm; mitochondrial outer membrane;
Biological process	oxidative phosphorylation; negative regulation of ATP citrate synthase activity; ATP biosynthetic process; positive regulation of high voltage-gated calcium channel activity; mitochondrion organization;
	Sources:Amigo / QuickGO
Orthologs
	2631
	14467
	ENSG00000146729
	ENSMUSG00000029432
	O75323
	O55126
	NM_001483; NM_001202469
	NM_008095
	NP_001189398; NP_001474
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

Protein NipSnap homolog 2 is a protein that in humans is encoded by the GBAS gene.^[5]^[6]^[7]

Chromosomal region 7p12, which contains GBAS, is amplified in approximately 40% of glioblastomas, the most common and malignant form of central nervous system tumor. The predicted 286-amino acid protein contains a signal peptide, a transmembrane domain, and 2 tyrosine phosphorylation sites. The GBAS transcript is expressed most abundantly in heart and skeletal muscle. GBAS protein might be involved in vesicular transport.^[7]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000146729 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000029432 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Wang XY, Smith DI, Liu W, James CD (Aug 1998). "GBAS, a novel gene encoding a protein with tyrosine phosphorylation sites and a transmembrane domain, is co-amplified with EGFR". Genomics. 49 (3): 448–51. doi:10.1006/geno.1998.5239. PMID 9615231.
^ Seroussi E, Pan HQ, Kedra D, Roe BA, Dumanski JP (Jul 1998). "Characterization of the human NIPSNAP1 gene from 22q12: a member of a novel gene family". Gene. 212 (1): 13–20. doi:10.1016/S0378-1119(98)00098-5. PMID 9661659.
^ ^a ^b "Entrez Gene: GBAS glioblastoma amplified sequence".

Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006". Nucleic Acids Res. 34 (Database issue): D415–8. doi:10.1093/nar/gkj139. PMC 1347501. PMID 16381901.
Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to Biology: A Functional Genomics Pipeline". Genome Res. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMC 528930. PMID 15489336.
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. PMC 528928. 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.
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. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Hartley JL, Temple GF, Brasch MA (2001). "DNA Cloning Using In Vitro Site-Specific Recombination". Genome Res. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948. PMID 11076863.

This article on a gene on human chromosome 7 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000146729 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000029432 – 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.

[pmid9615231-5] Wang XY, Smith DI, Liu W, James CD (Aug 1998). "GBAS, a novel gene encoding a protein with tyrosine phosphorylation sites and a transmembrane domain, is co-amplified with EGFR". Genomics. 49 (3): 448–51. doi:10.1006/geno.1998.5239. PMID 9615231.

[pmid9661659-6] Seroussi E, Pan HQ, Kedra D, Roe BA, Dumanski JP (Jul 1998). "Characterization of the human NIPSNAP1 gene from 22q12: a member of a novel gene family". Gene. 212 (1): 13–20. doi:10.1016/S0378-1119(98)00098-5. PMID 9661659.

[entrez-7] "Entrez Gene: GBAS glioblastoma amplified sequence".

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GBAS (gene)

References

Further reading