PABIR family member 2

PABIR2
Identifiers
Aliases	PABIR2, SPACIA2, family with sequence similarity 122B, PABIR family member 2, FAM122B
External IDs	MGI: 1926005; GeneCards: PABIR2
Gene location (Human)
Chr.	X chromosome (human)
End	134,797,232 bp
Gene location (Mouse)
Chr.	X chromosome (mouse)
End	52,358,682 bp
RNA expression pattern
	Top expressed in
	endothelial cell; ; germinal epithelium; ; pancreatic epithelial cell; ; Brodmann area 23; ; thymus; ; epithelium of nasopharynx; ; mucosa of ileum; ; secondary oocyte; ; palpebral conjunctiva; ; primary visual cortex;
	Top expressed in
	superior cervical ganglion; ; atrioventricular valve; ; zygote; ; umbilical cord; ; lumbar spinal ganglion; ; toe; ; secondary oocyte; ; atrium; ; dermis; ; second toe;
	More reference expression data
	n/a
Orthologs
Databases	NCBI: entry; OMA: entry
	159090
	78755
	ENSG00000156504
	ENSMUSG00000036022
	Q7Z309
	Q6NZE7
NM_001166599; NM_001166600; NM_001170756; NM_001170757; NM_145284;
	NM_001331088; NM_001331089; NM_001331090; NM_001331091; NM_001331092; NM_001331093; NM_001331094; NM_001387468; NM_001387469
	NM_001166365; NM_001166583; NM_030167
NP_001160071; NP_001160072; NP_001164227; NP_001164228; NP_001318017;
	NP_001318018; NP_001318019; NP_001318020; NP_001318021; NP_001318022; NP_001318023; NP_660327
	NP_001159837; NP_001160055; NP_084443
	Wikidata
View/Edit Human	View/Edit Mouse

PABIR family member 2 is a protein that in humans is encoded by the PABIR2 gene (previously FAM122B). Not much has been reported about the function of this protein, but it is predicted to act as a collagen trimer.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000156504 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000036022 – 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.
↑ Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, et al. (Dec 2002). "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.
1 2 "Entrez Gene: FAM122B family with sequence similarity 122B".

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.
Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, et al. (2001). "Toward a Catalog of Human Genes and Proteins: Sequencing and Analysis of 500 Novel Complete Protein Coding Human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.{{cite journal}}: CS1 maint: overridden setting (link)
Ota T, Suzuki Y, Nishikawa T, Otsuki T, Sugiyama T, Irie R, 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.{{cite journal}}: CS1 maint: overridden setting (link)
Gerhard DS, Wagner L, Feingold EA, Shenmen CM, Grouse LH, Schuler G, 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.{{cite journal}}: CS1 maint: overridden setting (link)
Wiemann S, Arlt D, Huber W, Wellenreuther R, Schleeger S, Mehrle A, 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.{{cite journal}}: CS1 maint: overridden setting (link)
Ross MT, Grafham DV, Coffey AJ, Scherer S, McLay K, Muzny D, et al. (2005). "The DNA sequence of the human X chromosome". Nature. 434 (7031): 325–37. Bibcode:2005Natur.434..325R. doi:10.1038/nature03440. PMC 2665286. PMID 15772651.{{cite journal}}: CS1 maint: overridden setting (link)
Mehrle A, Rosenfelder H, Schupp I, Del Val C, Arlt D, Hahne F, 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.{{cite journal}}: CS1 maint: overridden setting (link)
Beausoleil SA, Villén J, Gerber SA, Rush J, Gygi SP (2006). "A probability-based approach for high-throughput protein phosphorylation analysis and site localization". Nat. Biotechnol. 24 (10): 1285–92. doi:10.1038/nbt1240. PMID 16964243. S2CID 14294292.{{cite journal}}: CS1 maint: overridden setting (link)

This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by adding missing information.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000156504 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000036022 – 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.

[pmid12477932-5] Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, et al. (Dec 2002). "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.

[entrez-6] 1 2 "Entrez Gene: FAM122B family with sequence similarity 122B".

PABIR family member 2

See also

References

Further reading