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Protein FAM186B

From Wikipedia, the free encyclopedia

FAM186B

Identifiers

FAM186B, C12orf25, family with sequence similarity 186 member B

External IDs

MGI: 3647604 HomoloGene: 69502 GeneCards: FAM186B

Gene location (Human)

Chr.	Chromosome 12 (human)^[1]

Band	12q13.12	Start	49,582,885 bp^[1]
Band	12q13.12	End	49,605,639 bp^[1]

Gene location (Mouse)

Chr.	Chromosome 15 (mouse)^[2]

Band	15\|15 F1	Start	99,168,899 bp^[2]
Band	15\|15 F1	End	99,193,769 bp^[2]

RNA expression pattern

Human

Mouse (ortholog)

Top expressed in

sural nerve

striated muscle tissue

skeletal muscle tissue

stromal cell of endometrium

pharynx

thymus

body of pancreas

right lobe of liver

bone marrow

upper respiratory tract

Top expressed in

spermatid

spermatocyte

testicle

ovary

adrenal gland

olfactory bulb

hypothalamus

cerebellar cortex

neocortex

visual cortex

More reference expression data

n/a

Species

Human

Mouse


84070


545136


ENSG00000135436


ENSMUSG00000078907


Q8IYM0


D3Z420

RefSeq (mRNA)


NM_032130


NM_001081254

RefSeq (protein)


NP_115506


NP_001074723

Location (UCSC)

Chr 12: 49.58 – 49.61 Mb

Chr 15: 99.17 – 99.19 Mb

PubMed search

^[3]

^[4]

View/Edit Human

View/Edit Mouse

Protein FAM186B is a protein that in humans is encoded by the FAM186B gene.^[5]^[6]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000135436 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000078907 – 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.
^ Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Bocher M, Blocker H, Bauersachs S, Blum H, Lauber J, Dusterhoft A, Beyer A, Kohrer K, Strack N, Mewes HW, Ottenwalder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A (Mar 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.
^ "Entrez Gene: C12orf25 chromosome 12 open reading frame 25".

Further reading

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.
Simpson JC, Wellenreuther R, Poustka A, et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Rep. 1 (3): 287–92. doi:10.1093/embo-reports/kvd058. PMC 1083732. PMID 11256614.
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 12 is a stub. You can help Wikipedia by expanding it.

This page was last edited on 4 March 2023, at 01:09

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