CSMD2

CUB and sushi domain-containing protein 2 is a protein that in humans is encoded by the CSMD2 gene.[5][6][7]

CSMD2
Identifiers
Aliases	CSMD2, dJ1007G16.1, dJ1007G16.2, dJ947L8.1, CUB and Sushi multiple domains 2
External IDs	OMIM: 608398 MGI: 2386401 HomoloGene: 89034 GeneCards: CSMD2
Gene location (Human) Chr. Chromosome 1 (human)[1] Band 1p35.1 Start 33,513,999 bp[1] End 34,165,842 bp[1]
Gene location (Mouse) Chr. Chromosome 4 (mouse)[2] Band 4|4 D2.2 Start 127,987,857 bp[2] End 128,567,656 bp[2]
Orthologs
Species	Human	Mouse
Entrez	114784	329942
Ensembl	ENSG00000121904	ENSMUSG00000028804
UniProt	Q7Z408	V9GX34
RefSeq (mRNA)	NM_001281956 NM_052896	NM_001281955
RefSeq (protein)	NP_001268885 NP_443128	NP_001268884
Location (UCSC)	Chr 1: 33.51 – 34.17 Mb	Chr 4: 127.99 – 128.57 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. GRCh38: Ensembl release 89: ENSG00000121904 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000028804 - 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. Sun PC, Uppaluri R, Schmidt AP, Pashia ME, Quant EC, Sunwoo JB, Gollin SM, Scholnick SB (Jul 2001). "Transcript map of the 8p23 putative tumor suppressor region". Genomics. 75 (1–3): 17–25. doi:10.1006/geno.2001.6587. PMID 11472063.
6. Nagase T, Kikuno R, Ohara O (Sep 2001). "Prediction of the coding sequences of unidentified human genes. XXI. The complete sequences of 60 new cDNA clones from brain which code for large proteins". DNA Res. 8 (4): 179–87. doi:10.1093/dnares/8.4.179. PMID 11572484.
7. "Entrez Gene: CSMD2 CUB and Sushi multiple domains 2".

External links

• Human CSMD2 genome location and CSMD2 gene details page in the UCSC Genome Browser.

Further reading

• Gregory SG, Barlow KF, McLay KE, et al. (2006). "The DNA sequence and biological annotation of human chromosome 1". Nature. 441 (7091): 315–21. Bibcode:2006Natur.441..315G. doi:10.1038/nature04727. PMID 16710414.
• Jordanova A, Irobi J, Thomas FP, et al. (2006). "Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy". Nat. Genet. 38 (2): 197–202. doi:10.1038/ng1727. PMID 16429158. S2CID 16668375.
• 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.
• Lau WL, Scholnick SB (2004). "Identification of two new members of the CSMD gene family small star, filled". Genomics. 82 (3): 412–5. doi:10.1016/S0888-7543(03)00149-6. PMID 12906867.
• 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. PMC 139241. PMID 12477932.