CBWD1

COBW domain-containing protein 1 is a protein that is found in humans and mice. It is encoded by the CBWD1 gene.[5][6][7]

CBWD1
Identifiers
Aliases	CBWD1, COBP, COBW domain containing 1
External IDs	OMIM: 611078 MGI: 2385089 HomoloGene: 6843 GeneCards: CBWD1
Gene location (Human) Chr. Chromosome 9 (human)[1] Band 9p24.3 Start 121,038 bp[1] End 179,147 bp[1]
Gene location (Mouse) Chr. Chromosome 19 (mouse)[2] Band 19|19 B Start 24,919,916 bp[2] End 24,961,610 bp[2]
Orthologs
Species	Human	Mouse
Entrez	55871	226043
Ensembl	ENSG00000172785	ENSMUSG00000024878
UniProt	Q9BRT8	Q8VEH6
RefSeq (mRNA)	NM_001145355 NM_001145356 NM_018491	NM_146097
RefSeq (protein)	NP_001138827 NP_001138828 NP_060961	NP_666209
Location (UCSC)	Chr 9: 0.12 – 0.18 Mb	Chr 19: 24.92 – 24.96 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. GRCh38: Ensembl release 89: ENSG00000172785 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000024878 - 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. Wong A, Vallender EJ, Heretis K, Ilkin Y, Lahn BT, Martin CL, Ledbetter DH (Jul 2004). "Diverse fates of paralogs following segmental duplication of telomeric genes". Genomics. 84 (2): 239–47. doi:10.1016/j.ygeno.2004.03.001. PMID 15233989.
6. Fan Y, Newman T, Linardopoulou E, Trask BJ (Nov 2002). "Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions". Genome Res. 12 (11): 1663–72. doi:10.1101/gr.338402. PMC 187549. PMID 12421752.
7. "Entrez Gene: CBWD1 COBW domain containing 1".

External links

• Human CBWD1 genome location and CBWD1 gene details page in the UCSC Genome Browser.

Further reading

• Page N, Butlin D, Manyonda I, Lowry P (2000). "The development of a genetic profile of placental gene expression during the first trimester of pregnancy: a potential tool for identifying novel secreted markers". Fetal Diagn. Ther. 15 (4): 237–45. doi:10.1159/000021014. PMID 10867487.
• Hu RM, Han ZG, Song HD, et al. (2000). "Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning". Proc. Natl. Acad. Sci. U.S.A. 97 (17): 9543–8. doi:10.1073/pnas.160270997. PMC 16901. PMID 10931946.
• Shi J, Cai W, Chen X, et al. (2001). "Identification of dopamine responsive mRNAs in glial cells by suppression subtractive hybridization". Brain Res. 910 (1–2): 29–37. doi:10.1016/S0006-8993(01)02393-9. PMID 11489251.
• 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.
• Humphray SJ, Oliver K, Hunt AR, et al. (2004). "DNA sequence and analysis of human chromosome 9". Nature. 429 (6990): 369–74. doi:10.1038/nature02465. PMC 2734081. PMID 15164053.
• 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.
• Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Mol. Syst. Biol. 3 (1): 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.