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SPRYD7
Identifiers
Aliases	SPRYD7, C13orf1, CLLD6, SPRY domain containing 7
External IDs	OMIM: 607866; MGI: 1913924; HomoloGene: 10725; GeneCards: SPRYD7; OMA:SPRYD7 - orthologs
Gene location (Human) Chr. Chromosome 13 (human) Band 13q14.2 Start 49,912,702 bp End 49,936,490 bp
Gene location (Mouse) Chr. Chromosome 14 (mouse) Band 14|14 D1 Start 61,769,442 bp End 61,794,335 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in gastrocnemius muscle muscle of thigh gonad dorsolateral prefrontal cortex Brodmann area 9 cingulate gyrus anterior cingulate cortex endothelial cell middle temporal gyrus right frontal lobe Top expressed in dorsomedial hypothalamic nucleus ventral tegmental area spermatocyte triceps brachii muscle habenula paraventricular nucleus of hypothalamus temporal muscle sternocleidomastoid muscle dorsal tegmental nucleus lateral septal nucleus More reference expression data BioGPS More reference expression data
Orthologs Species Human Mouse Entrez 57213 66674 Ensembl ENSG00000123178 ENSMUSG00000021930 UniProt Q5W111 Q3TFQ1 RefSeq (mRNA) NM_001127482 NM_020456 NM_025697 NM_001310603 RefSeq (protein) NP_001120954 NP_065189 NP_001297532 NP_079973 Location (UCSC) Chr 13: 49.91 – 49.94 Mb Chr 14: 61.77 – 61.79 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

SPRY domain-containing protein 7 (SPRYD7) also known as chronic lymphocytic leukemia deletion region gene 6 protein (CLLD6) is a protein that in humans is encoded by the SPRYD7 gene.

References

1. ^ GRCh38: Ensembl release 89: ENSG00000123178 – Ensembl, May 2017
2. ^ GRCm38: Ensembl release 89: ENSMUSG00000021930 – 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. Mabuchi H, Fujii H, Calin G, Alder H, Negrini M, Rassenti L, Kipps TJ, Bullrich F, Croce CM (Apr 2001). "Cloning and characterization of CLLD6, CLLD7, and CLLD8, novel candidate genes for leukemogenesis at chromosome 13q14, a region commonly deleted in B-cell chronic lymphocytic leukemia". Cancer Res. 61 (7): 2870–7. PMID 11306461.
6. Tiazhelova TV, Ivanov DV, Makeeva NV, Kapanadze BI, Nikitin EA, Semov AB, Sangfeldt O, Grander D, Vorob'ev AI, Einhorn S, Iankovskii NK, Baranova AV (Dec 2001). "". Genetika. 37 (11): 1530–7. PMID 11771308.
7. "Entrez Gene: C13orf1 chromosome 13 open reading frame 1".

Further reading

• Andersson B, Wentland MA, Ricafrente JY, et al. (1996). "A "double adaptor" method for improved shotgun library construction". Anal. Biochem. 236 (1): 107–13. doi:10.1006/abio.1996.0138. PMID 8619474.
• Yu W, Andersson B, Worley KC, et al. (1997). "Large-Scale Concatenation cDNA Sequencing". Genome Res. 7 (4): 353–8. doi:10.1101/gr.7.4.353. PMC 139146. PMID 9110174.
• Mertens D, Wolf S, Schroeter P, et al. (2002). "Down-regulation of candidate tumor suppressor genes within chromosome band 13q14.3 is independent of the DNA methylation pattern in B-cell chronic lymphocytic leukemia". Blood. 99 (11): 4116–21. doi:10.1182/blood.V99.11.4116. PMID 12010815.
• 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.
• Gevaert K, Goethals M, Martens L, et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. 21 (5): 566–9. doi:10.1038/nbt810. PMID 12665801. S2CID 23783563.
• Dunham A, Matthews LH, Burton J, et al. (2004). "The DNA sequence and analysis of human chromosome 13". Nature. 428 (6982): 522–8. Bibcode:2004Natur.428..522D. doi:10.1038/nature02379. PMC 2665288. PMID 15057823.
• Gerhard DS, Wagner L, BB 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.

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