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LY9

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LY9
Identifiers
AliasesLY9, CD229, SLAMF3, hly9, mlymphocyte antigen 9
External IDsOMIM: 600684; MGI: 96885; HomoloGene: 1759; GeneCards: LY9; OMA:LY9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001033667
NM_001261456
NM_001261457
NM_002348

NM_001277968
NM_008534

RefSeq (protein)

NP_001028839
NP_001248385
NP_001248386
NP_002339

NP_001264897
NP_032560

Location (UCSC)Chr 1: 160.8 – 160.83 MbChr 1: 171.42 – 171.43 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

T-lymphocyte surface antigen Ly-9 is a protein that in humans is encoded by the LY9 gene.[5][6][7] LY9 has also recently been designated CD229 (cluster of differentiation 229).

Interactions

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LY9 has been shown to interact with SH2D1A.[8][9]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000122224Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000004707Ensembl, 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. ^ Sandrin MS, Henning MM, Lo MF, Baker E, Sutherland GR, McKenzie IF (Feb 1996). "Isolation and characterization of cDNA clones for Humly9: the human homologue of mouse Ly9". Immunogenetics. 43 (1–2): 13–9. doi:10.1007/bf00186599. PMID 8537117. S2CID 10045488.
  6. ^ Kingsmore SF, Souryal CA, Watson ML, Patel DD, Seldin MF (Aug 1995). "Physical and genetic linkage of the genes encoding Ly-9 and CD48 on mouse and human chromosomes 1". Immunogenetics. 42 (1): 59–62. doi:10.1007/BF00164988. PMID 7797269. S2CID 28529549.
  7. ^ "Entrez Gene: LY9 lymphocyte antigen 9".
  8. ^ Sayós J, Martín M, Chen A, Simarro M, Howie D, Morra M, Engel P, Terhorst C (Jun 2001). "Cell surface receptors Ly-9 and CD84 recruit the X-linked lymphoproliferative disease gene product SAP". Blood. 97 (12): 3867–3874. doi:10.1182/blood.V97.12.3867. PMID 11389028.
  9. ^ Morra M, Simarro-Grande M, Martin M, Chen AS, Lanyi A, Silander O, Calpe S, Davis J, Pawson T, Eck MJ, Sumegi J, Engel P, Li SC, Terhorst C (Sep 2001). "Characterization of SH2D1A missense mutations identified in X-linked lymphoproliferative disease patients" (PDF). J. Biol. Chem. 276 (39): 36809–36816. doi:10.1074/jbc.M101305200. PMID 11477068. S2CID 39889619.

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.