MARVELD2

MARVELD2
Identifiers
AliasesMARVELD2, DFNB49, MARVD2, MRVLDC2, Tric, MARVEL domain containing 2
External IDsMGI: 2446166 HomoloGene: 27037 GeneCards: MARVELD2
Gene location (Human)
Chr.Chromosome 5 (human)[1]
Band5q13.2Start69,415,065 bp[1]
End69,444,330 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

153562

218518

Ensembl

ENSG00000274671
ENSG00000152939

ENSMUSG00000021636

UniProt

Q8N4S9

Q3UZP0

RefSeq (mRNA)

NM_001038603
NM_001244734
NM_144724

NM_001038602
NM_178410

RefSeq (protein)

NP_001033692
NP_001231663

NP_001033691
NP_848497

Location (UCSC)Chr 5: 69.42 – 69.44 MbChr 13: 100.6 – 100.62 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

MARVEL domain-containing protein 2 is a protein that in humans is encoded by the MARVELD2 gene.[5][6]

References

  1. 1 2 3 ENSG00000152939 GRCh38: Ensembl release 89: ENSG00000274671, ENSG00000152939 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000021636 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. ↑ Riazuddin S, Ahmed ZM, Fanning AS, Lagziel A, Kitajiri S, Ramzan K, Khan SN, Chattaraj P, Friedman PL, Anderson JM, Belyantseva IA, Forge A, Riazuddin S, Friedman TB (Dec 2006). "Tricellulin is a tight-junction protein necessary for hearing". Am J Hum Genet. 79 (6): 1040–51. doi:10.1086/510022. PMC 1698716. PMID 17186462.
  6. ↑ "Entrez Gene: MARVELD2 MARVEL domain containing 2".

Further reading

  • Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983.
  • Ikenouchi J, Furuse M, Furuse K, et al. (2006). "Tricellulin constitutes a novel barrier at tricellular contacts of epithelial cells". J. Cell Biol. 171 (6): 939–45. doi:10.1083/jcb.200510043. PMC 2171318. PMID 16365161.
  • Zhang Y, Wolf-Yadlin A, Ross PL, et al. (2005). "Time-resolved mass spectrometry of tyrosine phosphorylation sites in the epidermal growth factor receptor signaling network reveals dynamic modules". Mol. Cell. Proteomics. 4 (9): 1240–50. doi:10.1074/mcp.M500089-MCP200. PMID 15951569.
  • Ramzan K, Shaikh RS, Ahmad J, et al. (2005). "A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1". Hum. Genet. 116 (1–2): 17–22. doi:10.1007/s00439-004-1205-8. PMID 15538632.
  • 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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.


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