DIAPH1

DIAPH1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesDIAPH1, DFNA1, DIA1, DRF1, LFHL1, hDIA1, SCBMS, diaphanous related formin 1, mDia1
External IDsOMIM: 602121; MGI: 1194490; HomoloGene: 129567; GeneCards: DIAPH1; OMA:DIAPH1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001314007
NM_001079812
NM_005219

NM_007858
NM_001305980
NM_001305981

RefSeq (protein)

NP_001073280
NP_001300936
NP_005210

NP_001292909
NP_001292910
NP_031884

Location (UCSC)Chr 5: 141.52 – 141.62 MbChr 18: 37.98 – 38.07 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Protein diaphanous homolog 1 is a protein that in humans is encoded by the DIAPH1 gene.[5][6][7]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000131504Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024456Ensembl, 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. ^ Lynch ED, Lee MK, Morrow JE, Welcsh PL, León PE, King MC (November 1997). "Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous". Science. 278 (5341): 1315–8. Bibcode:1997Sci...278.1315L. doi:10.1126/science.278.5341.1315. PMID 9360932.
  6. ^ Leon PE, Raventos H, Lynch E, Morrow J, King MC (June 1992). "The gene for an inherited form of deafness maps to chromosome 5q31". Proceedings of the National Academy of Sciences of the United States of America. 89 (11): 5181–4. Bibcode:1992PNAS...89.5181L. doi:10.1073/pnas.89.11.5181. PMC 49253. PMID 1350680.
  7. ^ "Entrez Gene: DIAPH1 diaphanous homolog 1 (Drosophila)".