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DYNC2H1

From Wikipedia, the free encyclopedia
DYNC2H1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesDYNC2H1, ATD3, DHC1b, DHC2, DNCH2, DYH1B, SRPS2B, SRTD3, hdhc11, dynein cytoplasmic 2 heavy chain 1
External IDsOMIM: 603297; MGI: 107736; HomoloGene: 14468; GeneCards: DYNC2H1; OMA:DYNC2H1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001080463
NM_001377
NM_024606

NM_029851
NM_001364519
NM_138307

RefSeq (protein)

NP_001073932
NP_001368

NP_084127
NP_001351448

Location (UCSC)Chr 11: 103.11 – 103.48 MbChr 9: 6.93 – 7.18 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Cytoplasmic dynein 2 heavy chain 1 is a protein that in humans is encoded by the DYNC2H1 gene.[5][6][7]

It is associated with Short rib-polydactyly syndrome type 3.[8]

It is also associated with Asphyxiating thoracic dysplasia.[9]


See also

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References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000187240Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000047193Ensembl, 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. ^ Koehler MR, Schmid M, Neesen J (Nov 1998). "Chromosomal localization of the human cytoplasmic dynein heavy chain gene DNCH2 to 11q21→q22.1". Cytogenet Cell Genet. 82 (1–2): 123–5. doi:10.1159/000015085. PMID 9763680. S2CID 46818608.
  6. ^ Neesen J, Koehler MR, Kirschner R, Steinlein C, Kreutzberger J, Engel W, Schmid M (Dec 1997). "Identification of dynein heavy chain genes expressed in human and mouse testis: chromosomal localization of an axonemal dynein gene". Gene. 200 (1–2): 193–202. doi:10.1016/S0378-1119(97)00417-4. PMID 9373155.
  7. ^ "Entrez Gene: DYNC2H1 dynein, cytoplasmic 2, heavy chain 1".
  8. ^ Merrill AE, Merriman B, Farrington-Rock C, et al. (April 2009). "Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome". Am. J. Hum. Genet. 84 (4): 542–9. doi:10.1016/j.ajhg.2009.03.015. PMC 2667993. PMID 19361615.
  9. ^ Dagoneau N, Goulet M, Geneviève D, et al. (May 2009). "DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III". Am. J. Hum. Genet. 84 (5): 706–11. doi:10.1016/j.ajhg.2009.04.016. PMC 2681009. PMID 19442771.

Further reading

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