DYX1C1

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Dyslexia susceptibility 1 candidate gene 1 protein is a protein that in humans is encoded by the DYX1C1 gene.[5][6] This protein contains 420 amino acids with 3 tetratricopeptide repeat (TPR) domains, thought to mediate protein–protein interactions.

AliasesDNAAF4, CILD25, DYX1, DYXC1, EKN1, RD, DYX1C1, dyslexia susceptibility 1 candidate 1, dynein axonemal assembly factor 4
End55,508,234 bp[1]
Quick facts DNAAF4, Identifiers ...
DNAAF4
Identifiers
AliasesDNAAF4, CILD25, DYX1, DYXC1, EKN1, RD, DYX1C1, dyslexia susceptibility 1 candidate 1, dynein axonemal assembly factor 4
External IDsOMIM: 608706; MGI: 1914935; HomoloGene: 12173; GeneCards: DNAAF4; OMA:DNAAF4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_130810
NM_001033559
NM_001033560

NM_001163725
NM_026314

RefSeq (protein)

NP_001028731
NP_001028732
NP_570722

NP_001157197
NP_080590

Location (UCSC)Chr 15: 55.41 – 55.51 MbChr 9: 72.87 – 72.88 Mb
PubMed search[3][4]
Wikidata
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Clinical significance

A mutation in the DYX1C1 gene has been associated with deficits in reading ability (dyslexia).[5][7]

References

Further reading

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