OFD1 Centriole and Centriolar Satellite Protein

Alternative Names

  • OFD1
  • OFD1 Gene
  • Chromosome X Open Reading Frame 5
  • CXORF5

Associated Diseases

Orofaciodigital Syndrome I
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OMIM Number

300170

NCBI Gene ID

8481

Uniprot ID

O75665

Length

39,253 bases

No. of Exons

27

No. of isoforms

3

Protein Name

Oral-facial-digital syndrome 1 protein

Molecular Mass

116671 Da

Amino Acid Count

1012

Genomic Location

chrX:13,734,725-13,773,977

Gene Map Locus
Xp22.2

Description

This gene is located on the X chromosome and encodes a centrosomal protein. A knockout mouse model has been used to study the effect of mutations in this gene. The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation. Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2. Many pseudogenes have been identified; a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_003611.3:c.1193_1196delSaudi ArabiaNC_000023.11:g.13755210AATC[1]PathogenicPathogenicOrofaciodigital Syndrome ING_008872.1:g.25498AATC[1]; NM_003611.3:c.1193_1196del; NP_003602.1:p.Gln398LeufsTer231226286841065
NM_003611.3:c.1469A>GUnited Arab EmiratesNC_000023.11:g.13757717A>GBenign, Uncertain SignificanceBenignNG_008872.1:g.28005A>G; NM_003611.3:c.1469A>G; NP_003602.1:p.Glu490Gly754484224211785
NM_003611.3:c.2757+1delUnited Arab EmiratesNC_000023.11:g.13767285delLikely PathogenicOrofaciodigital Syndrome ING_008872.1:g.37573del; NM_003611.3:c.2757+1del; NP_003602.1:p.?
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