Regulatory Factor X, 6

Alternative Names

  • RFX6
  • RFXDC1
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OMIM Number

612659

NCBI Gene ID

222546

Uniprot ID

Q8HWS3

Length

54,946 bases

No. of Exons

20

No. of isoforms

1

Protein Name

DNA-binding protein RFX6

Molecular Mass

102461 Da

Amino Acid Count

928

Genomic Location

chr6:116,877,217-116,932,162

Gene Map Locus
6q22.1

Description

The nuclear protein encoded by this gene is a member of the regulatory factor X (RFX) family of transcription factors. Studies in mice suggest that this gene is specifically required for the differentiation of islet cells for the production of insulin, but not for the differentiation of pancreatic polypeptide-producing cells. It regulates the transcription factors involved in beta-cell maturation and function, thus, restricting the expression of the beta-cell differentiation and specification genes. Mutations in this gene are associated with Mitchell-Riley syndrome, which is characterized by neonatal diabetes with pancreatic hypoplasia, duodenal and jejunal atresia, and gall bladder agenesis. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_173560.3:c.1153C>TUnited Arab EmiratesNC_000006.12:g.116919267C>TLikely PathogenicMitchell-Riley SyndromeNG_027699.1:g.47055C>T; NM_173560.3:c.1153C>T; NP_775831.2:p.Arg385Ter369489227
NM_173560.4:c.1384G>AQatarNC_000006.12:g.116922098G>AUncertain SignificanceType 2 Diabetes MellitusNG_027699.1:g.49886G>A; NM_173560.4:c.1384G>A; NP_775831.2:p.Val462Met1485759457
NM_173560.4:c.1673A>CQatarNC_000006.12:g.116924786A>CUncertain SignificanceType 2 Diabetes MellitusNG_027699.1:g.52574A>C; NM_173560.4:c.1673A>C; NP_775831.2:p.Asn558Thr1775673420
NM_173560.4:c.2390C>TQatarNC_000006.12:g.116927531C>TUncertain SignificanceType 2 Diabetes MellitusNG_027699.1:g.55319C>T; NM_173560.4:c.2390C>T; NP_775831.2:p.Ser797Leu762356403
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