USH2A gene

Alternative Names

  • USH2A
  • Usherin
  • USH2
  • US2
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OMIM Number

608400

NCBI Gene ID

7399

Uniprot ID

O75445

Length

800,558 bases

No. of Exons

72

No. of isoforms

3

Protein Name

Usherin

Molecular Mass

575600 Da

Amino Acid Count

5202

Genomic Location

chr1:215,622,890-216,423,447

Gene Map Locus
1q41

Description

This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs. The protein is found in the basement membrane, and may be important in development and homeostasis of the inner ear and retina. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_206933.2:c.11907delLebanonNC_000001.11:g.215728189delPathogenicUsher Syndrome, Type IIANG_009497.2:g.700260A>T; NM_206933.2:c.11907del; NP_996816.2:p.Ala3970LeufsTer14
NM_206933.2:c.1923T>AJordanNC_000001.11:g.216289328A>TPathogenicPathogenicRetinitis Pigmentosa 39NG_009497.1:g.139069T>A; NM_206933.2:c.1923T>A; NP_996816.2:p.Cys641Ter979000
NM_206933.2:c.4033G>CSaudi Arabiachr1:216198363PathogenicPathogenicRetinitis Pigmentosa 39NG_009497.1:g.230034G>C; NM_206933.2:c.4033G>C; NP_996816.2:p.Ala1345Pro979016
NM_206933.2:c.4707T>GLebanonNC_000001.11:g.216097134A>CPathogenicPathogenicUsher Syndrome, Type IIANG_009497.2:g.331315T>G; NM_206933.2:c.4707T>G; NP_996816.2:p.Tyr1569Ter867170
NM_206933.4:c.14031dupLebanonNC_000001.11:g.215671074dupPathogenicPathogenicUsher Syndrome, Type IIANG_009497.2:g.757375dup; NM_206933.4:c.14031dup; NP_996816.3:p.Ala4678fs39751798848426
NM_206933.4:c.14424C>ALebanonNC_000001.11:g.215648686G>TLikely Pathogenic, PathogenicPathogenicUsher Syndrome, Type IIANG_009497.2:g.779763C>A; NM_206933.4:c.14424C>A; NP_996816.3:p.Cys4808Ter1553250184552628
NM_206933.4:c.486-1G>CSaudi Arabiachr1:216418680PathogenicPathogenicUsher Syndrome, Type IIANG_009497.2:g.9769G>C; NM_206933.4:c.486-1G>C876657730228413
NM_206933.4:c.532dupLebanonNC_000001.11:g.216418633dupPathogenicPathogenicUsher Syndrome, Type IIANG_009497.2:g.9816dup; NM_206933.4:c.532dup; NP_996816.3:p.Thr178fs1571801788813346
NM_206933.4:c.8681G>AJordan; LebanonNC_000001.11:g.215877758C>TLikely Pathogenic, PathogenicPathogenicUsher Syndrome, Type IIANG_009497.2:g.550691G>A; NM_206933.4:c.8681G>A; NP_996816.3:p.Arg2894Lys1369414978495329
NM_206933.4:c.9860_9873delUnited Arab EmiratesNC_000001.11:g.215798993_215799006delLikely Pathogenic, PathogenicLikely PathogenicUsher Syndrome, Type IIANG_009497.2:g.629444_629457del; NM_206933.4:c.9860_9873del; NP_996816.3:p.His3287ProfsTer541388040238438035
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