Annotation Detail
Information
- Associated Genes
- GNPTAB
- Associated Variants
-
GNPTAB p.Asn148ThrfsTer4 (p.N148Tfs*4)
(
ENST00000299314.12,
ENST00000549940.5 )
GNPTAB p.Asn148ThrfsTer4 (p.N148Tfs*4) ( ENST00000299314.12, ENST00000549940.5 ) - Associated Disease
- Pseudo-Hurler polydystrophy Mucolipidosis type II
- Source Database
- ClinVar
- Description
- NM_024312.5(GNPTAB):c.441del (p.Asn148fs) AND multiple conditions
- ClinVar Allele ID
- 47682
- ClinVar RefSeq Alternation Syntax
- NM_024312.5:c.441del
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-12-23
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000673915
- ClinVar Disease
- Pseudo-Hurler polydystrophy
- ClinVar Disease
- Mucolipidosis type II
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs