Arterial Tortuosity Syndrome(ATS) Explore Disorder's Alias
An Autosomal recessive mode(s) within the Cardiovascular disorders category
Candidate Gene Information
An Autosomal recessive mode(s) within the Cardiovascular disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | SLC2A10/81031 | solute carrier family 2 member 10 | 20q13.12 | Chr20, NC_000020.11 (46708320..46736347) |
28028 nt | 7 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |