GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Lists of Rare Genetic Disorders      

Primary Sclerosing Cholangitis(PSC)      Explore Disorder's Alias
An Unknown mode(s) within the Liver disorders category
Reported Pathogenic variants
Candidate Gene Information
S.No. Name/GeneID Description Cytogentic Band Gene Location on genomic DNA Gene Length Exons Details Gene Cross-References
1 Snhg10/69434 small nucleolar RNA host gene 10 Chr12, NC_000078.7
(104996876..104998538, complement)
1663 nt 2 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

2 SEMA4D/10507 semaphorin 4D 9q22.2 Chr9, NC_000009.12
(89360787..89498113, complement)
137327 nt 34 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

3 GPR35/2859 G protein-coupled receptor 35 2q37.3 Chr2, NC_000002.12
(240605430..240633159)
27730 nt 7 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

4 STK4/6789 serine/threonine kinase 4 20q13.12 Chr20, NC_000020.11
(44966512..45080021)
113510 nt 15 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

Variant Information
Disorder Cross-References:      GARD          GTR          MalaCards          NORD     

Patient care services
Clinical Symptoms & Disabilities

Prevalence
Under development