VARIANT: 8643v1
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Entry
8643v1 Variant
Name
PTCH2 mutation
Gene
PTCH2
patched 2 [KO:
K11101
]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar:
603673
Network
nt06501
HH signaling
Disease
H00039
Basal cell carcinoma
Reference
PMID:
31781166
Authors
Sasai N, Toriyama M, Kondo T
Title
Hedgehog Signal and Genetic Disorders.
Journal
Front Genet 10:1103 (2019)
DOI:
10.3389/fgene.2019.01103
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