VARIANT: 6469v2
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Entry
6469v2 Variant
Name
SHH mutation
Gene
SHH
sonic hedgehog signaling molecule [KO:
K11988
]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar:
600725
Network
nt06501
HH signaling
Disease
H00267
Holoprosencephaly
H01027
Microphthalmia
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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