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1 protein found in SwissVar (0 variants)

with gene/protein name Q15465

Disclaimer: The query results are intended for research purposes only, not for clinical and diagnostic use.

Accession Entry name Disease Variants 3D mapping
(variant position)
Q15465 SHH_HUMAN microphthalmia, isolated, with coloboma, 5
Q15465 SHH_HUMAN holoprosencephaly 3
Q15465 SHH_HUMAN solitary median maxillary central incisor
Q15465 SHH_HUMAN triphalangeal thumb-polysyndactyly syndrome
Q15465 SHH_HUMAN preaxial polydactyly 2
Q15465 SHH_HUMAN hypoplasia or aplasia of tibia with polydactyly
Q15465 SHH_HUMAN laurin-sandrow syndrome