LMBR1 Chromosome 7

Limb development membrane protein 1
10 variants 10 Health Risk

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What This Gene Does
This gene encodes a member of the LMBR1-like membrane protein family. Another member of this protein family has been shown to be a lipocalin transmembrane receptor. A highly conserved, cis-acting regulatory module for the sonic hedgehog gene is located within an intron of this gene. Consequently, disruption of this genic region can alter sonic hedgehog expression and affect limb patterning, but it is not known if this gene functions directly in limb development. Mutations and chromosomal deletions and rearrangements in this genic region are associated with acheiropody and preaxial polydactyly, which likely result from altered sonic hedgehog expression. [provided by RefSeq, Jul 2008]
Associated Conditions (7)
Polydactyly of a triphalangeal thumb
Inborn genetic diseases
Skeletal dysplasia
Syndactyly type 4
Acheiropodia
Laurin-Sandrow syndrome
Triphalangeal thumb-polysyndactyly syndrome
Key Variants
All Variants (10)
RSID Category Clinical Significance Conditions
RS139646169 Health Risk Conflicting classifications of pathogenicity Polydactyly of a triphalangeal thumb, Inborn genetic diseases, Skeletal dysplasia
RS140722848 Health Risk Conflicting classifications of pathogenicity Polydactyly of a triphalangeal thumb, Syndactyly type 4, Acheiropodia
RS140806590 Health Risk Conflicting classifications of pathogenicity Polydactyly of a triphalangeal thumb, Polydactyly of a triphalangeal thumb
RS182641358 Health Risk Conflicting classifications of pathogenicity Polydactyly of a triphalangeal thumb, Inborn genetic diseases, Polydactyly of a triphalangeal thumb
RS201194692 Health Risk Conflicting classifications of pathogenicity Polydactyly of a triphalangeal thumb, Polydactyly of a triphalangeal thumb
RS367632078 Health Risk Conflicting classifications of pathogenicity Polydactyly of a triphalangeal thumb, Polydactyly of a triphalangeal thumb
RS369873566 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS376183960 Health Risk Conflicting classifications of pathogenicity
RS2536128236 Health Risk Likely pathogenic
RS752653908 Health Risk Pathogenic
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