Previous symbols: C7orf2. Aliases: ACHP, FLJ11665, ZRS.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Acheiropodia | causative germline |
mechanism: LMBR1 Exon 4 Region Deletion
|
| ZRS-Related Limb Malformation | causative germline |
mechanism: Pre-ZRS Single Nucleotide Variant; ZRS-Encompassing Duplication
subtype: Haas-Type Polysyndactyly; Isolated Triphalangeal Thumb; Laurin-Sandrow Syndrome; Preaxial Polydactyly Type 2; Triphalangeal Thumb-Polysyndactyly Syndrome; Werner Mesomelic Syndrome
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.