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Details of FERMT1 gene in Homo sapiens
IDs |
Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
| FERMT1 | C20orf42 | KIND1 | URP1 | Q9BQL6 | D3DW10 | Q8IX34 | --- |
Disease |
Disease |
OMIM id |
Kindler syndrome (KINDS) [MIM:173650]: Autosomal recessive skin disorder characterized by skin blistering |
progressive poikiloderma |
Orthologs in other species |
M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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