Gene
si:ch211-250k18.7
- ID
- ZDB-GENE-070912-246
- Name
- si:ch211-250k18.7
- Symbol
- si:ch211-250k18.7 Nomenclature History
- Previous Names
-
- si:ch211-250k18.3
- Type
- protein_coding_gene
- Location
- Chr: 22 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in Muckle-Wells syndrome; autoimmune disease (multiple); autosomal dominant nonsyndromic deafness 34; familial cold autoinflammatory syndrome (multiple); and urticaria. Orthologous to several human genes including NLRP1 (NLR family pyrin domain containing 1); NLRP12 (NLR family pyrin domain containing 12); and NLRP13 (NLR family pyrin domain containing 13).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
si:ch211-250k18.7-201
(1)
|
Ensembl | 4,695 nt |
Interactions and Pathways
No data available
Plasmids
No data available