Gene

si:ch211-76m11.3

ID
ZDB-GENE-041210-276
Name
si:ch211-76m11.3
Symbol
si:ch211-76m11.3 Nomenclature History
Previous Names
  • si:ch211-76m11.4
Type
protein_coding_gene
Location
Chr: 4 Mapping Details/Browsers
Description
Human ortholog(s) of this gene implicated in CINCA Syndrome; Muckle-Wells syndrome; autosomal dominant nonsyndromic deafness 34; familial cold autoinflammatory syndrome (multiple); and urticaria. Orthologous to several human genes including NLRP12 (NLR family pyrin domain containing 12); NLRP13 (NLR family pyrin domain containing 13); and NLRP14 (NLR family pyrin domain containing 14).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
No data available
Sequence Targeting Reagents
No data available
Human Disease
Associated With si:ch211-76m11.3 Human Ortholog
No data available
Associated With si:ch211-76m11.3 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 4
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA si:ch211-76m11.3-205 (1) Ensembl 3,243 nt
mRNA si:ch211-76m11.5-206 (1) Ensembl 2,624 nt
mRNA si:ch211-76m11.5-207 (1) Ensembl 3,516 nt
1 - 3 of 3
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
No data available
Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
Contained inBACCH211-76M11ZFIN Curated Data
1 - 1 of 1
Show
Sequences
Type Accession # Sequence Length (nt/aa) Analysis
GenomicGenBank:BX936384 (1)194634 nt
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
No data available
Citations
No data available