Gene

smarcad1a

ID
ZDB-GENE-050522-499
Name
SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 a
Symbol
smarcad1a Nomenclature History
Previous Names
  • smarcad1
  • wu:fi25c01
  • zgc:113183
Type
protein_coding_gene
Location
Chr: 8 Mapping Details/Browsers
Description
Predicted to be involved in ATP-dependent chromatin remodeling and DNA double-strand break processing. Predicted to localize to site of double-strand break. Human ortholog(s) of this gene implicated in BASAN syndrome and adermatoglyphia. Orthologous to human SMARCAD1 (SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1).
Genome Resources
Note
None
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With smarcad1a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
adermatoglyphia Alliance Adermatoglyphia 136000
BASAN syndrome Alliance Basan syndrome 129200
Huriez syndrome 181600
Associated With smarcad1a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR003892 Ubiquitin system component CUE
Homologous_superfamily IPR009060 UBA-like superfamily
Domain Details Per Protein
Protein Length UBA-like superfamily Ubiquitin system component CUE
UniProtKB:B0R061 972
UniProtKB:B0R060 385
UniProtKB:F6NTX5 154
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Ensembl Gene Tree
Citations