Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | EIF4H | contributors: mct - updated : 04-05-2020 |
HGNC name | eukaryotic translation initiation factor 4H |
HGNC id | 12741 |
|
DNA |
TYPE | functioning gene |
STRUCTURE | 22.72 kb 7 Exon(s) |
regulatory sequence | Binding site |
text structure | RNA binding sites |
MAPPING | cloned | Y | linked | status | provisional |
regionally located | in a region commonly deleted in Williams-Beuren syndrome |
RNA |
TRANSCRIPTS | type | messenger |
---|
EXPRESSION |
Type | ubiquitous |
expressed in | (based on citations) | ||||||||||||||||||||||||||||||
organ(s) |
|
tissue |
|
cell lineage
cell lines
| fluid/secretion
| |
at STAGE |
PROTEIN |
PHYSICAL PROPERTIES
STRUCTURE
| |
motifs/domains
| |
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HOMOLOGY |
interspecies | homolog to murine Wbscr1 |
intraspecies | homolog to RNA-binding proteins |
Homologene |
FAMILY |
CATEGORY | regulatory , RNA associated |
SUBCELLULAR LOCALIZATION | intracellular |
intracellular,cytoplasm,organelle,membrane | |
intracellular,cytoplasm,cytosolic | |
intracellular,nuclear envelope |
basic FUNCTION | |
| |
|
CELLULAR PROCESS | protein, translation/synthesis |
PHYSIOLOGICAL PROCESS |
PATHWAY |
metabolism |
signaling |
a component |
INTERACTION |
DNA |
RNA |
small molecule |
protein | |
| |
| |
| |
|
cell & other |
REGULATION |
ASSOCIATED DISORDERS |
corresponding disease(s) | WBS |
Susceptibility |
Variant & Polymorphism other | base-pair inversion polymorphism predisposing to primarily WBS- causing microdeletions |
Candidate gene
Marker
| Therapy target
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ANIMAL & CELL MODELS |