EEF1A2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 20[13]
- Cytogenetic location
- 20q13.33[17]
- Expressed in
- gastrocnemius muscle, apex of heart, muscle of thigh, paraflocculus of cerebellum, right hemisphere of cerebellum, frontal pole, thoracic diaphragm, Skeletal muscle tissue of rectus abdominis, Brodmann area 10, cerebellar vermis[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- autosomal dominant non-syndromic intellectual disability 38, undetermined early-onset epileptic encephalopathy[14][15]
- HomoloGene ID
- 121568[3]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en STNL
en DEE33
en EEF1A2
en EEF1AL
en EF1A
en EF-1-alpha-2
en EIEE33
en eukaryotic translation elongation factor 1 alpha 2
en HS1
en MRD38
en STN
ar EEF١A٢
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000101210
- Ensembl transcript ID
- ENST00000298049, ENST00000217182, ENST00000646335, ENST00000645357, ENST00000645586, ENST00000642899, ENST00000643976, ENST00000675519
- Entrez Gene ID
- 1917
- Exact match
- identifiers.org
- Freebase ID
- /m/03gxdqz
- HGNC ID
- 3192
- HGNC gene symbol
- EEF1A2
- Microsoft Academic ID (discontinued)
- 2777805120
- OMIM ID
- 602959
- RefSeq RNA ID
- NM_001958
- UMLS CUI
- C1414273
🔗 Connections
Expressed in 4
Chromosome 1
Found in taxon 1
Instance of 1
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