EFTUD2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 17
- Cytogenetic location
- 17q21.31
- Encodes
- Elongation factor Tu GTP binding domain containing 2, 116 kDa U5 small nuclear ribonucleoprotein component[14]
- Expressed in
- bone marrow cell, tibialis anterior muscle, ventricular zone, monocyte, mucosa of ileum, ganglionic eminence, skin of arm, gastrocnemius muscle, stromal cell of endometrium, islet of Langerhans
- Found in taxon
- Homo sapiens
- Genetic association
- mandibulofacial dysostosis-microcephaly syndrome
- HomoloGene ID
- 3133[3]
- Strand orientation
- reverse strand
🏷️ Also known as
en U5-116KD
en EFTUD2
en elongation factor Tu GTP binding domain containing 2
en MFDGA
en MFDM
en SNRNP116
en Snrp116
en Snu114
ar EFTUD٢
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000108883
- Ensembl transcript ID
- ENST00000593200, ENST00000402521, ENST00000426333, ENST00000585616, ENST00000585794, ENST00000586276, ENST00000586654, ENST00000586875, ENST00000587914, ENST00000587957, ENST00000588340, ENST00000588374, ENST00000589211, ENST00000589475, ENST00000589769, ENST00000589825, ENST00000590105, ENST00000590124, ENST00000590367, ENST00000590977, ENST00000591382, ENST00000591856, ENST00000592408, ENST00000592576, ENST00000592701, ENST00000593072
- Entrez Gene ID
- 9343
- Exact match
- identifiers.org
- Freebase ID
- /m/03gybbh
- HGNC ID
- 30858
- HGNC gene symbol
- EFTUD2
- OMIM ID
- 603892
- RefSeq RNA ID
- NM_001142605, NM_001258353, NM_001258354, NM_004247, XM_047437084
- UMLS CUI
- C1825036
🔗 Connections
Expressed in 5
Chromosome 1
Found in taxon 1
Instance of 1
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Summary
EFTUD2 is a gene[1].