FBXW11
protein-coding gene in the species Homo sapiens
Facts
12 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 5[14]
- Cytogenetic location
- 5q35.1[16]
- Expressed in
- corpus callosum, internal globus pallidus, islet of Langerhans, subthalamic nucleus, Brodmann area 23, cartilage tissue, pars compacta, superior vestibular nucleus, cerebellar vermis, endothelial cell[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[13]
- HomoloGene ID
- 76444[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en BTRC2
en BTRCP2
en F-box and WD repeat domain containing 11
en Fbw11
en FBW1B
en FBXW11
en FBXW1B
en Hos
en NEDJED
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000072803
- Ensembl transcript ID
- ENST00000523843, ENST00000265094, ENST00000296933, ENST00000393802, ENST00000517395, ENST00000518106, ENST00000518752, ENST00000519693, ENST00000520376, ENST00000522376, ENST00000522507, ENST00000522891
- Entrez Gene ID
- 23291
- Exact match
- identifiers.org
- Freebase ID
- /m/03g_zbf
- HGNC ID
- 13607
- HGNC gene symbol
- FBXW11
- Microsoft Academic ID (discontinued)
- 2777104241
- OMIM ID
- 605651
- RefSeq RNA ID
- NM_012300, NM_033644, NM_033645, XM_005265857, XM_017009279, NM_001378974, NM_001378975, NM_001378976, NM_001378977, NM_001378978, NM_001378979, NM_001378980, XM_047417023
- UMLS CUI
- C1539505
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