FBLN5
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 14[12]
- Cytogenetic location
- 14q32.12[16]
- Expressed in
- thoracic aorta, ascending aorta, Descending thoracic aorta, right lung, right coronary artery, stromal cell of endometrium, left coronary artery, gallbladder, popliteal artery, tibial arteries[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- age related macular degeneration, hereditary sensorimotor neuropathy with hyperelastic skin[13][14]
- HomoloGene ID
- 38170[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en UP50
en ADCL2
en ARCL1A
en ARMD3
en CMT1H
en DANCE
en EVEC
en FBLN5
en FIBL-5
en fibulin 5
en HNARMD
ar FBLN٥
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000140092
- Ensembl transcript ID
- ENST00000557570, ENST00000267620, ENST00000342058, ENST00000554121, ENST00000554468, ENST00000556154, ENST00000556961, ENST00000557088, ENST00000557462
- Entrez Gene ID
- 10516
- Exact match
- identifiers.org
- Freebase ID
- /m/02kg8k8
- HGNC ID
- 3602
- HGNC gene symbol
- FBLN5
- Microsoft Academic ID (discontinued)
- 2779001669
- OMIM ID
- 604580
- RefSeq RNA ID
- NM_006329, XM_011536356, NM_001384158, NM_001384159, NM_001384160, NM_001384161, NM_001384162
- UMLS CUI
- C1414541
🔗 Connections
Expressed in 6
Chromosome 1
Found in taxon 1
Instance of 1
← Genetic association 1
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