FBN2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 5[11]
- Cytogenetic location
- 5q23.3[14]
- Encodes
- fibrillin 2[9]
- Expressed in
- cartilage tissue, placenta, decidua, stromal cell of endometrium, right ventricle, embryo, monocyte, testicle, buccal mucosa cell, myocardium of left ventricle[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- morbid obesity[12]
- HomoloGene ID
- 1515[3]
- Strand orientation
- reverse strand[13]
🏷️ Also known as
en CCA
en DA9
en EOMD
en FBN2
en fibrillin 2
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000138829
- Ensembl transcript ID
- ENST00000262464, ENST00000502468, ENST00000507835, ENST00000508053, ENST00000508989, ENST00000511489, ENST00000514742
- Entrez Gene ID
- 2201
- Exact match
- identifiers.org
- Google Knowledge Graph ID
- /g/11fy_q9d7g
- HGNC ID
- 3604
- HGNC gene symbol
- FBN2
- OMIM ID
- 612570
- RefSeq RNA ID
- NM_001999, XM_017009228
- UMLS CUI
- C1414543
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