FBLN1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 22[13]
- Cytogenetic location
- 22q13.31[16]
- Expressed in
- canal of the cervix, gallbladder, vena cava, pericardium, gastric mucosa, ectocervix, vagina, left uterine tube, right auricle of heart, tendon of biceps brachii[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- bipolar disorder[14]
- HomoloGene ID
- 21295[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en FBLN
en FBLN1
en FIBL1
en fibulin 1
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000077942
- Ensembl transcript ID
- ENST00000484531, ENST00000262722, ENST00000327858, ENST00000340923, ENST00000402984, ENST00000411478, ENST00000437711, ENST00000439835, ENST00000442170, ENST00000445110, ENST00000450975, ENST00000451475, ENST00000454279, ENST00000455233, ENST00000460300, ENST00000460538, ENST00000465578, ENST00000476366
- Entrez Gene ID
- 2192
- Exact match
- identifiers.org
- Freebase ID
- /m/03cvz3m
- HGNC ID
- 3600
- HGNC gene symbol
- FBLN1
- Microsoft Academic ID (discontinued)
- 2779684723
- OMIM ID
- 135820
- UMLS CUI
- C1414539
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Summary
FBLN1 is a gene[1].