FREM2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 13[13]
- Cytogenetic location
- 13q13.3[16]
- Expressed in
- renal medulla, tibialis anterior muscle, deltoid muscle, pancreatic epithelial cell, metanephros, lower lobe of lung, vastus lateralis muscle, endometrium, human kidney, Skeletal muscle tissue of rectus abdominis[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- Fraser syndrome[14]
- HomoloGene ID
- 18454[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en CRYPTOP
en FRAS1 related extracellular matrix 2
en FRAS1 related extracellular matrix protein 2
en FRASRS2
en FREM2
ar FREM٢
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000150893
- Ensembl transcript ID
- ENST00000482551, ENST00000280481
- Entrez Gene ID
- 341640
- Exact match
- identifiers.org
- Freebase ID
- /m/03hn3v0
- HGNC ID
- 25396
- HGNC gene symbol
- FREM2
- OMIM ID
- 608945
- RefSeq RNA ID
- XR_941571, NM_207361, XM_017020554
- UMLS CUI
- C1539531
🔗 Connections
Expressed in 6
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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