LRIT3
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 4[12]
- Cytogenetic location
- 4q25[15]
- Expressed in
- testicle, superior frontal gyrus, cerebellar hemisphere, right hemisphere of cerebellum, primary visual cortex, Brodmann area 9, renal cortex, tibial nerve, granulocyte, right frontal lobe[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- congenital stationary night blindness 1F[13]
- HomoloGene ID
- 19426[3]
- Strand orientation
- forward strand[14]
🏷️ Also known as
en CSNB1F
en FIGLER4
en leucine rich repeat, Ig-like and transmembrane domains 3
en leucine-rich repeat, Ig-like and transmembrane domains 3
en LRIT3
ar LRIT٣
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000183423
- Ensembl transcript ID
- ENST00000594814, ENST00000327908
- Entrez Gene ID
- 345193
- Exact match
- identifiers.org
- Freebase ID
- /m/0wbjlzg
- HGNC ID
- 24783
- HGNC gene symbol
- LRIT3
- OMIM ID
- 615004
- RefSeq RNA ID
- NM_198506, XM_017008167, XM_017008168
- UMLS CUI
- C2239655
🔗 Connections
Expressed in 6
Chromosome 1
Found in taxon 1
Instance of 1
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