SEMA4A
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[11]
- Cytogenetic location
- 1q22[15]
- Encodes
- semaphorin 4A[9]
- Expressed in
- monocyte, granulocyte, bone marrow cell, blood, amygdala, nucleus accumbens, skin of abdomen, left lobe of thyroid gland, retinal pigment epithelium, cingulate gyrus[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- retinitis pigmentosa 35, cone-rod dystrophy 10[12][13]
- HomoloGene ID
- 8425[3]
- Strand orientation
- forward strand[14]
🏷️ Also known as
en SEMA4A
en CORD10
en RP35
en SEMB
en SEMAB
en semaphorin 4A
ar SEMA٤A
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000196189
- Ensembl transcript ID
- ENST00000633494, ENST00000355014, ENST00000368282, ENST00000368284, ENST00000368285, ENST00000414683, ENST00000435124, ENST00000438830, ENST00000462892, ENST00000466698, ENST00000469065, ENST00000470306, ENST00000484155, ENST00000485575, ENST00000487358
- Entrez Gene ID
- 64218
- Exact match
- identifiers.org
- Freebase ID
- /m/03hgqjc
- HGNC ID
- 10729
- HGNC gene symbol
- SEMA4A
- OMIM ID
- 607292
- RefSeq RNA ID
- NM_001193300, NM_001193301, NM_001193302, NM_022367, XM_011509871, XM_011509872, XM_011509874, XM_011509875, XM_011509878, NM_001370567, NM_001370568, NM_001370569, NM_001370571, XM_047427664, XM_047427670, XM_047427671, XM_047427677, XM_047427678
- UMLS CUI
- C1419947
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Instance of 1
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