SYNGAP1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 6[13]
- Cytogenetic location
- 6p21.32[16]
- Encodes
- Synaptic Ras GTPase activating protein 1[11]
- Expressed in
- pituitary gland, right uterine tube, anterior pituitary, right ovary, right hemisphere of cerebellum, body of uterus, left ovary, superior frontal gyrus, canal of the cervix, myometrium[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- autosomal dominant non-syndromic intellectual disability 5[14]
- HomoloGene ID
- 84739[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en MRD5
en RASA1
en RASA5
en synaptic Ras GTPase activating protein 1
en SYNGAP
en SYNGAP1
zh SYNGAP1基因
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000227460, ENSG00000197283
- Ensembl transcript ID
- ENST00000638127, ENST00000418600, ENST00000637721, ENST00000638142, ENST00000455687, ENST00000490978, ENST00000636075, ENST00000636640, ENST00000428982, ENST00000636193, ENST00000629380, ENST00000636436, ENST00000395071, ENST00000461459, ENST00000636443, ENST00000636116, ENST00000481000, ENST00000470232, ENST00000635885, ENST00000293748, ENST00000636146, ENST00000479510, ENST00000637490, ENST00000637911, ENST00000628646, ENST00000637671, ENST00000637052, ENST00000414753, ENST00000636731, ENST00000637587, ENST00000355818, ENST00000449372, ENST00000484671, ENST00000637194, ENST00000646630, ENST00000644458, ENST00000645250, ENST00000682587
- Entrez Gene ID
- 8831
- Exact match
- identifiers.org
- Freebase ID
- /m/03gyb0j
- HGNC ID
- 11497
- HGNC gene symbol
- SYNGAP1
- Microsoft Academic ID (discontinued)
- 2776053993
- OMIM ID
- 603384
- RefSeq RNA ID
- NM_006772, NM_001130066
- UMLS CUI
- C1420546
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