C9orf72
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 9[14]
- Cytogenetic location
- 9p21.2[17]
- Expressed in
- monocyte, mucosa of paranasal sinus, bronchial epithelial cell, cerebellar vermis, right lung, right uterine tube, cerebellar hemisphere, Brodmann area 23, right hemisphere of cerebellum, blood[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- frontotemporal dementia with motor neuron disease 1[15]
- HomoloGene ID
- 10137[3]
- Ortholog
- C9orf72, RGD1359108, zgc:100846[8][9][10]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en ALSFTD
en C9orf72
en C9orf72-SMCR8 complex subunit
en chromosome 9 open reading frame 72
en DENND9
en DENNL72
en FTDALS
en FTDALS1
fr Chromosome 9, phase de lecture ouverte 72
pt fase de leitura aberta 72 do cromossoma 9
🔖 Identifiers · 12
- OpenAlex ID
- C2777898937
- Ensembl gene ID
- ENSG00000147894
- Ensembl transcript ID
- ENST00000619707, ENST00000379995, ENST00000379997, ENST00000380003, ENST00000488117, ENST00000647196, ENST00000644136, ENST00000673600
- Entrez Gene ID
- 203228
- Exact match
- identifiers.org
- Freebase ID
- /m/0ndx18k
- HGNC ID
- 28337
- HGNC gene symbol
- C9orf72
- Microsoft Academic ID (discontinued)
- 2777898937
- OMIM ID
- 614260
- RefSeq RNA ID
- NM_145005, NM_001256054, NM_018325
- UMLS CUI
- C1428691
🔗 Connections
Expressed in 3
Chromosome 1
Encodes 1
Found in taxon 1
Instance of 1
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Summary
C9orf72 is a gene[1].