DNMT3B
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 20[12]
- Cytogenetic location
- 20q11.21[16]
- Expressed in
- secondary oocyte, hair follicle, sperm, embryo, gonad, testicle, ganglionic eminence, body of pancreas, ventricular zone, corpus epididymis[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- inflammatory bowel diseases, immunodeficiency-centromeric instability-facial anomalies syndrome[13][14]
- HomoloGene ID
- 56000[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en DNA (cytosine-5-)-methyltransferase 3 beta
en DNA methyltransferase 3 beta
en DNMT3B
en FSHD4
en ICF
en ICF1
en M.HsaIIIB
🔖 Identifiers · 13
- OpenAlex ID
- C2777142704
- Image (Wikimedia Commons)
- Protein DNMT3B PDB 1khc.png ↗
- Ensembl gene ID
- ENSG00000088305
- Ensembl transcript ID
- ENST00000456297, ENST00000201963, ENST00000328111, ENST00000348286, ENST00000353855, ENST00000443239
- Entrez Gene ID
- 1789
- Exact match
- identifiers.org
- Freebase ID
- /m/02vvw1t
- HGNC ID
- 2979
- HGNC gene symbol
- DNMT3B
- Microsoft Academic ID (discontinued)
- 2777142704
- OMIM ID
- 602900
- RefSeq RNA ID
- XR_936512, NM_001207055, NM_001207056, NM_006892, NM_175848, NM_175849, NM_175850, XM_011528653, XM_011528654, XR_936510, XR_936511
Show all 13 identifiers +1
- UMLS CUI
- C1333242
🔗 Connections
Expressed in 6
← Genetic association 2
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
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