MLH3
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 14[12]
- Cytogenetic location
- 14q24.3[16]
- Encodes
- MutL homolog 3, DNA mismatch repair protein Mlh3[9][10]
- Expressed in
- monocyte, ventricular zone, Achilles tendon, epithelium of colon, right lobe of thyroid gland, left lobe of thyroid gland, granulocyte, right adrenal cortex, tibial nerve, gastric mucosa[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- colorectal cancer, Lynch syndrome[13][14]
- HomoloGene ID
- 91153[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en HNPCC7
en MLH3
en mutL homolog 3
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000119684
- Ensembl transcript ID
- ENST00000557648, ENST00000355774, ENST00000380968, ENST00000553263, ENST00000553713, ENST00000554697, ENST00000555144, ENST00000555415, ENST00000555499, ENST00000555671, ENST00000556257, ENST00000556453
- Entrez Gene ID
- 27030
- Exact match
- identifiers.org
- Freebase ID
- /m/03g_zvh
- HGNC ID
- 7128
- HGNC gene symbol
- MLH3
- Microsoft Academic ID (discontinued)
- 2777526516
- OMIM ID
- 604395
- RefSeq RNA ID
- XR_245681, NM_001040108, NM_014381, XM_005267532, XM_005267533, XM_005267534, XM_006720116, XM_017021219, XR_001750225, XM_024449538, XM_047431265, XM_047431266, XM_047431267, XM_047431268, XM_047431269, XR_007064004, XR_007064005
- UMLS CUI
- C1334511
Press Enter · cited answer in seconds