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MLH1
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MLH1
Description
mutL homolog 1
Aliases
COCA2, FCC2, HNPCC, HNPCC2, hMLH1
Gene Identifiers
mRNA Identifiers
RefSeq (mRNA)
NM_000249.4; NM_001167617.2; NM_001167618.2; NM_001167619.2; NM_001258271.1; NM_001258273.1; NM_001258274.2; NM_001354615.1; NM_001354616.1; NM_001354617.1; NM_001354618.1; NM_001354619.1; NM_001354620.1; NM_001354621.1; NM_001354622.1; NM_001354623.1; NM_001354624.1; NM_001354625.1; NM_001354626.1; NM_001354627.1; NM_001354628.1; NM_001354629.1; NM_001354630.1; XM_005265161.2; XM_017006450.2
Protein Identifiers
RefSeq (protein)
NP_000240.1; NP_001161089.1; NP_001161090.1; NP_001161091.1; NP_001245200.1; NP_001245202.1; NP_001245203.1; NP_001341544.1; NP_001341545.1; NP_001341546.1; NP_001341547.1; NP_001341548.1; NP_001341549.1; NP_001341550.1; NP_001341551.1; NP_001341552.1; NP_001341553.1; NP_001341554.1; NP_001341555.1; NP_001341556.1; NP_001341557.1; NP_001341558.1; NP_001341559.1; XP_005265218.1; XP_016861939.1
Uniprot ID
P40692; P40692; P40692; A0A024R2S9; P40692; A0A024R2S9; P40692; Q59EG3; P40692; A0A024R2S9; P40692; A0A024R2S9
Ensembl protein ID
Protein Architecture
SMART
Disease Mapping
Druggability
- Fewer loss of function mutations
- Fewer damaging SNVs/indels
- Fewer structural variants