Homo sapiens mutL homolog 1 (MLH1), transcript variant 8, mRNA

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[Characteristics and clinical analysis of MLH1 c.463dupC gene mutation in a Lynch syndrome family]. [Zhonghua Yi Xue Za Zhi. 2024]
[Characteristics and clinical analysis of MLH1 c.463dupC gene mutation in a Lynch syndrome family].
Zhou DY, Liu C, Huang J, Xu N, Ji X, Yang KX, Peng JB, Pan H, Xu WJ, Zhu Z. Zhonghua Yi Xue Za Zhi. 2024 Feb 20; 104(7):547-551.
MLH1 Promotor Hypermethylation in Colorectal and Endometrial Carcinomas from Patients with Lynch Syndrome. [J Mol Diagn. 2024]
MLH1 Promotor Hypermethylation in Colorectal and Endometrial Carcinomas from Patients with Lynch Syndrome.
Helderman NC, Andini KD, van Leerdam ME, van Hest LP, Hoekman DR, Ahadova A, Bajwa-Ten Broeke SW, Bosse T, van der Logt EMJ, Imhann F, et al. J Mol Diagn. 2024 Feb; 26(2):106-114. Epub 2023 Dec 5.
MLH1 Promoter Methylation Could Be the Second Hit in Lynch Syndrome Carcinogenesis. [Genes (Basel). 2023]
MLH1 Promoter Methylation Could Be the Second Hit in Lynch Syndrome Carcinogenesis.
Carnevali IW, Cini G, Libera L, Sahnane N, Facchi S, Viel A, Sessa F, Tibiletti MG. Genes (Basel). 2023 Nov 9; 14(11). Epub 2023 Nov 9.

RefSeq alternative splicing
See 33 reference mRNA sequence splice variants for the MLH1 gene.
RefSeq protein product
See the reference protein sequence for DNA mismatch repair protein Mlh1 isoform 3 (NP_001341544.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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BioSystems
CCDS
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Components (Core)
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Functional Class
Functional class of the sequence domain architecture
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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Nucleotide