PMS2P11 PMS1 homolog 2, mismatch repair system component pseudogene 11 [Homo sapiens (human)] - Gene

Summary

Official Symbol: PMS2P11provided by HGNC
Official Full Name: PMS1 homolog 2, mismatch repair system component pseudogene 11provided by HGNC
Primary source: HGNC:HGNC:9125
See related: AllianceGenome:HGNC:9125
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: PMSR6; PMS2L11
Summary: Predicted to enable kinase activity. Predicted to be involved in mismatch repair. Predicted to be part of mismatch repair complex. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

Location:: 7q11.23

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	7	NC_000007.14 (77011447..77025554)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	7	NC_000007.13 (76640764..76654871)

Chromosome 7 - NC_000007.14 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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Readthrough DTX2P1-UPK3BP1-PMS2P11

Readthrough gene: DTX2P1-UPK3BP1-PMS2P11, Included gene: PMS2P9, Included gene: UPK3BP1, Included gene: DTX2P1

Other Names

postmeiotic segregation increased 2 pseudogene 11
postmeiotic segregation increased 2-like 11 pseudogene

Gene Ontology Provided by GOA

Function	Evidence Code	Pubs
enables kinase activity	IEA Inferred from Electronic Annotation more info

Process	Evidence Code	Pubs
involved_in phosphorylation	IEA Inferred from Electronic Annotation more info

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.