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Gene: PMS2P3 (PMS1 homolog 2, mismatch repair system component pseudogene 3) Homo sapiens

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Symbol:

PMS2P3

Name:

PMS1 homolog 2, mismatch repair system component pseudogene 3

RGD ID:

1606835

HGNC Page

HGNC:9128

Description:

Predicted to enable ATP hydrolysis activity and ATP-dependent DNA damage sensor activity. Predicted to be involved in mismatch repair and regulation of DNA-templated transcription. Predicted to be part of mismatch repair complex.

Type:

pseudo (Ensembl: lncRNA)

RefSeq Status:

VALIDATED

Previously known as:

MGC126647; PMS2L3; PMS2L9; PMS5; PMSR3

RGD Orthologs

Mouse

Alliance Orthologs

More Info

more info ...

Related Functional Gene:

PMS2

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	75,507,747 - 75,528,123 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	75,510,931 - 75,516,235 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh38.p14 Ensembl	7	75,490,413 - 75,528,172 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	75,137,069 - 75,157,453 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	74,975,005 - 74,995,330 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	7	70,004,871 - 70,025,253 (-)	NCBI		Celera
Cytogenetic Map	7	q11.23	NCBI
HuRef	7	70,239,269 - 70,243,167 (-)	NCBI		HuRef
HuRef	7	62,940,232 - 62,947,271 (-)	NCBI		HuRef
CHM1_1	7	75,067,163 - 75,087,539 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	7	76,795,078 - 76,815,462 (-)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	74,470,133 - 74,490,517 (-)	NCBI

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-epigallocatechin 3-gallate (EXP)

arsane (EXP)

arsenic atom (EXP)

bisphenol A (EXP)

CGP 52608 (EXP)

cobalt dichloride (EXP)

copper(II) sulfate (EXP)

doxorubicin (EXP)

hydrogen peroxide (EXP)

potassium chromate (EXP)

sunitinib (EXP)

tert-butyl hydroperoxide (EXP)

tunicamycin (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

biological_process (ND)

mismatch repair (IEA)

regulation of DNA-templated transcription (IEA)

Cellular Component

cellular_component (ND)

mismatch repair complex (IEA)

Molecular Function

ATP hydrolysis activity (IEA)

ATP-dependent DNA damage sensor activity (IEA)

molecular_function (ND)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:7980603	PMID:8586419	PMID:10737800	PMID:12477932	PMID:20819778	PMID:21873635	PMID:33961781

Genomics

Comparative Map Data

PMS2P3
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	75,507,747 - 75,528,123 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	75,510,931 - 75,516,235 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh38.p14 Ensembl	7	75,490,413 - 75,528,172 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	75,137,069 - 75,157,453 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	74,975,005 - 74,995,330 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	7	70,004,871 - 70,025,253 (-)	NCBI		Celera
Cytogenetic Map	7	q11.23	NCBI
HuRef	7	70,239,269 - 70,243,167 (-)	NCBI		HuRef
HuRef	7	62,940,232 - 62,947,271 (-)	NCBI		HuRef
CHM1_1	7	75,067,163 - 75,087,539 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	7	76,795,078 - 76,815,462 (-)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	74,470,133 - 74,490,517 (-)	NCBI

Gm12258
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	58,737,971 - 58,752,783 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	58,737,984 - 58,752,782 (+)	Ensembl		GRCm39 Ensembl
GRCm38	11	58,847,162 - 58,861,957 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	58,847,158 - 58,861,956 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	58,663,359 - 58,676,079 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	58,663,359 - 58,676,079 (+)	NCBI		MGSCv36	mm8
Celera	11	63,611,131 - 63,625,944 (+)	NCBI		Celera
Cytogenetic Map	11	B1.3	NCBI
cM Map	11	36.33	NCBI

Variants

Variants in PMS2P3
4 total Variants

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1593
Count of miRNA genes:	677
Interacting mature miRNAs:	745
Transcripts:	ENST00000275580, ENST00000301956, ENST00000394921, ENST00000418756, ENST00000422064, ENST00000430602, ENST00000434405, ENST00000437568, ENST00000438326, ENST00000529061, ENST00000533167
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2439	2788	2253	4974	1726	2351	6	624	1951	465	2270	7305	6471	53	3734	1	852	1744	1617	174	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NR_028059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC018720	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC211429	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC007683	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC014421	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC046153	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC087844	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC101598	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC143635	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BE938866	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471220	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	D38437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	D38498	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U38979	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000394921

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,528,051 (-)	Ensembl

Ensembl Acc Id:

ENST00000418756

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,528,123 (-)	Ensembl

Ensembl Acc Id:

ENST00000422064

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,512,589 - 75,528,148 (-)	Ensembl

Ensembl Acc Id:

ENST00000430602

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,527,836 (-)	Ensembl

Ensembl Acc Id:

ENST00000437568

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,511,017 - 75,528,088 (-)	Ensembl

Ensembl Acc Id:

ENST00000438326

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,516,043 - 75,525,955 (-)	Ensembl

Ensembl Acc Id:

ENST00000529061

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,510,931 - 75,516,235 (-)	Ensembl

Ensembl Acc Id:

ENST00000533167

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,510,676 - 75,527,853 (-)	Ensembl

Ensembl Acc Id:

ENST00000691440

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,512,124 - 75,528,103 (-)	Ensembl

Ensembl Acc Id:

ENST00000693762

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,528,132 (-)	Ensembl

Ensembl Acc Id:

ENST00000702274

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,528,096 (-)	Ensembl

Ensembl Acc Id:

ENST00000845724

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,502,855 - 75,528,138 (-)	Ensembl

Ensembl Acc Id:

ENST00000845725

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,490,413 - 75,512,638 (-)	Ensembl

Ensembl Acc Id:

ENST00000845726

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,528,172 (-)	Ensembl

Ensembl Acc Id:

ENST00000845727

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,751 - 75,528,146 (-)	Ensembl

Ensembl Acc Id:

ENST00000845728

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,528,118 (-)	Ensembl

Ensembl Acc Id:

ENST00000845729

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,528,121 (-)	Ensembl

Ensembl Acc Id:

ENST00000845730

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,528,118 (-)	Ensembl

Ensembl Acc Id:

ENST00000845731

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,528,103 (-)	Ensembl

Ensembl Acc Id:

ENST00000845732

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,528,103 (-)	Ensembl

Ensembl Acc Id:

ENST00000845733

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,528,099 (-)	Ensembl

Ensembl Acc Id:

ENST00000845734

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,527,990 (-)	Ensembl

Ensembl Acc Id:

ENST00000845735

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,527,963 (-)	Ensembl

Ensembl Acc Id:

ENST00000845736

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,749 - 75,527,899 (-)	Ensembl

Ensembl Acc Id:

ENST00000845737

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,527,889 (-)	Ensembl

Ensembl Acc Id:

ENST00000845738

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,527,885 (-)	Ensembl

Ensembl Acc Id:

ENST00000845739

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,527,868 (-)	Ensembl

Ensembl Acc Id:

ENST00000845740

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,527,673 (-)	Ensembl

Ensembl Acc Id:

ENST00000845741

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,527,606 (-)	Ensembl

Ensembl Acc Id:

ENST00000845742

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,510,741 - 75,527,965 (-)	Ensembl

Ensembl Acc Id:

ENST00000845743

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,510,680 - 75,527,869 (-)	Ensembl

Ensembl Acc Id:

ENST00000845746

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,512,124 - 75,528,121 (-)	Ensembl

Ensembl Acc Id:

ENST00000845747

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,512,119 - 75,527,896 (-)	Ensembl

Ensembl Acc Id:

ENST00000845748

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,512,100 - 75,527,849 (-)	Ensembl

Ensembl Acc Id:

ENST00000845878

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,502,855 - 75,514,779 (-)	Ensembl

Ensembl Acc Id:

ENST00000845951

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,746 - 75,514,850 (-)	Ensembl

Ensembl Acc Id:

ENST00000845952

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,514,825 (-)	Ensembl

Ensembl Acc Id:

ENST00000845954

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,514,762 (-)	Ensembl

Ensembl Acc Id:

ENST00000845969

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,510,677 - 75,516,178 (-)	Ensembl

Ensembl Acc Id:

ENST00000845970

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,545 - 75,512,390 (-)	Ensembl

Ensembl Acc Id:

ENST00000845972

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,512,124 - 75,515,765 (-)	Ensembl

Ensembl Acc Id:

ENST00000845973

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,747 - 75,511,302 (-)	Ensembl

Ensembl Acc Id:

ENST00000845974

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	75,507,750 - 75,511,114 (-)	Ensembl

RefSeq Acc Id:

NR_028059

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	75,507,747 - 75,528,123 (-)	NCBI
GRCh37	7	75,137,069 - 75,157,453 (-)	RGD
Celera	7	70,004,871 - 70,025,253 (-)	RGD
HuRef	7	70,226,268 - 70,243,191 (-)	NCBI
CHM1_1	7	75,067,163 - 75,087,539 (-)	NCBI
T2T-CHM13v2.0	7	76,795,078 - 76,815,462 (-)	NCBI
CRA_TCAGchr7v2	7	74,470,133 - 74,490,517 (-)	ENTREZGENE

Sequence:

show sequence

GCACTGCCCTCGCTTCCTGTGAGTCTTCAGGTCGCCGCTTGCTCTCGTTCCTAGGGTTTGGCCT
GCAGTGGACGAGCATCGCATAGCCTGCGGGGCTGGATGCTGACCGCCCGGGCCAGCACCTAGGC
GGACGCGGAGCTGTGCAGACCAGGGTTCGCGCGGGCCGGGTGGAGGCTCAAGCGGGGACCCCGG
AGCGTGAGCCCCGGAGTCGGCGGCGCTGGGGCCAGAGGGGCCGGGAGGGAGTCGGCTGAGGTGG
CGGCGGAGGCGAAGTGGCGGCGGAGGCGAAGGGGCGGCGGGACCCGGGCCTGGCCCGTATGTGT
CCTTGGCGGCCTAGACTAGGCCGTCGCTGTATGGTGAGCCCCAGGGAGGCGGATCTGGGCCCCC
AGAAGGACACCCGCCTGGATTTGCCCCGTAGGCCCGGCCCGGGCCCCTCGGGAGCAGAACAGCC
TTGGTGAGGTGGACAGGAGGGGACCTCGCGAGCAGACGCGCGCGCCAGCGACAGCAGCCCCGCC
CCGGCCTCTCGGGAGCCGGGGGGCAGAGGCTGCGGAGCCCCAGGAGGGTCTATCAGCCACAGTC
TCTGCATGTTTCCAAGAGCAACAGGAAATGAACACATTGCAGGGGCCAGTGTCATTCAAAGATG
TGGCTGTGGATTTCACCCAGGAGGAGTGGCGGCAACTGGACCCTGATGAGAAGATAGCATACGG
GGATGTGATGTTGGAGAACTACAGCCATCTAGTTTCTGTGGGGTATGATTATCACCAAGCCAAA
CATCATCATGGAGTGGAGGTGAAGGAAGTGGAGCAGGGAGAGGAGCCGTGGATAATGGAAGGTG
AATTTCCATGTCAACATAGTCCAGTACAGAACCTGCTAAGGCCATCAAACCTATTGATCGGAAG
TCAGTCCATCAGATTTGCTCTGGGCCAGTGGTACTGAGTCTAAGCACTGCAGTGAAGGAGTTAG
TAGAAAACAGTCTGGATGCTGGTGCCACTAATATTGATCTAAAGCTTAAGGACTATGGAGTGGA
TCTCATTGAAGTTTCAGACAATGGATGTGGGGTAGAAGAAGAAAACTTTGAAGGCTTAATCTCT
TTCAGCTCTGAAACATCACACATGTAAGATTCAAGAGTTTGCCGACCTAACTGAAGTTGAAACT
TTCGGTTTTCAGGGGGAAGCTCTGAGCTCACTGTGTGCACTGAGCGATGTCACCATTTCTACCT
GCCACGCGTCGGTGAAGGTTGGGACTCGACTGGTGTTTGATCACGATGGGAAAATCATCCAGGA
AACCCCCTACCCCCACCCCAGAGGGACCACAGTCAGCGTGAAGCAGTTATTTTCTACGCTACCT
GTGCGCCATAAGGAATTTCAAAGGAATATTAAGAAGACGTGCCTGCTTCCCCTTCGCCTTCTGC
CGTGATTGTCAGTTTCCTGAGGCCTCCCCAGCCATGCTTCCTGTACAGCCTGCAGAACTGTGAG
TCAATTAAACCTCTTTTCTTCATAAATTAAAAAAAAAAAAAAAAAA

hide sequence

Protein Sequences


GenBank Protein	AAA97459	(Get FASTA)	NCBI Sequence Viewer
	AAI01599	(Get FASTA)	NCBI Sequence Viewer
	BAA07472	(Get FASTA)	NCBI Sequence Viewer
	BAA07510	(Get FASTA)	NCBI Sequence Viewer
	EAW71765	(Get FASTA)	NCBI Sequence Viewer
	EAW71766	(Get FASTA)	NCBI Sequence Viewer
	Q13401	(Get FASTA)	NCBI Sequence Viewer

Protein Domains

KRAB

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q13401-F1-model_v2	AlphaFold	Q13401	1-168	view protein structure

Promoters

RGD ID:

6805553

Promoter ID:

HG_KWN:58124

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000275580, ENST00000301956, OTTHUMT00000342862, OTTHUMT00000342940, OTTHUMT00000342942, UC003UDN.1, UC003UDO.1, UC003UDP.1, UC003UDQ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	7	74,995,131 - 74,995,631 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:9128	AgrOrtholog
COSMIC	PMS2P3	COSMIC
Ensembl Genes	ENSG00000127957	Ensembl
	ENSG00000291092	Ensembl, ENTREZGENE
Ensembl Transcript	ENST00000845735	ENTREZGENE
Gene3D-CATH	3.30.565.10	UniProtKB/Swiss-Prot
	6.10.140.140	UniProtKB/Swiss-Prot
GTEx	ENSG00000127957	GTEx
	ENSG00000291092	GTEx
HGNC ID	HGNC:9128	ENTREZGENE
Human Proteome Map	PMS2P3	Human Proteome Map
InterPro	HATPase_C_sf	UniProtKB/Swiss-Prot
	KRAB	UniProtKB/Swiss-Prot
	KRAB_dom_sf	UniProtKB/Swiss-Prot
	MutL/Mlh/Pms	UniProtKB/Swiss-Prot
NCBI Gene	PMS2P3	ENTREZGENE
PANTHER	MISMATCH REPAIR ENDONUCLEASE PMS2	UniProtKB/Swiss-Prot
	PTHR10073	UniProtKB/Swiss-Prot
Pfam	HATPase_c_3	UniProtKB/Swiss-Prot
	KRAB	UniProtKB/Swiss-Prot
PharmGKB	PA33454	PharmGKB
PROSITE	KRAB	UniProtKB/Swiss-Prot
SMART	KRAB	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF109640	UniProtKB/Swiss-Prot
	SSF55874	UniProtKB/Swiss-Prot
UniProt	PM2P3_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary	A6NG70	UniProtKB/Swiss-Prot
	Q3MJ29	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-07-14	PMS2P3	PMS1 homolog 2, mismatch repair system component pseudogene 3		postmeiotic segregation increased 2 pseudogene 3	Symbol and/or name change	5135510	APPROVED
2011-07-27	PMS2P3	postmeiotic segregation increased 2 pseudogene 3	PMS2L3	postmeiotic segregation increased 2-like 3	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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