Epm2a (epilepsy, progressive myoclonic epilepsy, type 2 gene alpha) - Rat Genome Database

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Gene: Epm2a (epilepsy, progressive myoclonic epilepsy, type 2 gene alpha) Mus musculus
Analyze
Symbol: Epm2a
Name: epilepsy, progressive myoclonic epilepsy, type 2 gene alpha
RGD ID: 731931
MGI Page MGI
Description: Enables several functions, including glycogen (starch) synthase activity; phosphatase activity; and starch binding activity. Involved in carbohydrate phosphorylation and glycogen biosynthetic process. Acts upstream of or within several processes, including habituation; regulation of protein localization; and regulation of protein metabolic process. Located in several cellular components, including cytoplasmic side of endoplasmic reticulum membrane; dendrite; and perikaryon. Is active in cytosol. Is expressed in several structures, including brain. Used to study Lafora disease and lymphoma. Human ortholog(s) of this gene implicated in Lafora disease and progressive myoclonus epilepsy. Orthologous to human EPM2A (EPM2A glucan phosphatase, laforin).
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: glucan phosphatase; l; lafora PTPase; laforin; LAFPTPase; Tg(TcraK,TcrbK)TG-BFlv; TG-B
RGD Orthologs
Human
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Latest Assembly: GRCm39 - Mouse Genome Assembly GRCm39
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391011,218,435 - 11,335,408 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1011,219,148 - 11,335,388 (+)EnsemblGRCm39 Ensembl
GRCm381011,342,691 - 11,459,664 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1011,343,404 - 11,459,644 (+)EnsemblGRCm38mm10GRCm38
MGSCv371011,063,243 - 11,177,275 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361011,033,594 - 11,147,912 (+)NCBIMGSCv36mm8
Celera1011,232,470 - 11,346,997 (+)NCBICelera
Cytogenetic Map10A1NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
autophagosome assembly  (IMP)
autophagy  (IMP)
calcium ion transport  (IMP)
carbohydrate metabolic process  (IEA)
carbohydrate phosphorylation  (IMP)
dephosphorylation  (ISO)
glial cell proliferation  (IGI)
glycogen biosynthetic process  (IDA,IGI,IMP)
glycogen metabolic process  (IGI,IMP,ISO)
habituation  (IMP)
L-glutamate transmembrane transport  (IMP)
macromolecule metabolic process  (IMP)
mitochondrion organization  (IMP)
negative regulation of cell cycle  (IMP)
negative regulation of dephosphorylation  (ISO)
negative regulation of gene expression  (IMP)
negative regulation of peptidyl-serine phosphorylation  (IMP)
negative regulation of phosphatase activity  (ISO)
negative regulation of TOR signaling  (ISO)
nervous system development  (IMP)
peptidyl-tyrosine dephosphorylation  (ISO)
positive regulation of macroautophagy  (IGI,IMP,ISO)
proteasome-mediated ubiquitin-dependent protein catabolic process  (IMP)
protein dephosphorylation  (ISO)
regulation of cell growth  (IMP)
regulation of gene expression  (IMP)
regulation of glycogen (starch) synthase activity  (IMP)
regulation of phosphorylation  (IMP)
regulation of proteasomal protein catabolic process  (IMP)
regulation of protein import into nucleus  (IDA)
regulation of protein kinase activity  (IMP)
regulation of protein localization to plasma membrane  (IGI)
regulation of protein phosphorylation  (IMP)
regulation of protein ubiquitination  (IGI)
regulation of ubiquitin protein ligase activity  (IMP)
Wnt signaling pathway  (IMP)

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View

Mammalian Phenotype
abnormal brain wave pattern  (IAGP)
abnormal DNA methylation  (IAGP)
abnormal enzyme/coenzyme level  (IAGP)
abnormal exocrine pancreas morphology  (IAGP)
abnormal heart morphology  (IAGP)
abnormal pancreas morphology  (IAGP)
abnormal passive avoidance behavior  (IAGP)
abnormal Purkinje cell morphology  (IEA)
ataxia  (IAGP)
axon degeneration  (IAGP)
decreased grip strength  (IAGP)
hepatic steatosis  (IAGP)
hippocampal neuron degeneration  (IAGP)
hypoglycemia  (IAGP)
impaired balance  (IAGP)
impaired coordination  (IAGP)
improved glucose tolerance  (IAGP)
increased body fat mass  (IAGP)
increased body weight  (IAGP)
increased cardiac cell glucose uptake  (IAGP)
increased cardiac muscle glycogen level  (IAGP)
increased CD8-positive, alpha-beta T cell number  (IAGP)
increased circulating cholesterol level  (IAGP)
increased circulating free fatty acids level  (IAGP)
increased circulating ketone body level  (IAGP)
increased circulating triglyceride level  (IAGP)
increased energy expenditure  (IAGP)
increased fluid intake  (IAGP)
increased insulin sensitivity  (IAGP)
increased liver cholesterol level  (IAGP)
increased liver triglyceride level  (IAGP)
increased neuron apoptosis  (IAGP)
increased oxygen consumption  (IAGP)
increased respiratory quotient  (IAGP)
increased startle reflex  (IAGP)
increased T cell derived lymphoma incidence  (IAGP)
Lafora bodies  (IAGP)
muscle weakness  (IAGP)
myoclonus  (IAGP)
pancreas inflammation  (IAGP)
polyphagia  (IAGP)
premature death  (IAGP)
Purkinje cell degeneration  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. Regional and developmental expression of Epm2a gene and its evolutionary conservation. Ganesh S, etal., Biochem Biophys Res Commun 2001 May 25;283(5):1046-53.
2. Electronic Transfer of Homolog Data MGD and Homologene mouse data transfer
3. MGDs mouse GO annotations MGD data from the GO Consortium
4. MGD IEA MGD IEA
5. Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy. Minassian BA, etal., Nat Genet. 1998 Oct;20(2):171-4.
6. Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Okazaki Y, etal., Nature. 2002 Dec 5;420(6915):563-73.
7. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
8. Mouse MP Annotation Import Pipeline RGD automated import pipeline
9. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
10. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1532662   PMID:7594526   PMID:8889548   PMID:10092504   PMID:10349636   PMID:11042159   PMID:11076861   PMID:11217851   PMID:12019206   PMID:12391185   PMID:12915448   PMID:15102711  
PMID:15128765   PMID:15541350   PMID:16084644   PMID:16141072   PMID:16141073   PMID:16602821   PMID:16959610   PMID:16971387   PMID:17118331   PMID:17908927   PMID:17952067   PMID:18040046  
PMID:18519661   PMID:18824542   PMID:18852261   PMID:19036738   PMID:19529779   PMID:19542233   PMID:19805094   PMID:20453062   PMID:21267068   PMID:21493628   PMID:21552327   PMID:21677750  
PMID:21873635   PMID:21965301   PMID:22124153   PMID:22186021   PMID:22186026   PMID:22487859   PMID:22542948   PMID:22578008   PMID:22669944   PMID:22751135   PMID:22961547   PMID:23546741  
PMID:23663739   PMID:23851691   PMID:23913475   PMID:24068615   PMID:24131995   PMID:24209604   PMID:24430976   PMID:24472629   PMID:24838580   PMID:24914213   PMID:25309313   PMID:25416783  
PMID:26216881   PMID:26976331   PMID:27041370   PMID:27107699   PMID:27975203   PMID:28063983   PMID:28098937   PMID:28536304   PMID:28619201   PMID:28973665   PMID:29408991   PMID:31042462  
PMID:32785985   PMID:32817315   PMID:32892347   PMID:33092303   PMID:34043942   PMID:36511140  


Genomics

Comparative Map Data
Epm2a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391011,218,435 - 11,335,408 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1011,219,148 - 11,335,388 (+)EnsemblGRCm39 Ensembl
GRCm381011,342,691 - 11,459,664 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1011,343,404 - 11,459,644 (+)EnsemblGRCm38mm10GRCm38
MGSCv371011,063,243 - 11,177,275 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361011,033,594 - 11,147,912 (+)NCBIMGSCv36mm8
Celera1011,232,470 - 11,346,997 (+)NCBICelera
Cytogenetic Map10A1NCBI
EPM2A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386145,383,353 - 145,736,023 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl6145,382,535 - 145,736,023 (-)EnsemblGRCh38hg38GRCh38
GRCh376145,946,441 - 146,057,159 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366145,988,133 - 146,098,684 (-)NCBINCBI36Build 36hg18NCBI36
Build 346145,988,132 - 146,098,684NCBI
Celera6146,686,800 - 146,797,348 (-)NCBICelera
Cytogenetic Map6q24.3NCBI
HuRef6143,510,000 - 143,620,189 (-)NCBIHuRef
CHM1_16146,209,644 - 146,320,201 (-)NCBICHM1_1
T2T-CHM13v2.06146,574,195 - 146,956,629 (-)NCBIT2T-CHM13v2.0
Epm2a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.215,727,111 - 5,845,338 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl15,727,066 - 5,920,555 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx15,419,467 - 5,535,147 (+)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.0111,419,821 - 11,535,500 (+)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.015,701,665 - 5,817,345 (+)NCBIRnor_WKY
Rnor_6.015,448,958 - 5,571,512 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl15,448,958 - 5,571,512 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.017,100,639 - 7,223,403 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.116,051,557 - 6,172,313 (+)NCBI
Celera14,243,803 - 4,360,561 (+)NCBICelera
Cytogenetic Map1p13NCBI
Epm2a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543614,926,123 - 14,983,180 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495543614,925,452 - 14,982,357 (+)NCBIChiLan1.0ChiLan1.0
EPM2A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan16163,278,722 - 163,622,838 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v06143,179,097 - 143,525,223 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.16148,133,563 - 148,238,519 (-)NCBIpanpan1.1PanPan1.1panPan2
EPM2A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1136,835,775 - 36,977,653 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl136,870,594 - 36,931,847 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha137,577,467 - 37,858,360 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0136,862,309 - 37,141,316 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl137,028,269 - 37,141,626 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1136,732,602 - 37,013,661 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0136,604,089 - 36,884,723 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0137,104,772 - 37,201,859 (-)NCBIUU_Cfam_GSD_1.0
Epm2a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404946131,813,991 - 131,874,561 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936625738,124 - 821,566 (+)EnsemblSpeTri2.0
SpeTri2.0NW_004936625761,013 - 819,826 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FBXO30
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl119,806,765 - 19,893,339 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1119,806,363 - 19,893,350 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2122,050,546 - 22,135,943 (+)NCBISscrofa10.2Sscrofa10.2susScr3
EPM2A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11326,152,974 - 26,266,676 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1326,153,319 - 26,264,568 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666040202,127,578 - 202,247,016 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Epm2a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247538,715,898 - 8,804,194 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247538,715,898 - 8,805,728 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in Epm2a
3353 total Variants
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:932
Count of miRNA genes:552
Interacting mature miRNAs:688
Transcripts:ENSMUST00000069106, ENSMUST00000161438
Prediction methods:Miranda, Rnahybrid, Targetscan
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.


QTLs in Region (GRCm39)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
11532725Sluc44b_msusceptibility to lung cancer 44b (mouse)10126289265Mouse
11532724Sluc44c_msusceptibility to lung cancer 44c (mouse)10126289265Mouse
11532723Sluc44d_msusceptibility to lung cancer 44d (mouse)10126289265Mouse
11532722Sluc44e_msusceptibility to lung cancer 44e (mouse)10126289265Mouse
11532721Sluc44_msusceptibility to lung cancer 44 (mouse)10126289265Mouse
11532720Sluc44a_msusceptibility to lung cancer 44a (mouse)10126289265Mouse
11532718Sluc44f_msusceptibility to lung cancer 44f (mouse)10126289265Mouse
11532717Sluc44g_msusceptibility to lung cancer 44g (mouse)10126289265Mouse
11533917Mts2_mmammary tumor susceptibility 2 (mouse)10126289265Mouse
1300759Geot_mgeotaxia (mouse)Not determined10126289265Mouse
1300881Sluc29_msusceptibility to lung cancer 29 (mouse)Not determined10126289265Mouse
12879494Facq1_mfear acquisition QTL 1 (mouse)10131279130Mouse
15039341Nmrs28_mNAFLD-associated magnetic resonance shift 28 (mouse)1035100134351001Mouse
1357813Ath20_matherosclerosis 20 (mouse)Not determined10328318537283334Mouse
1300790Pgia6_mproteoglycan induced arthritis 6 (mouse)Not determined10381017137810295Mouse
1300997Eae15_msusceptibility to experimental allergic encephalomyelitis 15 (mouse)Not determined10440815438408276Mouse
13208561Wght8_mweight 8 (mouse)10495000043875996Mouse
1302092Ath11_matherosclerosis 11 (mouse)Not determined10615194558693521Mouse
1357740Obsty3_mobesity 3 (mouse)Not determined108235478116190980Mouse
1558865Lith21_mlithogenic gene 21 (mouse)Not determined10852500342525126Mouse
1301796Mop2_mmorphine preference 2 (mouse)Not determined10928911929028424Mouse
1301448Pas11_mpulmonary adenoma susceptibility 11 (mouse)Not determined10989026443890391Mouse
1301129Alcp15_malcohol preference locus 15 (mouse)Not determined10989026443890391Mouse
1302133Alcp16_malcohol preference locus 16 (mouse)Not determined10989026443890391Mouse
1301386Sysbp1_msystolic blood pressure 1 (mouse)Not determined101010826587401095Mouse


Expression


Sequence


Reference Sequences
RefSeq Acc Id: ENSMUST00000069106   ⟹   ENSMUSP00000066050
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl1011,219,148 - 11,335,388 (+)Ensembl
GRCm38.p6 Ensembl1011,343,404 - 11,459,644 (+)Ensembl
RefSeq Acc Id: ENSMUST00000161438
RefSeq Status:
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl1011,219,197 - 11,324,442 (+)Ensembl
GRCm38.p6 Ensembl1011,343,453 - 11,448,698 (+)Ensembl
RefSeq Acc Id: NM_010146   ⟹   NP_034276
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm391011,219,189 - 11,333,221 (+)NCBI
GRCm381011,343,445 - 11,457,477 (+)NCBI
MGSCv371011,063,243 - 11,177,275 (+)RGD
Celera1011,232,470 - 11,346,997 (+)RGD
cM Map10 ENTREZGENE
Sequence:
RefSeq Acc Id: XR_003948588
RefSeq Status:
Type: NON-CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm391011,218,435 - 11,335,408 (+)NCBI
GRCm381011,342,691 - 11,459,664 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_034276 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAD26336 (Get FASTA)   NCBI Sequence Viewer  
  BAC31004 (Get FASTA)   NCBI Sequence Viewer  
  EDL03516 (Get FASTA)   NCBI Sequence Viewer  
  Q9WUA5 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_034276   ⟸   NM_010146
- UniProtKB: Q8BY80 (UniProtKB/Swiss-Prot),   Q9WUA5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSMUSP00000066050   ⟸   ENSMUST00000069106
Protein Domains
CBM20   Tyrosine-protein phosphatase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9WUA5-F1-model_v2 AlphaFold Q9WUA5 1-330 view protein structure

Promoters
RGD ID:6819268
Promoter ID:MM_KWN:3541
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day0,   3T3L1_Day3,   3T3L1_Day4,   BoneMarrow_0Hour,   BoneMarrow_2Hour,   BoneMarrow_4Hour,   Brain,   ES_Cell,   Kidney,   Liver,   Lung,   MEF_B6
Transcripts:OTTMUST00000078597,   OTTMUST00000081636,   UC007EJU.1
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv361011,062,991 - 11,063,491 (+)MPROMDB
RGD ID:8671500
Promoter ID:EPDNEW_M13777
Type:initiation region
Name:Epm2a_1
Description:Mus musculus epilepsy, progressive myoclonic epilepsy, type 2gene alpha , mRNA.
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm381011,343,416 - 11,343,476EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene MGI:1341085 AgrOrtholog
Ensembl Genes ENSMUSG00000055493 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSMUSP00000066050 ENTREZGENE
  ENSMUSP00000066050.5 UniProtKB/Swiss-Prot
Ensembl Transcript ENSMUST00000069106 ENTREZGENE
  ENSMUST00000069106.5 UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot
  3.90.190.10 UniProtKB/Swiss-Prot
InterPro Carb-bd-like_fold UniProtKB/Swiss-Prot
  CBM20_laforin UniProtKB/Swiss-Prot
  CBM_fam20 UniProtKB/Swiss-Prot
  DSP_laforin-like UniProtKB/Swiss-Prot
  Dual-sp_phosphatase_cat-dom UniProtKB/Swiss-Prot
  Ig-like_fold UniProtKB/Swiss-Prot
  Laforin UniProtKB/Swiss-Prot
  Prot-tyrosine_phosphatase-like UniProtKB/Swiss-Prot
  Tyr_Pase_AS UniProtKB/Swiss-Prot
  TYR_PHOSPHATASE_dom UniProtKB/Swiss-Prot
  TYR_PHOSPHATASE_DUAL_dom UniProtKB/Swiss-Prot
KEGG Report mmu:13853 UniProtKB/Swiss-Prot
MGD MGI:1341085 ENTREZGENE
NCBI Gene 13853 ENTREZGENE
PANTHER LAFORIN UniProtKB/Swiss-Prot
  PTHR46864 UniProtKB/Swiss-Prot
Pfam CBM_20 UniProtKB/Swiss-Prot
  DSPc UniProtKB/Swiss-Prot
PhenoGen Epm2a PhenoGen
PROSITE CBM20 UniProtKB/Swiss-Prot
  TYR_PHOSPHATASE_1 UniProtKB/Swiss-Prot
  TYR_PHOSPHATASE_2 UniProtKB/Swiss-Prot
  TYR_PHOSPHATASE_DUAL UniProtKB/Swiss-Prot
SMART CBM_2 UniProtKB/Swiss-Prot
  DSPc UniProtKB/Swiss-Prot
Superfamily-SCOP SSF49452 UniProtKB/Swiss-Prot
  SSF52799 UniProtKB/Swiss-Prot
UniProt EPM2A_MOUSE UniProtKB/Swiss-Prot
  Q8BY80 ENTREZGENE
  Q9WUA5 ENTREZGENE
UniProt Secondary G5E8E2 UniProtKB/Swiss-Prot
  Q8BY80 UniProtKB/Swiss-Prot