Incidental Mutation 'IGL00341:Ptpn20'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ptpn20
Ensembl Gene ENSMUSG00000021940
Gene Nameprotein tyrosine phosphatase, non-receptor type 20
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL00341
Quality Score
Chromosomal Location33589207-33640754 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 33622619 bp
Amino Acid Change Arginine to Serine at position 167 (R167S)
Ref Sequence ENSEMBL: ENSMUSP00000022508 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022508] [ENSMUST00000226512] [ENSMUST00000227887]
Predicted Effect probably benign
Transcript: ENSMUST00000022508
AA Change: R167S

PolyPhen 2 Score 0.221 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000022508
Gene: ENSMUSG00000021940
AA Change: R167S

low complexity region 12 35 N/A INTRINSIC
PTPc 164 420 1.12e-120 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000226512
Predicted Effect probably benign
Transcript: ENSMUST00000227887
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene belongs to the family of classical tyrosine-specific protein tyrosine phosphatases. Many protein tyrosine phosphatases have been shown to regulate fundamental cellular processes. The encoded protein appears to be targeted to sites of actin polymerization. A pseudogene of this gene has been defined on chromosome 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgef5 T A 6: 43,280,269 Y519* probably null Het
Bahcc1 A G 11: 120,272,304 Y476C probably damaging Het
Bclaf1 A T 10: 20,325,999 E295D probably damaging Het
Bend3 A G 10: 43,511,543 D644G probably damaging Het
Ccdc122 G A 14: 77,091,739 M77I probably benign Het
Ccna1 A G 3: 55,050,655 V143A probably damaging Het
Dnah11 T C 12: 118,198,745 R30G probably benign Het
Hoxc4 A G 15: 103,035,838 D214G probably damaging Het
Itsn2 A T 12: 4,658,027 T778S possibly damaging Het
Kcnn2 A G 18: 45,677,071 probably benign Het
Krtap5-3 G T 7: 142,201,875 probably benign Het
Lgr5 G T 10: 115,454,464 Q516K possibly damaging Het
Lrpprc T C 17: 84,750,525 K759R possibly damaging Het
Mtfr2 A G 10: 20,357,648 D321G probably damaging Het
Nip7 A G 8: 107,057,170 Y45C possibly damaging Het
Olfr1216 T C 2: 89,013,924 I47V probably benign Het
Pak1ip1 A T 13: 41,008,018 T84S possibly damaging Het
Rab4b C T 7: 27,172,726 G190S probably damaging Het
Ropn1l T A 15: 31,443,349 D179V probably damaging Het
Shc2 C T 10: 79,621,069 R571Q probably damaging Het
Smad1 A G 8: 79,356,469 V134A probably damaging Het
Smad6 A G 9: 63,953,981 V344A probably damaging Het
Tet2 A G 3: 133,488,085 L196P possibly damaging Het
Tmem64 T A 4: 15,266,694 V248E probably damaging Het
Ttc7 C T 17: 87,363,564 T709I possibly damaging Het
Usp31 A G 7: 121,706,670 L195P probably damaging Het
Vmn2r112 G A 17: 22,618,936 V793I probably benign Het
Xpo5 T G 17: 46,225,047 L535R probably damaging Het
Ythdc2 A T 18: 44,850,397 M544L probably benign Het
Other mutations in Ptpn20
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01510:Ptpn20 APN 14 33638386 splice site probably null
R2057:Ptpn20 UTSW 14 33630985 missense probably damaging 0.98
R2262:Ptpn20 UTSW 14 33612311 missense probably benign
R3106:Ptpn20 UTSW 14 33612296 missense probably benign
R3430:Ptpn20 UTSW 14 33614528 missense possibly damaging 0.61
R4645:Ptpn20 UTSW 14 33631212 missense probably benign
R4928:Ptpn20 UTSW 14 33614489 missense probably benign 0.00
R4962:Ptpn20 UTSW 14 33614459 missense probably benign 0.02
R5087:Ptpn20 UTSW 14 33614441 missense possibly damaging 0.90
R5163:Ptpn20 UTSW 14 33631111 missense probably benign 0.07
R5275:Ptpn20 UTSW 14 33631192 missense probably benign 0.00
R6325:Ptpn20 UTSW 14 33631005 missense possibly damaging 0.52
R6651:Ptpn20 UTSW 14 33632940 missense probably damaging 1.00
R6831:Ptpn20 UTSW 14 33632925 missense probably damaging 1.00
R6903:Ptpn20 UTSW 14 33614504 missense probably damaging 0.98
R7034:Ptpn20 UTSW 14 33614435 makesense probably null
R7036:Ptpn20 UTSW 14 33614435 makesense probably null
R7265:Ptpn20 UTSW 14 33614524 missense probably benign 0.05
R7654:Ptpn20 UTSW 14 33638324 missense probably benign 0.18
R7735:Ptpn20 UTSW 14 33630945 missense probably damaging 1.00
R7761:Ptpn20 UTSW 14 33622552 missense probably benign 0.18
Posted On2015-08-05