Incidental Mutation 'R5222:Pstpip2'
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ID402395
Institutional Source Beutler Lab
Gene Symbol Pstpip2
Ensembl Gene ENSMUSG00000025429
Gene Nameproline-serine-threonine phosphatase-interacting protein 2
Synonymscmo
MMRRC Submission 042795-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R5222 (G1)
Quality Score225
Status Validated
Chromosome18
Chromosomal Location77794545-77882007 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 77874332 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Stop codon at position 267 (Y267*)
Ref Sequence ENSEMBL: ENSMUSP00000110389 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000114741]
Predicted Effect probably null
Transcript: ENSMUST00000114741
AA Change: Y267*
SMART Domains Protein: ENSMUSP00000110389
Gene: ENSMUSG00000025429
AA Change: Y267*

DomainStartEndE-ValueType
FCH 13 98 7.62e-16 SMART
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency 98% (52/53)
MGI Phenotype PHENOTYPE: Homozygous mutant animals develop osteomyelitis (bone inflammation). Tail kinks are observed starting at 6-8 weeks of age and chronic inflammation of the extremities and ears is subsequently seen. Extramedullary hematopoiesis in the spleen is observed. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930523C07Rik C A 1: 160,044,608 noncoding transcript Het
Acad11 G A 9: 104,097,377 A515T probably damaging Het
Angpt1 T C 15: 42,676,334 Y43C probably damaging Het
Arhgef33 A G 17: 80,337,314 Y24C probably damaging Het
Cd40 G C 2: 165,066,544 S180T probably benign Het
Cenpc1 A T 5: 86,037,747 S302T possibly damaging Het
Cit C A 5: 115,952,543 T932K probably benign Het
Col19a1 A C 1: 24,559,640 probably null Het
Dapk3 A G 10: 81,192,460 E288G probably damaging Het
Ddx60 T C 8: 61,984,158 F1002S probably damaging Het
Dgke G T 11: 89,050,394 T321K probably benign Het
Ebf2 T G 14: 67,313,594 probably benign Het
Enpp7 A G 11: 118,990,962 D311G probably benign Het
Epm2a A G 10: 11,448,749 E194G probably damaging Het
Esf1 A G 2: 140,158,583 Y428H possibly damaging Het
Esyt2 T C 12: 116,318,826 F132S probably damaging Het
Gm13101 T A 4: 143,964,792 I454F possibly damaging Het
Gm5455 T C 13: 110,304,960 noncoding transcript Het
Gria1 T A 11: 57,189,797 V202E probably benign Het
Lin9 T A 1: 180,669,198 L351I probably benign Het
Mark1 A T 1: 184,928,091 F123I probably damaging Het
Nectin4 T A 1: 171,385,257 probably null Het
Obscn T A 11: 59,044,145 T5220S possibly damaging Het
Olfr1 AGCGGTCGTAGGC AGC 11: 73,395,654 probably null Het
Olfr1370 T A 13: 21,072,569 H244L probably damaging Het
Olfr166 A C 16: 19,486,930 I31L probably benign Het
Pdcd1 A T 1: 94,052,450 V14E probably damaging Het
Pmel A G 10: 128,718,984 probably null Het
Prrx1 C T 1: 163,261,973 R95Q probably damaging Het
Ptprq A G 10: 107,662,564 I884T probably damaging Het
Rad17 G A 13: 100,633,891 T216I possibly damaging Het
Rif1 T C 2: 52,077,020 I107T probably benign Het
Rpp14 T C 14: 8,087,513 L69P probably damaging Het
Rtel1 G T 2: 181,346,983 probably benign Het
Sap130 C T 18: 31,666,703 T362M probably damaging Het
Scn11a A G 9: 119,815,202 probably null Het
Sec31a G T 5: 100,382,895 T243N probably benign Het
Slc5a9 T A 4: 111,898,611 H30L possibly damaging Het
Slco6b1 T A 1: 96,997,491 noncoding transcript Het
Smarca4 A G 9: 21,655,706 D694G probably benign Het
Spaca6 A G 17: 17,838,105 T213A probably benign Het
Tagap C A 17: 7,933,641 Q553K possibly damaging Het
Tagap A T 17: 7,933,642 Q553L possibly damaging Het
Tcf7l2 A G 19: 55,898,612 Q19R probably benign Het
Ttn A G 2: 76,878,853 probably benign Het
Ubr7 A T 12: 102,775,705 R399S probably benign Het
Uspl1 C A 5: 149,214,101 Q690K possibly damaging Het
Vps8 T A 16: 21,581,548 Y853* probably null Het
Vrk3 A T 7: 44,759,796 Q129L possibly damaging Het
Wapl T A 14: 34,736,685 C901* probably null Het
Other mutations in Pstpip2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00087:Pstpip2 APN 18 77874294 missense probably benign 0.00
IGL00264:Pstpip2 APN 18 77871559 splice site probably benign
IGL01373:Pstpip2 APN 18 77835216 nonsense probably null
IGL01866:Pstpip2 APN 18 77877625 missense probably benign 0.00
IGL02948:Pstpip2 APN 18 77854807 missense probably benign 0.00
R1853:Pstpip2 UTSW 18 77871799 missense probably damaging 1.00
R1854:Pstpip2 UTSW 18 77871799 missense probably damaging 1.00
R1916:Pstpip2 UTSW 18 77835192 missense probably damaging 0.99
R2402:Pstpip2 UTSW 18 77854864 missense possibly damaging 0.82
R2927:Pstpip2 UTSW 18 77861889 missense probably damaging 0.99
R3103:Pstpip2 UTSW 18 77871777 missense probably damaging 0.99
R4276:Pstpip2 UTSW 18 77861856 missense probably benign
R4881:Pstpip2 UTSW 18 77874332 nonsense probably null
R5361:Pstpip2 UTSW 18 77870378 missense probably damaging 0.99
R6397:Pstpip2 UTSW 18 77873379 missense probably benign 0.10
R7538:Pstpip2 UTSW 18 77871605 missense probably damaging 1.00
R7854:Pstpip2 UTSW 18 77874304 missense probably benign
R7885:Pstpip2 UTSW 18 77794722 missense probably benign
R7982:Pstpip2 UTSW 18 77879373 missense probably benign 0.06
X0065:Pstpip2 UTSW 18 77879361 missense probably benign 0.05
Predicted Primers PCR Primer
(F):5'- CATGGGACTTGGCATAGAGTTTC -3'
(R):5'- CACAGCAGGAGAGGTCATTG -3'

Sequencing Primer
(F):5'- GGCATAGAGTTTCTTAGTTCTAATCC -3'
(R):5'- CGGTCTCAAAAGCGATGGCATC -3'
Posted On2016-07-22