Incidental Mutation 'R7777:Pira2'
ID598953
Institutional Source Beutler Lab
Gene Symbol Pira2
Ensembl Gene ENSMUSG00000089942
Gene Namepaired-Ig-like receptor A2
Synonyms6M23
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.065) question?
Stock #R7777 (G1)
Quality Score225.009
Status Not validated
Chromosome7
Chromosomal Location3836812-3845051 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 3841697 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Tyrosine at position 445 (F445Y)
Ref Sequence ENSEMBL: ENSMUSP00000104255 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108615] [ENSMUST00000119469]
Predicted Effect probably benign
Transcript: ENSMUST00000108615
AA Change: F445Y

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000104255
Gene: ENSMUSG00000089942
AA Change: F445Y

DomainStartEndE-ValueType
low complexity region 8 17 N/A INTRINSIC
IG 34 118 2.39e-1 SMART
IG_like 129 220 1.94e1 SMART
IG 231 315 7.77e-1 SMART
IG 328 415 3.36e0 SMART
IG_like 435 502 3.18e0 SMART
IG 529 618 8.59e-3 SMART
low complexity region 654 663 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000119469
AA Change: F445Y

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000113857
Gene: ENSMUSG00000089942
AA Change: F445Y

DomainStartEndE-ValueType
low complexity region 8 17 N/A INTRINSIC
IG 34 118 2.39e-1 SMART
IG_like 129 220 1.94e1 SMART
IG 231 315 7.77e-1 SMART
IG 328 415 3.36e0 SMART
IG_like 435 502 3.18e0 SMART
IG 529 618 8.59e-3 SMART
low complexity region 637 646 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 100% (47/47)
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700022I11Rik C T 4: 42,970,171 Q53* probably null Het
1700022I11Rik T C 4: 42,971,095 S143P probably benign Het
Adam6b C T 12: 113,490,138 P192S possibly damaging Het
Arhgef10 A G 8: 14,945,373 T353A probably damaging Het
Cabyr A G 18: 12,744,771 D55G probably damaging Het
Dcaf4 T C 12: 83,537,959 V322A probably damaging Het
Ephb2 T A 4: 136,771,636 E44V possibly damaging Het
Fam3c T C 6: 22,328,574 I105V probably benign Het
Fras1 A G 5: 96,752,904 D2994G probably damaging Het
Fryl C T 5: 73,071,298 D1697N probably damaging Het
Gapdh A T 6: 125,162,948 Y164* probably null Het
Gm4353 T G 7: 116,083,763 Q194H possibly damaging Het
Ilvbl T A 10: 78,577,251 probably null Het
Ism2 T A 12: 87,286,884 probably null Het
Jak2 C T 19: 29,276,868 T196I probably benign Het
Lcor T G 19: 41,558,795 Y273D probably benign Het
Ldlrad4 G T 18: 68,235,669 A66S possibly damaging Het
Lysmd4 T A 7: 67,223,698 M27K possibly damaging Het
Muc3 G A 5: 137,146,716 silent Het
Olfr1023 A G 2: 85,887,607 E269G possibly damaging Het
Olfr539 T A 7: 140,667,941 I211N probably benign Het
Olfr747 A T 14: 50,680,804 Y277N probably damaging Het
Oscp1 T C 4: 126,064,981 probably null Het
Pkd2l2 C A 18: 34,416,860 P186Q probably damaging Het
Plcb1 G A 2: 135,220,757 G96R possibly damaging Het
Plcd3 G C 11: 103,074,655 R535G probably benign Het
Plcg1 A G 2: 160,754,603 M681V possibly damaging Het
Polr1b C A 2: 129,125,544 F952L probably damaging Het
Polrmt A T 10: 79,739,188 D836E probably benign Het
Pramef8 T C 4: 143,417,761 Y226H possibly damaging Het
Prkag1 A T 15: 98,814,597 I149N probably damaging Het
Prkci A T 3: 31,050,213 Q575L possibly damaging Het
Prss40 C T 1: 34,552,765 W276* probably null Het
Ptprn T C 1: 75,252,302 D823G possibly damaging Het
Radil A C 5: 142,543,548 F131C probably damaging Het
Rif1 A G 2: 52,116,356 I550V probably benign Het
Rmnd1 T C 10: 4,411,713 E320G probably damaging Het
Sec31b T A 19: 44,523,773 K561* probably null Het
Tbx5 A C 5: 119,883,167 T413P probably benign Het
Tmprss7 A G 16: 45,660,600 probably null Het
Tnfaip8l2 T C 3: 95,139,996 *185W probably null Het
Tpst2 A G 5: 112,309,694 E296G possibly damaging Het
Ubn2 T A 6: 38,490,753 S801T probably damaging Het
Usp34 A G 11: 23,382,638 S1141G Het
Uts2r A G 11: 121,161,453 N381S probably benign Het
Vmn2r44 G T 7: 8,378,315 T193K possibly damaging Het
Wdr18 T A 10: 79,966,050 M223K probably benign Het
Wdr64 T C 1: 175,789,998 C715R possibly damaging Het
Zfp672 A G 11: 58,317,255 F80S possibly damaging Het
Other mutations in Pira2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01349:Pira2 APN 7 3844139 missense probably damaging 1.00
IGL01810:Pira2 APN 7 3844612 missense probably damaging 1.00
IGL03167:Pira2 APN 7 3840920 missense probably damaging 0.98
IGL03171:Pira2 APN 7 3842605 missense probably damaging 1.00
BB009:Pira2 UTSW 7 3842436 critical splice donor site probably null
BB019:Pira2 UTSW 7 3842436 critical splice donor site probably null
PIT4260001:Pira2 UTSW 7 3842170 missense probably benign
PIT4260001:Pira2 UTSW 7 3842173 missense probably benign
PIT4260001:Pira2 UTSW 7 3842174 missense probably benign
R0517:Pira2 UTSW 7 3844197 splice site probably benign
R1565:Pira2 UTSW 7 3844549 missense probably damaging 1.00
R1870:Pira2 UTSW 7 3844453 missense probably damaging 1.00
R2143:Pira2 UTSW 7 3844345 missense probably damaging 1.00
R2144:Pira2 UTSW 7 3844345 missense probably damaging 1.00
R2145:Pira2 UTSW 7 3844345 missense probably damaging 1.00
R2149:Pira2 UTSW 7 3844171 missense probably damaging 1.00
R2171:Pira2 UTSW 7 3844418 missense probably benign 0.08
R3118:Pira2 UTSW 7 3841677 nonsense probably null
R4658:Pira2 UTSW 7 3840934 missense probably damaging 1.00
R5148:Pira2 UTSW 7 3844593 missense possibly damaging 0.62
R5228:Pira2 UTSW 7 3844374 missense probably benign 0.33
R5583:Pira2 UTSW 7 3842546 missense probably benign 0.34
R5974:Pira2 UTSW 7 3841577 missense probably benign 0.27
R6120:Pira2 UTSW 7 3841554 missense probably damaging 1.00
R6122:Pira2 UTSW 7 3842446 missense probably damaging 1.00
R6392:Pira2 UTSW 7 3843902 missense possibly damaging 0.72
R6658:Pira2 UTSW 7 3842301 missense probably benign 0.00
R6790:Pira2 UTSW 7 3842443 missense probably damaging 1.00
R6990:Pira2 UTSW 7 3841068 missense probably damaging 0.99
R7336:Pira2 UTSW 7 3844345 missense probably damaging 1.00
R7597:Pira2 UTSW 7 3842461 missense probably damaging 1.00
R7768:Pira2 UTSW 7 3841697 missense probably benign
R7861:Pira2 UTSW 7 3844544 missense probably damaging 1.00
R7932:Pira2 UTSW 7 3842436 critical splice donor site probably null
R7977:Pira2 UTSW 7 3841697 missense probably benign
R7984:Pira2 UTSW 7 3841697 missense probably benign
R7985:Pira2 UTSW 7 3841697 missense probably benign
R7987:Pira2 UTSW 7 3841697 missense probably benign
R8017:Pira2 UTSW 7 3841697 missense probably benign
R8017:Pira2 UTSW 7 3841697 missense probably benign
R8019:Pira2 UTSW 7 3841697 missense probably benign
R8389:Pira2 UTSW 7 3843889 missense probably damaging 1.00
Predicted Primers
Posted On2019-11-26