Incidental Mutation 'R7831:Itpr2'
ID 605617
Institutional Source Beutler Lab
Gene Symbol Itpr2
Ensembl Gene ENSMUSG00000030287
Gene Name inositol 1,4,5-triphosphate receptor 2
Synonyms Ip3r2, Itpr5
MMRRC Submission 045885-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7831 (G1)
Quality Score 225.009
Status Validated
Chromosome 6
Chromosomal Location 146009797-146403721 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 146193082 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 1672 (I1672F)
Ref Sequence ENSEMBL: ENSMUSP00000049584 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053273] [ENSMUST00000079573]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000053273
AA Change: I1672F

PolyPhen 2 Score 0.040 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000049584
Gene: ENSMUSG00000030287
AA Change: I1672F

DomainStartEndE-ValueType
low complexity region 68 80 N/A INTRINSIC
MIR 112 166 1.1e-5 SMART
MIR 173 223 8.9e-6 SMART
MIR 231 287 5.11e-6 SMART
MIR 294 402 3.73e-8 SMART
Pfam:RYDR_ITPR 473 670 1.5e-62 PFAM
low complexity region 882 890 N/A INTRINSIC
Pfam:RYDR_ITPR 1183 1346 1.6e-16 PFAM
low complexity region 1773 1785 N/A INTRINSIC
low complexity region 1897 1908 N/A INTRINSIC
Pfam:RIH_assoc 1912 2022 4.6e-34 PFAM
low complexity region 2088 2098 N/A INTRINSIC
transmembrane domain 2228 2250 N/A INTRINSIC
Pfam:Ion_trans 2260 2552 5.1e-20 PFAM
coiled coil region 2631 2686 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000079573
AA Change: I1639F

PolyPhen 2 Score 0.638 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000078526
Gene: ENSMUSG00000030287
AA Change: I1639F

DomainStartEndE-ValueType
low complexity region 68 80 N/A INTRINSIC
MIR 112 166 1.1e-5 SMART
MIR 198 254 5.11e-6 SMART
MIR 261 369 3.73e-8 SMART
Pfam:RYDR_ITPR 438 644 5.4e-75 PFAM
low complexity region 849 857 N/A INTRINSIC
Pfam:RYDR_ITPR 1148 1322 7.2e-60 PFAM
low complexity region 1740 1752 N/A INTRINSIC
Pfam:RIH_assoc 1875 1994 5.8e-35 PFAM
low complexity region 2055 2065 N/A INTRINSIC
transmembrane domain 2195 2217 N/A INTRINSIC
transmembrane domain 2230 2249 N/A INTRINSIC
low complexity region 2268 2279 N/A INTRINSIC
Pfam:Ion_trans 2281 2507 2.4e-12 PFAM
coiled coil region 2598 2653 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (87/87)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the inositol 1,4,5-triphosphate receptor family, whose members are second messenger intracellular calcium release channels. These proteins mediate a rise in cytoplasmic calcium in response to receptor activated production of inositol triphosphate. Inositol triphosphate receptor-mediated signaling is involved in many processes including cell migration, cell division, smooth muscle contraction, and neuronal signaling. This protein is a type 2 receptor that consists of a cytoplasmic amino-terminus that binds inositol triphosphate, six membrane-spanning helices that contribute to the ion pore, and a short cytoplasmic carboxy-terminus. A mutation in this gene has been associated with anhidrosis, suggesting that intracellular calcium release mediated by this protein is required for eccrine sweat production. [provided by RefSeq, Apr 2015]
PHENOTYPE: Homozygotes for a knock-out allele are viable and fertile but show decreased sweating and disturbed calcium signaling in sweat glands. Mice homozygous for a different knock-out allele have atrial myocytes that are significantly less prone to develop proarrhythmic disturbances in calcium signaling. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 85 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 G A 11: 9,247,404 (GRCm39) V2384I possibly damaging Het
Acsl1 A G 8: 46,972,043 (GRCm39) D297G probably benign Het
Ap2a1 C A 7: 44,550,436 (GRCm39) R944L probably damaging Het
Apbb1ip A G 2: 22,756,933 (GRCm39) Y398C probably damaging Het
Atp8a2 A T 14: 60,011,202 (GRCm39) V968D probably damaging Het
Becn1 T C 11: 101,181,279 (GRCm39) T341A probably benign Het
Card11 G T 5: 140,859,167 (GRCm39) S1126R possibly damaging Het
Ccdc51 T C 9: 108,921,058 (GRCm39) L315S probably damaging Het
Cdk12 T C 11: 98,140,653 (GRCm39) L1298P unknown Het
Cep170b A T 12: 112,711,234 (GRCm39) D1538V probably benign Het
Cfap52 A T 11: 67,826,782 (GRCm39) F348I possibly damaging Het
Clip1 A T 5: 123,751,342 (GRCm39) M813K Het
Col19a1 G A 1: 24,565,563 (GRCm39) T256I unknown Het
Col6a3 A T 1: 90,724,268 (GRCm39) C2027* probably null Het
Crisp4 A T 1: 18,199,013 (GRCm39) N140K probably benign Het
Crocc2 G T 1: 93,143,195 (GRCm39) A1266S probably benign Het
Cyfip2 G A 11: 46,087,273 (GRCm39) R1206C probably damaging Het
Cyp24a1 T A 2: 170,327,860 (GRCm39) M461L probably damaging Het
Cyp2a5 C T 7: 26,534,940 (GRCm39) T51I possibly damaging Het
Cyp2b19 C T 7: 26,466,565 (GRCm39) H398Y possibly damaging Het
Cyp4a29 G A 4: 115,107,367 (GRCm39) V234I probably benign Het
Dicer1 T G 12: 104,675,059 (GRCm39) K734N probably damaging Het
Dnai1 T C 4: 41,614,695 (GRCm39) probably null Het
Entpd3 G A 9: 120,373,025 (GRCm39) G14D probably damaging Het
Entrep3 G A 3: 89,091,520 (GRCm39) probably null Het
Ermp1 T C 19: 29,595,367 (GRCm39) T634A probably benign Het
Evc C T 5: 37,476,427 (GRCm39) G374D probably damaging Het
Fcgbp C A 7: 27,806,404 (GRCm39) T2124K probably damaging Het
Fgf8 G A 19: 45,730,876 (GRCm39) P50S probably benign Het
Fmnl1 C T 11: 103,088,999 (GRCm39) R1074W unknown Het
Galnt18 C T 7: 111,155,665 (GRCm39) V223M possibly damaging Het
Galnt2 A G 8: 125,058,817 (GRCm39) N295S probably benign Het
Grip1 T G 10: 119,854,011 (GRCm39) V600G probably damaging Het
Insm2 T A 12: 55,647,323 (GRCm39) C356S probably damaging Het
Kdm1b T G 13: 47,204,098 (GRCm39) N76K probably benign Het
Khnyn T A 14: 56,125,303 (GRCm39) probably null Het
Kidins220 C T 12: 25,111,230 (GRCm39) A1167V possibly damaging Het
Krt40 T C 11: 99,432,087 (GRCm39) D208G probably benign Het
Lars1 T A 18: 42,350,627 (GRCm39) D894V probably benign Het
Lmx1a A T 1: 167,668,521 (GRCm39) N266I probably benign Het
Mrgprb5 T A 7: 47,817,997 (GRCm39) K246M probably benign Het
Mrpl2 G A 17: 46,959,598 (GRCm39) G176R possibly damaging Het
Muc21 T A 17: 35,929,651 (GRCm39) T1512S unknown Het
Nell1 T A 7: 49,632,548 (GRCm39) F60L possibly damaging Het
Nnt G A 13: 119,506,630 (GRCm39) A453V possibly damaging Het
Opa1 A G 16: 29,467,755 (GRCm39) K940R probably benign Het
Opn5 A C 17: 42,891,510 (GRCm39) I309S probably null Het
Or1af1 C T 2: 37,109,723 (GRCm39) T74I probably damaging Het
Or1r1 A C 11: 73,875,257 (GRCm39) M59R probably damaging Het
Or2ag15 T A 7: 106,340,620 (GRCm39) I174F probably damaging Het
P3h3 T G 6: 124,832,118 (GRCm39) E256A possibly damaging Het
Pald1 G T 10: 61,191,593 (GRCm39) T65K probably damaging Het
Pcnx3 T C 19: 5,735,989 (GRCm39) Y279C probably damaging Het
Pik3c2b G A 1: 132,998,980 (GRCm39) S367N possibly damaging Het
Pik3cb T C 9: 98,970,666 (GRCm39) T342A probably benign Het
Pkd1l3 A T 8: 110,357,990 (GRCm39) E837D possibly damaging Het
Ppp2r2b T A 18: 42,834,597 (GRCm39) Y191F probably benign Het
Ppp4r4 G A 12: 103,557,080 (GRCm39) E439K possibly damaging Het
Ptprk A G 10: 28,444,404 (GRCm39) I946V possibly damaging Het
Ror1 A G 4: 100,298,295 (GRCm39) N556S probably benign Het
Ryr3 C T 2: 112,757,183 (GRCm39) A391T possibly damaging Het
Selp G A 1: 163,972,584 (GRCm39) probably null Het
Setx T C 2: 29,047,120 (GRCm39) L1866S probably damaging Het
Setx T A 2: 29,069,866 (GRCm39) V2557E possibly damaging Het
Slc66a3 T A 12: 17,047,632 (GRCm39) probably null Het
Slit2 A G 5: 48,402,025 (GRCm39) T805A probably benign Het
Sorbs3 T G 14: 70,440,481 (GRCm39) N89T possibly damaging Het
Sorl1 C A 9: 42,001,257 (GRCm39) V248L probably benign Het
Srebf2 T A 15: 82,066,288 (GRCm39) V612E probably damaging Het
Sv2c T A 13: 96,113,200 (GRCm39) Y583F probably damaging Het
Tada1 G T 1: 166,217,442 (GRCm39) R193I probably damaging Het
Tnrc6b C G 15: 80,764,580 (GRCm39) A694G possibly damaging Het
Ttll3 CAAAGTAA CAAAGTAAAGTAA 6: 113,376,118 (GRCm39) probably null Het
Ttn C T 2: 76,711,425 (GRCm39) G8372D unknown Het
Ube2g2 A G 10: 77,470,576 (GRCm39) T68A Het
Ubl7 T G 9: 57,821,918 (GRCm39) V89G possibly damaging Het
Ush2a T A 1: 188,492,038 (GRCm39) I3109N probably damaging Het
Utp20 T A 10: 88,598,632 (GRCm39) K115* probably null Het
Vmn2r26 T A 6: 124,016,758 (GRCm39) Y407* probably null Het
Yod1 G T 1: 130,646,986 (GRCm39) V288F probably damaging Het
Zbed5 A C 5: 129,930,798 (GRCm39) N249T possibly damaging Het
Zbtb5 T C 4: 44,995,244 (GRCm39) T47A probably damaging Het
Zcchc14 T C 8: 122,331,984 (GRCm39) T460A not run Het
Zfp712 A C 13: 67,200,483 (GRCm39) probably null Het
Zfyve16 A T 13: 92,658,836 (GRCm39) H358Q probably benign Het
Other mutations in Itpr2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00087:Itpr2 APN 6 146,298,510 (GRCm39) missense probably damaging 0.99
IGL00163:Itpr2 APN 6 146,292,334 (GRCm39) missense possibly damaging 0.88
IGL00229:Itpr2 APN 6 146,045,683 (GRCm39) missense probably damaging 1.00
IGL00712:Itpr2 APN 6 146,133,934 (GRCm39) missense possibly damaging 0.63
IGL00952:Itpr2 APN 6 146,060,459 (GRCm39) missense probably damaging 1.00
IGL00983:Itpr2 APN 6 146,212,479 (GRCm39) splice site probably benign
IGL01012:Itpr2 APN 6 146,246,659 (GRCm39) missense probably damaging 1.00
IGL01289:Itpr2 APN 6 146,014,033 (GRCm39) nonsense probably null
IGL01411:Itpr2 APN 6 146,277,560 (GRCm39) critical splice donor site probably null
IGL01557:Itpr2 APN 6 146,060,474 (GRCm39) missense probably damaging 0.99
IGL01669:Itpr2 APN 6 146,081,727 (GRCm39) missense probably damaging 1.00
IGL01809:Itpr2 APN 6 146,129,079 (GRCm39) missense probably damaging 1.00
IGL01814:Itpr2 APN 6 146,134,044 (GRCm39) missense probably benign 0.02
IGL02198:Itpr2 APN 6 146,224,725 (GRCm39) missense probably damaging 1.00
IGL02218:Itpr2 APN 6 146,141,760 (GRCm39) splice site probably benign
IGL02332:Itpr2 APN 6 146,328,040 (GRCm39) missense probably damaging 1.00
IGL02425:Itpr2 APN 6 146,292,819 (GRCm39) missense probably damaging 0.99
IGL02432:Itpr2 APN 6 146,226,671 (GRCm39) missense probably benign 0.05
IGL02726:Itpr2 APN 6 146,277,419 (GRCm39) missense probably benign 0.18
IGL02851:Itpr2 APN 6 146,287,477 (GRCm39) missense probably damaging 0.99
IGL02933:Itpr2 APN 6 146,214,402 (GRCm39) missense probably benign
IGL03015:Itpr2 APN 6 146,277,435 (GRCm39) missense probably benign
IGL03067:Itpr2 APN 6 146,226,680 (GRCm39) missense probably damaging 1.00
IGL03093:Itpr2 APN 6 146,281,008 (GRCm39) missense probably damaging 1.00
IGL03214:Itpr2 APN 6 146,081,742 (GRCm39) missense probably benign 0.02
IGL03275:Itpr2 APN 6 146,060,375 (GRCm39) splice site probably benign
IGL03332:Itpr2 APN 6 146,045,647 (GRCm39) missense probably damaging 0.98
IGL03352:Itpr2 APN 6 146,058,602 (GRCm39) missense probably damaging 1.00
IGL03377:Itpr2 APN 6 146,231,256 (GRCm39) missense probably benign
IGL03377:Itpr2 APN 6 146,231,213 (GRCm39) missense probably damaging 0.96
dollar_short UTSW 6 146,298,517 (GRCm39) nonsense probably null
enfermos UTSW 6 146,135,504 (GRCm39) missense probably damaging 0.98
Hopla UTSW 6 146,096,096 (GRCm39) missense probably damaging 0.98
P0029:Itpr2 UTSW 6 146,280,987 (GRCm39) missense probably damaging 1.00
PIT4431001:Itpr2 UTSW 6 146,256,218 (GRCm39) missense probably benign
PIT4453001:Itpr2 UTSW 6 146,274,671 (GRCm39) missense probably damaging 1.00
PIT4504001:Itpr2 UTSW 6 146,131,369 (GRCm39) missense probably damaging 0.99
R0040:Itpr2 UTSW 6 146,246,638 (GRCm39) missense probably damaging 1.00
R0040:Itpr2 UTSW 6 146,246,638 (GRCm39) missense probably damaging 1.00
R0048:Itpr2 UTSW 6 146,133,789 (GRCm39) splice site probably null
R0048:Itpr2 UTSW 6 146,133,789 (GRCm39) splice site probably null
R0055:Itpr2 UTSW 6 146,224,631 (GRCm39) missense probably benign 0.42
R0055:Itpr2 UTSW 6 146,224,631 (GRCm39) missense probably benign 0.42
R0088:Itpr2 UTSW 6 146,142,683 (GRCm39) missense probably benign
R0089:Itpr2 UTSW 6 146,251,520 (GRCm39) critical splice donor site probably null
R0114:Itpr2 UTSW 6 146,214,377 (GRCm39) missense probably damaging 1.00
R0125:Itpr2 UTSW 6 146,141,951 (GRCm39) missense probably benign 0.00
R0144:Itpr2 UTSW 6 146,228,653 (GRCm39) missense probably damaging 0.98
R0180:Itpr2 UTSW 6 146,403,407 (GRCm39) start gained probably benign
R0211:Itpr2 UTSW 6 146,096,111 (GRCm39) missense probably benign 0.17
R0305:Itpr2 UTSW 6 146,212,601 (GRCm39) missense possibly damaging 0.63
R0367:Itpr2 UTSW 6 146,135,506 (GRCm39) missense probably damaging 1.00
R0374:Itpr2 UTSW 6 146,260,890 (GRCm39) missense probably benign 0.00
R0391:Itpr2 UTSW 6 146,131,271 (GRCm39) missense probably damaging 1.00
R0450:Itpr2 UTSW 6 146,319,477 (GRCm39) missense possibly damaging 0.66
R0464:Itpr2 UTSW 6 146,277,387 (GRCm39) missense probably damaging 1.00
R0510:Itpr2 UTSW 6 146,319,477 (GRCm39) missense possibly damaging 0.66
R0532:Itpr2 UTSW 6 146,013,898 (GRCm39) missense probably damaging 1.00
R0625:Itpr2 UTSW 6 146,068,149 (GRCm39) missense probably benign
R0633:Itpr2 UTSW 6 146,275,954 (GRCm39) missense probably damaging 1.00
R0636:Itpr2 UTSW 6 146,072,910 (GRCm39) missense probably damaging 1.00
R1086:Itpr2 UTSW 6 146,251,543 (GRCm39) missense probably damaging 1.00
R1352:Itpr2 UTSW 6 146,013,240 (GRCm39) missense probably damaging 1.00
R1631:Itpr2 UTSW 6 146,081,788 (GRCm39) missense probably damaging 1.00
R1655:Itpr2 UTSW 6 146,277,646 (GRCm39) missense probably damaging 1.00
R1767:Itpr2 UTSW 6 146,251,566 (GRCm39) missense possibly damaging 0.91
R1779:Itpr2 UTSW 6 146,060,399 (GRCm39) nonsense probably null
R1796:Itpr2 UTSW 6 146,198,171 (GRCm39) missense probably benign
R1815:Itpr2 UTSW 6 146,260,914 (GRCm39) missense probably benign 0.08
R1827:Itpr2 UTSW 6 146,229,830 (GRCm39) missense probably damaging 1.00
R1828:Itpr2 UTSW 6 146,229,830 (GRCm39) missense probably damaging 1.00
R1884:Itpr2 UTSW 6 146,287,469 (GRCm39) missense probably benign 0.16
R1902:Itpr2 UTSW 6 146,131,201 (GRCm39) missense probably damaging 1.00
R1931:Itpr2 UTSW 6 146,141,852 (GRCm39) missense probably benign 0.41
R1964:Itpr2 UTSW 6 146,013,191 (GRCm39) missense probably damaging 1.00
R2010:Itpr2 UTSW 6 146,129,022 (GRCm39) splice site probably null
R2168:Itpr2 UTSW 6 146,013,176 (GRCm39) missense probably benign 0.05
R2179:Itpr2 UTSW 6 146,277,464 (GRCm39) missense probably benign
R2290:Itpr2 UTSW 6 146,324,326 (GRCm39) missense probably damaging 1.00
R2874:Itpr2 UTSW 6 146,327,996 (GRCm39) missense possibly damaging 0.73
R2888:Itpr2 UTSW 6 146,072,791 (GRCm39) missense probably damaging 1.00
R2897:Itpr2 UTSW 6 146,224,667 (GRCm39) missense probably damaging 1.00
R2897:Itpr2 UTSW 6 146,074,839 (GRCm39) missense probably benign 0.03
R2898:Itpr2 UTSW 6 146,224,667 (GRCm39) missense probably damaging 1.00
R2898:Itpr2 UTSW 6 146,074,839 (GRCm39) missense probably benign 0.03
R3024:Itpr2 UTSW 6 146,081,808 (GRCm39) missense probably benign 0.35
R3104:Itpr2 UTSW 6 146,214,335 (GRCm39) critical splice donor site probably null
R3607:Itpr2 UTSW 6 146,129,099 (GRCm39) missense probably damaging 0.98
R3732:Itpr2 UTSW 6 146,284,198 (GRCm39) missense probably damaging 1.00
R3732:Itpr2 UTSW 6 146,284,198 (GRCm39) missense probably damaging 1.00
R3733:Itpr2 UTSW 6 146,284,198 (GRCm39) missense probably damaging 1.00
R3792:Itpr2 UTSW 6 146,316,852 (GRCm39) missense probably damaging 1.00
R3806:Itpr2 UTSW 6 146,133,789 (GRCm39) splice site probably null
R3821:Itpr2 UTSW 6 146,319,224 (GRCm39) missense probably damaging 1.00
R3929:Itpr2 UTSW 6 146,275,857 (GRCm39) splice site probably null
R3958:Itpr2 UTSW 6 146,327,008 (GRCm39) missense probably damaging 0.97
R3959:Itpr2 UTSW 6 146,327,008 (GRCm39) missense probably damaging 0.97
R3960:Itpr2 UTSW 6 146,327,008 (GRCm39) missense probably damaging 0.97
R3960:Itpr2 UTSW 6 146,131,262 (GRCm39) missense probably damaging 1.00
R4074:Itpr2 UTSW 6 146,274,742 (GRCm39) splice site probably null
R4085:Itpr2 UTSW 6 146,045,746 (GRCm39) missense probably damaging 1.00
R4114:Itpr2 UTSW 6 146,327,008 (GRCm39) missense probably damaging 0.97
R4115:Itpr2 UTSW 6 146,327,008 (GRCm39) missense probably damaging 0.97
R4588:Itpr2 UTSW 6 146,142,694 (GRCm39) missense probably benign 0.33
R4663:Itpr2 UTSW 6 146,274,671 (GRCm39) missense probably damaging 1.00
R4673:Itpr2 UTSW 6 146,274,671 (GRCm39) missense probably damaging 1.00
R4684:Itpr2 UTSW 6 146,274,671 (GRCm39) missense probably damaging 1.00
R4686:Itpr2 UTSW 6 146,131,273 (GRCm39) missense probably damaging 1.00
R4713:Itpr2 UTSW 6 146,298,456 (GRCm39) missense probably damaging 1.00
R4713:Itpr2 UTSW 6 146,274,671 (GRCm39) missense probably damaging 1.00
R4729:Itpr2 UTSW 6 146,274,671 (GRCm39) missense probably damaging 1.00
R4732:Itpr2 UTSW 6 146,274,671 (GRCm39) missense probably damaging 1.00
R4733:Itpr2 UTSW 6 146,274,671 (GRCm39) missense probably damaging 1.00
R4801:Itpr2 UTSW 6 146,272,829 (GRCm39) missense probably damaging 1.00
R4802:Itpr2 UTSW 6 146,272,829 (GRCm39) missense probably damaging 1.00
R4877:Itpr2 UTSW 6 146,226,703 (GRCm39) missense probably damaging 1.00
R4970:Itpr2 UTSW 6 146,135,489 (GRCm39) missense possibly damaging 0.95
R4986:Itpr2 UTSW 6 146,141,840 (GRCm39) missense probably damaging 0.96
R5112:Itpr2 UTSW 6 146,135,489 (GRCm39) missense possibly damaging 0.95
R5200:Itpr2 UTSW 6 146,045,605 (GRCm39) critical splice donor site probably null
R5224:Itpr2 UTSW 6 146,068,149 (GRCm39) missense probably benign
R5243:Itpr2 UTSW 6 146,089,044 (GRCm39) missense probably damaging 1.00
R5348:Itpr2 UTSW 6 146,378,191 (GRCm39) missense possibly damaging 0.78
R5393:Itpr2 UTSW 6 146,277,653 (GRCm39) nonsense probably null
R5552:Itpr2 UTSW 6 146,195,578 (GRCm39) missense probably benign
R5579:Itpr2 UTSW 6 146,074,864 (GRCm39) nonsense probably null
R5744:Itpr2 UTSW 6 146,277,649 (GRCm39) missense probably damaging 1.00
R5825:Itpr2 UTSW 6 146,045,647 (GRCm39) missense probably damaging 0.98
R5910:Itpr2 UTSW 6 146,231,069 (GRCm39) missense probably benign 0.10
R5911:Itpr2 UTSW 6 146,214,441 (GRCm39) missense probably benign 0.42
R6044:Itpr2 UTSW 6 146,298,449 (GRCm39) missense probably null 0.98
R6072:Itpr2 UTSW 6 146,248,609 (GRCm39) missense probably damaging 0.98
R6191:Itpr2 UTSW 6 146,229,833 (GRCm39) missense probably benign 0.01
R6483:Itpr2 UTSW 6 146,013,975 (GRCm39) missense possibly damaging 0.52
R6511:Itpr2 UTSW 6 146,231,225 (GRCm39) missense probably damaging 1.00
R6524:Itpr2 UTSW 6 146,246,709 (GRCm39) missense probably benign 0.01
R6561:Itpr2 UTSW 6 146,135,504 (GRCm39) missense probably damaging 0.98
R6594:Itpr2 UTSW 6 146,091,978 (GRCm39) missense possibly damaging 0.71
R6603:Itpr2 UTSW 6 146,248,669 (GRCm39) missense probably damaging 0.98
R6736:Itpr2 UTSW 6 146,226,668 (GRCm39) missense probably damaging 1.00
R6783:Itpr2 UTSW 6 146,287,371 (GRCm39) critical splice donor site probably null
R6831:Itpr2 UTSW 6 146,013,927 (GRCm39) missense probably damaging 1.00
R6857:Itpr2 UTSW 6 146,298,517 (GRCm39) nonsense probably null
R7103:Itpr2 UTSW 6 146,226,572 (GRCm39) missense probably damaging 1.00
R7111:Itpr2 UTSW 6 146,226,554 (GRCm39) missense probably damaging 1.00
R7126:Itpr2 UTSW 6 146,259,294 (GRCm39) nonsense probably null
R7165:Itpr2 UTSW 6 146,195,589 (GRCm39) missense probably damaging 1.00
R7184:Itpr2 UTSW 6 146,212,585 (GRCm39) missense possibly damaging 0.79
R7249:Itpr2 UTSW 6 146,212,550 (GRCm39) missense probably damaging 1.00
R7292:Itpr2 UTSW 6 146,060,447 (GRCm39) missense possibly damaging 0.95
R7342:Itpr2 UTSW 6 146,228,685 (GRCm39) missense probably damaging 0.98
R7392:Itpr2 UTSW 6 146,260,838 (GRCm39) missense possibly damaging 0.95
R7414:Itpr2 UTSW 6 146,274,706 (GRCm39) missense probably benign 0.06
R7448:Itpr2 UTSW 6 146,231,006 (GRCm39) missense probably damaging 1.00
R7492:Itpr2 UTSW 6 146,292,436 (GRCm39) missense probably damaging 1.00
R7515:Itpr2 UTSW 6 146,228,608 (GRCm39) missense probably damaging 1.00
R7529:Itpr2 UTSW 6 146,096,096 (GRCm39) missense probably damaging 0.98
R7558:Itpr2 UTSW 6 146,292,363 (GRCm39) missense probably damaging 1.00
R7650:Itpr2 UTSW 6 146,135,492 (GRCm39) missense probably benign 0.36
R7678:Itpr2 UTSW 6 146,089,048 (GRCm39) missense probably benign 0.00
R7790:Itpr2 UTSW 6 146,126,274 (GRCm39) missense probably damaging 1.00
R7798:Itpr2 UTSW 6 146,287,513 (GRCm39) missense probably benign 0.06
R8023:Itpr2 UTSW 6 146,088,988 (GRCm39) missense probably damaging 0.97
R8046:Itpr2 UTSW 6 146,327,957 (GRCm39) missense probably damaging 0.96
R8236:Itpr2 UTSW 6 146,292,281 (GRCm39) critical splice donor site probably null
R8241:Itpr2 UTSW 6 146,320,013 (GRCm39) missense possibly damaging 0.90
R8245:Itpr2 UTSW 6 146,274,604 (GRCm39) missense probably damaging 0.98
R8324:Itpr2 UTSW 6 146,229,896 (GRCm39) missense probably damaging 0.97
R8339:Itpr2 UTSW 6 146,214,396 (GRCm39) missense probably benign 0.19
R8458:Itpr2 UTSW 6 146,135,464 (GRCm39) missense possibly damaging 0.62
R8506:Itpr2 UTSW 6 146,319,914 (GRCm39) critical splice donor site probably null
R8529:Itpr2 UTSW 6 146,231,051 (GRCm39) missense probably damaging 1.00
R8672:Itpr2 UTSW 6 146,276,016 (GRCm39) missense probably damaging 1.00
R8755:Itpr2 UTSW 6 146,133,926 (GRCm39) missense probably benign
R8816:Itpr2 UTSW 6 146,142,710 (GRCm39) missense probably damaging 0.98
R9160:Itpr2 UTSW 6 146,276,099 (GRCm39) missense probably damaging 1.00
R9273:Itpr2 UTSW 6 146,226,529 (GRCm39) missense probably damaging 1.00
R9284:Itpr2 UTSW 6 146,256,174 (GRCm39) missense probably benign 0.01
R9322:Itpr2 UTSW 6 146,226,587 (GRCm39) missense probably benign 0.19
R9357:Itpr2 UTSW 6 146,260,814 (GRCm39) missense probably damaging 1.00
R9424:Itpr2 UTSW 6 146,212,505 (GRCm39) missense probably damaging 0.98
R9438:Itpr2 UTSW 6 146,068,166 (GRCm39) missense probably benign
R9576:Itpr2 UTSW 6 146,212,505 (GRCm39) missense probably damaging 0.98
V8831:Itpr2 UTSW 6 146,287,380 (GRCm39) missense probably damaging 1.00
X0054:Itpr2 UTSW 6 146,224,734 (GRCm39) missense probably damaging 1.00
X0063:Itpr2 UTSW 6 146,081,851 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CGCGTTGCAATCCATAGATAC -3'
(R):5'- ACCTGAGAAACACTGGGATG -3'

Sequencing Primer
(F):5'- GCAATCCATAGATACAACATTCTGG -3'
(R):5'- ATATGCTGGTGTATAGTTTTCAGCC -3'
Posted On 2019-12-20