Incidental Mutation 'R4715:Ptprd'
ID 353933
Institutional Source Beutler Lab
Gene Symbol Ptprd
Ensembl Gene ENSMUSG00000028399
Gene Name protein tyrosine phosphatase, receptor type, D
Synonyms 1110002J03Rik, 3000002J10Rik, B230219D21Rik
MMRRC Submission 041982-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4715 (G1)
Quality Score 225
Status Validated
Chromosome 4
Chromosomal Location 75941238-78211961 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 76107333 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 543 (T543A)
Ref Sequence ENSEMBL: ENSMUSP00000102910 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050757] [ENSMUST00000098005] [ENSMUST00000102834] [ENSMUST00000107289] [ENSMUST00000173376] [ENSMUST00000174023] [ENSMUST00000174180] [ENSMUST00000174531] [ENSMUST00000174831]
AlphaFold Q64487
Predicted Effect probably benign
Transcript: ENSMUST00000050757
AA Change: T533A

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000058466
Gene: ENSMUSG00000028399
AA Change: T533A

DomainStartEndE-ValueType
IGc2 36 105 8.57e-12 SMART
IGc2 138 208 1.38e-15 SMART
IGc2 238 299 8.13e-4 SMART
FN3 313 392 7.92e-14 SMART
FN3 408 491 5.73e-11 SMART
IG_like 499 593 8.34e1 SMART
FN3 506 584 9.1e-14 SMART
FN3 597 674 1.21e0 SMART
transmembrane domain 847 869 N/A INTRINSIC
low complexity region 870 882 N/A INTRINSIC
PTPc 949 1207 6.38e-134 SMART
PTPc 1236 1498 9.17e-135 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000098005
AA Change: T543A

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000095614
Gene: ENSMUSG00000028399
AA Change: T543A

DomainStartEndE-ValueType
IGc2 36 105 8.57e-12 SMART
IGc2 138 214 8.5e-16 SMART
low complexity region 225 237 N/A INTRINSIC
IGc2 248 309 8.13e-4 SMART
FN3 323 402 7.92e-14 SMART
FN3 418 501 5.73e-11 SMART
IG_like 509 603 8.34e1 SMART
FN3 516 594 9.1e-14 SMART
FN3 607 684 1.21e0 SMART
transmembrane domain 857 879 N/A INTRINSIC
low complexity region 886 897 N/A INTRINSIC
PTPc 950 1208 6.38e-134 SMART
PTPc 1237 1499 9.17e-135 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000102834
AA Change: T296A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000099898
Gene: ENSMUSG00000028399
AA Change: T296A

DomainStartEndE-ValueType
IGc2 1 62 8.13e-4 SMART
FN3 76 155 7.92e-14 SMART
FN3 171 254 5.73e-11 SMART
IG_like 262 356 8.34e1 SMART
FN3 269 347 9.1e-14 SMART
FN3 360 437 1.21e0 SMART
transmembrane domain 610 632 N/A INTRINSIC
low complexity region 633 645 N/A INTRINSIC
PTPc 698 956 6.38e-134 SMART
PTPc 985 1247 9.17e-135 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000107289
AA Change: T543A

PolyPhen 2 Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000102910
Gene: ENSMUSG00000028399
AA Change: T543A

DomainStartEndE-ValueType
IGc2 36 105 8.57e-12 SMART
IGc2 138 214 8.5e-16 SMART
low complexity region 225 237 N/A INTRINSIC
IGc2 248 309 8.13e-4 SMART
FN3 323 402 7.92e-14 SMART
FN3 418 501 5.73e-11 SMART
IG_like 509 603 8.34e1 SMART
FN3 516 594 9.1e-14 SMART
FN3 609 696 2.72e-12 SMART
FN3 712 809 2.87e-11 SMART
FN3 824 904 4.96e-6 SMART
FN3 919 1003 4.12e-12 SMART
FN3 1018 1095 1.95e0 SMART
transmembrane domain 1268 1290 N/A INTRINSIC
low complexity region 1291 1303 N/A INTRINSIC
PTPc 1356 1614 6.38e-134 SMART
PTPc 1643 1905 9.17e-135 SMART
Predicted Effect unknown
Transcript: ENSMUST00000172811
AA Change: T21A
SMART Domains Protein: ENSMUSP00000134190
Gene: ENSMUSG00000028399
AA Change: T21A

DomainStartEndE-ValueType
FN3 1 73 1.29e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000173376
AA Change: T550A

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
SMART Domains Protein: ENSMUSP00000133468
Gene: ENSMUSG00000028399
AA Change: T550A

DomainStartEndE-ValueType
IGc2 43 112 8.57e-12 SMART
IGc2 145 221 8.5e-16 SMART
low complexity region 232 244 N/A INTRINSIC
IGc2 255 316 8.13e-4 SMART
FN3 330 409 7.92e-14 SMART
FN3 425 508 5.73e-11 SMART
IG_like 516 610 8.34e1 SMART
FN3 523 601 9.1e-14 SMART
FN3 614 691 1.21e0 SMART
transmembrane domain 864 886 N/A INTRINSIC
low complexity region 887 899 N/A INTRINSIC
PTPc 952 1210 6.38e-134 SMART
PTPc 1239 1501 9.17e-135 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000174023
AA Change: T540A

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000133562
Gene: ENSMUSG00000028399
AA Change: T540A

DomainStartEndE-ValueType
IGc2 36 105 8.57e-12 SMART
IGc2 138 211 4.88e-16 SMART
low complexity region 222 234 N/A INTRINSIC
IGc2 245 306 8.13e-4 SMART
FN3 320 399 7.92e-14 SMART
FN3 415 498 5.73e-11 SMART
IG_like 506 600 8.34e1 SMART
FN3 513 591 9.1e-14 SMART
FN3 604 681 1.21e0 SMART
transmembrane domain 853 875 N/A INTRINSIC
low complexity region 882 893 N/A INTRINSIC
PTPc 946 1204 6.38e-134 SMART
PTPc 1233 1495 9.17e-135 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000174180
AA Change: T530A

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000133973
Gene: ENSMUSG00000028399
AA Change: T530A

DomainStartEndE-ValueType
IGc2 36 105 8.57e-12 SMART
IGc2 138 205 2.09e-15 SMART
IGc2 235 296 8.13e-4 SMART
FN3 310 389 7.92e-14 SMART
FN3 405 488 5.73e-11 SMART
IG_like 496 590 8.34e1 SMART
FN3 503 581 9.1e-14 SMART
FN3 596 683 2.72e-12 SMART
FN3 699 787 6.15e-11 SMART
FN3 802 882 4.96e-6 SMART
FN3 897 981 4.12e-12 SMART
FN3 996 1073 1.95e0 SMART
transmembrane domain 1246 1268 N/A INTRINSIC
low complexity region 1269 1281 N/A INTRINSIC
PTPc 1334 1592 6.38e-134 SMART
PTPc 1621 1883 9.17e-135 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000174531
AA Change: T537A

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000134229
Gene: ENSMUSG00000028399
AA Change: T537A

DomainStartEndE-ValueType
IGc2 36 105 8.57e-12 SMART
IGc2 138 208 1.38e-15 SMART
low complexity region 219 231 N/A INTRINSIC
IGc2 242 303 8.13e-4 SMART
FN3 317 396 7.92e-14 SMART
FN3 412 495 5.73e-11 SMART
IG_like 503 597 8.34e1 SMART
FN3 510 588 9.1e-14 SMART
FN3 601 678 1.21e0 SMART
transmembrane domain 851 873 N/A INTRINSIC
low complexity region 874 886 N/A INTRINSIC
PTPc 939 1197 6.38e-134 SMART
PTPc 1226 1488 9.17e-135 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000174831
AA Change: T543A

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000133328
Gene: ENSMUSG00000028399
AA Change: T543A

DomainStartEndE-ValueType
IGc2 36 105 8.57e-12 SMART
IGc2 138 214 8.5e-16 SMART
low complexity region 225 237 N/A INTRINSIC
IGc2 248 309 8.13e-4 SMART
FN3 323 402 7.92e-14 SMART
FN3 418 501 5.73e-11 SMART
IG_like 509 603 8.34e1 SMART
FN3 516 594 9.1e-14 SMART
FN3 607 684 1.21e0 SMART
transmembrane domain 856 878 N/A INTRINSIC
low complexity region 885 896 N/A INTRINSIC
PTPc 949 1207 6.38e-134 SMART
PTPc 1236 1498 9.17e-135 SMART
Meta Mutation Damage Score 0.0787 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency 92% (86/93)
MGI Phenotype Strain: 2158795
PHENOTYPE: Homozygotes for a targeted null mutation exhibit impaired learning of spatial tasks, enhanced long-term potentiation at hippocampal synapses, and high mortality associated with reduced food intake. [provided by MGI curators]
Allele List at MGI

All alleles(9) : Targeted(4) Gene trapped(5)
 

Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc2 A C 19: 43,816,882 (GRCm38) E725A possibly damaging Het
Abcc5 G T 16: 20,398,876 (GRCm38) L362I probably damaging Het
Ammecr1l C T 18: 31,774,653 (GRCm38) R179* probably null Het
Arap2 G T 5: 62,749,094 (GRCm38) T194K probably benign Het
Atf2 C A 2: 73,823,300 (GRCm38) V282F probably damaging Het
Atp1a1 T C 3: 101,591,806 (GRCm38) E159G possibly damaging Het
B4galt2 T C 4: 117,877,179 (GRCm38) S258G possibly damaging Het
Bptf G T 11: 107,047,181 (GRCm38) H2695N probably damaging Het
Casq2 T C 3: 102,110,244 (GRCm38) V80A probably benign Het
Ccdc130 A G 8: 84,263,874 (GRCm38) I43T probably damaging Het
Cdc42ep3 G A 17: 79,335,458 (GRCm38) A11V probably benign Het
Cdh4 A T 2: 179,780,467 (GRCm38) H128L probably benign Het
Cdk5rap1 C A 2: 154,361,835 (GRCm38) *191L probably null Het
Cfdp1 G A 8: 111,830,891 (GRCm38) T206I probably benign Het
Cgn C A 3: 94,779,438 (GRCm38) G185W probably damaging Het
Clpx A C 9: 65,312,114 (GRCm38) R231S possibly damaging Het
Copg1 T A 6: 87,912,286 (GRCm38) L870* probably null Het
Cyp4a10 A T 4: 115,525,338 (GRCm38) D275V probably benign Het
Dip2a T C 10: 76,296,406 (GRCm38) T504A probably benign Het
Dmxl2 A C 9: 54,446,405 (GRCm38) probably null Het
Dnaaf5 A T 5: 139,178,000 (GRCm38) I671F probably damaging Het
Dnah14 A G 1: 181,757,223 (GRCm38) D3173G probably damaging Het
Dock2 T C 11: 34,294,118 (GRCm38) Y1074C probably damaging Het
Dthd1 A C 5: 62,888,187 (GRCm38) M765L probably benign Het
E2f3 A C 13: 29,911,275 (GRCm38) C220W probably damaging Het
Elf3 C T 1: 135,257,752 (GRCm38) S8N probably damaging Het
F2rl1 A T 13: 95,513,267 (GRCm38) V369E probably damaging Het
Fam214a T A 9: 75,012,968 (GRCm38) W799R probably damaging Het
Fpr-rs7 C T 17: 20,113,428 (GRCm38) G267R probably benign Het
Ggact A T 14: 122,891,635 (GRCm38) L56Q possibly damaging Het
Gm10698 A T 9: 33,728,488 (GRCm38) noncoding transcript Het
Gm5546 T C 3: 104,366,508 (GRCm38) noncoding transcript Het
Gm8267 A G 14: 44,717,835 (GRCm38) V243A probably benign Het
Gtf2h1 A G 7: 46,815,412 (GRCm38) T424A possibly damaging Het
Gucy1b2 A G 14: 62,423,017 (GRCm38) V140A possibly damaging Het
Htatip2 T C 7: 49,770,844 (GRCm38) L146P probably damaging Het
Htr1b T C 9: 81,631,510 (GRCm38) D348G possibly damaging Het
Ifi205 T C 1: 174,028,321 (GRCm38) I48V possibly damaging Het
Igkv18-36 C T 6: 69,992,591 (GRCm38) R72K probably damaging Het
Kcnk7 T C 19: 5,706,253 (GRCm38) L169P probably damaging Het
Klf17 T C 4: 117,760,536 (GRCm38) D208G probably benign Het
Ltn1 A G 16: 87,418,494 (GRCm38) F418L probably damaging Het
Map4k4 G A 1: 40,019,564 (GRCm38) V1040I probably damaging Het
Mark1 A G 1: 184,912,132 (GRCm38) V445A probably benign Het
Med11 T C 11: 70,453,196 (GRCm38) I114T probably benign Het
Moxd2 A G 6: 40,887,247 (GRCm38) V83A probably damaging Het
Mrpl33 A G 5: 31,616,358 (GRCm38) probably benign Het
Mrps27 A G 13: 99,414,815 (GRCm38) probably null Het
Nop58 T C 1: 59,696,026 (GRCm38) V75A probably benign Het
Olfr1290 A C 2: 111,489,744 (GRCm38) M138R probably benign Het
Olfr1339 T C 4: 118,734,655 (GRCm38) L42P probably damaging Het
Olfr136 A C 17: 38,335,840 (GRCm38) I228L possibly damaging Het
Olfr325 A G 11: 58,581,429 (GRCm38) D195G probably damaging Het
Olfr832 A G 9: 18,945,446 (GRCm38) H266R probably benign Het
Olfr844 C A 9: 19,319,147 (GRCm38) F210L probably benign Het
Pdzd2 G T 15: 12,419,516 (GRCm38) N263K possibly damaging Het
Podnl1 C A 8: 84,126,061 (GRCm38) probably benign Het
Prkd3 G T 17: 78,951,937 (GRCm38) H864N possibly damaging Het
Pum2 T A 12: 8,747,272 (GRCm38) I788N probably damaging Het
Ralgapa1 T A 12: 55,693,458 (GRCm38) N1328I probably damaging Het
Rhoc T C 3: 104,794,039 (GRCm38) L193P probably damaging Het
Rif1 T C 2: 52,073,139 (GRCm38) probably benign Het
Rspo2 A T 15: 43,075,904 (GRCm38) C163* probably null Het
Sco1 A G 11: 67,056,599 (GRCm38) Y204C probably damaging Het
Shc2 T C 10: 79,622,379 (GRCm38) K490R probably benign Het
Siglec1 T C 2: 131,074,436 (GRCm38) D1198G probably damaging Het
Slc25a18 T C 6: 120,786,090 (GRCm38) V31A probably damaging Het
Smpd5 A T 15: 76,295,693 (GRCm38) I112L probably benign Het
Synpr CT C 14: 13,285,198 (GRCm38) probably null Het
Tdrd9 T G 12: 112,041,689 (GRCm38) S988A probably benign Het
Tiam2 T A 17: 3,454,168 (GRCm38) F982I probably damaging Het
Tmc3 G A 7: 83,622,396 (GRCm38) V919I probably benign Het
Tmem200c A T 17: 68,840,470 (GRCm38) D16V probably damaging Het
Tmem37 A T 1: 120,068,205 (GRCm38) D47E probably damaging Het
Top3a T A 11: 60,742,997 (GRCm38) R733* probably null Het
Treh T C 9: 44,683,318 (GRCm38) V8A probably benign Het
Trim17 A C 11: 58,968,450 (GRCm38) probably benign Het
Ubash3b T C 9: 41,016,600 (GRCm38) K471E probably damaging Het
Usp8 T A 2: 126,729,222 (GRCm38) L144Q possibly damaging Het
Wnk2 T A 13: 49,147,232 (GRCm38) M1L unknown Het
Other mutations in Ptprd
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00964:Ptprd APN 4 75,998,556 (GRCm38) nonsense probably null
IGL01067:Ptprd APN 4 76,059,685 (GRCm38) missense probably damaging 1.00
IGL01121:Ptprd APN 4 75,954,201 (GRCm38) splice site probably benign
IGL01531:Ptprd APN 4 76,085,520 (GRCm38) missense probably damaging 0.98
IGL01661:Ptprd APN 4 75,954,083 (GRCm38) missense probably damaging 1.00
IGL01723:Ptprd APN 4 76,243,673 (GRCm38) missense probably damaging 1.00
IGL01735:Ptprd APN 4 76,136,820 (GRCm38) splice site probably null
IGL01810:Ptprd APN 4 76,140,507 (GRCm38) splice site probably benign
IGL01834:Ptprd APN 4 76,128,595 (GRCm38) missense probably damaging 1.00
IGL01835:Ptprd APN 4 76,246,821 (GRCm38) missense probably benign 0.02
IGL01867:Ptprd APN 4 76,243,647 (GRCm38) missense probably damaging 1.00
IGL02582:Ptprd APN 4 75,947,124 (GRCm38) missense probably damaging 1.00
IGL02591:Ptprd APN 4 75,982,050 (GRCm38) missense probably damaging 1.00
IGL02741:Ptprd APN 4 76,133,284 (GRCm38) missense probably damaging 1.00
IGL02866:Ptprd APN 4 76,050,437 (GRCm38) missense probably damaging 1.00
IGL02960:Ptprd APN 4 76,128,868 (GRCm38) missense probably damaging 1.00
IGL03155:Ptprd APN 4 76,066,219 (GRCm38) missense possibly damaging 0.95
IGL03230:Ptprd APN 4 76,050,417 (GRCm38) nonsense probably null
IGL03343:Ptprd APN 4 76,059,729 (GRCm38) missense probably damaging 1.00
unhurried UTSW 4 76,100,633 (GRCm38) nonsense probably null
ANU22:Ptprd UTSW 4 76,100,456 (GRCm38) missense probably damaging 0.99
F5493:Ptprd UTSW 4 76,084,408 (GRCm38) missense probably damaging 1.00
P0033:Ptprd UTSW 4 76,128,854 (GRCm38) nonsense probably null
R0044:Ptprd UTSW 4 76,086,329 (GRCm38) missense probably benign 0.08
R0044:Ptprd UTSW 4 76,086,329 (GRCm38) missense probably benign 0.08
R0076:Ptprd UTSW 4 75,947,039 (GRCm38) splice site probably benign
R0137:Ptprd UTSW 4 76,136,903 (GRCm38) missense probably benign 0.24
R0358:Ptprd UTSW 4 75,944,989 (GRCm38) missense probably damaging 1.00
R0365:Ptprd UTSW 4 76,136,846 (GRCm38) missense probably damaging 1.00
R0385:Ptprd UTSW 4 76,128,665 (GRCm38) missense probably damaging 1.00
R0601:Ptprd UTSW 4 76,100,474 (GRCm38) missense probably benign
R0646:Ptprd UTSW 4 76,084,403 (GRCm38) missense probably damaging 0.99
R0667:Ptprd UTSW 4 75,957,346 (GRCm38) missense probably damaging 1.00
R0707:Ptprd UTSW 4 75,957,239 (GRCm38) missense probably damaging 1.00
R0734:Ptprd UTSW 4 76,140,597 (GRCm38) missense probably damaging 1.00
R0827:Ptprd UTSW 4 76,128,915 (GRCm38) missense probably damaging 0.98
R0932:Ptprd UTSW 4 76,136,885 (GRCm38) missense probably damaging 1.00
R1069:Ptprd UTSW 4 76,100,633 (GRCm38) nonsense probably null
R1069:Ptprd UTSW 4 75,998,487 (GRCm38) splice site probably benign
R1086:Ptprd UTSW 4 76,133,258 (GRCm38) missense probably damaging 1.00
R1439:Ptprd UTSW 4 76,066,200 (GRCm38) missense probably damaging 1.00
R1440:Ptprd UTSW 4 76,084,552 (GRCm38) missense probably damaging 0.98
R1688:Ptprd UTSW 4 75,982,684 (GRCm38) missense probably damaging 1.00
R1858:Ptprd UTSW 4 75,947,147 (GRCm38) missense probably damaging 1.00
R2001:Ptprd UTSW 4 75,954,122 (GRCm38) missense probably damaging 1.00
R2020:Ptprd UTSW 4 76,133,161 (GRCm38) missense probably damaging 1.00
R2023:Ptprd UTSW 4 75,957,104 (GRCm38) missense probably damaging 1.00
R2413:Ptprd UTSW 4 76,133,200 (GRCm38) missense probably damaging 1.00
R2510:Ptprd UTSW 4 76,086,011 (GRCm38) critical splice donor site probably null
R2914:Ptprd UTSW 4 75,947,101 (GRCm38) missense probably damaging 1.00
R2971:Ptprd UTSW 4 76,107,324 (GRCm38) missense probably benign 0.10
R3051:Ptprd UTSW 4 76,100,630 (GRCm38) missense probably damaging 1.00
R3433:Ptprd UTSW 4 76,086,011 (GRCm38) critical splice donor site probably null
R3964:Ptprd UTSW 4 76,059,836 (GRCm38) splice site probably benign
R4009:Ptprd UTSW 4 75,956,397 (GRCm38) missense possibly damaging 0.94
R4394:Ptprd UTSW 4 76,128,685 (GRCm38) missense probably damaging 1.00
R4420:Ptprd UTSW 4 76,039,377 (GRCm38) missense possibly damaging 0.92
R4424:Ptprd UTSW 4 76,102,963 (GRCm38) missense probably benign 0.22
R4575:Ptprd UTSW 4 76,243,786 (GRCm38) missense possibly damaging 0.55
R4578:Ptprd UTSW 4 76,243,786 (GRCm38) missense possibly damaging 0.55
R4782:Ptprd UTSW 4 76,091,532 (GRCm38) missense probably benign 0.01
R4785:Ptprd UTSW 4 76,140,553 (GRCm38) missense probably benign 0.05
R4799:Ptprd UTSW 4 76,091,532 (GRCm38) missense probably benign 0.01
R4944:Ptprd UTSW 4 76,128,899 (GRCm38) missense probably damaging 1.00
R4950:Ptprd UTSW 4 76,140,515 (GRCm38) splice site probably null
R4969:Ptprd UTSW 4 76,133,305 (GRCm38) missense probably damaging 1.00
R5153:Ptprd UTSW 4 76,012,102 (GRCm38) missense probably damaging 1.00
R5164:Ptprd UTSW 4 76,100,758 (GRCm38) splice site probably null
R5287:Ptprd UTSW 4 75,954,168 (GRCm38) nonsense probably null
R5305:Ptprd UTSW 4 75,982,626 (GRCm38) missense probably damaging 1.00
R5362:Ptprd UTSW 4 76,128,813 (GRCm38) missense probably damaging 1.00
R5403:Ptprd UTSW 4 75,954,168 (GRCm38) nonsense probably null
R5531:Ptprd UTSW 4 76,059,667 (GRCm38) critical splice donor site probably null
R5543:Ptprd UTSW 4 76,059,753 (GRCm38) missense probably damaging 1.00
R5634:Ptprd UTSW 4 76,072,018 (GRCm38) missense probably benign 0.01
R5719:Ptprd UTSW 4 76,054,602 (GRCm38) critical splice acceptor site probably null
R5884:Ptprd UTSW 4 75,982,690 (GRCm38) missense probably damaging 1.00
R6247:Ptprd UTSW 4 76,066,291 (GRCm38) missense probably benign 0.06
R6250:Ptprd UTSW 4 76,128,995 (GRCm38) missense probably damaging 1.00
R6335:Ptprd UTSW 4 75,954,183 (GRCm38) missense probably damaging 1.00
R6352:Ptprd UTSW 4 76,091,552 (GRCm38) splice site probably null
R6533:Ptprd UTSW 4 76,128,528 (GRCm38) missense probably damaging 1.00
R6756:Ptprd UTSW 4 75,955,299 (GRCm38) missense probably damaging 1.00
R6782:Ptprd UTSW 4 76,325,140 (GRCm38) splice site probably null
R7131:Ptprd UTSW 4 76,066,340 (GRCm38) missense probably damaging 1.00
R7170:Ptprd UTSW 4 76,071,962 (GRCm38) missense probably benign 0.06
R7233:Ptprd UTSW 4 76,059,783 (GRCm38) missense probably benign 0.00
R7246:Ptprd UTSW 4 76,128,676 (GRCm38) missense probably damaging 1.00
R7413:Ptprd UTSW 4 76,246,839 (GRCm38) missense probably benign 0.00
R7428:Ptprd UTSW 4 76,086,468 (GRCm38) missense probably benign 0.03
R7442:Ptprd UTSW 4 76,059,821 (GRCm38) nonsense probably null
R7491:Ptprd UTSW 4 76,133,155 (GRCm38) missense probably benign 0.23
R7526:Ptprd UTSW 4 76,066,327 (GRCm38) missense probably benign 0.00
R7609:Ptprd UTSW 4 76,072,003 (GRCm38) missense probably benign 0.03
R7612:Ptprd UTSW 4 76,086,459 (GRCm38) missense probably benign 0.45
R7659:Ptprd UTSW 4 76,128,916 (GRCm38) missense probably benign 0.03
R7743:Ptprd UTSW 4 76,086,089 (GRCm38) missense probably damaging 1.00
R7748:Ptprd UTSW 4 76,099,504 (GRCm38) missense probably null 0.39
R7788:Ptprd UTSW 4 75,998,604 (GRCm38) missense probably damaging 1.00
R7836:Ptprd UTSW 4 75,982,644 (GRCm38) missense probably damaging 0.99
R7937:Ptprd UTSW 4 76,095,535 (GRCm38) missense probably benign 0.00
R8000:Ptprd UTSW 4 76,066,242 (GRCm38) missense possibly damaging 0.95
R8018:Ptprd UTSW 4 76,085,520 (GRCm38) missense probably damaging 0.98
R8072:Ptprd UTSW 4 76,086,036 (GRCm38) missense probably benign 0.01
R8119:Ptprd UTSW 4 76,129,026 (GRCm38) missense probably benign 0.00
R8350:Ptprd UTSW 4 75,950,661 (GRCm38) missense probably damaging 1.00
R8387:Ptprd UTSW 4 75,955,289 (GRCm38) missense probably damaging 1.00
R8458:Ptprd UTSW 4 76,066,259 (GRCm38) missense probably benign 0.00
R8529:Ptprd UTSW 4 76,129,025 (GRCm38) missense probably damaging 1.00
R8699:Ptprd UTSW 4 76,041,392 (GRCm38) missense probably benign
R8924:Ptprd UTSW 4 75,998,499 (GRCm38) critical splice donor site probably null
R8984:Ptprd UTSW 4 75,945,014 (GRCm38) missense probably damaging 1.00
R9024:Ptprd UTSW 4 75,956,330 (GRCm38) missense probably damaging 1.00
R9204:Ptprd UTSW 4 75,954,078 (GRCm38) missense possibly damaging 0.46
R9206:Ptprd UTSW 4 75,954,078 (GRCm38) missense possibly damaging 0.46
R9259:Ptprd UTSW 4 76,071,963 (GRCm38) missense probably damaging 0.99
R9311:Ptprd UTSW 4 76,133,083 (GRCm38) missense probably benign 0.25
R9417:Ptprd UTSW 4 75,947,098 (GRCm38) missense probably damaging 0.99
R9427:Ptprd UTSW 4 76,133,203 (GRCm38) missense probably benign 0.01
R9579:Ptprd UTSW 4 75,954,078 (GRCm38) missense possibly damaging 0.46
R9580:Ptprd UTSW 4 75,954,078 (GRCm38) missense possibly damaging 0.46
R9701:Ptprd UTSW 4 75,998,659 (GRCm38) missense probably damaging 1.00
RF016:Ptprd UTSW 4 76,128,655 (GRCm38) missense probably benign 0.01
RF023:Ptprd UTSW 4 76,128,565 (GRCm38) missense probably damaging 0.98
Z1176:Ptprd UTSW 4 76,133,214 (GRCm38) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GCTGTGACCTGATGATTGAATAG -3'
(R):5'- GAGGCCCTTACATCTCAGATG -3'

Sequencing Primer
(F):5'- GACCTGATGATTGAATAGTATCTAGC -3'
(R):5'- CTCAGATGATGTAAGAGCCTTGTTC -3'
Posted On 2015-10-21