Incidental Mutation 'R2078:Plch1'
ID 229262
Institutional Source Beutler Lab
Gene Symbol Plch1
Ensembl Gene ENSMUSG00000036834
Gene Name phospholipase C, eta 1
Synonyms Plcl3, PLCeta1
MMRRC Submission 040083-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.198) question?
Stock # R2078 (G1)
Quality Score 225
Status Not validated
Chromosome 3
Chromosomal Location 63603655-63806893 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 63609364 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 948 (S948P)
Ref Sequence ENSEMBL: ENSMUSP00000123921 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000048134] [ENSMUST00000059973] [ENSMUST00000084105] [ENSMUST00000159676] [ENSMUST00000177143] [ENSMUST00000160638] [ENSMUST00000162269] [ENSMUST00000175947]
AlphaFold Q4KWH5
Predicted Effect probably benign
Transcript: ENSMUST00000048134
AA Change: S909P

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000047693
Gene: ENSMUSG00000036834
AA Change: S909P

DomainStartEndE-ValueType
PH 3 112 2.37e-6 SMART
EFh 128 156 2.41e-4 SMART
EFh 164 193 1.54e-2 SMART
Pfam:EF-hand_like 198 280 2.2e-26 PFAM
PLCXc 281 426 3.13e-71 SMART
low complexity region 440 453 N/A INTRINSIC
low complexity region 564 581 N/A INTRINSIC
PLCYc 583 696 3.4e-49 SMART
C2 715 823 5.47e-22 SMART
low complexity region 979 997 N/A INTRINSIC
low complexity region 1079 1091 N/A INTRINSIC
low complexity region 1420 1435 N/A INTRINSIC
low complexity region 1543 1557 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000059973
AA Change: S947P

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000058524
Gene: ENSMUSG00000036834
AA Change: S947P

DomainStartEndE-ValueType
PH 21 130 1.1e-8 SMART
EFh 146 174 1.1e-6 SMART
EFh 182 211 7.6e-5 SMART
Pfam:EF-hand_like 216 298 4.5e-24 PFAM
PLCXc 299 444 1.6e-73 SMART
low complexity region 458 471 N/A INTRINSIC
low complexity region 582 599 N/A INTRINSIC
PLCYc 601 714 1.7e-51 SMART
C2 733 841 3.7e-24 SMART
low complexity region 1017 1035 N/A INTRINSIC
low complexity region 1117 1129 N/A INTRINSIC
low complexity region 1458 1473 N/A INTRINSIC
low complexity region 1581 1595 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000084105
AA Change: S948P

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000081122
Gene: ENSMUSG00000036834
AA Change: S948P

DomainStartEndE-ValueType
PH 21 130 2.37e-6 SMART
EFh 146 174 2.41e-4 SMART
EFh 182 211 1.54e-2 SMART
Pfam:EF-hand_like 216 298 2.4e-27 PFAM
PLCXc 299 444 3.13e-71 SMART
low complexity region 458 471 N/A INTRINSIC
low complexity region 583 600 N/A INTRINSIC
PLCYc 602 715 3.4e-49 SMART
C2 734 842 5.47e-22 SMART
low complexity region 1018 1036 N/A INTRINSIC
low complexity region 1118 1130 N/A INTRINSIC
low complexity region 1459 1474 N/A INTRINSIC
low complexity region 1582 1596 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159374
Predicted Effect probably benign
Transcript: ENSMUST00000159676
AA Change: S948P

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000124632
Gene: ENSMUSG00000036834
AA Change: S948P

DomainStartEndE-ValueType
PH 21 130 2.37e-6 SMART
EFh 146 174 2.41e-4 SMART
EFh 182 211 1.54e-2 SMART
Pfam:EF-hand_like 216 298 1.8e-26 PFAM
PLCXc 299 444 3.13e-71 SMART
low complexity region 458 471 N/A INTRINSIC
low complexity region 583 600 N/A INTRINSIC
PLCYc 602 715 3.4e-49 SMART
C2 734 842 5.47e-22 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159982
Predicted Effect probably benign
Transcript: ENSMUST00000177143
AA Change: S939P

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000135424
Gene: ENSMUSG00000036834
AA Change: S939P

DomainStartEndE-ValueType
PH 33 142 2.37e-6 SMART
EFh 158 186 2.41e-4 SMART
EFh 194 223 1.54e-2 SMART
Pfam:EF-hand_like 228 310 2.3e-26 PFAM
PLCXc 311 456 3.13e-71 SMART
low complexity region 470 483 N/A INTRINSIC
low complexity region 594 611 N/A INTRINSIC
PLCYc 613 726 3.4e-49 SMART
C2 745 853 5.47e-22 SMART
low complexity region 1009 1027 N/A INTRINSIC
low complexity region 1109 1121 N/A INTRINSIC
low complexity region 1450 1465 N/A INTRINSIC
low complexity region 1573 1587 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000160638
AA Change: S948P

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000123921
Gene: ENSMUSG00000036834
AA Change: S948P

DomainStartEndE-ValueType
PH 21 130 2.37e-6 SMART
EFh 146 174 2.41e-4 SMART
EFh 182 211 1.54e-2 SMART
Pfam:EF-hand_like 216 298 5.3e-28 PFAM
PLCXc 299 444 3.13e-71 SMART
low complexity region 458 471 N/A INTRINSIC
low complexity region 583 600 N/A INTRINSIC
PLCYc 602 715 3.4e-49 SMART
C2 734 842 5.47e-22 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000162269
AA Change: S948P

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000124463
Gene: ENSMUSG00000036834
AA Change: S948P

DomainStartEndE-ValueType
PH 21 130 2.37e-6 SMART
EFh 146 174 2.41e-4 SMART
EFh 182 211 1.54e-2 SMART
Pfam:EF-hand_like 216 298 1.7e-26 PFAM
PLCXc 299 444 3.13e-71 SMART
low complexity region 458 471 N/A INTRINSIC
low complexity region 583 600 N/A INTRINSIC
PLCYc 602 715 3.4e-49 SMART
C2 734 842 5.47e-22 SMART
Predicted Effect unknown
Transcript: ENSMUST00000176861
AA Change: S34P
Predicted Effect unknown
Transcript: ENSMUST00000175947
AA Change: S927P
SMART Domains Protein: ENSMUSP00000135353
Gene: ENSMUSG00000036834
AA Change: S927P

DomainStartEndE-ValueType
PH 21 130 2.37e-6 SMART
EFh 146 174 2.41e-4 SMART
EFh 182 211 1.54e-2 SMART
Pfam:EF-hand_like 216 298 1.2e-26 PFAM
PLCXc 299 444 3.13e-71 SMART
low complexity region 458 471 N/A INTRINSIC
low complexity region 582 599 N/A INTRINSIC
PLCYc 601 714 3.4e-49 SMART
C2 733 841 5.47e-22 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] PLCH1 is a member of the PLC-eta family of the phosphoinositide-specific phospholipase C (PLC) superfamily of enzymes that cleave phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) to generate second messengers inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DAG) (Hwang et al., 2005 [PubMed 15702972]).[supplied by OMIM, Jun 2009]
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb6 C A 1: 75,148,780 (GRCm39) G55C probably damaging Het
Acss3 T C 10: 106,802,902 (GRCm39) T448A possibly damaging Het
Atxn7 A G 14: 14,052,975 (GRCm38) N138D probably damaging Het
Cacna2d4 A T 6: 119,315,077 (GRCm39) D869V probably benign Het
Cps1 T G 1: 67,196,965 (GRCm39) Y339D probably damaging Het
Cps1 T C 1: 67,234,424 (GRCm39) I937T possibly damaging Het
Dlgap4 T C 2: 156,604,746 (GRCm39) S261P probably damaging Het
Dusp6 T C 10: 99,099,686 (GRCm39) Y45H probably damaging Het
Ebag9 A G 15: 44,500,200 (GRCm39) N157S probably damaging Het
Exoc4 A G 6: 33,887,522 (GRCm39) D770G probably benign Het
Ezr A G 17: 7,050,041 (GRCm39) M1T probably null Het
Fat4 A G 3: 38,943,822 (GRCm39) N905S probably damaging Het
Fcrlb C G 1: 170,735,650 (GRCm39) R208P probably damaging Het
Flnb T C 14: 7,927,466 (GRCm38) V1892A probably damaging Het
Gas2 G A 7: 51,547,073 (GRCm39) V75M probably benign Het
Gda T A 19: 21,378,036 (GRCm39) D267V probably damaging Het
Gper1 A T 5: 139,411,888 (GRCm39) I78F probably benign Het
Hectd1 A C 12: 51,795,325 (GRCm39) I2368S probably damaging Het
Katna1 C T 10: 7,619,333 (GRCm39) P114S probably benign Het
Lce3c G A 3: 92,852,758 (GRCm39) S73N unknown Het
Lrfn3 A T 7: 30,059,879 (GRCm39) D115E possibly damaging Het
Lrrc47 C A 4: 154,103,888 (GRCm39) T505K probably damaging Het
Mertk C T 2: 128,636,378 (GRCm39) T784I probably damaging Het
Mettl21e T A 1: 44,245,662 (GRCm39) I195F possibly damaging Het
Mff T C 1: 82,719,642 (GRCm39) S207P probably damaging Het
Mtmr6 A G 14: 60,529,436 (GRCm39) probably null Het
Myh9 T C 15: 77,648,112 (GRCm39) K1788R probably benign Het
Narf A G 11: 121,136,220 (GRCm39) T199A probably benign Het
Neurod6 A G 6: 55,655,954 (GRCm39) S228P probably benign Het
Notch4 A T 17: 34,787,689 (GRCm39) probably null Het
Nyap2 T C 1: 81,169,696 (GRCm39) L151P probably damaging Het
Or5b21 T A 19: 12,839,751 (GRCm39) V204E probably benign Het
P2ry1 A G 3: 60,911,118 (GRCm39) I86V probably damaging Het
Pafah1b2 G T 9: 45,880,127 (GRCm39) D183E probably damaging Het
Phldb1 T C 9: 44,619,276 (GRCm39) E179G probably damaging Het
Piezo2 T C 18: 63,250,791 (GRCm39) E436G probably damaging Het
Pkhd1l1 A G 15: 44,391,163 (GRCm39) I1514V probably benign Het
Rfc5 A G 5: 117,518,868 (GRCm39) V296A probably benign Het
Rnf150 A T 8: 83,730,234 (GRCm39) I255F probably damaging Het
Rsbn1 A G 3: 103,868,839 (GRCm39) D626G probably damaging Het
Sfswap A G 5: 129,593,171 (GRCm39) D346G possibly damaging Het
Slc38a11 A T 2: 65,160,728 (GRCm39) F289I possibly damaging Het
Terf2ip A G 8: 112,742,035 (GRCm39) N243S probably benign Het
Tmed5 A T 5: 108,272,471 (GRCm39) V209E probably damaging Het
Tmem63b A G 17: 45,974,462 (GRCm39) S603P possibly damaging Het
Tomm20 T C 8: 127,663,822 (GRCm39) M121V possibly damaging Het
Tspan33 G A 6: 29,709,970 (GRCm39) V45I probably benign Het
Usp17la A T 7: 104,508,600 (GRCm39) M1L probably benign Het
Vsig8 C A 1: 172,390,856 (GRCm39) D301E probably benign Het
Vwa8 T A 14: 79,145,597 (GRCm39) H91Q probably damaging Het
Other mutations in Plch1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01397:Plch1 APN 3 63,639,150 (GRCm39) splice site probably null
IGL01542:Plch1 APN 3 63,639,070 (GRCm39) missense probably damaging 0.99
IGL01999:Plch1 APN 3 63,660,728 (GRCm39) missense probably damaging 1.00
IGL02153:Plch1 APN 3 63,688,772 (GRCm39) missense probably damaging 1.00
IGL02203:Plch1 APN 3 63,606,160 (GRCm39) missense possibly damaging 0.46
IGL02220:Plch1 APN 3 63,606,382 (GRCm39) missense probably damaging 0.97
IGL02259:Plch1 APN 3 63,630,170 (GRCm39) critical splice donor site probably null
IGL02268:Plch1 APN 3 63,606,704 (GRCm39) makesense probably null
IGL02411:Plch1 APN 3 63,605,177 (GRCm39) splice site probably null
IGL02472:Plch1 APN 3 63,609,270 (GRCm39) missense probably damaging 1.00
IGL02477:Plch1 APN 3 63,660,714 (GRCm39) missense probably damaging 1.00
IGL02503:Plch1 APN 3 63,605,285 (GRCm39) missense probably damaging 1.00
IGL02800:Plch1 APN 3 63,605,899 (GRCm39) missense probably benign 0.21
IGL03167:Plch1 APN 3 63,630,165 (GRCm39) splice site probably benign
IGL03182:Plch1 APN 3 63,610,015 (GRCm39) nonsense probably null
IGL03197:Plch1 APN 3 63,660,591 (GRCm39) missense probably damaging 1.00
IGL03251:Plch1 APN 3 63,691,423 (GRCm39) missense possibly damaging 0.93
BB009:Plch1 UTSW 3 63,609,402 (GRCm39) missense probably benign 0.05
BB019:Plch1 UTSW 3 63,609,402 (GRCm39) missense probably benign 0.05
R0335:Plch1 UTSW 3 63,618,399 (GRCm39) missense probably damaging 1.00
R0347:Plch1 UTSW 3 63,660,737 (GRCm39) missense probably damaging 1.00
R0631:Plch1 UTSW 3 63,606,640 (GRCm39) missense probably benign 0.23
R0687:Plch1 UTSW 3 63,623,450 (GRCm39) missense probably damaging 1.00
R0738:Plch1 UTSW 3 63,609,974 (GRCm39) intron probably benign
R0883:Plch1 UTSW 3 63,660,677 (GRCm39) missense probably damaging 1.00
R1437:Plch1 UTSW 3 63,604,954 (GRCm39) missense probably benign 0.37
R1678:Plch1 UTSW 3 63,648,115 (GRCm39) missense probably damaging 1.00
R1738:Plch1 UTSW 3 63,626,659 (GRCm39) missense probably benign 0.12
R1929:Plch1 UTSW 3 63,651,956 (GRCm39) missense probably damaging 1.00
R1955:Plch1 UTSW 3 63,662,688 (GRCm39) missense probably damaging 0.98
R2112:Plch1 UTSW 3 63,630,227 (GRCm39) missense probably damaging 1.00
R2158:Plch1 UTSW 3 63,628,655 (GRCm39) missense probably benign 0.00
R2165:Plch1 UTSW 3 63,605,903 (GRCm39) missense probably benign 0.01
R2259:Plch1 UTSW 3 63,605,398 (GRCm39) missense possibly damaging 0.94
R2271:Plch1 UTSW 3 63,651,956 (GRCm39) missense probably damaging 1.00
R3110:Plch1 UTSW 3 63,616,952 (GRCm39) missense probably damaging 1.00
R3112:Plch1 UTSW 3 63,616,952 (GRCm39) missense probably damaging 1.00
R3407:Plch1 UTSW 3 63,606,768 (GRCm39) unclassified probably benign
R3408:Plch1 UTSW 3 63,606,768 (GRCm39) unclassified probably benign
R3791:Plch1 UTSW 3 63,606,944 (GRCm39) missense probably benign
R3793:Plch1 UTSW 3 63,605,252 (GRCm39) missense probably damaging 0.96
R3928:Plch1 UTSW 3 63,675,044 (GRCm39) missense probably damaging 1.00
R4211:Plch1 UTSW 3 63,618,640 (GRCm39) missense probably damaging 1.00
R4212:Plch1 UTSW 3 63,778,180 (GRCm39) start gained probably benign
R4223:Plch1 UTSW 3 63,609,321 (GRCm39) missense probably damaging 1.00
R4491:Plch1 UTSW 3 63,648,160 (GRCm39) missense probably damaging 1.00
R4589:Plch1 UTSW 3 63,688,928 (GRCm39) missense probably damaging 1.00
R4656:Plch1 UTSW 3 63,611,598 (GRCm39) missense probably damaging 1.00
R4701:Plch1 UTSW 3 63,606,917 (GRCm39) splice site probably null
R4716:Plch1 UTSW 3 63,688,967 (GRCm39) missense probably damaging 1.00
R4772:Plch1 UTSW 3 63,660,746 (GRCm39) missense probably damaging 1.00
R4902:Plch1 UTSW 3 63,648,264 (GRCm39) intron probably benign
R5058:Plch1 UTSW 3 63,630,202 (GRCm39) missense probably damaging 1.00
R5092:Plch1 UTSW 3 63,606,131 (GRCm39) missense probably benign 0.02
R5093:Plch1 UTSW 3 63,681,136 (GRCm39) missense probably damaging 0.99
R5210:Plch1 UTSW 3 63,607,199 (GRCm39) critical splice donor site probably null
R5368:Plch1 UTSW 3 63,609,394 (GRCm39) missense possibly damaging 0.82
R5373:Plch1 UTSW 3 63,605,499 (GRCm39) missense probably benign 0.01
R5374:Plch1 UTSW 3 63,605,499 (GRCm39) missense probably benign 0.01
R5501:Plch1 UTSW 3 63,615,162 (GRCm39) missense probably damaging 1.00
R5606:Plch1 UTSW 3 63,648,108 (GRCm39) missense probably benign 0.35
R5738:Plch1 UTSW 3 63,681,076 (GRCm39) missense probably damaging 1.00
R5835:Plch1 UTSW 3 63,604,943 (GRCm39) missense probably benign
R6106:Plch1 UTSW 3 63,609,444 (GRCm39) missense probably damaging 1.00
R6107:Plch1 UTSW 3 63,609,444 (GRCm39) missense probably damaging 1.00
R6108:Plch1 UTSW 3 63,609,444 (GRCm39) missense probably damaging 1.00
R6110:Plch1 UTSW 3 63,606,279 (GRCm39) missense possibly damaging 0.62
R6116:Plch1 UTSW 3 63,609,444 (GRCm39) missense probably damaging 1.00
R6147:Plch1 UTSW 3 63,630,302 (GRCm39) missense probably damaging 1.00
R6195:Plch1 UTSW 3 63,648,210 (GRCm39) missense probably damaging 1.00
R6315:Plch1 UTSW 3 63,688,811 (GRCm39) nonsense probably null
R6316:Plch1 UTSW 3 63,688,811 (GRCm39) nonsense probably null
R6317:Plch1 UTSW 3 63,688,811 (GRCm39) nonsense probably null
R6318:Plch1 UTSW 3 63,688,811 (GRCm39) nonsense probably null
R6324:Plch1 UTSW 3 63,688,811 (GRCm39) nonsense probably null
R6325:Plch1 UTSW 3 63,688,811 (GRCm39) nonsense probably null
R6326:Plch1 UTSW 3 63,688,811 (GRCm39) nonsense probably null
R6479:Plch1 UTSW 3 63,651,931 (GRCm39) missense probably benign 0.06
R6544:Plch1 UTSW 3 63,758,399 (GRCm39) missense probably damaging 1.00
R6767:Plch1 UTSW 3 63,662,765 (GRCm39) missense probably damaging 1.00
R6829:Plch1 UTSW 3 63,604,939 (GRCm39) missense probably damaging 0.99
R6891:Plch1 UTSW 3 63,605,504 (GRCm39) missense probably benign
R6893:Plch1 UTSW 3 63,660,562 (GRCm39) nonsense probably null
R6921:Plch1 UTSW 3 63,615,155 (GRCm39) missense possibly damaging 0.90
R7298:Plch1 UTSW 3 63,623,458 (GRCm39) nonsense probably null
R7396:Plch1 UTSW 3 63,606,375 (GRCm39) missense probably benign 0.00
R7420:Plch1 UTSW 3 63,630,278 (GRCm39) missense probably damaging 1.00
R7566:Plch1 UTSW 3 63,688,663 (GRCm39) splice site probably null
R7572:Plch1 UTSW 3 63,648,105 (GRCm39) missense possibly damaging 0.89
R7649:Plch1 UTSW 3 63,605,590 (GRCm39) nonsense probably null
R7696:Plch1 UTSW 3 63,662,726 (GRCm39) missense probably benign
R7851:Plch1 UTSW 3 63,605,855 (GRCm39) missense probably damaging 0.99
R7853:Plch1 UTSW 3 63,681,068 (GRCm39) missense probably benign 0.44
R7932:Plch1 UTSW 3 63,609,402 (GRCm39) missense probably benign 0.05
R7983:Plch1 UTSW 3 63,615,164 (GRCm39) missense probably damaging 1.00
R8057:Plch1 UTSW 3 63,605,557 (GRCm39) missense probably benign
R8066:Plch1 UTSW 3 63,618,478 (GRCm39) nonsense probably null
R8206:Plch1 UTSW 3 63,610,047 (GRCm39) splice site probably null
R8678:Plch1 UTSW 3 63,623,468 (GRCm39) nonsense probably null
R8731:Plch1 UTSW 3 63,605,059 (GRCm39) missense probably benign 0.37
R8739:Plch1 UTSW 3 63,778,106 (GRCm39) missense possibly damaging 0.66
R8853:Plch1 UTSW 3 63,688,967 (GRCm39) missense probably damaging 1.00
R8875:Plch1 UTSW 3 63,618,391 (GRCm39) missense probably damaging 1.00
R8945:Plch1 UTSW 3 63,639,039 (GRCm39) missense probably benign 0.02
R8947:Plch1 UTSW 3 63,691,547 (GRCm39) missense probably damaging 0.99
R8953:Plch1 UTSW 3 63,639,126 (GRCm39) missense possibly damaging 0.94
R9065:Plch1 UTSW 3 63,674,924 (GRCm39) missense probably damaging 1.00
R9068:Plch1 UTSW 3 63,612,036 (GRCm39) missense probably damaging 1.00
R9188:Plch1 UTSW 3 63,639,075 (GRCm39) missense probably null 1.00
R9238:Plch1 UTSW 3 63,606,412 (GRCm39) missense possibly damaging 0.53
R9478:Plch1 UTSW 3 63,606,825 (GRCm39) missense probably benign 0.01
R9526:Plch1 UTSW 3 63,758,549 (GRCm39) intron probably benign
R9539:Plch1 UTSW 3 63,691,427 (GRCm39) missense probably null 0.01
R9634:Plch1 UTSW 3 63,605,152 (GRCm39) missense probably damaging 1.00
R9643:Plch1 UTSW 3 63,660,747 (GRCm39) missense
R9659:Plch1 UTSW 3 63,681,136 (GRCm39) missense probably benign 0.17
R9711:Plch1 UTSW 3 63,615,176 (GRCm39) missense probably damaging 1.00
R9788:Plch1 UTSW 3 63,681,136 (GRCm39) missense probably benign 0.17
R9799:Plch1 UTSW 3 63,605,591 (GRCm39) missense possibly damaging 0.89
RF018:Plch1 UTSW 3 63,628,636 (GRCm39) missense probably damaging 1.00
X0028:Plch1 UTSW 3 63,651,930 (GRCm39) missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- GGGACCAAACTGCAGCTTAG -3'
(R):5'- TGTCCTCAGAACAGACAGCTCC -3'

Sequencing Primer
(F):5'- CAAACTGCAGCTTAGAGAATCTG -3'
(R):5'- GACAGCTCCAAGGCCTGAAG -3'
Posted On 2014-09-17