Incidental Mutation 'R5071:Fryl'
ID 388758
Institutional Source Beutler Lab
Gene Symbol Fryl
Ensembl Gene ENSMUSG00000070733
Gene Name FRY like transcription coactivator
Synonyms 9030227G01Rik, 2310004H21Rik, 2510002A14Rik
MMRRC Submission 042661-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.740) question?
Stock # R5071 (G1)
Quality Score 225
Status Not validated
Chromosome 5
Chromosomal Location 73177534-73414042 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 73232110 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Leucine at position 1550 (P1550L)
Ref Sequence ENSEMBL: ENSMUSP00000098687 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094700] [ENSMUST00000101127]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000094700
AA Change: P1550L

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000092289
Gene: ENSMUSG00000070733
AA Change: P1550L

DomainStartEndE-ValueType
Pfam:MOR2-PAG1_N 117 649 5.7e-176 PFAM
low complexity region 873 884 N/A INTRINSIC
Pfam:MOR2-PAG1_mid 896 1141 1.3e-5 PFAM
Pfam:MOR2-PAG1_mid 1145 1331 2e-19 PFAM
Pfam:MOR2-PAG1_mid 1351 1450 1.2e-5 PFAM
low complexity region 1476 1487 N/A INTRINSIC
low complexity region 1530 1548 N/A INTRINSIC
Pfam:MOR2-PAG1_mid 1590 1660 1.1e-5 PFAM
Pfam:MOR2-PAG1_mid 1725 1866 3.2e-15 PFAM
low complexity region 1973 1984 N/A INTRINSIC
Pfam:MOR2-PAG1_C 2002 2255 9.9e-78 PFAM
low complexity region 2329 2341 N/A INTRINSIC
low complexity region 2473 2482 N/A INTRINSIC
low complexity region 2485 2500 N/A INTRINSIC
low complexity region 2523 2534 N/A INTRINSIC
coiled coil region 2625 2649 N/A INTRINSIC
low complexity region 2827 2841 N/A INTRINSIC
coiled coil region 2854 2893 N/A INTRINSIC
coiled coil region 2963 2989 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000101127
AA Change: P1550L

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000098687
Gene: ENSMUSG00000070733
AA Change: P1550L

DomainStartEndE-ValueType
Pfam:MOR2-PAG1_N 116 649 3e-172 PFAM
low complexity region 873 884 N/A INTRINSIC
Pfam:MOR2-PAG1_mid 898 1115 7.8e-6 PFAM
Pfam:MOR2-PAG1_mid 1147 1331 9.5e-19 PFAM
Pfam:MOR2-PAG1_mid 1351 1503 1.1e-5 PFAM
low complexity region 1530 1548 N/A INTRINSIC
Pfam:MOR2-PAG1_mid 1589 1664 6e-6 PFAM
Pfam:MOR2-PAG1_mid 1725 1866 1.6e-14 PFAM
low complexity region 1973 1984 N/A INTRINSIC
Pfam:MOR2-PAG1_C 1998 2260 4.4e-76 PFAM
low complexity region 2329 2341 N/A INTRINSIC
low complexity region 2473 2482 N/A INTRINSIC
low complexity region 2485 2500 N/A INTRINSIC
low complexity region 2523 2534 N/A INTRINSIC
coiled coil region 2625 2649 N/A INTRINSIC
low complexity region 2827 2841 N/A INTRINSIC
coiled coil region 2854 2893 N/A INTRINSIC
coiled coil region 2963 2989 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000156661
Predicted Effect noncoding transcript
Transcript: ENSMUST00000175890
Predicted Effect probably benign
Transcript: ENSMUST00000201277
Predicted Effect unknown
Transcript: ENSMUST00000202381
AA Change: P419L
Predicted Effect noncoding transcript
Transcript: ENSMUST00000202413
Predicted Effect probably benign
Transcript: ENSMUST00000202697
Meta Mutation Damage Score 0.1496 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.0%
  • 20x: 94.3%
Validation Efficiency
MGI Phenotype PHENOTYPE: Most mice homozygous for a knock-out allele exhibit postnatal lethality and defects in kidney development; rare survivors display growth retardation, decreased body weight, and premature death associated with chronic hydronephrosis. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 95 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy8 A T 15: 64,659,207 (GRCm39) W528R probably damaging Het
Agbl1 A G 7: 76,071,665 (GRCm39) E329G probably damaging Het
Agbl5 G A 5: 31,060,403 (GRCm39) R141Q probably damaging Het
AI182371 A T 2: 34,975,227 (GRCm39) I334N probably benign Het
Aldh1b1 A G 4: 45,803,383 (GRCm39) probably null Het
Armc9 G A 1: 86,113,838 (GRCm39) M298I probably benign Het
Atp8a1 T A 5: 67,973,066 (GRCm39) K27N probably benign Het
BC004004 G A 17: 29,513,389 (GRCm39) probably null Het
Ccdc83 A T 7: 89,899,737 (GRCm39) F45Y probably damaging Het
Cct8l1 G A 5: 25,721,881 (GRCm39) V199I probably benign Het
Cdc23 C A 18: 34,784,742 (GRCm39) V7L unknown Het
Cdh17 G T 4: 11,810,325 (GRCm39) G672V probably damaging Het
Cdh5 C A 8: 104,867,334 (GRCm39) T537K probably damaging Het
Chd1 T A 17: 15,982,667 (GRCm39) S1377R probably benign Het
Chd2 T C 7: 73,079,437 (GRCm39) N1821S probably benign Het
Cnot3 A G 7: 3,653,860 (GRCm39) K4R probably damaging Het
Colq T A 14: 31,250,789 (GRCm39) I339F possibly damaging Het
Coq2 A T 5: 100,815,816 (GRCm39) L121Q probably damaging Het
Csnk1e G A 15: 79,305,072 (GRCm39) R342* probably null Het
Cstl1 A T 2: 148,592,847 (GRCm39) M1L probably benign Het
Cwh43 A G 5: 73,581,256 (GRCm39) probably null Het
Cyp2a22 A T 7: 26,631,906 (GRCm39) F450Y probably benign Het
Cyp2d10 C T 15: 82,287,954 (GRCm39) R383H probably benign Het
Cyp4a29 A G 4: 115,104,860 (GRCm39) T123A probably benign Het
Dgkh T C 14: 78,841,972 (GRCm39) K417E probably damaging Het
Dnah11 A T 12: 118,046,188 (GRCm39) L1750* probably null Het
Edn1 A G 13: 42,457,153 (GRCm39) E62G probably damaging Het
Eef1akmt1 A G 14: 57,803,464 (GRCm39) L30P probably damaging Het
Fbxo42 T C 4: 140,926,256 (GRCm39) W313R probably damaging Het
Fign A T 2: 63,810,037 (GRCm39) L411* probably null Het
Fitm1 T A 14: 55,813,230 (GRCm39) V31E possibly damaging Het
Gabrd A C 4: 155,471,619 (GRCm39) F228C probably damaging Het
Gm5916 A C 9: 36,039,964 (GRCm39) L8R probably benign Het
Gpr108 A G 17: 57,542,335 (GRCm39) S557P probably damaging Het
Gpr75 C A 11: 30,842,380 (GRCm39) N428K probably damaging Het
H2-M5 T G 17: 37,298,076 (GRCm39) probably null Het
Hdac6 A G X: 7,811,036 (GRCm39) F104L probably damaging Homo
Homer3 T C 8: 70,744,005 (GRCm39) V243A probably benign Het
Hspg2 T C 4: 137,267,541 (GRCm39) S2050P probably damaging Het
Hydin A G 8: 111,265,105 (GRCm39) N2763D probably benign Het
Ifi203 T C 1: 173,762,676 (GRCm39) Q152R possibly damaging Het
Ifi44 T C 3: 151,455,269 (GRCm39) probably benign Het
Ifi47 A G 11: 48,986,361 (GRCm39) T43A probably benign Het
Ighv1-24 A G 12: 114,736,748 (GRCm39) Y51H probably benign Het
Inf2 A T 12: 112,578,473 (GRCm39) probably null Het
Insl6 T C 19: 29,302,655 (GRCm39) R21G probably benign Het
Kif19a G A 11: 114,658,053 (GRCm39) M37I probably benign Het
Ltbp3 T C 19: 5,806,851 (GRCm39) C1043R probably damaging Het
Mpeg1 T A 19: 12,438,545 (GRCm39) M1K probably null Het
Mrtfa A G 15: 80,906,627 (GRCm39) V91A probably damaging Het
Muc21 G A 17: 35,931,444 (GRCm39) probably benign Het
Ncald A T 15: 37,397,478 (GRCm39) H67Q probably damaging Het
Nek9 C A 12: 85,374,233 (GRCm39) R268L possibly damaging Het
Nudt5 T A 2: 5,869,198 (GRCm39) H141Q probably benign Het
Numbl G A 7: 26,980,415 (GRCm39) D466N probably damaging Het
Or14c46 A G 7: 85,918,799 (GRCm39) I66T probably damaging Het
Or2l5 A G 16: 19,333,777 (GRCm39) I203T probably benign Het
Or4c100 T C 2: 88,356,385 (GRCm39) S153P probably damaging Het
Or51l14 A T 7: 103,100,617 (GRCm39) E24D probably benign Het
Or52n2c A C 7: 104,574,700 (GRCm39) N90K probably benign Het
Or6x1 T C 9: 40,098,960 (GRCm39) L183S probably damaging Het
Or8h10 A T 2: 86,808,666 (GRCm39) V158D possibly damaging Het
Pik3c2g T A 6: 139,665,873 (GRCm39) C65S probably null Het
Plagl1 A G 10: 13,003,005 (GRCm39) Y91C probably damaging Het
Polr1a A G 6: 71,908,693 (GRCm39) N506S possibly damaging Het
Pomt2 A C 12: 87,180,234 (GRCm39) C256G probably damaging Het
Psg29 T A 7: 16,945,763 (GRCm39) D444E probably damaging Het
Ptgs1 A T 2: 36,141,272 (GRCm39) N573I probably damaging Het
Ptprf C A 4: 118,069,196 (GRCm39) G1624W probably damaging Het
Rbm38 C T 2: 172,863,875 (GRCm39) P15S probably benign Het
Rc3h1 A G 1: 160,787,047 (GRCm39) D814G possibly damaging Het
Rnf40 T C 7: 127,196,458 (GRCm39) L802P probably damaging Het
Rusc2 A G 4: 43,415,240 (GRCm39) D182G probably benign Het
Setd1b A G 5: 123,298,977 (GRCm39) probably benign Het
Slc4a2 G A 5: 24,643,760 (GRCm39) S855N probably benign Het
Slc8a2 T C 7: 15,884,508 (GRCm39) L626P possibly damaging Het
Slirp A G 12: 87,490,784 (GRCm39) T29A probably damaging Het
Smarcc2 A G 10: 128,299,809 (GRCm39) D158G probably damaging Het
Sptbn1 A G 11: 30,063,854 (GRCm39) probably null Het
St3gal5 T C 6: 72,109,037 (GRCm39) C42R probably damaging Het
Syt7 T C 19: 10,420,792 (GRCm39) S397P possibly damaging Het
Tenm2 T A 11: 35,959,208 (GRCm39) T1114S probably damaging Het
Thada T A 17: 84,693,960 (GRCm39) D1263V probably damaging Het
Tmco3 G T 8: 13,342,860 (GRCm39) E199* probably null Het
Tpcn1 A T 5: 120,686,334 (GRCm39) probably null Het
Tppp2 G A 14: 52,157,912 (GRCm39) R119Q probably benign Het
Trim30d A C 7: 104,137,165 (GRCm39) V13G probably damaging Het
Ubxn2b A T 4: 6,214,746 (GRCm39) Q260L probably damaging Het
Ufl1 A G 4: 25,254,780 (GRCm39) Y559H probably benign Het
Usp5 A G 6: 124,803,342 (GRCm39) F7L probably benign Het
Utrn A T 10: 12,259,948 (GRCm39) probably null Het
Vmn1r28 A T 6: 58,242,894 (GRCm39) I246F probably benign Het
Vmn2r2 C A 3: 64,024,321 (GRCm39) M753I probably benign Het
Zbtb26 T C 2: 37,325,941 (GRCm39) H365R probably benign Het
Zfp976 A T 7: 42,262,354 (GRCm39) Y494* probably null Het
Other mutations in Fryl
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00819:Fryl APN 5 73,305,451 (GRCm39) missense possibly damaging 0.92
IGL01518:Fryl APN 5 73,244,305 (GRCm39) missense possibly damaging 0.76
IGL01545:Fryl APN 5 73,211,940 (GRCm39) missense probably damaging 1.00
IGL01646:Fryl APN 5 73,179,844 (GRCm39) critical splice donor site probably null
IGL01938:Fryl APN 5 73,279,707 (GRCm39) missense probably damaging 0.98
IGL01962:Fryl APN 5 73,190,134 (GRCm39) missense possibly damaging 0.62
IGL02064:Fryl APN 5 73,282,112 (GRCm39) unclassified probably benign
IGL02148:Fryl APN 5 73,233,302 (GRCm39) missense probably benign 0.35
IGL02418:Fryl APN 5 73,267,519 (GRCm39) splice site probably benign
IGL02431:Fryl APN 5 73,255,651 (GRCm39) missense probably benign 0.02
IGL02513:Fryl APN 5 73,222,636 (GRCm39) missense probably damaging 1.00
IGL02557:Fryl APN 5 73,255,736 (GRCm39) missense probably damaging 1.00
IGL02625:Fryl APN 5 73,227,220 (GRCm39) intron probably benign
IGL02642:Fryl APN 5 73,252,809 (GRCm39) missense probably benign
IGL02657:Fryl APN 5 73,212,203 (GRCm39) missense probably benign 0.01
IGL02706:Fryl APN 5 73,250,506 (GRCm39) missense probably benign 0.45
IGL03022:Fryl APN 5 73,216,726 (GRCm39) missense possibly damaging 0.82
IGL03144:Fryl APN 5 73,258,798 (GRCm39) missense probably null 0.22
IGL03155:Fryl APN 5 73,234,038 (GRCm39) missense probably benign
IGL03183:Fryl APN 5 73,234,038 (GRCm39) missense probably benign
IGL03275:Fryl APN 5 73,305,376 (GRCm39) missense possibly damaging 0.47
IGL03310:Fryl APN 5 73,293,659 (GRCm39) splice site probably benign
IGL03341:Fryl APN 5 73,234,038 (GRCm39) missense probably benign
IGL03343:Fryl APN 5 73,234,038 (GRCm39) missense probably benign
IGL03350:Fryl APN 5 73,290,649 (GRCm39) missense probably damaging 0.99
IGL03357:Fryl APN 5 73,211,402 (GRCm39) missense probably damaging 1.00
IGL03374:Fryl APN 5 73,267,624 (GRCm39) splice site probably benign
IGL03375:Fryl APN 5 73,245,792 (GRCm39) missense possibly damaging 0.91
bedeviled UTSW 5 73,216,843 (GRCm39) missense probably damaging 1.00
Besotted UTSW 5 73,230,255 (GRCm39) missense probably damaging 1.00
R0062:Fryl UTSW 5 73,179,621 (GRCm39) missense probably benign 0.02
R0062:Fryl UTSW 5 73,179,621 (GRCm39) missense probably benign 0.02
R0308:Fryl UTSW 5 73,198,947 (GRCm39) splice site probably benign
R0312:Fryl UTSW 5 73,230,231 (GRCm39) missense probably damaging 1.00
R0415:Fryl UTSW 5 73,255,757 (GRCm39) missense probably damaging 0.99
R0440:Fryl UTSW 5 73,244,315 (GRCm39) missense possibly damaging 0.91
R0446:Fryl UTSW 5 73,254,760 (GRCm39) missense possibly damaging 0.91
R0566:Fryl UTSW 5 73,221,840 (GRCm39) splice site probably benign
R0567:Fryl UTSW 5 73,222,734 (GRCm39) missense possibly damaging 0.50
R0606:Fryl UTSW 5 73,282,077 (GRCm39) missense probably benign 0.15
R0619:Fryl UTSW 5 73,226,074 (GRCm39) missense probably benign 0.22
R0654:Fryl UTSW 5 73,240,715 (GRCm39) missense probably benign 0.17
R0658:Fryl UTSW 5 73,222,702 (GRCm39) missense probably damaging 1.00
R0707:Fryl UTSW 5 73,240,715 (GRCm39) missense probably benign 0.17
R0744:Fryl UTSW 5 73,246,424 (GRCm39) unclassified probably benign
R0745:Fryl UTSW 5 73,228,469 (GRCm39) missense probably damaging 0.96
R0833:Fryl UTSW 5 73,246,424 (GRCm39) unclassified probably benign
R0885:Fryl UTSW 5 73,246,539 (GRCm39) missense probably damaging 0.97
R0894:Fryl UTSW 5 73,198,675 (GRCm39) splice site probably benign
R1076:Fryl UTSW 5 73,282,016 (GRCm39) unclassified probably benign
R1241:Fryl UTSW 5 73,267,614 (GRCm39) missense probably damaging 1.00
R1241:Fryl UTSW 5 73,222,268 (GRCm39) splice site probably benign
R1394:Fryl UTSW 5 73,230,255 (GRCm39) missense probably damaging 1.00
R1395:Fryl UTSW 5 73,230,255 (GRCm39) missense probably damaging 1.00
R1608:Fryl UTSW 5 73,232,094 (GRCm39) nonsense probably null
R1664:Fryl UTSW 5 73,216,778 (GRCm39) missense probably damaging 1.00
R1745:Fryl UTSW 5 73,190,204 (GRCm39) splice site probably benign
R1937:Fryl UTSW 5 73,290,710 (GRCm39) missense probably damaging 1.00
R1969:Fryl UTSW 5 73,255,609 (GRCm39) missense probably benign 0.18
R1993:Fryl UTSW 5 73,265,836 (GRCm39) missense probably damaging 1.00
R1994:Fryl UTSW 5 73,265,836 (GRCm39) missense probably damaging 1.00
R2029:Fryl UTSW 5 73,179,465 (GRCm39) nonsense probably null
R2036:Fryl UTSW 5 73,265,305 (GRCm39) critical splice donor site probably null
R2036:Fryl UTSW 5 73,179,887 (GRCm39) missense probably benign
R2088:Fryl UTSW 5 73,222,804 (GRCm39) missense probably benign 0.02
R2105:Fryl UTSW 5 73,279,642 (GRCm39) missense probably benign
R2106:Fryl UTSW 5 73,255,674 (GRCm39) missense probably damaging 1.00
R2186:Fryl UTSW 5 73,222,318 (GRCm39) missense probably damaging 1.00
R2239:Fryl UTSW 5 73,265,890 (GRCm39) missense probably damaging 0.99
R2256:Fryl UTSW 5 73,230,187 (GRCm39) missense possibly damaging 0.47
R2257:Fryl UTSW 5 73,230,187 (GRCm39) missense possibly damaging 0.47
R2280:Fryl UTSW 5 73,198,707 (GRCm39) missense possibly damaging 0.47
R2281:Fryl UTSW 5 73,198,707 (GRCm39) missense possibly damaging 0.47
R2911:Fryl UTSW 5 73,207,799 (GRCm39) missense probably damaging 0.99
R3019:Fryl UTSW 5 73,240,193 (GRCm39) missense probably benign 0.01
R3416:Fryl UTSW 5 73,265,417 (GRCm39) missense possibly damaging 0.84
R3783:Fryl UTSW 5 73,258,819 (GRCm39) missense probably benign
R3787:Fryl UTSW 5 73,258,819 (GRCm39) missense probably benign
R3837:Fryl UTSW 5 73,228,608 (GRCm39) missense probably benign 0.03
R3969:Fryl UTSW 5 73,269,766 (GRCm39) missense probably damaging 0.97
R4387:Fryl UTSW 5 73,243,903 (GRCm39) missense possibly damaging 0.91
R4502:Fryl UTSW 5 73,245,740 (GRCm39) missense probably damaging 1.00
R4658:Fryl UTSW 5 73,238,396 (GRCm39) missense probably damaging 1.00
R4664:Fryl UTSW 5 73,248,022 (GRCm39) missense possibly damaging 0.80
R4690:Fryl UTSW 5 73,257,636 (GRCm39) missense probably benign
R4700:Fryl UTSW 5 73,222,881 (GRCm39) missense possibly damaging 0.88
R4709:Fryl UTSW 5 73,238,315 (GRCm39) missense probably benign 0.03
R4807:Fryl UTSW 5 73,198,705 (GRCm39) missense probably benign 0.00
R4912:Fryl UTSW 5 73,226,125 (GRCm39) frame shift probably null
R4948:Fryl UTSW 5 73,246,473 (GRCm39) missense probably benign 0.08
R4959:Fryl UTSW 5 73,192,401 (GRCm39) missense probably benign 0.00
R5062:Fryl UTSW 5 73,233,236 (GRCm39) missense possibly damaging 0.89
R5067:Fryl UTSW 5 73,215,098 (GRCm39) missense probably benign 0.13
R5072:Fryl UTSW 5 73,232,110 (GRCm39) missense probably damaging 0.99
R5073:Fryl UTSW 5 73,232,110 (GRCm39) missense probably damaging 0.99
R5074:Fryl UTSW 5 73,232,110 (GRCm39) missense probably damaging 0.99
R5139:Fryl UTSW 5 73,248,061 (GRCm39) missense probably damaging 1.00
R5172:Fryl UTSW 5 73,259,016 (GRCm39) missense possibly damaging 0.95
R5187:Fryl UTSW 5 73,243,943 (GRCm39) missense possibly damaging 0.95
R5272:Fryl UTSW 5 73,222,479 (GRCm39) nonsense probably null
R5275:Fryl UTSW 5 73,270,134 (GRCm39) missense probably damaging 1.00
R5295:Fryl UTSW 5 73,270,134 (GRCm39) missense probably damaging 1.00
R5344:Fryl UTSW 5 73,262,117 (GRCm39) missense probably damaging 1.00
R5355:Fryl UTSW 5 73,231,247 (GRCm39) missense probably damaging 1.00
R5716:Fryl UTSW 5 73,257,808 (GRCm39) missense probably benign
R5778:Fryl UTSW 5 73,230,121 (GRCm39) missense probably damaging 1.00
R5810:Fryl UTSW 5 73,248,098 (GRCm39) missense probably benign 0.06
R5934:Fryl UTSW 5 73,248,060 (GRCm39) missense probably damaging 1.00
R5948:Fryl UTSW 5 73,254,715 (GRCm39) critical splice donor site probably null
R6005:Fryl UTSW 5 73,240,638 (GRCm39) missense probably damaging 1.00
R6026:Fryl UTSW 5 73,257,340 (GRCm39) missense probably benign 0.04
R6045:Fryl UTSW 5 73,275,894 (GRCm39) missense probably damaging 0.99
R6185:Fryl UTSW 5 73,270,131 (GRCm39) missense probably benign 0.43
R6247:Fryl UTSW 5 73,222,824 (GRCm39) missense probably damaging 0.98
R6294:Fryl UTSW 5 73,349,102 (GRCm39) intron probably benign
R6310:Fryl UTSW 5 73,349,104 (GRCm39) intron probably benign
R6429:Fryl UTSW 5 73,248,094 (GRCm39) missense possibly damaging 0.84
R6568:Fryl UTSW 5 73,216,859 (GRCm39) missense probably damaging 1.00
R6636:Fryl UTSW 5 73,290,655 (GRCm39) missense probably benign 0.01
R6664:Fryl UTSW 5 73,289,824 (GRCm39) missense probably damaging 1.00
R6732:Fryl UTSW 5 73,212,124 (GRCm39) missense probably damaging 1.00
R6750:Fryl UTSW 5 73,179,575 (GRCm39) missense probably damaging 1.00
R6805:Fryl UTSW 5 73,222,437 (GRCm39) missense probably benign 0.03
R6823:Fryl UTSW 5 73,222,560 (GRCm39) missense probably damaging 0.99
R6855:Fryl UTSW 5 73,216,843 (GRCm39) missense probably damaging 1.00
R6858:Fryl UTSW 5 73,222,375 (GRCm39) missense probably damaging 1.00
R6868:Fryl UTSW 5 73,226,146 (GRCm39) missense probably damaging 1.00
R6898:Fryl UTSW 5 73,179,485 (GRCm39) missense probably damaging 0.96
R6908:Fryl UTSW 5 73,179,554 (GRCm39) missense probably damaging 1.00
R6958:Fryl UTSW 5 73,231,272 (GRCm39) missense possibly damaging 0.89
R6980:Fryl UTSW 5 73,207,773 (GRCm39) missense probably benign 0.06
R7036:Fryl UTSW 5 73,212,951 (GRCm39) missense probably benign 0.03
R7065:Fryl UTSW 5 73,248,099 (GRCm39) missense probably damaging 0.96
R7097:Fryl UTSW 5 73,231,251 (GRCm39) missense probably benign 0.31
R7171:Fryl UTSW 5 73,279,653 (GRCm39) missense probably damaging 0.97
R7191:Fryl UTSW 5 73,230,255 (GRCm39) missense probably damaging 1.00
R7207:Fryl UTSW 5 73,222,438 (GRCm39) missense probably benign
R7236:Fryl UTSW 5 73,265,821 (GRCm39) missense possibly damaging 0.66
R7334:Fryl UTSW 5 73,204,839 (GRCm39) splice site probably null
R7425:Fryl UTSW 5 73,262,091 (GRCm39) missense probably damaging 1.00
R7452:Fryl UTSW 5 73,181,331 (GRCm39) missense probably damaging 1.00
R7479:Fryl UTSW 5 73,254,904 (GRCm39) missense possibly damaging 0.71
R7535:Fryl UTSW 5 73,255,539 (GRCm39) missense probably benign 0.15
R7538:Fryl UTSW 5 73,180,019 (GRCm39) missense probably benign 0.09
R7544:Fryl UTSW 5 73,238,382 (GRCm39) missense probably benign
R7548:Fryl UTSW 5 73,349,105 (GRCm39) missense unknown
R7565:Fryl UTSW 5 73,191,063 (GRCm39) missense probably benign 0.18
R7572:Fryl UTSW 5 73,245,739 (GRCm39) missense possibly damaging 0.91
R7582:Fryl UTSW 5 73,179,843 (GRCm39) critical splice donor site probably null
R7630:Fryl UTSW 5 73,267,588 (GRCm39) missense possibly damaging 0.62
R7774:Fryl UTSW 5 73,240,727 (GRCm39) missense probably benign 0.12
R7777:Fryl UTSW 5 73,228,641 (GRCm39) missense probably damaging 0.98
R7917:Fryl UTSW 5 73,211,875 (GRCm39) missense probably damaging 1.00
R7920:Fryl UTSW 5 73,259,150 (GRCm39) splice site probably null
R8110:Fryl UTSW 5 73,290,620 (GRCm39) missense probably benign 0.10
R8120:Fryl UTSW 5 73,228,527 (GRCm39) missense probably benign 0.01
R8143:Fryl UTSW 5 73,207,682 (GRCm39) missense probably benign 0.00
R8207:Fryl UTSW 5 73,257,843 (GRCm39) splice site probably null
R8263:Fryl UTSW 5 73,238,348 (GRCm39) missense probably damaging 1.00
R8350:Fryl UTSW 5 73,226,073 (GRCm39) missense probably benign
R8359:Fryl UTSW 5 73,233,276 (GRCm39) missense probably benign 0.39
R8387:Fryl UTSW 5 73,293,663 (GRCm39) critical splice donor site probably null
R8403:Fryl UTSW 5 73,275,790 (GRCm39) makesense probably null
R8450:Fryl UTSW 5 73,226,073 (GRCm39) missense probably benign
R8514:Fryl UTSW 5 73,242,699 (GRCm39) missense probably benign
R8536:Fryl UTSW 5 73,257,696 (GRCm39) missense probably damaging 0.99
R8703:Fryl UTSW 5 73,247,997 (GRCm39) missense probably damaging 0.99
R8708:Fryl UTSW 5 73,289,905 (GRCm39) missense probably benign 0.01
R8783:Fryl UTSW 5 73,226,185 (GRCm39) missense probably benign 0.45
R9028:Fryl UTSW 5 73,255,609 (GRCm39) missense probably benign 0.18
R9045:Fryl UTSW 5 73,182,118 (GRCm39) missense
R9063:Fryl UTSW 5 73,238,346 (GRCm39) missense possibly damaging 0.70
R9096:Fryl UTSW 5 73,265,920 (GRCm39) missense probably benign 0.01
R9244:Fryl UTSW 5 73,348,862 (GRCm39) intron probably benign
R9345:Fryl UTSW 5 73,207,754 (GRCm39) missense probably benign
R9381:Fryl UTSW 5 73,240,637 (GRCm39) missense probably benign 0.24
R9386:Fryl UTSW 5 73,349,152 (GRCm39) missense unknown
R9401:Fryl UTSW 5 73,222,563 (GRCm39) nonsense probably null
R9497:Fryl UTSW 5 73,215,134 (GRCm39) missense
R9514:Fryl UTSW 5 73,262,115 (GRCm39) missense probably damaging 1.00
R9570:Fryl UTSW 5 73,179,498 (GRCm39) missense probably benign 0.02
R9654:Fryl UTSW 5 73,275,801 (GRCm39) missense probably benign
R9665:Fryl UTSW 5 73,222,299 (GRCm39) missense probably damaging 1.00
R9685:Fryl UTSW 5 73,216,879 (GRCm39) missense probably damaging 0.99
R9798:Fryl UTSW 5 73,192,402 (GRCm39) missense probably benign
Z1088:Fryl UTSW 5 73,248,081 (GRCm39) missense probably damaging 1.00
Z1088:Fryl UTSW 5 73,248,052 (GRCm39) missense probably damaging 0.99
Z1176:Fryl UTSW 5 73,230,180 (GRCm39) missense probably benign
Z1177:Fryl UTSW 5 73,198,938 (GRCm39) critical splice acceptor site probably null
Predicted Primers PCR Primer
(F):5'- TACACTGTGCGGTGTCAGAC -3'
(R):5'- GTGTTAATAACCTTTCTGCCTTGG -3'

Sequencing Primer
(F):5'- TGTCAGACAGTGTCTAGGAAGCTG -3'
(R):5'- GCCTTGGTCTCCCTAGAAAATGTG -3'
Posted On 2016-06-06