Incidental Mutation 'R7378:Fras1'
ID 572460
Institutional Source Beutler Lab
Gene Symbol Fras1
Ensembl Gene ENSMUSG00000034687
Gene Name Fraser extracellular matrix complex subunit 1
Synonyms bl, E130113P14Rik
MMRRC Submission 045460-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7378 (G1)
Quality Score 225.009
Status Validated
Chromosome 5
Chromosomal Location 96521814-96932587 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 96744644 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Arginine at position 560 (C560R)
Ref Sequence ENSEMBL: ENSMUSP00000043250 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036019]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000036019
AA Change: C560R

PolyPhen 2 Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000043250
Gene: ENSMUSG00000034687
AA Change: C560R

DomainStartEndE-ValueType
signal peptide 1 25 N/A INTRINSIC
VWC 27 86 9.23e-9 SMART
VWC 94 151 9.37e-10 SMART
VWC 158 215 8.61e-9 SMART
VWC 220 277 7.1e-10 SMART
VWC 284 341 7.8e-7 SMART
VWC 365 415 1.93e-1 SMART
FU 408 459 3.33e-1 SMART
FU 461 504 9.12e-8 SMART
EGF_like 466 495 6.67e1 SMART
FU 506 552 6.01e-8 SMART
FU 554 598 2.21e-6 SMART
FU 601 646 1.28e-11 SMART
FU 648 704 4.19e-7 SMART
FU 707 752 9.12e-8 SMART
FU 754 799 1.11e-6 SMART
EGF_like 759 790 7.23e1 SMART
FU 802 851 5.44e-6 SMART
EGF_like 807 842 4.55e1 SMART
FU 853 899 7.4e-8 SMART
FU 902 947 4.78e-2 SMART
FU 951 996 4.52e-12 SMART
EGF_like 956 987 2.75e1 SMART
FU 998 1041 1.38e-7 SMART
FU 1045 1088 9.7e-3 SMART
EGF_like 1057 1096 3.16e1 SMART
Pfam:Cadherin_3 1098 1198 5.2e-12 PFAM
Pfam:Cadherin_3 1167 1309 6.5e-27 PFAM
Pfam:Cadherin_3 1278 1442 7e-24 PFAM
Pfam:Cadherin_3 1411 1560 1.3e-23 PFAM
Pfam:Cadherin_3 1561 1693 6.4e-15 PFAM
Pfam:Cadherin_3 1695 1814 1.1e-10 PFAM
Pfam:Cadherin_3 1780 1940 1.6e-18 PFAM
Pfam:Cadherin_3 1906 2061 2.8e-22 PFAM
Pfam:Cadherin_3 2063 2181 3.3e-18 PFAM
Pfam:Cadherin_3 2172 2295 1.4e-26 PFAM
Pfam:Cadherin_3 2296 2408 2.3e-31 PFAM
Pfam:Cadherin_3 2413 2540 7.9e-23 PFAM
Calx_beta 2544 2648 1.23e-10 SMART
Calx_beta 2661 2772 3.3e-11 SMART
Calx_beta 2787 2892 1.21e-9 SMART
Calx_beta 2907 3009 4.45e-3 SMART
Calx_beta 3027 3131 1.5e-14 SMART
Blast:Calx_beta 3162 3187 1e-5 BLAST
transmembrane domain 3902 3924 N/A INTRINSIC
low complexity region 3927 3935 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 99% (138/140)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
PHENOTYPE: Mice homozygous for mutations at this locus display a significant amount of embryonic lethality due to hemorrhaging of embryonic blisters. Survival is variable on genetic backgrounds. Kidney development is severely affected and syndactyly is common. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 142 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 A C 6: 128,523,210 (GRCm39) probably null Het
Aars1 A G 8: 111,768,974 (GRCm39) Y258C probably damaging Het
Acaa2 A T 18: 74,938,943 (GRCm39) Y376F probably benign Het
Adcy1 C T 11: 7,119,543 (GRCm39) S1062F possibly damaging Het
Adgrb3 A T 1: 25,571,000 (GRCm39) C492* probably null Het
Adgrg6 A G 10: 14,411,636 (GRCm39) F22S probably benign Het
Adh1 A G 3: 137,994,648 (GRCm39) probably null Het
Afm T A 5: 90,699,259 (GRCm39) C568S probably benign Het
Ago4 C T 4: 126,405,257 (GRCm39) E439K probably benign Het
Aifm2 T G 10: 61,563,496 (GRCm39) V122G possibly damaging Het
Akap6 A G 12: 53,189,357 (GRCm39) N2257S probably benign Het
Ap3m2 A G 8: 23,294,026 (GRCm39) I8T probably benign Het
Apc2 C A 10: 80,147,228 (GRCm39) L761I probably damaging Het
Asap2 A G 12: 21,162,052 (GRCm39) D3G probably benign Het
Asxl1 T C 2: 153,243,913 (GRCm39) C1489R probably damaging Het
Atm T G 9: 53,364,737 (GRCm39) probably null Het
Bmal1 C A 7: 112,898,415 (GRCm39) T281K probably benign Het
Bpifa6 C A 2: 153,828,353 (GRCm39) A153E probably damaging Het
Cav2 A G 6: 17,282,059 (GRCm39) T106A probably benign Het
Cavin4 A G 4: 48,663,631 (GRCm39) N4D probably benign Het
Cenpc1 T C 5: 86,194,358 (GRCm39) N136S probably benign Het
Cfap45 T A 1: 172,365,910 (GRCm39) probably null Het
Col3a1 G A 1: 45,366,807 (GRCm39) probably null Het
Crocc2 C T 1: 93,121,809 (GRCm39) L653F probably damaging Het
Cry2 A G 2: 92,244,009 (GRCm39) L388P probably damaging Het
Cstb T C 10: 78,262,822 (GRCm39) F43S probably damaging Het
Ctcfl A G 2: 172,954,051 (GRCm39) Y349H probably damaging Het
Ctu2 T A 8: 123,208,238 (GRCm39) V485D probably damaging Het
Cwc25 A C 11: 97,638,823 (GRCm39) L367R possibly damaging Het
Dock4 T A 12: 40,838,243 (GRCm39) H1061Q possibly damaging Het
Dpy19l3 C A 7: 35,452,067 (GRCm39) V26L probably benign Het
Efcab3 T C 11: 104,605,528 (GRCm39) I298T probably benign Het
Elmo1 A T 13: 20,465,105 (GRCm39) I225F probably benign Het
Ep300 T C 15: 81,534,746 (GRCm39) S2268P probably damaging Het
F2r C T 13: 95,754,836 (GRCm39) C16Y probably damaging Het
Fbxo33 C A 12: 59,251,157 (GRCm39) E453* probably null Het
Flot1 A T 17: 36,136,405 (GRCm39) D186V probably damaging Het
Fmn2 CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC 1: 174,436,769 (GRCm39) probably benign Het
Get3 A T 8: 85,746,492 (GRCm39) F119I probably benign Het
Gfi1 A T 5: 107,871,095 (GRCm39) S165T possibly damaging Het
Gli2 T C 1: 118,776,222 (GRCm39) D400G probably damaging Het
Gm37240 T A 3: 84,879,944 (GRCm39) probably null Het
Gml C T 15: 74,688,970 (GRCm39) V27I possibly damaging Het
Htt A T 5: 34,961,143 (GRCm39) I257F probably benign Het
Hycc2 T C 1: 58,569,193 (GRCm39) K462R probably benign Het
Ier5 C T 1: 154,974,438 (GRCm39) V247M probably damaging Het
Ift46 C T 9: 44,689,892 (GRCm39) probably benign Het
Il12b A G 11: 44,298,721 (GRCm39) T59A probably benign Het
Insr A G 8: 3,248,231 (GRCm39) L438P probably damaging Het
Iqgap2 C T 13: 95,869,398 (GRCm39) probably null Het
Irx4 A T 13: 73,415,672 (GRCm39) T154S possibly damaging Het
Itgbl1 A G 14: 124,094,901 (GRCm39) K309E probably benign Het
Kcns2 T A 15: 34,839,849 (GRCm39) L404* probably null Het
Kif2c T C 4: 117,019,226 (GRCm39) E644G possibly damaging Het
Klhl22 T C 16: 17,594,669 (GRCm39) L266P probably damaging Het
Krt71 T A 15: 101,646,764 (GRCm39) K315* probably null Het
Lca5 T C 9: 83,277,583 (GRCm39) N587S probably benign Het
Lrp1b T A 2: 41,185,681 (GRCm39) M1459L Het
Lrrtm2 T C 18: 35,346,645 (GRCm39) K219R probably damaging Het
Mcmbp T C 7: 128,306,241 (GRCm39) D459G probably damaging Het
Megf8 A G 7: 25,048,367 (GRCm39) H1680R probably damaging Het
Mia3 A G 1: 183,115,629 (GRCm39) S301P probably benign Het
Mtrr A G 13: 68,712,521 (GRCm39) Y622H probably damaging Het
Myo7b T A 18: 32,099,292 (GRCm39) Q1710L probably damaging Het
Nab1 T C 1: 52,520,154 (GRCm39) N276D probably damaging Het
Nalcn C T 14: 123,540,302 (GRCm39) R1127H probably damaging Het
Nbas T A 12: 13,324,220 (GRCm39) I110N probably damaging Het
Nfe2l3 C T 6: 51,434,276 (GRCm39) Q279* probably null Het
Nlrp9c C T 7: 26,064,440 (GRCm39) E963K probably benign Het
Nsmaf A G 4: 6,416,586 (GRCm39) V569A probably benign Het
Or10ak14 T C 4: 118,611,372 (GRCm39) Y123C possibly damaging Het
Or13c3 C T 4: 52,856,421 (GRCm39) V31I probably benign Het
Or52a5b T A 7: 103,417,137 (GRCm39) I156F probably benign Het
Or52n5 A T 7: 104,588,638 (GRCm39) I302F probably benign Het
Or5ac17 T A 16: 59,036,283 (GRCm39) D231V probably benign Het
Or5p4 T C 7: 107,680,399 (GRCm39) S133P not run Het
Or7e166 A T 9: 19,624,183 (GRCm39) D20V probably damaging Het
Or7g32 T A 9: 19,408,398 (GRCm39) M118K probably damaging Het
Or8d1b T A 9: 38,887,017 (GRCm39) V15E probably benign Het
Or8k28 T C 2: 86,286,412 (GRCm39) T68A probably benign Het
Paf1 A G 7: 28,096,353 (GRCm39) Y322C probably damaging Het
Pcdha2 C A 18: 37,072,438 (GRCm39) A23D possibly damaging Het
Pcdhb6 G A 18: 37,468,225 (GRCm39) C382Y probably damaging Het
Pdzd7 C T 19: 45,034,045 (GRCm39) G13D probably damaging Het
Pik3r2 T C 8: 71,222,025 (GRCm39) N586S probably benign Het
Pik3r3 T A 4: 116,128,027 (GRCm39) D119E probably benign Het
Pkd2l1 T A 19: 44,142,154 (GRCm39) I535F probably benign Het
Ppfia3 T C 7: 45,010,870 (GRCm39) probably null Het
Ppl T A 16: 4,930,860 (GRCm39) Q53L possibly damaging Het
Rimbp3 T G 16: 17,029,068 (GRCm39) S831A probably benign Het
Rnps1 A G 17: 24,637,504 (GRCm39) T49A unknown Het
Rpl7a T A 2: 26,802,019 (GRCm39) probably null Het
Rrm2b T A 15: 37,931,891 (GRCm39) E248D probably benign Het
Sdhaf4 A G 1: 24,035,439 (GRCm39) F70L probably damaging Het
Sel1l3 A T 5: 53,273,751 (GRCm39) S1038R probably benign Het
Selenoo T A 15: 88,973,681 (GRCm39) F124I probably benign Het
Setbp1 A T 18: 78,900,701 (GRCm39) Y989N probably damaging Het
Slc1a7 A G 4: 107,859,400 (GRCm39) E163G possibly damaging Het
Slc22a2 T C 17: 12,831,278 (GRCm39) F356S probably damaging Het
Slc24a4 C T 12: 102,205,435 (GRCm39) P378L probably benign Het
Slc4a1ap A G 5: 31,684,871 (GRCm39) D169G probably benign Het
Slc4a7 T A 14: 14,757,421 (GRCm38) V422D probably damaging Het
Slitrk6 T C 14: 110,987,295 (GRCm39) Y804C probably damaging Het
Smarcad1 T A 6: 65,087,360 (GRCm39) H906Q probably benign Het
Smn1 A G 13: 100,264,373 (GRCm39) T109A probably damaging Het
Sntb2 A G 8: 107,707,944 (GRCm39) N236S probably damaging Het
Spag9 T A 11: 94,005,177 (GRCm39) probably null Het
Spg11 C A 2: 121,888,910 (GRCm39) G2154W probably damaging Het
Srsf6 T C 2: 162,776,489 (GRCm39) S278P unknown Het
Stag3 G A 5: 138,280,222 (GRCm39) R29H probably benign Het
Stambp C T 6: 83,540,888 (GRCm39) V98I not run Het
Styxl2 G T 1: 165,939,632 (GRCm39) S58* probably null Het
Suco T C 1: 161,689,780 (GRCm39) D89G possibly damaging Het
Suox C T 10: 128,506,910 (GRCm39) V373I probably benign Het
Sv2b T A 7: 74,797,476 (GRCm39) probably null Het
Tatdn2 T C 6: 113,681,662 (GRCm39) L565P probably damaging Het
Tbpl2 T A 2: 23,984,712 (GRCm39) E145V probably benign Het
Tlr1 T C 5: 65,082,571 (GRCm39) I669V not run Het
Tmc1 A T 19: 20,845,753 (GRCm39) F157I probably damaging Het
Tmem26 T G 10: 68,559,922 (GRCm39) probably null Het
Tmem33 A T 5: 67,443,476 (GRCm39) I218F probably benign Het
Tmem94 T A 11: 115,685,000 (GRCm39) D862E probably damaging Het
Tnr T C 1: 159,712,432 (GRCm39) probably null Het
Tnrc6c T C 11: 117,632,606 (GRCm39) S1103P probably benign Het
Tomm70a T A 16: 56,966,407 (GRCm39) Y453* probably null Het
Trabd C A 15: 88,969,493 (GRCm39) R229S possibly damaging Het
Trappc10 T C 10: 78,029,252 (GRCm39) D1095G probably damaging Het
Trim27 A G 13: 21,376,631 (GRCm39) T460A possibly damaging Het
Tsen54 T G 11: 115,712,531 (GRCm39) D433E probably benign Het
Ubap2 A G 4: 41,235,515 (GRCm39) probably null Het
Vat1l A T 8: 115,016,132 (GRCm39) N341Y possibly damaging Het
Vmn2r82 C G 10: 79,232,276 (GRCm39) Y758* probably null Het
Vps16 T G 2: 130,280,099 (GRCm39) V108G probably damaging Het
Vps53 T A 11: 75,967,900 (GRCm39) I585F possibly damaging Het
Wrnip1 G A 13: 33,000,264 (GRCm39) V424M probably benign Het
Yif1a G A 19: 5,139,818 (GRCm39) V88M possibly damaging Het
Zfat T C 15: 68,052,969 (GRCm39) Y275C probably damaging Het
Zfhx3 A G 8: 109,519,880 (GRCm39) E334G probably damaging Het
Zfp277 T C 12: 40,365,852 (GRCm39) D539G possibly damaging Het
Zfp292 A T 4: 34,808,384 (GRCm39) N1558K probably benign Het
Zfp3 A G 11: 70,662,899 (GRCm39) K286R probably benign Het
Zfp366 T C 13: 99,366,023 (GRCm39) C395R probably damaging Het
Other mutations in Fras1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00332:Fras1 APN 5 96,887,217 (GRCm39) missense possibly damaging 0.55
IGL00507:Fras1 APN 5 96,926,048 (GRCm39) missense probably damaging 1.00
IGL00672:Fras1 APN 5 96,907,309 (GRCm39) splice site probably benign
IGL00772:Fras1 APN 5 96,783,971 (GRCm39) missense probably benign 0.42
IGL00844:Fras1 APN 5 96,682,712 (GRCm39) splice site probably benign
IGL00913:Fras1 APN 5 96,842,935 (GRCm39) missense probably damaging 0.99
IGL00959:Fras1 APN 5 96,929,140 (GRCm39) missense probably damaging 0.96
IGL00966:Fras1 APN 5 96,703,080 (GRCm39) missense probably benign 0.00
IGL01296:Fras1 APN 5 96,821,557 (GRCm39) missense probably null 0.58
IGL01307:Fras1 APN 5 96,929,551 (GRCm39) missense probably benign
IGL01481:Fras1 APN 5 96,805,100 (GRCm39) missense probably damaging 1.00
IGL01525:Fras1 APN 5 96,887,195 (GRCm39) missense probably damaging 0.99
IGL01599:Fras1 APN 5 96,857,750 (GRCm39) missense possibly damaging 0.94
IGL01646:Fras1 APN 5 96,906,007 (GRCm39) missense probably benign 0.29
IGL01795:Fras1 APN 5 96,925,904 (GRCm39) missense probably damaging 1.00
IGL01867:Fras1 APN 5 96,735,990 (GRCm39) missense probably benign
IGL01869:Fras1 APN 5 96,856,642 (GRCm39) splice site probably benign
IGL01923:Fras1 APN 5 96,883,139 (GRCm39) missense probably damaging 1.00
IGL01982:Fras1 APN 5 96,887,107 (GRCm39) missense possibly damaging 0.46
IGL02109:Fras1 APN 5 96,848,382 (GRCm39) missense probably benign
IGL02132:Fras1 APN 5 96,929,496 (GRCm39) nonsense probably null
IGL02171:Fras1 APN 5 96,883,040 (GRCm39) missense probably benign 0.15
IGL02213:Fras1 APN 5 96,793,730 (GRCm39) nonsense probably null
IGL02277:Fras1 APN 5 96,735,977 (GRCm39) missense probably benign 0.00
IGL02507:Fras1 APN 5 96,805,267 (GRCm39) missense possibly damaging 0.95
IGL02589:Fras1 APN 5 96,917,372 (GRCm39) missense probably damaging 1.00
IGL02671:Fras1 APN 5 96,876,475 (GRCm39) missense possibly damaging 0.91
IGL02677:Fras1 APN 5 96,692,883 (GRCm39) missense probably damaging 1.00
IGL02691:Fras1 APN 5 96,892,564 (GRCm39) missense possibly damaging 0.68
IGL02741:Fras1 APN 5 96,839,230 (GRCm39) missense probably benign 0.35
IGL02836:Fras1 APN 5 96,682,725 (GRCm39) missense possibly damaging 0.67
IGL02850:Fras1 APN 5 96,926,034 (GRCm39) missense probably damaging 1.00
IGL02998:Fras1 APN 5 96,850,040 (GRCm39) missense possibly damaging 0.82
IGL03040:Fras1 APN 5 96,857,960 (GRCm39) missense probably benign
IGL03078:Fras1 APN 5 96,783,994 (GRCm39) missense probably damaging 1.00
IGL03096:Fras1 APN 5 96,912,760 (GRCm39) missense probably damaging 1.00
IGL03102:Fras1 APN 5 96,874,394 (GRCm39) missense probably benign 0.11
IGL03183:Fras1 APN 5 96,881,640 (GRCm39) splice site probably benign
IGL03189:Fras1 APN 5 96,890,930 (GRCm39) missense probably benign 0.00
IGL03193:Fras1 APN 5 96,925,965 (GRCm39) missense probably damaging 0.99
IGL03292:Fras1 APN 5 96,855,350 (GRCm39) missense probably damaging 1.00
IGL03328:Fras1 APN 5 96,929,619 (GRCm39) missense probably damaging 0.96
IGL03335:Fras1 APN 5 96,881,803 (GRCm39) splice site probably benign
IGL03394:Fras1 APN 5 96,815,336 (GRCm39) missense probably damaging 0.98
IGL03404:Fras1 APN 5 96,876,440 (GRCm39) missense probably damaging 0.99
baby_ruth UTSW 5 96,856,617 (GRCm39) missense probably benign 0.01
BB002:Fras1 UTSW 5 96,929,443 (GRCm39) missense probably damaging 0.96
BB012:Fras1 UTSW 5 96,929,443 (GRCm39) missense probably damaging 0.96
G1patch:Fras1 UTSW 5 96,929,199 (GRCm39) missense possibly damaging 0.91
I0000:Fras1 UTSW 5 96,888,688 (GRCm39) missense probably damaging 0.99
PIT4581001:Fras1 UTSW 5 96,703,160 (GRCm39) missense probably benign 0.01
R0028:Fras1 UTSW 5 96,825,175 (GRCm39) missense probably benign 0.07
R0049:Fras1 UTSW 5 96,924,481 (GRCm39) missense probably benign 0.07
R0049:Fras1 UTSW 5 96,924,481 (GRCm39) missense probably benign 0.07
R0099:Fras1 UTSW 5 96,762,776 (GRCm39) critical splice donor site probably null
R0109:Fras1 UTSW 5 96,857,936 (GRCm39) missense probably benign 0.01
R0158:Fras1 UTSW 5 96,924,493 (GRCm39) missense possibly damaging 0.83
R0268:Fras1 UTSW 5 96,884,868 (GRCm39) missense probably damaging 0.99
R0305:Fras1 UTSW 5 96,744,747 (GRCm39) missense probably benign
R0352:Fras1 UTSW 5 96,874,399 (GRCm39) missense probably damaging 0.97
R0359:Fras1 UTSW 5 96,910,449 (GRCm39) missense probably damaging 0.98
R0371:Fras1 UTSW 5 96,703,190 (GRCm39) missense possibly damaging 0.90
R0379:Fras1 UTSW 5 96,903,368 (GRCm39) nonsense probably null
R0395:Fras1 UTSW 5 96,917,512 (GRCm39) missense possibly damaging 0.50
R0417:Fras1 UTSW 5 96,839,231 (GRCm39) missense probably benign 0.18
R0454:Fras1 UTSW 5 96,910,524 (GRCm39) missense probably damaging 0.96
R0456:Fras1 UTSW 5 96,862,202 (GRCm39) splice site probably null
R0456:Fras1 UTSW 5 96,702,647 (GRCm39) missense probably damaging 1.00
R0464:Fras1 UTSW 5 96,784,662 (GRCm39) missense probably damaging 0.98
R0613:Fras1 UTSW 5 96,848,347 (GRCm39) splice site probably benign
R0652:Fras1 UTSW 5 96,929,199 (GRCm39) missense possibly damaging 0.91
R0675:Fras1 UTSW 5 96,815,246 (GRCm39) splice site probably benign
R0765:Fras1 UTSW 5 96,700,655 (GRCm39) missense probably benign 0.00
R0783:Fras1 UTSW 5 96,916,289 (GRCm39) missense probably damaging 1.00
R0811:Fras1 UTSW 5 96,900,857 (GRCm39) missense probably benign 0.35
R0812:Fras1 UTSW 5 96,900,857 (GRCm39) missense probably benign 0.35
R0943:Fras1 UTSW 5 96,874,402 (GRCm39) missense probably benign 0.00
R1037:Fras1 UTSW 5 96,862,322 (GRCm39) missense probably damaging 0.97
R1104:Fras1 UTSW 5 96,856,530 (GRCm39) missense probably benign 0.00
R1108:Fras1 UTSW 5 96,790,488 (GRCm39) missense probably damaging 0.99
R1332:Fras1 UTSW 5 96,855,167 (GRCm39) missense probably benign 0.00
R1336:Fras1 UTSW 5 96,855,167 (GRCm39) missense probably benign 0.00
R1458:Fras1 UTSW 5 96,748,592 (GRCm39) missense probably benign 0.00
R1495:Fras1 UTSW 5 96,676,445 (GRCm39) missense possibly damaging 0.49
R1499:Fras1 UTSW 5 96,891,046 (GRCm39) missense probably benign 0.31
R1528:Fras1 UTSW 5 96,784,678 (GRCm39) missense probably damaging 0.99
R1532:Fras1 UTSW 5 96,861,855 (GRCm39) missense probably damaging 1.00
R1556:Fras1 UTSW 5 96,890,921 (GRCm39) missense possibly damaging 0.88
R1625:Fras1 UTSW 5 96,857,837 (GRCm39) missense possibly damaging 0.94
R1625:Fras1 UTSW 5 96,861,849 (GRCm39) missense probably damaging 1.00
R1645:Fras1 UTSW 5 96,848,445 (GRCm39) missense possibly damaging 0.90
R1647:Fras1 UTSW 5 96,874,472 (GRCm39) critical splice donor site probably null
R1648:Fras1 UTSW 5 96,874,472 (GRCm39) critical splice donor site probably null
R1661:Fras1 UTSW 5 96,746,768 (GRCm39) missense probably damaging 1.00
R1665:Fras1 UTSW 5 96,746,768 (GRCm39) missense probably damaging 1.00
R1682:Fras1 UTSW 5 96,793,732 (GRCm39) missense probably benign 0.00
R1701:Fras1 UTSW 5 96,748,643 (GRCm39) missense probably benign 0.00
R1716:Fras1 UTSW 5 96,700,584 (GRCm39) missense probably benign 0.10
R1718:Fras1 UTSW 5 96,702,748 (GRCm39) splice site probably null
R1800:Fras1 UTSW 5 96,857,741 (GRCm39) missense probably benign
R1806:Fras1 UTSW 5 96,912,835 (GRCm39) missense possibly damaging 0.88
R1806:Fras1 UTSW 5 96,861,829 (GRCm39) splice site probably benign
R1822:Fras1 UTSW 5 96,918,547 (GRCm39) missense probably damaging 1.00
R1823:Fras1 UTSW 5 96,918,547 (GRCm39) missense probably damaging 1.00
R1824:Fras1 UTSW 5 96,918,547 (GRCm39) missense probably damaging 1.00
R1847:Fras1 UTSW 5 96,897,282 (GRCm39) splice site probably null
R1929:Fras1 UTSW 5 96,815,296 (GRCm39) missense probably benign 0.24
R1951:Fras1 UTSW 5 96,860,242 (GRCm39) missense probably benign 0.38
R2093:Fras1 UTSW 5 96,929,062 (GRCm39) missense probably damaging 1.00
R2283:Fras1 UTSW 5 96,802,164 (GRCm39) missense probably benign 0.10
R2884:Fras1 UTSW 5 96,848,127 (GRCm39) missense probably benign 0.07
R2913:Fras1 UTSW 5 96,881,774 (GRCm39) missense probably benign
R2914:Fras1 UTSW 5 96,881,774 (GRCm39) missense probably benign
R3054:Fras1 UTSW 5 96,912,802 (GRCm39) missense probably damaging 0.99
R3117:Fras1 UTSW 5 96,919,571 (GRCm39) missense probably damaging 1.00
R3118:Fras1 UTSW 5 96,919,571 (GRCm39) missense probably damaging 1.00
R3691:Fras1 UTSW 5 96,929,371 (GRCm39) missense probably benign 0.02
R3714:Fras1 UTSW 5 96,793,829 (GRCm39) critical splice donor site probably null
R3715:Fras1 UTSW 5 96,793,829 (GRCm39) critical splice donor site probably null
R3801:Fras1 UTSW 5 96,881,791 (GRCm39) missense probably benign 0.26
R3961:Fras1 UTSW 5 96,825,244 (GRCm39) critical splice donor site probably null
R4065:Fras1 UTSW 5 96,918,542 (GRCm39) missense possibly damaging 0.64
R4066:Fras1 UTSW 5 96,918,542 (GRCm39) missense possibly damaging 0.64
R4076:Fras1 UTSW 5 96,891,017 (GRCm39) missense probably damaging 1.00
R4124:Fras1 UTSW 5 96,918,512 (GRCm39) missense probably benign 0.05
R4127:Fras1 UTSW 5 96,918,512 (GRCm39) missense probably benign 0.05
R4153:Fras1 UTSW 5 96,924,594 (GRCm39) missense probably benign 0.17
R4233:Fras1 UTSW 5 96,862,235 (GRCm39) missense possibly damaging 0.91
R4273:Fras1 UTSW 5 96,762,763 (GRCm39) missense probably benign 0.00
R4355:Fras1 UTSW 5 96,848,101 (GRCm39) missense probably benign
R4401:Fras1 UTSW 5 96,790,479 (GRCm39) missense probably damaging 0.97
R4402:Fras1 UTSW 5 96,790,479 (GRCm39) missense probably damaging 0.97
R4403:Fras1 UTSW 5 96,790,479 (GRCm39) missense probably damaging 0.97
R4505:Fras1 UTSW 5 96,929,207 (GRCm39) missense probably damaging 1.00
R4548:Fras1 UTSW 5 96,857,754 (GRCm39) missense probably benign 0.00
R4559:Fras1 UTSW 5 96,929,148 (GRCm39) missense probably damaging 1.00
R4629:Fras1 UTSW 5 96,924,593 (GRCm39) missense probably benign 0.00
R4637:Fras1 UTSW 5 96,925,947 (GRCm39) missense probably damaging 1.00
R4678:Fras1 UTSW 5 96,848,427 (GRCm39) missense probably benign 0.13
R4707:Fras1 UTSW 5 96,883,097 (GRCm39) missense probably damaging 0.96
R4735:Fras1 UTSW 5 96,736,022 (GRCm39) missense probably benign 0.00
R4756:Fras1 UTSW 5 96,929,518 (GRCm39) missense probably benign 0.00
R4762:Fras1 UTSW 5 96,879,477 (GRCm39) missense probably benign
R4820:Fras1 UTSW 5 96,876,512 (GRCm39) missense probably benign 0.00
R4847:Fras1 UTSW 5 96,692,851 (GRCm39) missense possibly damaging 0.94
R4857:Fras1 UTSW 5 96,926,018 (GRCm39) missense probably benign 0.00
R4909:Fras1 UTSW 5 96,856,617 (GRCm39) missense probably benign 0.01
R4931:Fras1 UTSW 5 96,784,699 (GRCm39) missense probably benign 0.02
R4938:Fras1 UTSW 5 96,924,583 (GRCm39) missense probably damaging 0.99
R4952:Fras1 UTSW 5 96,795,357 (GRCm39) missense probably benign 0.01
R4965:Fras1 UTSW 5 96,874,439 (GRCm39) missense possibly damaging 0.95
R4989:Fras1 UTSW 5 96,798,541 (GRCm39) missense possibly damaging 0.75
R5151:Fras1 UTSW 5 96,792,969 (GRCm39) missense probably damaging 1.00
R5168:Fras1 UTSW 5 96,856,616 (GRCm39) missense probably benign 0.00
R5182:Fras1 UTSW 5 96,784,032 (GRCm39) nonsense probably null
R5214:Fras1 UTSW 5 96,917,452 (GRCm39) missense probably damaging 1.00
R5220:Fras1 UTSW 5 96,916,222 (GRCm39) missense probably damaging 1.00
R5235:Fras1 UTSW 5 96,748,609 (GRCm39) missense probably benign 0.02
R5242:Fras1 UTSW 5 96,805,109 (GRCm39) missense probably benign 0.11
R5253:Fras1 UTSW 5 96,888,884 (GRCm39) missense probably damaging 0.99
R5260:Fras1 UTSW 5 96,883,046 (GRCm39) missense possibly damaging 0.79
R5301:Fras1 UTSW 5 96,805,125 (GRCm39) missense possibly damaging 0.88
R5411:Fras1 UTSW 5 96,793,019 (GRCm39) missense probably benign 0.00
R5467:Fras1 UTSW 5 96,927,912 (GRCm39) missense probably benign 0.04
R5543:Fras1 UTSW 5 96,676,394 (GRCm39) missense probably benign 0.01
R5555:Fras1 UTSW 5 96,825,236 (GRCm39) missense probably benign 0.34
R5602:Fras1 UTSW 5 96,884,880 (GRCm39) missense probably damaging 1.00
R5664:Fras1 UTSW 5 96,876,394 (GRCm39) missense possibly damaging 0.91
R5695:Fras1 UTSW 5 96,929,203 (GRCm39) missense probably damaging 1.00
R5717:Fras1 UTSW 5 96,929,596 (GRCm39) missense possibly damaging 0.93
R5742:Fras1 UTSW 5 96,916,240 (GRCm39) missense possibly damaging 0.50
R5759:Fras1 UTSW 5 96,857,775 (GRCm39) missense probably benign 0.02
R5766:Fras1 UTSW 5 96,879,548 (GRCm39) missense possibly damaging 0.91
R5890:Fras1 UTSW 5 96,793,807 (GRCm39) missense probably benign
R6052:Fras1 UTSW 5 96,912,725 (GRCm39) missense probably damaging 1.00
R6058:Fras1 UTSW 5 96,857,844 (GRCm39) missense probably benign
R6256:Fras1 UTSW 5 96,881,702 (GRCm39) missense possibly damaging 0.84
R6306:Fras1 UTSW 5 96,912,805 (GRCm39) missense probably damaging 1.00
R6494:Fras1 UTSW 5 96,907,423 (GRCm39) missense possibly damaging 0.59
R6638:Fras1 UTSW 5 96,905,953 (GRCm39) missense possibly damaging 0.94
R6647:Fras1 UTSW 5 96,883,061 (GRCm39) missense probably damaging 1.00
R6725:Fras1 UTSW 5 96,929,199 (GRCm39) missense possibly damaging 0.91
R6769:Fras1 UTSW 5 96,746,800 (GRCm39) missense possibly damaging 0.60
R6771:Fras1 UTSW 5 96,746,800 (GRCm39) missense possibly damaging 0.60
R6837:Fras1 UTSW 5 96,874,832 (GRCm39) missense probably damaging 0.99
R6841:Fras1 UTSW 5 96,876,410 (GRCm39) missense probably damaging 0.99
R6863:Fras1 UTSW 5 96,691,165 (GRCm39) missense probably benign 0.19
R6868:Fras1 UTSW 5 96,830,237 (GRCm39) missense probably benign 0.38
R6936:Fras1 UTSW 5 96,916,211 (GRCm39) missense possibly damaging 0.92
R6997:Fras1 UTSW 5 96,762,732 (GRCm39) nonsense probably null
R7023:Fras1 UTSW 5 96,857,943 (GRCm39) missense probably benign 0.00
R7091:Fras1 UTSW 5 96,856,535 (GRCm39) missense probably benign
R7102:Fras1 UTSW 5 96,718,900 (GRCm39) missense probably benign
R7120:Fras1 UTSW 5 96,900,819 (GRCm39) nonsense probably null
R7124:Fras1 UTSW 5 96,862,260 (GRCm39) missense probably damaging 1.00
R7129:Fras1 UTSW 5 96,929,143 (GRCm39) missense probably benign 0.00
R7173:Fras1 UTSW 5 96,925,937 (GRCm39) missense probably damaging 1.00
R7174:Fras1 UTSW 5 96,903,436 (GRCm39) critical splice donor site probably null
R7185:Fras1 UTSW 5 96,784,635 (GRCm39) missense probably damaging 1.00
R7191:Fras1 UTSW 5 96,762,771 (GRCm39) missense probably benign 0.05
R7216:Fras1 UTSW 5 96,887,173 (GRCm39) missense probably damaging 1.00
R7222:Fras1 UTSW 5 96,784,668 (GRCm39) missense probably benign 0.00
R7222:Fras1 UTSW 5 96,784,045 (GRCm39) missense probably damaging 1.00
R7320:Fras1 UTSW 5 96,857,745 (GRCm39) missense probably benign 0.03
R7335:Fras1 UTSW 5 96,884,829 (GRCm39) missense possibly damaging 0.82
R7394:Fras1 UTSW 5 96,860,309 (GRCm39) nonsense probably null
R7412:Fras1 UTSW 5 96,762,748 (GRCm39) missense probably benign 0.06
R7422:Fras1 UTSW 5 96,821,458 (GRCm39) missense probably benign 0.21
R7552:Fras1 UTSW 5 96,916,297 (GRCm39) missense probably damaging 1.00
R7559:Fras1 UTSW 5 96,888,713 (GRCm39) missense possibly damaging 0.82
R7575:Fras1 UTSW 5 96,691,173 (GRCm39) missense probably benign 0.02
R7578:Fras1 UTSW 5 96,832,296 (GRCm39) missense probably damaging 1.00
R7600:Fras1 UTSW 5 96,832,295 (GRCm39) missense probably damaging 1.00
R7669:Fras1 UTSW 5 96,840,483 (GRCm39) missense probably benign 0.01
R7710:Fras1 UTSW 5 96,792,962 (GRCm39) nonsense probably null
R7722:Fras1 UTSW 5 96,917,413 (GRCm39) missense probably damaging 1.00
R7726:Fras1 UTSW 5 96,860,310 (GRCm39) missense probably benign 0.41
R7745:Fras1 UTSW 5 96,874,754 (GRCm39) missense probably benign 0.11
R7777:Fras1 UTSW 5 96,900,763 (GRCm39) missense probably damaging 1.00
R7923:Fras1 UTSW 5 96,887,177 (GRCm39) missense probably damaging 1.00
R7925:Fras1 UTSW 5 96,929,443 (GRCm39) missense probably damaging 0.96
R8000:Fras1 UTSW 5 96,910,536 (GRCm39) missense probably damaging 0.96
R8056:Fras1 UTSW 5 96,892,633 (GRCm39) missense probably damaging 1.00
R8058:Fras1 UTSW 5 96,842,778 (GRCm39) missense probably benign
R8117:Fras1 UTSW 5 96,855,245 (GRCm39) missense probably damaging 1.00
R8157:Fras1 UTSW 5 96,702,714 (GRCm39) missense probably benign 0.00
R8312:Fras1 UTSW 5 96,736,050 (GRCm39) missense probably benign
R8315:Fras1 UTSW 5 96,891,041 (GRCm39) missense probably damaging 0.97
R8412:Fras1 UTSW 5 96,744,711 (GRCm39) missense probably benign 0.00
R8546:Fras1 UTSW 5 96,857,825 (GRCm39) missense probably benign 0.00
R8705:Fras1 UTSW 5 96,839,260 (GRCm39) missense probably benign 0.01
R8790:Fras1 UTSW 5 96,903,236 (GRCm39) missense probably damaging 1.00
R8848:Fras1 UTSW 5 96,929,207 (GRCm39) missense probably damaging 1.00
R8855:Fras1 UTSW 5 96,917,465 (GRCm39) missense
R8871:Fras1 UTSW 5 96,855,257 (GRCm39) missense probably benign 0.34
R8894:Fras1 UTSW 5 96,907,402 (GRCm39) missense probably damaging 1.00
R8904:Fras1 UTSW 5 96,929,138 (GRCm39) missense probably benign 0.16
R8910:Fras1 UTSW 5 96,715,855 (GRCm39) missense probably benign 0.01
R8916:Fras1 UTSW 5 96,900,774 (GRCm39) missense probably damaging 1.00
R8929:Fras1 UTSW 5 96,917,366 (GRCm39) missense probably damaging 0.98
R8995:Fras1 UTSW 5 96,860,415 (GRCm39) missense possibly damaging 0.83
R9016:Fras1 UTSW 5 96,783,923 (GRCm39) missense probably damaging 0.96
R9021:Fras1 UTSW 5 96,888,609 (GRCm39) missense probably damaging 1.00
R9038:Fras1 UTSW 5 96,874,742 (GRCm39) missense probably benign 0.25
R9204:Fras1 UTSW 5 96,883,022 (GRCm39) missense probably damaging 1.00
R9222:Fras1 UTSW 5 96,805,087 (GRCm39) missense probably benign 0.15
R9231:Fras1 UTSW 5 96,692,904 (GRCm39) missense probably damaging 1.00
R9238:Fras1 UTSW 5 96,832,220 (GRCm39) missense possibly damaging 0.90
R9257:Fras1 UTSW 5 96,910,359 (GRCm39) missense probably damaging 1.00
R9302:Fras1 UTSW 5 96,682,751 (GRCm39) missense probably damaging 1.00
R9329:Fras1 UTSW 5 96,884,813 (GRCm39) missense probably damaging 1.00
R9361:Fras1 UTSW 5 96,924,557 (GRCm39) missense probably damaging 1.00
R9430:Fras1 UTSW 5 96,929,251 (GRCm39) missense probably benign 0.00
R9431:Fras1 UTSW 5 96,900,873 (GRCm39) missense possibly damaging 0.71
R9474:Fras1 UTSW 5 96,887,124 (GRCm39) missense probably benign 0.00
R9475:Fras1 UTSW 5 96,927,929 (GRCm39) missense probably damaging 0.96
R9497:Fras1 UTSW 5 96,884,895 (GRCm39) missense probably damaging 1.00
R9597:Fras1 UTSW 5 96,888,551 (GRCm39) missense probably damaging 1.00
R9650:Fras1 UTSW 5 96,910,387 (GRCm39) missense probably damaging 1.00
R9694:Fras1 UTSW 5 96,929,545 (GRCm39) missense probably benign 0.03
R9779:Fras1 UTSW 5 96,717,353 (GRCm39) missense probably damaging 0.99
Z1088:Fras1 UTSW 5 96,891,070 (GRCm39) missense probably damaging 0.97
Z1088:Fras1 UTSW 5 96,906,001 (GRCm39) missense probably benign
Z1176:Fras1 UTSW 5 96,906,001 (GRCm39) missense probably benign
Z1177:Fras1 UTSW 5 96,848,110 (GRCm39) missense possibly damaging 0.71
Z1177:Fras1 UTSW 5 96,839,316 (GRCm39) missense probably damaging 1.00
Z1177:Fras1 UTSW 5 96,906,001 (GRCm39) missense probably benign
Z1177:Fras1 UTSW 5 96,888,842 (GRCm39) missense possibly damaging 0.95
Z1177:Fras1 UTSW 5 96,888,670 (GRCm39) missense probably benign 0.18
Predicted Primers PCR Primer
(F):5'- TGTTGAATTGGAAACACTGGTG -3'
(R):5'- GCTGCTGCTAATGATGATAATGTCTC -3'

Sequencing Primer
(F):5'- TGTGTTCAGTGACTAAGTATCCC -3'
(R):5'- TGATGATAATGTCTCAACTCCTACC -3'
Posted On 2019-09-13