Incidental Mutation 'R1772:Fcgbp'
ID 196696
Institutional Source Beutler Lab
Gene Symbol Fcgbp
Ensembl Gene ENSMUSG00000047730
Gene Name Fc fragment of IgG binding protein
Synonyms A430096B05Rik
MMRRC Submission 039803-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1772 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 27770661-27820287 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 27804600 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Lysine at position 1903 (Q1903K)
Ref Sequence ENSEMBL: ENSMUSP00000114271 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076648] [ENSMUST00000138392]
AlphaFold E9Q0B5
Predicted Effect probably benign
Transcript: ENSMUST00000076648
AA Change: Q1903K

PolyPhen 2 Score 0.066 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000075945
Gene: ENSMUSG00000047730
AA Change: Q1903K

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
FOLN 27 49 2.3e-4 SMART
VWD 46 211 5.26e-45 SMART
low complexity region 226 237 N/A INTRINSIC
C8 251 326 1.17e-34 SMART
Pfam:TIL 329 383 1.2e-12 PFAM
VWC 385 431 2.34e-1 SMART
FOLN 418 441 3.48e1 SMART
VWD 438 603 6.85e-35 SMART
C8 642 717 1.4e-32 SMART
Pfam:TIL 720 773 4.7e-14 PFAM
VWC 775 829 9.42e-1 SMART
VWD 824 990 7.86e-44 SMART
C8 1034 1109 1.66e-34 SMART
Pfam:TIL 1112 1165 6.7e-13 PFAM
VWC 1167 1225 9.8e-3 SMART
FOLN 1198 1220 9.55e-1 SMART
FOLN 1224 1246 2.41e0 SMART
VWD 1243 1411 6.59e-37 SMART
C8 1451 1527 5.6e-32 SMART
low complexity region 1541 1551 N/A INTRINSIC
EGF_like 1558 1581 6.15e1 SMART
VWC 1589 1682 1.6e-2 SMART
VWD 1640 1807 5.15e-39 SMART
C8 1839 1914 4.62e-33 SMART
EGF_like 1942 1965 4.46e1 SMART
VWC 1972 2064 1.92e-1 SMART
VWD 2024 2180 6.34e-39 SMART
low complexity region 2201 2214 N/A INTRINSIC
C8 2221 2296 3.7e-32 SMART
Pfam:TIL 2299 2352 5e-12 PFAM
VWC 2354 2413 8.29e-1 SMART
FOLN 2385 2407 4.96e1 SMART
VWD 2404 2566 1.89e-5 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000138392
AA Change: Q1903K

PolyPhen 2 Score 0.901 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000114271
Gene: ENSMUSG00000047730
AA Change: Q1903K

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
FOLN 27 49 2.3e-4 SMART
VWD 46 211 5.26e-45 SMART
low complexity region 226 237 N/A INTRINSIC
C8 251 326 1.17e-34 SMART
Pfam:TIL 329 383 8.4e-13 PFAM
VWC 385 431 2.34e-1 SMART
FOLN 418 441 3.48e1 SMART
VWD 438 603 7.99e-36 SMART
C8 642 717 1.4e-32 SMART
Pfam:TIL 720 773 3.3e-14 PFAM
VWC 775 829 9.42e-1 SMART
VWD 824 990 7.86e-44 SMART
C8 1034 1109 1.66e-34 SMART
Pfam:TIL 1112 1165 6.9e-13 PFAM
VWC 1167 1225 9.8e-3 SMART
FOLN 1198 1220 9.55e-1 SMART
FOLN 1224 1246 2.41e0 SMART
VWD 1243 1411 6.59e-37 SMART
C8 1451 1527 5.6e-32 SMART
low complexity region 1541 1551 N/A INTRINSIC
EGF_like 1558 1581 6.15e1 SMART
VWC 1589 1682 1.6e-2 SMART
VWD 1640 1807 5.15e-39 SMART
C8 1839 1914 4.62e-33 SMART
EGF_like 1942 1965 4.46e1 SMART
VWC 1972 2064 1.92e-1 SMART
VWD 2024 2180 6.34e-39 SMART
low complexity region 2201 2214 N/A INTRINSIC
C8 2221 2296 3.7e-32 SMART
Pfam:TIL 2299 2352 1e-11 PFAM
VWC 2354 2413 8.29e-1 SMART
FOLN 2385 2407 4.96e1 SMART
VWD 2404 2566 1.89e-5 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148946
Meta Mutation Damage Score 0.1349 question?
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 97.0%
  • 10x: 95.6%
  • 20x: 93.5%
Validation Efficiency 97% (107/110)
Allele List at MGI
Other mutations in this stock
Total: 106 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgb G T 10: 10,258,465 (GRCm39) probably benign Het
Aldh1a7 T C 19: 20,693,383 (GRCm39) K179E probably damaging Het
Angptl7 G A 4: 148,581,883 (GRCm39) R168C probably damaging Het
Atp8b1 T A 18: 64,706,563 (GRCm39) I208F possibly damaging Het
Bco1 A G 8: 117,857,347 (GRCm39) Y438C probably benign Het
Bltp1 T C 3: 37,013,581 (GRCm39) S1937P probably damaging Het
Btrc A C 19: 45,501,100 (GRCm39) K218Q probably damaging Het
Cct8l1 G A 5: 25,722,697 (GRCm39) V471M probably damaging Het
Cd180 C T 13: 102,842,750 (GRCm39) L599F probably benign Het
Cd300e T C 11: 114,945,344 (GRCm39) N150S probably benign Het
Clcn1 C A 6: 42,271,079 (GRCm39) T281K probably damaging Het
Cnnm3 T C 1: 36,558,038 (GRCm39) S417P probably damaging Het
Cspg4 T A 9: 56,804,776 (GRCm39) S1862R probably benign Het
Cspg5 A T 9: 110,091,206 (GRCm39) N432Y probably damaging Het
Cyp2r1 T A 7: 114,152,451 (GRCm39) I169F probably damaging Het
D130043K22Rik T A 13: 25,059,982 (GRCm39) S618T probably damaging Het
Diaph3 G A 14: 87,202,985 (GRCm39) P635L probably damaging Het
Dlg1 A G 16: 31,484,485 (GRCm39) I38V possibly damaging Het
Dlk1 T G 12: 109,425,685 (GRCm39) V186G probably damaging Het
Dmxl2 T C 9: 54,330,508 (GRCm39) probably benign Het
Dnajc17 G A 2: 119,014,164 (GRCm39) R132* probably null Het
Dock9 G T 14: 121,847,210 (GRCm39) N1042K probably benign Het
Dok7 A T 5: 35,243,994 (GRCm39) Q511L probably damaging Het
Espnl G A 1: 91,272,325 (GRCm39) E562K possibly damaging Het
Evi5 G A 5: 107,943,707 (GRCm39) T562I probably benign Het
Exd2 T A 12: 80,536,253 (GRCm39) D294E probably benign Het
Fbn1 A T 2: 125,245,148 (GRCm39) D246E possibly damaging Het
Fbxw16 A T 9: 109,268,650 (GRCm39) W247R possibly damaging Het
Fcer1a A G 1: 173,053,004 (GRCm39) I64T probably benign Het
Fmn1 A G 2: 113,195,700 (GRCm39) S467G unknown Het
Fndc7 T A 3: 108,777,850 (GRCm39) T369S probably damaging Het
Fnta T C 8: 26,490,994 (GRCm39) probably benign Het
Gak A T 5: 108,754,758 (GRCm39) H289Q probably damaging Het
Gas2l3 A G 10: 89,252,876 (GRCm39) probably benign Het
Gbp8 T C 5: 105,163,987 (GRCm39) N437S probably benign Het
Gk5 G A 9: 96,032,850 (GRCm39) probably null Het
Hid1 A T 11: 115,239,299 (GRCm39) V788E probably damaging Het
Hmcn1 T C 1: 150,439,319 (GRCm39) T5505A probably damaging Het
Igf1r T A 7: 67,844,822 (GRCm39) M865K probably benign Het
Katnal2 G A 18: 77,090,233 (GRCm39) T258I probably damaging Het
Kdm3b A T 18: 34,936,557 (GRCm39) I280L probably benign Het
Kif24 A G 4: 41,409,787 (GRCm39) V382A probably damaging Het
Kif2a A T 13: 107,114,640 (GRCm39) probably benign Het
Klhl10 A G 11: 100,333,022 (GRCm39) I56V probably benign Het
Klk6 C T 7: 43,478,695 (GRCm39) Q201* probably null Het
Klra3 A T 6: 130,300,671 (GRCm39) S233T probably benign Het
Krt9 A T 11: 100,082,131 (GRCm39) M223K probably damaging Het
Lama4 G A 10: 38,936,220 (GRCm39) E632K probably benign Het
Lamb1 T C 12: 31,328,524 (GRCm39) Y163H probably damaging Het
Lipo3 A G 19: 33,764,821 (GRCm39) I11T probably benign Het
Lix1l T A 3: 96,531,207 (GRCm39) H333Q possibly damaging Het
Mal2 T A 15: 54,451,783 (GRCm39) M68K probably damaging Het
Map2k2 T C 10: 80,956,934 (GRCm39) I104T probably damaging Het
Matn2 T C 15: 34,428,931 (GRCm39) V765A probably damaging Het
Mptx2 T A 1: 173,102,040 (GRCm39) K216N probably damaging Het
Mup5 C T 4: 61,750,578 (GRCm39) probably null Het
Mycbp2 A G 14: 103,419,855 (GRCm39) Y2494H probably damaging Het
Myh3 G A 11: 66,990,220 (GRCm39) D1622N probably benign Het
Myo6 T C 9: 80,177,331 (GRCm39) I609T possibly damaging Het
Ndst1 G A 18: 60,835,909 (GRCm39) T458I probably damaging Het
Neb A T 2: 52,125,689 (GRCm39) Y3622N probably damaging Het
Ntm A G 9: 29,090,396 (GRCm39) Y108H probably benign Het
Or13c3 T G 4: 52,855,730 (GRCm39) K261T probably benign Het
Or1a1b T C 11: 74,097,398 (GRCm39) I215V probably benign Het
Or52e19 T C 7: 102,959,449 (GRCm39) Y174H possibly damaging Het
Pappa2 T A 1: 158,641,938 (GRCm39) I1373F possibly damaging Het
Pear1 A G 3: 87,661,799 (GRCm39) probably benign Het
Phc3 C T 3: 31,015,969 (GRCm39) A81T probably damaging Het
Pmepa1 A G 2: 173,076,153 (GRCm39) S105P probably damaging Het
Ppp6r1 T C 7: 4,645,030 (GRCm39) I248V probably benign Het
Prdm4 G A 10: 85,729,256 (GRCm39) T717I probably damaging Het
Prom1 T C 5: 44,168,566 (GRCm39) T669A probably benign Het
Ptpn5 T A 7: 46,740,516 (GRCm39) I96F probably benign Het
Ptpro T C 6: 137,407,741 (GRCm39) L922P probably damaging Het
Reck A T 4: 43,890,982 (GRCm39) H40L probably benign Het
Rreb1 T A 13: 38,114,899 (GRCm39) C753S probably benign Het
Sacs T C 14: 61,448,346 (GRCm39) L3464P probably damaging Het
Samsn1 A T 16: 75,667,663 (GRCm39) D304E probably benign Het
Scgb2b3 T C 7: 31,059,621 (GRCm39) N51S possibly damaging Het
Shroom3 T C 5: 93,088,515 (GRCm39) S341P probably damaging Het
Siglece T C 7: 43,308,717 (GRCm39) D212G probably damaging Het
Sirpa A G 2: 129,458,376 (GRCm39) T331A probably damaging Het
Spata21 T C 4: 140,838,607 (GRCm39) S553P possibly damaging Het
Speer4b T A 5: 27,705,236 (GRCm39) probably benign Het
Srgap2 T C 1: 131,247,376 (GRCm39) D552G probably damaging Het
Stab2 A G 10: 86,790,098 (GRCm39) I556T probably benign Het
Strip1 C T 3: 107,534,047 (GRCm39) probably null Het
Stxbp6 T A 12: 44,949,653 (GRCm39) D92V probably damaging Het
Styx A G 14: 45,594,215 (GRCm39) K46E probably damaging Het
Supt20 T A 3: 54,617,841 (GRCm39) V314E probably damaging Het
Syne2 T A 12: 75,985,503 (GRCm39) D1650E probably benign Het
Szt2 T A 4: 118,262,714 (GRCm39) K21M probably damaging Het
Tbx4 A T 11: 85,802,033 (GRCm39) H222L probably damaging Het
Tcstv1b T A 13: 120,634,725 (GRCm39) D2E probably benign Het
Tmx3 A T 18: 90,551,121 (GRCm39) I254L probably benign Het
Tns2 C T 15: 102,017,369 (GRCm39) R281C probably damaging Het
Trpv2 A T 11: 62,485,052 (GRCm39) probably benign Het
Ubap2 A G 4: 41,202,380 (GRCm39) S683P probably benign Het
Ube2d3 C T 3: 135,170,972 (GRCm39) R139W probably benign Het
Ubox5 G T 2: 130,433,794 (GRCm39) Q518K probably benign Het
Usp42 T C 5: 143,702,857 (GRCm39) N588S probably damaging Het
Vars2 G A 17: 35,970,976 (GRCm39) T618M probably damaging Het
Wfdc17 A T 11: 83,595,730 (GRCm39) N65Y probably damaging Het
Zbtb38 G A 9: 96,570,094 (GRCm39) P330L probably damaging Het
Zfp385a C T 15: 103,224,308 (GRCm39) probably null Het
Zfp637 T A 6: 117,822,373 (GRCm39) L167H probably damaging Het
Other mutations in Fcgbp
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00309:Fcgbp APN 7 27,784,555 (GRCm39) missense probably damaging 1.00
IGL00331:Fcgbp APN 7 27,800,966 (GRCm39) splice site probably benign
IGL00335:Fcgbp APN 7 27,785,560 (GRCm39) missense possibly damaging 0.90
IGL00470:Fcgbp APN 7 27,774,511 (GRCm39) nonsense probably null
IGL00491:Fcgbp APN 7 27,792,827 (GRCm39) missense probably damaging 1.00
IGL00498:Fcgbp APN 7 27,791,222 (GRCm39) missense probably damaging 1.00
IGL01296:Fcgbp APN 7 27,789,072 (GRCm39) missense probably benign 0.15
IGL01582:Fcgbp APN 7 27,793,067 (GRCm39) missense probably benign 0.19
IGL01929:Fcgbp APN 7 27,803,388 (GRCm39) missense probably damaging 1.00
IGL02024:Fcgbp APN 7 27,805,799 (GRCm39) missense probably damaging 1.00
IGL02027:Fcgbp APN 7 27,774,629 (GRCm39) missense probably damaging 1.00
IGL02140:Fcgbp APN 7 27,791,379 (GRCm39) missense probably damaging 1.00
IGL02162:Fcgbp APN 7 27,774,660 (GRCm39) missense probably damaging 1.00
IGL02345:Fcgbp APN 7 27,771,068 (GRCm39) splice site probably benign
IGL02377:Fcgbp APN 7 27,806,395 (GRCm39) missense possibly damaging 0.67
IGL02389:Fcgbp APN 7 27,774,596 (GRCm39) missense probably damaging 1.00
IGL02423:Fcgbp APN 7 27,789,378 (GRCm39) missense probably benign 0.02
IGL02523:Fcgbp APN 7 27,804,157 (GRCm39) missense possibly damaging 0.89
IGL02561:Fcgbp APN 7 27,800,599 (GRCm39) intron probably benign
IGL02631:Fcgbp APN 7 27,784,723 (GRCm39) missense probably damaging 1.00
IGL02716:Fcgbp APN 7 27,800,859 (GRCm39) missense probably damaging 0.98
IGL02836:Fcgbp APN 7 27,816,783 (GRCm39) missense possibly damaging 0.91
IGL02957:Fcgbp APN 7 27,791,272 (GRCm39) nonsense probably null
IGL02971:Fcgbp APN 7 27,800,898 (GRCm39) missense probably damaging 1.00
IGL03284:Fcgbp APN 7 27,784,857 (GRCm39) missense possibly damaging 0.93
IGL03379:Fcgbp APN 7 27,789,342 (GRCm39) missense possibly damaging 0.76
bilge UTSW 7 27,816,762 (GRCm39) missense probably benign 0.00
R6548_fcgbp_365 UTSW 7 27,791,343 (GRCm39) missense probably benign 0.00
swill UTSW 7 27,789,159 (GRCm39) missense probably damaging 1.00
G1citation:Fcgbp UTSW 7 27,806,781 (GRCm39) missense probably damaging 1.00
IGL02796:Fcgbp UTSW 7 27,800,576 (GRCm39) intron probably benign
PIT4486001:Fcgbp UTSW 7 27,774,698 (GRCm39) missense possibly damaging 0.52
R0277:Fcgbp UTSW 7 27,784,918 (GRCm39) critical splice donor site probably null
R0387:Fcgbp UTSW 7 27,790,879 (GRCm39) splice site probably benign
R0586:Fcgbp UTSW 7 27,789,138 (GRCm39) missense probably damaging 1.00
R0981:Fcgbp UTSW 7 27,784,535 (GRCm39) nonsense probably null
R0987:Fcgbp UTSW 7 27,793,599 (GRCm39) missense probably damaging 1.00
R1240:Fcgbp UTSW 7 27,819,950 (GRCm39) missense probably damaging 1.00
R1394:Fcgbp UTSW 7 27,792,804 (GRCm39) missense probably damaging 0.98
R1395:Fcgbp UTSW 7 27,792,804 (GRCm39) missense probably damaging 0.98
R1438:Fcgbp UTSW 7 27,803,158 (GRCm39) nonsense probably null
R1474:Fcgbp UTSW 7 27,791,273 (GRCm39) missense probably benign 0.00
R1521:Fcgbp UTSW 7 27,774,585 (GRCm39) missense probably benign 0.00
R1740:Fcgbp UTSW 7 27,800,674 (GRCm39) missense possibly damaging 0.87
R1750:Fcgbp UTSW 7 27,792,868 (GRCm39) nonsense probably null
R1804:Fcgbp UTSW 7 27,785,564 (GRCm39) missense probably benign
R1808:Fcgbp UTSW 7 27,784,515 (GRCm39) missense probably benign 0.04
R1819:Fcgbp UTSW 7 27,784,708 (GRCm39) missense probably benign 0.00
R1934:Fcgbp UTSW 7 27,806,518 (GRCm39) missense probably damaging 1.00
R1972:Fcgbp UTSW 7 27,793,617 (GRCm39) missense probably benign 0.11
R2051:Fcgbp UTSW 7 27,819,785 (GRCm39) missense probably damaging 0.97
R2072:Fcgbp UTSW 7 27,819,814 (GRCm39) missense probably damaging 0.98
R2074:Fcgbp UTSW 7 27,819,814 (GRCm39) missense probably damaging 0.98
R2124:Fcgbp UTSW 7 27,791,444 (GRCm39) missense probably benign 0.03
R2155:Fcgbp UTSW 7 27,806,628 (GRCm39) missense probably benign 0.00
R3015:Fcgbp UTSW 7 27,774,838 (GRCm39) splice site probably benign
R3037:Fcgbp UTSW 7 27,802,127 (GRCm39) missense possibly damaging 0.62
R3151:Fcgbp UTSW 7 27,816,665 (GRCm39) missense probably damaging 1.00
R3176:Fcgbp UTSW 7 27,791,086 (GRCm39) missense probably damaging 0.99
R3177:Fcgbp UTSW 7 27,791,086 (GRCm39) missense probably damaging 0.99
R3276:Fcgbp UTSW 7 27,791,086 (GRCm39) missense probably damaging 0.99
R3277:Fcgbp UTSW 7 27,791,086 (GRCm39) missense probably damaging 0.99
R3623:Fcgbp UTSW 7 27,800,701 (GRCm39) missense probably damaging 1.00
R3730:Fcgbp UTSW 7 27,784,882 (GRCm39) missense possibly damaging 0.82
R3935:Fcgbp UTSW 7 27,774,824 (GRCm39) missense probably benign 0.00
R3936:Fcgbp UTSW 7 27,774,824 (GRCm39) missense probably benign 0.00
R4041:Fcgbp UTSW 7 27,813,404 (GRCm39) missense probably benign 0.01
R4056:Fcgbp UTSW 7 27,803,541 (GRCm39) missense probably benign 0.09
R4057:Fcgbp UTSW 7 27,803,541 (GRCm39) missense probably benign 0.09
R4705:Fcgbp UTSW 7 27,806,721 (GRCm39) missense probably benign 0.44
R4708:Fcgbp UTSW 7 27,794,386 (GRCm39) missense probably benign 0.00
R4710:Fcgbp UTSW 7 27,794,386 (GRCm39) missense probably benign 0.00
R4779:Fcgbp UTSW 7 27,794,362 (GRCm39) missense probably damaging 1.00
R4820:Fcgbp UTSW 7 27,813,383 (GRCm39) missense probably damaging 1.00
R4863:Fcgbp UTSW 7 27,785,769 (GRCm39) missense probably benign 0.33
R4926:Fcgbp UTSW 7 27,785,660 (GRCm39) missense probably damaging 0.99
R4947:Fcgbp UTSW 7 27,789,237 (GRCm39) missense probably benign 0.00
R4979:Fcgbp UTSW 7 27,816,995 (GRCm39) missense probably benign 0.06
R5002:Fcgbp UTSW 7 27,785,528 (GRCm39) splice site probably null
R5219:Fcgbp UTSW 7 27,803,510 (GRCm39) missense probably damaging 1.00
R5241:Fcgbp UTSW 7 27,784,624 (GRCm39) missense probably damaging 1.00
R5301:Fcgbp UTSW 7 27,793,099 (GRCm39) missense possibly damaging 0.93
R5306:Fcgbp UTSW 7 27,791,243 (GRCm39) missense probably damaging 1.00
R5335:Fcgbp UTSW 7 27,789,159 (GRCm39) missense probably damaging 1.00
R5399:Fcgbp UTSW 7 27,804,480 (GRCm39) missense probably benign 0.05
R5418:Fcgbp UTSW 7 27,784,738 (GRCm39) missense probably damaging 1.00
R5527:Fcgbp UTSW 7 27,793,060 (GRCm39) missense probably benign
R5583:Fcgbp UTSW 7 27,791,004 (GRCm39) missense probably damaging 1.00
R5698:Fcgbp UTSW 7 27,791,447 (GRCm39) missense possibly damaging 0.95
R5780:Fcgbp UTSW 7 27,784,643 (GRCm39) missense probably benign 0.02
R5813:Fcgbp UTSW 7 27,800,919 (GRCm39) missense possibly damaging 0.64
R5910:Fcgbp UTSW 7 27,784,928 (GRCm39) splice site probably benign
R5936:Fcgbp UTSW 7 27,786,117 (GRCm39) missense probably damaging 0.98
R5992:Fcgbp UTSW 7 27,819,959 (GRCm39) missense probably benign 0.05
R6091:Fcgbp UTSW 7 27,804,390 (GRCm39) missense possibly damaging 0.90
R6372:Fcgbp UTSW 7 27,806,433 (GRCm39) missense probably damaging 1.00
R6488:Fcgbp UTSW 7 27,792,963 (GRCm39) missense probably damaging 0.96
R6548:Fcgbp UTSW 7 27,791,343 (GRCm39) missense probably benign 0.00
R6553:Fcgbp UTSW 7 27,813,404 (GRCm39) missense possibly damaging 0.79
R6585:Fcgbp UTSW 7 27,813,404 (GRCm39) missense possibly damaging 0.79
R6695:Fcgbp UTSW 7 27,785,695 (GRCm39) nonsense probably null
R6711:Fcgbp UTSW 7 27,789,098 (GRCm39) missense probably damaging 0.99
R6803:Fcgbp UTSW 7 27,802,637 (GRCm39) missense probably benign 0.00
R6822:Fcgbp UTSW 7 27,806,781 (GRCm39) missense probably damaging 1.00
R6907:Fcgbp UTSW 7 27,784,443 (GRCm39) missense probably damaging 1.00
R6912:Fcgbp UTSW 7 27,789,129 (GRCm39) missense probably benign 0.15
R6924:Fcgbp UTSW 7 27,793,248 (GRCm39) missense probably benign
R6943:Fcgbp UTSW 7 27,791,477 (GRCm39) missense probably benign 0.22
R7060:Fcgbp UTSW 7 27,791,358 (GRCm39) missense probably benign 0.20
R7103:Fcgbp UTSW 7 27,784,387 (GRCm39) missense probably benign 0.00
R7208:Fcgbp UTSW 7 27,803,446 (GRCm39) missense probably benign 0.01
R7291:Fcgbp UTSW 7 27,800,817 (GRCm39) missense probably benign 0.00
R7301:Fcgbp UTSW 7 27,792,861 (GRCm39) missense possibly damaging 0.65
R7404:Fcgbp UTSW 7 27,800,932 (GRCm39) missense probably damaging 1.00
R7426:Fcgbp UTSW 7 27,785,949 (GRCm39) missense probably benign 0.00
R7459:Fcgbp UTSW 7 27,806,710 (GRCm39) missense possibly damaging 0.65
R7475:Fcgbp UTSW 7 27,802,401 (GRCm39) missense probably damaging 0.99
R7505:Fcgbp UTSW 7 27,789,099 (GRCm39) missense probably damaging 0.97
R7517:Fcgbp UTSW 7 27,784,794 (GRCm39) missense probably damaging 1.00
R7519:Fcgbp UTSW 7 27,785,724 (GRCm39) missense probably damaging 1.00
R7524:Fcgbp UTSW 7 27,802,391 (GRCm39) missense probably damaging 1.00
R7649:Fcgbp UTSW 7 27,790,928 (GRCm39) missense possibly damaging 0.88
R7782:Fcgbp UTSW 7 27,784,460 (GRCm39) nonsense probably null
R7820:Fcgbp UTSW 7 27,819,784 (GRCm39) missense probably benign 0.01
R7831:Fcgbp UTSW 7 27,806,404 (GRCm39) missense probably damaging 0.98
R7835:Fcgbp UTSW 7 27,816,632 (GRCm39) missense possibly damaging 0.64
R7947:Fcgbp UTSW 7 27,803,595 (GRCm39) critical splice donor site probably null
R8086:Fcgbp UTSW 7 27,813,389 (GRCm39) missense probably damaging 1.00
R8137:Fcgbp UTSW 7 27,804,496 (GRCm39) missense probably damaging 1.00
R8154:Fcgbp UTSW 7 27,784,507 (GRCm39) missense probably benign 0.00
R8169:Fcgbp UTSW 7 27,784,919 (GRCm39) critical splice donor site probably null
R8176:Fcgbp UTSW 7 27,791,174 (GRCm39) missense possibly damaging 0.88
R8193:Fcgbp UTSW 7 27,804,276 (GRCm39) missense probably damaging 1.00
R8313:Fcgbp UTSW 7 27,785,769 (GRCm39) missense probably benign 0.00
R8350:Fcgbp UTSW 7 27,793,614 (GRCm39) missense probably benign 0.02
R8382:Fcgbp UTSW 7 27,816,762 (GRCm39) missense probably benign 0.00
R8393:Fcgbp UTSW 7 27,806,815 (GRCm39) missense probably benign 0.18
R8438:Fcgbp UTSW 7 27,789,231 (GRCm39) missense probably benign 0.25
R8489:Fcgbp UTSW 7 27,804,435 (GRCm39) missense possibly damaging 0.94
R8495:Fcgbp UTSW 7 27,785,978 (GRCm39) missense probably damaging 1.00
R8707:Fcgbp UTSW 7 27,819,920 (GRCm39) missense probably benign 0.01
R8736:Fcgbp UTSW 7 27,805,621 (GRCm39) missense probably benign 0.05
R8816:Fcgbp UTSW 7 27,784,412 (GRCm39) missense probably benign 0.09
R8905:Fcgbp UTSW 7 27,785,934 (GRCm39) missense probably damaging 1.00
R9031:Fcgbp UTSW 7 27,790,908 (GRCm39) missense possibly damaging 0.89
R9063:Fcgbp UTSW 7 27,791,277 (GRCm39) missense probably damaging 1.00
R9180:Fcgbp UTSW 7 27,803,198 (GRCm39) nonsense probably null
R9262:Fcgbp UTSW 7 27,819,952 (GRCm39) missense probably damaging 1.00
R9439:Fcgbp UTSW 7 27,803,436 (GRCm39) missense possibly damaging 0.60
R9526:Fcgbp UTSW 7 27,790,937 (GRCm39) missense probably damaging 1.00
R9603:Fcgbp UTSW 7 27,802,563 (GRCm39) missense probably damaging 1.00
R9635:Fcgbp UTSW 7 27,800,832 (GRCm39) missense probably benign 0.40
R9703:Fcgbp UTSW 7 27,806,400 (GRCm39) missense probably damaging 0.98
R9711:Fcgbp UTSW 7 27,793,000 (GRCm39) missense probably benign 0.00
R9733:Fcgbp UTSW 7 27,803,012 (GRCm39) missense probably damaging 1.00
RF002:Fcgbp UTSW 7 27,789,180 (GRCm39) missense probably benign
X0028:Fcgbp UTSW 7 27,803,445 (GRCm39) missense possibly damaging 0.48
Z1186:Fcgbp UTSW 7 27,791,072 (GRCm39) missense probably benign
Z1186:Fcgbp UTSW 7 27,789,180 (GRCm39) missense probably benign
Z1186:Fcgbp UTSW 7 27,785,616 (GRCm39) missense probably benign
Z1186:Fcgbp UTSW 7 27,803,309 (GRCm39) missense probably benign 0.09
Z1186:Fcgbp UTSW 7 27,792,770 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- TGCCCTTCCATCTGGACCAGAAAC -3'
(R):5'- GGGTTCCTTGCTGAGTAACTGTCAC -3'

Sequencing Primer
(F):5'- CTGGACCAGAAACTCAGTGTTTAC -3'
(R):5'- GCTGAGTAACTGTCACTATCCAAG -3'
Posted On 2014-05-23