Incidental Mutation 'R8137:Fcgbp'
ID 632302
Institutional Source Beutler Lab
Gene Symbol Fcgbp
Ensembl Gene ENSMUSG00000047730
Gene Name Fc fragment of IgG binding protein
Synonyms A430096B05Rik
MMRRC Submission 067565-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8137 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 27770661-27820287 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 27804496 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Serine at position 1868 (Y1868S)
Ref Sequence ENSEMBL: ENSMUSP00000075945 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076648] [ENSMUST00000138392]
AlphaFold E9Q0B5
Predicted Effect probably damaging
Transcript: ENSMUST00000076648
AA Change: Y1868S

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000075945
Gene: ENSMUSG00000047730
AA Change: Y1868S

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 probably damaging
Transcript: ENSMUST00000138392
AA Change: Y1868S

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000114271
Gene: ENSMUSG00000047730
AA Change: Y1868S

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
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.6%
  • 10x: 98.8%
  • 20x: 96.4%
Validation Efficiency 100% (56/56)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ankfn1 T G 11: 89,344,003 (GRCm39) Q326H probably benign Het
Carf G A 1: 60,187,124 (GRCm39) V576I probably benign Het
Ccnl1 C T 3: 65,865,291 (GRCm39) D87N possibly damaging Het
Cgref1 T A 5: 31,091,749 (GRCm39) D111V possibly damaging Het
Cnot4 G A 6: 35,023,222 (GRCm39) P567S unknown Het
Cyp7b1 A T 3: 18,151,765 (GRCm39) D149E probably benign Het
Dcc A T 18: 71,511,783 (GRCm39) D877E probably benign Het
Dhx8 T A 11: 101,654,808 (GRCm39) I1032N probably damaging Het
Dnah7b A G 1: 46,272,913 (GRCm39) Y2347C probably damaging Het
Dtx3 A G 10: 127,029,041 (GRCm39) S63P possibly damaging Het
Dyrk2 C T 10: 118,695,789 (GRCm39) E490K probably benign Het
Foxa2 T C 2: 147,885,768 (GRCm39) H355R probably benign Het
Fpr-rs7 A G 17: 20,334,055 (GRCm39) V145A possibly damaging Het
Gm14137 A T 2: 119,005,837 (GRCm39) E132V probably benign Het
Gpn2 T C 4: 133,315,873 (GRCm39) S211P possibly damaging Het
Greb1l A T 18: 10,474,357 (GRCm39) Q224L possibly damaging Het
Gspt1 A G 16: 11,058,532 (GRCm39) V144A probably benign Het
Ifi204 A G 1: 173,589,188 (GRCm39) I81T possibly damaging Het
Il27ra T A 8: 84,767,720 (GRCm39) probably null Het
Kif21a T C 15: 90,852,645 (GRCm39) T862A probably benign Het
Klf2 T C 8: 73,074,088 (GRCm39) probably null Het
Kmt2e A G 5: 23,706,952 (GRCm39) Y1505C probably damaging Het
Mcm9 T C 10: 53,499,076 (GRCm39) T216A Het
Muc16 T C 9: 18,556,972 (GRCm39) E3107G unknown Het
Ncor2 C T 5: 125,114,957 (GRCm39) V169I Het
Oas3 T C 5: 120,915,565 (GRCm39) Q42R probably benign Het
Or2l5 A G 16: 19,333,846 (GRCm39) V180A possibly damaging Het
Or4p8 T C 2: 88,727,013 (GRCm39) *309W probably null Het
Pde10a A G 17: 9,193,647 (GRCm39) Y693C possibly damaging Het
Pde11a T C 2: 76,041,383 (GRCm39) E429G possibly damaging Het
Pramel23 A G 4: 143,425,835 (GRCm39) F36S probably damaging Het
Pygo1 A G 9: 72,852,140 (GRCm39) H109R probably damaging Het
Rbsn A T 6: 92,167,003 (GRCm39) V547D probably benign Het
Ros1 A G 10: 52,001,933 (GRCm39) I1084T possibly damaging Het
Sis T C 3: 72,796,378 (GRCm39) D1801G probably benign Het
Slco4c1 C T 1: 96,748,970 (GRCm39) G649E probably damaging Het
Spmip10 A G 18: 56,727,653 (GRCm39) D117G probably damaging Het
Sptbn2 A T 19: 4,787,431 (GRCm39) I914F possibly damaging Het
Srebf2 C T 15: 82,062,966 (GRCm39) R468C probably damaging Het
Strc C T 2: 121,197,219 (GRCm39) G1503R probably damaging Het
Sv2c T A 13: 96,225,171 (GRCm39) Y46F probably damaging Het
Tctn3 A T 19: 40,593,785 (GRCm39) W462R probably damaging Het
Tjp3 T C 10: 81,109,525 (GRCm39) D857G probably benign Het
Tor1aip2 C T 1: 155,939,414 (GRCm39) T242I possibly damaging Het
Ttn T A 2: 76,800,273 (GRCm39) I312F unknown Het
Vezt T C 10: 93,775,154 (GRCm39) N94D Het
Vmn2r105 T C 17: 20,454,966 (GRCm39) N57D probably benign Het
Wdr59 T C 8: 112,212,011 (GRCm39) D353G Het
Ykt6 T C 11: 5,909,368 (GRCm39) V59A probably damaging Het
Ypel3 T G 7: 126,377,269 (GRCm39) V54G possibly damaging Het
Zfp386 T A 12: 116,023,268 (GRCm39) C329S possibly damaging Het
Zfp451 A T 1: 33,821,156 (GRCm39) L232H possibly damaging Het
Zfp648 A G 1: 154,081,110 (GRCm39) H423R probably damaging Het
Zfp729b T C 13: 67,740,861 (GRCm39) Y468C 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
R1772:Fcgbp UTSW 7 27,804,600 (GRCm39) missense possibly damaging 0.90
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
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'- ACGATGACCTGACTGCAGTG -3'
(R):5'- CCAAGGTGTATCTCTGTCAGGAG -3'

Sequencing Primer
(F):5'- AAACCTGAGGGCTGGAAAGTG -3'
(R):5'- ATCTCTGTCAGGAGGTGGAG -3'
Posted On 2020-06-30