Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
T |
7: 119,993,587 (GRCm39) |
K1269M |
possibly damaging |
Het |
Adgrl2 |
A |
T |
3: 148,564,585 (GRCm39) |
Y332N |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,627,777 (GRCm39) |
V3695I |
probably benign |
Het |
Aldh1l1 |
A |
T |
6: 90,575,257 (GRCm39) |
Y848F |
probably damaging |
Het |
Ambra1 |
T |
C |
2: 91,598,103 (GRCm39) |
V88A |
possibly damaging |
Het |
Ankrd12 |
C |
T |
17: 66,292,160 (GRCm39) |
R1091Q |
probably damaging |
Het |
Apob |
T |
G |
12: 8,055,087 (GRCm39) |
V1362G |
probably damaging |
Het |
Arhgap17 |
A |
G |
7: 122,905,661 (GRCm39) |
L328P |
probably damaging |
Het |
Arhgap27 |
A |
C |
11: 103,235,367 (GRCm39) |
V9G |
probably benign |
Het |
Arhgap33 |
A |
T |
7: 30,232,434 (GRCm39) |
D34E |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,873,259 (GRCm39) |
D14G |
probably benign |
Het |
Atf6b |
T |
C |
17: 34,872,703 (GRCm39) |
Y575H |
probably damaging |
Het |
Bcl2l2 |
T |
G |
14: 55,122,058 (GRCm39) |
S74A |
probably benign |
Het |
Begain |
T |
C |
12: 109,004,794 (GRCm39) |
T73A |
possibly damaging |
Het |
Bicdl1 |
C |
T |
5: 115,808,340 (GRCm39) |
R264Q |
probably damaging |
Het |
Ccdc180 |
A |
G |
4: 45,914,588 (GRCm39) |
D701G |
probably benign |
Het |
Cd200r4 |
G |
T |
16: 44,653,529 (GRCm39) |
V146L |
probably damaging |
Het |
Cd226 |
G |
A |
18: 89,265,322 (GRCm39) |
C200Y |
probably damaging |
Het |
Cdcp3 |
T |
C |
7: 130,879,352 (GRCm39) |
|
probably null |
Het |
Cdhr18 |
T |
C |
14: 13,866,032 (GRCm38) |
T286A |
|
Het |
Cdk12 |
A |
G |
11: 98,115,451 (GRCm39) |
N864S |
unknown |
Het |
Clcnkb |
A |
T |
4: 141,135,946 (GRCm39) |
L413Q |
probably damaging |
Het |
Cldn10 |
T |
C |
14: 119,099,255 (GRCm39) |
V123A |
possibly damaging |
Het |
Cnn1 |
T |
A |
9: 22,017,078 (GRCm39) |
|
probably null |
Het |
Cpa5 |
C |
A |
6: 30,630,829 (GRCm39) |
Q364K |
probably benign |
Het |
Cstdc5 |
T |
C |
16: 36,187,809 (GRCm39) |
I19V |
probably benign |
Het |
Ddx11 |
A |
G |
17: 66,437,766 (GRCm39) |
E164G |
probably benign |
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
Drc7 |
T |
A |
8: 95,804,549 (GRCm39) |
Y855N |
probably damaging |
Het |
Fam20b |
C |
A |
1: 156,529,968 (GRCm39) |
|
probably null |
Het |
Fip1l1 |
T |
A |
5: 74,748,736 (GRCm39) |
|
probably null |
Het |
Flt4 |
A |
G |
11: 49,525,125 (GRCm39) |
D657G |
probably null |
Het |
Fmo3 |
T |
A |
1: 162,781,857 (GRCm39) |
T499S |
possibly damaging |
Het |
Fyco1 |
C |
T |
9: 123,651,491 (GRCm39) |
G1190S |
probably benign |
Het |
Galnt17 |
C |
A |
5: 131,335,590 (GRCm39) |
|
probably benign |
Het |
Ggcx |
T |
C |
6: 72,404,987 (GRCm39) |
I465T |
probably damaging |
Het |
Gm7361 |
T |
A |
5: 26,466,116 (GRCm39) |
N159K |
probably damaging |
Het |
Golgb1 |
A |
G |
16: 36,695,663 (GRCm39) |
N54S |
unknown |
Het |
Grin2c |
G |
A |
11: 115,141,876 (GRCm39) |
P848S |
probably damaging |
Het |
Grina |
T |
C |
15: 76,133,287 (GRCm39) |
V285A |
probably damaging |
Het |
Gtpbp6 |
A |
G |
5: 110,252,478 (GRCm39) |
L381P |
probably damaging |
Het |
Herc2 |
G |
T |
7: 55,832,388 (GRCm39) |
G3028V |
probably damaging |
Het |
Ibsp |
A |
T |
5: 104,458,297 (GRCm39) |
Y278F |
probably damaging |
Het |
Ints4 |
T |
A |
7: 97,184,433 (GRCm39) |
L846* |
probably null |
Het |
Kif17 |
A |
G |
4: 138,021,077 (GRCm39) |
K849E |
probably benign |
Het |
Krt77 |
G |
A |
15: 101,777,806 (GRCm39) |
P83L |
probably benign |
Het |
Ky |
T |
G |
9: 102,419,491 (GRCm39) |
D499E |
probably damaging |
Het |
Lrp3 |
A |
T |
7: 34,902,051 (GRCm39) |
M610K |
probably damaging |
Het |
Lrrfip1 |
T |
A |
1: 91,019,338 (GRCm39) |
D156E |
probably benign |
Het |
Map6 |
C |
A |
7: 98,918,257 (GRCm39) |
H343Q |
probably benign |
Het |
Micu2 |
G |
T |
14: 58,191,606 (GRCm39) |
D148E |
probably benign |
Het |
Mks1 |
T |
A |
11: 87,747,428 (GRCm39) |
S153T |
probably benign |
Het |
Msantd5f3 |
A |
G |
4: 73,573,157 (GRCm39) |
Y132C |
probably damaging |
Het |
Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,214,363 (GRCm39) |
|
probably null |
Het |
Myh9 |
T |
C |
15: 77,667,672 (GRCm39) |
K587R |
probably benign |
Het |
Neb |
T |
C |
2: 52,086,368 (GRCm39) |
Y5478C |
probably damaging |
Het |
Nelfe |
G |
A |
17: 35,069,912 (GRCm39) |
|
probably null |
Het |
Nps |
T |
A |
7: 134,870,510 (GRCm39) |
L11I |
probably damaging |
Het |
Nsd1 |
A |
T |
13: 55,394,283 (GRCm39) |
D731V |
probably damaging |
Het |
Nup50 |
A |
G |
15: 84,817,859 (GRCm39) |
T93A |
probably benign |
Het |
Nup98 |
A |
T |
7: 101,844,248 (GRCm39) |
F29Y |
unknown |
Het |
Oprd1 |
A |
G |
4: 131,841,112 (GRCm39) |
I282T |
probably damaging |
Het |
Or4c103 |
T |
C |
2: 88,513,767 (GRCm39) |
H103R |
possibly damaging |
Het |
Or5p50 |
T |
C |
7: 107,421,782 (GRCm39) |
N298S |
probably benign |
Het |
Or6b3 |
A |
T |
1: 92,439,573 (GRCm39) |
M59K |
probably benign |
Het |
Or6d12 |
A |
G |
6: 116,492,936 (GRCm39) |
Y66C |
probably damaging |
Het |
Osbp2 |
T |
C |
11: 3,662,134 (GRCm39) |
I240V |
probably damaging |
Het |
Otub2 |
C |
A |
12: 103,359,163 (GRCm39) |
P84Q |
probably benign |
Het |
Parp9 |
A |
T |
16: 35,777,360 (GRCm39) |
I435F |
probably benign |
Het |
Pcdh18 |
C |
T |
3: 49,709,923 (GRCm39) |
R464H |
probably benign |
Het |
Pcsk6 |
G |
T |
7: 65,675,156 (GRCm39) |
|
probably null |
Het |
Ptgs2 |
G |
A |
1: 149,978,512 (GRCm39) |
R208Q |
probably benign |
Het |
Rab11b |
G |
A |
17: 33,968,841 (GRCm39) |
R51C |
probably damaging |
Het |
Rad1 |
A |
G |
15: 10,493,343 (GRCm39) |
I257V |
probably benign |
Het |
Rbms3 |
C |
T |
9: 116,415,085 (GRCm39) |
|
probably null |
Het |
Rxfp2 |
A |
T |
5: 149,983,364 (GRCm39) |
I300L |
probably benign |
Het |
Rxfp2 |
C |
A |
5: 149,983,368 (GRCm39) |
T301K |
probably benign |
Het |
Sars2 |
G |
T |
7: 28,443,733 (GRCm39) |
A112S |
probably benign |
Het |
Scn10a |
T |
C |
9: 119,442,616 (GRCm39) |
D1543G |
probably damaging |
Het |
Serpinb1b |
A |
G |
13: 33,271,406 (GRCm39) |
H59R |
probably benign |
Het |
Sgsm2 |
T |
A |
11: 74,745,319 (GRCm39) |
D661V |
possibly damaging |
Het |
Smad6 |
C |
A |
9: 63,927,688 (GRCm39) |
V207L |
probably damaging |
Het |
Son |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCAGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,183 (GRCm39) |
|
probably benign |
Het |
Spata31h1 |
A |
T |
10: 82,125,161 (GRCm39) |
D2616E |
probably benign |
Het |
Tenm2 |
C |
T |
11: 35,939,956 (GRCm39) |
R1390Q |
probably damaging |
Het |
Tmem132a |
T |
A |
19: 10,844,295 (GRCm39) |
Q101L |
probably damaging |
Het |
Tmem151a |
A |
G |
19: 5,132,801 (GRCm39) |
V135A |
probably damaging |
Het |
Trappc10 |
T |
C |
10: 78,046,262 (GRCm39) |
K443E |
probably damaging |
Het |
Trrap |
A |
T |
5: 144,779,517 (GRCm39) |
N3161I |
possibly damaging |
Het |
Tspan32 |
G |
T |
7: 142,558,863 (GRCm39) |
R6L |
possibly damaging |
Het |
Tut7 |
C |
G |
13: 59,936,364 (GRCm39) |
D1246H |
probably damaging |
Het |
Ugt2a2 |
T |
C |
5: 87,608,468 (GRCm39) |
D457G |
possibly damaging |
Het |
Ulk2 |
A |
T |
11: 61,725,657 (GRCm39) |
S140T |
possibly damaging |
Het |
Upf1 |
C |
T |
8: 70,792,695 (GRCm39) |
A338T |
possibly damaging |
Het |
Usp43 |
C |
T |
11: 67,774,110 (GRCm39) |
R460Q |
probably null |
Het |
Uxs1 |
A |
G |
1: 43,856,118 (GRCm39) |
|
probably benign |
Het |
Vmn1r59 |
A |
G |
7: 5,457,725 (GRCm39) |
C12R |
probably damaging |
Het |
Wdr64 |
A |
G |
1: 175,617,499 (GRCm39) |
D693G |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,920,839 (GRCm39) |
|
probably null |
Het |
Wnt2 |
G |
T |
6: 18,028,046 (GRCm39) |
R63S |
probably benign |
Het |
Zfp418 |
A |
T |
7: 7,184,562 (GRCm39) |
Q175L |
probably benign |
Het |
|
Other mutations in Cfhr4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00906:Cfhr4
|
APN |
1 |
139,659,312 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01088:Cfhr4
|
APN |
1 |
139,625,823 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01419:Cfhr4
|
APN |
1 |
139,667,382 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01552:Cfhr4
|
APN |
1 |
139,667,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01924:Cfhr4
|
APN |
1 |
139,666,944 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02032:Cfhr4
|
APN |
1 |
139,702,284 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02254:Cfhr4
|
APN |
1 |
139,661,143 (GRCm39) |
splice site |
probably benign |
|
IGL02318:Cfhr4
|
APN |
1 |
139,708,835 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02527:Cfhr4
|
APN |
1 |
139,680,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02531:Cfhr4
|
APN |
1 |
139,702,307 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02587:Cfhr4
|
APN |
1 |
139,629,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02644:Cfhr4
|
APN |
1 |
139,708,905 (GRCm39) |
start codon destroyed |
probably null |
0.63 |
IGL02852:Cfhr4
|
APN |
1 |
139,701,754 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02963:Cfhr4
|
APN |
1 |
139,659,334 (GRCm39) |
nonsense |
probably null |
|
IGL03084:Cfhr4
|
APN |
1 |
139,708,880 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0131:Cfhr4
|
UTSW |
1 |
139,682,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R0131:Cfhr4
|
UTSW |
1 |
139,682,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R0132:Cfhr4
|
UTSW |
1 |
139,682,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R0549:Cfhr4
|
UTSW |
1 |
139,667,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Cfhr4
|
UTSW |
1 |
139,667,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R0610:Cfhr4
|
UTSW |
1 |
139,629,584 (GRCm39) |
missense |
probably benign |
0.20 |
R1341:Cfhr4
|
UTSW |
1 |
139,660,131 (GRCm39) |
missense |
probably damaging |
0.98 |
R1460:Cfhr4
|
UTSW |
1 |
139,625,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R1544:Cfhr4
|
UTSW |
1 |
139,664,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R1873:Cfhr4
|
UTSW |
1 |
139,702,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R2032:Cfhr4
|
UTSW |
1 |
139,660,993 (GRCm39) |
splice site |
probably benign |
|
R2111:Cfhr4
|
UTSW |
1 |
139,702,417 (GRCm39) |
splice site |
probably benign |
|
R2179:Cfhr4
|
UTSW |
1 |
139,659,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Cfhr4
|
UTSW |
1 |
139,680,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R4356:Cfhr4
|
UTSW |
1 |
139,660,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R4747:Cfhr4
|
UTSW |
1 |
139,625,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R4838:Cfhr4
|
UTSW |
1 |
139,661,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R4867:Cfhr4
|
UTSW |
1 |
139,702,213 (GRCm39) |
critical splice donor site |
probably null |
|
R4910:Cfhr4
|
UTSW |
1 |
139,702,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R4911:Cfhr4
|
UTSW |
1 |
139,702,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R5050:Cfhr4
|
UTSW |
1 |
139,664,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R5120:Cfhr4
|
UTSW |
1 |
139,680,841 (GRCm39) |
missense |
probably benign |
0.39 |
R5259:Cfhr4
|
UTSW |
1 |
139,668,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R5504:Cfhr4
|
UTSW |
1 |
139,629,558 (GRCm39) |
missense |
probably benign |
0.18 |
R5825:Cfhr4
|
UTSW |
1 |
139,702,336 (GRCm39) |
splice site |
probably null |
|
R5949:Cfhr4
|
UTSW |
1 |
139,660,887 (GRCm39) |
missense |
probably damaging |
0.98 |
R6140:Cfhr4
|
UTSW |
1 |
139,660,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R6200:Cfhr4
|
UTSW |
1 |
139,682,073 (GRCm39) |
missense |
probably damaging |
0.97 |
R6254:Cfhr4
|
UTSW |
1 |
139,682,128 (GRCm39) |
missense |
probably damaging |
0.98 |
R6255:Cfhr4
|
UTSW |
1 |
139,680,749 (GRCm39) |
nonsense |
probably null |
|
R6334:Cfhr4
|
UTSW |
1 |
139,701,662 (GRCm39) |
splice site |
probably null |
|
R6611:Cfhr4
|
UTSW |
1 |
139,660,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Cfhr4
|
UTSW |
1 |
139,625,859 (GRCm39) |
missense |
probably benign |
0.20 |
R6800:Cfhr4
|
UTSW |
1 |
139,629,719 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6895:Cfhr4
|
UTSW |
1 |
139,668,210 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6904:Cfhr4
|
UTSW |
1 |
139,659,391 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6994:Cfhr4
|
UTSW |
1 |
139,664,668 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7173:Cfhr4
|
UTSW |
1 |
139,659,415 (GRCm39) |
nonsense |
probably null |
|
R7184:Cfhr4
|
UTSW |
1 |
139,660,822 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7192:Cfhr4
|
UTSW |
1 |
139,667,033 (GRCm39) |
missense |
probably damaging |
0.96 |
R7302:Cfhr4
|
UTSW |
1 |
139,667,436 (GRCm39) |
splice site |
probably null |
|
R7308:Cfhr4
|
UTSW |
1 |
139,682,041 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7735:Cfhr4
|
UTSW |
1 |
139,660,039 (GRCm39) |
critical splice donor site |
probably null |
|
R8006:Cfhr4
|
UTSW |
1 |
139,664,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R8045:Cfhr4
|
UTSW |
1 |
139,661,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R8188:Cfhr4
|
UTSW |
1 |
139,625,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R8339:Cfhr4
|
UTSW |
1 |
139,660,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R9156:Cfhr4
|
UTSW |
1 |
139,660,085 (GRCm39) |
missense |
probably damaging |
0.96 |
R9339:Cfhr4
|
UTSW |
1 |
139,682,044 (GRCm39) |
missense |
probably benign |
0.26 |
R9520:Cfhr4
|
UTSW |
1 |
139,682,135 (GRCm39) |
missense |
probably damaging |
0.99 |
R9525:Cfhr4
|
UTSW |
1 |
139,702,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R9554:Cfhr4
|
UTSW |
1 |
139,668,169 (GRCm39) |
missense |
probably benign |
0.04 |
R9635:Cfhr4
|
UTSW |
1 |
139,701,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R9669:Cfhr4
|
UTSW |
1 |
139,708,872 (GRCm39) |
missense |
probably damaging |
0.96 |
R9737:Cfhr4
|
UTSW |
1 |
139,708,872 (GRCm39) |
missense |
probably damaging |
0.96 |
X0009:Cfhr4
|
UTSW |
1 |
139,661,287 (GRCm39) |
missense |
probably benign |
0.08 |
X0024:Cfhr4
|
UTSW |
1 |
139,661,247 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Cfhr4
|
UTSW |
1 |
139,681,999 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Cfhr4
|
UTSW |
1 |
139,661,186 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cfhr4
|
UTSW |
1 |
139,625,994 (GRCm39) |
missense |
probably benign |
0.13 |
|