Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
T |
19: 8,992,615 (GRCm39) |
D4633V |
probably damaging |
Het |
Akap6 |
T |
C |
12: 53,187,578 (GRCm39) |
F1664S |
possibly damaging |
Het |
Arhgef28 |
T |
C |
13: 98,103,604 (GRCm39) |
M803V |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,008,134 (GRCm39) |
|
probably null |
Het |
Bltp2 |
A |
T |
11: 78,158,993 (GRCm39) |
Q433L |
probably damaging |
Het |
Ccdc73 |
T |
A |
2: 104,761,390 (GRCm39) |
L130* |
probably null |
Het |
Ccdc73 |
A |
G |
2: 104,829,504 (GRCm39) |
E1059G |
probably damaging |
Het |
Ccer2 |
A |
C |
7: 28,456,708 (GRCm39) |
S151R |
possibly damaging |
Het |
Cep128 |
T |
A |
12: 91,197,603 (GRCm39) |
H406L |
probably benign |
Het |
Cep135 |
A |
G |
5: 76,745,275 (GRCm39) |
D229G |
probably benign |
Het |
Cpvl |
T |
A |
6: 53,931,596 (GRCm39) |
D103V |
probably benign |
Het |
Crppa |
T |
A |
12: 36,571,995 (GRCm39) |
L301Q |
probably damaging |
Het |
Cstdc6 |
C |
A |
16: 36,142,194 (GRCm39) |
G61C |
probably damaging |
Het |
Disp3 |
G |
A |
4: 148,343,210 (GRCm39) |
A567V |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,343,737 (GRCm39) |
I2379T |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,072,027 (GRCm39) |
Y2433C |
probably damaging |
Het |
Dock3 |
A |
G |
9: 106,985,620 (GRCm39) |
I85T |
probably benign |
Het |
Dock9 |
A |
C |
14: 121,829,242 (GRCm39) |
S1380A |
probably benign |
Het |
Erbin |
T |
C |
13: 104,022,711 (GRCm39) |
T43A |
probably benign |
Het |
Fastkd3 |
T |
C |
13: 68,733,360 (GRCm39) |
V502A |
possibly damaging |
Het |
Fn1 |
T |
C |
1: 71,690,784 (GRCm39) |
H59R |
probably damaging |
Het |
Fsd2 |
A |
G |
7: 81,209,407 (GRCm39) |
V145A |
possibly damaging |
Het |
Fzr1 |
A |
G |
10: 81,206,153 (GRCm39) |
V178A |
probably damaging |
Het |
Gnpnat1 |
T |
C |
14: 45,618,455 (GRCm39) |
R116G |
probably damaging |
Het |
Grm7 |
T |
A |
6: 110,891,472 (GRCm39) |
V235E |
probably damaging |
Het |
Hdac4 |
A |
C |
1: 91,862,367 (GRCm39) |
N1002K |
probably damaging |
Het |
Hey1 |
C |
T |
3: 8,729,957 (GRCm39) |
A167T |
probably benign |
Het |
Hrnr |
A |
G |
3: 93,239,911 (GRCm39) |
N3383S |
unknown |
Het |
Ints2 |
A |
T |
11: 86,108,626 (GRCm39) |
V907D |
probably benign |
Het |
Jchain |
T |
A |
5: 88,669,326 (GRCm39) |
Q109L |
probably damaging |
Het |
Klhdc7a |
A |
T |
4: 139,693,335 (GRCm39) |
Y537* |
probably null |
Het |
Klra1 |
C |
T |
6: 130,354,742 (GRCm39) |
S92N |
probably benign |
Het |
Krt31 |
C |
T |
11: 99,940,406 (GRCm39) |
G150S |
probably benign |
Het |
Lrrc71 |
G |
A |
3: 87,649,950 (GRCm39) |
T326M |
probably benign |
Het |
Lrrn4 |
T |
C |
2: 132,712,363 (GRCm39) |
T487A |
probably benign |
Het |
Map4k5 |
T |
G |
12: 69,889,686 (GRCm39) |
R198S |
probably damaging |
Het |
Men1 |
G |
A |
19: 6,388,867 (GRCm39) |
C354Y |
probably damaging |
Het |
Ms4a18 |
A |
T |
19: 10,991,019 (GRCm39) |
V25E |
probably damaging |
Het |
Mutyh |
T |
A |
4: 116,676,565 (GRCm39) |
S512R |
possibly damaging |
Het |
Myh10 |
G |
T |
11: 68,705,322 (GRCm39) |
A1947S |
possibly damaging |
Het |
Nfasc |
T |
C |
1: 132,538,624 (GRCm39) |
D427G |
probably damaging |
Het |
Nlrp9c |
A |
G |
7: 26,077,481 (GRCm39) |
M767T |
probably benign |
Het |
Nrbp1 |
T |
C |
5: 31,402,735 (GRCm39) |
L185P |
probably damaging |
Het |
Pcdh9 |
G |
A |
14: 94,125,741 (GRCm39) |
P143L |
probably damaging |
Het |
Pcsk6 |
A |
T |
7: 65,577,035 (GRCm39) |
M158L |
possibly damaging |
Het |
Pkd1 |
G |
T |
17: 24,795,566 (GRCm39) |
|
probably null |
Het |
Plk4 |
A |
T |
3: 40,760,252 (GRCm39) |
S383C |
possibly damaging |
Het |
Plxna2 |
T |
C |
1: 194,326,297 (GRCm39) |
L77P |
probably damaging |
Het |
Pnpla6 |
A |
T |
8: 3,592,370 (GRCm39) |
T1209S |
probably benign |
Het |
Prdm2 |
A |
G |
4: 142,859,079 (GRCm39) |
S1404P |
possibly damaging |
Het |
Preb |
T |
C |
5: 31,116,157 (GRCm39) |
D150G |
probably damaging |
Het |
Prrt2 |
A |
G |
7: 126,617,902 (GRCm39) |
V59A |
probably benign |
Het |
Prss40 |
T |
C |
1: 34,597,095 (GRCm39) |
N151S |
possibly damaging |
Het |
Ptprt |
G |
T |
2: 161,400,818 (GRCm39) |
A1053D |
probably damaging |
Het |
Ptprt |
A |
G |
2: 161,608,241 (GRCm39) |
V685A |
possibly damaging |
Het |
Rnaset2b |
T |
A |
17: 7,263,876 (GRCm39) |
V87E |
probably benign |
Het |
Rnf213 |
G |
A |
11: 119,331,933 (GRCm39) |
E2381K |
probably damaging |
Het |
Sectm1a |
A |
T |
11: 120,960,506 (GRCm39) |
I103N |
probably damaging |
Het |
Selp |
T |
A |
1: 163,970,327 (GRCm39) |
L597Q |
probably damaging |
Het |
Sema6a |
T |
C |
18: 47,433,209 (GRCm39) |
D74G |
probably damaging |
Het |
Serpinb9b |
T |
C |
13: 33,213,542 (GRCm39) |
V33A |
probably benign |
Het |
Setd1b |
A |
T |
5: 123,285,769 (GRCm39) |
T272S |
unknown |
Het |
Sgf29 |
G |
C |
7: 126,248,649 (GRCm39) |
|
probably null |
Het |
Slc4a10 |
C |
A |
2: 62,098,548 (GRCm39) |
Q561K |
probably damaging |
Het |
Slc4a5 |
T |
C |
6: 83,250,214 (GRCm39) |
I649T |
possibly damaging |
Het |
Slc5a7 |
A |
G |
17: 54,600,863 (GRCm39) |
Y91H |
probably damaging |
Het |
Styxl1 |
T |
C |
5: 135,785,976 (GRCm39) |
Y23C |
probably damaging |
Het |
Tbc1d24 |
A |
G |
17: 24,425,846 (GRCm39) |
V490A |
possibly damaging |
Het |
Tbpl2 |
A |
T |
2: 23,984,744 (GRCm39) |
F133L |
probably benign |
Het |
Tnfrsf22 |
T |
C |
7: 143,192,126 (GRCm39) |
|
probably benign |
Het |
Top2b |
A |
G |
14: 16,398,916 (GRCm38) |
E512G |
probably damaging |
Het |
Trgc3 |
C |
A |
13: 19,445,164 (GRCm39) |
F37L |
probably damaging |
Het |
Ttc17 |
T |
A |
2: 94,194,690 (GRCm39) |
H561L |
probably benign |
Het |
Ttll4 |
G |
T |
1: 74,724,527 (GRCm39) |
V566L |
possibly damaging |
Het |
Ubqlnl |
A |
G |
7: 103,797,692 (GRCm39) |
Y602H |
probably benign |
Het |
Vmn1r231 |
T |
A |
17: 21,110,212 (GRCm39) |
E234D |
probably damaging |
Het |
Wbp11 |
A |
G |
6: 136,797,583 (GRCm39) |
S279P |
probably damaging |
Het |
Wdr6 |
A |
G |
9: 108,453,733 (GRCm39) |
L50P |
probably damaging |
Het |
Zfp715 |
A |
C |
7: 42,948,073 (GRCm39) |
I629S |
possibly damaging |
Het |
|
Other mutations in Rfx4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Rfx4
|
APN |
10 |
84,676,063 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00334:Rfx4
|
APN |
10 |
84,615,917 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00928:Rfx4
|
APN |
10 |
84,675,978 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01063:Rfx4
|
APN |
10 |
84,704,246 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01490:Rfx4
|
APN |
10 |
84,676,715 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02390:Rfx4
|
APN |
10 |
84,676,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02454:Rfx4
|
APN |
10 |
84,675,970 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0099:Rfx4
|
UTSW |
10 |
84,730,168 (GRCm39) |
missense |
probably benign |
|
R0503:Rfx4
|
UTSW |
10 |
84,730,196 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0924:Rfx4
|
UTSW |
10 |
84,704,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R0930:Rfx4
|
UTSW |
10 |
84,704,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R1386:Rfx4
|
UTSW |
10 |
84,699,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R1715:Rfx4
|
UTSW |
10 |
84,680,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R1738:Rfx4
|
UTSW |
10 |
84,716,839 (GRCm39) |
critical splice donor site |
probably null |
|
R3717:Rfx4
|
UTSW |
10 |
84,716,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R4231:Rfx4
|
UTSW |
10 |
84,650,558 (GRCm39) |
missense |
probably benign |
0.03 |
R4300:Rfx4
|
UTSW |
10 |
84,740,966 (GRCm39) |
missense |
probably damaging |
0.98 |
R4581:Rfx4
|
UTSW |
10 |
84,680,164 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4582:Rfx4
|
UTSW |
10 |
84,680,164 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4618:Rfx4
|
UTSW |
10 |
84,716,760 (GRCm39) |
missense |
probably benign |
0.01 |
R5156:Rfx4
|
UTSW |
10 |
84,704,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R5185:Rfx4
|
UTSW |
10 |
84,699,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5377:Rfx4
|
UTSW |
10 |
84,696,406 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5601:Rfx4
|
UTSW |
10 |
84,634,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5879:Rfx4
|
UTSW |
10 |
84,650,625 (GRCm39) |
critical splice donor site |
probably null |
|
R5996:Rfx4
|
UTSW |
10 |
84,675,881 (GRCm39) |
nonsense |
probably null |
|
R6358:Rfx4
|
UTSW |
10 |
84,680,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Rfx4
|
UTSW |
10 |
84,676,092 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7248:Rfx4
|
UTSW |
10 |
84,740,919 (GRCm39) |
missense |
probably benign |
0.05 |
R7427:Rfx4
|
UTSW |
10 |
84,731,876 (GRCm39) |
missense |
probably benign |
0.28 |
R7428:Rfx4
|
UTSW |
10 |
84,731,876 (GRCm39) |
missense |
probably benign |
0.28 |
R7514:Rfx4
|
UTSW |
10 |
84,716,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R7576:Rfx4
|
UTSW |
10 |
84,699,213 (GRCm39) |
missense |
probably damaging |
0.98 |
R8002:Rfx4
|
UTSW |
10 |
84,676,721 (GRCm39) |
missense |
probably damaging |
0.97 |
R8838:Rfx4
|
UTSW |
10 |
84,676,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R8938:Rfx4
|
UTSW |
10 |
84,675,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R9359:Rfx4
|
UTSW |
10 |
84,740,921 (GRCm39) |
missense |
probably benign |
0.00 |
R9513:Rfx4
|
UTSW |
10 |
84,674,050 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
RF010:Rfx4
|
UTSW |
10 |
84,694,351 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF014:Rfx4
|
UTSW |
10 |
84,694,353 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF015:Rfx4
|
UTSW |
10 |
84,694,353 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF023:Rfx4
|
UTSW |
10 |
84,694,349 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF030:Rfx4
|
UTSW |
10 |
84,694,344 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF035:Rfx4
|
UTSW |
10 |
84,694,344 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF046:Rfx4
|
UTSW |
10 |
84,694,345 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF060:Rfx4
|
UTSW |
10 |
84,694,358 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF062:Rfx4
|
UTSW |
10 |
84,694,345 (GRCm39) |
critical splice acceptor site |
probably benign |
|
X0024:Rfx4
|
UTSW |
10 |
84,615,938 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1177:Rfx4
|
UTSW |
10 |
84,731,955 (GRCm39) |
missense |
probably benign |
0.30 |
Z1177:Rfx4
|
UTSW |
10 |
84,650,548 (GRCm39) |
missense |
possibly damaging |
0.85 |
|