Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alg6 |
T |
A |
4: 99,634,584 (GRCm39) |
C109S |
probably damaging |
Het |
Arhgdia |
C |
A |
11: 120,471,039 (GRCm39) |
E53D |
probably benign |
Het |
Ccr4 |
A |
C |
9: 114,321,401 (GRCm39) |
C221W |
probably damaging |
Het |
Ces2a |
G |
A |
8: 105,466,910 (GRCm39) |
|
probably null |
Het |
Chpf2 |
G |
T |
5: 24,796,709 (GRCm39) |
E552* |
probably null |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Dnmt1 |
C |
T |
9: 20,838,442 (GRCm39) |
R207H |
probably benign |
Het |
Dock2 |
A |
G |
11: 34,451,168 (GRCm39) |
|
probably null |
Het |
Esr1 |
A |
T |
10: 4,951,346 (GRCm39) |
T575S |
probably benign |
Het |
Fancc |
A |
G |
13: 63,545,965 (GRCm39) |
C93R |
probably damaging |
Het |
Foxj3 |
A |
T |
4: 119,482,114 (GRCm39) |
R523W |
unknown |
Het |
Fryl |
C |
T |
5: 73,227,220 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
A |
C |
2: 82,779,836 (GRCm39) |
H194P |
probably benign |
Het |
Gaa |
G |
A |
11: 119,165,559 (GRCm39) |
V350I |
probably damaging |
Het |
Gpn3 |
T |
A |
5: 122,519,257 (GRCm39) |
I152N |
probably damaging |
Het |
H2-M10.3 |
T |
A |
17: 36,678,417 (GRCm39) |
H136L |
probably benign |
Het |
H4c16 |
C |
T |
6: 136,781,335 (GRCm39) |
|
probably benign |
Het |
Hspg2 |
A |
G |
4: 137,239,953 (GRCm39) |
D507G |
probably damaging |
Het |
Jcad |
A |
G |
18: 4,674,422 (GRCm39) |
E728G |
probably benign |
Het |
Kat14 |
G |
A |
2: 144,244,365 (GRCm39) |
R406H |
possibly damaging |
Het |
Kcnma1 |
G |
T |
14: 23,413,900 (GRCm39) |
D863E |
probably damaging |
Het |
Lrp1 |
A |
G |
10: 127,410,355 (GRCm39) |
Y1464H |
probably damaging |
Het |
Map4 |
T |
C |
9: 109,893,485 (GRCm39) |
S584P |
probably damaging |
Het |
Nlrp4f |
G |
A |
13: 65,347,085 (GRCm39) |
L58F |
probably damaging |
Het |
Nlrp6 |
A |
G |
7: 140,503,413 (GRCm39) |
I506M |
probably benign |
Het |
Nudt17 |
G |
A |
3: 96,613,780 (GRCm39) |
R266W |
probably damaging |
Het |
Or4a47 |
A |
G |
2: 89,665,740 (GRCm39) |
L183P |
probably damaging |
Het |
Or4a69 |
A |
G |
2: 89,313,018 (GRCm39) |
S154P |
probably damaging |
Het |
Or52h9 |
A |
G |
7: 104,202,780 (GRCm39) |
Y218C |
probably damaging |
Het |
Plcb4 |
A |
G |
2: 135,803,714 (GRCm39) |
E529G |
probably benign |
Het |
Prss32 |
A |
T |
17: 24,075,210 (GRCm39) |
I187F |
possibly damaging |
Het |
Prss55 |
A |
T |
14: 64,316,818 (GRCm39) |
I108K |
probably damaging |
Het |
Rho |
A |
T |
6: 115,912,158 (GRCm39) |
M207L |
possibly damaging |
Het |
Slc12a1 |
A |
G |
2: 125,012,611 (GRCm39) |
D291G |
probably damaging |
Het |
Slco2b1 |
A |
C |
7: 99,309,330 (GRCm39) |
|
probably null |
Het |
Stx11 |
T |
A |
10: 12,817,661 (GRCm39) |
D21V |
possibly damaging |
Het |
Svep1 |
T |
A |
4: 58,115,807 (GRCm39) |
Y962F |
possibly damaging |
Het |
Tbx5 |
G |
T |
5: 119,974,972 (GRCm39) |
|
probably benign |
Het |
Tcf12 |
C |
A |
9: 71,830,039 (GRCm39) |
G141W |
probably damaging |
Het |
Tmtc2 |
A |
G |
10: 105,206,407 (GRCm39) |
M296T |
probably damaging |
Het |
Trim13 |
T |
A |
14: 61,842,999 (GRCm39) |
S339T |
probably benign |
Het |
Ugt1a7c |
A |
G |
1: 88,023,239 (GRCm39) |
K133E |
possibly damaging |
Het |
Usp40 |
A |
G |
1: 87,877,739 (GRCm39) |
V1050A |
probably benign |
Het |
Vmn2r86 |
T |
G |
10: 130,288,781 (GRCm39) |
N240T |
probably damaging |
Het |
Wdr36 |
T |
C |
18: 32,992,314 (GRCm39) |
V617A |
possibly damaging |
Het |
Wdr38 |
A |
T |
2: 38,888,424 (GRCm39) |
N7I |
probably damaging |
Het |
Wdr6 |
T |
C |
9: 108,452,704 (GRCm39) |
Y393C |
probably damaging |
Het |
Zfp619 |
A |
T |
7: 39,183,609 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Rcl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Rcl1
|
APN |
19 |
29,098,662 (GRCm39) |
splice site |
probably null |
|
IGL01514:Rcl1
|
APN |
19 |
29,120,698 (GRCm39) |
utr 3 prime |
probably benign |
|
R0512:Rcl1
|
UTSW |
19 |
29,105,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R2249:Rcl1
|
UTSW |
19 |
29,099,268 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3610:Rcl1
|
UTSW |
19 |
29,095,630 (GRCm39) |
missense |
probably benign |
0.00 |
R4415:Rcl1
|
UTSW |
19 |
29,095,762 (GRCm39) |
missense |
probably benign |
0.01 |
R5324:Rcl1
|
UTSW |
19 |
29,105,401 (GRCm39) |
missense |
probably benign |
0.23 |
R5679:Rcl1
|
UTSW |
19 |
29,098,658 (GRCm39) |
splice site |
probably null |
|
R5988:Rcl1
|
UTSW |
19 |
29,099,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R7332:Rcl1
|
UTSW |
19 |
29,108,096 (GRCm39) |
missense |
probably benign |
0.03 |
R7936:Rcl1
|
UTSW |
19 |
29,095,805 (GRCm39) |
splice site |
probably null |
|
R8353:Rcl1
|
UTSW |
19 |
29,093,159 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8453:Rcl1
|
UTSW |
19 |
29,093,159 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9282:Rcl1
|
UTSW |
19 |
29,093,170 (GRCm39) |
missense |
probably damaging |
0.99 |
R9747:Rcl1
|
UTSW |
19 |
29,105,482 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Rcl1
|
UTSW |
19 |
29,079,017 (GRCm39) |
missense |
probably benign |
|
|