Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410004P03Rik |
A |
G |
12: 17,057,179 (GRCm39) |
F106S |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,581,957 (GRCm39) |
F4696I |
probably benign |
Het |
Ank2 |
T |
C |
3: 126,756,047 (GRCm39) |
I1073V |
probably damaging |
Het |
Card11 |
A |
T |
5: 140,884,033 (GRCm39) |
D415E |
probably damaging |
Het |
Clec16a |
G |
A |
16: 10,390,792 (GRCm39) |
|
probably null |
Het |
Coro2a |
T |
C |
4: 46,540,504 (GRCm39) |
T472A |
probably benign |
Het |
D130043K22Rik |
T |
A |
13: 25,069,574 (GRCm39) |
F878I |
probably damaging |
Het |
D5Ertd579e |
G |
T |
5: 36,787,127 (GRCm39) |
D80E |
probably damaging |
Het |
Ddrgk1 |
A |
T |
2: 130,506,481 (GRCm39) |
V2E |
possibly damaging |
Het |
Disp1 |
T |
C |
1: 182,867,896 (GRCm39) |
H1508R |
probably benign |
Het |
Dmtf1 |
T |
C |
5: 9,176,656 (GRCm39) |
N344S |
probably benign |
Het |
Eml5 |
A |
G |
12: 98,829,388 (GRCm39) |
V503A |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,406,429 (GRCm39) |
H1060R |
probably benign |
Het |
Fbxw8 |
C |
T |
5: 118,251,814 (GRCm39) |
R233Q |
probably damaging |
Het |
Fer1l4 |
T |
C |
2: 155,890,211 (GRCm39) |
K238R |
probably damaging |
Het |
Flg |
T |
A |
3: 93,187,357 (GRCm39) |
S270T |
probably benign |
Het |
Gm10801 |
TC |
TCGCC |
2: 98,494,151 (GRCm39) |
|
probably benign |
Het |
Gm3604 |
A |
T |
13: 62,519,659 (GRCm39) |
V32D |
probably damaging |
Het |
Gnl2 |
T |
G |
4: 124,948,022 (GRCm39) |
|
probably null |
Het |
Gpr162 |
A |
G |
6: 124,838,204 (GRCm39) |
S149P |
probably damaging |
Het |
Il2ra |
T |
A |
2: 11,652,790 (GRCm39) |
|
probably benign |
Het |
Kics2 |
T |
C |
10: 121,586,810 (GRCm39) |
L375P |
probably damaging |
Het |
Kmt5b |
T |
A |
19: 3,854,499 (GRCm39) |
M254K |
probably damaging |
Het |
Lrriq3 |
T |
C |
3: 154,835,039 (GRCm39) |
I258T |
probably benign |
Het |
Mbnl1 |
T |
C |
3: 60,523,165 (GRCm39) |
L328S |
probably damaging |
Het |
Mboat2 |
A |
G |
12: 25,001,430 (GRCm39) |
D277G |
possibly damaging |
Het |
Mug2 |
A |
G |
6: 122,014,005 (GRCm39) |
I364V |
probably benign |
Het |
Myh7 |
G |
A |
14: 55,226,315 (GRCm39) |
R442C |
probably damaging |
Het |
Nin |
A |
G |
12: 70,090,511 (GRCm39) |
L968P |
probably damaging |
Het |
Or1l8 |
T |
C |
2: 36,817,404 (GRCm39) |
T241A |
probably damaging |
Het |
Or5w14 |
A |
T |
2: 87,542,188 (GRCm39) |
Y21N |
probably benign |
Het |
Or8g53 |
T |
G |
9: 39,683,916 (GRCm39) |
Y60S |
probably damaging |
Het |
Per1 |
C |
T |
11: 68,993,730 (GRCm39) |
P403S |
probably damaging |
Het |
Ppip5k2 |
T |
C |
1: 97,661,730 (GRCm39) |
I723V |
possibly damaging |
Het |
Ptprg |
A |
G |
14: 12,153,943 (GRCm38) |
T555A |
probably benign |
Het |
Rgsl1 |
C |
T |
1: 153,703,194 (GRCm39) |
M187I |
probably benign |
Het |
Sec31a |
A |
G |
5: 100,517,453 (GRCm39) |
|
probably null |
Het |
Sptbn5 |
C |
T |
2: 119,889,898 (GRCm39) |
|
probably benign |
Het |
Sry |
C |
G |
Y: 2,662,975 (GRCm39) |
Q228H |
unknown |
Het |
Stx1b |
G |
A |
7: 127,407,077 (GRCm39) |
T206I |
possibly damaging |
Het |
Tsc22d4 |
T |
A |
5: 137,757,351 (GRCm39) |
M35K |
probably damaging |
Het |
Zc2hc1c |
A |
G |
12: 85,343,218 (GRCm39) |
K452E |
probably damaging |
Het |
Zfp386 |
A |
G |
12: 116,024,133 (GRCm39) |
N582S |
possibly damaging |
Het |
Zfp457 |
A |
G |
13: 67,440,976 (GRCm39) |
V437A |
possibly damaging |
Het |
Zfyve26 |
G |
A |
12: 79,315,501 (GRCm39) |
S1325F |
probably damaging |
Het |
|
Other mutations in Zfp599 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00580:Zfp599
|
APN |
9 |
22,160,768 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00845:Zfp599
|
APN |
9 |
22,162,814 (GRCm39) |
splice site |
probably benign |
|
R0136:Zfp599
|
UTSW |
9 |
22,161,038 (GRCm39) |
missense |
probably benign |
0.13 |
R0239:Zfp599
|
UTSW |
9 |
22,161,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Zfp599
|
UTSW |
9 |
22,161,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0421:Zfp599
|
UTSW |
9 |
22,161,843 (GRCm39) |
splice site |
probably benign |
|
R1699:Zfp599
|
UTSW |
9 |
22,161,700 (GRCm39) |
missense |
probably benign |
0.20 |
R1723:Zfp599
|
UTSW |
9 |
22,169,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Zfp599
|
UTSW |
9 |
22,162,845 (GRCm39) |
missense |
probably benign |
0.00 |
R4231:Zfp599
|
UTSW |
9 |
22,161,041 (GRCm39) |
nonsense |
probably null |
|
R4233:Zfp599
|
UTSW |
9 |
22,161,041 (GRCm39) |
nonsense |
probably null |
|
R4236:Zfp599
|
UTSW |
9 |
22,161,041 (GRCm39) |
nonsense |
probably null |
|
R4931:Zfp599
|
UTSW |
9 |
22,169,419 (GRCm39) |
missense |
probably damaging |
0.98 |
R5117:Zfp599
|
UTSW |
9 |
22,161,396 (GRCm39) |
nonsense |
probably null |
|
R5615:Zfp599
|
UTSW |
9 |
22,165,165 (GRCm39) |
missense |
probably benign |
|
R5759:Zfp599
|
UTSW |
9 |
22,160,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R5915:Zfp599
|
UTSW |
9 |
22,161,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R6188:Zfp599
|
UTSW |
9 |
22,161,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R6657:Zfp599
|
UTSW |
9 |
22,161,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Zfp599
|
UTSW |
9 |
22,161,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Zfp599
|
UTSW |
9 |
22,160,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R7071:Zfp599
|
UTSW |
9 |
22,169,392 (GRCm39) |
missense |
probably benign |
0.38 |
R7643:Zfp599
|
UTSW |
9 |
22,161,188 (GRCm39) |
missense |
probably benign |
0.19 |
R7714:Zfp599
|
UTSW |
9 |
22,161,811 (GRCm39) |
missense |
probably benign |
0.07 |
R7951:Zfp599
|
UTSW |
9 |
22,160,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7967:Zfp599
|
UTSW |
9 |
22,160,830 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8014:Zfp599
|
UTSW |
9 |
22,160,777 (GRCm39) |
missense |
probably benign |
0.03 |
R8187:Zfp599
|
UTSW |
9 |
22,161,111 (GRCm39) |
nonsense |
probably null |
|
R9562:Zfp599
|
UTSW |
9 |
22,160,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R9684:Zfp599
|
UTSW |
9 |
22,160,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R9722:Zfp599
|
UTSW |
9 |
22,160,741 (GRCm39) |
missense |
probably damaging |
0.96 |
RF005:Zfp599
|
UTSW |
9 |
22,165,180 (GRCm39) |
missense |
probably benign |
0.03 |
RF024:Zfp599
|
UTSW |
9 |
22,165,180 (GRCm39) |
missense |
probably benign |
0.03 |
|