Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm5 |
C |
A |
7: 119,137,374 (GRCm39) |
P397T |
probably damaging |
Het |
Adamts14 |
C |
T |
10: 61,106,781 (GRCm39) |
R113K |
probably benign |
Het |
Baiap2 |
G |
A |
11: 119,897,201 (GRCm39) |
V519I |
probably benign |
Het |
Ccna1 |
C |
T |
3: 54,953,069 (GRCm39) |
A233T |
probably benign |
Het |
Cdon |
T |
C |
9: 35,389,931 (GRCm39) |
Y862H |
probably damaging |
Het |
Crygc |
C |
T |
1: 65,111,030 (GRCm39) |
A86T |
probably benign |
Het |
Cyb5d2 |
T |
G |
11: 72,669,662 (GRCm39) |
N232T |
probably benign |
Het |
Dnah14 |
C |
A |
1: 181,465,412 (GRCm39) |
H1193N |
probably benign |
Het |
Dnah17 |
T |
G |
11: 117,992,201 (GRCm39) |
E1170A |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,162,806 (GRCm39) |
Y384C |
probably damaging |
Het |
Fat4 |
G |
A |
3: 39,053,278 (GRCm39) |
V4091I |
probably benign |
Het |
Fbxl12 |
C |
A |
9: 20,550,160 (GRCm39) |
R165L |
possibly damaging |
Het |
G6pc2 |
A |
G |
2: 69,050,441 (GRCm39) |
Y22C |
probably benign |
Het |
Gpihbp1 |
A |
T |
15: 75,469,828 (GRCm39) |
Q181L |
possibly damaging |
Het |
H2bc4 |
C |
T |
13: 23,868,552 (GRCm39) |
S113L |
probably damaging |
Het |
Hhatl |
A |
T |
9: 121,619,965 (GRCm39) |
|
probably benign |
Het |
Iars1 |
C |
A |
13: 49,841,738 (GRCm39) |
S75R |
probably benign |
Het |
Igfn1 |
T |
A |
1: 135,902,573 (GRCm39) |
I375F |
possibly damaging |
Het |
Itih4 |
A |
G |
14: 30,618,529 (GRCm39) |
I647V |
probably benign |
Het |
Jmjd1c |
T |
A |
10: 67,060,616 (GRCm39) |
C703S |
probably benign |
Het |
L3mbtl2 |
C |
T |
15: 81,569,615 (GRCm39) |
T619I |
possibly damaging |
Het |
Lct |
T |
C |
1: 128,231,684 (GRCm39) |
T722A |
possibly damaging |
Het |
Meioc |
C |
T |
11: 102,567,686 (GRCm39) |
Q827* |
probably null |
Het |
Meis2 |
T |
C |
2: 115,694,986 (GRCm39) |
S386G |
probably benign |
Het |
Mroh8 |
T |
A |
2: 157,071,876 (GRCm39) |
D543V |
probably damaging |
Het |
Ms4a13 |
C |
T |
19: 11,161,200 (GRCm39) |
R113H |
probably benign |
Het |
Myrfl |
T |
C |
10: 116,613,325 (GRCm39) |
Y826C |
probably benign |
Het |
Nf1 |
T |
C |
11: 79,366,711 (GRCm39) |
|
probably benign |
Het |
Nrg3 |
A |
C |
14: 38,093,243 (GRCm39) |
L542R |
probably benign |
Het |
Or13j1 |
T |
C |
4: 43,706,455 (GRCm39) |
T38A |
probably damaging |
Het |
Or2y8 |
T |
A |
11: 52,036,340 (GRCm39) |
T6S |
probably benign |
Het |
Or6c65 |
T |
A |
10: 129,603,674 (GRCm39) |
I103K |
probably damaging |
Het |
Pcdh15 |
A |
G |
10: 74,419,978 (GRCm39) |
N1212S |
probably damaging |
Het |
Pcsk5 |
G |
A |
19: 17,443,472 (GRCm39) |
T1229I |
probably benign |
Het |
Pkd1l3 |
A |
T |
8: 110,374,946 (GRCm39) |
H1483L |
probably benign |
Het |
Polr3b |
T |
A |
10: 84,532,879 (GRCm39) |
L840* |
probably null |
Het |
Psd4 |
A |
T |
2: 24,287,440 (GRCm39) |
R457S |
probably benign |
Het |
Relch |
T |
C |
1: 105,678,121 (GRCm39) |
S1149P |
possibly damaging |
Het |
Rgs12 |
A |
G |
5: 35,186,915 (GRCm39) |
S194G |
|
Het |
Rps3 |
A |
G |
7: 99,132,797 (GRCm39) |
|
probably null |
Het |
Saxo4 |
T |
C |
19: 10,455,602 (GRCm39) |
I216V |
probably benign |
Het |
Sgcb |
G |
T |
5: 73,793,036 (GRCm39) |
N255K |
probably benign |
Het |
Sla2 |
A |
G |
2: 156,717,799 (GRCm39) |
Y158H |
probably damaging |
Het |
Sla2 |
G |
A |
2: 156,717,823 (GRCm39) |
Q150* |
probably null |
Het |
Slc12a2 |
T |
A |
18: 58,012,455 (GRCm39) |
Y193N |
possibly damaging |
Het |
Supt16 |
G |
T |
14: 52,409,960 (GRCm39) |
T749K |
probably damaging |
Het |
Uqcrc2 |
A |
G |
7: 120,239,500 (GRCm39) |
E104G |
probably damaging |
Het |
Vasp |
T |
C |
7: 18,994,563 (GRCm39) |
N251S |
unknown |
Het |
Vmn1r72 |
A |
G |
7: 11,403,965 (GRCm39) |
M161T |
probably benign |
Het |
Zc3h18 |
T |
C |
8: 123,134,989 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp981 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02647:Zfp981
|
APN |
4 |
146,621,709 (GRCm39) |
nonsense |
probably null |
|
R0003:Zfp981
|
UTSW |
4 |
146,622,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Zfp981
|
UTSW |
4 |
146,622,221 (GRCm39) |
missense |
probably benign |
|
R2989:Zfp981
|
UTSW |
4 |
146,622,347 (GRCm39) |
missense |
probably benign |
0.40 |
R4158:Zfp981
|
UTSW |
4 |
146,622,339 (GRCm39) |
missense |
probably benign |
0.07 |
R4158:Zfp981
|
UTSW |
4 |
146,622,080 (GRCm39) |
missense |
probably benign |
|
R4778:Zfp981
|
UTSW |
4 |
146,622,112 (GRCm39) |
missense |
probably benign |
|
R5148:Zfp981
|
UTSW |
4 |
146,621,357 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5352:Zfp981
|
UTSW |
4 |
146,621,462 (GRCm39) |
missense |
probably benign |
0.29 |
R6252:Zfp981
|
UTSW |
4 |
146,621,970 (GRCm39) |
missense |
probably benign |
0.22 |
R6674:Zfp981
|
UTSW |
4 |
146,619,950 (GRCm39) |
missense |
probably damaging |
0.98 |
R6765:Zfp981
|
UTSW |
4 |
146,622,363 (GRCm39) |
missense |
probably benign |
0.34 |
R7288:Zfp981
|
UTSW |
4 |
146,622,100 (GRCm39) |
missense |
probably benign |
0.32 |
R7816:Zfp981
|
UTSW |
4 |
146,622,100 (GRCm39) |
missense |
probably benign |
0.32 |
R7835:Zfp981
|
UTSW |
4 |
146,622,333 (GRCm39) |
missense |
probably benign |
0.01 |
R8020:Zfp981
|
UTSW |
4 |
146,621,825 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8805:Zfp981
|
UTSW |
4 |
146,622,410 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9145:Zfp981
|
UTSW |
4 |
146,622,410 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9324:Zfp981
|
UTSW |
4 |
146,619,884 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9471:Zfp981
|
UTSW |
4 |
146,622,080 (GRCm39) |
missense |
probably benign |
|
Z1176:Zfp981
|
UTSW |
4 |
146,621,547 (GRCm39) |
missense |
probably damaging |
0.96 |
|