Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd13c |
T |
A |
3: 157,653,571 (GRCm39) |
N136K |
probably damaging |
Het |
Aph1b |
A |
T |
9: 66,697,955 (GRCm39) |
|
probably benign |
Het |
Atf7ip |
A |
G |
6: 136,583,718 (GRCm39) |
K1250E |
probably damaging |
Het |
Atp8b2 |
T |
C |
3: 89,857,160 (GRCm39) |
N400S |
probably damaging |
Het |
Brca2 |
C |
A |
5: 150,462,126 (GRCm39) |
S630Y |
probably damaging |
Het |
Chd6 |
T |
A |
2: 160,807,595 (GRCm39) |
E1873V |
probably damaging |
Het |
Chrna10 |
T |
C |
7: 101,761,236 (GRCm39) |
|
probably benign |
Het |
Col6a3 |
A |
G |
1: 90,739,328 (GRCm39) |
L907P |
probably damaging |
Het |
Cxcr6 |
A |
G |
9: 123,639,770 (GRCm39) |
N264S |
probably damaging |
Het |
Cyria |
A |
G |
12: 12,414,752 (GRCm39) |
T248A |
possibly damaging |
Het |
Dgkg |
A |
G |
16: 22,388,980 (GRCm39) |
|
probably benign |
Het |
Dpysl2 |
T |
G |
14: 67,061,839 (GRCm39) |
M256L |
probably benign |
Het |
Dsp |
G |
T |
13: 38,380,499 (GRCm39) |
E1816* |
probably null |
Het |
Fam13b |
T |
C |
18: 34,587,709 (GRCm39) |
K530E |
probably damaging |
Het |
Fastk |
T |
C |
5: 24,648,090 (GRCm39) |
H242R |
probably damaging |
Het |
Fbxw28 |
A |
T |
9: 109,166,420 (GRCm39) |
H145Q |
possibly damaging |
Het |
Heatr6 |
T |
C |
11: 83,669,718 (GRCm39) |
L910P |
probably damaging |
Het |
Hmcn2 |
A |
G |
2: 31,343,617 (GRCm39) |
T4642A |
possibly damaging |
Het |
Hspg2 |
A |
G |
4: 137,235,700 (GRCm39) |
T167A |
probably benign |
Het |
Igsf10 |
A |
G |
3: 59,238,111 (GRCm39) |
L690P |
probably benign |
Het |
Klhdc10 |
G |
A |
6: 30,439,865 (GRCm39) |
|
probably null |
Het |
Krt31 |
A |
G |
11: 99,939,222 (GRCm39) |
Y232H |
probably damaging |
Het |
Lsm3 |
A |
G |
6: 91,493,070 (GRCm39) |
|
probably benign |
Het |
Mfn2 |
T |
A |
4: 147,969,947 (GRCm39) |
I375F |
probably damaging |
Het |
Mfrp |
A |
T |
9: 44,014,171 (GRCm39) |
I180F |
probably damaging |
Het |
Msh3 |
T |
C |
13: 92,485,820 (GRCm39) |
E168G |
possibly damaging |
Het |
Naa16 |
A |
T |
14: 79,622,108 (GRCm39) |
V77D |
probably damaging |
Het |
Nav2 |
T |
C |
7: 49,208,521 (GRCm39) |
S1570P |
probably damaging |
Het |
Niban3 |
A |
G |
8: 72,055,504 (GRCm39) |
R305G |
possibly damaging |
Het |
Numa1 |
C |
T |
7: 101,649,439 (GRCm39) |
R1057* |
probably null |
Het |
Nup210l |
G |
A |
3: 90,030,099 (GRCm39) |
A271T |
probably damaging |
Het |
Ogdh |
T |
C |
11: 6,305,400 (GRCm39) |
V965A |
probably damaging |
Het |
Or10h28 |
C |
A |
17: 33,488,639 (GRCm39) |
Q314K |
probably benign |
Het |
Or4m1 |
A |
T |
14: 50,557,473 (GRCm39) |
V273E |
probably damaging |
Het |
Or6c219 |
A |
G |
10: 129,781,772 (GRCm39) |
L53P |
probably damaging |
Het |
Or7g21 |
A |
T |
9: 19,032,671 (GRCm39) |
N140I |
probably damaging |
Het |
Or8b51 |
T |
A |
9: 38,569,362 (GRCm39) |
I109F |
probably damaging |
Het |
Pdp2 |
A |
T |
8: 105,321,531 (GRCm39) |
Q460L |
probably benign |
Het |
Pex5l |
T |
C |
3: 33,047,141 (GRCm39) |
T270A |
probably benign |
Het |
Pkp4 |
C |
T |
2: 59,140,598 (GRCm39) |
Q435* |
probably null |
Het |
Prss32 |
G |
A |
17: 24,075,096 (GRCm39) |
V149M |
probably benign |
Het |
Riox2 |
C |
A |
16: 59,309,780 (GRCm39) |
P378Q |
probably benign |
Het |
Rita1 |
C |
T |
5: 120,747,858 (GRCm39) |
A147T |
probably damaging |
Het |
Rsph4a |
T |
A |
10: 33,781,521 (GRCm39) |
S124T |
possibly damaging |
Het |
Sdccag8 |
G |
A |
1: 176,652,321 (GRCm39) |
R24H |
possibly damaging |
Het |
Slc22a1 |
C |
A |
17: 12,894,387 (GRCm39) |
G54* |
probably null |
Het |
Slc24a5 |
C |
T |
2: 124,927,567 (GRCm39) |
|
probably benign |
Het |
Tex101 |
C |
T |
7: 24,367,750 (GRCm39) |
V201M |
probably damaging |
Het |
Tmprss7 |
T |
C |
16: 45,501,956 (GRCm39) |
Y223C |
probably damaging |
Het |
Trpc4ap |
T |
C |
2: 155,492,388 (GRCm39) |
E382G |
probably damaging |
Het |
Uggt1 |
A |
T |
1: 36,223,565 (GRCm39) |
Y575N |
probably damaging |
Het |
Vmn2r70 |
T |
C |
7: 85,214,376 (GRCm39) |
I259V |
probably damaging |
Het |
Xpo1 |
T |
A |
11: 23,227,065 (GRCm39) |
N131K |
probably damaging |
Het |
Zfp579 |
C |
T |
7: 4,997,432 (GRCm39) |
V160M |
probably benign |
Het |
Zfp697 |
A |
G |
3: 98,332,766 (GRCm39) |
D64G |
probably benign |
Het |
|
Other mutations in Zfp974 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00836:Zfp974
|
APN |
7 |
27,610,315 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01805:Zfp974
|
APN |
7 |
27,611,689 (GRCm39) |
splice site |
probably benign |
|
IGL02449:Zfp974
|
APN |
7 |
27,611,152 (GRCm39) |
missense |
probably benign |
|
R0362:Zfp974
|
UTSW |
7 |
27,626,819 (GRCm39) |
splice site |
probably benign |
|
R0372:Zfp974
|
UTSW |
7 |
27,620,120 (GRCm39) |
critical splice donor site |
probably null |
|
R0379:Zfp974
|
UTSW |
7 |
27,610,357 (GRCm39) |
missense |
probably damaging |
0.98 |
R0699:Zfp974
|
UTSW |
7 |
27,611,416 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0791:Zfp974
|
UTSW |
7 |
27,609,510 (GRCm39) |
nonsense |
probably null |
|
R1411:Zfp974
|
UTSW |
7 |
27,610,634 (GRCm39) |
missense |
probably benign |
0.00 |
R1567:Zfp974
|
UTSW |
7 |
27,610,148 (GRCm39) |
missense |
probably damaging |
0.99 |
R1747:Zfp974
|
UTSW |
7 |
27,610,506 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1837:Zfp974
|
UTSW |
7 |
27,609,781 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1838:Zfp974
|
UTSW |
7 |
27,609,781 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1839:Zfp974
|
UTSW |
7 |
27,609,781 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2311:Zfp974
|
UTSW |
7 |
27,609,866 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4006:Zfp974
|
UTSW |
7 |
27,611,677 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4303:Zfp974
|
UTSW |
7 |
27,609,657 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4541:Zfp974
|
UTSW |
7 |
27,625,829 (GRCm39) |
missense |
probably damaging |
0.99 |
R4771:Zfp974
|
UTSW |
7 |
27,625,733 (GRCm39) |
missense |
probably damaging |
0.96 |
R4889:Zfp974
|
UTSW |
7 |
27,610,244 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5332:Zfp974
|
UTSW |
7 |
27,625,715 (GRCm39) |
missense |
probably benign |
0.01 |
R5537:Zfp974
|
UTSW |
7 |
27,611,671 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R5906:Zfp974
|
UTSW |
7 |
27,610,230 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5908:Zfp974
|
UTSW |
7 |
27,610,382 (GRCm39) |
missense |
probably benign |
0.01 |
R6419:Zfp974
|
UTSW |
7 |
27,610,940 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6654:Zfp974
|
UTSW |
7 |
27,625,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6731:Zfp974
|
UTSW |
7 |
27,611,074 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7162:Zfp974
|
UTSW |
7 |
27,610,944 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7316:Zfp974
|
UTSW |
7 |
27,609,863 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7484:Zfp974
|
UTSW |
7 |
27,611,559 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7663:Zfp974
|
UTSW |
7 |
27,611,110 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7664:Zfp974
|
UTSW |
7 |
27,610,137 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8052:Zfp974
|
UTSW |
7 |
27,610,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R8698:Zfp974
|
UTSW |
7 |
27,610,361 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8700:Zfp974
|
UTSW |
7 |
27,609,472 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8938:Zfp974
|
UTSW |
7 |
27,610,311 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8972:Zfp974
|
UTSW |
7 |
27,610,589 (GRCm39) |
missense |
probably benign |
0.06 |
R9212:Zfp974
|
UTSW |
7 |
27,610,052 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9236:Zfp974
|
UTSW |
7 |
27,610,342 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9335:Zfp974
|
UTSW |
7 |
27,611,476 (GRCm39) |
missense |
probably benign |
0.02 |
R9436:Zfp974
|
UTSW |
7 |
27,611,094 (GRCm39) |
missense |
probably benign |
0.24 |
R9740:Zfp974
|
UTSW |
7 |
27,610,025 (GRCm39) |
missense |
probably damaging |
1.00 |
|