Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930402F06Rik |
C |
A |
2: 35,266,309 (GRCm39) |
M120I |
probably damaging |
Het |
4933427D14Rik |
A |
T |
11: 72,082,342 (GRCm39) |
L328Q |
probably damaging |
Het |
Adgrv1 |
A |
C |
13: 81,709,704 (GRCm39) |
|
probably null |
Het |
Ankrd46 |
A |
T |
15: 36,484,279 (GRCm39) |
|
probably benign |
Het |
Arhgef18 |
A |
T |
8: 3,494,979 (GRCm39) |
M413L |
probably benign |
Het |
Atp6v1e1 |
G |
A |
6: 120,781,044 (GRCm39) |
T87M |
probably null |
Het |
Bap1 |
T |
C |
14: 30,980,402 (GRCm39) |
|
probably benign |
Het |
Brf1 |
A |
G |
12: 112,929,507 (GRCm39) |
L385P |
probably benign |
Het |
C1qtnf1 |
A |
T |
11: 118,338,938 (GRCm39) |
N203Y |
probably damaging |
Het |
Catsperb |
A |
T |
12: 101,569,025 (GRCm39) |
N899I |
probably damaging |
Het |
Ccnjl |
A |
C |
11: 43,470,718 (GRCm39) |
D162A |
probably damaging |
Het |
Cd248 |
A |
C |
19: 5,119,195 (GRCm39) |
I348L |
probably benign |
Het |
Cdc20 |
T |
C |
4: 118,293,029 (GRCm39) |
T265A |
probably benign |
Het |
Cdca5 |
T |
A |
19: 6,140,427 (GRCm39) |
L196* |
probably null |
Het |
Cdk4 |
T |
A |
10: 126,900,444 (GRCm39) |
|
probably benign |
Het |
Cldn10 |
G |
A |
14: 119,025,725 (GRCm39) |
G53S |
possibly damaging |
Het |
Clec4b2 |
G |
T |
6: 123,177,999 (GRCm39) |
E105* |
probably null |
Het |
Dapk1 |
T |
A |
13: 60,909,600 (GRCm39) |
D1404E |
probably benign |
Het |
Dnah1 |
T |
C |
14: 30,989,496 (GRCm39) |
Y3308C |
probably damaging |
Het |
Dnah17 |
A |
C |
11: 117,969,419 (GRCm39) |
Y2260D |
probably damaging |
Het |
Dock8 |
T |
G |
19: 25,159,001 (GRCm39) |
S1720A |
probably benign |
Het |
Erc1 |
A |
G |
6: 119,754,947 (GRCm39) |
|
probably null |
Het |
Ergic1 |
A |
G |
17: 26,848,597 (GRCm39) |
I66V |
probably benign |
Het |
Fam186a |
T |
C |
15: 99,843,158 (GRCm39) |
T1029A |
possibly damaging |
Het |
Fat4 |
A |
T |
3: 39,034,781 (GRCm39) |
Y2811F |
probably damaging |
Het |
Flt3 |
A |
G |
5: 147,306,110 (GRCm39) |
M310T |
probably damaging |
Het |
Ganab |
T |
A |
19: 8,892,355 (GRCm39) |
C844S |
probably benign |
Het |
Gas2l2 |
C |
A |
11: 83,320,041 (GRCm39) |
V72F |
probably damaging |
Het |
Gm14401 |
T |
A |
2: 176,778,573 (GRCm39) |
C220S |
probably damaging |
Het |
Hmmr |
A |
T |
11: 40,619,261 (GRCm39) |
V73E |
probably benign |
Het |
Idi2l |
T |
G |
13: 8,990,637 (GRCm39) |
|
probably benign |
Het |
Ifih1 |
G |
T |
2: 62,465,358 (GRCm39) |
|
probably benign |
Het |
Jak3 |
A |
G |
8: 72,138,048 (GRCm39) |
E833G |
probably damaging |
Het |
Lama2 |
TTTGCGCATT |
TTT |
10: 26,919,639 (GRCm39) |
|
probably null |
Het |
Ldb1 |
G |
A |
19: 46,023,132 (GRCm39) |
A217V |
probably benign |
Het |
Lrrc8c |
A |
G |
5: 105,755,955 (GRCm39) |
T577A |
probably benign |
Het |
Mfn1 |
T |
A |
3: 32,600,711 (GRCm39) |
|
probably benign |
Het |
Mki67 |
G |
A |
7: 135,298,474 (GRCm39) |
P2187S |
probably damaging |
Het |
Mrc1 |
T |
A |
2: 14,323,952 (GRCm39) |
D1096E |
probably benign |
Het |
Msi1 |
A |
G |
5: 115,573,654 (GRCm39) |
|
probably benign |
Het |
Msto1 |
T |
A |
3: 88,819,559 (GRCm39) |
I152F |
probably benign |
Het |
Myo9a |
A |
G |
9: 59,803,800 (GRCm39) |
R2060G |
probably benign |
Het |
Nnt |
A |
T |
13: 119,541,107 (GRCm39) |
C44* |
probably null |
Het |
Nup210l |
A |
G |
3: 90,100,378 (GRCm39) |
D1468G |
probably damaging |
Het |
Or1j16 |
T |
C |
2: 36,530,906 (GRCm39) |
L285P |
probably damaging |
Het |
Or4c10b |
A |
G |
2: 89,711,476 (GRCm39) |
E102G |
probably benign |
Het |
Or5d46 |
C |
A |
2: 88,174,686 (GRCm39) |
C129F |
possibly damaging |
Het |
Or7a40 |
T |
C |
16: 16,491,482 (GRCm39) |
D121G |
probably damaging |
Het |
P2rx3 |
G |
A |
2: 84,855,270 (GRCm39) |
T62I |
probably damaging |
Het |
Pabpc4l |
G |
T |
3: 46,401,578 (GRCm39) |
T22K |
probably damaging |
Het |
Pcdha7 |
A |
G |
18: 37,108,646 (GRCm39) |
D557G |
probably damaging |
Het |
Pcdhb20 |
A |
G |
18: 37,639,298 (GRCm39) |
K608R |
possibly damaging |
Het |
Pcnx1 |
A |
G |
12: 81,964,939 (GRCm39) |
S369G |
probably damaging |
Het |
Plod1 |
T |
C |
4: 148,004,736 (GRCm39) |
I455V |
probably benign |
Het |
Prune2 |
A |
T |
19: 17,099,219 (GRCm39) |
E1574D |
probably benign |
Het |
Ptar1 |
T |
A |
19: 23,680,472 (GRCm39) |
L96H |
probably damaging |
Het |
Rabgap1 |
T |
C |
2: 37,450,583 (GRCm39) |
S904P |
probably benign |
Het |
Rps6ka4 |
C |
T |
19: 6,815,467 (GRCm39) |
V176I |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Runx1t1 |
T |
A |
4: 13,771,459 (GRCm39) |
M1K |
probably null |
Het |
Serinc4 |
T |
A |
2: 121,282,905 (GRCm39) |
Y419F |
probably damaging |
Het |
Serpina12 |
A |
T |
12: 104,004,056 (GRCm39) |
M192K |
possibly damaging |
Het |
Spata21 |
T |
A |
4: 140,832,261 (GRCm39) |
M474K |
probably damaging |
Het |
Stpg1 |
T |
C |
4: 135,246,676 (GRCm39) |
S135P |
possibly damaging |
Het |
Tdrkh |
A |
G |
3: 94,336,671 (GRCm39) |
D481G |
probably damaging |
Het |
Ube2e1 |
A |
C |
14: 18,285,268 (GRCm38) |
S68R |
probably damaging |
Het |
Vcpip1 |
A |
C |
1: 9,817,572 (GRCm39) |
N270K |
probably damaging |
Het |
Vmn2r79 |
T |
C |
7: 86,650,675 (GRCm39) |
F154L |
probably benign |
Het |
Vwa3b |
A |
G |
1: 37,153,684 (GRCm39) |
|
probably benign |
Het |
Xdh |
C |
A |
17: 74,207,703 (GRCm39) |
V885L |
probably benign |
Het |
Zfp141 |
A |
T |
7: 42,125,629 (GRCm39) |
V281D |
probably benign |
Het |
Zfp345 |
G |
A |
2: 150,314,608 (GRCm39) |
R310C |
probably benign |
Het |
Zfp760 |
G |
A |
17: 21,942,229 (GRCm39) |
C468Y |
probably benign |
Het |
|
Other mutations in Zfp317 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02425:Zfp317
|
APN |
9 |
19,554,909 (GRCm39) |
nonsense |
probably null |
|
R1520:Zfp317
|
UTSW |
9 |
19,559,144 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1646:Zfp317
|
UTSW |
9 |
19,558,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:Zfp317
|
UTSW |
9 |
19,553,280 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2029:Zfp317
|
UTSW |
9 |
19,556,532 (GRCm39) |
missense |
probably benign |
0.13 |
R2364:Zfp317
|
UTSW |
9 |
19,559,031 (GRCm39) |
missense |
probably benign |
0.01 |
R4006:Zfp317
|
UTSW |
9 |
19,559,333 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4031:Zfp317
|
UTSW |
9 |
19,558,008 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4293:Zfp317
|
UTSW |
9 |
19,557,990 (GRCm39) |
splice site |
probably null |
|
R5593:Zfp317
|
UTSW |
9 |
19,558,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R6077:Zfp317
|
UTSW |
9 |
19,558,184 (GRCm39) |
missense |
probably benign |
0.00 |
R6573:Zfp317
|
UTSW |
9 |
19,556,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R6652:Zfp317
|
UTSW |
9 |
19,558,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Zfp317
|
UTSW |
9 |
19,559,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R6875:Zfp317
|
UTSW |
9 |
19,554,961 (GRCm39) |
missense |
probably damaging |
0.98 |
R7688:Zfp317
|
UTSW |
9 |
19,559,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Zfp317
|
UTSW |
9 |
19,553,265 (GRCm39) |
missense |
probably benign |
0.00 |
R8900:Zfp317
|
UTSW |
9 |
19,558,708 (GRCm39) |
nonsense |
probably null |
|
R8927:Zfp317
|
UTSW |
9 |
19,552,521 (GRCm39) |
start codon destroyed |
probably null |
|
R8928:Zfp317
|
UTSW |
9 |
19,552,521 (GRCm39) |
start codon destroyed |
probably null |
|
R9052:Zfp317
|
UTSW |
9 |
19,556,568 (GRCm39) |
missense |
probably benign |
0.03 |
R9176:Zfp317
|
UTSW |
9 |
19,559,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Zfp317
|
UTSW |
9 |
19,558,442 (GRCm39) |
nonsense |
probably null |
|
R9212:Zfp317
|
UTSW |
9 |
19,558,442 (GRCm39) |
nonsense |
probably null |
|
Z1177:Zfp317
|
UTSW |
9 |
19,558,326 (GRCm39) |
missense |
probably damaging |
1.00 |
|