Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030C10Rik |
A |
T |
12: 20,865,089 (GRCm39) |
|
noncoding transcript |
Het |
Aars1 |
G |
A |
8: 111,781,715 (GRCm39) |
G929D |
probably damaging |
Het |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Actn4 |
A |
T |
7: 28,598,082 (GRCm39) |
L506Q |
probably damaging |
Het |
Adam26a |
A |
T |
8: 44,023,475 (GRCm39) |
F5Y |
probably benign |
Het |
Adamts5 |
G |
A |
16: 85,696,954 (GRCm39) |
Q68* |
probably null |
Het |
Adcy9 |
A |
G |
16: 4,116,618 (GRCm39) |
I871T |
probably benign |
Het |
Ak5 |
A |
T |
3: 152,361,514 (GRCm39) |
L136H |
probably damaging |
Het |
Ap1g2 |
A |
G |
14: 55,342,483 (GRCm39) |
|
probably null |
Het |
Ap2a1 |
G |
A |
7: 44,555,805 (GRCm39) |
T355M |
probably damaging |
Het |
Ap3s2 |
T |
C |
7: 79,564,989 (GRCm39) |
D60G |
possibly damaging |
Het |
Apold1 |
G |
A |
6: 134,960,558 (GRCm39) |
R4Q |
probably benign |
Het |
Atp13a5 |
G |
T |
16: 29,152,846 (GRCm39) |
Q207K |
possibly damaging |
Het |
BC035947 |
A |
C |
1: 78,474,666 (GRCm39) |
I622S |
probably damaging |
Het |
Bmper |
G |
T |
9: 23,289,021 (GRCm39) |
V339F |
probably benign |
Het |
Btbd8 |
C |
T |
5: 107,655,176 (GRCm39) |
Q992* |
probably null |
Het |
C1ra |
A |
G |
6: 124,499,293 (GRCm39) |
D493G |
probably damaging |
Het |
C3 |
C |
T |
17: 57,533,830 (GRCm39) |
|
probably null |
Het |
Cabp4 |
T |
A |
19: 4,187,120 (GRCm39) |
I209F |
possibly damaging |
Het |
Cacna1s |
A |
T |
1: 136,007,342 (GRCm39) |
H453L |
probably damaging |
Het |
Camk2g |
A |
G |
14: 20,842,652 (GRCm39) |
V32A |
probably benign |
Het |
Ccdc175 |
G |
A |
12: 72,206,527 (GRCm39) |
R240C |
probably damaging |
Het |
Cdk13 |
C |
T |
13: 17,946,988 (GRCm39) |
S590N |
possibly damaging |
Het |
Cfap45 |
A |
T |
1: 172,357,443 (GRCm39) |
T24S |
probably benign |
Het |
Clca3a1 |
T |
G |
3: 144,730,324 (GRCm39) |
K174Q |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,529,058 (GRCm39) |
|
probably benign |
Het |
Colgalt1 |
A |
T |
8: 72,073,277 (GRCm39) |
I323F |
possibly damaging |
Het |
Cpeb3 |
A |
T |
19: 37,152,059 (GRCm39) |
S106T |
probably damaging |
Het |
Cpeb3 |
T |
C |
19: 37,151,633 (GRCm39) |
S248G |
possibly damaging |
Het |
Ctcfl |
C |
T |
2: 172,937,191 (GRCm39) |
A576T |
probably benign |
Het |
Cyp4f16 |
T |
G |
17: 32,769,295 (GRCm39) |
V395G |
possibly damaging |
Het |
Dchs1 |
C |
T |
7: 105,415,462 (GRCm39) |
G605S |
probably damaging |
Het |
Egflam |
A |
T |
15: 7,249,110 (GRCm39) |
F903I |
probably damaging |
Het |
Eif5a |
G |
A |
11: 69,808,311 (GRCm39) |
A62V |
possibly damaging |
Het |
Fam217a |
A |
G |
13: 35,094,389 (GRCm39) |
S609P |
probably damaging |
Het |
Fhad1 |
T |
A |
4: 141,712,822 (GRCm39) |
I206F |
probably benign |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,856,617 (GRCm39) |
M2000K |
probably benign |
Het |
Frmd5 |
C |
T |
2: 121,422,134 (GRCm39) |
|
probably null |
Het |
Gle1 |
T |
C |
2: 29,826,092 (GRCm39) |
L57P |
probably benign |
Het |
Glrx3 |
C |
A |
7: 137,046,765 (GRCm39) |
N52K |
probably damaging |
Het |
Grin3b |
A |
G |
10: 79,812,938 (GRCm39) |
*1004W |
probably null |
Het |
Hectd4 |
T |
A |
5: 121,401,954 (GRCm39) |
F347L |
probably benign |
Het |
Htra1 |
G |
A |
7: 130,586,802 (GRCm39) |
V462I |
probably benign |
Het |
Itga11 |
A |
G |
9: 62,662,581 (GRCm39) |
Y518C |
probably damaging |
Het |
Krtap15-1 |
T |
C |
16: 88,626,253 (GRCm39) |
F88L |
probably benign |
Het |
Ktn1 |
A |
T |
14: 47,943,917 (GRCm39) |
R866W |
probably damaging |
Het |
Lamb1 |
G |
A |
12: 31,338,280 (GRCm39) |
R483H |
probably damaging |
Het |
Megf6 |
C |
T |
4: 154,349,848 (GRCm39) |
R983C |
probably damaging |
Het |
Mybpc3 |
T |
A |
2: 90,965,157 (GRCm39) |
D1075E |
probably benign |
Het |
Myo7b |
A |
T |
18: 32,097,489 (GRCm39) |
N1792K |
probably benign |
Het |
Nabp2 |
A |
T |
10: 128,237,556 (GRCm39) |
|
probably benign |
Het |
Neil3 |
A |
G |
8: 54,091,928 (GRCm39) |
C7R |
probably damaging |
Het |
Nxpe2 |
T |
A |
9: 48,230,897 (GRCm39) |
I491F |
possibly damaging |
Het |
Obscn |
A |
G |
11: 58,952,291 (GRCm39) |
V4292A |
possibly damaging |
Het |
Ogfod3 |
A |
G |
11: 121,088,318 (GRCm39) |
S139P |
probably damaging |
Het |
Oog2 |
T |
C |
4: 143,921,669 (GRCm39) |
I211T |
possibly damaging |
Het |
Oosp1 |
T |
C |
19: 11,666,080 (GRCm39) |
D70G |
probably benign |
Het |
Or10j2 |
A |
T |
1: 173,098,546 (GRCm39) |
D268V |
probably damaging |
Het |
Or1ab2 |
A |
G |
8: 72,863,425 (GRCm39) |
N5S |
probably damaging |
Het |
Or56a42-ps1 |
C |
A |
7: 104,777,435 (GRCm39) |
V70L |
probably benign |
Het |
Or6c210 |
A |
G |
10: 129,496,589 (GRCm39) |
I305V |
probably benign |
Het |
Padi3 |
T |
C |
4: 140,522,937 (GRCm39) |
D345G |
probably damaging |
Het |
Pcyt2 |
A |
G |
11: 120,506,246 (GRCm39) |
F71L |
probably benign |
Het |
Pi4k2b |
T |
C |
5: 52,911,971 (GRCm39) |
|
probably benign |
Het |
Pigr |
A |
C |
1: 130,776,195 (GRCm39) |
T577P |
possibly damaging |
Het |
Pirb |
G |
A |
7: 3,722,361 (GRCm39) |
Q161* |
probably null |
Het |
Pnlip |
A |
G |
19: 58,664,672 (GRCm39) |
E204G |
possibly damaging |
Het |
Pop7 |
G |
T |
5: 137,500,161 (GRCm39) |
D57E |
probably benign |
Het |
Ppfia4 |
A |
T |
1: 134,260,239 (GRCm39) |
I8N |
probably damaging |
Het |
Pprc1 |
A |
G |
19: 46,052,758 (GRCm39) |
T759A |
probably damaging |
Het |
Prom1 |
T |
C |
5: 44,202,894 (GRCm39) |
N213S |
probably benign |
Het |
Prop1 |
GCTTCACT |
GCTTCACTTCACT |
11: 50,842,863 (GRCm39) |
|
probably null |
Het |
Prop1 |
A |
T |
11: 50,842,872 (GRCm39) |
L105H |
probably damaging |
Het |
Pwp2 |
A |
T |
10: 78,018,328 (GRCm39) |
M121K |
possibly damaging |
Het |
Rap1gds1 |
A |
T |
3: 138,689,509 (GRCm39) |
M161K |
possibly damaging |
Het |
Rps6kb2 |
T |
A |
19: 4,207,002 (GRCm39) |
|
probably benign |
Het |
Rxfp1 |
A |
G |
3: 79,552,109 (GRCm39) |
S731P |
probably benign |
Het |
Scfd1 |
T |
C |
12: 51,437,195 (GRCm39) |
V137A |
probably benign |
Het |
Slc6a15 |
G |
A |
10: 103,240,275 (GRCm39) |
D333N |
probably damaging |
Het |
Sqor |
T |
C |
2: 122,627,101 (GRCm39) |
V74A |
possibly damaging |
Het |
Stil |
T |
A |
4: 114,881,422 (GRCm39) |
Y655* |
probably null |
Het |
Syt14 |
A |
T |
1: 192,581,167 (GRCm39) |
I468K |
probably damaging |
Het |
Tbc1d31 |
T |
C |
15: 57,825,661 (GRCm39) |
|
probably null |
Het |
Tspyl5 |
A |
T |
15: 33,686,995 (GRCm39) |
S317T |
probably damaging |
Het |
Ttf1 |
C |
T |
2: 28,954,668 (GRCm39) |
H11Y |
possibly damaging |
Het |
Ttf2 |
T |
C |
3: 100,861,631 (GRCm39) |
T620A |
probably damaging |
Het |
Usp32 |
G |
A |
11: 84,946,598 (GRCm39) |
Q269* |
probably null |
Het |
Vsig10 |
T |
A |
5: 117,476,308 (GRCm39) |
V254E |
probably benign |
Het |
Wdr6 |
C |
T |
9: 108,450,187 (GRCm39) |
A1114T |
probably benign |
Het |
Zfp280d |
A |
G |
9: 72,238,714 (GRCm39) |
S63G |
probably damaging |
Het |
Zfp934 |
T |
C |
13: 62,665,768 (GRCm39) |
H291R |
probably damaging |
Het |
|
Other mutations in Zfp607b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02090:Zfp607b
|
APN |
7 |
27,398,140 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02114:Zfp607b
|
APN |
7 |
27,403,150 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03171:Zfp607b
|
APN |
7 |
27,393,020 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03329:Zfp607b
|
APN |
7 |
27,403,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0988:Zfp607b
|
UTSW |
7 |
27,402,401 (GRCm39) |
missense |
probably benign |
0.34 |
R1518:Zfp607b
|
UTSW |
7 |
27,398,087 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1672:Zfp607b
|
UTSW |
7 |
27,391,948 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1733:Zfp607b
|
UTSW |
7 |
27,391,949 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1992:Zfp607b
|
UTSW |
7 |
27,401,949 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2849:Zfp607b
|
UTSW |
7 |
27,401,819 (GRCm39) |
missense |
probably benign |
0.00 |
R3879:Zfp607b
|
UTSW |
7 |
27,403,476 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4117:Zfp607b
|
UTSW |
7 |
27,398,107 (GRCm39) |
missense |
probably damaging |
0.97 |
R4439:Zfp607b
|
UTSW |
7 |
27,402,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Zfp607b
|
UTSW |
7 |
27,403,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Zfp607b
|
UTSW |
7 |
27,402,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R5095:Zfp607b
|
UTSW |
7 |
27,393,061 (GRCm39) |
intron |
probably benign |
|
R5301:Zfp607b
|
UTSW |
7 |
27,403,172 (GRCm39) |
missense |
probably benign |
|
R5422:Zfp607b
|
UTSW |
7 |
27,401,813 (GRCm39) |
missense |
probably benign |
0.00 |
R5538:Zfp607b
|
UTSW |
7 |
27,402,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R5546:Zfp607b
|
UTSW |
7 |
27,402,032 (GRCm39) |
missense |
probably benign |
0.19 |
R5644:Zfp607b
|
UTSW |
7 |
27,403,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R5649:Zfp607b
|
UTSW |
7 |
27,403,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R5692:Zfp607b
|
UTSW |
7 |
27,402,889 (GRCm39) |
missense |
probably benign |
0.17 |
R5945:Zfp607b
|
UTSW |
7 |
27,401,841 (GRCm39) |
missense |
probably benign |
0.06 |
R6695:Zfp607b
|
UTSW |
7 |
27,403,464 (GRCm39) |
missense |
probably benign |
0.04 |
R7402:Zfp607b
|
UTSW |
7 |
27,392,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R7515:Zfp607b
|
UTSW |
7 |
27,402,921 (GRCm39) |
missense |
probably benign |
0.03 |
R8402:Zfp607b
|
UTSW |
7 |
27,402,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R8954:Zfp607b
|
UTSW |
7 |
27,403,387 (GRCm39) |
missense |
probably benign |
0.00 |
R9494:Zfp607b
|
UTSW |
7 |
27,403,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R9554:Zfp607b
|
UTSW |
7 |
27,402,464 (GRCm39) |
missense |
probably damaging |
0.99 |
R9727:Zfp607b
|
UTSW |
7 |
27,403,125 (GRCm39) |
missense |
probably benign |
|
Z1177:Zfp607b
|
UTSW |
7 |
27,401,819 (GRCm39) |
missense |
probably benign |
0.00 |
|