Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933428M09Rik |
G |
T |
X: 138,080,282 (GRCm39) |
G16* |
probably null |
Het |
Abhd11 |
T |
A |
5: 135,040,398 (GRCm39) |
W144R |
probably damaging |
Het |
Abhd2 |
A |
G |
7: 78,973,378 (GRCm39) |
E119G |
probably benign |
Het |
Acbd3 |
A |
G |
1: 180,553,938 (GRCm39) |
Y91C |
probably benign |
Het |
Aox4 |
C |
A |
1: 58,285,400 (GRCm39) |
S628* |
probably null |
Het |
Bahcc1 |
T |
A |
11: 120,165,285 (GRCm39) |
Y905* |
probably null |
Het |
Baiap2l2 |
T |
G |
15: 79,154,687 (GRCm39) |
S211R |
probably benign |
Het |
Cab39l |
T |
A |
14: 59,764,258 (GRCm39) |
Y206* |
probably null |
Het |
Cacna1i |
A |
T |
15: 80,275,041 (GRCm39) |
T1830S |
possibly damaging |
Het |
Catsperg1 |
A |
T |
7: 28,889,723 (GRCm39) |
L793* |
probably null |
Het |
Cdh10 |
G |
T |
15: 18,966,108 (GRCm39) |
V198F |
probably damaging |
Het |
Cenpk |
A |
T |
13: 104,385,917 (GRCm39) |
I271F |
probably damaging |
Het |
Chchd4 |
A |
T |
6: 91,442,260 (GRCm39) |
C53S |
probably damaging |
Het |
Cluh |
T |
G |
11: 74,550,531 (GRCm39) |
C252W |
probably damaging |
Het |
Cmklr1 |
G |
T |
5: 113,752,710 (GRCm39) |
A97E |
probably damaging |
Het |
Coil |
C |
A |
11: 88,871,987 (GRCm39) |
A116D |
possibly damaging |
Het |
Eif1ad9 |
A |
G |
12: 88,296,196 (GRCm39) |
H58R |
probably benign |
Het |
F830045P16Rik |
C |
A |
2: 129,305,493 (GRCm39) |
V294F |
probably damaging |
Het |
Fgd6 |
T |
A |
10: 93,969,939 (GRCm39) |
M1196K |
possibly damaging |
Het |
Gabra5 |
G |
A |
7: 57,140,604 (GRCm39) |
S31L |
probably benign |
Het |
Gm7135 |
A |
T |
1: 97,362,790 (GRCm39) |
|
noncoding transcript |
Het |
Gon4l |
C |
A |
3: 88,794,882 (GRCm39) |
T695K |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,491,614 (GRCm39) |
H3684R |
possibly damaging |
Het |
Ica1l |
T |
A |
1: 60,054,917 (GRCm39) |
M105L |
probably benign |
Het |
Ift70a1 |
A |
G |
2: 75,811,147 (GRCm39) |
L312P |
probably damaging |
Het |
Igkv8-24 |
A |
T |
6: 70,194,386 (GRCm39) |
V7D |
probably damaging |
Het |
Klf10 |
G |
A |
15: 38,296,331 (GRCm39) |
R420W |
probably damaging |
Het |
Klrc2 |
C |
A |
6: 129,633,843 (GRCm39) |
W177C |
probably damaging |
Het |
Krit1 |
T |
A |
5: 3,856,451 (GRCm39) |
C15* |
probably null |
Het |
Lamc1 |
C |
A |
1: 153,103,442 (GRCm39) |
V1375L |
probably damaging |
Het |
Lrrc37a |
C |
T |
11: 103,347,780 (GRCm39) |
V2972I |
unknown |
Het |
Mapkapk5 |
T |
C |
5: 121,672,492 (GRCm39) |
D13G |
probably damaging |
Het |
Mcph1 |
T |
A |
8: 18,838,489 (GRCm39) |
L804I |
probably damaging |
Het |
Mdn1 |
C |
T |
4: 32,723,690 (GRCm39) |
P2542L |
probably damaging |
Het |
Mrto4 |
A |
G |
4: 139,075,770 (GRCm39) |
Y119H |
probably benign |
Het |
Nbeal2 |
G |
T |
9: 110,461,158 (GRCm39) |
A1635E |
possibly damaging |
Het |
Ndc1 |
T |
C |
4: 107,246,773 (GRCm39) |
S399P |
probably benign |
Het |
Ndufv2 |
A |
G |
17: 66,394,424 (GRCm39) |
I147T |
probably damaging |
Het |
Neb |
C |
A |
2: 52,052,142 (GRCm39) |
E382* |
probably null |
Het |
Nhsl3 |
C |
T |
4: 129,116,478 (GRCm39) |
E729K |
probably damaging |
Het |
Nme8 |
T |
A |
13: 19,880,861 (GRCm39) |
I32F |
probably damaging |
Het |
Obox5 |
T |
A |
7: 15,491,793 (GRCm39) |
|
probably null |
Het |
Or8g23 |
A |
G |
9: 38,971,065 (GRCm39) |
V299A |
probably benign |
Het |
Pcdhb19 |
A |
T |
18: 37,630,939 (GRCm39) |
M245L |
probably benign |
Het |
Pex5l |
A |
T |
3: 33,061,477 (GRCm39) |
|
probably null |
Het |
Phrf1 |
T |
G |
7: 140,840,616 (GRCm39) |
D1270E |
probably damaging |
Het |
Pik3r5 |
A |
G |
11: 68,382,790 (GRCm39) |
K277E |
possibly damaging |
Het |
Ppan |
T |
C |
9: 20,802,221 (GRCm39) |
V204A |
possibly damaging |
Het |
Ppp1r9a |
A |
T |
6: 5,115,367 (GRCm39) |
N830I |
probably damaging |
Het |
Pxn |
C |
G |
5: 115,682,974 (GRCm39) |
A92G |
probably benign |
Het |
Qsox1 |
A |
G |
1: 155,666,742 (GRCm39) |
V249A |
probably benign |
Het |
Rgl3 |
T |
A |
9: 21,898,944 (GRCm39) |
*88C |
probably null |
Het |
Rps6kc1 |
A |
T |
1: 190,515,802 (GRCm39) |
W975R |
probably damaging |
Het |
Sash1 |
G |
T |
10: 8,656,368 (GRCm39) |
A208D |
possibly damaging |
Het |
Simc1 |
A |
T |
13: 54,687,709 (GRCm39) |
|
probably benign |
Het |
Sox7 |
T |
C |
14: 64,185,449 (GRCm39) |
Y162H |
probably damaging |
Het |
Srp72 |
T |
A |
5: 77,128,375 (GRCm39) |
L171H |
probably damaging |
Het |
Stab1 |
T |
A |
14: 30,881,476 (GRCm39) |
Y577F |
probably benign |
Het |
Stam2 |
G |
A |
2: 52,626,305 (GRCm39) |
|
probably benign |
Het |
Tagln |
T |
C |
9: 45,842,177 (GRCm39) |
T139A |
probably benign |
Het |
Thbs3 |
T |
C |
3: 89,130,471 (GRCm39) |
|
probably null |
Het |
Tmem216 |
G |
A |
19: 10,529,155 (GRCm39) |
T131M |
possibly damaging |
Het |
Tmprss11c |
A |
G |
5: 86,404,249 (GRCm39) |
V142A |
probably benign |
Het |
Trarg1 |
C |
G |
11: 76,585,102 (GRCm39) |
A164G |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ubtf |
T |
C |
11: 102,199,128 (GRCm39) |
M511V |
probably null |
Het |
Ugt2b36 |
A |
T |
5: 87,214,114 (GRCm39) |
V510E |
probably damaging |
Het |
Vars2 |
G |
C |
17: 35,969,041 (GRCm39) |
P887A |
probably damaging |
Het |
Vmn2r80 |
A |
G |
10: 79,004,980 (GRCm39) |
M206V |
possibly damaging |
Het |
Zbtb5 |
A |
G |
4: 44,993,990 (GRCm39) |
F465L |
probably benign |
Het |
Zfp119a |
G |
A |
17: 56,172,425 (GRCm39) |
Q473* |
probably null |
Het |
Zfp998 |
A |
T |
13: 66,581,787 (GRCm39) |
L28H |
probably damaging |
Het |
Zmym6 |
C |
A |
4: 126,999,167 (GRCm39) |
N450K |
possibly damaging |
Het |
|
Other mutations in Zfp607a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00164:Zfp607a
|
APN |
7 |
27,577,214 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01019:Zfp607a
|
APN |
7 |
27,578,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01412:Zfp607a
|
APN |
7 |
27,578,109 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03206:Zfp607a
|
APN |
7 |
27,577,248 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0071:Zfp607a
|
UTSW |
7 |
27,577,694 (GRCm39) |
missense |
probably damaging |
0.96 |
R0304:Zfp607a
|
UTSW |
7 |
27,578,637 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0685:Zfp607a
|
UTSW |
7 |
27,577,901 (GRCm39) |
missense |
probably damaging |
0.97 |
R0726:Zfp607a
|
UTSW |
7 |
27,578,574 (GRCm39) |
missense |
probably benign |
0.00 |
R1201:Zfp607a
|
UTSW |
7 |
27,578,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R1304:Zfp607a
|
UTSW |
7 |
27,565,000 (GRCm39) |
missense |
probably benign |
0.00 |
R1648:Zfp607a
|
UTSW |
7 |
27,578,493 (GRCm39) |
missense |
probably benign |
0.02 |
R1732:Zfp607a
|
UTSW |
7 |
27,577,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R2194:Zfp607a
|
UTSW |
7 |
27,578,805 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3793:Zfp607a
|
UTSW |
7 |
27,578,331 (GRCm39) |
missense |
probably benign |
0.01 |
R3808:Zfp607a
|
UTSW |
7 |
27,578,826 (GRCm39) |
missense |
probably benign |
0.01 |
R4296:Zfp607a
|
UTSW |
7 |
27,565,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Zfp607a
|
UTSW |
7 |
27,578,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Zfp607a
|
UTSW |
7 |
27,578,078 (GRCm39) |
missense |
probably benign |
0.23 |
R4915:Zfp607a
|
UTSW |
7 |
27,577,985 (GRCm39) |
missense |
probably benign |
0.00 |
R4950:Zfp607a
|
UTSW |
7 |
27,578,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R5123:Zfp607a
|
UTSW |
7 |
27,578,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R5270:Zfp607a
|
UTSW |
7 |
27,577,730 (GRCm39) |
nonsense |
probably null |
|
R5403:Zfp607a
|
UTSW |
7 |
27,578,744 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6010:Zfp607a
|
UTSW |
7 |
27,577,254 (GRCm39) |
nonsense |
probably null |
|
R6224:Zfp607a
|
UTSW |
7 |
27,578,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R6939:Zfp607a
|
UTSW |
7 |
27,578,473 (GRCm39) |
nonsense |
probably null |
|
R6953:Zfp607a
|
UTSW |
7 |
27,577,790 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7082:Zfp607a
|
UTSW |
7 |
27,578,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7781:Zfp607a
|
UTSW |
7 |
27,565,000 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7909:Zfp607a
|
UTSW |
7 |
27,578,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Zfp607a
|
UTSW |
7 |
27,578,868 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8224:Zfp607a
|
UTSW |
7 |
27,577,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R8949:Zfp607a
|
UTSW |
7 |
27,577,944 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8962:Zfp607a
|
UTSW |
7 |
27,578,786 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9178:Zfp607a
|
UTSW |
7 |
27,577,382 (GRCm39) |
missense |
probably benign |
0.00 |
R9802:Zfp607a
|
UTSW |
7 |
27,578,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|