Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl6a |
G |
A |
3: 32,772,194 (GRCm39) |
R164H |
probably damaging |
Het |
Afg3l2 |
A |
G |
18: 67,573,269 (GRCm39) |
Y178H |
probably benign |
Het |
Agtr1a |
A |
G |
13: 30,566,016 (GRCm39) |
*360W |
probably null |
Het |
Arfgef1 |
A |
G |
1: 10,209,109 (GRCm39) |
V1830A |
probably benign |
Het |
Asic2 |
A |
T |
11: 81,858,806 (GRCm39) |
S69T |
probably benign |
Het |
Axin1 |
A |
T |
17: 26,401,531 (GRCm39) |
N368Y |
probably damaging |
Het |
Brme1 |
A |
G |
8: 84,898,473 (GRCm39) |
E537G |
probably damaging |
Het |
Ces1d |
G |
A |
8: 93,904,756 (GRCm39) |
P328L |
probably benign |
Het |
Cndp2 |
T |
A |
18: 84,686,203 (GRCm39) |
K461* |
probably null |
Het |
Cntnap5c |
A |
T |
17: 58,620,852 (GRCm39) |
H977L |
probably benign |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Glg1 |
T |
C |
8: 111,896,194 (GRCm39) |
T177A |
possibly damaging |
Het |
Gm7168 |
T |
C |
17: 14,169,824 (GRCm39) |
V397A |
probably benign |
Het |
Hif1a |
T |
A |
12: 73,988,533 (GRCm39) |
D535E |
probably benign |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Ice1 |
T |
C |
13: 70,763,219 (GRCm39) |
E173G |
possibly damaging |
Het |
Ighmbp2 |
A |
G |
19: 3,329,909 (GRCm39) |
V115A |
probably damaging |
Het |
Irf2 |
A |
T |
8: 47,271,831 (GRCm39) |
E101D |
possibly damaging |
Het |
Kat8 |
G |
A |
7: 127,523,988 (GRCm39) |
E343K |
probably damaging |
Het |
Kyat1 |
C |
T |
2: 30,078,123 (GRCm39) |
C127Y |
probably damaging |
Het |
Mrgpra4 |
T |
C |
7: 47,630,755 (GRCm39) |
H282R |
probably benign |
Het |
Npsr1 |
C |
A |
9: 24,225,096 (GRCm39) |
P368Q |
probably damaging |
Het |
Nwd1 |
G |
A |
8: 73,401,872 (GRCm39) |
V839M |
probably damaging |
Het |
Or51a43 |
T |
A |
7: 103,717,930 (GRCm39) |
M103L |
probably damaging |
Het |
Or6n2 |
G |
T |
1: 173,897,436 (GRCm39) |
D191Y |
probably damaging |
Het |
P4ha3 |
A |
G |
7: 99,955,198 (GRCm39) |
D351G |
probably benign |
Het |
Pard3b |
T |
A |
1: 62,479,160 (GRCm39) |
|
probably null |
Het |
Pgap6 |
CGGGG |
CGGGGG |
17: 26,339,536 (GRCm39) |
|
probably null |
Het |
Pik3c2b |
G |
T |
1: 133,031,574 (GRCm39) |
G1505W |
probably damaging |
Het |
Plppr5 |
A |
T |
3: 117,414,714 (GRCm39) |
I112L |
probably benign |
Het |
Potefam1 |
T |
A |
2: 111,034,468 (GRCm39) |
T355S |
probably benign |
Het |
Ptprq |
A |
G |
10: 107,522,226 (GRCm39) |
I575T |
possibly damaging |
Het |
Ranbp3l |
A |
G |
15: 9,029,656 (GRCm39) |
E46G |
probably damaging |
Het |
Rbm46 |
A |
G |
3: 82,772,640 (GRCm39) |
V164A |
possibly damaging |
Het |
Sap25 |
A |
G |
5: 137,639,713 (GRCm39) |
E13G |
probably benign |
Het |
Setbp1 |
A |
T |
18: 78,899,860 (GRCm39) |
V1269E |
possibly damaging |
Het |
Smgc |
T |
A |
15: 91,726,109 (GRCm39) |
S18R |
possibly damaging |
Het |
Snrk |
T |
C |
9: 121,993,072 (GRCm39) |
I345T |
probably benign |
Het |
Sp4 |
T |
A |
12: 118,262,976 (GRCm39) |
I357F |
possibly damaging |
Het |
Sra1 |
A |
G |
18: 36,808,031 (GRCm39) |
L399P |
probably damaging |
Het |
Stat6 |
A |
G |
10: 127,494,242 (GRCm39) |
T658A |
probably benign |
Het |
Sv2a |
G |
A |
3: 96,092,339 (GRCm39) |
R13H |
probably benign |
Het |
Thoc3 |
G |
T |
13: 54,608,014 (GRCm39) |
T310N |
probably damaging |
Het |
Tox3 |
A |
C |
8: 91,074,489 (GRCm39) |
|
probably null |
Het |
Trpc6 |
A |
G |
9: 8,680,550 (GRCm39) |
E848G |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,538,590 (GRCm39) |
T34703S |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,776,312 (GRCm39) |
I1577V |
probably damaging |
Het |
Ubqln3 |
G |
A |
7: 103,790,674 (GRCm39) |
P472L |
probably benign |
Het |
Ugt2b36 |
C |
T |
5: 87,240,297 (GRCm39) |
W29* |
probably null |
Het |
Wdr17 |
C |
T |
8: 55,113,806 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zfp790 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Zfp790
|
APN |
7 |
29,527,988 (GRCm39) |
missense |
probably benign |
0.32 |
IGL00979:Zfp790
|
APN |
7 |
29,529,034 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02286:Zfp790
|
APN |
7 |
29,529,160 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL03136:Zfp790
|
APN |
7 |
29,529,320 (GRCm39) |
nonsense |
probably null |
|
R0021:Zfp790
|
UTSW |
7 |
29,525,113 (GRCm39) |
unclassified |
probably benign |
|
R0077:Zfp790
|
UTSW |
7 |
29,524,300 (GRCm39) |
missense |
probably damaging |
0.98 |
R1477:Zfp790
|
UTSW |
7 |
29,522,525 (GRCm39) |
start gained |
probably benign |
|
R1572:Zfp790
|
UTSW |
7 |
29,527,564 (GRCm39) |
missense |
probably benign |
0.33 |
R2015:Zfp790
|
UTSW |
7 |
29,528,286 (GRCm39) |
missense |
probably benign |
0.29 |
R4941:Zfp790
|
UTSW |
7 |
29,528,916 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5019:Zfp790
|
UTSW |
7 |
29,529,192 (GRCm39) |
missense |
probably benign |
0.00 |
R5159:Zfp790
|
UTSW |
7 |
29,529,192 (GRCm39) |
missense |
probably benign |
0.00 |
R5160:Zfp790
|
UTSW |
7 |
29,529,192 (GRCm39) |
missense |
probably benign |
0.00 |
R5954:Zfp790
|
UTSW |
7 |
29,528,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R6025:Zfp790
|
UTSW |
7 |
29,528,970 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6312:Zfp790
|
UTSW |
7 |
29,527,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7392:Zfp790
|
UTSW |
7 |
29,528,050 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7623:Zfp790
|
UTSW |
7 |
29,525,130 (GRCm39) |
nonsense |
probably null |
|
R8036:Zfp790
|
UTSW |
7 |
29,528,346 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8175:Zfp790
|
UTSW |
7 |
29,529,205 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8898:Zfp790
|
UTSW |
7 |
29,522,525 (GRCm39) |
start gained |
probably benign |
|
R8988:Zfp790
|
UTSW |
7 |
29,527,593 (GRCm39) |
missense |
probably benign |
|
R9176:Zfp790
|
UTSW |
7 |
29,529,387 (GRCm39) |
missense |
probably benign |
0.04 |
R9404:Zfp790
|
UTSW |
7 |
29,525,185 (GRCm39) |
missense |
probably benign |
|
R9519:Zfp790
|
UTSW |
7 |
29,522,567 (GRCm39) |
missense |
unknown |
|
Z1186:Zfp790
|
UTSW |
7 |
29,529,109 (GRCm39) |
missense |
possibly damaging |
0.53 |
Z1186:Zfp790
|
UTSW |
7 |
29,529,258 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1186:Zfp790
|
UTSW |
7 |
29,529,208 (GRCm39) |
missense |
possibly damaging |
0.72 |
|