Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adtrp |
A |
T |
13: 41,931,078 (GRCm39) |
S170T |
probably benign |
Het |
Cep55 |
C |
A |
19: 38,061,887 (GRCm39) |
Q443K |
probably damaging |
Het |
Ces1c |
T |
C |
8: 93,833,301 (GRCm39) |
E388G |
probably benign |
Het |
Chd9 |
T |
C |
8: 91,752,020 (GRCm39) |
S1753P |
possibly damaging |
Het |
Cse1l |
T |
A |
2: 166,769,724 (GRCm39) |
I343N |
probably damaging |
Het |
Ctif |
T |
G |
18: 75,570,247 (GRCm39) |
M551L |
possibly damaging |
Het |
Cyp2c29 |
A |
G |
19: 39,310,143 (GRCm39) |
|
probably benign |
Het |
Filip1 |
G |
A |
9: 79,725,226 (GRCm39) |
T1131I |
probably damaging |
Het |
Gm13941 |
G |
A |
2: 110,922,193 (GRCm39) |
|
probably benign |
Het |
Klc3 |
T |
C |
7: 19,130,220 (GRCm39) |
E319G |
possibly damaging |
Het |
Lonrf1 |
T |
C |
8: 36,697,231 (GRCm39) |
|
probably benign |
Het |
Lrba |
A |
G |
3: 86,267,089 (GRCm39) |
E1593G |
probably benign |
Het |
Mroh5 |
G |
A |
15: 73,664,638 (GRCm39) |
|
probably benign |
Het |
Mthfr |
T |
A |
4: 148,125,727 (GRCm39) |
M20K |
probably benign |
Het |
Nsd2 |
C |
A |
5: 34,040,347 (GRCm39) |
N960K |
possibly damaging |
Het |
Osgin1 |
T |
A |
8: 120,171,785 (GRCm39) |
V193E |
probably damaging |
Het |
Pced1a |
A |
T |
2: 130,261,098 (GRCm39) |
C420S |
probably benign |
Het |
Pkd2l1 |
C |
T |
19: 44,146,075 (GRCm39) |
|
probably null |
Het |
Plekhg5 |
C |
A |
4: 152,186,498 (GRCm39) |
|
probably null |
Het |
Prkg2 |
A |
G |
5: 99,172,400 (GRCm39) |
V105A |
probably benign |
Het |
Rab11fip3 |
A |
G |
17: 26,286,599 (GRCm39) |
I518T |
probably benign |
Het |
Rapgef5 |
T |
A |
12: 117,677,917 (GRCm39) |
V150D |
probably damaging |
Het |
Sema4c |
A |
G |
1: 36,593,001 (GRCm39) |
|
probably benign |
Het |
Slc27a2 |
A |
G |
2: 126,422,837 (GRCm39) |
E354G |
probably damaging |
Het |
Slc28a3 |
A |
T |
13: 58,722,114 (GRCm39) |
L257I |
probably benign |
Het |
Slc2a8 |
G |
T |
2: 32,863,636 (GRCm39) |
Q469K |
probably damaging |
Het |
Slc44a1 |
T |
C |
4: 53,553,550 (GRCm39) |
V519A |
possibly damaging |
Het |
Slco6d1 |
A |
G |
1: 98,359,955 (GRCm39) |
|
probably null |
Het |
Strap |
T |
C |
6: 137,722,521 (GRCm39) |
S219P |
probably damaging |
Het |
Tjp1 |
T |
C |
7: 64,950,967 (GRCm39) |
I1636V |
probably benign |
Het |
Tle1 |
G |
A |
4: 72,087,355 (GRCm39) |
R126C |
possibly damaging |
Het |
Traf3 |
T |
A |
12: 111,205,501 (GRCm39) |
I94N |
probably damaging |
Het |
Trps1 |
G |
T |
15: 50,710,266 (GRCm39) |
T28K |
probably benign |
Het |
Unc13c |
T |
A |
9: 73,643,985 (GRCm39) |
T1160S |
probably damaging |
Het |
Vapb |
G |
A |
2: 173,619,964 (GRCm39) |
V228M |
probably benign |
Het |
Wdr3 |
A |
T |
3: 100,055,424 (GRCm39) |
D506E |
probably damaging |
Het |
Zfp51 |
A |
T |
17: 21,683,714 (GRCm39) |
M110L |
probably benign |
Het |
Zfp687 |
G |
A |
3: 94,919,727 (GRCm39) |
A15V |
probably damaging |
Het |
Zkscan6 |
A |
G |
11: 65,719,287 (GRCm39) |
T436A |
possibly damaging |
Het |
|
Other mutations in Zfp119a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0421:Zfp119a
|
UTSW |
17 |
56,172,248 (GRCm39) |
nonsense |
probably null |
|
R1385:Zfp119a
|
UTSW |
17 |
56,172,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R1600:Zfp119a
|
UTSW |
17 |
56,175,355 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2310:Zfp119a
|
UTSW |
17 |
56,172,440 (GRCm39) |
missense |
probably benign |
0.00 |
R2924:Zfp119a
|
UTSW |
17 |
56,175,343 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3910:Zfp119a
|
UTSW |
17 |
56,173,520 (GRCm39) |
missense |
probably benign |
|
R4594:Zfp119a
|
UTSW |
17 |
56,173,325 (GRCm39) |
missense |
probably benign |
|
R5217:Zfp119a
|
UTSW |
17 |
56,172,425 (GRCm39) |
nonsense |
probably null |
|
R5321:Zfp119a
|
UTSW |
17 |
56,172,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R5392:Zfp119a
|
UTSW |
17 |
56,173,328 (GRCm39) |
missense |
probably benign |
0.03 |
R5678:Zfp119a
|
UTSW |
17 |
56,175,336 (GRCm39) |
missense |
probably benign |
0.03 |
R7033:Zfp119a
|
UTSW |
17 |
56,173,009 (GRCm39) |
missense |
probably benign |
0.04 |
R7355:Zfp119a
|
UTSW |
17 |
56,173,287 (GRCm39) |
nonsense |
probably null |
|
R7489:Zfp119a
|
UTSW |
17 |
56,173,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R8130:Zfp119a
|
UTSW |
17 |
56,172,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8940:Zfp119a
|
UTSW |
17 |
56,172,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R9542:Zfp119a
|
UTSW |
17 |
56,172,593 (GRCm39) |
nonsense |
probably null |
|
Z1176:Zfp119a
|
UTSW |
17 |
56,173,011 (GRCm39) |
missense |
possibly damaging |
0.61 |
|