Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
T |
C |
2: 68,569,855 (GRCm39) |
S524P |
possibly damaging |
Het |
Aplf |
A |
C |
6: 87,635,184 (GRCm39) |
|
probably null |
Het |
Asb5 |
A |
C |
8: 55,037,827 (GRCm39) |
H173P |
|
Het |
Atp6v0a2 |
A |
G |
5: 124,779,443 (GRCm39) |
E186G |
probably damaging |
Het |
Bbs2 |
A |
T |
8: 94,816,388 (GRCm39) |
|
probably null |
Het |
Chrm5 |
A |
G |
2: 112,310,301 (GRCm39) |
S272P |
probably benign |
Het |
Chrna6 |
T |
C |
8: 27,897,392 (GRCm39) |
I162V |
probably damaging |
Het |
Cldn6 |
T |
A |
17: 23,900,581 (GRCm39) |
C182S |
probably damaging |
Het |
Cysltr2 |
A |
G |
14: 73,267,203 (GRCm39) |
I169T |
probably benign |
Het |
Ddx11 |
T |
C |
17: 66,437,543 (GRCm39) |
|
probably null |
Het |
Efhc1 |
A |
T |
1: 21,049,685 (GRCm39) |
Y515F |
probably damaging |
Het |
Elmo1 |
A |
G |
13: 20,773,812 (GRCm39) |
|
probably null |
Het |
Ep300 |
T |
C |
15: 81,470,887 (GRCm39) |
S20P |
unknown |
Het |
Gfpt2 |
T |
G |
11: 49,715,268 (GRCm39) |
I421R |
probably damaging |
Het |
Gm14226 |
T |
A |
2: 154,866,630 (GRCm39) |
C196S |
possibly damaging |
Het |
Grm8 |
T |
C |
6: 27,363,671 (GRCm39) |
R615G |
possibly damaging |
Het |
Hic1 |
C |
T |
11: 75,057,042 (GRCm39) |
V616M |
possibly damaging |
Het |
Ing1 |
A |
G |
8: 11,611,814 (GRCm39) |
E178G |
probably benign |
Het |
Kansl3 |
A |
T |
1: 36,387,758 (GRCm39) |
L530H |
probably damaging |
Het |
Kcna5 |
A |
T |
6: 126,511,768 (GRCm39) |
L120* |
probably null |
Het |
Kcnt1 |
T |
G |
2: 25,791,901 (GRCm39) |
I617S |
probably benign |
Het |
Lama1 |
T |
A |
17: 68,111,468 (GRCm39) |
S2240T |
|
Het |
Lcn2 |
T |
C |
2: 32,277,927 (GRCm39) |
D55G |
probably benign |
Het |
Ldlrad4 |
G |
T |
18: 68,368,740 (GRCm39) |
A66S |
possibly damaging |
Het |
Matn2 |
A |
T |
15: 34,399,223 (GRCm39) |
H370L |
possibly damaging |
Het |
Mettl23 |
T |
G |
11: 116,740,096 (GRCm39) |
V189G |
probably benign |
Het |
Mpp4 |
G |
A |
1: 59,162,672 (GRCm39) |
T543M |
not run |
Het |
Odf4 |
A |
T |
11: 68,812,898 (GRCm39) |
S253R |
probably benign |
Het |
Or10d4 |
C |
A |
9: 39,580,534 (GRCm39) |
F60L |
possibly damaging |
Het |
Or11h23 |
G |
T |
14: 50,947,928 (GRCm39) |
C47F |
possibly damaging |
Het |
Or7d9 |
A |
G |
9: 20,193,708 (GRCm39) |
|
probably benign |
Het |
Or8b36 |
T |
A |
9: 37,937,963 (GRCm39) |
I287N |
probably damaging |
Het |
Or8g21 |
T |
A |
9: 38,906,203 (GRCm39) |
H176L |
probably damaging |
Het |
Pcdha11 |
A |
T |
18: 37,145,733 (GRCm39) |
Y608F |
possibly damaging |
Het |
Pcdhga5 |
A |
G |
18: 37,828,578 (GRCm39) |
D342G |
probably damaging |
Het |
Pde6d |
A |
G |
1: 86,471,250 (GRCm39) |
S143P |
probably damaging |
Het |
Plec |
A |
T |
15: 76,061,135 (GRCm39) |
I2934N |
probably damaging |
Het |
Primpol |
G |
T |
8: 47,039,459 (GRCm39) |
P387Q |
probably damaging |
Het |
Prkcd |
C |
T |
14: 30,327,772 (GRCm39) |
|
probably null |
Het |
Prph2 |
T |
C |
17: 47,221,732 (GRCm39) |
L37S |
possibly damaging |
Het |
Prrt4 |
A |
G |
6: 29,177,718 (GRCm39) |
L17P |
probably damaging |
Het |
Pycr3 |
T |
C |
15: 75,790,138 (GRCm39) |
D171G |
probably damaging |
Het |
Rapsn |
A |
G |
2: 90,875,293 (GRCm39) |
T359A |
probably benign |
Het |
Setd6 |
A |
T |
8: 96,442,866 (GRCm39) |
H101L |
probably benign |
Het |
Sez6 |
T |
C |
11: 77,865,375 (GRCm39) |
S671P |
probably damaging |
Het |
Son |
T |
C |
16: 91,453,416 (GRCm39) |
L721S |
probably damaging |
Het |
Spata31d1b |
A |
T |
13: 59,865,047 (GRCm39) |
R732W |
possibly damaging |
Het |
Srd5a3 |
T |
A |
5: 76,302,618 (GRCm39) |
F328I |
probably damaging |
Het |
Tfap2b |
G |
A |
1: 19,304,531 (GRCm39) |
G447D |
probably damaging |
Het |
Thoc3 |
A |
C |
13: 54,611,591 (GRCm39) |
F232C |
probably damaging |
Het |
Tmem69 |
A |
G |
4: 116,410,595 (GRCm39) |
L125P |
probably damaging |
Het |
Tnfsf13 |
C |
T |
11: 69,575,989 (GRCm39) |
V33M |
probably damaging |
Het |
Togaram2 |
T |
A |
17: 72,011,746 (GRCm39) |
M476K |
probably benign |
Het |
Tube1 |
A |
G |
10: 39,018,294 (GRCm39) |
I124V |
probably benign |
Het |
Uevld |
A |
T |
7: 46,576,100 (GRCm39) |
I462N |
probably damaging |
Het |
Utrn |
G |
A |
10: 12,362,354 (GRCm39) |
R2660C |
probably damaging |
Het |
Vcan |
T |
C |
13: 89,836,773 (GRCm39) |
T2924A |
probably damaging |
Het |
Vmn2r120 |
T |
C |
17: 57,832,942 (GRCm39) |
Y79C |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,275,587 (GRCm39) |
V790A |
probably benign |
Het |
Zfp874b |
A |
G |
13: 67,622,093 (GRCm39) |
F402L |
probably benign |
Het |
Zfp978 |
T |
C |
4: 147,469,760 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zfp936 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02231:Zfp936
|
APN |
7 |
42,836,909 (GRCm39) |
splice site |
probably null |
|
IGL02245:Zfp936
|
APN |
7 |
42,836,722 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02335:Zfp936
|
APN |
7 |
42,836,691 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Zfp936
|
UTSW |
7 |
42,838,913 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0437:Zfp936
|
UTSW |
7 |
42,838,734 (GRCm39) |
missense |
probably benign |
0.00 |
R3899:Zfp936
|
UTSW |
7 |
42,839,158 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4120:Zfp936
|
UTSW |
7 |
42,839,630 (GRCm39) |
missense |
probably benign |
0.10 |
R4406:Zfp936
|
UTSW |
7 |
42,839,748 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4959:Zfp936
|
UTSW |
7 |
42,839,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Zfp936
|
UTSW |
7 |
42,836,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R5163:Zfp936
|
UTSW |
7 |
42,839,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R5182:Zfp936
|
UTSW |
7 |
42,839,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R5292:Zfp936
|
UTSW |
7 |
42,838,759 (GRCm39) |
nonsense |
probably null |
|
R5668:Zfp936
|
UTSW |
7 |
42,839,858 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6057:Zfp936
|
UTSW |
7 |
42,839,787 (GRCm39) |
missense |
probably benign |
0.00 |
R6901:Zfp936
|
UTSW |
7 |
42,839,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R7139:Zfp936
|
UTSW |
7 |
42,839,715 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7258:Zfp936
|
UTSW |
7 |
42,839,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R7440:Zfp936
|
UTSW |
7 |
42,836,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7537:Zfp936
|
UTSW |
7 |
42,839,239 (GRCm39) |
nonsense |
probably null |
|
R7561:Zfp936
|
UTSW |
7 |
42,839,339 (GRCm39) |
missense |
probably damaging |
0.98 |
R7662:Zfp936
|
UTSW |
7 |
42,839,336 (GRCm39) |
nonsense |
probably null |
|
R7775:Zfp936
|
UTSW |
7 |
42,839,720 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8016:Zfp936
|
UTSW |
7 |
42,838,848 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8121:Zfp936
|
UTSW |
7 |
42,839,547 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9012:Zfp936
|
UTSW |
7 |
42,839,416 (GRCm39) |
nonsense |
probably null |
|
R9058:Zfp936
|
UTSW |
7 |
42,839,196 (GRCm39) |
missense |
probably benign |
0.32 |
R9188:Zfp936
|
UTSW |
7 |
42,839,768 (GRCm39) |
missense |
probably benign |
0.00 |
R9236:Zfp936
|
UTSW |
7 |
42,836,922 (GRCm39) |
missense |
probably benign |
0.00 |
R9596:Zfp936
|
UTSW |
7 |
42,839,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|