Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
C |
T |
8: 41,208,953 (GRCm39) |
P740S |
probably benign |
Het |
Arfgef1 |
G |
T |
1: 10,283,419 (GRCm39) |
H163Q |
probably benign |
Het |
Arih2 |
C |
G |
9: 108,488,938 (GRCm39) |
R260P |
probably damaging |
Het |
Atp6v1h |
T |
A |
1: 5,187,699 (GRCm39) |
D222E |
probably damaging |
Het |
Auts2 |
T |
C |
5: 131,490,155 (GRCm39) |
T165A |
|
Het |
BC034090 |
A |
G |
1: 155,099,049 (GRCm39) |
S579P |
probably benign |
Het |
Bpifb9b |
T |
A |
2: 154,160,766 (GRCm39) |
S546T |
probably benign |
Het |
C4b |
C |
T |
17: 34,952,159 (GRCm39) |
V1229I |
probably benign |
Het |
Cadps2 |
T |
C |
6: 23,344,262 (GRCm39) |
D895G |
probably benign |
Het |
Cby2 |
A |
G |
14: 75,820,838 (GRCm39) |
S296P |
probably damaging |
Het |
Cep112 |
T |
C |
11: 108,328,076 (GRCm39) |
S51P |
probably damaging |
Het |
Cep164 |
T |
C |
9: 45,717,708 (GRCm39) |
H545R |
unknown |
Het |
Creb3l1 |
C |
T |
2: 91,822,231 (GRCm39) |
|
probably null |
Het |
Crlf1 |
T |
A |
8: 70,951,316 (GRCm39) |
I65K |
probably benign |
Het |
Crybg3 |
T |
C |
16: 59,421,256 (GRCm39) |
M1V |
probably null |
Het |
Cyb5d1 |
T |
A |
11: 69,285,830 (GRCm39) |
I69L |
probably damaging |
Het |
D430041D05Rik |
T |
C |
2: 104,088,337 (GRCm39) |
D213G |
probably benign |
Het |
Dennd5a |
C |
G |
7: 109,498,930 (GRCm39) |
|
probably null |
Het |
Dennd5a |
T |
A |
7: 109,498,942 (GRCm39) |
M998L |
probably benign |
Het |
E2f1 |
T |
A |
2: 154,402,755 (GRCm39) |
E382D |
probably benign |
Het |
Enpep |
T |
A |
3: 129,102,772 (GRCm39) |
T395S |
probably benign |
Het |
Gm20939 |
A |
G |
17: 95,182,977 (GRCm39) |
E71G |
probably damaging |
Het |
Hs1bp3 |
T |
A |
12: 8,386,273 (GRCm39) |
V225E |
probably benign |
Het |
Icam5 |
T |
C |
9: 20,943,427 (GRCm39) |
M1T |
probably null |
Het |
Ifi205 |
T |
C |
1: 173,844,997 (GRCm39) |
I262V |
probably benign |
Het |
Iqce |
T |
C |
5: 140,677,380 (GRCm39) |
Y147C |
probably damaging |
Het |
Kcnh2 |
C |
T |
5: 24,538,003 (GRCm39) |
G120E |
probably damaging |
Het |
Kif3c |
A |
G |
12: 3,417,505 (GRCm39) |
T509A |
probably benign |
Het |
Napepld |
A |
T |
5: 21,875,490 (GRCm39) |
N351K |
probably benign |
Het |
Ndufaf3 |
C |
A |
9: 108,443,357 (GRCm39) |
|
probably null |
Het |
Nlrp9b |
C |
T |
7: 19,757,336 (GRCm39) |
T191I |
probably damaging |
Het |
Oog2 |
T |
C |
4: 143,921,789 (GRCm39) |
L233P |
probably damaging |
Het |
Or1a1b |
T |
A |
11: 74,097,289 (GRCm39) |
Y251F |
probably damaging |
Het |
Or2g1 |
T |
C |
17: 38,106,992 (GRCm39) |
I219T |
probably damaging |
Het |
Or2n1d |
A |
T |
17: 38,646,320 (GRCm39) |
T91S |
possibly damaging |
Het |
Or2w1 |
T |
A |
13: 21,317,131 (GRCm39) |
F62Y |
possibly damaging |
Het |
Preb |
A |
G |
5: 31,112,995 (GRCm39) |
F416L |
probably benign |
Het |
Prickle2 |
C |
T |
6: 92,397,243 (GRCm39) |
V217I |
probably benign |
Het |
Prss45 |
T |
A |
9: 110,668,278 (GRCm39) |
I157N |
probably damaging |
Het |
Ranbp17 |
T |
C |
11: 33,429,232 (GRCm39) |
T338A |
probably benign |
Het |
Snd1 |
T |
C |
6: 28,745,206 (GRCm39) |
F517S |
probably damaging |
Het |
Srpk2 |
A |
T |
5: 23,719,671 (GRCm39) |
F578I |
probably damaging |
Het |
Stx2 |
A |
T |
5: 129,076,601 (GRCm39) |
D27E |
probably benign |
Het |
Tgfbrap1 |
A |
G |
1: 43,093,695 (GRCm39) |
I599T |
probably benign |
Het |
Trim25 |
G |
T |
11: 88,900,167 (GRCm39) |
E305* |
probably null |
Het |
Ttll7 |
T |
A |
3: 146,673,768 (GRCm39) |
I821N |
probably benign |
Het |
Wdfy3 |
A |
G |
5: 102,089,358 (GRCm39) |
L612P |
probably damaging |
Het |
Zcchc9 |
T |
A |
13: 91,954,186 (GRCm39) |
D23V |
|
Het |
Zfyve26 |
T |
C |
12: 79,315,231 (GRCm39) |
D1415G |
possibly damaging |
Het |
Zpbp2 |
C |
T |
11: 98,442,141 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp141 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00593:Zfp141
|
APN |
7 |
42,124,731 (GRCm39) |
nonsense |
probably null |
|
IGL00595:Zfp141
|
APN |
7 |
42,126,079 (GRCm39) |
missense |
probably benign |
0.08 |
R0577:Zfp141
|
UTSW |
7 |
42,125,938 (GRCm39) |
missense |
probably benign |
0.14 |
R0883:Zfp141
|
UTSW |
7 |
42,125,480 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1701:Zfp141
|
UTSW |
7 |
42,125,470 (GRCm39) |
missense |
probably benign |
0.35 |
R2290:Zfp141
|
UTSW |
7 |
42,124,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R4176:Zfp141
|
UTSW |
7 |
42,125,705 (GRCm39) |
missense |
probably benign |
0.04 |
R4719:Zfp141
|
UTSW |
7 |
42,126,111 (GRCm39) |
splice site |
probably null |
|
R4897:Zfp141
|
UTSW |
7 |
42,125,629 (GRCm39) |
missense |
probably benign |
0.24 |
R5372:Zfp141
|
UTSW |
7 |
42,126,620 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5438:Zfp141
|
UTSW |
7 |
42,138,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R5447:Zfp141
|
UTSW |
7 |
42,124,983 (GRCm39) |
nonsense |
probably null |
|
R5743:Zfp141
|
UTSW |
7 |
42,125,855 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5969:Zfp141
|
UTSW |
7 |
42,138,912 (GRCm39) |
missense |
probably damaging |
0.98 |
R6731:Zfp141
|
UTSW |
7 |
42,138,924 (GRCm39) |
missense |
probably damaging |
0.99 |
R7127:Zfp141
|
UTSW |
7 |
42,124,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R7474:Zfp141
|
UTSW |
7 |
42,125,678 (GRCm39) |
nonsense |
probably null |
|
R7572:Zfp141
|
UTSW |
7 |
42,124,856 (GRCm39) |
missense |
probably benign |
0.03 |
R7830:Zfp141
|
UTSW |
7 |
42,124,612 (GRCm39) |
missense |
probably benign |
0.01 |
R7890:Zfp141
|
UTSW |
7 |
42,125,903 (GRCm39) |
missense |
probably damaging |
0.99 |
R8133:Zfp141
|
UTSW |
7 |
42,124,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Zfp141
|
UTSW |
7 |
42,125,687 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9238:Zfp141
|
UTSW |
7 |
42,125,111 (GRCm39) |
nonsense |
probably null |
|
R9245:Zfp141
|
UTSW |
7 |
42,124,821 (GRCm39) |
nonsense |
probably null |
|
R9339:Zfp141
|
UTSW |
7 |
42,125,639 (GRCm39) |
missense |
probably damaging |
0.98 |
R9498:Zfp141
|
UTSW |
7 |
42,125,770 (GRCm39) |
missense |
probably benign |
0.07 |
|