Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
A |
G |
3: 124,206,180 (GRCm39) |
I336T |
probably benign |
Het |
4930519P11Rik |
T |
C |
2: 154,455,107 (GRCm39) |
Y84C |
unknown |
Het |
4930568D16Rik |
C |
T |
2: 35,244,606 (GRCm39) |
G249S |
probably damaging |
Het |
AAdacl4fm3 |
A |
T |
4: 144,430,047 (GRCm39) |
L314Q |
probably damaging |
Het |
Adprhl1 |
C |
T |
8: 13,298,682 (GRCm39) |
V83I |
probably damaging |
Het |
Agbl1 |
T |
A |
7: 76,348,585 (GRCm39) |
V894E |
unknown |
Het |
Amigo3 |
T |
C |
9: 107,931,867 (GRCm39) |
L430P |
probably benign |
Het |
Aoc1 |
A |
G |
6: 48,883,146 (GRCm39) |
I341V |
probably benign |
Het |
Bod1l |
A |
G |
5: 41,990,055 (GRCm39) |
S223P |
probably benign |
Het |
Cacnb3 |
T |
C |
15: 98,537,819 (GRCm39) |
|
probably null |
Het |
Ccdc63 |
G |
T |
5: 122,247,335 (GRCm39) |
N503K |
probably damaging |
Het |
Ccdc83 |
T |
A |
7: 89,879,120 (GRCm39) |
I225F |
probably damaging |
Het |
Cd200r1 |
A |
G |
16: 44,610,050 (GRCm39) |
T90A |
possibly damaging |
Het |
Cd8a |
A |
G |
6: 71,350,799 (GRCm39) |
N88S |
probably benign |
Het |
Cep170 |
A |
G |
1: 176,567,642 (GRCm39) |
V152A |
|
Het |
Chid1 |
T |
C |
7: 141,109,518 (GRCm39) |
M123V |
probably benign |
Het |
Cnnm4 |
T |
C |
1: 36,538,603 (GRCm39) |
V595A |
probably benign |
Het |
Coro7 |
A |
G |
16: 4,449,870 (GRCm39) |
L630P |
probably damaging |
Het |
Cpvl |
A |
G |
6: 53,908,890 (GRCm39) |
|
probably null |
Het |
Edem3 |
A |
T |
1: 151,687,347 (GRCm39) |
K762* |
probably null |
Het |
Elp6 |
T |
A |
9: 110,141,627 (GRCm39) |
|
probably null |
Het |
Emilin3 |
A |
T |
2: 160,752,718 (GRCm39) |
Y77* |
probably null |
Het |
Fam234b |
T |
A |
6: 135,220,912 (GRCm39) |
I641N |
probably benign |
Het |
Farsa |
T |
C |
8: 85,590,781 (GRCm39) |
|
probably null |
Het |
Foxf2 |
T |
C |
13: 31,811,182 (GRCm39) |
S374P |
probably benign |
Het |
Gm11596 |
A |
T |
11: 99,683,667 (GRCm39) |
I151N |
unknown |
Het |
Gm9817 |
C |
T |
13: 45,232,427 (GRCm39) |
Q77* |
probably null |
Het |
Gon4l |
A |
G |
3: 88,803,102 (GRCm39) |
K1238E |
probably benign |
Het |
H13 |
A |
G |
2: 152,537,431 (GRCm39) |
Y292C |
probably damaging |
Het |
Hip1r |
A |
G |
5: 124,139,504 (GRCm39) |
N928S |
probably benign |
Het |
Jak3 |
A |
C |
8: 72,131,686 (GRCm39) |
T125P |
probably benign |
Het |
Krt7 |
A |
C |
15: 101,311,913 (GRCm39) |
K124Q |
possibly damaging |
Het |
Ldc1 |
T |
C |
4: 130,114,169 (GRCm39) |
N83D |
probably damaging |
Het |
Lrrc66 |
G |
A |
5: 73,764,664 (GRCm39) |
S793F |
probably damaging |
Het |
Mycbp2 |
C |
T |
14: 103,485,840 (GRCm39) |
V1074I |
probably damaging |
Het |
Nckap5 |
T |
C |
1: 125,954,581 (GRCm39) |
D657G |
probably benign |
Het |
Nt5el |
A |
G |
13: 105,218,793 (GRCm39) |
I42M |
probably damaging |
Het |
Or5b113 |
T |
A |
19: 13,342,598 (GRCm39) |
V202E |
probably benign |
Het |
Or8k21 |
T |
C |
2: 86,145,034 (GRCm39) |
I199V |
probably benign |
Het |
Osbpl7 |
A |
G |
11: 96,941,548 (GRCm39) |
S24G |
probably benign |
Het |
Pcm1 |
G |
T |
8: 41,762,610 (GRCm39) |
E1385* |
probably null |
Het |
Poc5 |
A |
G |
13: 96,547,143 (GRCm39) |
T469A |
probably damaging |
Het |
Ppp3ca |
A |
G |
3: 136,596,222 (GRCm39) |
T296A |
probably benign |
Het |
Prl6a1 |
T |
C |
13: 27,502,125 (GRCm39) |
I164T |
probably damaging |
Het |
Psmd6 |
GCAGAGCGGGCAGGGCATCTCACTGACCCTGTCACCTACCCAGAGCGGGCAGGGCATCTCACTGACCCTGTCACCTACCCAGAGCGGGCAGGGCATCTCACTGACC |
GCAGAGCGGGCAGGGCATCTCACTGACCCTGTCACCTACCCAGAGCGGGCAGGGCATCTCACTGACC |
14: 14,119,882 (GRCm38) |
|
probably null |
Het |
Rnf149 |
A |
C |
1: 39,604,299 (GRCm39) |
M188R |
possibly damaging |
Het |
Rpl10l |
T |
C |
12: 66,331,041 (GRCm39) |
I31V |
probably benign |
Het |
Serinc5 |
T |
C |
13: 92,797,592 (GRCm39) |
S32P |
probably damaging |
Het |
Sirt1 |
T |
A |
10: 63,162,562 (GRCm39) |
K137M |
possibly damaging |
Het |
Smc4 |
A |
G |
3: 68,923,496 (GRCm39) |
Y251C |
probably damaging |
Het |
Sod3 |
A |
C |
5: 52,525,643 (GRCm39) |
E114A |
possibly damaging |
Het |
Tgfbr3 |
A |
G |
5: 107,288,368 (GRCm39) |
V431A |
probably benign |
Het |
Tlr4 |
T |
C |
4: 66,757,836 (GRCm39) |
S210P |
probably damaging |
Het |
Trub2 |
G |
T |
2: 29,676,520 (GRCm39) |
T70N |
probably benign |
Het |
Tsga10 |
A |
T |
1: 37,874,323 (GRCm39) |
C159S |
unknown |
Het |
Vmn1r15 |
A |
T |
6: 57,235,644 (GRCm39) |
I171F |
probably benign |
Het |
Vmn2r50 |
T |
A |
7: 9,771,562 (GRCm39) |
H713L |
possibly damaging |
Het |
Zcchc14 |
T |
C |
8: 122,378,514 (GRCm39) |
S43G |
unknown |
Het |
Zfp638 |
T |
C |
6: 83,956,196 (GRCm39) |
I1601T |
probably damaging |
Het |
|
Other mutations in Iqcf4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01329:Iqcf4
|
APN |
9 |
106,447,832 (GRCm39) |
missense |
probably benign |
0.12 |
R0781:Iqcf4
|
UTSW |
9 |
106,445,860 (GRCm39) |
missense |
probably benign |
0.06 |
R1764:Iqcf4
|
UTSW |
9 |
106,445,893 (GRCm39) |
missense |
probably benign |
0.12 |
R4525:Iqcf4
|
UTSW |
9 |
106,447,827 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4703:Iqcf4
|
UTSW |
9 |
106,445,519 (GRCm39) |
splice site |
probably null |
|
R5823:Iqcf4
|
UTSW |
9 |
106,445,800 (GRCm39) |
missense |
probably benign |
0.00 |
R6298:Iqcf4
|
UTSW |
9 |
106,445,874 (GRCm39) |
missense |
probably benign |
0.25 |
R7780:Iqcf4
|
UTSW |
9 |
106,445,860 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7818:Iqcf4
|
UTSW |
9 |
106,447,738 (GRCm39) |
nonsense |
probably null |
|
R8694:Iqcf4
|
UTSW |
9 |
106,448,111 (GRCm39) |
start gained |
probably benign |
|
R9435:Iqcf4
|
UTSW |
9 |
106,445,652 (GRCm39) |
missense |
possibly damaging |
0.95 |
RF003:Iqcf4
|
UTSW |
9 |
106,447,806 (GRCm39) |
small insertion |
probably benign |
|
RF007:Iqcf4
|
UTSW |
9 |
106,447,808 (GRCm39) |
small insertion |
probably benign |
|
RF016:Iqcf4
|
UTSW |
9 |
106,447,808 (GRCm39) |
small insertion |
probably benign |
|
RF028:Iqcf4
|
UTSW |
9 |
106,447,813 (GRCm39) |
small insertion |
probably benign |
|
RF031:Iqcf4
|
UTSW |
9 |
106,447,814 (GRCm39) |
small insertion |
probably benign |
|
RF036:Iqcf4
|
UTSW |
9 |
106,447,810 (GRCm39) |
small insertion |
probably benign |
|
RF041:Iqcf4
|
UTSW |
9 |
106,447,812 (GRCm39) |
nonsense |
probably null |
|
RF042:Iqcf4
|
UTSW |
9 |
106,447,804 (GRCm39) |
small insertion |
probably benign |
|
RF043:Iqcf4
|
UTSW |
9 |
106,447,812 (GRCm39) |
small insertion |
probably benign |
|
RF045:Iqcf4
|
UTSW |
9 |
106,447,809 (GRCm39) |
small insertion |
probably benign |
|
RF046:Iqcf4
|
UTSW |
9 |
106,447,809 (GRCm39) |
small insertion |
probably benign |
|
RF047:Iqcf4
|
UTSW |
9 |
106,447,811 (GRCm39) |
small insertion |
probably benign |
|
RF063:Iqcf4
|
UTSW |
9 |
106,447,816 (GRCm39) |
small insertion |
probably benign |
|
|