Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd2 |
T |
C |
15: 91,033,232 (GRCm39) |
D728G |
probably benign |
Het |
Adig |
A |
T |
2: 158,347,727 (GRCm39) |
D48V |
probably damaging |
Het |
Adig |
A |
C |
2: 158,349,890 (GRCm39) |
*57S |
probably null |
Het |
Amigo3 |
A |
G |
9: 107,932,020 (GRCm39) |
D481G |
probably damaging |
Het |
Atf6b |
T |
A |
17: 34,872,968 (GRCm39) |
M628K |
probably damaging |
Het |
Atoh8 |
A |
G |
6: 72,212,129 (GRCm39) |
L7P |
probably damaging |
Het |
Bcl9 |
A |
G |
3: 97,115,959 (GRCm39) |
S912P |
probably damaging |
Het |
Card9 |
T |
A |
2: 26,247,310 (GRCm39) |
I280F |
probably damaging |
Het |
Ccr9 |
A |
G |
9: 123,609,085 (GRCm39) |
T256A |
probably benign |
Het |
Cd300lg |
T |
C |
11: 101,939,590 (GRCm39) |
I306T |
probably damaging |
Het |
Cfap65 |
T |
A |
1: 74,960,769 (GRCm39) |
M734L |
probably benign |
Het |
Cobll1 |
A |
G |
2: 64,929,356 (GRCm39) |
S657P |
probably damaging |
Het |
Comp |
A |
G |
8: 70,831,285 (GRCm39) |
N384S |
probably damaging |
Het |
Cps1 |
T |
A |
1: 67,191,445 (GRCm39) |
V209D |
possibly damaging |
Het |
Cwc22 |
A |
T |
2: 77,759,803 (GRCm39) |
D81E |
possibly damaging |
Het |
D630045J12Rik |
G |
A |
6: 38,167,512 (GRCm39) |
P1030L |
possibly damaging |
Het |
Dcn |
A |
G |
10: 97,343,637 (GRCm39) |
Y199C |
probably damaging |
Het |
Exosc3 |
A |
T |
4: 45,316,969 (GRCm39) |
I228N |
probably damaging |
Het |
Fbxo10 |
T |
C |
4: 45,062,178 (GRCm39) |
H116R |
probably benign |
Het |
Fbxo21 |
T |
A |
5: 118,146,108 (GRCm39) |
I577N |
probably damaging |
Het |
Flnc |
A |
T |
6: 29,447,815 (GRCm39) |
Q1206L |
probably benign |
Het |
Fubp3 |
T |
C |
2: 31,503,056 (GRCm39) |
F480L |
probably benign |
Het |
Fzd5 |
T |
C |
1: 64,775,110 (GRCm39) |
N217S |
possibly damaging |
Het |
Gcg |
T |
C |
2: 62,306,133 (GRCm39) |
M155V |
probably null |
Het |
Gm7298 |
G |
A |
6: 121,756,604 (GRCm39) |
|
probably benign |
Het |
Gpr160 |
T |
A |
3: 30,950,038 (GRCm39) |
L37I |
probably benign |
Het |
Grik1 |
G |
A |
16: 87,848,379 (GRCm39) |
H130Y |
|
Het |
Hydin |
T |
A |
8: 111,233,580 (GRCm39) |
I1806N |
probably damaging |
Het |
Isl1 |
A |
T |
13: 116,444,902 (GRCm39) |
C42* |
probably null |
Het |
Itpr2 |
T |
C |
6: 146,226,529 (GRCm39) |
D1405G |
probably damaging |
Het |
Kat6b |
A |
G |
14: 21,711,551 (GRCm39) |
N682D |
probably benign |
Het |
Kcnh6 |
C |
G |
11: 105,924,860 (GRCm39) |
H941Q |
possibly damaging |
Het |
Kprp |
A |
C |
3: 92,733,000 (GRCm39) |
C17G |
probably damaging |
Het |
Lsm14a |
T |
C |
7: 34,088,225 (GRCm39) |
|
probably benign |
Het |
Mrgpra2a |
G |
T |
7: 47,076,307 (GRCm39) |
T317K |
probably benign |
Het |
Myh11 |
A |
G |
16: 14,054,283 (GRCm39) |
V360A |
|
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Oaf |
G |
A |
9: 43,133,966 (GRCm39) |
P252S |
probably benign |
Het |
Obox2 |
T |
G |
7: 15,131,290 (GRCm39) |
V132G |
unknown |
Het |
Or51v8 |
T |
A |
7: 103,319,633 (GRCm39) |
T202S |
probably benign |
Het |
Or52b1 |
A |
G |
7: 104,978,646 (GRCm39) |
L251P |
probably damaging |
Het |
Or5b109 |
C |
T |
19: 13,212,268 (GRCm39) |
S218L |
probably damaging |
Het |
Or5b12 |
T |
C |
19: 12,897,446 (GRCm39) |
T76A |
possibly damaging |
Het |
Pld2 |
T |
A |
11: 70,448,234 (GRCm39) |
S894T |
probably benign |
Het |
Plxna1 |
G |
T |
6: 89,296,364 (GRCm39) |
S1893R |
possibly damaging |
Het |
Prkd1 |
T |
C |
12: 50,472,232 (GRCm39) |
E227G |
possibly damaging |
Het |
Prox1 |
T |
C |
1: 189,893,242 (GRCm39) |
N401S |
possibly damaging |
Het |
Prune2 |
T |
C |
19: 17,095,690 (GRCm39) |
V398A |
possibly damaging |
Het |
Rasgef1a |
A |
G |
6: 118,063,223 (GRCm39) |
N285D |
probably benign |
Het |
Rbbp5 |
A |
G |
1: 132,420,304 (GRCm39) |
K179R |
probably benign |
Het |
Rp9 |
G |
A |
9: 22,379,573 (GRCm39) |
|
probably benign |
Het |
Slc15a2 |
A |
G |
16: 36,574,090 (GRCm39) |
F588L |
probably benign |
Het |
Sptan1 |
T |
A |
2: 29,880,977 (GRCm39) |
D415E |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 4,990,901 (GRCm39) |
K593E |
probably benign |
Het |
Tab1 |
A |
G |
15: 80,041,904 (GRCm39) |
T341A |
probably benign |
Het |
Tmc4 |
T |
C |
7: 3,670,552 (GRCm39) |
E513G |
probably damaging |
Het |
Tmem131l |
A |
C |
3: 83,848,244 (GRCm39) |
V302G |
probably damaging |
Het |
Tnip1 |
G |
A |
11: 54,807,783 (GRCm39) |
H553Y |
possibly damaging |
Het |
Tns2 |
C |
T |
15: 102,021,478 (GRCm39) |
P1048S |
probably damaging |
Het |
Twsg1 |
C |
T |
17: 66,233,306 (GRCm39) |
V215I |
probably damaging |
Het |
Txnl1 |
G |
A |
18: 63,825,325 (GRCm39) |
|
probably benign |
Het |
Unc13c |
A |
G |
9: 73,839,862 (GRCm39) |
Y330H |
possibly damaging |
Het |
Utrn |
A |
T |
10: 12,509,707 (GRCm39) |
W2422R |
probably damaging |
Het |
Vmn2r112 |
T |
A |
17: 22,837,721 (GRCm39) |
D727E |
probably damaging |
Het |
Vmn2r59 |
G |
T |
7: 41,695,286 (GRCm39) |
C375* |
probably null |
Het |
Vopp1 |
G |
T |
6: 57,731,575 (GRCm39) |
Q139K |
possibly damaging |
Het |
Vwa5b1 |
T |
C |
4: 138,316,005 (GRCm39) |
D579G |
probably damaging |
Het |
Wdr6 |
A |
G |
9: 108,450,691 (GRCm39) |
Y971H |
probably benign |
Het |
Zfp354c |
A |
G |
11: 50,706,059 (GRCm39) |
F339L |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,317,610 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Garem1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00504:Garem1
|
APN |
18 |
21,281,714 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01588:Garem1
|
APN |
18 |
21,262,854 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02171:Garem1
|
APN |
18 |
21,262,298 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02270:Garem1
|
APN |
18 |
21,281,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03149:Garem1
|
APN |
18 |
21,264,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R0136:Garem1
|
UTSW |
18 |
21,263,048 (GRCm39) |
missense |
probably damaging |
0.96 |
R0285:Garem1
|
UTSW |
18 |
21,262,669 (GRCm39) |
missense |
probably benign |
|
R0361:Garem1
|
UTSW |
18 |
21,432,801 (GRCm39) |
nonsense |
probably null |
|
R1068:Garem1
|
UTSW |
18 |
21,301,812 (GRCm39) |
missense |
probably benign |
0.00 |
R1537:Garem1
|
UTSW |
18 |
21,301,931 (GRCm39) |
splice site |
probably null |
|
R1726:Garem1
|
UTSW |
18 |
21,281,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R1826:Garem1
|
UTSW |
18 |
21,262,509 (GRCm39) |
missense |
probably benign |
0.00 |
R2140:Garem1
|
UTSW |
18 |
21,262,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R3714:Garem1
|
UTSW |
18 |
21,281,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R3937:Garem1
|
UTSW |
18 |
21,281,863 (GRCm39) |
nonsense |
probably null |
|
R4362:Garem1
|
UTSW |
18 |
21,369,172 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4441:Garem1
|
UTSW |
18 |
21,301,807 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4747:Garem1
|
UTSW |
18 |
21,263,000 (GRCm39) |
missense |
probably benign |
|
R4814:Garem1
|
UTSW |
18 |
21,281,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Garem1
|
UTSW |
18 |
21,262,825 (GRCm39) |
missense |
probably benign |
0.01 |
R4838:Garem1
|
UTSW |
18 |
21,280,950 (GRCm39) |
missense |
probably benign |
0.00 |
R5805:Garem1
|
UTSW |
18 |
21,281,492 (GRCm39) |
missense |
probably benign |
0.04 |
R5963:Garem1
|
UTSW |
18 |
21,262,487 (GRCm39) |
missense |
probably benign |
0.45 |
R5982:Garem1
|
UTSW |
18 |
21,281,408 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6134:Garem1
|
UTSW |
18 |
21,262,881 (GRCm39) |
missense |
probably benign |
0.00 |
R6242:Garem1
|
UTSW |
18 |
21,262,229 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6453:Garem1
|
UTSW |
18 |
21,281,796 (GRCm39) |
missense |
probably damaging |
0.99 |
R6485:Garem1
|
UTSW |
18 |
21,262,894 (GRCm39) |
missense |
probably benign |
0.00 |
R6596:Garem1
|
UTSW |
18 |
21,281,796 (GRCm39) |
missense |
probably damaging |
0.99 |
R6662:Garem1
|
UTSW |
18 |
21,281,304 (GRCm39) |
missense |
probably benign |
0.45 |
R6883:Garem1
|
UTSW |
18 |
21,262,769 (GRCm39) |
missense |
probably benign |
|
R6937:Garem1
|
UTSW |
18 |
21,280,827 (GRCm39) |
missense |
probably benign |
0.00 |
R7027:Garem1
|
UTSW |
18 |
21,263,051 (GRCm39) |
missense |
probably benign |
|
R7256:Garem1
|
UTSW |
18 |
21,281,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R7534:Garem1
|
UTSW |
18 |
21,432,973 (GRCm39) |
start gained |
probably benign |
|
R7620:Garem1
|
UTSW |
18 |
21,262,898 (GRCm39) |
missense |
probably benign |
|
R7869:Garem1
|
UTSW |
18 |
21,432,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R7963:Garem1
|
UTSW |
18 |
21,281,844 (GRCm39) |
missense |
probably damaging |
0.98 |
R8058:Garem1
|
UTSW |
18 |
21,281,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R8953:Garem1
|
UTSW |
18 |
21,264,388 (GRCm39) |
critical splice donor site |
probably null |
|
R9411:Garem1
|
UTSW |
18 |
21,369,057 (GRCm39) |
critical splice donor site |
probably null |
|
R9475:Garem1
|
UTSW |
18 |
21,281,370 (GRCm39) |
missense |
probably benign |
0.00 |
R9789:Garem1
|
UTSW |
18 |
21,262,985 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1176:Garem1
|
UTSW |
18 |
21,281,382 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Garem1
|
UTSW |
18 |
21,262,849 (GRCm39) |
missense |
probably damaging |
1.00 |
|