Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars2 |
T |
A |
17: 45,818,523 (GRCm39) |
C103S |
probably damaging |
Het |
Adamts20 |
T |
C |
15: 94,236,349 (GRCm39) |
S841G |
probably benign |
Het |
Add3 |
T |
A |
19: 53,222,332 (GRCm39) |
V313E |
possibly damaging |
Het |
Ahr |
G |
T |
12: 35,562,771 (GRCm39) |
|
probably benign |
Het |
Ankrd12 |
T |
A |
17: 66,356,874 (GRCm39) |
M48L |
probably benign |
Het |
Apaf1 |
A |
C |
10: 90,859,580 (GRCm39) |
|
probably null |
Het |
Bank1 |
T |
C |
3: 135,989,772 (GRCm39) |
H106R |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,868,260 (GRCm39) |
|
probably benign |
Het |
Castor1 |
A |
G |
11: 4,170,141 (GRCm39) |
E73G |
probably benign |
Het |
Ccdc170 |
C |
T |
10: 4,511,016 (GRCm39) |
H692Y |
possibly damaging |
Het |
Cd93 |
A |
G |
2: 148,284,071 (GRCm39) |
I425T |
probably benign |
Het |
Celsr1 |
A |
C |
15: 85,914,772 (GRCm39) |
L1067R |
possibly damaging |
Het |
Clca3a2 |
A |
T |
3: 144,519,447 (GRCm39) |
|
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,251,990 (GRCm39) |
S549P |
unknown |
Het |
Col6a4 |
A |
G |
9: 105,952,138 (GRCm39) |
S587P |
possibly damaging |
Het |
Crebbp |
C |
A |
16: 3,903,187 (GRCm39) |
M2017I |
probably benign |
Het |
Crybg1 |
A |
C |
10: 43,874,103 (GRCm39) |
F1002V |
probably benign |
Het |
Ctif |
T |
C |
18: 75,654,458 (GRCm39) |
E356G |
probably damaging |
Het |
Dbx2 |
T |
C |
15: 95,530,239 (GRCm39) |
K243E |
probably damaging |
Het |
Dgkh |
C |
T |
14: 78,853,957 (GRCm39) |
V394I |
probably damaging |
Het |
Dnaja4 |
T |
A |
9: 54,621,638 (GRCm39) |
M321K |
probably benign |
Het |
Dock9 |
T |
C |
14: 121,866,324 (GRCm39) |
N593S |
probably damaging |
Het |
Dot1l |
T |
A |
10: 80,626,560 (GRCm39) |
S1260R |
probably damaging |
Het |
Eea1 |
A |
T |
10: 95,831,510 (GRCm39) |
L200F |
probably damaging |
Het |
Elp2 |
T |
G |
18: 24,765,833 (GRCm39) |
F658V |
probably benign |
Het |
Fbxw15 |
G |
A |
9: 109,394,468 (GRCm39) |
Q116* |
probably null |
Het |
Fstl5 |
A |
T |
3: 76,615,416 (GRCm39) |
N826Y |
probably damaging |
Het |
Galp |
T |
C |
7: 6,214,347 (GRCm39) |
S60P |
possibly damaging |
Het |
Gsdmc |
T |
C |
15: 63,649,902 (GRCm39) |
M330V |
probably benign |
Het |
Hectd2 |
T |
C |
19: 36,562,862 (GRCm39) |
F175L |
probably benign |
Het |
Hmbs |
A |
G |
9: 44,248,102 (GRCm39) |
I318T |
possibly damaging |
Het |
Ifi205 |
T |
C |
1: 173,855,841 (GRCm39) |
D63G |
probably benign |
Het |
Il10ra |
T |
A |
9: 45,167,396 (GRCm39) |
Q387L |
probably damaging |
Het |
Kcnj14 |
C |
A |
7: 45,469,388 (GRCm39) |
G39V |
probably benign |
Het |
Kpna1 |
T |
C |
16: 35,836,381 (GRCm39) |
|
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,331,996 (GRCm39) |
D1586E |
probably damaging |
Het |
Lrrc45 |
A |
G |
11: 120,607,947 (GRCm39) |
I243V |
probably benign |
Het |
Lrrc7 |
T |
C |
3: 157,946,138 (GRCm39) |
K187R |
probably benign |
Het |
Mamdc4 |
G |
T |
2: 25,453,371 (GRCm39) |
T1216N |
probably damaging |
Het |
Map1a |
A |
C |
2: 121,134,145 (GRCm39) |
K1654Q |
probably benign |
Het |
Mta2 |
G |
A |
19: 8,924,104 (GRCm39) |
V195M |
probably damaging |
Het |
Nav2 |
G |
T |
7: 49,208,561 (GRCm39) |
R1583L |
probably damaging |
Het |
Or2y1g |
A |
T |
11: 49,171,247 (GRCm39) |
T91S |
probably benign |
Het |
Or4c112 |
A |
T |
2: 88,854,308 (GRCm39) |
L13Q |
probably damaging |
Het |
Or9i14 |
T |
C |
19: 13,792,735 (GRCm39) |
Y73C |
probably damaging |
Het |
Osbpl1a |
T |
A |
18: 13,002,074 (GRCm39) |
|
probably benign |
Het |
Pcdh17 |
T |
C |
14: 84,685,084 (GRCm39) |
V517A |
possibly damaging |
Het |
Pcdhb14 |
T |
A |
18: 37,583,157 (GRCm39) |
C754* |
probably null |
Het |
Pkd1 |
T |
C |
17: 24,791,988 (GRCm39) |
V1225A |
probably damaging |
Het |
Plekhm3 |
T |
C |
1: 64,960,802 (GRCm39) |
N485D |
probably benign |
Het |
Plekho1 |
A |
C |
3: 95,902,995 (GRCm39) |
S14A |
unknown |
Het |
Ppp2r3d |
A |
T |
9: 101,090,006 (GRCm39) |
C106S |
probably benign |
Het |
Ppp6c |
A |
C |
2: 39,094,928 (GRCm39) |
L99R |
probably damaging |
Het |
Pramel27 |
A |
G |
4: 143,578,345 (GRCm39) |
S202G |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,653,091 (GRCm39) |
Y3855* |
probably null |
Het |
Ptpru |
A |
T |
4: 131,503,565 (GRCm39) |
I1155N |
possibly damaging |
Het |
Reln |
C |
T |
5: 22,216,059 (GRCm39) |
G1042D |
probably damaging |
Het |
Sall4 |
A |
G |
2: 168,596,773 (GRCm39) |
V689A |
probably benign |
Het |
Sec31b |
C |
T |
19: 44,507,741 (GRCm39) |
G768S |
probably damaging |
Het |
Serpinb10 |
T |
A |
1: 107,474,549 (GRCm39) |
V237D |
probably benign |
Het |
Serpinb9 |
T |
G |
13: 33,199,579 (GRCm39) |
D291E |
probably benign |
Het |
Slc12a7 |
T |
G |
13: 73,954,089 (GRCm39) |
|
probably benign |
Het |
Slfn8 |
A |
T |
11: 82,907,902 (GRCm39) |
F214I |
probably damaging |
Het |
Slu7 |
A |
T |
11: 43,328,952 (GRCm39) |
D58V |
probably damaging |
Het |
Smu1 |
T |
C |
4: 40,745,558 (GRCm39) |
Y254C |
probably damaging |
Het |
Snapc4 |
A |
T |
2: 26,260,805 (GRCm39) |
Y479* |
probably null |
Het |
Specc1l |
A |
G |
10: 75,066,640 (GRCm39) |
N30D |
probably benign |
Het |
Spopfm1 |
A |
C |
3: 94,173,153 (GRCm39) |
S50R |
possibly damaging |
Het |
Tbck |
T |
C |
3: 132,428,130 (GRCm39) |
|
probably null |
Het |
Tcf7l1 |
T |
C |
6: 72,610,259 (GRCm39) |
Y246C |
probably damaging |
Het |
Tmem43 |
C |
T |
6: 91,463,897 (GRCm39) |
R391W |
possibly damaging |
Het |
Trav7-1 |
T |
G |
14: 52,892,566 (GRCm39) |
S40A |
possibly damaging |
Het |
Trim45 |
T |
A |
3: 100,832,440 (GRCm39) |
Y224* |
probably null |
Het |
Trio |
A |
T |
15: 27,852,097 (GRCm39) |
I798N |
possibly damaging |
Het |
Trnau1ap |
A |
T |
4: 132,056,662 (GRCm39) |
|
probably null |
Het |
Vmn1r213 |
T |
C |
13: 23,196,043 (GRCm39) |
S209P |
probably damaging |
Het |
Ythdf1 |
G |
T |
2: 180,552,857 (GRCm39) |
R453S |
probably damaging |
Het |
|
Other mutations in Gm7298 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0030:Gm7298
|
UTSW |
6 |
121,751,009 (GRCm39) |
missense |
probably benign |
|
R4978:Gm7298
|
UTSW |
6 |
121,710,076 (GRCm39) |
critical splice donor site |
probably null |
|
R4980:Gm7298
|
UTSW |
6 |
121,736,198 (GRCm39) |
splice site |
probably null |
|
R6000:Gm7298
|
UTSW |
6 |
121,742,038 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6160:Gm7298
|
UTSW |
6 |
121,741,886 (GRCm39) |
missense |
probably benign |
0.28 |
R6180:Gm7298
|
UTSW |
6 |
121,737,782 (GRCm39) |
missense |
probably benign |
0.01 |
R6243:Gm7298
|
UTSW |
6 |
121,756,096 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6266:Gm7298
|
UTSW |
6 |
121,759,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R6268:Gm7298
|
UTSW |
6 |
121,756,032 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6363:Gm7298
|
UTSW |
6 |
121,765,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R6364:Gm7298
|
UTSW |
6 |
121,756,402 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6527:Gm7298
|
UTSW |
6 |
121,746,669 (GRCm39) |
missense |
probably benign |
0.01 |
R6538:Gm7298
|
UTSW |
6 |
121,753,132 (GRCm39) |
missense |
probably damaging |
0.98 |
R6801:Gm7298
|
UTSW |
6 |
121,752,768 (GRCm39) |
missense |
probably benign |
0.03 |
R6884:Gm7298
|
UTSW |
6 |
121,737,480 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6935:Gm7298
|
UTSW |
6 |
121,744,653 (GRCm39) |
missense |
probably benign |
0.02 |
R7051:Gm7298
|
UTSW |
6 |
121,751,993 (GRCm39) |
critical splice donor site |
probably null |
|
R7144:Gm7298
|
UTSW |
6 |
121,738,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R7178:Gm7298
|
UTSW |
6 |
121,762,855 (GRCm39) |
missense |
probably damaging |
0.98 |
R7398:Gm7298
|
UTSW |
6 |
121,758,912 (GRCm39) |
missense |
probably benign |
0.02 |
R7706:Gm7298
|
UTSW |
6 |
121,712,570 (GRCm39) |
missense |
probably damaging |
0.96 |
R7793:Gm7298
|
UTSW |
6 |
121,737,563 (GRCm39) |
critical splice donor site |
probably null |
|
R7829:Gm7298
|
UTSW |
6 |
121,742,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:Gm7298
|
UTSW |
6 |
121,759,741 (GRCm39) |
nonsense |
probably null |
|
R8010:Gm7298
|
UTSW |
6 |
121,712,542 (GRCm39) |
missense |
probably benign |
|
R8167:Gm7298
|
UTSW |
6 |
121,761,414 (GRCm39) |
nonsense |
probably null |
|
R8188:Gm7298
|
UTSW |
6 |
121,763,537 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8248:Gm7298
|
UTSW |
6 |
121,764,402 (GRCm39) |
missense |
probably benign |
0.02 |
R8669:Gm7298
|
UTSW |
6 |
121,742,002 (GRCm39) |
missense |
probably benign |
|
R8806:Gm7298
|
UTSW |
6 |
121,761,641 (GRCm39) |
synonymous |
silent |
|
R8867:Gm7298
|
UTSW |
6 |
121,748,788 (GRCm39) |
missense |
probably benign |
|
R8907:Gm7298
|
UTSW |
6 |
121,741,817 (GRCm39) |
missense |
probably benign |
0.10 |
R8930:Gm7298
|
UTSW |
6 |
121,742,030 (GRCm39) |
missense |
probably benign |
0.01 |
R8932:Gm7298
|
UTSW |
6 |
121,742,030 (GRCm39) |
missense |
probably benign |
0.01 |
R8947:Gm7298
|
UTSW |
6 |
121,757,553 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9016:Gm7298
|
UTSW |
6 |
121,758,800 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9040:Gm7298
|
UTSW |
6 |
121,764,438 (GRCm39) |
missense |
probably benign |
0.20 |
R9154:Gm7298
|
UTSW |
6 |
121,756,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Gm7298
|
UTSW |
6 |
121,756,604 (GRCm39) |
intron |
probably benign |
|
R9371:Gm7298
|
UTSW |
6 |
121,744,541 (GRCm39) |
missense |
probably benign |
0.02 |
R9372:Gm7298
|
UTSW |
6 |
121,748,746 (GRCm39) |
missense |
probably benign |
0.21 |
R9490:Gm7298
|
UTSW |
6 |
121,751,083 (GRCm39) |
missense |
probably benign |
0.00 |
R9649:Gm7298
|
UTSW |
6 |
121,764,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Gm7298
|
UTSW |
6 |
121,741,834 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Gm7298
|
UTSW |
6 |
121,741,829 (GRCm39) |
missense |
probably benign |
0.03 |
|