Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
C |
A |
3: 59,843,843 (GRCm39) |
P179Q |
probably damaging |
Het |
Abcc1 |
C |
T |
16: 14,290,794 (GRCm39) |
T1468I |
probably damaging |
Het |
Adrb3 |
A |
C |
8: 27,718,099 (GRCm39) |
C117G |
probably benign |
Het |
Aff4 |
A |
T |
11: 53,302,721 (GRCm39) |
S1065C |
possibly damaging |
Het |
Agrn |
G |
A |
4: 156,256,825 (GRCm39) |
A1260V |
probably benign |
Het |
Auts2 |
A |
G |
5: 131,488,963 (GRCm39) |
|
probably null |
Het |
BC005537 |
T |
A |
13: 24,993,916 (GRCm39) |
H159Q |
probably benign |
Het |
Cacna2d4 |
A |
G |
6: 119,274,488 (GRCm39) |
D625G |
probably benign |
Het |
Cd72 |
A |
G |
4: 43,450,174 (GRCm39) |
Y245H |
probably damaging |
Het |
Ceacam20 |
G |
T |
7: 19,710,109 (GRCm39) |
V378L |
probably damaging |
Het |
Chpf |
C |
T |
1: 75,455,436 (GRCm39) |
R105K |
probably null |
Het |
Chst9 |
A |
T |
18: 15,585,365 (GRCm39) |
Y399* |
probably null |
Het |
Cntn5 |
A |
G |
9: 10,145,386 (GRCm39) |
I108T |
possibly damaging |
Het |
Col14a1 |
A |
G |
15: 55,291,324 (GRCm39) |
T931A |
unknown |
Het |
D630045J12Rik |
T |
C |
6: 38,105,410 (GRCm39) |
H1890R |
probably damaging |
Het |
Dkk2 |
T |
C |
3: 131,880,739 (GRCm39) |
I128T |
probably benign |
Het |
Ece2 |
C |
T |
16: 20,430,534 (GRCm39) |
P54S |
probably damaging |
Het |
Fhip2a |
T |
C |
19: 57,372,697 (GRCm39) |
|
probably null |
Het |
Fry |
A |
T |
5: 150,322,998 (GRCm39) |
T1050S |
probably benign |
Het |
Gfra2 |
A |
G |
14: 71,133,397 (GRCm39) |
K76E |
probably damaging |
Het |
Gpr180 |
G |
A |
14: 118,391,302 (GRCm39) |
G235R |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,369,003 (GRCm39) |
Q403R |
probably null |
Het |
Hes5 |
A |
G |
4: 155,045,502 (GRCm39) |
N17S |
probably benign |
Het |
Insrr |
T |
A |
3: 87,707,735 (GRCm39) |
L59H |
probably damaging |
Het |
Irs1 |
A |
C |
1: 82,266,290 (GRCm39) |
I642S |
probably damaging |
Het |
Mettl22 |
T |
C |
16: 8,306,633 (GRCm39) |
V363A |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,028,238 (GRCm39) |
H983R |
possibly damaging |
Het |
Nynrin |
T |
G |
14: 56,100,587 (GRCm39) |
S126A |
probably damaging |
Het |
Nynrin |
A |
T |
14: 56,102,517 (GRCm39) |
M729L |
probably benign |
Het |
Or51v14 |
G |
A |
7: 103,261,347 (GRCm39) |
T71I |
possibly damaging |
Het |
Or7e178 |
A |
C |
9: 20,226,015 (GRCm39) |
I67S |
possibly damaging |
Het |
Otof |
C |
T |
5: 30,537,538 (GRCm39) |
G1257D |
probably benign |
Het |
Pals2 |
A |
T |
6: 50,171,527 (GRCm39) |
E392V |
probably benign |
Het |
Pcdhgc5 |
A |
G |
18: 37,954,175 (GRCm39) |
E483G |
probably benign |
Het |
Phldb2 |
T |
C |
16: 45,680,747 (GRCm39) |
E20G |
possibly damaging |
Het |
Ptprz1 |
A |
G |
6: 23,001,662 (GRCm39) |
I1251V |
probably benign |
Het |
Rfx2 |
A |
T |
17: 57,110,605 (GRCm39) |
M127K |
probably benign |
Het |
Slc9a3 |
A |
G |
13: 74,312,407 (GRCm39) |
N668S |
probably benign |
Het |
Smg6 |
G |
A |
11: 74,929,465 (GRCm39) |
V965M |
probably damaging |
Het |
Spen |
A |
T |
4: 141,202,314 (GRCm39) |
H2104Q |
possibly damaging |
Het |
Svep1 |
C |
T |
4: 58,069,396 (GRCm39) |
E2797K |
possibly damaging |
Het |
Svep1 |
T |
C |
4: 58,087,815 (GRCm39) |
S1755G |
probably benign |
Het |
Sycp2 |
A |
C |
2: 177,996,770 (GRCm39) |
S1144R |
probably damaging |
Het |
Tsen54 |
T |
A |
11: 115,711,804 (GRCm39) |
L407* |
probably null |
Het |
Uba1y |
T |
A |
Y: 828,806 (GRCm39) |
I538K |
possibly damaging |
Het |
Vil1 |
C |
A |
1: 74,463,136 (GRCm39) |
H440N |
probably benign |
Het |
|
Other mutations in Gigyf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Gigyf1
|
APN |
5 |
137,521,007 (GRCm39) |
unclassified |
probably benign |
|
IGL00326:Gigyf1
|
APN |
5 |
137,517,210 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL00935:Gigyf1
|
APN |
5 |
137,523,096 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01717:Gigyf1
|
APN |
5 |
137,523,953 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02090:Gigyf1
|
APN |
5 |
137,523,826 (GRCm39) |
splice site |
probably null |
|
IGL02354:Gigyf1
|
APN |
5 |
137,517,989 (GRCm39) |
splice site |
probably benign |
|
IGL02361:Gigyf1
|
APN |
5 |
137,517,989 (GRCm39) |
splice site |
probably benign |
|
IGL03370:Gigyf1
|
APN |
5 |
137,523,952 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4354001:Gigyf1
|
UTSW |
5 |
137,522,366 (GRCm39) |
missense |
unknown |
|
R1415:Gigyf1
|
UTSW |
5 |
137,517,478 (GRCm39) |
splice site |
probably null |
|
R1764:Gigyf1
|
UTSW |
5 |
137,520,770 (GRCm39) |
unclassified |
probably benign |
|
R2259:Gigyf1
|
UTSW |
5 |
137,518,594 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2260:Gigyf1
|
UTSW |
5 |
137,518,594 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4656:Gigyf1
|
UTSW |
5 |
137,523,477 (GRCm39) |
nonsense |
probably null |
|
R4717:Gigyf1
|
UTSW |
5 |
137,523,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Gigyf1
|
UTSW |
5 |
137,523,032 (GRCm39) |
missense |
probably benign |
0.39 |
R4733:Gigyf1
|
UTSW |
5 |
137,523,032 (GRCm39) |
missense |
probably benign |
0.39 |
R4942:Gigyf1
|
UTSW |
5 |
137,523,952 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5338:Gigyf1
|
UTSW |
5 |
137,521,422 (GRCm39) |
unclassified |
probably benign |
|
R5503:Gigyf1
|
UTSW |
5 |
137,521,729 (GRCm39) |
unclassified |
probably benign |
|
R5790:Gigyf1
|
UTSW |
5 |
137,522,517 (GRCm39) |
unclassified |
probably benign |
|
R5888:Gigyf1
|
UTSW |
5 |
137,523,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R5955:Gigyf1
|
UTSW |
5 |
137,521,769 (GRCm39) |
splice site |
probably null |
|
R6544:Gigyf1
|
UTSW |
5 |
137,523,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R7227:Gigyf1
|
UTSW |
5 |
137,522,085 (GRCm39) |
missense |
unknown |
|
R7493:Gigyf1
|
UTSW |
5 |
137,523,795 (GRCm39) |
missense |
probably damaging |
0.98 |
R7660:Gigyf1
|
UTSW |
5 |
137,519,231 (GRCm39) |
missense |
probably benign |
0.23 |
R7959:Gigyf1
|
UTSW |
5 |
137,522,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R8026:Gigyf1
|
UTSW |
5 |
137,523,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R8552:Gigyf1
|
UTSW |
5 |
137,521,401 (GRCm39) |
unclassified |
probably benign |
|
R8936:Gigyf1
|
UTSW |
5 |
137,523,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R9622:Gigyf1
|
UTSW |
5 |
137,522,926 (GRCm39) |
nonsense |
probably null |
|
|