Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430033K04Rik |
G |
T |
5: 138,646,006 (GRCm39) |
K630N |
probably damaging |
Het |
Acss2 |
C |
A |
2: 155,398,283 (GRCm39) |
L335I |
probably benign |
Het |
Alg6 |
A |
T |
4: 99,641,023 (GRCm39) |
|
probably benign |
Het |
Atp8b3 |
C |
T |
10: 80,359,681 (GRCm39) |
M984I |
probably benign |
Het |
Bsn |
G |
T |
9: 107,981,277 (GRCm39) |
|
probably null |
Het |
Ccdc88a |
T |
C |
11: 29,432,651 (GRCm39) |
I1219T |
probably benign |
Het |
Cdhr4 |
G |
A |
9: 107,870,150 (GRCm39) |
E52K |
probably benign |
Het |
Ces1a |
T |
A |
8: 93,747,532 (GRCm39) |
N500Y |
probably damaging |
Het |
Chd3 |
G |
T |
11: 69,240,703 (GRCm39) |
R1579S |
probably benign |
Het |
Chrnb3 |
T |
C |
8: 27,875,118 (GRCm39) |
L39P |
probably damaging |
Het |
Ckm |
A |
G |
7: 19,154,209 (GRCm39) |
K319E |
probably damaging |
Het |
Cnot6 |
C |
T |
11: 49,593,363 (GRCm39) |
|
probably null |
Het |
Copg1 |
A |
G |
6: 87,884,528 (GRCm39) |
|
probably benign |
Het |
Dbn1 |
A |
T |
13: 55,624,042 (GRCm39) |
I350N |
possibly damaging |
Het |
Dnah2 |
A |
G |
11: 69,356,457 (GRCm39) |
S2135P |
possibly damaging |
Het |
Dsg2 |
C |
A |
18: 20,734,444 (GRCm39) |
D807E |
probably benign |
Het |
Foxi1 |
A |
G |
11: 34,157,972 (GRCm39) |
F18L |
probably damaging |
Het |
Galnt3 |
C |
A |
2: 65,923,954 (GRCm39) |
R438L |
probably damaging |
Het |
Glod4 |
T |
A |
11: 76,134,397 (GRCm39) |
D25V |
probably damaging |
Het |
Golga4 |
T |
A |
9: 118,388,076 (GRCm39) |
S1733T |
probably benign |
Het |
H2-M10.3 |
C |
T |
17: 36,678,722 (GRCm39) |
|
probably null |
Het |
Hemgn |
T |
C |
4: 46,396,477 (GRCm39) |
E253G |
probably damaging |
Het |
Itsn1 |
G |
A |
16: 91,696,537 (GRCm39) |
V47M |
probably damaging |
Het |
Kif5b |
A |
G |
18: 6,208,257 (GRCm39) |
V947A |
probably benign |
Het |
Kif9 |
A |
G |
9: 110,318,935 (GRCm39) |
H133R |
probably benign |
Het |
Lce1l |
T |
C |
3: 92,757,781 (GRCm39) |
T26A |
unknown |
Het |
Macf1 |
T |
C |
4: 123,387,781 (GRCm39) |
E1172G |
probably damaging |
Het |
Nkx3-2 |
C |
T |
5: 41,921,281 (GRCm39) |
V3M |
probably damaging |
Het |
Nr2e1 |
G |
A |
10: 42,454,187 (GRCm39) |
T49I |
probably benign |
Het |
Oc90 |
A |
G |
15: 65,764,242 (GRCm39) |
L138P |
probably damaging |
Het |
Or7g12 |
T |
G |
9: 18,899,278 (GRCm39) |
|
probably null |
Het |
Or8g34 |
C |
T |
9: 39,373,527 (GRCm39) |
R264* |
probably null |
Het |
Orc4 |
G |
A |
2: 48,827,501 (GRCm39) |
P31S |
probably benign |
Het |
Pabir3 |
G |
A |
X: 52,382,376 (GRCm39) |
R94H |
possibly damaging |
Het |
Paqr3 |
T |
A |
5: 97,251,220 (GRCm39) |
N168I |
possibly damaging |
Het |
Pcdhac1 |
T |
A |
18: 37,224,432 (GRCm39) |
I415N |
probably damaging |
Het |
Pdik1l |
T |
C |
4: 134,006,207 (GRCm39) |
N75S |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,549,924 (GRCm39) |
H1005R |
probably damaging |
Het |
Plekhn1 |
T |
C |
4: 156,309,988 (GRCm39) |
S109G |
probably damaging |
Het |
Prkch |
A |
G |
12: 73,749,612 (GRCm39) |
T402A |
possibly damaging |
Het |
Ptger4 |
C |
A |
15: 5,271,860 (GRCm39) |
R253L |
probably damaging |
Het |
Rabac1 |
A |
T |
7: 24,669,585 (GRCm39) |
Y173* |
probably null |
Het |
Rapsn |
G |
A |
2: 90,873,557 (GRCm39) |
V288M |
possibly damaging |
Het |
Rnf26rt |
C |
T |
6: 76,473,792 (GRCm39) |
V275I |
probably benign |
Het |
Sec31a |
A |
G |
5: 100,513,817 (GRCm39) |
S993P |
probably damaging |
Het |
Septin4 |
A |
G |
11: 87,458,883 (GRCm39) |
H419R |
probably benign |
Het |
Serpine1 |
G |
A |
5: 137,098,322 (GRCm39) |
A117V |
probably damaging |
Het |
Sh3tc2 |
A |
G |
18: 62,120,764 (GRCm39) |
|
probably null |
Het |
Sipa1l2 |
T |
C |
8: 126,218,965 (GRCm39) |
D124G |
probably benign |
Het |
Slc6a12 |
T |
A |
6: 121,330,489 (GRCm39) |
|
probably null |
Het |
Stk11 |
A |
G |
10: 79,952,435 (GRCm39) |
|
probably benign |
Het |
Tcaf3 |
A |
G |
6: 42,566,930 (GRCm39) |
Y720H |
probably damaging |
Het |
Tmem38a |
C |
T |
8: 73,326,005 (GRCm39) |
P20S |
possibly damaging |
Het |
Tmprss11a |
C |
T |
5: 86,568,055 (GRCm39) |
R224K |
probably damaging |
Het |
Tmprss15 |
C |
T |
16: 78,754,244 (GRCm39) |
S988N |
probably benign |
Het |
Txn2 |
A |
T |
15: 77,799,643 (GRCm39) |
|
probably null |
Het |
Ugt1a10 |
T |
A |
1: 87,983,919 (GRCm39) |
V239E |
probably damaging |
Het |
Vmn2r102 |
A |
G |
17: 19,901,475 (GRCm39) |
Y534C |
probably damaging |
Het |
Vmn2r78 |
A |
T |
7: 86,603,466 (GRCm39) |
D548V |
probably damaging |
Het |
|
Other mutations in Serpina9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01020:Serpina9
|
APN |
12 |
103,974,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02228:Serpina9
|
APN |
12 |
103,974,859 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02692:Serpina9
|
APN |
12 |
103,974,665 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03149:Serpina9
|
APN |
12 |
103,974,869 (GRCm39) |
nonsense |
probably null |
|
IGL03134:Serpina9
|
UTSW |
12 |
103,967,696 (GRCm39) |
missense |
probably null |
0.18 |
R0119:Serpina9
|
UTSW |
12 |
103,967,729 (GRCm39) |
missense |
probably benign |
0.18 |
R0299:Serpina9
|
UTSW |
12 |
103,967,729 (GRCm39) |
missense |
probably benign |
0.18 |
R0499:Serpina9
|
UTSW |
12 |
103,967,729 (GRCm39) |
missense |
probably benign |
0.18 |
R1477:Serpina9
|
UTSW |
12 |
103,963,362 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1912:Serpina9
|
UTSW |
12 |
103,967,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Serpina9
|
UTSW |
12 |
103,974,568 (GRCm39) |
missense |
probably benign |
0.04 |
R2221:Serpina9
|
UTSW |
12 |
103,964,523 (GRCm39) |
missense |
probably damaging |
0.98 |
R2413:Serpina9
|
UTSW |
12 |
103,967,485 (GRCm39) |
critical splice donor site |
probably null |
|
R3939:Serpina9
|
UTSW |
12 |
103,975,151 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R5242:Serpina9
|
UTSW |
12 |
103,974,644 (GRCm39) |
missense |
probably benign |
0.09 |
R5589:Serpina9
|
UTSW |
12 |
103,967,728 (GRCm39) |
missense |
probably benign |
0.00 |
R5900:Serpina9
|
UTSW |
12 |
103,975,130 (GRCm39) |
nonsense |
probably null |
|
R6171:Serpina9
|
UTSW |
12 |
103,974,678 (GRCm39) |
nonsense |
probably null |
|
R6195:Serpina9
|
UTSW |
12 |
103,967,666 (GRCm39) |
missense |
probably damaging |
0.96 |
R6566:Serpina9
|
UTSW |
12 |
103,963,296 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6995:Serpina9
|
UTSW |
12 |
103,967,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Serpina9
|
UTSW |
12 |
103,967,575 (GRCm39) |
missense |
probably damaging |
0.98 |
R7808:Serpina9
|
UTSW |
12 |
103,967,484 (GRCm39) |
critical splice donor site |
probably null |
|
R7860:Serpina9
|
UTSW |
12 |
103,967,680 (GRCm39) |
missense |
probably benign |
0.01 |
R7935:Serpina9
|
UTSW |
12 |
103,964,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R9041:Serpina9
|
UTSW |
12 |
103,967,737 (GRCm39) |
missense |
|
|
Z1176:Serpina9
|
UTSW |
12 |
103,967,543 (GRCm39) |
missense |
probably damaging |
1.00 |
|