Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563I02Rik |
T |
A |
14: 60,325,668 (GRCm39) |
|
probably benign |
Het |
Abtb1 |
A |
C |
6: 88,813,349 (GRCm39) |
L439R |
probably damaging |
Het |
Adcy10 |
A |
G |
1: 165,345,829 (GRCm39) |
T293A |
probably damaging |
Het |
Agl |
A |
T |
3: 116,581,961 (GRCm39) |
V306D |
possibly damaging |
Het |
Alpk2 |
T |
A |
18: 65,511,147 (GRCm39) |
T17S |
probably damaging |
Het |
Ar |
T |
A |
X: 97,194,937 (GRCm39) |
M517K |
probably benign |
Het |
Atg9b |
A |
G |
5: 24,591,393 (GRCm39) |
V735A |
possibly damaging |
Het |
BB014433 |
C |
A |
8: 15,091,717 (GRCm39) |
A379S |
probably benign |
Het |
Ccdc33 |
A |
G |
9: 57,989,305 (GRCm39) |
S123P |
probably damaging |
Het |
Ccl2 |
G |
T |
11: 81,927,427 (GRCm39) |
|
probably null |
Het |
Cct2 |
T |
C |
10: 116,888,922 (GRCm39) |
R526G |
probably null |
Het |
Cep55 |
T |
C |
19: 38,051,082 (GRCm39) |
M164T |
probably benign |
Het |
Clec2d |
G |
A |
6: 129,161,214 (GRCm39) |
A104T |
probably benign |
Het |
Cyp3a11 |
A |
G |
5: 145,805,357 (GRCm39) |
L220P |
possibly damaging |
Het |
Dgkk |
T |
A |
X: 6,741,487 (GRCm39) |
D102E |
probably damaging |
Het |
Emcn |
T |
C |
3: 137,109,778 (GRCm39) |
I140T |
possibly damaging |
Het |
Exoc2 |
T |
A |
13: 31,048,867 (GRCm39) |
I729L |
probably benign |
Het |
Fbxl20 |
T |
C |
11: 97,981,675 (GRCm39) |
I338V |
probably benign |
Het |
Gucy2c |
G |
A |
6: 136,679,758 (GRCm39) |
T943I |
probably damaging |
Het |
Hdac9 |
C |
T |
12: 34,457,801 (GRCm39) |
V251I |
probably benign |
Het |
Hoxa10 |
T |
C |
6: 52,209,616 (GRCm39) |
E52G |
probably damaging |
Het |
Il17rb |
A |
T |
14: 29,728,038 (GRCm39) |
S56R |
probably benign |
Het |
Knl1 |
A |
G |
2: 118,902,481 (GRCm39) |
D1394G |
probably damaging |
Het |
Kpna1 |
G |
A |
16: 35,851,591 (GRCm39) |
A392T |
probably damaging |
Het |
Krt6b |
A |
G |
15: 101,587,557 (GRCm39) |
V179A |
probably damaging |
Het |
Lpar5 |
A |
T |
6: 125,058,098 (GRCm39) |
|
probably null |
Het |
Marchf7 |
A |
G |
2: 60,060,190 (GRCm39) |
R106G |
probably benign |
Het |
Mtus1 |
C |
T |
8: 41,535,812 (GRCm39) |
V635M |
probably damaging |
Het |
Myl1 |
T |
C |
1: 66,983,974 (GRCm39) |
K31E |
possibly damaging |
Het |
Myt1l |
T |
A |
12: 29,876,969 (GRCm39) |
L207I |
unknown |
Het |
Naalad2 |
A |
T |
9: 18,287,829 (GRCm39) |
V267E |
possibly damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,376,188 (GRCm39) |
I950T |
possibly damaging |
Het |
Ppp1r9a |
G |
T |
6: 5,154,074 (GRCm39) |
R1081L |
probably benign |
Het |
Rc3h1 |
T |
C |
1: 160,791,112 (GRCm39) |
I932T |
probably benign |
Het |
Rubcnl |
G |
A |
14: 75,279,832 (GRCm39) |
R405Q |
probably benign |
Het |
Sgsm3 |
A |
G |
15: 80,888,069 (GRCm39) |
E53G |
probably damaging |
Het |
Slco1a8 |
T |
G |
6: 141,938,087 (GRCm39) |
E277D |
possibly damaging |
Het |
Spin2g |
A |
T |
X: 33,656,599 (GRCm39) |
I171N |
possibly damaging |
Het |
Srsf6 |
G |
A |
2: 162,773,619 (GRCm39) |
S10N |
probably damaging |
Het |
Tesl2 |
T |
A |
X: 23,825,173 (GRCm39) |
M1L |
probably null |
Het |
Thoc2l |
T |
A |
5: 104,667,286 (GRCm39) |
Y603N |
probably damaging |
Het |
Tnn |
A |
T |
1: 159,975,035 (GRCm39) |
C131S |
probably damaging |
Het |
Tnnt2 |
A |
G |
1: 135,771,529 (GRCm39) |
|
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Vmn1r86 |
T |
C |
7: 12,836,847 (GRCm39) |
I10V |
probably benign |
Het |
Xpot |
T |
C |
10: 121,458,765 (GRCm39) |
R20G |
probably damaging |
Het |
Zfp735 |
T |
A |
11: 73,602,222 (GRCm39) |
L389I |
possibly damaging |
Het |
Zfp735 |
T |
G |
11: 73,602,223 (GRCm39) |
L389* |
probably null |
Het |
|
Other mutations in Saxo5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02418:Saxo5
|
APN |
8 |
3,526,080 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02717:Saxo5
|
APN |
8 |
3,536,970 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4131001:Saxo5
|
UTSW |
8 |
3,526,062 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1842:Saxo5
|
UTSW |
8 |
3,533,668 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1928:Saxo5
|
UTSW |
8 |
3,536,947 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2202:Saxo5
|
UTSW |
8 |
3,529,028 (GRCm39) |
missense |
probably benign |
0.01 |
R2224:Saxo5
|
UTSW |
8 |
3,529,249 (GRCm39) |
missense |
probably benign |
0.11 |
R4162:Saxo5
|
UTSW |
8 |
3,529,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R4413:Saxo5
|
UTSW |
8 |
3,533,529 (GRCm39) |
missense |
probably damaging |
0.99 |
R4441:Saxo5
|
UTSW |
8 |
3,526,105 (GRCm39) |
missense |
probably damaging |
0.97 |
R4807:Saxo5
|
UTSW |
8 |
3,529,004 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4869:Saxo5
|
UTSW |
8 |
3,537,148 (GRCm39) |
missense |
probably damaging |
0.98 |
R5753:Saxo5
|
UTSW |
8 |
3,534,112 (GRCm39) |
missense |
probably benign |
|
R6457:Saxo5
|
UTSW |
8 |
3,529,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:Saxo5
|
UTSW |
8 |
3,526,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7186:Saxo5
|
UTSW |
8 |
3,529,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R7386:Saxo5
|
UTSW |
8 |
3,537,079 (GRCm39) |
missense |
probably benign |
|
R7609:Saxo5
|
UTSW |
8 |
3,526,057 (GRCm39) |
missense |
probably benign |
0.02 |
R7738:Saxo5
|
UTSW |
8 |
3,533,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R9000:Saxo5
|
UTSW |
8 |
3,526,083 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9169:Saxo5
|
UTSW |
8 |
3,525,967 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9473:Saxo5
|
UTSW |
8 |
3,529,232 (GRCm39) |
missense |
probably benign |
0.03 |
R9732:Saxo5
|
UTSW |
8 |
3,526,167 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1177:Saxo5
|
UTSW |
8 |
3,526,213 (GRCm39) |
missense |
probably benign |
0.45 |
|