Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam10 |
A |
T |
9: 70,610,713 (GRCm39) |
H67L |
probably damaging |
Het |
Adgrb1 |
C |
T |
15: 74,412,326 (GRCm39) |
T435I |
probably damaging |
Het |
Adgrd1 |
T |
A |
5: 129,256,325 (GRCm39) |
F652Y |
probably damaging |
Het |
Adgrl4 |
T |
A |
3: 151,205,991 (GRCm39) |
F250Y |
possibly damaging |
Het |
Aebp2 |
C |
T |
6: 140,588,010 (GRCm39) |
A360V |
probably benign |
Het |
AW551984 |
A |
C |
9: 39,504,220 (GRCm39) |
M582R |
probably benign |
Het |
B430306N03Rik |
T |
C |
17: 48,624,020 (GRCm39) |
V107A |
probably benign |
Het |
Cage1 |
T |
C |
13: 38,206,505 (GRCm39) |
N447D |
probably damaging |
Het |
Col17a1 |
T |
C |
19: 47,657,071 (GRCm39) |
D524G |
probably benign |
Het |
Dpp6 |
A |
T |
5: 27,743,022 (GRCm39) |
I218F |
probably benign |
Het |
Ep300 |
T |
G |
15: 81,512,621 (GRCm39) |
|
probably benign |
Het |
Ephb2 |
C |
T |
4: 136,421,225 (GRCm39) |
C375Y |
probably damaging |
Het |
Fastk |
A |
G |
5: 24,649,051 (GRCm39) |
V112A |
probably damaging |
Het |
Fbxo11 |
T |
A |
17: 88,301,187 (GRCm39) |
R775S |
possibly damaging |
Het |
Fbxw20 |
A |
G |
9: 109,062,886 (GRCm39) |
|
probably null |
Het |
Hamp2 |
G |
T |
7: 30,622,122 (GRCm39) |
A50E |
probably damaging |
Het |
Il22b |
C |
A |
10: 118,130,902 (GRCm39) |
|
probably benign |
Het |
Ints1 |
G |
A |
5: 139,737,715 (GRCm39) |
R2139C |
probably damaging |
Het |
Itgae |
T |
A |
11: 72,994,720 (GRCm39) |
V24E |
probably benign |
Het |
Jakmip3 |
G |
A |
7: 138,609,075 (GRCm39) |
V60M |
possibly damaging |
Het |
Kcnk10 |
A |
C |
12: 98,485,099 (GRCm39) |
|
probably benign |
Het |
Klra1 |
A |
T |
6: 130,352,293 (GRCm39) |
C150S |
probably damaging |
Het |
Lhx9 |
A |
T |
1: 138,759,172 (GRCm39) |
V376E |
probably damaging |
Het |
Mdm1 |
T |
A |
10: 117,983,970 (GRCm39) |
F199I |
probably damaging |
Het |
Nipal3 |
G |
T |
4: 135,194,163 (GRCm39) |
T290K |
possibly damaging |
Het |
Obsl1 |
C |
T |
1: 75,480,464 (GRCm39) |
E387K |
probably damaging |
Het |
Or8b43 |
A |
G |
9: 38,360,693 (GRCm39) |
H175R |
probably damaging |
Het |
Oxct1 |
A |
G |
15: 4,120,711 (GRCm39) |
Y265C |
probably damaging |
Het |
Pccb |
G |
A |
9: 100,867,243 (GRCm39) |
H411Y |
probably damaging |
Het |
Pkp1 |
A |
G |
1: 135,814,485 (GRCm39) |
S279P |
probably benign |
Het |
Prdm14 |
C |
A |
1: 13,195,663 (GRCm39) |
G133C |
probably benign |
Het |
Prkaa2 |
A |
T |
4: 104,897,285 (GRCm39) |
N309K |
probably benign |
Het |
Shc2 |
T |
C |
10: 79,458,102 (GRCm39) |
D527G |
probably damaging |
Het |
Shkbp1 |
C |
T |
7: 27,042,064 (GRCm39) |
|
probably benign |
Het |
Skil |
T |
C |
3: 31,151,856 (GRCm39) |
V126A |
possibly damaging |
Het |
Slc25a36 |
A |
T |
9: 96,975,122 (GRCm39) |
|
probably benign |
Het |
Slc2a13 |
T |
C |
15: 91,227,924 (GRCm39) |
T423A |
probably benign |
Het |
Spty2d1 |
A |
G |
7: 46,657,892 (GRCm39) |
|
probably benign |
Het |
Stag1 |
A |
G |
9: 100,769,442 (GRCm39) |
D519G |
probably benign |
Het |
Tmprss2 |
G |
T |
16: 97,400,479 (GRCm39) |
|
probably benign |
Het |
Trim66 |
G |
T |
7: 109,060,109 (GRCm39) |
T759K |
possibly damaging |
Het |
Trpc4ap |
C |
A |
2: 155,481,467 (GRCm39) |
A530S |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,642,099 (GRCm39) |
D11625E |
probably damaging |
Het |
Ube4b |
T |
C |
4: 149,483,141 (GRCm39) |
I42M |
possibly damaging |
Het |
Ubxn10 |
A |
G |
4: 138,448,584 (GRCm39) |
S31P |
probably benign |
Het |
Vmn1r234 |
A |
G |
17: 21,449,269 (GRCm39) |
Y61C |
probably benign |
Het |
|
Other mutations in Ubxn7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00821:Ubxn7
|
APN |
16 |
32,188,216 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02183:Ubxn7
|
APN |
16 |
32,188,201 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02690:Ubxn7
|
APN |
16 |
32,200,423 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03133:Ubxn7
|
APN |
16 |
32,200,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Ubxn7
|
UTSW |
16 |
32,178,864 (GRCm39) |
missense |
probably benign |
0.05 |
R0583:Ubxn7
|
UTSW |
16 |
32,194,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Ubxn7
|
UTSW |
16 |
32,186,235 (GRCm39) |
intron |
probably benign |
|
R0787:Ubxn7
|
UTSW |
16 |
32,200,581 (GRCm39) |
splice site |
probably benign |
|
R1658:Ubxn7
|
UTSW |
16 |
32,200,054 (GRCm39) |
splice site |
probably null |
|
R1916:Ubxn7
|
UTSW |
16 |
32,200,577 (GRCm39) |
splice site |
probably benign |
|
R2070:Ubxn7
|
UTSW |
16 |
32,191,287 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2071:Ubxn7
|
UTSW |
16 |
32,191,287 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3031:Ubxn7
|
UTSW |
16 |
32,194,125 (GRCm39) |
missense |
probably benign |
0.34 |
R3871:Ubxn7
|
UTSW |
16 |
32,200,248 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4994:Ubxn7
|
UTSW |
16 |
32,200,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R5629:Ubxn7
|
UTSW |
16 |
32,151,117 (GRCm39) |
missense |
unknown |
|
R6334:Ubxn7
|
UTSW |
16 |
32,191,007 (GRCm39) |
splice site |
probably null |
|
R6599:Ubxn7
|
UTSW |
16 |
32,203,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R8230:Ubxn7
|
UTSW |
16 |
32,194,094 (GRCm39) |
missense |
probably benign |
0.08 |
R8714:Ubxn7
|
UTSW |
16 |
32,186,229 (GRCm39) |
critical splice donor site |
probably benign |
|
R9234:Ubxn7
|
UTSW |
16 |
32,178,895 (GRCm39) |
critical splice donor site |
probably null |
|
R9633:Ubxn7
|
UTSW |
16 |
32,200,248 (GRCm39) |
missense |
probably benign |
0.08 |
R9778:Ubxn7
|
UTSW |
16 |
32,200,471 (GRCm39) |
missense |
probably benign |
0.20 |
|