Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm3 |
T |
C |
3: 59,784,571 (GRCm39) |
L348P |
probably damaging |
Het |
Adamts15 |
C |
A |
9: 30,816,111 (GRCm39) |
C616F |
probably damaging |
Het |
Adarb1 |
T |
C |
10: 77,158,099 (GRCm39) |
N116S |
probably damaging |
Het |
Add2 |
C |
T |
6: 86,095,639 (GRCm39) |
S437L |
probably damaging |
Het |
Adra1d |
T |
A |
2: 131,388,069 (GRCm39) |
R495S |
probably benign |
Het |
Agk |
C |
T |
6: 40,364,429 (GRCm39) |
T309I |
probably damaging |
Het |
Aqr |
T |
C |
2: 113,992,133 (GRCm39) |
Y81C |
probably damaging |
Het |
Bak1 |
G |
A |
17: 27,240,242 (GRCm39) |
Q142* |
probably null |
Het |
Bckdha |
A |
G |
7: 25,330,845 (GRCm39) |
V307A |
probably damaging |
Het |
Camk2n2 |
C |
A |
16: 20,438,948 (GRCm39) |
G72V |
probably benign |
Het |
Cd276 |
A |
T |
9: 58,434,845 (GRCm39) |
|
probably benign |
Het |
Cd2ap |
G |
A |
17: 43,149,649 (GRCm39) |
Q122* |
probably null |
Het |
Cdan1 |
T |
A |
2: 120,561,907 (GRCm39) |
|
probably benign |
Het |
Cdh3 |
T |
C |
8: 107,263,547 (GRCm39) |
S156P |
probably benign |
Het |
Chil4 |
T |
A |
3: 106,117,959 (GRCm39) |
|
probably benign |
Het |
Col11a1 |
C |
T |
3: 113,951,791 (GRCm39) |
R1074C |
probably damaging |
Het |
Depp1 |
G |
A |
6: 116,628,683 (GRCm39) |
V9M |
possibly damaging |
Het |
Fcrlb |
T |
C |
1: 170,735,096 (GRCm39) |
T344A |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,861,829 (GRCm39) |
|
probably benign |
Het |
Fras1 |
G |
T |
5: 96,912,835 (GRCm39) |
V3380F |
possibly damaging |
Het |
Galnt9 |
A |
G |
5: 110,767,119 (GRCm39) |
D530G |
possibly damaging |
Het |
Gja10 |
A |
T |
4: 32,601,135 (GRCm39) |
S416R |
probably benign |
Het |
Gm10549 |
T |
A |
18: 33,603,841 (GRCm39) |
V108E |
unknown |
Het |
Hook3 |
A |
T |
8: 26,558,687 (GRCm39) |
L59Q |
probably damaging |
Het |
Hpf1 |
T |
A |
8: 61,353,154 (GRCm39) |
D178E |
probably benign |
Het |
Hsd17b7 |
T |
C |
1: 169,788,698 (GRCm39) |
N173S |
possibly damaging |
Het |
Hsph1 |
A |
G |
5: 149,553,454 (GRCm39) |
F236L |
probably damaging |
Het |
Kcnk12 |
G |
T |
17: 88,053,537 (GRCm39) |
T375K |
probably benign |
Het |
Klra3 |
A |
T |
6: 130,304,033 (GRCm39) |
S220T |
probably damaging |
Het |
Lhx1 |
A |
T |
11: 84,414,967 (GRCm39) |
L12Q |
probably damaging |
Het |
Lnx1 |
A |
G |
5: 74,766,710 (GRCm39) |
L468P |
probably damaging |
Het |
Ltbp3 |
T |
A |
19: 5,803,970 (GRCm39) |
C827* |
probably null |
Het |
Mical1 |
C |
T |
10: 41,354,210 (GRCm39) |
A53V |
probably damaging |
Het |
Mmp10 |
A |
T |
9: 7,506,502 (GRCm39) |
H326L |
probably benign |
Het |
Mpl |
A |
T |
4: 118,300,729 (GRCm39) |
M600K |
possibly damaging |
Het |
Muc5b |
T |
A |
7: 141,419,230 (GRCm39) |
D4004E |
possibly damaging |
Het |
Myo5b |
A |
T |
18: 74,710,680 (GRCm39) |
H98L |
possibly damaging |
Het |
Nbeal1 |
A |
G |
1: 60,323,251 (GRCm39) |
T2110A |
probably damaging |
Het |
Nedd4l |
C |
A |
18: 65,345,862 (GRCm39) |
R825S |
probably damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Or4k35 |
A |
T |
2: 111,100,622 (GRCm39) |
I30N |
possibly damaging |
Het |
Or52e19 |
T |
A |
7: 102,959,432 (GRCm39) |
L168Q |
probably damaging |
Het |
Or8k41 |
A |
T |
2: 86,313,483 (GRCm39) |
I201N |
probably damaging |
Het |
Otog |
A |
T |
7: 45,940,361 (GRCm39) |
|
probably null |
Het |
Parp2 |
T |
A |
14: 51,056,836 (GRCm39) |
L320H |
probably damaging |
Het |
Poglut3 |
T |
C |
9: 53,307,150 (GRCm39) |
Y365H |
probably damaging |
Het |
Pola2 |
C |
T |
19: 5,993,250 (GRCm39) |
|
probably null |
Het |
Poln |
A |
T |
5: 34,264,494 (GRCm39) |
|
probably benign |
Het |
Pomt1 |
T |
A |
2: 32,131,680 (GRCm39) |
V123E |
probably damaging |
Het |
Prom2 |
T |
C |
2: 127,374,802 (GRCm39) |
Y578C |
probably damaging |
Het |
Prss23 |
T |
C |
7: 89,159,599 (GRCm39) |
T157A |
probably damaging |
Het |
Sdk1 |
T |
A |
5: 141,598,950 (GRCm39) |
V205E |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 142,147,681 (GRCm39) |
K1771R |
probably benign |
Het |
Sidt1 |
A |
T |
16: 44,102,234 (GRCm39) |
S309T |
possibly damaging |
Het |
Sirpa |
T |
A |
2: 129,457,432 (GRCm39) |
F169I |
probably damaging |
Het |
Slc8a1 |
T |
C |
17: 81,955,916 (GRCm39) |
N374S |
probably damaging |
Het |
Sp110 |
C |
T |
1: 85,523,831 (GRCm39) |
|
probably null |
Het |
Stard9 |
A |
G |
2: 120,509,934 (GRCm39) |
|
probably null |
Het |
Synpr |
A |
G |
14: 13,563,082 (GRCm38) |
N105S |
probably damaging |
Het |
Tbc1d16 |
T |
C |
11: 119,046,927 (GRCm39) |
Y440C |
probably damaging |
Het |
Trabd |
A |
G |
15: 88,969,824 (GRCm39) |
I313V |
possibly damaging |
Het |
Trappc10 |
T |
C |
10: 78,046,610 (GRCm39) |
R430G |
probably damaging |
Het |
Trim50 |
A |
G |
5: 135,387,743 (GRCm39) |
E145G |
probably benign |
Het |
Uba3 |
A |
G |
6: 97,176,230 (GRCm39) |
V92A |
possibly damaging |
Het |
Uhmk1 |
T |
C |
1: 170,038,628 (GRCm39) |
K153R |
probably damaging |
Het |
Vmn2r3 |
T |
C |
3: 64,194,810 (GRCm39) |
K8R |
possibly damaging |
Het |
Vmn2r3 |
T |
A |
3: 64,182,893 (GRCm39) |
M269L |
probably benign |
Het |
Xpot |
G |
T |
10: 121,443,543 (GRCm39) |
|
probably benign |
Het |
Zfp128 |
A |
G |
7: 12,624,949 (GRCm39) |
Y439C |
probably benign |
Het |
Zfy1 |
T |
A |
Y: 725,620 (GRCm39) |
H715L |
possibly damaging |
Het |
Zmym1 |
A |
C |
4: 126,941,872 (GRCm39) |
L839V |
probably damaging |
Het |
|
Other mutations in Uba2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00704:Uba2
|
APN |
7 |
33,858,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01593:Uba2
|
APN |
7 |
33,845,689 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02268:Uba2
|
APN |
7 |
33,842,161 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03399:Uba2
|
APN |
7 |
33,843,939 (GRCm39) |
missense |
probably damaging |
1.00 |
Divided
|
UTSW |
7 |
33,864,860 (GRCm39) |
missense |
probably damaging |
1.00 |
Minus
|
UTSW |
7 |
33,845,687 (GRCm39) |
nonsense |
probably null |
|
Subtracted
|
UTSW |
7 |
33,850,239 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0242:Uba2
|
UTSW |
7 |
33,854,054 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0242:Uba2
|
UTSW |
7 |
33,854,054 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0270:Uba2
|
UTSW |
7 |
33,850,281 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0390:Uba2
|
UTSW |
7 |
33,850,446 (GRCm39) |
missense |
probably benign |
0.10 |
R0603:Uba2
|
UTSW |
7 |
33,861,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R1066:Uba2
|
UTSW |
7 |
33,858,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Uba2
|
UTSW |
7 |
33,850,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R1896:Uba2
|
UTSW |
7 |
33,850,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R2210:Uba2
|
UTSW |
7 |
33,862,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R3618:Uba2
|
UTSW |
7 |
33,853,907 (GRCm39) |
critical splice donor site |
probably null |
|
R3779:Uba2
|
UTSW |
7 |
33,854,071 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3793:Uba2
|
UTSW |
7 |
33,845,722 (GRCm39) |
missense |
probably damaging |
0.97 |
R4607:Uba2
|
UTSW |
7 |
33,854,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R4608:Uba2
|
UTSW |
7 |
33,854,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R5938:Uba2
|
UTSW |
7 |
33,864,915 (GRCm39) |
splice site |
probably null |
|
R6404:Uba2
|
UTSW |
7 |
33,853,985 (GRCm39) |
missense |
probably damaging |
0.98 |
R7050:Uba2
|
UTSW |
7 |
33,845,687 (GRCm39) |
nonsense |
probably null |
|
R7181:Uba2
|
UTSW |
7 |
33,840,854 (GRCm39) |
missense |
probably benign |
0.01 |
R7369:Uba2
|
UTSW |
7 |
33,850,239 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7622:Uba2
|
UTSW |
7 |
33,864,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R7727:Uba2
|
UTSW |
7 |
33,850,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R7807:Uba2
|
UTSW |
7 |
33,862,638 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8038:Uba2
|
UTSW |
7 |
33,847,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R8057:Uba2
|
UTSW |
7 |
33,867,835 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8120:Uba2
|
UTSW |
7 |
33,867,812 (GRCm39) |
missense |
probably benign |
|
R8253:Uba2
|
UTSW |
7 |
33,850,323 (GRCm39) |
missense |
probably damaging |
0.96 |
R8961:Uba2
|
UTSW |
7 |
33,855,642 (GRCm39) |
intron |
probably benign |
|
R8988:Uba2
|
UTSW |
7 |
33,853,987 (GRCm39) |
missense |
probably benign |
|
R9672:Uba2
|
UTSW |
7 |
33,856,749 (GRCm39) |
missense |
probably benign |
0.29 |
X0026:Uba2
|
UTSW |
7 |
33,853,904 (GRCm39) |
splice site |
probably null |
|
|