Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
A |
3: 121,881,128 (GRCm39) |
N514K |
probably benign |
Het |
Adss1 |
A |
T |
12: 112,602,882 (GRCm39) |
R358W |
probably damaging |
Het |
Anxa8 |
T |
A |
14: 33,819,932 (GRCm39) |
I307N |
probably damaging |
Het |
Atad5 |
T |
A |
11: 79,986,845 (GRCm39) |
I644N |
probably damaging |
Het |
Atp5f1a |
G |
T |
18: 77,868,938 (GRCm39) |
L437F |
probably damaging |
Het |
Babam1 |
A |
G |
8: 71,855,684 (GRCm39) |
K259R |
possibly damaging |
Het |
BC048562 |
T |
G |
9: 108,323,054 (GRCm39) |
F130V |
probably damaging |
Het |
Btf3l4b |
T |
A |
13: 96,217,621 (GRCm39) |
K73* |
probably null |
Het |
Camsap2 |
T |
A |
1: 136,202,640 (GRCm39) |
|
probably null |
Het |
Ccne2 |
A |
G |
4: 11,192,881 (GRCm39) |
I27M |
probably benign |
Het |
Cd302 |
A |
G |
2: 60,082,793 (GRCm39) |
V177A |
possibly damaging |
Het |
Cfap46 |
T |
C |
7: 139,222,461 (GRCm39) |
K1172R |
|
Het |
Cic |
T |
C |
7: 24,991,117 (GRCm39) |
W2141R |
probably damaging |
Het |
Cpeb3 |
A |
G |
19: 37,151,473 (GRCm39) |
V301A |
possibly damaging |
Het |
Cpsf3 |
A |
G |
12: 21,350,112 (GRCm39) |
K277R |
possibly damaging |
Het |
Cstl1 |
A |
G |
2: 148,592,926 (GRCm39) |
H27R |
possibly damaging |
Het |
Dapk1 |
T |
A |
13: 60,866,125 (GRCm39) |
I188K |
possibly damaging |
Het |
Dock6 |
T |
C |
9: 21,729,111 (GRCm39) |
T1301A |
probably benign |
Het |
Eml5 |
A |
T |
12: 98,848,292 (GRCm39) |
C133* |
probably null |
Het |
Ermap |
T |
A |
4: 119,042,744 (GRCm39) |
I260F |
probably damaging |
Het |
Fbxw22 |
T |
G |
9: 109,215,653 (GRCm39) |
E198D |
possibly damaging |
Het |
Flt4 |
T |
C |
11: 49,516,241 (GRCm39) |
Y115H |
possibly damaging |
Het |
Fmo9 |
A |
C |
1: 166,494,794 (GRCm39) |
I369S |
probably damaging |
Het |
Frmd4a |
T |
A |
2: 4,157,904 (GRCm39) |
S6T |
probably benign |
Het |
Golga5 |
A |
T |
12: 102,443,057 (GRCm39) |
I330L |
probably benign |
Het |
Helq |
C |
A |
5: 100,927,158 (GRCm39) |
V643F |
probably damaging |
Het |
Ino80d |
A |
T |
1: 63,104,969 (GRCm39) |
L369H |
probably damaging |
Het |
Kank1 |
A |
T |
19: 25,388,798 (GRCm39) |
M824L |
probably benign |
Het |
Lilrb4b |
T |
C |
10: 51,356,801 (GRCm39) |
|
probably benign |
Het |
Ltbp4 |
T |
A |
7: 27,021,578 (GRCm39) |
D1003V |
probably damaging |
Het |
Mapk8ip2 |
T |
C |
15: 89,341,886 (GRCm39) |
S366P |
probably damaging |
Het |
Mdga1 |
T |
C |
17: 30,069,512 (GRCm39) |
H178R |
probably benign |
Het |
Mlh3 |
A |
G |
12: 85,292,613 (GRCm39) |
V1266A |
possibly damaging |
Het |
Nrp1 |
A |
G |
8: 129,089,859 (GRCm39) |
E78G |
probably damaging |
Het |
Or1l4 |
A |
T |
2: 37,091,255 (GRCm39) |
M1L |
probably benign |
Het |
Or4z4 |
A |
T |
19: 12,076,826 (GRCm39) |
M59K |
probably damaging |
Het |
Or5d16 |
A |
G |
2: 87,773,297 (GRCm39) |
V225A |
probably benign |
Het |
Or8k33 |
A |
G |
2: 86,383,818 (GRCm39) |
S217P |
possibly damaging |
Het |
Ovch2 |
A |
G |
7: 107,395,815 (GRCm39) |
S68P |
probably damaging |
Het |
Pappa2 |
T |
A |
1: 158,672,614 (GRCm39) |
I1110F |
probably damaging |
Het |
Pcyox1 |
A |
C |
6: 86,369,241 (GRCm39) |
L195R |
possibly damaging |
Het |
Pde11a |
A |
G |
2: 75,848,217 (GRCm39) |
L870P |
probably damaging |
Het |
Pgpep1 |
G |
A |
8: 71,103,418 (GRCm39) |
T152M |
probably damaging |
Het |
Pik3c2a |
A |
T |
7: 115,945,413 (GRCm39) |
D1464E |
probably damaging |
Het |
Plcb1 |
A |
G |
2: 135,167,610 (GRCm39) |
K468R |
possibly damaging |
Het |
Postn |
C |
T |
3: 54,292,659 (GRCm39) |
T742I |
probably benign |
Het |
Ppm1j |
T |
A |
3: 104,691,057 (GRCm39) |
Y274N |
probably damaging |
Het |
Ppp2cb |
T |
C |
8: 34,090,038 (GRCm39) |
C32R |
possibly damaging |
Het |
Prmt9 |
T |
A |
8: 78,282,374 (GRCm39) |
Y90* |
probably null |
Het |
Ptk2 |
T |
C |
15: 73,146,346 (GRCm39) |
Y441C |
probably damaging |
Het |
Rabggta |
T |
A |
14: 55,957,083 (GRCm39) |
I266L |
probably benign |
Het |
Rft1 |
C |
T |
14: 30,398,812 (GRCm39) |
R261W |
probably damaging |
Het |
Rsrc1 |
C |
T |
3: 67,197,680 (GRCm39) |
A195V |
probably damaging |
Het |
Rtkn2 |
T |
G |
10: 67,871,677 (GRCm39) |
L355R |
possibly damaging |
Het |
Runx1t1 |
A |
T |
4: 13,875,477 (GRCm39) |
D427V |
possibly damaging |
Het |
Slc15a4 |
T |
G |
5: 127,673,812 (GRCm39) |
H534P |
probably benign |
Het |
Slc16a7 |
T |
C |
10: 125,066,880 (GRCm39) |
N253S |
probably damaging |
Het |
Slc29a1 |
A |
G |
17: 45,897,063 (GRCm39) |
S408P |
probably damaging |
Het |
Slc52a2 |
G |
A |
15: 76,424,406 (GRCm39) |
A215T |
probably damaging |
Het |
Smc1b |
T |
A |
15: 85,011,995 (GRCm39) |
I126L |
probably damaging |
Het |
Sycp2 |
A |
T |
2: 178,023,650 (GRCm39) |
N455K |
probably benign |
Het |
Tbck |
T |
C |
3: 132,543,738 (GRCm39) |
V863A |
probably benign |
Het |
Tfap2c |
A |
G |
2: 172,395,347 (GRCm39) |
M263V |
probably benign |
Het |
Tmem45a |
A |
G |
16: 56,627,134 (GRCm39) |
V245A |
probably damaging |
Het |
Top2a |
C |
T |
11: 98,897,790 (GRCm39) |
G759D |
probably damaging |
Het |
Traf5 |
A |
G |
1: 191,729,489 (GRCm39) |
S218P |
|
Het |
Tsfm |
T |
C |
10: 126,866,502 (GRCm39) |
R20G |
probably benign |
Het |
Usp34 |
T |
A |
11: 23,422,951 (GRCm39) |
D3108E |
|
Het |
Wnt11 |
A |
G |
7: 98,495,796 (GRCm39) |
Y100C |
probably damaging |
Het |
Zbtb49 |
A |
G |
5: 38,370,931 (GRCm39) |
C317R |
probably benign |
Het |
|
Other mutations in Ugt2a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0131:Ugt2a2
|
UTSW |
5 |
87,622,720 (GRCm39) |
nonsense |
probably null |
|
R0132:Ugt2a2
|
UTSW |
5 |
87,622,720 (GRCm39) |
nonsense |
probably null |
|
R0233:Ugt2a2
|
UTSW |
5 |
87,622,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Ugt2a2
|
UTSW |
5 |
87,612,007 (GRCm39) |
missense |
probably benign |
0.38 |
R0732:Ugt2a2
|
UTSW |
5 |
87,608,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R0841:Ugt2a2
|
UTSW |
5 |
87,622,648 (GRCm39) |
missense |
probably benign |
0.00 |
R1168:Ugt2a2
|
UTSW |
5 |
87,613,427 (GRCm39) |
splice site |
probably null |
|
R1433:Ugt2a2
|
UTSW |
5 |
87,611,965 (GRCm39) |
missense |
probably damaging |
0.98 |
R1552:Ugt2a2
|
UTSW |
5 |
87,609,880 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1795:Ugt2a2
|
UTSW |
5 |
87,622,315 (GRCm39) |
missense |
probably benign |
|
R1986:Ugt2a2
|
UTSW |
5 |
87,608,438 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2967:Ugt2a2
|
UTSW |
5 |
87,622,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R3053:Ugt2a2
|
UTSW |
5 |
87,622,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R4641:Ugt2a2
|
UTSW |
5 |
87,610,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Ugt2a2
|
UTSW |
5 |
87,622,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R5098:Ugt2a2
|
UTSW |
5 |
87,612,040 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5725:Ugt2a2
|
UTSW |
5 |
87,622,755 (GRCm39) |
missense |
probably damaging |
0.98 |
R6243:Ugt2a2
|
UTSW |
5 |
87,610,818 (GRCm39) |
missense |
probably benign |
0.13 |
R6502:Ugt2a2
|
UTSW |
5 |
87,608,318 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6650:Ugt2a2
|
UTSW |
5 |
87,622,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R7097:Ugt2a2
|
UTSW |
5 |
87,608,255 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7122:Ugt2a2
|
UTSW |
5 |
87,608,255 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7134:Ugt2a2
|
UTSW |
5 |
87,608,435 (GRCm39) |
missense |
probably benign |
0.12 |
R7205:Ugt2a2
|
UTSW |
5 |
87,608,468 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7476:Ugt2a2
|
UTSW |
5 |
87,622,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Ugt2a2
|
UTSW |
5 |
87,622,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R8222:Ugt2a2
|
UTSW |
5 |
87,608,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R8694:Ugt2a2
|
UTSW |
5 |
87,612,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Ugt2a2
|
UTSW |
5 |
87,608,270 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9119:Ugt2a2
|
UTSW |
5 |
87,610,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Ugt2a2
|
UTSW |
5 |
87,613,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R9302:Ugt2a2
|
UTSW |
5 |
87,609,940 (GRCm39) |
nonsense |
probably null |
|
R9556:Ugt2a2
|
UTSW |
5 |
87,609,821 (GRCm39) |
missense |
probably damaging |
1.00 |
|