Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810064F22Rik |
C |
T |
9: 22,119,367 (GRCm39) |
|
noncoding transcript |
Het |
2610021A01Rik |
T |
G |
7: 41,275,858 (GRCm39) |
I520M |
probably damaging |
Het |
Ackr4 |
A |
G |
9: 103,976,831 (GRCm39) |
F39L |
probably damaging |
Het |
Adgre5 |
C |
T |
8: 84,460,126 (GRCm39) |
S92N |
probably damaging |
Het |
Adrb2 |
T |
C |
18: 62,312,762 (GRCm39) |
D21G |
probably benign |
Het |
Akr1c6 |
G |
A |
13: 4,486,372 (GRCm39) |
E60K |
probably benign |
Het |
Bcl7c |
T |
A |
7: 127,306,503 (GRCm39) |
N96I |
possibly damaging |
Het |
Brca1 |
A |
T |
11: 101,422,969 (GRCm39) |
S106R |
possibly damaging |
Het |
C6 |
A |
T |
15: 4,764,717 (GRCm39) |
T138S |
probably benign |
Het |
Cul3 |
T |
C |
1: 80,300,564 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
T |
A |
17: 31,022,217 (GRCm39) |
M3939K |
probably damaging |
Het |
Dock4 |
T |
A |
12: 40,681,626 (GRCm39) |
|
probably benign |
Het |
Dsc2 |
T |
G |
18: 20,183,116 (GRCm39) |
T101P |
probably damaging |
Het |
Dynlt1b |
T |
C |
17: 6,697,649 (GRCm39) |
|
probably benign |
Het |
E330013P04Rik |
A |
G |
19: 60,150,354 (GRCm39) |
|
noncoding transcript |
Het |
Fggy |
A |
G |
4: 95,585,238 (GRCm39) |
E39G |
probably benign |
Het |
Fhip1a |
A |
G |
3: 85,572,797 (GRCm39) |
V952A |
possibly damaging |
Het |
Fmo6 |
A |
T |
1: 162,753,795 (GRCm39) |
C116S |
probably benign |
Het |
Gadd45a |
A |
G |
6: 67,013,813 (GRCm39) |
I44T |
possibly damaging |
Het |
Gmps |
A |
G |
3: 63,883,743 (GRCm39) |
|
probably benign |
Het |
Gnmt |
A |
G |
17: 47,037,271 (GRCm39) |
L171P |
probably damaging |
Het |
Hnrnpm |
G |
A |
17: 33,868,976 (GRCm39) |
R523C |
probably damaging |
Het |
Inpp5a |
T |
C |
7: 139,105,654 (GRCm39) |
Y202H |
probably damaging |
Het |
Kank3 |
C |
T |
17: 34,036,450 (GRCm39) |
S106F |
probably damaging |
Het |
Lmcd1 |
A |
G |
6: 112,305,658 (GRCm39) |
D253G |
probably benign |
Het |
Lrrk2 |
A |
T |
15: 91,613,284 (GRCm39) |
I803F |
possibly damaging |
Het |
Mybpc2 |
T |
C |
7: 44,156,311 (GRCm39) |
K834R |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,500,129 (GRCm39) |
|
probably benign |
Het |
Myh4 |
A |
T |
11: 67,133,689 (GRCm39) |
N243Y |
probably damaging |
Het |
Myorg |
A |
G |
4: 41,497,996 (GRCm39) |
Y545H |
probably damaging |
Het |
Nfatc1 |
C |
T |
18: 80,679,110 (GRCm39) |
M759I |
probably benign |
Het |
Nipal4 |
A |
G |
11: 46,041,139 (GRCm39) |
I352T |
possibly damaging |
Het |
Nomo1 |
A |
G |
7: 45,683,329 (GRCm39) |
E25G |
possibly damaging |
Het |
Or10j27 |
A |
G |
1: 172,958,020 (GRCm39) |
S255P |
probably benign |
Het |
Or13a19 |
T |
C |
7: 139,903,065 (GRCm39) |
I151T |
probably benign |
Het |
Or14j7 |
A |
G |
17: 38,234,591 (GRCm39) |
I45V |
probably damaging |
Het |
Or1e32 |
T |
C |
11: 73,705,050 (GRCm39) |
N286S |
probably damaging |
Het |
Or4c116 |
T |
A |
2: 88,942,419 (GRCm39) |
I146L |
probably benign |
Het |
Or5p66 |
T |
C |
7: 107,886,264 (GRCm39) |
D23G |
probably benign |
Het |
Pabpn1l |
A |
G |
8: 123,349,183 (GRCm39) |
V78A |
probably benign |
Het |
Pde6b |
T |
A |
5: 108,568,203 (GRCm39) |
I327N |
possibly damaging |
Het |
Phrf1 |
T |
C |
7: 140,834,768 (GRCm39) |
|
probably benign |
Het |
Pkm |
C |
T |
9: 59,575,818 (GRCm39) |
|
probably benign |
Het |
Plxna2 |
G |
A |
1: 194,482,863 (GRCm39) |
V1519I |
probably benign |
Het |
Ppp2cb |
T |
C |
8: 34,105,689 (GRCm39) |
|
probably null |
Het |
Prickle2 |
A |
G |
6: 92,387,984 (GRCm39) |
Y473H |
probably benign |
Het |
Prpf3 |
A |
G |
3: 95,751,535 (GRCm39) |
W389R |
probably damaging |
Het |
Psme4 |
G |
A |
11: 30,765,264 (GRCm39) |
E544K |
possibly damaging |
Het |
Relb |
A |
T |
7: 19,345,767 (GRCm39) |
D395E |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,307,389 (GRCm39) |
N683S |
probably benign |
Het |
Rtel1 |
T |
C |
2: 180,964,596 (GRCm39) |
C102R |
probably benign |
Het |
Sel1l3 |
C |
T |
5: 53,301,379 (GRCm39) |
|
probably benign |
Het |
Slc8a2 |
A |
G |
7: 15,878,887 (GRCm39) |
T458A |
probably benign |
Het |
Smc3 |
T |
A |
19: 53,629,340 (GRCm39) |
M931K |
probably benign |
Het |
Sorbs2 |
T |
C |
8: 46,249,539 (GRCm39) |
V795A |
probably benign |
Het |
Tgm3 |
A |
G |
2: 129,854,326 (GRCm39) |
S2G |
probably benign |
Het |
Tpbpa |
T |
C |
13: 61,087,867 (GRCm39) |
T75A |
probably damaging |
Het |
Trub1 |
A |
G |
19: 57,473,495 (GRCm39) |
|
probably benign |
Het |
Ugt2a3 |
A |
G |
5: 87,475,065 (GRCm39) |
V393A |
possibly damaging |
Het |
Vav3 |
T |
A |
3: 109,470,151 (GRCm39) |
M532K |
possibly damaging |
Het |
Zfp616 |
A |
T |
11: 73,975,850 (GRCm39) |
K706N |
probably damaging |
Het |
Zkscan1 |
T |
C |
5: 138,091,432 (GRCm39) |
F55S |
probably damaging |
Het |
|
Other mutations in Uggt2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Uggt2
|
APN |
14 |
119,286,688 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00430:Uggt2
|
APN |
14 |
119,263,841 (GRCm39) |
nonsense |
probably null |
|
IGL00433:Uggt2
|
APN |
14 |
119,250,899 (GRCm39) |
missense |
probably benign |
|
IGL00572:Uggt2
|
APN |
14 |
119,280,203 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00577:Uggt2
|
APN |
14 |
119,272,312 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL00671:Uggt2
|
APN |
14 |
119,280,211 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01482:Uggt2
|
APN |
14 |
119,295,057 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01630:Uggt2
|
APN |
14 |
119,280,184 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01787:Uggt2
|
APN |
14 |
119,319,146 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02063:Uggt2
|
APN |
14 |
119,326,605 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02809:Uggt2
|
APN |
14 |
119,328,150 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02894:Uggt2
|
APN |
14 |
119,319,211 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03062:Uggt2
|
APN |
14 |
119,312,758 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03139:Uggt2
|
APN |
14 |
119,332,722 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03142:Uggt2
|
APN |
14 |
119,235,603 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03168:Uggt2
|
APN |
14 |
119,315,080 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03348:Uggt2
|
APN |
14 |
119,308,300 (GRCm39) |
missense |
probably benign |
0.38 |
P0014:Uggt2
|
UTSW |
14 |
119,281,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Uggt2
|
UTSW |
14 |
119,287,075 (GRCm39) |
missense |
probably benign |
0.07 |
R0063:Uggt2
|
UTSW |
14 |
119,244,542 (GRCm39) |
splice site |
probably benign |
|
R0063:Uggt2
|
UTSW |
14 |
119,244,542 (GRCm39) |
splice site |
probably benign |
|
R0383:Uggt2
|
UTSW |
14 |
119,286,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Uggt2
|
UTSW |
14 |
119,312,741 (GRCm39) |
critical splice donor site |
probably null |
|
R0472:Uggt2
|
UTSW |
14 |
119,332,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Uggt2
|
UTSW |
14 |
119,332,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Uggt2
|
UTSW |
14 |
119,295,010 (GRCm39) |
missense |
probably benign |
0.27 |
R0788:Uggt2
|
UTSW |
14 |
119,332,812 (GRCm39) |
splice site |
probably benign |
|
R1567:Uggt2
|
UTSW |
14 |
119,246,505 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1627:Uggt2
|
UTSW |
14 |
119,295,075 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1682:Uggt2
|
UTSW |
14 |
119,292,055 (GRCm39) |
missense |
probably benign |
0.19 |
R1746:Uggt2
|
UTSW |
14 |
119,250,915 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Uggt2
|
UTSW |
14 |
119,298,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Uggt2
|
UTSW |
14 |
119,298,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1799:Uggt2
|
UTSW |
14 |
119,269,688 (GRCm39) |
missense |
probably benign |
0.00 |
R1894:Uggt2
|
UTSW |
14 |
119,287,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R1918:Uggt2
|
UTSW |
14 |
119,245,467 (GRCm39) |
splice site |
probably benign |
|
R2149:Uggt2
|
UTSW |
14 |
119,312,757 (GRCm39) |
missense |
probably benign |
0.02 |
R2168:Uggt2
|
UTSW |
14 |
119,256,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R2219:Uggt2
|
UTSW |
14 |
119,312,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R2220:Uggt2
|
UTSW |
14 |
119,312,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:Uggt2
|
UTSW |
14 |
119,232,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R2331:Uggt2
|
UTSW |
14 |
119,264,011 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2904:Uggt2
|
UTSW |
14 |
119,296,521 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2906:Uggt2
|
UTSW |
14 |
119,256,919 (GRCm39) |
missense |
probably benign |
0.00 |
R2907:Uggt2
|
UTSW |
14 |
119,256,919 (GRCm39) |
missense |
probably benign |
0.00 |
R2908:Uggt2
|
UTSW |
14 |
119,256,919 (GRCm39) |
missense |
probably benign |
0.00 |
R2998:Uggt2
|
UTSW |
14 |
119,286,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R3407:Uggt2
|
UTSW |
14 |
119,328,682 (GRCm39) |
missense |
probably benign |
0.39 |
R3722:Uggt2
|
UTSW |
14 |
119,278,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R3749:Uggt2
|
UTSW |
14 |
119,295,084 (GRCm39) |
missense |
probably benign |
0.13 |
R4015:Uggt2
|
UTSW |
14 |
119,263,845 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4016:Uggt2
|
UTSW |
14 |
119,263,845 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4017:Uggt2
|
UTSW |
14 |
119,263,845 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4206:Uggt2
|
UTSW |
14 |
119,286,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R4536:Uggt2
|
UTSW |
14 |
119,256,970 (GRCm39) |
missense |
probably benign |
|
R4642:Uggt2
|
UTSW |
14 |
119,272,347 (GRCm39) |
missense |
probably benign |
0.00 |
R4654:Uggt2
|
UTSW |
14 |
119,269,670 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4770:Uggt2
|
UTSW |
14 |
119,266,466 (GRCm39) |
splice site |
probably null |
|
R4810:Uggt2
|
UTSW |
14 |
119,250,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Uggt2
|
UTSW |
14 |
119,239,259 (GRCm39) |
missense |
probably damaging |
0.99 |
R4856:Uggt2
|
UTSW |
14 |
119,273,376 (GRCm39) |
splice site |
probably null |
|
R4886:Uggt2
|
UTSW |
14 |
119,273,376 (GRCm39) |
splice site |
probably null |
|
R4888:Uggt2
|
UTSW |
14 |
119,315,062 (GRCm39) |
critical splice donor site |
probably null |
|
R4888:Uggt2
|
UTSW |
14 |
119,286,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R4895:Uggt2
|
UTSW |
14 |
119,256,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R5353:Uggt2
|
UTSW |
14 |
119,319,182 (GRCm39) |
missense |
probably benign |
0.00 |
R5423:Uggt2
|
UTSW |
14 |
119,256,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R5476:Uggt2
|
UTSW |
14 |
119,328,121 (GRCm39) |
missense |
probably benign |
0.01 |
R5561:Uggt2
|
UTSW |
14 |
119,278,939 (GRCm39) |
missense |
probably benign |
0.02 |
R5607:Uggt2
|
UTSW |
14 |
119,326,611 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5608:Uggt2
|
UTSW |
14 |
119,326,611 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5625:Uggt2
|
UTSW |
14 |
119,315,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R5698:Uggt2
|
UTSW |
14 |
119,280,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R5986:Uggt2
|
UTSW |
14 |
119,286,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Uggt2
|
UTSW |
14 |
119,308,238 (GRCm39) |
missense |
probably benign |
0.06 |
R6031:Uggt2
|
UTSW |
14 |
119,308,238 (GRCm39) |
missense |
probably benign |
0.06 |
R6056:Uggt2
|
UTSW |
14 |
119,273,381 (GRCm39) |
critical splice donor site |
probably null |
|
R6289:Uggt2
|
UTSW |
14 |
119,279,014 (GRCm39) |
missense |
probably damaging |
0.99 |
R6480:Uggt2
|
UTSW |
14 |
119,294,976 (GRCm39) |
missense |
probably benign |
0.01 |
R6515:Uggt2
|
UTSW |
14 |
119,315,131 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6706:Uggt2
|
UTSW |
14 |
119,308,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R6745:Uggt2
|
UTSW |
14 |
119,280,022 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6819:Uggt2
|
UTSW |
14 |
119,263,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6879:Uggt2
|
UTSW |
14 |
119,239,271 (GRCm39) |
missense |
probably benign |
0.10 |
R7117:Uggt2
|
UTSW |
14 |
119,251,938 (GRCm39) |
missense |
probably benign |
0.25 |
R7183:Uggt2
|
UTSW |
14 |
119,257,049 (GRCm39) |
splice site |
probably null |
|
R7337:Uggt2
|
UTSW |
14 |
119,323,587 (GRCm39) |
missense |
probably benign |
0.28 |
R7342:Uggt2
|
UTSW |
14 |
119,232,384 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7615:Uggt2
|
UTSW |
14 |
119,326,681 (GRCm39) |
missense |
probably benign |
0.12 |
R7625:Uggt2
|
UTSW |
14 |
119,263,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R7685:Uggt2
|
UTSW |
14 |
119,312,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Uggt2
|
UTSW |
14 |
119,235,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R7891:Uggt2
|
UTSW |
14 |
119,280,059 (GRCm39) |
missense |
probably benign |
0.09 |
R7938:Uggt2
|
UTSW |
14 |
119,296,519 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8050:Uggt2
|
UTSW |
14 |
119,263,834 (GRCm39) |
missense |
probably damaging |
0.98 |
R9007:Uggt2
|
UTSW |
14 |
119,326,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R9080:Uggt2
|
UTSW |
14 |
119,295,017 (GRCm39) |
missense |
probably benign |
0.42 |
R9203:Uggt2
|
UTSW |
14 |
119,294,975 (GRCm39) |
missense |
probably benign |
0.08 |
R9215:Uggt2
|
UTSW |
14 |
119,279,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R9324:Uggt2
|
UTSW |
14 |
119,312,741 (GRCm39) |
critical splice donor site |
probably null |
|
R9459:Uggt2
|
UTSW |
14 |
119,286,595 (GRCm39) |
missense |
probably benign |
0.02 |
R9647:Uggt2
|
UTSW |
14 |
119,256,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R9781:Uggt2
|
UTSW |
14 |
119,232,384 (GRCm39) |
missense |
possibly damaging |
0.56 |
Z1177:Uggt2
|
UTSW |
14 |
119,244,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|