Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg4 |
A |
T |
X: 56,013,487 (GRCm39) |
I2838F |
probably damaging |
Het |
Agbl2 |
G |
A |
2: 90,621,962 (GRCm39) |
V150I |
probably damaging |
Het |
Ambra1 |
T |
C |
2: 91,740,652 (GRCm39) |
S924P |
probably damaging |
Het |
Arfgap3 |
T |
C |
15: 83,206,808 (GRCm39) |
D260G |
probably benign |
Het |
Bag3 |
AAAGG |
AAAGGAAGG |
7: 128,147,493 (GRCm39) |
|
probably null |
Het |
Bag3 |
TAAAG |
TAAAGAAAG |
7: 128,147,492 (GRCm39) |
|
probably null |
Het |
Cacnb3 |
T |
C |
15: 98,539,068 (GRCm39) |
V167A |
probably benign |
Het |
Carm1 |
C |
T |
9: 21,497,478 (GRCm39) |
R347W |
probably damaging |
Het |
Ccdc30 |
A |
T |
4: 119,181,778 (GRCm39) |
F577I |
possibly damaging |
Het |
Ces3a |
T |
A |
8: 105,777,199 (GRCm39) |
V174E |
probably damaging |
Het |
Cobl |
T |
C |
11: 12,325,830 (GRCm39) |
Y215C |
probably damaging |
Het |
Cybrd1 |
A |
T |
2: 70,948,470 (GRCm39) |
M3L |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,336,212 (GRCm39) |
V98A |
probably benign |
Het |
Dsg1c |
G |
A |
18: 20,415,115 (GRCm39) |
|
probably null |
Het |
Eif4a1 |
A |
T |
11: 69,561,089 (GRCm39) |
V72E |
probably damaging |
Het |
Fmn1 |
A |
T |
2: 113,195,400 (GRCm39) |
I367F |
unknown |
Het |
Fnbp1l |
A |
C |
3: 122,345,799 (GRCm39) |
W229G |
probably damaging |
Het |
Inka1 |
C |
T |
9: 107,862,253 (GRCm39) |
R23Q |
probably damaging |
Het |
Ints6 |
A |
T |
14: 62,934,386 (GRCm39) |
I707K |
probably benign |
Het |
Ipo8 |
T |
C |
6: 148,723,207 (GRCm39) |
D70G |
probably benign |
Het |
Kif20b |
T |
C |
19: 34,927,900 (GRCm39) |
L1014P |
probably damaging |
Het |
Kif9 |
T |
C |
9: 110,348,208 (GRCm39) |
L677P |
probably damaging |
Het |
Mbd1 |
A |
G |
18: 74,410,438 (GRCm39) |
K414E |
possibly damaging |
Het |
Mfsd1 |
T |
A |
3: 67,504,046 (GRCm39) |
M346K |
possibly damaging |
Het |
Mthfr |
T |
C |
4: 148,139,518 (GRCm39) |
I66T |
probably damaging |
Het |
Myh10 |
T |
G |
11: 68,681,037 (GRCm39) |
L989R |
possibly damaging |
Het |
Ncan |
G |
A |
8: 70,564,801 (GRCm39) |
T271I |
probably damaging |
Het |
Or10ag53 |
A |
C |
2: 87,083,243 (GRCm39) |
T321P |
probably benign |
Het |
Or9s23 |
A |
G |
1: 92,501,675 (GRCm39) |
T261A |
probably damaging |
Het |
Pate2 |
C |
T |
9: 35,582,262 (GRCm39) |
T80I |
probably damaging |
Het |
Pcdhb15 |
A |
G |
18: 37,607,442 (GRCm39) |
T225A |
possibly damaging |
Het |
Pde4dip |
C |
A |
3: 97,661,784 (GRCm39) |
L640F |
probably damaging |
Het |
Plch1 |
A |
G |
3: 63,606,768 (GRCm39) |
|
probably benign |
Het |
Pus3 |
C |
T |
9: 35,478,021 (GRCm39) |
R418C |
probably damaging |
Het |
Sall2 |
G |
T |
14: 52,565,561 (GRCm39) |
N24K |
probably benign |
Het |
Sh3bp4 |
G |
T |
1: 89,072,769 (GRCm39) |
C539F |
possibly damaging |
Het |
Smco3 |
A |
G |
6: 136,808,425 (GRCm39) |
S150P |
probably benign |
Het |
Spag17 |
G |
T |
3: 99,992,615 (GRCm39) |
A1704S |
probably benign |
Het |
Tecta |
A |
T |
9: 42,249,150 (GRCm39) |
I1904N |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,536,281 (GRCm39) |
K33280* |
probably null |
Het |
Vmn1r21 |
C |
T |
6: 57,820,877 (GRCm39) |
G189D |
probably damaging |
Het |
Zbtb10 |
A |
G |
3: 9,329,926 (GRCm39) |
N428S |
probably damaging |
Het |
Zfp407 |
G |
A |
18: 84,576,997 (GRCm39) |
A1372V |
probably benign |
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 |
|
R0940:Uggt2
|
UTSW |
14 |
119,328,604 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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 |
|