Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Add2 |
A |
T |
6: 86,086,728 (GRCm39) |
D296V |
probably damaging |
Het |
Ak9 |
A |
G |
10: 41,233,559 (GRCm39) |
E599G |
possibly damaging |
Het |
Ank3 |
A |
T |
10: 69,822,293 (GRCm39) |
I1604F |
probably benign |
Het |
Arid4a |
A |
G |
12: 71,109,980 (GRCm39) |
D107G |
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,019,770 (GRCm39) |
T2060A |
probably damaging |
Het |
Btn2a2 |
A |
T |
13: 23,666,978 (GRCm39) |
I209N |
probably benign |
Het |
Cenps |
C |
A |
4: 149,214,658 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
A |
G |
15: 47,596,901 (GRCm39) |
V1979A |
probably damaging |
Het |
Cyp4a12b |
C |
T |
4: 115,271,714 (GRCm39) |
R142* |
probably null |
Het |
Ddx23 |
A |
T |
15: 98,556,121 (GRCm39) |
S66T |
unknown |
Het |
Efcab2 |
A |
G |
1: 178,303,439 (GRCm39) |
K121R |
probably benign |
Het |
Epb41l1 |
T |
A |
2: 156,345,708 (GRCm39) |
V237D |
probably damaging |
Het |
Epb41l1 |
G |
T |
2: 156,366,903 (GRCm39) |
A579S |
probably benign |
Het |
Epn1 |
G |
A |
7: 5,096,911 (GRCm39) |
R231H |
probably damaging |
Het |
Fbrs |
T |
C |
7: 127,086,924 (GRCm39) |
S649P |
probably damaging |
Het |
Fezf1 |
A |
G |
6: 23,247,427 (GRCm39) |
V216A |
probably benign |
Het |
Gen1 |
A |
T |
12: 11,310,897 (GRCm39) |
S112T |
probably damaging |
Het |
Glrx2 |
A |
G |
1: 143,620,872 (GRCm39) |
N84D |
probably benign |
Het |
Gm1818 |
T |
G |
12: 48,602,719 (GRCm39) |
|
noncoding transcript |
Het |
Hira |
C |
A |
16: 18,753,815 (GRCm39) |
T553K |
possibly damaging |
Het |
Hnrnph3 |
A |
G |
10: 62,851,374 (GRCm39) |
|
probably benign |
Het |
Ighv12-3 |
A |
T |
12: 114,330,204 (GRCm39) |
F97Y |
probably benign |
Het |
Jcad |
A |
G |
18: 4,674,554 (GRCm39) |
Q772R |
probably damaging |
Het |
Lamb3 |
A |
G |
1: 193,014,670 (GRCm39) |
T610A |
probably benign |
Het |
Map3k19 |
T |
C |
1: 127,750,477 (GRCm39) |
D958G |
probably benign |
Het |
Map4k4 |
G |
A |
1: 40,039,082 (GRCm39) |
|
probably benign |
Het |
Mocos |
T |
C |
18: 24,834,444 (GRCm39) |
V827A |
possibly damaging |
Het |
Ms4a10 |
T |
A |
19: 10,941,486 (GRCm39) |
D161V |
probably damaging |
Het |
Myh9 |
A |
G |
15: 77,657,532 (GRCm39) |
I1071T |
possibly damaging |
Het |
Myo15a |
A |
G |
11: 60,370,246 (GRCm39) |
E1002G |
possibly damaging |
Het |
Neurod6 |
G |
A |
6: 55,656,002 (GRCm39) |
H212Y |
probably damaging |
Het |
Or2v1 |
A |
T |
11: 49,025,399 (GRCm39) |
I95F |
probably damaging |
Het |
Or52z13 |
T |
A |
7: 103,247,174 (GRCm39) |
I217N |
probably damaging |
Het |
Or5b12 |
T |
C |
19: 12,897,194 (GRCm39) |
N160D |
probably benign |
Het |
Pcdhb17 |
T |
C |
18: 37,620,133 (GRCm39) |
V641A |
probably benign |
Het |
Ppp3ca |
A |
T |
3: 136,634,332 (GRCm39) |
M431L |
probably benign |
Het |
Ptprk |
A |
T |
10: 28,461,671 (GRCm39) |
I69F |
probably damaging |
Het |
Rab34 |
G |
T |
11: 78,081,094 (GRCm39) |
|
probably benign |
Het |
Rb1cc1 |
A |
G |
1: 6,318,406 (GRCm39) |
N619S |
probably benign |
Het |
Rps6kc1 |
A |
G |
1: 190,617,617 (GRCm39) |
V129A |
probably benign |
Het |
Siglecf |
C |
T |
7: 43,005,351 (GRCm39) |
T437M |
probably benign |
Het |
Slc25a2 |
T |
C |
18: 37,771,335 (GRCm39) |
N65D |
probably benign |
Het |
Spire1 |
A |
G |
18: 67,639,779 (GRCm39) |
S245P |
probably benign |
Het |
Sptb |
A |
T |
12: 76,679,158 (GRCm39) |
M99K |
probably benign |
Het |
Tacc1 |
G |
T |
8: 25,672,011 (GRCm39) |
L406I |
possibly damaging |
Het |
Tas2r140 |
T |
C |
6: 40,468,476 (GRCm39) |
I102T |
probably benign |
Het |
Trappc11 |
A |
T |
8: 47,949,952 (GRCm39) |
|
probably null |
Het |
Trbv11 |
A |
G |
6: 41,084,153 (GRCm39) |
|
noncoding transcript |
Het |
Trmt11 |
A |
G |
10: 30,436,838 (GRCm39) |
Y301H |
probably benign |
Het |
Tspo |
A |
G |
15: 83,456,441 (GRCm39) |
T75A |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,710,569 (GRCm39) |
|
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,462,030 (GRCm39) |
Q1210R |
probably damaging |
Het |
Zhx3 |
A |
T |
2: 160,623,937 (GRCm39) |
Y77N |
probably damaging |
Het |
|
Other mutations in Rnf169 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01476:Rnf169
|
APN |
7 |
99,604,691 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02344:Rnf169
|
APN |
7 |
99,575,642 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03066:Rnf169
|
APN |
7 |
99,574,760 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0201:Rnf169
|
UTSW |
7 |
99,575,210 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1087:Rnf169
|
UTSW |
7 |
99,592,204 (GRCm39) |
missense |
probably benign |
0.01 |
R1289:Rnf169
|
UTSW |
7 |
99,574,943 (GRCm39) |
missense |
probably benign |
0.01 |
R1476:Rnf169
|
UTSW |
7 |
99,574,535 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1912:Rnf169
|
UTSW |
7 |
99,575,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R1964:Rnf169
|
UTSW |
7 |
99,574,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R2057:Rnf169
|
UTSW |
7 |
99,574,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R2342:Rnf169
|
UTSW |
7 |
99,574,652 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4755:Rnf169
|
UTSW |
7 |
99,574,930 (GRCm39) |
missense |
probably benign |
0.01 |
R4801:Rnf169
|
UTSW |
7 |
99,575,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Rnf169
|
UTSW |
7 |
99,575,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5391:Rnf169
|
UTSW |
7 |
99,584,367 (GRCm39) |
critical splice donor site |
probably null |
|
R5395:Rnf169
|
UTSW |
7 |
99,584,367 (GRCm39) |
critical splice donor site |
probably null |
|
R5643:Rnf169
|
UTSW |
7 |
99,576,338 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5817:Rnf169
|
UTSW |
7 |
99,574,976 (GRCm39) |
missense |
probably benign |
0.02 |
R6009:Rnf169
|
UTSW |
7 |
99,576,330 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6453:Rnf169
|
UTSW |
7 |
99,584,434 (GRCm39) |
missense |
probably benign |
0.01 |
R7238:Rnf169
|
UTSW |
7 |
99,574,954 (GRCm39) |
missense |
probably benign |
0.10 |
R7500:Rnf169
|
UTSW |
7 |
99,629,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R8194:Rnf169
|
UTSW |
7 |
99,575,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R9227:Rnf169
|
UTSW |
7 |
99,574,699 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9469:Rnf169
|
UTSW |
7 |
99,575,567 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9548:Rnf169
|
UTSW |
7 |
99,574,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R9729:Rnf169
|
UTSW |
7 |
99,575,477 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Rnf169
|
UTSW |
7 |
99,575,068 (GRCm39) |
missense |
not run |
|
|