Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
C |
11: 109,844,445 (GRCm39) |
D862G |
possibly damaging |
Het |
Abcg2 |
C |
T |
6: 58,655,336 (GRCm39) |
Q109* |
probably null |
Het |
Acbd7 |
A |
G |
2: 3,341,455 (GRCm39) |
Y33C |
probably damaging |
Het |
Actl7a |
A |
G |
4: 56,744,310 (GRCm39) |
D279G |
probably damaging |
Het |
Akr1c18 |
A |
T |
13: 4,194,328 (GRCm39) |
Y110* |
probably null |
Het |
Akt1 |
T |
C |
12: 112,623,704 (GRCm39) |
K276E |
probably damaging |
Het |
Bcas2 |
A |
G |
3: 103,084,608 (GRCm39) |
|
probably benign |
Het |
C9 |
T |
A |
15: 6,516,297 (GRCm39) |
Y367N |
probably damaging |
Het |
Cd163 |
A |
G |
6: 124,296,022 (GRCm39) |
T789A |
probably benign |
Het |
Cers6 |
T |
A |
2: 68,938,789 (GRCm39) |
S344T |
probably benign |
Het |
Clcn4 |
A |
G |
7: 7,294,681 (GRCm39) |
V329A |
probably damaging |
Het |
Crisp3 |
A |
C |
17: 40,546,804 (GRCm39) |
V38G |
probably damaging |
Het |
Cyp2b23 |
A |
G |
7: 26,380,821 (GRCm39) |
F135L |
probably benign |
Het |
Cyrib |
A |
T |
15: 63,828,447 (GRCm39) |
|
probably null |
Het |
Ddr2 |
A |
T |
1: 169,816,089 (GRCm39) |
C539* |
probably null |
Het |
Efna5 |
T |
A |
17: 62,914,458 (GRCm39) |
D189V |
probably damaging |
Het |
Endov |
G |
T |
11: 119,390,675 (GRCm39) |
V70F |
probably damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Frem3 |
A |
T |
8: 81,340,026 (GRCm39) |
H773L |
probably benign |
Het |
Gm43302 |
T |
A |
5: 105,365,352 (GRCm39) |
Q552L |
possibly damaging |
Het |
Gramd1a |
A |
T |
7: 30,833,908 (GRCm39) |
W506R |
probably damaging |
Het |
Hmcn1 |
C |
T |
1: 150,570,600 (GRCm39) |
V2188I |
possibly damaging |
Het |
Ifit1bl2 |
A |
G |
19: 34,597,458 (GRCm39) |
F53L |
probably benign |
Het |
Kat8 |
G |
A |
7: 127,523,988 (GRCm39) |
E343K |
probably damaging |
Het |
Kif5a |
GGGTTGGT |
GGGT |
10: 127,066,898 (GRCm39) |
|
probably null |
Het |
Krt16 |
A |
G |
11: 100,139,272 (GRCm39) |
Y149H |
probably damaging |
Het |
Mreg |
A |
G |
1: 72,201,527 (GRCm39) |
I155T |
probably damaging |
Het |
Nans |
T |
C |
4: 46,499,083 (GRCm39) |
F130S |
probably benign |
Het |
Nox4 |
T |
C |
7: 86,954,181 (GRCm39) |
|
probably benign |
Het |
Or3a1d |
C |
A |
11: 74,237,954 (GRCm39) |
W32L |
possibly damaging |
Het |
Or52ad1 |
A |
T |
7: 102,995,826 (GRCm39) |
M103K |
possibly damaging |
Het |
Or56a3 |
C |
A |
7: 104,740,309 (GRCm39) |
C179F |
probably damaging |
Het |
Or5k15 |
A |
T |
16: 58,709,976 (GRCm39) |
Y202* |
probably null |
Het |
Pgap6 |
CGGGG |
CGGGGG |
17: 26,339,536 (GRCm39) |
|
probably null |
Het |
Pkd1 |
A |
G |
17: 24,784,497 (GRCm39) |
T348A |
probably benign |
Het |
Poteg |
T |
C |
8: 27,940,020 (GRCm39) |
|
probably null |
Het |
Prom1 |
T |
G |
5: 44,172,236 (GRCm39) |
N585T |
probably benign |
Het |
Rfc1 |
T |
C |
5: 65,434,769 (GRCm39) |
S666G |
probably null |
Het |
Rilp |
A |
G |
11: 75,403,687 (GRCm39) |
|
probably benign |
Het |
Serpina3i |
A |
G |
12: 104,231,759 (GRCm39) |
E132G |
probably benign |
Het |
Serpina3m |
T |
C |
12: 104,360,170 (GRCm39) |
V414A |
probably damaging |
Het |
Sfrp4 |
T |
C |
13: 19,807,868 (GRCm39) |
F89S |
probably damaging |
Het |
Stat5a |
A |
G |
11: 100,772,900 (GRCm39) |
H692R |
probably benign |
Het |
Tex29 |
A |
T |
8: 11,904,279 (GRCm39) |
|
probably benign |
Het |
Tmc5 |
T |
A |
7: 118,271,416 (GRCm39) |
F910I |
probably damaging |
Het |
Tusc3 |
G |
A |
8: 39,538,651 (GRCm39) |
G230D |
possibly damaging |
Het |
Ubqln3 |
G |
A |
7: 103,790,674 (GRCm39) |
P472L |
probably benign |
Het |
Upb1 |
A |
T |
10: 75,264,105 (GRCm39) |
I184F |
probably damaging |
Het |
Vamp4 |
T |
C |
1: 162,401,932 (GRCm39) |
F5L |
possibly damaging |
Het |
Zfp583 |
C |
A |
7: 6,326,674 (GRCm39) |
Q68H |
probably damaging |
Het |
Zfp831 |
A |
C |
2: 174,487,200 (GRCm39) |
H625P |
probably benign |
Het |
Zfp941 |
G |
A |
7: 140,392,763 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Krtap5-2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01958:Krtap5-2
|
APN |
7 |
141,729,459 (GRCm39) |
nonsense |
probably null |
|
IGL02064:Krtap5-2
|
APN |
7 |
141,729,468 (GRCm39) |
missense |
unknown |
|
IGL03214:Krtap5-2
|
APN |
7 |
141,728,751 (GRCm39) |
missense |
unknown |
|
IGL03326:Krtap5-2
|
APN |
7 |
141,729,100 (GRCm39) |
nonsense |
probably null |
|
R1196:Krtap5-2
|
UTSW |
7 |
141,728,620 (GRCm39) |
nonsense |
probably null |
|
R2327:Krtap5-2
|
UTSW |
7 |
141,728,748 (GRCm39) |
missense |
unknown |
|
R5166:Krtap5-2
|
UTSW |
7 |
141,728,721 (GRCm39) |
missense |
unknown |
|
R6356:Krtap5-2
|
UTSW |
7 |
141,729,119 (GRCm39) |
intron |
probably benign |
|
R6364:Krtap5-2
|
UTSW |
7 |
141,728,800 (GRCm39) |
nonsense |
probably null |
|
R6593:Krtap5-2
|
UTSW |
7 |
141,728,697 (GRCm39) |
missense |
unknown |
|
R7193:Krtap5-2
|
UTSW |
7 |
141,728,980 (GRCm39) |
small deletion |
probably benign |
|
R7740:Krtap5-2
|
UTSW |
7 |
141,728,699 (GRCm39) |
missense |
unknown |
|
R7748:Krtap5-2
|
UTSW |
7 |
141,728,845 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R7753:Krtap5-2
|
UTSW |
7 |
141,729,136 (GRCm39) |
small deletion |
probably benign |
|
R8307:Krtap5-2
|
UTSW |
7 |
141,728,586 (GRCm39) |
missense |
unknown |
|
R8446:Krtap5-2
|
UTSW |
7 |
141,728,845 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8767:Krtap5-2
|
UTSW |
7 |
141,728,845 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9100:Krtap5-2
|
UTSW |
7 |
141,728,836 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9689:Krtap5-2
|
UTSW |
7 |
141,729,029 (GRCm39) |
missense |
unknown |
|
Z1177:Krtap5-2
|
UTSW |
7 |
141,729,518 (GRCm39) |
missense |
unknown |
|
|