Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd6 |
T |
C |
4: 32,822,232 (GRCm39) |
H179R |
probably damaging |
Het |
Apbb2 |
G |
T |
5: 66,460,021 (GRCm39) |
P692Q |
probably damaging |
Het |
Arhgap40 |
A |
G |
2: 158,391,567 (GRCm39) |
N627D |
possibly damaging |
Het |
Asns |
G |
A |
6: 7,676,076 (GRCm39) |
R465* |
probably null |
Het |
Bdkrb1 |
G |
A |
12: 105,570,562 (GRCm39) |
V43I |
probably benign |
Het |
Bod1 |
T |
C |
11: 31,621,514 (GRCm39) |
D63G |
possibly damaging |
Het |
Ccdc39 |
T |
C |
3: 33,880,629 (GRCm39) |
K446R |
probably damaging |
Het |
Csnka2ip |
T |
A |
16: 64,298,310 (GRCm39) |
K685* |
probably null |
Het |
Dennd5a |
A |
T |
7: 109,517,808 (GRCm39) |
D609E |
probably benign |
Het |
Dhx34 |
G |
C |
7: 15,952,274 (GRCm39) |
T117S |
probably benign |
Het |
Dpp4 |
A |
T |
2: 62,182,630 (GRCm39) |
D550E |
probably benign |
Het |
Enah |
C |
T |
1: 181,784,066 (GRCm39) |
R81K |
unknown |
Het |
Epha5 |
G |
T |
5: 84,298,254 (GRCm39) |
A383E |
probably damaging |
Het |
Epha5 |
C |
T |
5: 84,298,255 (GRCm39) |
A383T |
probably damaging |
Het |
Etnppl |
A |
T |
3: 130,423,212 (GRCm39) |
M298L |
probably benign |
Het |
Fam81a |
G |
A |
9: 70,017,556 (GRCm39) |
R130* |
probably null |
Het |
Fbxl3 |
A |
C |
14: 103,332,839 (GRCm39) |
H46Q |
probably benign |
Het |
Gal3st1 |
A |
G |
11: 3,948,509 (GRCm39) |
I239V |
possibly damaging |
Het |
Htra4 |
T |
C |
8: 25,523,612 (GRCm39) |
I318V |
probably benign |
Het |
Igdcc4 |
A |
G |
9: 65,038,932 (GRCm39) |
T906A |
possibly damaging |
Het |
Il7r |
T |
C |
15: 9,516,543 (GRCm39) |
N86S |
probably benign |
Het |
Mettl17 |
A |
G |
14: 52,127,063 (GRCm39) |
N231D |
probably benign |
Het |
Mki67 |
T |
C |
7: 135,299,040 (GRCm39) |
D1998G |
probably benign |
Het |
Myh15 |
G |
T |
16: 48,940,417 (GRCm39) |
R789L |
possibly damaging |
Het |
Myh7 |
A |
G |
14: 55,224,860 (GRCm39) |
V569A |
probably benign |
Het |
Nell1 |
A |
G |
7: 50,503,588 (GRCm39) |
I617M |
probably damaging |
Het |
Nlrp1b |
C |
G |
11: 71,072,512 (GRCm39) |
E444Q |
probably benign |
Het |
Or10ak16 |
T |
C |
4: 118,750,402 (GRCm39) |
S41P |
probably damaging |
Het |
Or2b4 |
T |
A |
17: 38,116,660 (GRCm39) |
L208* |
probably null |
Het |
Or2y8 |
T |
A |
11: 52,035,677 (GRCm39) |
I227F |
possibly damaging |
Het |
Psmd2 |
T |
C |
16: 20,478,709 (GRCm39) |
S603P |
probably damaging |
Het |
Slc4a2 |
T |
A |
5: 24,644,055 (GRCm39) |
I913N |
possibly damaging |
Het |
Smyd4 |
T |
C |
11: 75,291,164 (GRCm39) |
Y589H |
probably damaging |
Het |
Spag17 |
A |
G |
3: 100,000,992 (GRCm39) |
E1850G |
probably damaging |
Het |
Srsf11 |
A |
T |
3: 157,718,427 (GRCm39) |
|
probably benign |
Het |
Stra6 |
A |
T |
9: 58,058,687 (GRCm39) |
N488I |
possibly damaging |
Het |
Supt20 |
C |
T |
3: 54,614,362 (GRCm39) |
Q160* |
probably null |
Het |
Tbc1d2b |
G |
A |
9: 90,104,393 (GRCm39) |
P583L |
possibly damaging |
Het |
Uchl1 |
T |
A |
5: 66,839,808 (GRCm39) |
F117I |
probably damaging |
Het |
Usf1 |
T |
A |
1: 171,245,677 (GRCm39) |
N307K |
probably benign |
Het |
Zfp994 |
T |
A |
17: 22,419,926 (GRCm39) |
H341L |
probably damaging |
Het |
|
Other mutations in H2-T15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01859:H2-T15
|
APN |
17 |
36,368,903 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02007:H2-T15
|
APN |
17 |
36,367,222 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1829:H2-T15
|
UTSW |
17 |
36,368,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R1944:H2-T15
|
UTSW |
17 |
36,368,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R4117:H2-T15
|
UTSW |
17 |
36,368,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:H2-T15
|
UTSW |
17 |
36,368,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R4626:H2-T15
|
UTSW |
17 |
36,368,788 (GRCm39) |
frame shift |
probably null |
|
R4649:H2-T15
|
UTSW |
17 |
36,368,768 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4864:H2-T15
|
UTSW |
17 |
36,369,253 (GRCm39) |
utr 3 prime |
probably benign |
|
R5412:H2-T15
|
UTSW |
17 |
36,366,936 (GRCm39) |
missense |
probably benign |
0.01 |
R5430:H2-T15
|
UTSW |
17 |
36,366,967 (GRCm39) |
missense |
probably benign |
0.00 |
R5547:H2-T15
|
UTSW |
17 |
36,368,796 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5896:H2-T15
|
UTSW |
17 |
36,367,236 (GRCm39) |
missense |
probably benign |
0.01 |
R5974:H2-T15
|
UTSW |
17 |
36,367,677 (GRCm39) |
missense |
probably benign |
0.05 |
R6456:H2-T15
|
UTSW |
17 |
36,367,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R7073:H2-T15
|
UTSW |
17 |
36,369,235 (GRCm39) |
missense |
unknown |
|
R7217:H2-T15
|
UTSW |
17 |
36,367,235 (GRCm39) |
missense |
probably benign |
0.01 |
R7652:H2-T15
|
UTSW |
17 |
36,367,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8267:H2-T15
|
UTSW |
17 |
36,367,675 (GRCm39) |
missense |
possibly damaging |
0.52 |
|