Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg1 |
C |
T |
17: 31,317,269 (GRCm39) |
R194* |
probably null |
Het |
Actl6a |
A |
G |
3: 32,766,262 (GRCm39) |
T39A |
possibly damaging |
Het |
Adamts6 |
T |
A |
13: 104,550,257 (GRCm39) |
C624* |
probably null |
Het |
Adgrl1 |
T |
C |
8: 84,664,564 (GRCm39) |
|
probably null |
Het |
Ap3m2 |
A |
G |
8: 23,289,674 (GRCm39) |
V143A |
probably benign |
Het |
Ap5m1 |
T |
C |
14: 49,311,218 (GRCm39) |
V96A |
probably damaging |
Het |
Aqp5 |
T |
A |
15: 99,489,424 (GRCm39) |
V91E |
probably damaging |
Het |
Atp6v0b |
A |
T |
4: 117,742,350 (GRCm39) |
I181N |
probably damaging |
Het |
Ccp110 |
T |
A |
7: 118,322,241 (GRCm39) |
M632K |
probably benign |
Het |
Cd44 |
A |
T |
2: 102,672,604 (GRCm39) |
|
probably null |
Het |
Cidea |
G |
A |
18: 67,491,854 (GRCm39) |
R38Q |
probably damaging |
Het |
Cnn3 |
T |
C |
3: 121,245,042 (GRCm39) |
I86T |
probably benign |
Het |
Col14a1 |
C |
A |
15: 55,252,016 (GRCm39) |
D557E |
unknown |
Het |
Col6a6 |
T |
C |
9: 105,566,760 (GRCm39) |
Y2245C |
probably damaging |
Het |
Dhrs4 |
A |
T |
14: 55,725,092 (GRCm39) |
N196Y |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 31,093,901 (GRCm39) |
V4665A |
possibly damaging |
Het |
Dpep2 |
T |
C |
8: 106,716,113 (GRCm39) |
T267A |
|
Het |
Dtx3l |
T |
A |
16: 35,759,120 (GRCm39) |
Q43L |
probably benign |
Het |
Ednrb |
A |
G |
14: 104,080,738 (GRCm39) |
S59P |
probably benign |
Het |
Eml4 |
A |
G |
17: 83,758,126 (GRCm39) |
T435A |
probably benign |
Het |
Fam135b |
A |
T |
15: 71,333,925 (GRCm39) |
F1090I |
probably benign |
Het |
Filip1 |
A |
G |
9: 79,726,225 (GRCm39) |
V798A |
probably benign |
Het |
Fnip1 |
T |
G |
11: 54,356,228 (GRCm39) |
|
probably benign |
Het |
Gabrb2 |
C |
T |
11: 42,378,050 (GRCm39) |
Q89* |
probably null |
Het |
Gtf2ird1 |
A |
T |
5: 134,392,063 (GRCm39) |
V882E |
probably benign |
Het |
Gucy1a2 |
T |
A |
9: 3,532,804 (GRCm39) |
M1K |
probably null |
Het |
Ift70b |
A |
G |
2: 75,766,963 (GRCm39) |
S597P |
possibly damaging |
Het |
Igkv10-96 |
T |
A |
6: 68,609,025 (GRCm39) |
D90V |
possibly damaging |
Het |
Igkv4-54 |
G |
A |
6: 69,608,740 (GRCm39) |
R60C |
probably benign |
Het |
Igkv7-33 |
G |
T |
6: 70,035,847 (GRCm39) |
A45D |
probably damaging |
Het |
Klk1b22 |
A |
T |
7: 43,762,168 (GRCm39) |
I15F |
possibly damaging |
Het |
Lamp3 |
T |
A |
16: 19,518,490 (GRCm39) |
D249V |
probably benign |
Het |
Lrrfip2 |
T |
C |
9: 111,022,149 (GRCm39) |
V125A |
possibly damaging |
Het |
Mprip |
G |
A |
11: 59,643,756 (GRCm39) |
R638H |
possibly damaging |
Het |
Muc5ac |
A |
G |
7: 141,349,589 (GRCm39) |
M501V |
probably benign |
Het |
Myo5a |
C |
T |
9: 75,111,034 (GRCm39) |
P1509S |
probably damaging |
Het |
Oit3 |
A |
G |
10: 59,259,852 (GRCm39) |
V517A |
probably benign |
Het |
Or8g21 |
A |
T |
9: 38,906,027 (GRCm39) |
S235T |
not run |
Het |
Pcdhb18 |
T |
A |
18: 37,623,512 (GRCm39) |
F281I |
probably damaging |
Het |
Pkd1 |
C |
A |
17: 24,809,881 (GRCm39) |
Q3520K |
probably benign |
Het |
Plxnb1 |
T |
A |
9: 108,929,525 (GRCm39) |
I127N |
probably damaging |
Het |
Ppfia2 |
A |
T |
10: 106,655,390 (GRCm39) |
N319I |
probably damaging |
Het |
Pxn |
T |
C |
5: 115,686,665 (GRCm39) |
S386P |
possibly damaging |
Het |
Ralgps2 |
C |
T |
1: 156,714,738 (GRCm39) |
V104I |
probably benign |
Het |
Rp1 |
C |
T |
1: 4,417,924 (GRCm39) |
V1063I |
probably benign |
Het |
Slc10a5 |
A |
T |
3: 10,399,532 (GRCm39) |
F376Y |
probably damaging |
Het |
Snd1 |
T |
A |
6: 28,527,724 (GRCm39) |
I277N |
probably damaging |
Het |
Spc25 |
A |
G |
2: 69,036,406 (GRCm39) |
|
probably null |
Het |
Tex29 |
A |
G |
8: 11,894,055 (GRCm39) |
N6D |
unknown |
Het |
Top6bl |
T |
A |
19: 4,748,514 (GRCm39) |
R61S |
unknown |
Het |
Ttc6 |
G |
A |
12: 57,721,435 (GRCm39) |
A975T |
probably damaging |
Het |
Uba6 |
T |
C |
5: 86,320,560 (GRCm39) |
E13G |
probably damaging |
Het |
Ugcg |
T |
G |
4: 59,211,927 (GRCm39) |
C98G |
possibly damaging |
Het |
Ugt2b36 |
T |
A |
5: 87,240,190 (GRCm39) |
D65V |
probably damaging |
Het |
Unc93b1 |
A |
T |
19: 3,985,243 (GRCm39) |
D17V |
not run |
Het |
Usf1 |
G |
T |
1: 171,245,462 (GRCm39) |
W291C |
unknown |
Het |
Vps29 |
T |
C |
5: 122,500,180 (GRCm39) |
W97R |
possibly damaging |
Het |
Zbtb6 |
T |
C |
2: 37,319,577 (GRCm39) |
E117G |
probably damaging |
Het |
Zfp735 |
A |
C |
11: 73,601,629 (GRCm39) |
D191A |
probably benign |
Het |
|
Other mutations in Ngdn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00924:Ngdn
|
APN |
14 |
55,260,626 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01301:Ngdn
|
APN |
14 |
55,254,571 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02350:Ngdn
|
APN |
14 |
55,259,393 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02357:Ngdn
|
APN |
14 |
55,259,393 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU18:Ngdn
|
UTSW |
14 |
55,254,571 (GRCm39) |
missense |
probably benign |
0.15 |
PIT4651001:Ngdn
|
UTSW |
14 |
55,253,657 (GRCm39) |
missense |
probably benign |
0.05 |
R2062:Ngdn
|
UTSW |
14 |
55,259,564 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2251:Ngdn
|
UTSW |
14 |
55,260,852 (GRCm39) |
critical splice donor site |
probably null |
|
R5167:Ngdn
|
UTSW |
14 |
55,259,656 (GRCm39) |
nonsense |
probably null |
|
R5492:Ngdn
|
UTSW |
14 |
55,260,509 (GRCm39) |
missense |
probably benign |
0.00 |
R6174:Ngdn
|
UTSW |
14 |
55,259,556 (GRCm39) |
missense |
probably benign |
0.38 |
R6712:Ngdn
|
UTSW |
14 |
55,253,645 (GRCm39) |
missense |
probably benign |
0.18 |
R8303:Ngdn
|
UTSW |
14 |
55,260,602 (GRCm39) |
missense |
probably benign |
0.01 |
R9587:Ngdn
|
UTSW |
14 |
55,254,578 (GRCm39) |
missense |
probably benign |
0.03 |
R9669:Ngdn
|
UTSW |
14 |
55,259,339 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9737:Ngdn
|
UTSW |
14 |
55,259,339 (GRCm39) |
missense |
possibly damaging |
0.56 |
X0025:Ngdn
|
UTSW |
14 |
55,259,372 (GRCm39) |
missense |
possibly damaging |
0.71 |
Z1177:Ngdn
|
UTSW |
14 |
55,259,401 (GRCm39) |
missense |
probably null |
1.00 |
|