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 |
Ngdn |
A |
G |
14: 55,258,554 (GRCm39) |
Y63C |
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 |
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 Ugcg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01447:Ugcg
|
APN |
4 |
59,213,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01768:Ugcg
|
APN |
4 |
59,217,216 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02636:Ugcg
|
APN |
4 |
59,207,763 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02672:Ugcg
|
APN |
4 |
59,218,587 (GRCm39) |
splice site |
probably benign |
|
IGL02798:Ugcg
|
APN |
4 |
59,220,346 (GRCm39) |
missense |
probably damaging |
1.00 |
congee
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
cream_o_wheat
|
UTSW |
4 |
59,220,387 (GRCm39) |
missense |
possibly damaging |
0.91 |
gruel
|
UTSW |
4 |
59,189,690 (GRCm39) |
missense |
probably benign |
|
Porridge
|
UTSW |
4 |
59,219,530 (GRCm39) |
missense |
possibly damaging |
0.86 |
slop
|
UTSW |
4 |
59,211,883 (GRCm39) |
missense |
probably benign |
0.16 |
wheatina
|
UTSW |
4 |
59,220,272 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4382001:Ugcg
|
UTSW |
4 |
59,213,246 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0013:Ugcg
|
UTSW |
4 |
59,213,931 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0013:Ugcg
|
UTSW |
4 |
59,213,931 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0068:Ugcg
|
UTSW |
4 |
59,217,130 (GRCm39) |
missense |
probably benign |
0.16 |
R0068:Ugcg
|
UTSW |
4 |
59,217,130 (GRCm39) |
missense |
probably benign |
0.16 |
R0119:Ugcg
|
UTSW |
4 |
59,217,036 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0230:Ugcg
|
UTSW |
4 |
59,189,739 (GRCm39) |
nonsense |
probably null |
|
R0299:Ugcg
|
UTSW |
4 |
59,217,036 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0384:Ugcg
|
UTSW |
4 |
59,220,387 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0499:Ugcg
|
UTSW |
4 |
59,217,036 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0645:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0688:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0726:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0802:Ugcg
|
UTSW |
4 |
59,189,685 (GRCm39) |
missense |
probably benign |
0.00 |
R0803:Ugcg
|
UTSW |
4 |
59,189,685 (GRCm39) |
missense |
probably benign |
0.00 |
R0811:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0812:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0828:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0831:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0944:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0945:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R0947:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1104:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1209:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1210:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1252:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1253:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1255:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1488:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1490:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1548:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1698:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1771:Ugcg
|
UTSW |
4 |
59,207,775 (GRCm39) |
missense |
probably benign |
0.05 |
R1776:Ugcg
|
UTSW |
4 |
59,207,775 (GRCm39) |
missense |
probably benign |
0.05 |
R1781:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1794:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R1840:Ugcg
|
UTSW |
4 |
59,219,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R1942:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2228:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2229:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2237:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2239:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2314:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2337:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2338:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2340:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2422:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2426:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R2433:Ugcg
|
UTSW |
4 |
59,207,876 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2680:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3076:Ugcg
|
UTSW |
4 |
59,213,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R3078:Ugcg
|
UTSW |
4 |
59,213,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R3689:Ugcg
|
UTSW |
4 |
59,211,883 (GRCm39) |
missense |
probably benign |
0.16 |
R3732:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3732:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3733:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3766:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3767:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3768:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3769:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3771:Ugcg
|
UTSW |
4 |
59,189,690 (GRCm39) |
missense |
probably benign |
|
R3847:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3848:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3916:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3917:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3958:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R3959:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4023:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4024:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4025:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4065:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4066:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
R4427:Ugcg
|
UTSW |
4 |
59,219,555 (GRCm39) |
missense |
probably benign |
0.02 |
R5842:Ugcg
|
UTSW |
4 |
59,219,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6012:Ugcg
|
UTSW |
4 |
59,220,272 (GRCm39) |
missense |
probably damaging |
0.96 |
R6080:Ugcg
|
UTSW |
4 |
59,218,524 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6762:Ugcg
|
UTSW |
4 |
59,219,530 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7194:Ugcg
|
UTSW |
4 |
59,213,210 (GRCm39) |
missense |
probably damaging |
0.99 |
R7286:Ugcg
|
UTSW |
4 |
59,217,111 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7362:Ugcg
|
UTSW |
4 |
59,217,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7472:Ugcg
|
UTSW |
4 |
59,217,156 (GRCm39) |
missense |
probably benign |
|
R7638:Ugcg
|
UTSW |
4 |
59,220,299 (GRCm39) |
missense |
probably benign |
0.26 |
R8170:Ugcg
|
UTSW |
4 |
59,211,974 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8488:Ugcg
|
UTSW |
4 |
59,213,896 (GRCm39) |
missense |
probably benign |
0.00 |
R8793:Ugcg
|
UTSW |
4 |
59,207,794 (GRCm39) |
missense |
probably benign |
0.22 |
R9441:Ugcg
|
UTSW |
4 |
59,207,843 (GRCm39) |
missense |
probably damaging |
1.00 |
Y4336:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
Y4337:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|