Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy2 |
A |
C |
13: 68,878,486 (GRCm39) |
I384S |
probably damaging |
Het |
Atxn7 |
T |
C |
14: 14,087,273 (GRCm38) |
|
probably benign |
Het |
Blm |
A |
T |
7: 80,143,895 (GRCm39) |
V848D |
probably damaging |
Het |
Cul1 |
G |
T |
6: 47,478,143 (GRCm39) |
L175F |
probably damaging |
Het |
Cyp4a29 |
A |
G |
4: 115,108,368 (GRCm39) |
H364R |
possibly damaging |
Het |
Ddx60 |
A |
G |
8: 62,465,483 (GRCm39) |
D1380G |
probably damaging |
Het |
Det1 |
A |
T |
7: 78,493,372 (GRCm39) |
C211S |
possibly damaging |
Het |
Dnaaf9 |
A |
G |
2: 130,559,200 (GRCm39) |
Y822H |
probably damaging |
Het |
F5 |
A |
C |
1: 164,020,801 (GRCm39) |
Q1092P |
probably damaging |
Het |
Fam117b |
A |
C |
1: 59,992,119 (GRCm39) |
Y256S |
probably benign |
Het |
Fbxl13 |
A |
G |
5: 21,728,796 (GRCm39) |
|
probably null |
Het |
Galnt7 |
A |
G |
8: 57,979,212 (GRCm39) |
I637T |
probably benign |
Het |
H2-T24 |
T |
A |
17: 36,317,671 (GRCm39) |
K120N |
unknown |
Het |
Hes2 |
A |
G |
4: 152,244,269 (GRCm39) |
K18R |
probably damaging |
Het |
Icam5 |
A |
T |
9: 20,945,097 (GRCm39) |
Q220L |
probably benign |
Het |
Kdm8 |
G |
A |
7: 125,054,278 (GRCm39) |
A170T |
probably benign |
Het |
Krt40 |
G |
A |
11: 99,430,711 (GRCm39) |
A321V |
probably damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,828,979 (GRCm39) |
V45D |
probably damaging |
Het |
Mbip |
A |
G |
12: 56,382,597 (GRCm39) |
Y290H |
probably damaging |
Het |
Mical1 |
A |
G |
10: 41,354,195 (GRCm39) |
Y48C |
probably damaging |
Het |
Mslnl |
T |
C |
17: 25,963,051 (GRCm39) |
S300P |
probably benign |
Het |
Nanog |
T |
C |
6: 122,688,731 (GRCm39) |
L104P |
probably damaging |
Het |
Or10ak11 |
T |
C |
4: 118,687,238 (GRCm39) |
Y132C |
probably damaging |
Het |
Or4c113 |
A |
T |
2: 88,885,457 (GRCm39) |
H104Q |
probably damaging |
Het |
Or4f60 |
T |
A |
2: 111,902,007 (GRCm39) |
Y307F |
probably benign |
Het |
Or52n2c |
A |
T |
7: 104,574,580 (GRCm39) |
N130K |
probably benign |
Het |
Oxgr1 |
C |
A |
14: 120,260,199 (GRCm39) |
E3* |
probably null |
Het |
Pam16 |
A |
T |
16: 4,434,671 (GRCm39) |
|
probably benign |
Het |
Plcb1 |
A |
T |
2: 134,655,606 (GRCm39) |
|
probably benign |
Het |
Slc25a32 |
A |
T |
15: 38,969,359 (GRCm39) |
V58E |
probably benign |
Het |
Slc2a12 |
G |
T |
10: 22,541,134 (GRCm39) |
V330F |
probably damaging |
Het |
Slit1 |
T |
C |
19: 41,591,881 (GRCm39) |
E1247G |
possibly damaging |
Het |
Supt5 |
A |
T |
7: 28,019,508 (GRCm39) |
C519S |
possibly damaging |
Het |
Szt2 |
A |
G |
4: 118,221,922 (GRCm39) |
|
probably benign |
Het |
Tas2r118 |
A |
G |
6: 23,969,180 (GRCm39) |
W294R |
possibly damaging |
Het |
Tmem132c |
T |
C |
5: 127,640,784 (GRCm39) |
I985T |
probably benign |
Het |
Tmem87b |
T |
C |
2: 128,665,019 (GRCm39) |
V61A |
probably benign |
Het |
Trhr2 |
G |
A |
8: 123,085,220 (GRCm39) |
|
probably benign |
Het |
Ttc28 |
A |
G |
5: 111,381,208 (GRCm39) |
D1209G |
probably benign |
Het |
Uchl5 |
A |
G |
1: 143,677,940 (GRCm39) |
E148G |
probably benign |
Het |
Wdr62 |
T |
C |
7: 29,970,199 (GRCm39) |
I203V |
possibly damaging |
Het |
Wnk1 |
T |
C |
6: 119,931,148 (GRCm39) |
I799V |
possibly damaging |
Het |
|
Other mutations in Tex21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00472:Tex21
|
APN |
12 |
76,253,571 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00923:Tex21
|
APN |
12 |
76,291,885 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01062:Tex21
|
APN |
12 |
76,245,718 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01063:Tex21
|
APN |
12 |
76,245,592 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02624:Tex21
|
APN |
12 |
76,261,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03349:Tex21
|
APN |
12 |
76,268,365 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03412:Tex21
|
APN |
12 |
76,291,780 (GRCm39) |
critical splice donor site |
probably null |
|
ihop
|
UTSW |
12 |
76,286,229 (GRCm39) |
critical splice donor site |
probably null |
|
R0189:Tex21
|
UTSW |
12 |
76,286,307 (GRCm39) |
missense |
probably benign |
0.13 |
R0730:Tex21
|
UTSW |
12 |
76,250,940 (GRCm39) |
missense |
probably benign |
0.25 |
R1521:Tex21
|
UTSW |
12 |
76,251,044 (GRCm39) |
missense |
probably benign |
0.38 |
R1572:Tex21
|
UTSW |
12 |
76,253,665 (GRCm39) |
missense |
probably benign |
0.03 |
R1700:Tex21
|
UTSW |
12 |
76,268,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R1941:Tex21
|
UTSW |
12 |
76,268,458 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4654:Tex21
|
UTSW |
12 |
76,263,860 (GRCm39) |
missense |
probably benign |
0.32 |
R4943:Tex21
|
UTSW |
12 |
76,268,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Tex21
|
UTSW |
12 |
76,245,707 (GRCm39) |
missense |
probably benign |
0.00 |
R6262:Tex21
|
UTSW |
12 |
76,259,306 (GRCm39) |
missense |
probably damaging |
0.99 |
R6738:Tex21
|
UTSW |
12 |
76,286,283 (GRCm39) |
missense |
probably benign |
0.12 |
R6759:Tex21
|
UTSW |
12 |
76,251,086 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6890:Tex21
|
UTSW |
12 |
76,286,229 (GRCm39) |
critical splice donor site |
probably null |
|
R8910:Tex21
|
UTSW |
12 |
76,263,533 (GRCm39) |
unclassified |
probably benign |
|
R9547:Tex21
|
UTSW |
12 |
76,253,591 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Tex21
|
UTSW |
12 |
76,250,894 (GRCm39) |
missense |
probably damaging |
1.00 |
|