Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700101I19Rik |
T |
C |
1: 34,618,370 (GRCm39) |
|
probably benign |
Het |
Abca15 |
T |
G |
7: 119,960,643 (GRCm39) |
Y702D |
probably damaging |
Het |
Abcc8 |
T |
C |
7: 45,754,088 (GRCm39) |
K1576R |
probably benign |
Het |
Acot12 |
T |
A |
13: 91,905,711 (GRCm39) |
|
probably benign |
Het |
Adamts13 |
A |
G |
2: 26,895,202 (GRCm39) |
I1098V |
probably benign |
Het |
Adcy6 |
C |
T |
15: 98,496,857 (GRCm39) |
V471M |
probably damaging |
Het |
Ccdc170 |
C |
A |
10: 4,508,550 (GRCm39) |
D591E |
probably benign |
Het |
Corin |
A |
C |
5: 72,462,354 (GRCm39) |
D826E |
probably damaging |
Het |
Cpsf2 |
T |
G |
12: 101,956,098 (GRCm39) |
N300K |
possibly damaging |
Het |
Csmd2 |
C |
T |
4: 128,262,923 (GRCm39) |
T703I |
probably benign |
Het |
D130043K22Rik |
T |
A |
13: 25,041,139 (GRCm39) |
L187Q |
probably damaging |
Het |
D430041D05Rik |
G |
T |
2: 104,088,511 (GRCm39) |
S155* |
probably null |
Het |
Dmrtc2 |
C |
T |
7: 24,572,001 (GRCm39) |
P32L |
probably damaging |
Het |
Dsel |
G |
A |
1: 111,787,791 (GRCm39) |
R915* |
probably null |
Het |
Fam124b |
T |
C |
1: 80,190,852 (GRCm39) |
Y177C |
possibly damaging |
Het |
Fam171b |
G |
A |
2: 83,707,072 (GRCm39) |
W314* |
probably null |
Het |
Gpn1 |
G |
T |
5: 31,655,745 (GRCm39) |
D103Y |
probably damaging |
Het |
Gpr89 |
A |
T |
3: 96,800,865 (GRCm39) |
F88I |
probably damaging |
Het |
Ifi27l2a |
T |
C |
12: 103,403,792 (GRCm39) |
|
probably benign |
Het |
Kdm4d |
A |
G |
9: 14,375,493 (GRCm39) |
Y122H |
probably damaging |
Het |
Oas1d |
G |
A |
5: 121,054,907 (GRCm39) |
V160I |
probably benign |
Het |
Or5b108 |
A |
G |
19: 13,168,598 (GRCm39) |
D189G |
possibly damaging |
Het |
Or7e170 |
A |
T |
9: 19,794,844 (GRCm39) |
Y252* |
probably null |
Het |
Poglut3 |
T |
C |
9: 53,299,879 (GRCm39) |
|
probably null |
Het |
Rrp1b |
C |
T |
17: 32,271,793 (GRCm39) |
P288S |
probably benign |
Het |
Sin3b |
A |
G |
8: 73,471,133 (GRCm39) |
K360R |
probably benign |
Het |
Sympk |
A |
G |
7: 18,781,498 (GRCm39) |
D818G |
probably benign |
Het |
Tep1 |
C |
T |
14: 51,088,096 (GRCm39) |
V814M |
probably damaging |
Het |
Tpsg1 |
T |
C |
17: 25,592,196 (GRCm39) |
V17A |
probably benign |
Het |
|
Other mutations in Tecpr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01759:Tecpr2
|
APN |
12 |
110,897,826 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02114:Tecpr2
|
APN |
12 |
110,935,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02813:Tecpr2
|
APN |
12 |
110,899,626 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Tecpr2
|
APN |
12 |
110,934,183 (GRCm39) |
missense |
probably benign |
|
IGL03085:Tecpr2
|
APN |
12 |
110,921,260 (GRCm39) |
splice site |
probably benign |
|
IGL03290:Tecpr2
|
APN |
12 |
110,934,267 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0362:Tecpr2
|
UTSW |
12 |
110,935,374 (GRCm39) |
missense |
probably damaging |
0.96 |
R0486:Tecpr2
|
UTSW |
12 |
110,862,803 (GRCm39) |
missense |
probably benign |
0.01 |
R0662:Tecpr2
|
UTSW |
12 |
110,862,662 (GRCm39) |
missense |
probably benign |
0.02 |
R0787:Tecpr2
|
UTSW |
12 |
110,912,777 (GRCm39) |
missense |
probably benign |
0.30 |
R1147:Tecpr2
|
UTSW |
12 |
110,907,872 (GRCm39) |
splice site |
probably benign |
|
R1454:Tecpr2
|
UTSW |
12 |
110,935,387 (GRCm39) |
missense |
probably benign |
0.00 |
R1513:Tecpr2
|
UTSW |
12 |
110,921,234 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1567:Tecpr2
|
UTSW |
12 |
110,908,030 (GRCm39) |
critical splice donor site |
probably null |
|
R1569:Tecpr2
|
UTSW |
12 |
110,911,321 (GRCm39) |
critical splice donor site |
probably null |
|
R1818:Tecpr2
|
UTSW |
12 |
110,892,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Tecpr2
|
UTSW |
12 |
110,899,498 (GRCm39) |
missense |
probably benign |
|
R1897:Tecpr2
|
UTSW |
12 |
110,899,681 (GRCm39) |
missense |
probably benign |
|
R1903:Tecpr2
|
UTSW |
12 |
110,914,346 (GRCm39) |
missense |
probably damaging |
0.98 |
R1939:Tecpr2
|
UTSW |
12 |
110,899,603 (GRCm39) |
missense |
probably damaging |
0.98 |
R1982:Tecpr2
|
UTSW |
12 |
110,921,219 (GRCm39) |
missense |
probably benign |
0.07 |
R2073:Tecpr2
|
UTSW |
12 |
110,934,863 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2393:Tecpr2
|
UTSW |
12 |
110,892,836 (GRCm39) |
missense |
probably damaging |
0.99 |
R2443:Tecpr2
|
UTSW |
12 |
110,862,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Tecpr2
|
UTSW |
12 |
110,899,752 (GRCm39) |
missense |
probably benign |
|
R4564:Tecpr2
|
UTSW |
12 |
110,921,219 (GRCm39) |
missense |
probably benign |
0.07 |
R4723:Tecpr2
|
UTSW |
12 |
110,899,410 (GRCm39) |
missense |
probably benign |
0.01 |
R4835:Tecpr2
|
UTSW |
12 |
110,921,164 (GRCm39) |
missense |
probably benign |
0.00 |
R4847:Tecpr2
|
UTSW |
12 |
110,906,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R4911:Tecpr2
|
UTSW |
12 |
110,897,921 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5179:Tecpr2
|
UTSW |
12 |
110,911,127 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5266:Tecpr2
|
UTSW |
12 |
110,881,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Tecpr2
|
UTSW |
12 |
110,881,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R5486:Tecpr2
|
UTSW |
12 |
110,899,449 (GRCm39) |
missense |
probably benign |
0.03 |
R5490:Tecpr2
|
UTSW |
12 |
110,881,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R5627:Tecpr2
|
UTSW |
12 |
110,907,916 (GRCm39) |
missense |
probably damaging |
0.97 |
R5836:Tecpr2
|
UTSW |
12 |
110,897,945 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6052:Tecpr2
|
UTSW |
12 |
110,885,325 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6084:Tecpr2
|
UTSW |
12 |
110,895,543 (GRCm39) |
missense |
probably damaging |
0.98 |
R6306:Tecpr2
|
UTSW |
12 |
110,911,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R6563:Tecpr2
|
UTSW |
12 |
110,895,521 (GRCm39) |
missense |
probably benign |
0.00 |
R6936:Tecpr2
|
UTSW |
12 |
110,911,297 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6977:Tecpr2
|
UTSW |
12 |
110,906,200 (GRCm39) |
missense |
probably benign |
0.17 |
R7110:Tecpr2
|
UTSW |
12 |
110,885,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Tecpr2
|
UTSW |
12 |
110,881,806 (GRCm39) |
missense |
probably damaging |
0.97 |
R7353:Tecpr2
|
UTSW |
12 |
110,934,278 (GRCm39) |
missense |
probably benign |
0.06 |
R7362:Tecpr2
|
UTSW |
12 |
110,907,910 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7366:Tecpr2
|
UTSW |
12 |
110,881,914 (GRCm39) |
critical splice donor site |
probably null |
|
R7404:Tecpr2
|
UTSW |
12 |
110,898,038 (GRCm39) |
missense |
probably benign |
0.00 |
R7478:Tecpr2
|
UTSW |
12 |
110,934,873 (GRCm39) |
missense |
probably benign |
0.36 |
R7774:Tecpr2
|
UTSW |
12 |
110,899,606 (GRCm39) |
missense |
probably benign |
0.00 |
R7922:Tecpr2
|
UTSW |
12 |
110,899,076 (GRCm39) |
frame shift |
probably null |
|
R7997:Tecpr2
|
UTSW |
12 |
110,900,037 (GRCm39) |
missense |
probably benign |
0.02 |
R8037:Tecpr2
|
UTSW |
12 |
110,902,854 (GRCm39) |
missense |
probably benign |
0.03 |
R8038:Tecpr2
|
UTSW |
12 |
110,902,854 (GRCm39) |
missense |
probably benign |
0.03 |
R8393:Tecpr2
|
UTSW |
12 |
110,911,191 (GRCm39) |
missense |
probably damaging |
0.99 |
R8411:Tecpr2
|
UTSW |
12 |
110,898,154 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8726:Tecpr2
|
UTSW |
12 |
110,904,668 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9155:Tecpr2
|
UTSW |
12 |
110,881,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9259:Tecpr2
|
UTSW |
12 |
110,897,867 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9279:Tecpr2
|
UTSW |
12 |
110,895,505 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9562:Tecpr2
|
UTSW |
12 |
110,914,141 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1176:Tecpr2
|
UTSW |
12 |
110,862,744 (GRCm39) |
missense |
probably damaging |
0.99 |
|