Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519G04Rik |
T |
C |
5: 115,001,569 (GRCm39) |
M22T |
probably benign |
Het |
A930018M24Rik |
A |
G |
14: 51,134,576 (GRCm39) |
L22P |
probably damaging |
Het |
Aipl1 |
A |
T |
11: 71,927,538 (GRCm39) |
M59K |
probably damaging |
Het |
Atg2b |
T |
C |
12: 105,589,747 (GRCm39) |
I1835V |
probably damaging |
Het |
Cacna1i |
A |
T |
15: 80,274,056 (GRCm39) |
|
probably benign |
Het |
Cacna1i |
T |
C |
15: 80,205,389 (GRCm39) |
V115A |
probably damaging |
Het |
Catsperb |
T |
A |
12: 101,554,361 (GRCm39) |
M685K |
probably damaging |
Het |
Cdh10 |
T |
A |
15: 18,986,853 (GRCm39) |
Y361* |
probably null |
Het |
Clcn4 |
C |
T |
7: 7,296,981 (GRCm39) |
C219Y |
probably damaging |
Het |
Cpeb2 |
G |
A |
5: 43,443,080 (GRCm39) |
V924M |
probably damaging |
Het |
Cpxm2 |
T |
C |
7: 131,745,411 (GRCm39) |
E138G |
probably benign |
Het |
Dennd1a |
T |
C |
2: 37,748,441 (GRCm39) |
Y346C |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 30,854,638 (GRCm39) |
L100Q |
probably benign |
Het |
Dnajc6 |
A |
C |
4: 101,456,334 (GRCm39) |
N76T |
probably damaging |
Het |
Ehbp1 |
A |
G |
11: 22,009,231 (GRCm39) |
L954P |
probably damaging |
Het |
Eral1 |
A |
T |
11: 77,966,232 (GRCm39) |
D315E |
probably benign |
Het |
Fbln2 |
G |
T |
6: 91,240,365 (GRCm39) |
E724* |
probably null |
Het |
Fyco1 |
A |
G |
9: 123,656,247 (GRCm39) |
|
probably benign |
Het |
Fzd3 |
T |
A |
14: 65,473,173 (GRCm39) |
E198D |
probably damaging |
Het |
Fzd9 |
T |
C |
5: 135,279,408 (GRCm39) |
N159S |
probably damaging |
Het |
Galnt6 |
T |
A |
15: 100,601,259 (GRCm39) |
Q340L |
probably benign |
Het |
Gm20939 |
C |
T |
17: 95,184,522 (GRCm39) |
A390V |
probably damaging |
Het |
Gm5435 |
T |
G |
12: 82,542,464 (GRCm39) |
|
noncoding transcript |
Het |
Gm9949 |
A |
C |
18: 62,317,089 (GRCm39) |
|
probably benign |
Het |
Gprc5b |
G |
A |
7: 118,582,984 (GRCm39) |
T295I |
probably benign |
Het |
Gria2 |
G |
T |
3: 80,598,704 (GRCm39) |
Q777K |
probably damaging |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Haao |
T |
C |
17: 84,142,318 (GRCm39) |
T174A |
probably benign |
Het |
Hes6 |
A |
T |
1: 91,340,858 (GRCm39) |
M1K |
probably null |
Het |
Hook3 |
G |
T |
8: 26,600,780 (GRCm39) |
Q43K |
probably benign |
Het |
Klhl35 |
T |
C |
7: 99,120,902 (GRCm39) |
V390A |
probably damaging |
Het |
Myh9 |
G |
T |
15: 77,656,057 (GRCm39) |
T1151K |
probably damaging |
Het |
Nbn |
A |
T |
4: 15,981,668 (GRCm39) |
I587F |
possibly damaging |
Het |
Nek4 |
A |
G |
14: 30,704,408 (GRCm39) |
D696G |
probably damaging |
Het |
Niban1 |
A |
T |
1: 151,591,424 (GRCm39) |
Y522F |
possibly damaging |
Het |
Nlrp2 |
T |
C |
7: 5,311,724 (GRCm39) |
D52G |
probably damaging |
Het |
Oit3 |
G |
T |
10: 59,263,896 (GRCm39) |
R413S |
probably damaging |
Het |
Or4k48 |
T |
A |
2: 111,476,027 (GRCm39) |
H105L |
probably damaging |
Het |
Or6c1b |
A |
G |
10: 129,273,580 (GRCm39) |
M300V |
probably benign |
Het |
Otof |
T |
C |
5: 30,528,349 (GRCm39) |
T1870A |
probably benign |
Het |
Pdgfd |
T |
C |
9: 6,293,939 (GRCm39) |
|
probably null |
Het |
Pitrm1 |
T |
C |
13: 6,613,506 (GRCm39) |
V526A |
possibly damaging |
Het |
Pknox1 |
T |
C |
17: 31,814,256 (GRCm39) |
S194P |
probably damaging |
Het |
Plekhg5 |
T |
C |
4: 152,181,266 (GRCm39) |
S8P |
probably benign |
Het |
Ppp1r13b |
T |
C |
12: 111,807,416 (GRCm39) |
E157G |
probably damaging |
Het |
Psmd3 |
C |
T |
11: 98,585,051 (GRCm39) |
R466W |
probably damaging |
Het |
Ptgfrn |
A |
G |
3: 100,967,967 (GRCm39) |
F542S |
possibly damaging |
Het |
Ptgs1 |
A |
T |
2: 36,135,214 (GRCm39) |
M393L |
possibly damaging |
Het |
Qpct |
T |
A |
17: 79,371,492 (GRCm39) |
S87T |
probably benign |
Het |
Qtrt1 |
T |
A |
9: 21,330,607 (GRCm39) |
V269D |
probably benign |
Het |
Rassf9 |
C |
G |
10: 102,380,821 (GRCm39) |
R68G |
probably damaging |
Het |
Relch |
A |
G |
1: 105,647,259 (GRCm39) |
Y707C |
probably damaging |
Het |
Rif1 |
A |
G |
2: 51,963,235 (GRCm39) |
E25G |
probably damaging |
Het |
Rnf213 |
T |
C |
11: 119,305,352 (GRCm39) |
F528L |
probably benign |
Het |
Sgip1 |
T |
C |
4: 102,823,457 (GRCm39) |
S693P |
probably benign |
Het |
She |
A |
G |
3: 89,761,921 (GRCm39) |
D460G |
probably benign |
Het |
Sipa1l1 |
G |
T |
12: 82,387,935 (GRCm39) |
V54L |
probably benign |
Het |
Slc8a3 |
T |
A |
12: 81,251,781 (GRCm39) |
D640V |
possibly damaging |
Het |
Smurf1 |
T |
A |
5: 144,819,323 (GRCm39) |
E601D |
probably damaging |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Synpo2l |
A |
G |
14: 20,711,346 (GRCm39) |
S425P |
probably damaging |
Het |
Tbck |
T |
C |
3: 132,421,454 (GRCm39) |
V187A |
possibly damaging |
Het |
Tcf23 |
A |
T |
5: 31,126,175 (GRCm39) |
H18L |
probably benign |
Het |
Tcp11l2 |
A |
G |
10: 84,420,808 (GRCm39) |
S16G |
probably damaging |
Het |
Tekt2 |
T |
A |
4: 126,217,200 (GRCm39) |
M233L |
probably benign |
Het |
Tex14 |
T |
C |
11: 87,427,634 (GRCm39) |
S29P |
probably damaging |
Het |
Tlr5 |
G |
A |
1: 182,802,575 (GRCm39) |
M626I |
probably benign |
Het |
Tnn |
A |
T |
1: 159,952,985 (GRCm39) |
V685D |
probably damaging |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Trhr |
G |
A |
15: 44,060,497 (GRCm39) |
V6I |
probably benign |
Het |
Trim30c |
C |
T |
7: 104,032,158 (GRCm39) |
R301Q |
probably benign |
Het |
Usp51 |
T |
C |
X: 151,790,988 (GRCm39) |
I194T |
probably benign |
Het |
Vmn2r63 |
A |
G |
7: 42,553,550 (GRCm39) |
S569P |
probably benign |
Het |
Vps26a |
T |
G |
10: 62,300,459 (GRCm39) |
I236L |
probably benign |
Het |
Zc3h7b |
C |
T |
15: 81,661,289 (GRCm39) |
P376L |
probably benign |
Het |
Zcchc14 |
T |
C |
8: 122,330,718 (GRCm39) |
M882V |
probably benign |
Het |
Zfhx2 |
A |
G |
14: 55,302,545 (GRCm39) |
V1813A |
probably benign |
Het |
Zswim2 |
C |
T |
2: 83,745,626 (GRCm39) |
G604D |
possibly damaging |
Het |
Zzef1 |
C |
T |
11: 72,739,559 (GRCm39) |
Q669* |
probably null |
Het |
|
Other mutations in Tjp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01151:Tjp2
|
APN |
19 |
24,116,174 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01412:Tjp2
|
APN |
19 |
24,078,139 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01681:Tjp2
|
APN |
19 |
24,112,213 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02044:Tjp2
|
APN |
19 |
24,098,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02212:Tjp2
|
APN |
19 |
24,116,150 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02629:Tjp2
|
APN |
19 |
24,099,743 (GRCm39) |
splice site |
probably benign |
|
IGL02819:Tjp2
|
APN |
19 |
24,091,469 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02931:Tjp2
|
APN |
19 |
24,073,996 (GRCm39) |
missense |
probably benign |
0.11 |
PIT4402001:Tjp2
|
UTSW |
19 |
24,075,493 (GRCm39) |
nonsense |
probably null |
|
R0032:Tjp2
|
UTSW |
19 |
24,086,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R0667:Tjp2
|
UTSW |
19 |
24,086,113 (GRCm39) |
missense |
probably benign |
0.36 |
R0674:Tjp2
|
UTSW |
19 |
24,108,680 (GRCm39) |
missense |
probably benign |
0.37 |
R0749:Tjp2
|
UTSW |
19 |
24,099,636 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1185:Tjp2
|
UTSW |
19 |
24,108,527 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1185:Tjp2
|
UTSW |
19 |
24,108,527 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1185:Tjp2
|
UTSW |
19 |
24,108,527 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1571:Tjp2
|
UTSW |
19 |
24,078,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R1624:Tjp2
|
UTSW |
19 |
24,108,776 (GRCm39) |
missense |
probably benign |
0.01 |
R1658:Tjp2
|
UTSW |
19 |
24,090,311 (GRCm39) |
missense |
probably damaging |
0.99 |
R1851:Tjp2
|
UTSW |
19 |
24,076,899 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1968:Tjp2
|
UTSW |
19 |
24,088,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R2068:Tjp2
|
UTSW |
19 |
24,099,687 (GRCm39) |
missense |
probably benign |
0.22 |
R2273:Tjp2
|
UTSW |
19 |
24,090,171 (GRCm39) |
missense |
probably benign |
|
R2994:Tjp2
|
UTSW |
19 |
24,090,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R3767:Tjp2
|
UTSW |
19 |
24,078,190 (GRCm39) |
missense |
probably benign |
0.01 |
R3770:Tjp2
|
UTSW |
19 |
24,078,190 (GRCm39) |
missense |
probably benign |
0.01 |
R4077:Tjp2
|
UTSW |
19 |
24,086,182 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4079:Tjp2
|
UTSW |
19 |
24,086,182 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4505:Tjp2
|
UTSW |
19 |
24,086,195 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4720:Tjp2
|
UTSW |
19 |
24,078,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R4739:Tjp2
|
UTSW |
19 |
24,097,475 (GRCm39) |
splice site |
probably null |
|
R4745:Tjp2
|
UTSW |
19 |
24,074,030 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4858:Tjp2
|
UTSW |
19 |
24,099,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R5290:Tjp2
|
UTSW |
19 |
24,108,568 (GRCm39) |
missense |
probably benign |
|
R5887:Tjp2
|
UTSW |
19 |
24,073,963 (GRCm39) |
missense |
probably benign |
|
R5988:Tjp2
|
UTSW |
19 |
24,091,464 (GRCm39) |
missense |
probably benign |
|
R6144:Tjp2
|
UTSW |
19 |
24,097,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R6163:Tjp2
|
UTSW |
19 |
24,103,068 (GRCm39) |
critical splice donor site |
probably null |
|
R6183:Tjp2
|
UTSW |
19 |
24,078,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R6242:Tjp2
|
UTSW |
19 |
24,076,967 (GRCm39) |
splice site |
probably null |
|
R6683:Tjp2
|
UTSW |
19 |
24,098,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R6866:Tjp2
|
UTSW |
19 |
24,079,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R7025:Tjp2
|
UTSW |
19 |
24,110,052 (GRCm39) |
missense |
probably benign |
0.28 |
R7153:Tjp2
|
UTSW |
19 |
24,079,345 (GRCm39) |
missense |
probably benign |
0.40 |
R7514:Tjp2
|
UTSW |
19 |
24,088,886 (GRCm39) |
missense |
probably benign |
0.03 |
R8004:Tjp2
|
UTSW |
19 |
24,091,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R8505:Tjp2
|
UTSW |
19 |
24,088,438 (GRCm39) |
missense |
probably null |
1.00 |
R8527:Tjp2
|
UTSW |
19 |
24,088,937 (GRCm39) |
missense |
probably damaging |
0.99 |
R8710:Tjp2
|
UTSW |
19 |
24,072,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R9718:Tjp2
|
UTSW |
19 |
24,078,207 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Tjp2
|
UTSW |
19 |
24,075,391 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tjp2
|
UTSW |
19 |
24,108,729 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Tjp2
|
UTSW |
19 |
24,072,824 (GRCm39) |
missense |
possibly damaging |
0.74 |
|