Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12b |
A |
G |
12: 70,216,039 (GRCm39) |
T199A |
probably benign |
Het |
Ank2 |
A |
G |
3: 126,737,121 (GRCm39) |
F2921S |
unknown |
Het |
Atg12 |
A |
G |
18: 46,874,505 (GRCm39) |
S37P |
probably benign |
Het |
Bnip3l |
G |
A |
14: 67,246,214 (GRCm39) |
P7L |
possibly damaging |
Het |
Cdh5 |
A |
G |
8: 104,863,329 (GRCm39) |
D413G |
probably damaging |
Het |
Cdk8 |
A |
G |
5: 146,236,539 (GRCm39) |
N318S |
probably benign |
Het |
Clasp2 |
T |
A |
9: 113,590,665 (GRCm39) |
L68* |
probably null |
Het |
Cntnap2 |
CCACATAAACAACACACA |
CCACA |
6: 45,992,373 (GRCm39) |
|
probably null |
Het |
Cpne9 |
A |
C |
6: 113,267,401 (GRCm39) |
N194T |
probably damaging |
Het |
Cpxm1 |
A |
G |
2: 130,235,302 (GRCm39) |
|
probably null |
Het |
Crtc1 |
T |
C |
8: 70,840,205 (GRCm39) |
N556S |
probably damaging |
Het |
Gm12888 |
A |
T |
4: 121,175,520 (GRCm39) |
C87* |
probably null |
Het |
Hivep2 |
A |
G |
10: 14,019,583 (GRCm39) |
E2118G |
probably damaging |
Het |
Hrh4 |
A |
G |
18: 13,155,270 (GRCm39) |
N270D |
possibly damaging |
Het |
Iqsec1 |
G |
A |
6: 90,671,672 (GRCm39) |
Q77* |
probably null |
Het |
Lars1 |
A |
G |
18: 42,350,649 (GRCm39) |
W887R |
probably damaging |
Het |
Lgr5 |
A |
G |
10: 115,288,527 (GRCm39) |
Y706H |
probably damaging |
Het |
Ltn1 |
A |
T |
16: 87,222,524 (GRCm39) |
F170I |
probably damaging |
Het |
Msrb1 |
T |
C |
17: 24,958,535 (GRCm39) |
S40P |
probably damaging |
Het |
Myh6 |
T |
C |
14: 55,189,759 (GRCm39) |
I1096V |
probably benign |
Het |
Myh7b |
A |
G |
2: 155,455,963 (GRCm39) |
Y116C |
probably damaging |
Het |
Ndrg2 |
T |
C |
14: 52,148,238 (GRCm39) |
H41R |
possibly damaging |
Het |
Or5an11 |
A |
G |
19: 12,245,869 (GRCm39) |
T92A |
probably benign |
Het |
Spag17 |
A |
G |
3: 99,934,526 (GRCm39) |
T603A |
possibly damaging |
Het |
Sugp1 |
T |
A |
8: 70,505,256 (GRCm39) |
H74Q |
probably benign |
Het |
Tsnaxip1 |
A |
G |
8: 106,568,390 (GRCm39) |
E358G |
possibly damaging |
Het |
Unc5d |
T |
A |
8: 29,214,332 (GRCm39) |
H410L |
probably benign |
Het |
Usp1 |
T |
C |
4: 98,819,672 (GRCm39) |
V378A |
probably benign |
Het |
Wdtc1 |
A |
G |
4: 133,022,604 (GRCm39) |
S581P |
probably damaging |
Het |
Zfp947 |
A |
G |
17: 22,365,341 (GRCm39) |
V111A |
probably benign |
Het |
|
Other mutations in Tjp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00420:Tjp1
|
APN |
7 |
64,950,967 (GRCm39) |
missense |
probably benign |
|
IGL00848:Tjp1
|
APN |
7 |
64,952,942 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01363:Tjp1
|
APN |
7 |
64,952,713 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01526:Tjp1
|
APN |
7 |
64,972,406 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01607:Tjp1
|
APN |
7 |
64,985,926 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02223:Tjp1
|
APN |
7 |
64,972,349 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02341:Tjp1
|
APN |
7 |
64,962,382 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02347:Tjp1
|
APN |
7 |
64,950,812 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02452:Tjp1
|
APN |
7 |
64,962,403 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02512:Tjp1
|
APN |
7 |
64,993,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02552:Tjp1
|
APN |
7 |
64,949,530 (GRCm39) |
nonsense |
probably null |
|
IGL02707:Tjp1
|
APN |
7 |
64,979,430 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02707:Tjp1
|
APN |
7 |
64,979,431 (GRCm39) |
nonsense |
probably null |
|
IGL02939:Tjp1
|
APN |
7 |
64,964,638 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03139:Tjp1
|
APN |
7 |
64,990,182 (GRCm39) |
splice site |
probably benign |
|
IGL03273:Tjp1
|
APN |
7 |
64,949,547 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Tjp1
|
APN |
7 |
64,964,717 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4453001:Tjp1
|
UTSW |
7 |
64,993,362 (GRCm39) |
critical splice donor site |
probably null |
|
R0012:Tjp1
|
UTSW |
7 |
64,979,523 (GRCm39) |
splice site |
probably benign |
|
R0012:Tjp1
|
UTSW |
7 |
64,979,523 (GRCm39) |
splice site |
probably benign |
|
R0390:Tjp1
|
UTSW |
7 |
64,964,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R0519:Tjp1
|
UTSW |
7 |
64,952,669 (GRCm39) |
missense |
probably benign |
|
R0653:Tjp1
|
UTSW |
7 |
64,964,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1163:Tjp1
|
UTSW |
7 |
64,972,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Tjp1
|
UTSW |
7 |
64,952,669 (GRCm39) |
missense |
probably benign |
|
R1634:Tjp1
|
UTSW |
7 |
64,952,700 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1767:Tjp1
|
UTSW |
7 |
64,962,301 (GRCm39) |
critical splice donor site |
probably null |
|
R1771:Tjp1
|
UTSW |
7 |
64,962,753 (GRCm39) |
missense |
probably benign |
0.45 |
R1794:Tjp1
|
UTSW |
7 |
64,972,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Tjp1
|
UTSW |
7 |
64,969,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Tjp1
|
UTSW |
7 |
64,973,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R1981:Tjp1
|
UTSW |
7 |
64,962,603 (GRCm39) |
missense |
probably damaging |
0.99 |
R2086:Tjp1
|
UTSW |
7 |
64,962,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R2310:Tjp1
|
UTSW |
7 |
64,979,490 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2942:Tjp1
|
UTSW |
7 |
64,967,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R3974:Tjp1
|
UTSW |
7 |
64,947,387 (GRCm39) |
nonsense |
probably null |
|
R4295:Tjp1
|
UTSW |
7 |
64,972,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4296:Tjp1
|
UTSW |
7 |
64,968,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R4567:Tjp1
|
UTSW |
7 |
64,956,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R4574:Tjp1
|
UTSW |
7 |
64,972,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4910:Tjp1
|
UTSW |
7 |
64,993,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R4958:Tjp1
|
UTSW |
7 |
64,985,850 (GRCm39) |
nonsense |
probably null |
|
R5267:Tjp1
|
UTSW |
7 |
64,972,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R5371:Tjp1
|
UTSW |
7 |
64,963,059 (GRCm39) |
nonsense |
probably null |
|
R5422:Tjp1
|
UTSW |
7 |
64,952,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R5514:Tjp1
|
UTSW |
7 |
65,004,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Tjp1
|
UTSW |
7 |
64,962,191 (GRCm39) |
splice site |
probably null |
|
R5693:Tjp1
|
UTSW |
7 |
64,992,411 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5933:Tjp1
|
UTSW |
7 |
64,952,600 (GRCm39) |
missense |
probably benign |
0.29 |
R6043:Tjp1
|
UTSW |
7 |
64,973,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R6416:Tjp1
|
UTSW |
7 |
64,962,953 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6491:Tjp1
|
UTSW |
7 |
64,986,865 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6525:Tjp1
|
UTSW |
7 |
64,993,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R6658:Tjp1
|
UTSW |
7 |
64,950,825 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6917:Tjp1
|
UTSW |
7 |
64,949,436 (GRCm39) |
missense |
probably damaging |
0.99 |
R6960:Tjp1
|
UTSW |
7 |
64,952,763 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7235:Tjp1
|
UTSW |
7 |
64,968,321 (GRCm39) |
missense |
probably benign |
0.16 |
R7274:Tjp1
|
UTSW |
7 |
65,177,400 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7471:Tjp1
|
UTSW |
7 |
64,964,438 (GRCm39) |
missense |
probably damaging |
0.99 |
R7475:Tjp1
|
UTSW |
7 |
64,972,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R7479:Tjp1
|
UTSW |
7 |
64,950,928 (GRCm39) |
missense |
probably damaging |
0.98 |
R8035:Tjp1
|
UTSW |
7 |
64,992,450 (GRCm39) |
missense |
probably benign |
0.34 |
R8195:Tjp1
|
UTSW |
7 |
64,993,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R8276:Tjp1
|
UTSW |
7 |
64,993,544 (GRCm39) |
intron |
probably benign |
|
R8817:Tjp1
|
UTSW |
7 |
64,952,810 (GRCm39) |
missense |
probably benign |
0.41 |
R8869:Tjp1
|
UTSW |
7 |
64,986,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R9043:Tjp1
|
UTSW |
7 |
64,962,679 (GRCm39) |
missense |
probably benign |
0.03 |
R9079:Tjp1
|
UTSW |
7 |
64,950,966 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9081:Tjp1
|
UTSW |
7 |
64,964,010 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9095:Tjp1
|
UTSW |
7 |
64,952,745 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9145:Tjp1
|
UTSW |
7 |
64,952,564 (GRCm39) |
missense |
probably benign |
0.00 |
R9215:Tjp1
|
UTSW |
7 |
64,962,595 (GRCm39) |
missense |
probably benign |
|
R9581:Tjp1
|
UTSW |
7 |
64,949,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Tjp1
|
UTSW |
7 |
64,962,644 (GRCm39) |
missense |
probably benign |
|
X0022:Tjp1
|
UTSW |
7 |
64,952,589 (GRCm39) |
missense |
possibly damaging |
0.75 |
X0027:Tjp1
|
UTSW |
7 |
64,964,507 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Tjp1
|
UTSW |
7 |
64,993,480 (GRCm39) |
missense |
probably damaging |
1.00 |
|