Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,266,233 (GRCm39) |
I3071V |
probably benign |
Het |
Abcb8 |
C |
T |
5: 24,605,137 (GRCm39) |
R108C |
possibly damaging |
Het |
Abr |
T |
C |
11: 76,354,403 (GRCm39) |
N236S |
probably damaging |
Het |
Adcy6 |
T |
C |
15: 98,501,870 (GRCm39) |
Y248C |
probably damaging |
Het |
Armc8 |
A |
G |
9: 99,378,202 (GRCm39) |
|
probably null |
Het |
Chd6 |
A |
T |
2: 160,807,185 (GRCm39) |
S2010T |
probably benign |
Het |
Dcc |
G |
A |
18: 71,708,153 (GRCm39) |
T521I |
probably damaging |
Het |
Dmrtb1 |
G |
A |
4: 107,541,366 (GRCm39) |
|
probably benign |
Het |
Evc |
A |
G |
5: 37,477,584 (GRCm39) |
V365A |
possibly damaging |
Het |
Gata4 |
A |
G |
14: 63,478,594 (GRCm39) |
Y2H |
probably damaging |
Het |
Gpc1 |
A |
G |
1: 92,785,621 (GRCm39) |
N437S |
probably damaging |
Het |
Lifr |
T |
C |
15: 7,205,041 (GRCm39) |
V426A |
probably damaging |
Het |
Lpin3 |
A |
G |
2: 160,737,320 (GRCm39) |
I122M |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,597,181 (GRCm39) |
N3174D |
possibly damaging |
Het |
Myo6 |
G |
A |
9: 80,173,462 (GRCm39) |
R534H |
probably damaging |
Het |
Nectin2 |
T |
C |
7: 19,458,794 (GRCm39) |
D339G |
probably benign |
Het |
Oprd1 |
G |
A |
4: 131,871,721 (GRCm39) |
|
probably benign |
Het |
Or6c66 |
T |
C |
10: 129,461,396 (GRCm39) |
D178G |
probably damaging |
Het |
Orc1 |
G |
A |
4: 108,470,276 (GRCm39) |
V751I |
probably benign |
Het |
Pacs2 |
T |
C |
12: 113,013,526 (GRCm39) |
S175P |
probably damaging |
Het |
Pik3r5 |
C |
T |
11: 68,385,077 (GRCm39) |
R661C |
probably damaging |
Het |
Plscr5 |
A |
T |
9: 92,087,564 (GRCm39) |
K178* |
probably null |
Het |
Prkar1b |
A |
G |
5: 139,113,400 (GRCm39) |
V40A |
possibly damaging |
Het |
Ptprf |
G |
A |
4: 118,093,374 (GRCm39) |
R90* |
probably null |
Het |
Rasef |
T |
C |
4: 73,688,076 (GRCm39) |
M26V |
probably damaging |
Het |
Rfx1 |
C |
A |
8: 84,800,533 (GRCm39) |
Q45K |
unknown |
Het |
Rnf183 |
A |
G |
4: 62,346,753 (GRCm39) |
V15A |
possibly damaging |
Het |
Slc10a2 |
C |
A |
8: 5,155,128 (GRCm39) |
C19F |
probably damaging |
Het |
Slc14a2 |
T |
A |
18: 78,190,229 (GRCm39) |
I907F |
probably benign |
Het |
Snx16 |
T |
C |
3: 10,485,318 (GRCm39) |
I293V |
probably benign |
Het |
Srcap |
C |
A |
7: 127,118,988 (GRCm39) |
A97E |
probably damaging |
Het |
Thyn1 |
G |
T |
9: 26,916,511 (GRCm39) |
|
probably null |
Het |
Tiparp |
T |
C |
3: 65,460,913 (GRCm39) |
I634T |
possibly damaging |
Het |
Tmem168 |
T |
C |
6: 13,602,320 (GRCm39) |
M349V |
probably benign |
Het |
Tyro3 |
T |
G |
2: 119,641,349 (GRCm39) |
F519L |
probably damaging |
Het |
Vmn1r167 |
A |
T |
7: 23,204,646 (GRCm39) |
Y123* |
probably null |
Het |
Vmn1r183 |
C |
T |
7: 23,754,227 (GRCm39) |
T10I |
possibly damaging |
Het |
Zfp654 |
T |
C |
16: 64,606,289 (GRCm39) |
T97A |
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 |
|
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 |
|
R9738:Tjp1
|
UTSW |
7 |
64,986,380 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|