Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm3 |
T |
A |
3: 59,776,435 (GRCm39) |
|
probably null |
Het |
Adam3 |
T |
A |
8: 25,184,321 (GRCm39) |
I560L |
probably benign |
Het |
Agxt |
T |
C |
1: 93,063,436 (GRCm39) |
F113L |
probably benign |
Het |
Aknad1 |
T |
A |
3: 108,688,568 (GRCm39) |
|
probably null |
Het |
Alpk2 |
T |
A |
18: 65,399,357 (GRCm39) |
K2074* |
probably null |
Het |
Apob |
A |
G |
12: 8,057,848 (GRCm39) |
Y2077C |
probably damaging |
Het |
Arhgap17 |
A |
T |
7: 122,907,600 (GRCm39) |
L254Q |
probably damaging |
Het |
Arhgap26 |
T |
A |
18: 39,126,690 (GRCm39) |
|
probably benign |
Het |
Arhgef5 |
A |
G |
6: 43,249,762 (GRCm39) |
D171G |
probably benign |
Het |
Arid1b |
T |
A |
17: 5,392,478 (GRCm39) |
S2003T |
probably damaging |
Het |
Armc5 |
T |
G |
7: 127,839,900 (GRCm39) |
L406R |
possibly damaging |
Het |
Arsb |
T |
C |
13: 93,908,485 (GRCm39) |
V67A |
probably benign |
Het |
Aspm |
A |
G |
1: 139,419,281 (GRCm39) |
Y2982C |
probably damaging |
Het |
Bltp1 |
C |
A |
3: 37,052,348 (GRCm39) |
T3016K |
probably damaging |
Het |
Btbd7 |
A |
G |
12: 102,774,307 (GRCm39) |
L487P |
probably damaging |
Het |
Card11 |
C |
G |
5: 140,860,169 (GRCm39) |
D1063H |
probably damaging |
Het |
Ccdc186 |
G |
A |
19: 56,787,123 (GRCm39) |
T615M |
probably damaging |
Het |
Cd101 |
T |
A |
3: 100,901,205 (GRCm39) |
T960S |
probably benign |
Het |
Cdca7l |
C |
A |
12: 117,837,520 (GRCm39) |
S191* |
probably null |
Het |
Cemip |
A |
T |
7: 83,646,619 (GRCm39) |
I143N |
probably damaging |
Het |
Cep170 |
C |
T |
1: 176,609,829 (GRCm39) |
E161K |
possibly damaging |
Het |
Cfhr4 |
T |
G |
1: 139,702,301 (GRCm39) |
D61A |
probably damaging |
Het |
Chrm2 |
A |
T |
6: 36,501,168 (GRCm39) |
T342S |
probably benign |
Het |
Cib2 |
A |
G |
9: 54,457,163 (GRCm39) |
F34L |
probably benign |
Het |
Cnot1 |
A |
T |
8: 96,459,859 (GRCm39) |
I1836N |
probably benign |
Het |
Col4a3 |
C |
A |
1: 82,650,400 (GRCm39) |
P552Q |
unknown |
Het |
Cp |
T |
A |
3: 20,043,388 (GRCm39) |
|
probably benign |
Het |
Cul3 |
C |
T |
1: 80,267,806 (GRCm39) |
V112I |
probably benign |
Het |
Dcdc5 |
A |
G |
2: 106,195,895 (GRCm39) |
|
noncoding transcript |
Het |
Disp1 |
A |
T |
1: 182,917,027 (GRCm39) |
V133E |
probably damaging |
Het |
Dlg4 |
A |
G |
11: 69,921,751 (GRCm39) |
D30G |
probably damaging |
Het |
Dop1a |
C |
T |
9: 86,374,114 (GRCm39) |
T191I |
probably damaging |
Het |
Enam |
T |
G |
5: 88,650,173 (GRCm39) |
S561A |
probably benign |
Het |
Fbxw8 |
G |
T |
5: 118,263,092 (GRCm39) |
|
probably null |
Het |
Filip1 |
A |
G |
9: 79,725,214 (GRCm39) |
V1135A |
probably benign |
Het |
Galnt6 |
T |
C |
15: 100,614,059 (GRCm39) |
T81A |
probably benign |
Het |
Ghdc |
T |
C |
11: 100,657,814 (GRCm39) |
K472E |
probably benign |
Het |
Gm10568 |
T |
G |
1: 3,751,164 (GRCm39) |
|
noncoding transcript |
Het |
Gm4953 |
T |
A |
1: 158,995,929 (GRCm39) |
|
noncoding transcript |
Het |
Gm6871 |
T |
A |
7: 41,223,016 (GRCm39) |
H24L |
probably benign |
Het |
Gpr155 |
G |
A |
2: 73,197,882 (GRCm39) |
Q413* |
probably null |
Het |
Grhl2 |
A |
G |
15: 37,291,920 (GRCm39) |
|
probably null |
Het |
Ighv1-31 |
G |
C |
12: 114,793,128 (GRCm39) |
S36* |
probably null |
Het |
Ighv8-5 |
A |
G |
12: 115,031,462 (GRCm39) |
S26P |
probably damaging |
Het |
Igkv17-134 |
A |
C |
6: 67,697,910 (GRCm39) |
|
probably benign |
Het |
Igkv5-48 |
A |
C |
6: 69,703,833 (GRCm39) |
L24R |
probably damaging |
Het |
Isg20l2 |
T |
A |
3: 87,846,570 (GRCm39) |
V340E |
probably damaging |
Het |
Lrrtm1 |
A |
G |
6: 77,221,884 (GRCm39) |
Y447C |
probably damaging |
Het |
Ltbp1 |
T |
C |
17: 75,634,287 (GRCm39) |
S855P |
probably damaging |
Het |
Mgat4e |
A |
T |
1: 134,469,602 (GRCm39) |
N147K |
probably damaging |
Het |
Mlc1 |
A |
G |
15: 88,842,415 (GRCm39) |
L315P |
possibly damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,076,292 (GRCm39) |
V322A |
probably benign |
Het |
Mroh7 |
T |
C |
4: 106,567,152 (GRCm39) |
|
probably null |
Het |
Mybpc1 |
T |
A |
10: 88,391,586 (GRCm39) |
K304* |
probably null |
Het |
Nlrp14 |
A |
C |
7: 106,785,790 (GRCm39) |
D622A |
possibly damaging |
Het |
Nlrp1b |
T |
A |
11: 71,108,103 (GRCm39) |
H466L |
probably benign |
Het |
Nlrp4d |
T |
A |
7: 10,112,336 (GRCm39) |
|
noncoding transcript |
Het |
Nrxn3 |
A |
G |
12: 89,227,130 (GRCm39) |
E628G |
possibly damaging |
Het |
Nup133 |
T |
C |
8: 124,653,870 (GRCm39) |
R530G |
possibly damaging |
Het |
Nup98 |
A |
G |
7: 101,845,007 (GRCm39) |
S21P |
unknown |
Het |
Or2h2b-ps1 |
T |
C |
17: 37,480,934 (GRCm39) |
I202V |
probably benign |
Het |
Or2l13b |
T |
C |
16: 19,348,768 (GRCm39) |
T301A |
probably benign |
Het |
Or4f14b |
A |
T |
2: 111,775,423 (GRCm39) |
I126K |
possibly damaging |
Het |
Or52e8 |
G |
A |
7: 104,624,686 (GRCm39) |
P169S |
possibly damaging |
Het |
Or5k1 |
T |
A |
16: 58,617,805 (GRCm39) |
T135S |
probably benign |
Het |
Or6c66 |
T |
C |
10: 129,461,676 (GRCm39) |
T85A |
probably damaging |
Het |
Or8c11 |
T |
A |
9: 38,290,038 (GRCm39) |
V287E |
probably null |
Het |
Otog |
A |
T |
7: 45,913,486 (GRCm39) |
Y773F |
probably damaging |
Het |
Otog |
A |
T |
7: 45,947,958 (GRCm39) |
I2320F |
probably damaging |
Het |
Otogl |
T |
C |
10: 107,715,378 (GRCm39) |
S433G |
probably benign |
Het |
Pcdhb17 |
A |
T |
18: 37,618,212 (GRCm39) |
M1L |
possibly damaging |
Het |
Pde7b |
T |
A |
10: 20,600,480 (GRCm39) |
|
probably benign |
Het |
Pgm1 |
T |
C |
4: 99,820,724 (GRCm39) |
V207A |
probably damaging |
Het |
Pkd1 |
T |
A |
17: 24,791,661 (GRCm39) |
V1116E |
probably damaging |
Het |
Pkd1l1 |
T |
A |
11: 8,879,360 (GRCm39) |
Y497F |
possibly damaging |
Het |
Pomgnt2 |
T |
C |
9: 121,812,013 (GRCm39) |
N256S |
probably benign |
Het |
Pot1a |
A |
T |
6: 25,746,020 (GRCm39) |
|
probably benign |
Het |
Prdm9 |
T |
C |
17: 15,764,585 (GRCm39) |
T732A |
probably benign |
Het |
Prg4 |
T |
A |
1: 150,331,574 (GRCm39) |
|
probably benign |
Het |
Ptpro |
T |
C |
6: 137,345,336 (GRCm39) |
V114A |
probably damaging |
Het |
Pyurf |
A |
G |
6: 57,668,933 (GRCm39) |
S20P |
unknown |
Het |
Rasgrf1 |
A |
G |
9: 89,858,805 (GRCm39) |
T488A |
probably benign |
Het |
Rassf8 |
A |
T |
6: 145,761,006 (GRCm39) |
K111* |
probably null |
Het |
Reps1 |
A |
T |
10: 17,983,436 (GRCm39) |
E426D |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,730,666 (GRCm39) |
K982R |
probably damaging |
Het |
Rps23 |
T |
C |
13: 91,071,871 (GRCm39) |
|
probably null |
Het |
Scamp4 |
T |
A |
10: 80,445,505 (GRCm39) |
V56E |
probably damaging |
Het |
Serpina1c |
C |
T |
12: 103,861,291 (GRCm39) |
V408I |
probably benign |
Het |
Sigirr |
A |
G |
7: 140,673,701 (GRCm39) |
W49R |
probably damaging |
Het |
Slc17a6 |
A |
T |
7: 51,308,489 (GRCm39) |
H271L |
possibly damaging |
Het |
Slc7a5 |
G |
T |
8: 122,611,861 (GRCm39) |
T389K |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,191,999 (GRCm39) |
H945L |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,523,549 (GRCm39) |
S662P |
probably damaging |
Het |
Snta1 |
C |
A |
2: 154,218,938 (GRCm39) |
E466* |
probably null |
Het |
Sowaha |
A |
G |
11: 53,369,272 (GRCm39) |
L488P |
probably damaging |
Het |
Spata17 |
C |
A |
1: 186,926,208 (GRCm39) |
V41F |
probably damaging |
Het |
Spta1 |
T |
A |
1: 174,045,429 (GRCm39) |
|
probably null |
Het |
Srrm2 |
T |
A |
17: 24,034,362 (GRCm39) |
|
probably benign |
Het |
Stard13 |
T |
C |
5: 150,985,992 (GRCm39) |
N388S |
probably benign |
Het |
Stmn3 |
T |
C |
2: 180,950,630 (GRCm39) |
K59E |
probably damaging |
Het |
Sval1 |
A |
G |
6: 41,932,378 (GRCm39) |
N76S |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,096,276 (GRCm39) |
H1448R |
possibly damaging |
Het |
Sycp2 |
A |
T |
2: 178,000,017 (GRCm39) |
D986E |
probably benign |
Het |
Sytl5 |
C |
T |
X: 9,781,841 (GRCm39) |
P181L |
possibly damaging |
Het |
Tbkbp1 |
G |
A |
11: 97,029,956 (GRCm39) |
S400L |
probably benign |
Het |
Tesc |
G |
T |
5: 118,194,531 (GRCm39) |
|
probably benign |
Het |
Tlr11 |
C |
A |
14: 50,600,346 (GRCm39) |
F777L |
probably benign |
Het |
Tmem156 |
A |
G |
5: 65,248,805 (GRCm39) |
|
probably benign |
Het |
Top3a |
A |
G |
11: 60,643,204 (GRCm39) |
|
probably benign |
Het |
Tpcn1 |
A |
G |
5: 120,694,584 (GRCm39) |
W162R |
probably damaging |
Het |
Tpd52l2 |
A |
T |
2: 181,157,005 (GRCm39) |
|
probably benign |
Het |
Trim80 |
G |
A |
11: 115,337,281 (GRCm39) |
G381D |
probably damaging |
Het |
Ugt1a10 |
C |
T |
1: 88,142,845 (GRCm39) |
P113L |
probably damaging |
Het |
Vmn2r117 |
TC |
T |
17: 23,698,487 (GRCm39) |
|
probably null |
Het |
Vmn2r56 |
T |
A |
7: 12,449,462 (GRCm39) |
I259F |
possibly damaging |
Het |
Vmn2r59 |
T |
C |
7: 41,693,077 (GRCm39) |
T508A |
probably benign |
Het |
Wdr73 |
A |
G |
7: 80,541,456 (GRCm39) |
V362A |
probably damaging |
Het |
Zdhhc21 |
G |
T |
4: 82,738,568 (GRCm39) |
T207K |
possibly damaging |
Het |
Zfp120 |
T |
A |
2: 149,959,872 (GRCm39) |
Q150L |
probably damaging |
Het |
Zfp212 |
C |
A |
6: 47,908,433 (GRCm39) |
Q471K |
possibly damaging |
Het |
Zfp804b |
C |
T |
5: 6,820,540 (GRCm39) |
G841D |
possibly damaging |
Het |
Znfx1 |
A |
T |
2: 166,878,724 (GRCm39) |
M1884K |
probably damaging |
Het |
Znfx1 |
G |
T |
2: 166,879,402 (GRCm39) |
A1658D |
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 |
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 |
|
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 |
|