Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts4 |
A |
G |
1: 171,083,905 (GRCm39) |
T492A |
probably damaging |
Het |
Afg3l2 |
A |
T |
18: 67,548,643 (GRCm39) |
L529* |
probably null |
Het |
Ak9 |
A |
G |
10: 41,213,572 (GRCm39) |
E259G |
probably damaging |
Het |
Apol11b |
T |
A |
15: 77,519,772 (GRCm39) |
I103F |
probably damaging |
Het |
Atp7b |
T |
C |
8: 22,501,667 (GRCm39) |
M864V |
possibly damaging |
Het |
Atp8a2 |
A |
G |
14: 60,324,073 (GRCm39) |
L60P |
probably damaging |
Het |
Begain |
T |
C |
12: 109,000,033 (GRCm39) |
Y451C |
probably damaging |
Het |
Bmpr1b |
A |
T |
3: 141,586,124 (GRCm39) |
I46N |
probably benign |
Het |
Bms1 |
T |
A |
6: 118,360,742 (GRCm39) |
K1242M |
probably damaging |
Het |
Calcoco1 |
A |
G |
15: 102,622,358 (GRCm39) |
L254P |
probably damaging |
Het |
Ccdc112 |
A |
T |
18: 46,424,173 (GRCm39) |
N188K |
possibly damaging |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cdkal1 |
A |
G |
13: 29,901,774 (GRCm39) |
V132A |
possibly damaging |
Het |
Cdo1 |
A |
G |
18: 46,853,369 (GRCm39) |
C130R |
probably damaging |
Het |
Cep295nl |
G |
T |
11: 118,223,474 (GRCm39) |
R457S |
probably damaging |
Het |
Cntn1 |
A |
T |
15: 92,148,829 (GRCm39) |
I359F |
probably benign |
Het |
Csnk1g1 |
T |
C |
9: 65,939,606 (GRCm39) |
V435A |
probably damaging |
Het |
Csnka2ip |
A |
G |
16: 64,298,855 (GRCm39) |
V59A |
probably benign |
Het |
Ddr2 |
A |
T |
1: 169,823,170 (GRCm39) |
Y371* |
probably null |
Het |
Dicer1 |
T |
C |
12: 104,688,410 (GRCm39) |
E389G |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,366,400 (GRCm39) |
I1901V |
probably damaging |
Het |
Fanci |
T |
A |
7: 79,088,056 (GRCm39) |
I903N |
probably damaging |
Het |
Fastk |
T |
C |
5: 24,646,529 (GRCm39) |
Q471R |
probably damaging |
Het |
Flvcr1 |
A |
T |
1: 190,757,577 (GRCm39) |
N238K |
probably damaging |
Het |
Gsdmc3 |
A |
T |
15: 63,740,965 (GRCm39) |
L61H |
probably damaging |
Het |
H2-M10.5 |
T |
A |
17: 37,084,836 (GRCm39) |
C187S |
probably damaging |
Het |
Hmcn2 |
T |
C |
2: 31,283,055 (GRCm39) |
I1977T |
probably damaging |
Het |
Itpr2 |
T |
A |
6: 146,260,914 (GRCm39) |
I905F |
probably benign |
Het |
Jmy |
C |
T |
13: 93,590,585 (GRCm39) |
G506D |
probably damaging |
Het |
Klf4 |
G |
T |
4: 55,530,977 (GRCm39) |
R45S |
probably benign |
Het |
Klhdc7b |
A |
G |
15: 89,271,800 (GRCm39) |
E894G |
probably damaging |
Het |
Klra7 |
T |
C |
6: 130,201,070 (GRCm39) |
I229V |
probably benign |
Het |
Krt35 |
T |
C |
11: 99,986,565 (GRCm39) |
T150A |
probably benign |
Het |
Krtap20-1 |
T |
C |
16: 88,812,337 (GRCm39) |
|
probably benign |
Het |
Lmbrd1 |
T |
A |
1: 24,724,642 (GRCm39) |
N75K |
possibly damaging |
Het |
Lss |
T |
C |
10: 76,388,798 (GRCm39) |
S700P |
probably damaging |
Het |
Ltbp1 |
A |
T |
17: 75,559,375 (GRCm39) |
Q288L |
probably benign |
Het |
Mical2 |
A |
G |
7: 112,012,109 (GRCm39) |
E653G |
probably damaging |
Het |
Mphosph10 |
G |
T |
7: 64,041,918 (GRCm39) |
Q9K |
probably benign |
Het |
Muc15 |
T |
A |
2: 110,561,603 (GRCm39) |
L13Q |
probably damaging |
Het |
Ncf4 |
A |
G |
15: 78,134,602 (GRCm39) |
D18G |
probably benign |
Het |
Nipsnap1 |
A |
G |
11: 4,839,101 (GRCm39) |
Y127C |
probably damaging |
Het |
Nrbp1 |
T |
A |
5: 31,403,157 (GRCm39) |
I210N |
probably damaging |
Het |
Nudt12 |
G |
A |
17: 59,317,131 (GRCm39) |
P172L |
probably damaging |
Het |
Or8g18 |
T |
C |
9: 39,149,286 (GRCm39) |
I145V |
probably benign |
Het |
Otud4 |
T |
A |
8: 80,366,618 (GRCm39) |
Y28* |
probably null |
Het |
Pdcd2l |
G |
A |
7: 33,885,826 (GRCm39) |
T286I |
probably benign |
Het |
Pgbd1 |
A |
G |
13: 21,607,342 (GRCm39) |
V284A |
probably damaging |
Het |
Phlpp2 |
C |
A |
8: 110,666,855 (GRCm39) |
T1128K |
probably damaging |
Het |
Pik3cb |
A |
G |
9: 98,975,148 (GRCm39) |
V244A |
possibly damaging |
Het |
Pld1 |
A |
G |
3: 28,163,917 (GRCm39) |
I783M |
probably benign |
Het |
Plk5 |
T |
C |
10: 80,199,855 (GRCm39) |
V454A |
probably benign |
Het |
Prkci |
T |
C |
3: 31,092,644 (GRCm39) |
S309P |
probably damaging |
Het |
Prx |
A |
T |
7: 27,216,090 (GRCm39) |
D197V |
probably damaging |
Het |
Ptpn5 |
A |
G |
7: 46,728,589 (GRCm39) |
L537P |
probably benign |
Het |
Rev3l |
T |
A |
10: 39,698,867 (GRCm39) |
N1121K |
probably benign |
Het |
Rock2 |
T |
A |
12: 17,022,727 (GRCm39) |
D1055E |
probably benign |
Het |
Rrp1b |
T |
C |
17: 32,275,785 (GRCm39) |
V444A |
probably benign |
Het |
Rsf1 |
CG |
CGACGGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
GGCGGCGGCGGCGGCGGCGGCGGCGGCGGC |
GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
GCG |
GCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
S1pr2 |
G |
A |
9: 20,879,388 (GRCm39) |
R147* |
probably null |
Het |
Serpinb9b |
A |
T |
13: 33,223,887 (GRCm39) |
I360F |
probably damaging |
Het |
Smc6 |
T |
C |
12: 11,344,602 (GRCm39) |
|
probably null |
Het |
Srsf11 |
C |
T |
3: 157,722,064 (GRCm39) |
|
probably benign |
Het |
Sstr1 |
T |
C |
12: 58,260,264 (GRCm39) |
F296L |
possibly damaging |
Het |
Tecrl |
T |
A |
5: 83,427,081 (GRCm39) |
I356L |
probably benign |
Het |
Tln2 |
A |
G |
9: 67,136,705 (GRCm39) |
I2348T |
probably damaging |
Het |
Tmed11 |
T |
A |
5: 108,925,291 (GRCm39) |
I174L |
probably benign |
Het |
Tmem132a |
G |
A |
19: 10,838,931 (GRCm39) |
Q504* |
probably null |
Het |
Unc5c |
A |
T |
3: 141,463,518 (GRCm39) |
D213V |
probably damaging |
Het |
Utp25 |
A |
C |
1: 192,800,591 (GRCm39) |
S410A |
probably benign |
Het |
Vgll4 |
T |
C |
6: 114,841,020 (GRCm39) |
D92G |
probably benign |
Het |
Vps37a |
T |
C |
8: 40,965,162 (GRCm39) |
F5L |
probably benign |
Het |
Zdhhc20 |
A |
T |
14: 58,127,600 (GRCm39) |
V13E |
probably benign |
Het |
Zeb1 |
G |
A |
18: 5,767,898 (GRCm39) |
C803Y |
probably damaging |
Het |
Zmym1 |
T |
C |
4: 126,942,814 (GRCm39) |
T427A |
possibly damaging |
Het |
|
Other mutations in Lct |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00777:Lct
|
APN |
1 |
128,215,293 (GRCm39) |
missense |
probably benign |
0.09 |
IGL00970:Lct
|
APN |
1 |
128,231,805 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01022:Lct
|
APN |
1 |
128,228,596 (GRCm39) |
missense |
probably benign |
|
IGL01878:Lct
|
APN |
1 |
128,222,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01892:Lct
|
APN |
1 |
128,235,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02307:Lct
|
APN |
1 |
128,214,327 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02434:Lct
|
APN |
1 |
128,231,527 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02559:Lct
|
APN |
1 |
128,222,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02623:Lct
|
APN |
1 |
128,235,988 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02818:Lct
|
APN |
1 |
128,227,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02949:Lct
|
APN |
1 |
128,240,869 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02951:Lct
|
APN |
1 |
128,227,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03087:Lct
|
APN |
1 |
128,228,112 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03227:Lct
|
APN |
1 |
128,255,426 (GRCm39) |
missense |
probably benign |
0.09 |
ANU18:Lct
|
UTSW |
1 |
128,235,784 (GRCm39) |
nonsense |
probably null |
|
R0071:Lct
|
UTSW |
1 |
128,219,755 (GRCm39) |
nonsense |
probably null |
|
R0071:Lct
|
UTSW |
1 |
128,219,755 (GRCm39) |
nonsense |
probably null |
|
R0135:Lct
|
UTSW |
1 |
128,212,860 (GRCm39) |
missense |
probably damaging |
0.98 |
R0145:Lct
|
UTSW |
1 |
128,255,632 (GRCm39) |
missense |
probably benign |
0.00 |
R0179:Lct
|
UTSW |
1 |
128,255,422 (GRCm39) |
missense |
probably benign |
|
R0331:Lct
|
UTSW |
1 |
128,226,479 (GRCm39) |
splice site |
probably benign |
|
R0366:Lct
|
UTSW |
1 |
128,214,199 (GRCm39) |
missense |
probably benign |
0.03 |
R0399:Lct
|
UTSW |
1 |
128,228,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Lct
|
UTSW |
1 |
128,228,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R0548:Lct
|
UTSW |
1 |
128,212,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Lct
|
UTSW |
1 |
128,235,971 (GRCm39) |
missense |
probably benign |
0.00 |
R0755:Lct
|
UTSW |
1 |
128,221,872 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0839:Lct
|
UTSW |
1 |
128,214,346 (GRCm39) |
missense |
probably benign |
0.00 |
R1128:Lct
|
UTSW |
1 |
128,229,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R1135:Lct
|
UTSW |
1 |
128,221,861 (GRCm39) |
critical splice donor site |
probably null |
|
R1321:Lct
|
UTSW |
1 |
128,227,759 (GRCm39) |
missense |
probably benign |
|
R1448:Lct
|
UTSW |
1 |
128,235,559 (GRCm39) |
missense |
probably damaging |
0.99 |
R1450:Lct
|
UTSW |
1 |
128,235,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Lct
|
UTSW |
1 |
128,221,932 (GRCm39) |
missense |
probably benign |
0.25 |
R1582:Lct
|
UTSW |
1 |
128,228,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1668:Lct
|
UTSW |
1 |
128,215,459 (GRCm39) |
splice site |
probably null |
|
R1757:Lct
|
UTSW |
1 |
128,228,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R1775:Lct
|
UTSW |
1 |
128,228,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Lct
|
UTSW |
1 |
128,255,679 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1932:Lct
|
UTSW |
1 |
128,221,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R2325:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R2381:Lct
|
UTSW |
1 |
128,231,858 (GRCm39) |
nonsense |
probably null |
|
R3001:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3002:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3003:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Lct
|
UTSW |
1 |
128,229,109 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3082:Lct
|
UTSW |
1 |
128,215,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3684:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3726:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3887:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3888:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4019:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Lct
|
UTSW |
1 |
128,212,918 (GRCm39) |
missense |
probably benign |
0.00 |
R4226:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4409:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4514:Lct
|
UTSW |
1 |
128,228,251 (GRCm39) |
missense |
probably benign |
|
R4570:Lct
|
UTSW |
1 |
128,227,641 (GRCm39) |
missense |
probably benign |
0.01 |
R4776:Lct
|
UTSW |
1 |
128,228,124 (GRCm39) |
missense |
probably damaging |
0.99 |
R5001:Lct
|
UTSW |
1 |
128,235,978 (GRCm39) |
missense |
probably damaging |
0.96 |
R5021:Lct
|
UTSW |
1 |
128,228,302 (GRCm39) |
missense |
probably benign |
0.38 |
R5318:Lct
|
UTSW |
1 |
128,232,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Lct
|
UTSW |
1 |
128,226,266 (GRCm39) |
missense |
probably benign |
0.06 |
R5385:Lct
|
UTSW |
1 |
128,239,354 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5499:Lct
|
UTSW |
1 |
128,214,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R5508:Lct
|
UTSW |
1 |
128,221,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Lct
|
UTSW |
1 |
128,222,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R5724:Lct
|
UTSW |
1 |
128,228,073 (GRCm39) |
missense |
probably benign |
|
R6026:Lct
|
UTSW |
1 |
128,227,755 (GRCm39) |
missense |
probably benign |
|
R6044:Lct
|
UTSW |
1 |
128,235,717 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6175:Lct
|
UTSW |
1 |
128,255,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Lct
|
UTSW |
1 |
128,231,974 (GRCm39) |
missense |
probably benign |
0.01 |
R6412:Lct
|
UTSW |
1 |
128,255,455 (GRCm39) |
missense |
probably benign |
0.00 |
R6480:Lct
|
UTSW |
1 |
128,222,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R6526:Lct
|
UTSW |
1 |
128,228,215 (GRCm39) |
missense |
probably benign |
0.05 |
R6620:Lct
|
UTSW |
1 |
128,222,809 (GRCm39) |
critical splice donor site |
probably null |
|
R7214:Lct
|
UTSW |
1 |
128,228,197 (GRCm39) |
missense |
probably benign |
0.00 |
R7308:Lct
|
UTSW |
1 |
128,246,824 (GRCm39) |
missense |
probably benign |
0.00 |
R7577:Lct
|
UTSW |
1 |
128,228,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R7626:Lct
|
UTSW |
1 |
128,212,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R7737:Lct
|
UTSW |
1 |
128,226,430 (GRCm39) |
missense |
probably benign |
0.12 |
R7901:Lct
|
UTSW |
1 |
128,216,722 (GRCm39) |
missense |
probably benign |
0.44 |
R8033:Lct
|
UTSW |
1 |
128,212,996 (GRCm39) |
missense |
probably benign |
0.03 |
R8373:Lct
|
UTSW |
1 |
128,231,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R8504:Lct
|
UTSW |
1 |
128,215,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R8751:Lct
|
UTSW |
1 |
128,221,534 (GRCm39) |
missense |
probably benign |
0.18 |
R8781:Lct
|
UTSW |
1 |
128,215,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8797:Lct
|
UTSW |
1 |
128,231,684 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8926:Lct
|
UTSW |
1 |
128,228,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R8949:Lct
|
UTSW |
1 |
128,221,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R8992:Lct
|
UTSW |
1 |
128,228,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Lct
|
UTSW |
1 |
128,227,894 (GRCm39) |
missense |
probably benign |
0.03 |
R9260:Lct
|
UTSW |
1 |
128,227,704 (GRCm39) |
nonsense |
probably null |
|
R9416:Lct
|
UTSW |
1 |
128,228,329 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9531:Lct
|
UTSW |
1 |
128,235,598 (GRCm39) |
missense |
probably benign |
0.00 |
X0052:Lct
|
UTSW |
1 |
128,235,367 (GRCm39) |
missense |
probably damaging |
1.00 |
YA93:Lct
|
UTSW |
1 |
128,229,057 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Lct
|
UTSW |
1 |
128,215,348 (GRCm39) |
nonsense |
probably null |
|
|