Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alox8 |
G |
T |
11: 69,087,864 (GRCm39) |
Q147K |
probably benign |
Het |
Ankib1 |
T |
A |
5: 3,784,152 (GRCm39) |
M275L |
possibly damaging |
Het |
Asb2 |
G |
A |
12: 103,287,922 (GRCm39) |
P546S |
possibly damaging |
Het |
B9d1 |
T |
C |
11: 61,398,449 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,557,257 (GRCm39) |
D1957G |
possibly damaging |
Het |
Cryzl2 |
T |
C |
1: 157,299,970 (GRCm39) |
V44A |
possibly damaging |
Het |
Fbxw19 |
A |
C |
9: 109,312,347 (GRCm39) |
|
probably benign |
Het |
Gabrb3 |
T |
C |
7: 57,466,163 (GRCm39) |
F326L |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm11168 |
T |
C |
9: 3,005,204 (GRCm39) |
C16R |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Gm7808 |
T |
A |
9: 19,839,542 (GRCm39) |
|
probably benign |
Het |
Gpam |
T |
C |
19: 55,071,806 (GRCm39) |
I312V |
probably benign |
Het |
H2-M10.5 |
A |
G |
17: 37,084,708 (GRCm39) |
Y144C |
probably damaging |
Het |
Hivep3 |
T |
C |
4: 119,952,424 (GRCm39) |
S247P |
possibly damaging |
Het |
Hs3st4 |
T |
G |
7: 123,996,536 (GRCm39) |
C401G |
probably damaging |
Het |
Klhl2 |
A |
G |
8: 65,212,858 (GRCm39) |
V227A |
probably damaging |
Het |
Lipm |
T |
A |
19: 34,093,911 (GRCm39) |
L276Q |
possibly damaging |
Het |
Lmf2 |
T |
A |
15: 89,236,621 (GRCm39) |
H515L |
probably damaging |
Het |
Mccc1 |
G |
A |
3: 36,030,041 (GRCm39) |
S423L |
probably damaging |
Het |
Mettl21e |
G |
A |
1: 44,250,193 (GRCm39) |
S71L |
probably null |
Het |
Muc16 |
T |
A |
9: 18,406,839 (GRCm39) |
H251L |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,059,852 (GRCm39) |
|
probably benign |
Het |
Ntf5 |
T |
C |
7: 45,065,450 (GRCm39) |
I194T |
probably damaging |
Het |
Or10ag58 |
T |
C |
2: 87,265,314 (GRCm39) |
I161T |
possibly damaging |
Het |
Or1o4 |
A |
G |
17: 37,590,891 (GRCm39) |
V140A |
possibly damaging |
Het |
Or2w6 |
T |
C |
13: 21,842,953 (GRCm39) |
D180G |
possibly damaging |
Het |
Or4x11 |
T |
C |
2: 89,867,478 (GRCm39) |
S72P |
probably damaging |
Het |
Or9m1 |
A |
T |
2: 87,733,675 (GRCm39) |
L115* |
probably null |
Het |
Pigv |
T |
C |
4: 133,392,428 (GRCm39) |
I247M |
probably benign |
Het |
Pik3r5 |
A |
G |
11: 68,383,356 (GRCm39) |
N392D |
probably benign |
Het |
Postn |
A |
G |
3: 54,290,901 (GRCm39) |
|
probably null |
Het |
Prl2c5 |
G |
A |
13: 13,360,402 (GRCm39) |
S23N |
probably benign |
Het |
Prpf40b |
T |
C |
15: 99,204,413 (GRCm39) |
C220R |
possibly damaging |
Het |
Pzp |
A |
G |
6: 128,472,261 (GRCm39) |
S843P |
probably damaging |
Het |
Rpl23 |
C |
A |
11: 97,669,177 (GRCm39) |
R85L |
probably benign |
Het |
Shcbp1 |
A |
G |
8: 4,799,721 (GRCm39) |
S252P |
probably damaging |
Het |
Slc26a7 |
C |
T |
4: 14,519,388 (GRCm39) |
|
probably null |
Het |
Sptbn4 |
T |
C |
7: 27,063,571 (GRCm39) |
E2285G |
probably damaging |
Het |
Telo2 |
G |
T |
17: 25,320,332 (GRCm39) |
T784K |
probably benign |
Het |
Tnfrsf19 |
C |
T |
14: 61,234,093 (GRCm39) |
V136M |
probably damaging |
Het |
Trpm5 |
T |
A |
7: 142,628,234 (GRCm39) |
I22F |
probably damaging |
Het |
Trpv6 |
G |
T |
6: 41,603,801 (GRCm39) |
|
probably benign |
Het |
Vmn1r173 |
T |
G |
7: 23,401,877 (GRCm39) |
H37Q |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Xpo6 |
T |
A |
7: 125,773,365 (GRCm39) |
H20L |
probably benign |
Het |
Zfp462 |
T |
C |
4: 55,010,613 (GRCm39) |
Y860H |
probably 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 |
|
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 |
R1815:Lct
|
UTSW |
1 |
128,227,896 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|