Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
A |
G |
15: 64,659,251 (GRCm39) |
V513A |
probably damaging |
Het |
Adgrl4 |
G |
A |
3: 151,223,410 (GRCm39) |
W621* |
probably null |
Het |
Ap4m1 |
A |
G |
5: 138,170,437 (GRCm39) |
|
probably benign |
Het |
Atp6v1b2 |
T |
C |
8: 69,554,026 (GRCm39) |
Y68H |
probably damaging |
Het |
AY761185 |
T |
A |
8: 21,434,556 (GRCm39) |
|
probably null |
Het |
C3ar1 |
T |
C |
6: 122,828,013 (GRCm39) |
D68G |
probably damaging |
Het |
Cdh10 |
A |
T |
15: 18,985,259 (GRCm39) |
I308F |
probably damaging |
Het |
Coq8a |
A |
T |
1: 180,006,552 (GRCm39) |
S112T |
probably benign |
Het |
Dmgdh |
A |
T |
13: 93,845,706 (GRCm39) |
E453D |
probably benign |
Het |
Fryl |
C |
A |
5: 73,290,655 (GRCm39) |
R83L |
probably benign |
Het |
Gm4861 |
C |
T |
3: 137,256,760 (GRCm39) |
|
probably null |
Het |
Gnai1 |
T |
C |
5: 18,478,472 (GRCm39) |
D231G |
probably damaging |
Het |
Hfe |
C |
G |
13: 23,890,778 (GRCm39) |
E120D |
possibly damaging |
Het |
Hfe |
T |
C |
13: 23,890,779 (GRCm39) |
E120G |
possibly damaging |
Het |
Hgd |
A |
G |
16: 37,435,736 (GRCm39) |
N149S |
possibly damaging |
Het |
Kcnb1 |
T |
C |
2: 166,947,774 (GRCm39) |
D358G |
probably damaging |
Het |
Lama2 |
C |
A |
10: 27,000,564 (GRCm39) |
V1653L |
probably benign |
Het |
Lamc1 |
A |
T |
1: 153,117,721 (GRCm39) |
I947N |
possibly damaging |
Het |
Lamp3 |
A |
G |
16: 19,519,983 (GRCm39) |
F67L |
probably benign |
Het |
Muc4 |
C |
T |
16: 32,575,255 (GRCm39) |
P1280L |
probably benign |
Het |
Muc5ac |
T |
C |
7: 141,372,342 (GRCm39) |
Y2659H |
possibly damaging |
Het |
Nmbr |
T |
C |
10: 14,645,978 (GRCm39) |
S168P |
probably benign |
Het |
Nsl1 |
A |
G |
1: 190,807,324 (GRCm39) |
T168A |
probably benign |
Het |
Or2g7 |
G |
A |
17: 38,378,115 (GRCm39) |
D18N |
probably damaging |
Het |
Or4a27 |
T |
C |
2: 88,559,185 (GRCm39) |
I253V |
probably benign |
Het |
Or5b113 |
T |
C |
19: 13,342,589 (GRCm39) |
V199A |
probably benign |
Het |
Or8s5 |
A |
G |
15: 98,238,831 (GRCm39) |
F13S |
probably benign |
Het |
Pde1c |
A |
C |
6: 56,157,087 (GRCm39) |
V191G |
probably damaging |
Het |
Proc |
T |
A |
18: 32,256,813 (GRCm39) |
I285F |
probably benign |
Het |
R3hdm1 |
GAA |
GAAA |
1: 128,090,548 (GRCm39) |
|
probably null |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Homo |
Spa17 |
A |
T |
9: 37,523,270 (GRCm39) |
S6T |
probably benign |
Het |
Spp1 |
T |
C |
5: 104,588,396 (GRCm39) |
V267A |
possibly damaging |
Het |
Stk17b |
A |
T |
1: 53,800,247 (GRCm39) |
Y244N |
probably damaging |
Het |
Tal1 |
A |
G |
4: 114,925,789 (GRCm39) |
N286S |
probably damaging |
Het |
Tgm7 |
T |
A |
2: 120,931,571 (GRCm39) |
R197S |
probably damaging |
Het |
Tmcc3 |
T |
A |
10: 94,414,286 (GRCm39) |
V27E |
probably benign |
Het |
Topaz1 |
A |
T |
9: 122,578,851 (GRCm39) |
Q587L |
probably benign |
Het |
Trim33 |
C |
T |
3: 103,261,035 (GRCm39) |
A1061V |
probably damaging |
Het |
Ttll1 |
C |
G |
15: 83,384,147 (GRCm39) |
W160S |
probably damaging |
Het |
Utp25 |
A |
T |
1: 192,796,075 (GRCm39) |
F197I |
probably damaging |
Het |
Wnt7a |
A |
G |
6: 91,371,540 (GRCm39) |
Y141H |
probably benign |
Het |
|
Other mutations in Ltbp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00471:Ltbp2
|
APN |
12 |
84,837,838 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00938:Ltbp2
|
APN |
12 |
84,878,573 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01397:Ltbp2
|
APN |
12 |
84,837,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01570:Ltbp2
|
APN |
12 |
84,840,807 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01631:Ltbp2
|
APN |
12 |
84,855,920 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01662:Ltbp2
|
APN |
12 |
84,856,020 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01728:Ltbp2
|
APN |
12 |
84,837,783 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01839:Ltbp2
|
APN |
12 |
84,840,432 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01946:Ltbp2
|
APN |
12 |
84,877,522 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01977:Ltbp2
|
APN |
12 |
84,876,973 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02220:Ltbp2
|
APN |
12 |
84,876,083 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02340:Ltbp2
|
APN |
12 |
84,839,729 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02430:Ltbp2
|
APN |
12 |
84,846,175 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02492:Ltbp2
|
APN |
12 |
84,856,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02517:Ltbp2
|
APN |
12 |
84,832,091 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02794:Ltbp2
|
APN |
12 |
84,838,709 (GRCm39) |
missense |
probably damaging |
1.00 |
deft
|
UTSW |
12 |
84,900,686 (GRCm39) |
missense |
probably damaging |
0.98 |
masterful
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
practiced
|
UTSW |
12 |
84,856,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R0045:Ltbp2
|
UTSW |
12 |
84,860,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R0045:Ltbp2
|
UTSW |
12 |
84,856,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R0091:Ltbp2
|
UTSW |
12 |
84,840,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Ltbp2
|
UTSW |
12 |
84,846,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0166:Ltbp2
|
UTSW |
12 |
84,833,132 (GRCm39) |
missense |
probably benign |
0.28 |
R0265:Ltbp2
|
UTSW |
12 |
84,832,743 (GRCm39) |
splice site |
probably null |
|
R0394:Ltbp2
|
UTSW |
12 |
84,853,198 (GRCm39) |
splice site |
probably benign |
|
R0535:Ltbp2
|
UTSW |
12 |
84,837,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R0535:Ltbp2
|
UTSW |
12 |
84,831,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Ltbp2
|
UTSW |
12 |
84,860,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Ltbp2
|
UTSW |
12 |
84,860,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Ltbp2
|
UTSW |
12 |
84,838,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Ltbp2
|
UTSW |
12 |
84,877,555 (GRCm39) |
nonsense |
probably null |
|
R1880:Ltbp2
|
UTSW |
12 |
84,876,045 (GRCm39) |
missense |
probably benign |
0.45 |
R1894:Ltbp2
|
UTSW |
12 |
84,834,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R1900:Ltbp2
|
UTSW |
12 |
84,877,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Ltbp2
|
UTSW |
12 |
84,876,879 (GRCm39) |
missense |
probably benign |
0.01 |
R1912:Ltbp2
|
UTSW |
12 |
84,832,637 (GRCm39) |
missense |
probably damaging |
0.98 |
R1993:Ltbp2
|
UTSW |
12 |
84,855,220 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1995:Ltbp2
|
UTSW |
12 |
84,855,220 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2069:Ltbp2
|
UTSW |
12 |
84,840,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2126:Ltbp2
|
UTSW |
12 |
84,832,483 (GRCm39) |
splice site |
probably null |
|
R2139:Ltbp2
|
UTSW |
12 |
84,862,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R2341:Ltbp2
|
UTSW |
12 |
84,855,937 (GRCm39) |
missense |
probably benign |
0.08 |
R2511:Ltbp2
|
UTSW |
12 |
84,851,183 (GRCm39) |
splice site |
probably null |
|
R3737:Ltbp2
|
UTSW |
12 |
84,851,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R3738:Ltbp2
|
UTSW |
12 |
84,851,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R3739:Ltbp2
|
UTSW |
12 |
84,851,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R3889:Ltbp2
|
UTSW |
12 |
84,831,681 (GRCm39) |
unclassified |
probably benign |
|
R4034:Ltbp2
|
UTSW |
12 |
84,851,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4542:Ltbp2
|
UTSW |
12 |
84,878,593 (GRCm39) |
nonsense |
probably null |
|
R4621:Ltbp2
|
UTSW |
12 |
84,856,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Ltbp2
|
UTSW |
12 |
84,856,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Ltbp2
|
UTSW |
12 |
84,840,414 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5080:Ltbp2
|
UTSW |
12 |
84,850,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5116:Ltbp2
|
UTSW |
12 |
84,856,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R5351:Ltbp2
|
UTSW |
12 |
84,837,132 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5445:Ltbp2
|
UTSW |
12 |
84,856,428 (GRCm39) |
missense |
probably null |
1.00 |
R5608:Ltbp2
|
UTSW |
12 |
84,834,238 (GRCm39) |
splice site |
probably null |
|
R5784:Ltbp2
|
UTSW |
12 |
84,915,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5838:Ltbp2
|
UTSW |
12 |
84,835,875 (GRCm39) |
missense |
probably benign |
0.16 |
R5859:Ltbp2
|
UTSW |
12 |
84,840,837 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6004:Ltbp2
|
UTSW |
12 |
84,922,923 (GRCm39) |
missense |
probably benign |
0.00 |
R6028:Ltbp2
|
UTSW |
12 |
84,831,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6347:Ltbp2
|
UTSW |
12 |
84,900,686 (GRCm39) |
missense |
probably damaging |
0.98 |
R6615:Ltbp2
|
UTSW |
12 |
84,860,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6637:Ltbp2
|
UTSW |
12 |
84,922,612 (GRCm39) |
missense |
probably benign |
0.00 |
R6755:Ltbp2
|
UTSW |
12 |
84,841,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6759:Ltbp2
|
UTSW |
12 |
84,834,184 (GRCm39) |
missense |
probably damaging |
0.99 |
R6806:Ltbp2
|
UTSW |
12 |
84,856,012 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6968:Ltbp2
|
UTSW |
12 |
84,835,857 (GRCm39) |
critical splice donor site |
probably null |
|
R7084:Ltbp2
|
UTSW |
12 |
84,915,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Ltbp2
|
UTSW |
12 |
84,834,166 (GRCm39) |
nonsense |
probably null |
|
R7374:Ltbp2
|
UTSW |
12 |
84,876,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R7501:Ltbp2
|
UTSW |
12 |
84,877,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R7523:Ltbp2
|
UTSW |
12 |
84,837,808 (GRCm39) |
missense |
probably benign |
0.00 |
R7754:Ltbp2
|
UTSW |
12 |
84,860,012 (GRCm39) |
critical splice donor site |
probably null |
|
R7827:Ltbp2
|
UTSW |
12 |
84,836,655 (GRCm39) |
missense |
probably benign |
0.19 |
R8042:Ltbp2
|
UTSW |
12 |
84,838,673 (GRCm39) |
missense |
probably damaging |
0.99 |
R8110:Ltbp2
|
UTSW |
12 |
84,850,676 (GRCm39) |
nonsense |
probably null |
|
R8411:Ltbp2
|
UTSW |
12 |
84,833,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8688:Ltbp2
|
UTSW |
12 |
84,850,578 (GRCm39) |
missense |
probably benign |
0.20 |
R8711:Ltbp2
|
UTSW |
12 |
84,900,515 (GRCm39) |
missense |
probably benign |
0.00 |
R8712:Ltbp2
|
UTSW |
12 |
84,853,124 (GRCm39) |
missense |
probably benign |
0.08 |
R8893:Ltbp2
|
UTSW |
12 |
84,875,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R8978:Ltbp2
|
UTSW |
12 |
84,834,164 (GRCm39) |
missense |
probably benign |
0.00 |
R9016:Ltbp2
|
UTSW |
12 |
84,856,467 (GRCm39) |
missense |
probably benign |
0.02 |
R9123:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9129:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9132:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9144:Ltbp2
|
UTSW |
12 |
84,856,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R9150:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9152:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9156:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9157:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9158:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9159:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9160:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9199:Ltbp2
|
UTSW |
12 |
84,832,750 (GRCm39) |
missense |
probably benign |
0.09 |
R9212:Ltbp2
|
UTSW |
12 |
84,839,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9276:Ltbp2
|
UTSW |
12 |
84,876,885 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9276:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9278:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9279:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9280:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9281:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9312:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9313:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9331:Ltbp2
|
UTSW |
12 |
84,922,965 (GRCm39) |
missense |
probably benign |
|
R9355:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9375:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9377:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9378:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9450:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9457:Ltbp2
|
UTSW |
12 |
84,835,927 (GRCm39) |
missense |
probably benign |
0.19 |
R9486:Ltbp2
|
UTSW |
12 |
84,878,648 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9505:Ltbp2
|
UTSW |
12 |
84,900,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R9512:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9581:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9582:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9645:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9747:Ltbp2
|
UTSW |
12 |
84,915,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R9792:Ltbp2
|
UTSW |
12 |
84,876,128 (GRCm39) |
missense |
probably damaging |
0.99 |
R9795:Ltbp2
|
UTSW |
12 |
84,876,128 (GRCm39) |
missense |
probably damaging |
0.99 |
X0017:Ltbp2
|
UTSW |
12 |
84,875,302 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Ltbp2
|
UTSW |
12 |
84,876,973 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ltbp2
|
UTSW |
12 |
84,922,627 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Ltbp2
|
UTSW |
12 |
84,876,090 (GRCm39) |
missense |
possibly damaging |
0.87 |
|