Other mutations in this stock |
Total: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
T |
C |
16: 14,207,744 (GRCm39) |
V41A |
probably benign |
Het |
Acad11 |
A |
G |
9: 103,972,762 (GRCm39) |
Q367R |
probably benign |
Het |
Ackr4 |
A |
G |
9: 103,976,203 (GRCm39) |
V248A |
possibly damaging |
Het |
Adamts14 |
T |
C |
10: 61,038,666 (GRCm39) |
E945G |
probably damaging |
Het |
Ano2 |
A |
G |
6: 125,959,728 (GRCm39) |
M663V |
probably damaging |
Het |
Apc2 |
T |
A |
10: 80,142,090 (GRCm39) |
C336* |
probably null |
Het |
Arhgap17 |
A |
G |
7: 122,893,741 (GRCm39) |
S560P |
probably benign |
Het |
Arl5a |
T |
C |
2: 52,295,026 (GRCm39) |
D128G |
probably damaging |
Het |
Atp6v0a2 |
C |
A |
5: 124,795,046 (GRCm39) |
R678S |
probably benign |
Het |
B4galnt2 |
C |
A |
11: 95,782,735 (GRCm39) |
A26S |
probably benign |
Het |
C1qtnf1 |
A |
T |
11: 118,337,454 (GRCm39) |
T95S |
possibly damaging |
Het |
Ccdc188 |
T |
A |
16: 18,036,784 (GRCm39) |
F241L |
probably benign |
Het |
Cdh19 |
A |
T |
1: 110,853,597 (GRCm39) |
D281E |
probably benign |
Het |
Cdk5rap2 |
T |
C |
4: 70,273,050 (GRCm39) |
E241G |
probably damaging |
Het |
Cherp |
A |
T |
8: 73,216,246 (GRCm39) |
|
probably null |
Het |
Cpne9 |
T |
A |
6: 113,267,361 (GRCm39) |
|
probably benign |
Het |
Cthrc1 |
A |
T |
15: 38,940,537 (GRCm39) |
R47W |
possibly damaging |
Het |
Dcaf13 |
A |
G |
15: 38,986,663 (GRCm39) |
E145G |
probably benign |
Het |
Dcaf4 |
T |
A |
12: 83,584,817 (GRCm39) |
|
probably null |
Het |
Dgka |
A |
C |
10: 128,568,979 (GRCm39) |
|
probably benign |
Het |
Dhrs13 |
T |
A |
11: 77,925,351 (GRCm39) |
F157L |
probably damaging |
Het |
Dnajb5 |
A |
T |
4: 42,956,577 (GRCm39) |
Y88F |
probably damaging |
Het |
Dpp8 |
A |
G |
9: 64,944,280 (GRCm39) |
T16A |
probably damaging |
Het |
Dscc1 |
A |
T |
15: 54,952,448 (GRCm39) |
I91K |
possibly damaging |
Het |
Efemp2 |
T |
A |
19: 5,525,091 (GRCm39) |
|
probably benign |
Het |
Elf2 |
T |
C |
3: 51,163,874 (GRCm39) |
T504A |
possibly damaging |
Het |
Elk3 |
G |
A |
10: 93,101,022 (GRCm39) |
S243F |
probably damaging |
Het |
Ell2 |
A |
G |
13: 75,898,112 (GRCm39) |
D93G |
probably damaging |
Het |
Eln |
G |
T |
5: 134,741,252 (GRCm39) |
|
probably benign |
Het |
Eme1 |
C |
T |
11: 94,541,256 (GRCm39) |
D189N |
possibly damaging |
Het |
Epb41l2 |
A |
G |
10: 25,319,668 (GRCm39) |
E167G |
possibly damaging |
Het |
Exoc5 |
A |
T |
14: 49,273,544 (GRCm39) |
|
probably benign |
Het |
Fam170b |
A |
G |
14: 32,558,271 (GRCm39) |
K369E |
unknown |
Het |
Fam187b |
T |
A |
7: 30,676,579 (GRCm39) |
C29* |
probably null |
Het |
Fam20c |
T |
C |
5: 138,752,392 (GRCm39) |
S260P |
possibly damaging |
Het |
Fam216b |
G |
A |
14: 78,324,114 (GRCm39) |
A21V |
possibly damaging |
Het |
Fam98a |
A |
T |
17: 75,845,482 (GRCm39) |
Y421* |
probably null |
Het |
Farp2 |
T |
C |
1: 93,504,222 (GRCm39) |
V333A |
probably damaging |
Het |
Fcgr1 |
T |
C |
3: 96,199,628 (GRCm39) |
Y93C |
probably damaging |
Het |
Fgd2 |
A |
T |
17: 29,584,526 (GRCm39) |
I157F |
probably damaging |
Het |
Frmd4b |
T |
A |
6: 97,302,387 (GRCm39) |
|
probably benign |
Het |
Fut9 |
T |
C |
4: 25,620,526 (GRCm39) |
D96G |
possibly damaging |
Het |
Glt8d1 |
G |
A |
14: 30,732,367 (GRCm39) |
|
probably null |
Het |
Gm7579 |
T |
A |
7: 141,766,121 (GRCm39) |
C176S |
unknown |
Het |
Gmpr2 |
A |
G |
14: 55,915,445 (GRCm39) |
E272G |
probably damaging |
Het |
Grin2b |
T |
C |
6: 135,710,927 (GRCm39) |
H873R |
probably damaging |
Het |
Gtf2i |
C |
T |
5: 134,271,027 (GRCm39) |
|
probably benign |
Het |
Htr3b |
A |
T |
9: 48,858,931 (GRCm39) |
V69E |
probably benign |
Het |
Icam5 |
A |
G |
9: 20,946,894 (GRCm39) |
N474S |
probably benign |
Het |
Itgal |
T |
A |
7: 126,913,232 (GRCm39) |
S610T |
probably damaging |
Het |
Jag1 |
T |
A |
2: 136,929,000 (GRCm39) |
I819L |
probably damaging |
Het |
Kif9 |
A |
T |
9: 110,340,408 (GRCm39) |
E467V |
probably benign |
Het |
Krit1 |
T |
C |
5: 3,873,694 (GRCm39) |
L491P |
possibly damaging |
Het |
Lipo2 |
T |
G |
19: 33,724,302 (GRCm39) |
I155L |
possibly damaging |
Het |
Lmbr1 |
A |
G |
5: 29,497,207 (GRCm39) |
F65L |
possibly damaging |
Het |
Lsp1 |
G |
A |
7: 142,042,687 (GRCm39) |
|
probably benign |
Het |
Mgat5 |
T |
A |
1: 127,339,985 (GRCm39) |
D455E |
probably damaging |
Het |
Mical2 |
A |
T |
7: 111,917,657 (GRCm39) |
Y338F |
probably damaging |
Het |
Mre11a |
T |
G |
9: 14,726,505 (GRCm39) |
S396A |
probably benign |
Het |
Mrtfa |
G |
A |
15: 80,901,375 (GRCm39) |
T372I |
probably damaging |
Het |
Mtarc2 |
T |
C |
1: 184,573,536 (GRCm39) |
N121D |
probably benign |
Het |
Myo3a |
C |
T |
2: 22,436,370 (GRCm39) |
|
probably benign |
Het |
Naca |
T |
C |
10: 127,876,224 (GRCm39) |
|
probably benign |
Het |
Nav1 |
A |
T |
1: 135,395,381 (GRCm39) |
I996K |
possibly damaging |
Het |
Ncbp1 |
A |
G |
4: 46,170,551 (GRCm39) |
N742S |
probably benign |
Het |
Ndufaf3 |
G |
A |
9: 108,444,122 (GRCm39) |
A2V |
probably benign |
Het |
Niban3 |
C |
A |
8: 72,051,779 (GRCm39) |
A38E |
probably benign |
Het |
Ntn5 |
G |
T |
7: 45,336,105 (GRCm39) |
A47S |
probably damaging |
Het |
Or10ag57 |
T |
A |
2: 87,218,298 (GRCm39) |
I83N |
probably damaging |
Het |
Or1e25 |
G |
A |
11: 73,494,218 (GRCm39) |
E271K |
probably benign |
Het |
Or1e32 |
T |
C |
11: 73,705,443 (GRCm39) |
H155R |
probably benign |
Het |
Or2a7 |
T |
A |
6: 43,151,541 (GRCm39) |
V207E |
possibly damaging |
Het |
Or6c207 |
T |
C |
10: 129,105,021 (GRCm39) |
Y57C |
possibly damaging |
Het |
Or9i1 |
G |
T |
19: 13,839,643 (GRCm39) |
C162F |
probably benign |
Het |
Otud7a |
T |
A |
7: 63,377,220 (GRCm39) |
L203* |
probably null |
Het |
Pakap |
A |
G |
4: 57,856,752 (GRCm39) |
T694A |
probably benign |
Het |
Pcdhb13 |
A |
G |
18: 37,576,984 (GRCm39) |
Y454C |
probably damaging |
Het |
Pdzph1 |
C |
T |
17: 59,261,474 (GRCm39) |
V853M |
possibly damaging |
Het |
Plec |
A |
G |
15: 76,056,453 (GRCm39) |
S4517P |
probably damaging |
Het |
Pm20d2 |
C |
T |
4: 33,181,746 (GRCm39) |
E286K |
probably damaging |
Het |
Polr2i |
T |
A |
7: 29,932,170 (GRCm39) |
|
probably null |
Het |
Ppp1r12b |
A |
G |
1: 134,704,217 (GRCm39) |
L879P |
probably damaging |
Het |
Prf1 |
C |
A |
10: 61,139,501 (GRCm39) |
Y486* |
probably null |
Het |
Qsox2 |
T |
G |
2: 26,104,056 (GRCm39) |
T325P |
probably damaging |
Het |
Rab1b |
G |
T |
19: 5,150,684 (GRCm39) |
|
probably benign |
Het |
Rbm19 |
T |
C |
5: 120,266,381 (GRCm39) |
|
probably null |
Het |
Rhobtb2 |
A |
G |
14: 70,031,397 (GRCm39) |
V576A |
probably benign |
Het |
Rnps1 |
G |
A |
17: 24,643,411 (GRCm39) |
V215M |
probably damaging |
Het |
Rps11 |
A |
G |
7: 44,773,706 (GRCm39) |
|
probably benign |
Het |
Serpinb3d |
C |
T |
1: 107,007,077 (GRCm39) |
M210I |
probably damaging |
Het |
Sgsm1 |
T |
C |
5: 113,458,428 (GRCm39) |
T17A |
probably benign |
Het |
Slc6a3 |
A |
G |
13: 73,686,761 (GRCm39) |
T43A |
probably damaging |
Het |
Sox4 |
C |
G |
13: 29,136,887 (GRCm39) |
A40P |
probably damaging |
Het |
Spry2 |
A |
T |
14: 106,130,744 (GRCm39) |
D147E |
possibly damaging |
Het |
Stpg1 |
A |
G |
4: 135,246,742 (GRCm39) |
N157D |
possibly damaging |
Het |
Sumf1 |
T |
C |
6: 108,150,375 (GRCm39) |
D152G |
probably benign |
Het |
Tbr1 |
T |
C |
2: 61,641,964 (GRCm39) |
S410P |
possibly damaging |
Het |
Tdrd6 |
A |
G |
17: 43,940,274 (GRCm39) |
V258A |
probably damaging |
Het |
Tirap |
C |
T |
9: 35,100,057 (GRCm39) |
G209D |
probably damaging |
Het |
Tnfrsf8 |
A |
T |
4: 145,023,431 (GRCm39) |
V134D |
probably damaging |
Het |
Tnr |
A |
G |
1: 159,677,905 (GRCm39) |
T97A |
probably benign |
Het |
Tspan32 |
T |
A |
7: 142,569,347 (GRCm39) |
F135L |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,619,400 (GRCm39) |
K16021E |
probably damaging |
Het |
Tusc3 |
T |
A |
8: 39,564,122 (GRCm39) |
I251N |
probably damaging |
Het |
Usp38 |
A |
T |
8: 81,731,995 (GRCm39) |
I305N |
probably damaging |
Het |
Usp4 |
T |
A |
9: 108,248,080 (GRCm39) |
|
probably null |
Het |
Usp5 |
A |
T |
6: 124,794,387 (GRCm39) |
D764E |
probably damaging |
Het |
Vangl2 |
A |
T |
1: 171,832,224 (GRCm39) |
V544E |
probably damaging |
Het |
Vmn1r29 |
T |
C |
6: 58,284,757 (GRCm39) |
V159A |
probably benign |
Het |
Vmn2r16 |
T |
A |
5: 109,511,762 (GRCm39) |
F656L |
probably damaging |
Het |
Wdfy3 |
T |
A |
5: 102,054,051 (GRCm39) |
I1590F |
possibly damaging |
Het |
Xpo1 |
T |
A |
11: 23,230,402 (GRCm39) |
V263E |
probably damaging |
Het |
Zbtb38 |
A |
G |
9: 96,568,007 (GRCm39) |
S1026P |
probably damaging |
Het |
Zfp407 |
A |
T |
18: 84,580,692 (GRCm39) |
D140E |
possibly damaging |
Het |
Zfp637 |
T |
A |
6: 117,822,647 (GRCm39) |
Y258* |
probably null |
Het |
Zfp951 |
T |
A |
5: 104,962,438 (GRCm39) |
Q376L |
possibly damaging |
Het |
|
Other mutations in Vldlr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01346:Vldlr
|
APN |
19 |
27,217,081 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01575:Vldlr
|
APN |
19 |
27,224,031 (GRCm39) |
missense |
probably benign |
|
IGL01626:Vldlr
|
APN |
19 |
27,221,173 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02213:Vldlr
|
APN |
19 |
27,218,726 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02365:Vldlr
|
APN |
19 |
27,223,025 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02488:Vldlr
|
APN |
19 |
27,215,675 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Vldlr
|
APN |
19 |
27,215,485 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02947:Vldlr
|
APN |
19 |
27,217,120 (GRCm39) |
missense |
probably benign |
0.03 |
disturbed
|
UTSW |
19 |
27,216,204 (GRCm39) |
nonsense |
probably null |
|
r26
|
UTSW |
19 |
27,223,054 (GRCm39) |
missense |
probably damaging |
0.99 |
spotty
|
UTSW |
19 |
27,216,192 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4142001:Vldlr
|
UTSW |
19 |
27,212,269 (GRCm39) |
missense |
probably benign |
0.05 |
R0195:Vldlr
|
UTSW |
19 |
27,215,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R0288:Vldlr
|
UTSW |
19 |
27,218,051 (GRCm39) |
splice site |
probably benign |
|
R0536:Vldlr
|
UTSW |
19 |
27,217,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R0537:Vldlr
|
UTSW |
19 |
27,225,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R0542:Vldlr
|
UTSW |
19 |
27,213,655 (GRCm39) |
missense |
probably benign |
0.01 |
R0624:Vldlr
|
UTSW |
19 |
27,215,663 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0726:Vldlr
|
UTSW |
19 |
27,215,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R1017:Vldlr
|
UTSW |
19 |
27,218,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Vldlr
|
UTSW |
19 |
27,218,691 (GRCm39) |
missense |
probably benign |
0.01 |
R1148:Vldlr
|
UTSW |
19 |
27,218,691 (GRCm39) |
missense |
probably benign |
0.01 |
R1443:Vldlr
|
UTSW |
19 |
27,217,121 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1493:Vldlr
|
UTSW |
19 |
27,218,691 (GRCm39) |
missense |
probably benign |
0.01 |
R1520:Vldlr
|
UTSW |
19 |
27,224,466 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1520:Vldlr
|
UTSW |
19 |
27,217,943 (GRCm39) |
missense |
probably damaging |
0.99 |
R1657:Vldlr
|
UTSW |
19 |
27,223,070 (GRCm39) |
missense |
probably benign |
0.00 |
R1901:Vldlr
|
UTSW |
19 |
27,218,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R2047:Vldlr
|
UTSW |
19 |
27,212,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:Vldlr
|
UTSW |
19 |
27,215,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R2273:Vldlr
|
UTSW |
19 |
27,225,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R2423:Vldlr
|
UTSW |
19 |
27,213,688 (GRCm39) |
missense |
possibly damaging |
0.49 |
R3196:Vldlr
|
UTSW |
19 |
27,220,554 (GRCm39) |
missense |
probably damaging |
0.98 |
R3752:Vldlr
|
UTSW |
19 |
27,215,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Vldlr
|
UTSW |
19 |
27,195,021 (GRCm39) |
missense |
probably damaging |
0.99 |
R3835:Vldlr
|
UTSW |
19 |
27,212,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Vldlr
|
UTSW |
19 |
27,215,713 (GRCm39) |
missense |
probably benign |
|
R4301:Vldlr
|
UTSW |
19 |
27,215,802 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4470:Vldlr
|
UTSW |
19 |
27,212,219 (GRCm39) |
missense |
probably damaging |
0.96 |
R4541:Vldlr
|
UTSW |
19 |
27,216,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4765:Vldlr
|
UTSW |
19 |
27,217,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Vldlr
|
UTSW |
19 |
27,217,290 (GRCm39) |
missense |
probably damaging |
0.97 |
R4795:Vldlr
|
UTSW |
19 |
27,216,252 (GRCm39) |
splice site |
probably null |
|
R4839:Vldlr
|
UTSW |
19 |
27,215,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Vldlr
|
UTSW |
19 |
27,215,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R5134:Vldlr
|
UTSW |
19 |
27,216,212 (GRCm39) |
nonsense |
probably null |
|
R5281:Vldlr
|
UTSW |
19 |
27,221,631 (GRCm39) |
missense |
probably benign |
0.44 |
R5466:Vldlr
|
UTSW |
19 |
27,217,243 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5514:Vldlr
|
UTSW |
19 |
27,221,624 (GRCm39) |
missense |
probably damaging |
0.97 |
R5886:Vldlr
|
UTSW |
19 |
27,221,171 (GRCm39) |
missense |
probably benign |
0.03 |
R5889:Vldlr
|
UTSW |
19 |
27,217,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R6110:Vldlr
|
UTSW |
19 |
27,215,477 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6343:Vldlr
|
UTSW |
19 |
27,223,049 (GRCm39) |
missense |
probably damaging |
0.99 |
R6833:Vldlr
|
UTSW |
19 |
27,217,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R6838:Vldlr
|
UTSW |
19 |
27,225,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R7169:Vldlr
|
UTSW |
19 |
27,221,728 (GRCm39) |
missense |
probably benign |
|
R7197:Vldlr
|
UTSW |
19 |
27,212,241 (GRCm39) |
missense |
probably benign |
0.36 |
R7304:Vldlr
|
UTSW |
19 |
27,216,004 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7403:Vldlr
|
UTSW |
19 |
27,213,674 (GRCm39) |
nonsense |
probably null |
|
R7658:Vldlr
|
UTSW |
19 |
27,220,536 (GRCm39) |
missense |
probably benign |
0.33 |
R7754:Vldlr
|
UTSW |
19 |
27,195,015 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R8105:Vldlr
|
UTSW |
19 |
27,216,204 (GRCm39) |
nonsense |
probably null |
|
R8377:Vldlr
|
UTSW |
19 |
27,212,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R8529:Vldlr
|
UTSW |
19 |
27,207,656 (GRCm39) |
missense |
probably benign |
0.03 |
R8777:Vldlr
|
UTSW |
19 |
27,217,946 (GRCm39) |
missense |
probably benign |
0.00 |
R8777-TAIL:Vldlr
|
UTSW |
19 |
27,217,946 (GRCm39) |
missense |
probably benign |
0.00 |
R9380:Vldlr
|
UTSW |
19 |
27,216,192 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9400:Vldlr
|
UTSW |
19 |
27,216,175 (GRCm39) |
missense |
probably damaging |
0.99 |
R9483:Vldlr
|
UTSW |
19 |
27,224,031 (GRCm39) |
missense |
probably benign |
0.00 |
R9502:Vldlr
|
UTSW |
19 |
27,218,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R9509:Vldlr
|
UTSW |
19 |
27,221,687 (GRCm39) |
missense |
probably benign |
0.44 |
R9630:Vldlr
|
UTSW |
19 |
27,207,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R9767:Vldlr
|
UTSW |
19 |
27,212,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R9768:Vldlr
|
UTSW |
19 |
27,218,720 (GRCm39) |
missense |
possibly damaging |
0.47 |
|