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 |
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 |
Vldlr |
G |
A |
19: 27,212,219 (GRCm39) |
V78M |
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 Cdh19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00772:Cdh19
|
APN |
1 |
110,876,982 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00863:Cdh19
|
APN |
1 |
110,876,874 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01537:Cdh19
|
APN |
1 |
110,847,341 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02108:Cdh19
|
APN |
1 |
110,817,461 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02125:Cdh19
|
APN |
1 |
110,857,614 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02234:Cdh19
|
APN |
1 |
110,859,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02251:Cdh19
|
APN |
1 |
110,882,382 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02275:Cdh19
|
APN |
1 |
110,853,616 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03203:Cdh19
|
APN |
1 |
110,817,828 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0539:Cdh19
|
UTSW |
1 |
110,852,892 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0612:Cdh19
|
UTSW |
1 |
110,820,900 (GRCm39) |
splice site |
probably benign |
|
R1028:Cdh19
|
UTSW |
1 |
110,882,314 (GRCm39) |
missense |
probably benign |
0.03 |
R1627:Cdh19
|
UTSW |
1 |
110,847,375 (GRCm39) |
missense |
probably benign |
0.16 |
R1728:Cdh19
|
UTSW |
1 |
110,821,114 (GRCm39) |
missense |
probably damaging |
0.98 |
R1729:Cdh19
|
UTSW |
1 |
110,821,114 (GRCm39) |
missense |
probably damaging |
0.98 |
R1730:Cdh19
|
UTSW |
1 |
110,821,114 (GRCm39) |
missense |
probably damaging |
0.98 |
R1739:Cdh19
|
UTSW |
1 |
110,821,114 (GRCm39) |
missense |
probably damaging |
0.98 |
R1762:Cdh19
|
UTSW |
1 |
110,821,114 (GRCm39) |
missense |
probably damaging |
0.98 |
R1783:Cdh19
|
UTSW |
1 |
110,821,114 (GRCm39) |
missense |
probably damaging |
0.98 |
R1785:Cdh19
|
UTSW |
1 |
110,821,114 (GRCm39) |
missense |
probably damaging |
0.98 |
R1974:Cdh19
|
UTSW |
1 |
110,817,889 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2119:Cdh19
|
UTSW |
1 |
110,847,320 (GRCm39) |
missense |
probably benign |
0.00 |
R3026:Cdh19
|
UTSW |
1 |
110,882,418 (GRCm39) |
missense |
probably benign |
0.03 |
R3037:Cdh19
|
UTSW |
1 |
110,882,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R3612:Cdh19
|
UTSW |
1 |
110,821,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R4254:Cdh19
|
UTSW |
1 |
110,852,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R4368:Cdh19
|
UTSW |
1 |
110,817,442 (GRCm39) |
nonsense |
probably null |
|
R4624:Cdh19
|
UTSW |
1 |
110,859,981 (GRCm39) |
missense |
probably benign |
0.25 |
R4648:Cdh19
|
UTSW |
1 |
110,852,907 (GRCm39) |
missense |
probably benign |
0.04 |
R4720:Cdh19
|
UTSW |
1 |
110,823,111 (GRCm39) |
critical splice donor site |
probably null |
|
R4766:Cdh19
|
UTSW |
1 |
110,820,990 (GRCm39) |
missense |
probably benign |
0.39 |
R4937:Cdh19
|
UTSW |
1 |
110,817,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R4968:Cdh19
|
UTSW |
1 |
110,852,958 (GRCm39) |
missense |
probably benign |
0.08 |
R4970:Cdh19
|
UTSW |
1 |
110,882,354 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5095:Cdh19
|
UTSW |
1 |
110,882,391 (GRCm39) |
missense |
probably benign |
|
R5112:Cdh19
|
UTSW |
1 |
110,882,354 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5586:Cdh19
|
UTSW |
1 |
110,857,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Cdh19
|
UTSW |
1 |
110,852,787 (GRCm39) |
missense |
probably benign |
0.00 |
R6595:Cdh19
|
UTSW |
1 |
110,853,517 (GRCm39) |
missense |
probably benign |
0.15 |
R6997:Cdh19
|
UTSW |
1 |
110,882,596 (GRCm39) |
start gained |
probably benign |
|
R7240:Cdh19
|
UTSW |
1 |
110,821,137 (GRCm39) |
missense |
probably benign |
|
R8252:Cdh19
|
UTSW |
1 |
110,817,615 (GRCm39) |
missense |
probably benign |
0.00 |
R8299:Cdh19
|
UTSW |
1 |
110,847,278 (GRCm39) |
missense |
probably benign |
0.01 |
R8416:Cdh19
|
UTSW |
1 |
110,853,610 (GRCm39) |
missense |
probably benign |
0.13 |
R8766:Cdh19
|
UTSW |
1 |
110,817,844 (GRCm39) |
missense |
probably benign |
0.33 |
R9090:Cdh19
|
UTSW |
1 |
110,876,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R9177:Cdh19
|
UTSW |
1 |
110,877,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R9266:Cdh19
|
UTSW |
1 |
110,817,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R9268:Cdh19
|
UTSW |
1 |
110,877,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Cdh19
|
UTSW |
1 |
110,876,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R9533:Cdh19
|
UTSW |
1 |
110,817,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R9560:Cdh19
|
UTSW |
1 |
110,821,004 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9765:Cdh19
|
UTSW |
1 |
110,823,111 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Cdh19
|
UTSW |
1 |
110,859,944 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Cdh19
|
UTSW |
1 |
110,823,117 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cdh19
|
UTSW |
1 |
110,821,036 (GRCm39) |
missense |
probably benign |
0.00 |
|