Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410137M14Rik |
A |
G |
17: 37,288,965 (GRCm39) |
|
probably benign |
Het |
Abcb1b |
C |
T |
5: 8,874,803 (GRCm39) |
R488C |
probably benign |
Het |
Adam34 |
T |
C |
8: 44,105,274 (GRCm39) |
I124V |
probably benign |
Het |
Aicda |
T |
A |
6: 122,538,244 (GRCm39) |
V134D |
possibly damaging |
Het |
Akt2 |
T |
A |
7: 27,336,625 (GRCm39) |
|
probably null |
Het |
Aldh1a3 |
T |
C |
7: 66,055,769 (GRCm39) |
R341G |
probably damaging |
Het |
Ankrd12 |
G |
T |
17: 66,338,569 (GRCm39) |
|
probably null |
Het |
Anxa11 |
A |
G |
14: 25,874,721 (GRCm39) |
Y244C |
probably damaging |
Het |
Atp2c2 |
G |
A |
8: 120,475,048 (GRCm39) |
R551Q |
probably damaging |
Het |
B4galt3 |
C |
A |
1: 171,101,613 (GRCm39) |
H196N |
probably damaging |
Het |
Bcl11a |
G |
T |
11: 24,113,343 (GRCm39) |
G229W |
probably damaging |
Het |
Brip1 |
A |
G |
11: 85,952,703 (GRCm39) |
V1026A |
probably benign |
Het |
Cacna1h |
A |
T |
17: 25,603,987 (GRCm39) |
S1282T |
probably benign |
Het |
Calcr |
T |
C |
6: 3,717,133 (GRCm39) |
Y109C |
probably damaging |
Het |
Ccdc39 |
T |
C |
3: 33,890,882 (GRCm39) |
I241V |
probably damaging |
Het |
Ccdc9 |
A |
G |
7: 16,018,194 (GRCm39) |
|
probably benign |
Het |
Cdk17 |
G |
A |
10: 93,064,624 (GRCm39) |
D298N |
probably damaging |
Het |
Cdkl3 |
A |
G |
11: 51,918,020 (GRCm39) |
*354W |
probably null |
Het |
Celf6 |
A |
T |
9: 59,511,610 (GRCm39) |
Y401F |
possibly damaging |
Het |
Clec4a4 |
C |
T |
6: 122,990,766 (GRCm39) |
L169F |
probably damaging |
Het |
Col14a1 |
T |
C |
15: 55,327,082 (GRCm39) |
F1411L |
unknown |
Het |
Col4a2 |
G |
T |
8: 11,493,352 (GRCm39) |
G1354W |
probably damaging |
Het |
Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
Cst13 |
A |
T |
2: 148,665,202 (GRCm39) |
R66W |
probably damaging |
Het |
Depp1 |
G |
A |
6: 116,628,683 (GRCm39) |
V9M |
possibly damaging |
Het |
Dhx8 |
A |
G |
11: 101,641,797 (GRCm39) |
T632A |
probably benign |
Het |
Disp1 |
A |
G |
1: 182,869,906 (GRCm39) |
F838S |
possibly damaging |
Het |
Dlg1 |
A |
G |
16: 31,672,664 (GRCm39) |
H599R |
probably benign |
Het |
Dnah12 |
T |
A |
14: 26,503,744 (GRCm39) |
V1654E |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,343,817 (GRCm39) |
L2406F |
probably benign |
Het |
Fam98b |
C |
G |
2: 117,098,300 (GRCm39) |
R257G |
probably damaging |
Het |
Fbn2 |
A |
T |
18: 58,214,471 (GRCm39) |
C900* |
probably null |
Het |
Fgf1 |
A |
G |
18: 38,980,138 (GRCm39) |
Y79H |
possibly damaging |
Het |
Foxn1 |
C |
A |
11: 78,249,630 (GRCm39) |
A632S |
probably benign |
Het |
Fsip2 |
T |
G |
2: 82,807,823 (GRCm39) |
S1381A |
probably benign |
Het |
Gtf2b |
G |
A |
3: 142,484,081 (GRCm39) |
G85D |
probably benign |
Het |
Gyg1 |
C |
A |
3: 20,204,703 (GRCm39) |
G161C |
probably damaging |
Het |
Hemgn |
G |
T |
4: 46,396,301 (GRCm39) |
L312I |
possibly damaging |
Het |
Hic2 |
T |
C |
16: 17,075,324 (GRCm39) |
M51T |
possibly damaging |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Hpx |
C |
T |
7: 105,241,633 (GRCm39) |
R287H |
probably damaging |
Het |
Igf2bp3 |
C |
T |
6: 49,065,488 (GRCm39) |
G468E |
possibly damaging |
Het |
Il5ra |
C |
A |
6: 106,689,402 (GRCm39) |
E397* |
probably null |
Het |
Itfg1 |
A |
T |
8: 86,502,827 (GRCm39) |
S246R |
probably benign |
Het |
Kdm2a |
A |
T |
19: 4,412,898 (GRCm39) |
D29E |
probably damaging |
Het |
Lamc2 |
T |
G |
1: 153,009,452 (GRCm39) |
E784D |
possibly damaging |
Het |
Lrp2 |
A |
T |
2: 69,297,372 (GRCm39) |
N3196K |
possibly damaging |
Het |
Lyzl1 |
T |
A |
18: 4,181,962 (GRCm39) |
C96* |
probably null |
Het |
Maf1 |
A |
G |
15: 76,236,718 (GRCm39) |
T17A |
probably benign |
Het |
Map1b |
T |
C |
13: 99,567,591 (GRCm39) |
D1710G |
unknown |
Het |
Megf8 |
C |
T |
7: 25,049,222 (GRCm39) |
T1773I |
probably damaging |
Het |
Mei1 |
T |
C |
15: 81,987,450 (GRCm39) |
M414T |
probably benign |
Het |
Myo15a |
A |
G |
11: 60,396,860 (GRCm39) |
N2643S |
probably benign |
Het |
Ndufa9 |
A |
G |
6: 126,821,772 (GRCm39) |
Y64H |
probably damaging |
Het |
Neb |
A |
T |
2: 52,101,579 (GRCm39) |
L4354* |
probably null |
Het |
Nom1 |
T |
A |
5: 29,644,972 (GRCm39) |
I480N |
probably damaging |
Het |
Nrxn3 |
C |
T |
12: 89,315,082 (GRCm39) |
T331M |
probably damaging |
Het |
Or1a1 |
G |
T |
11: 74,087,150 (GRCm39) |
V274L |
possibly damaging |
Het |
Or1j16 |
G |
T |
2: 36,530,201 (GRCm39) |
R50M |
possibly damaging |
Het |
Or4f14b |
A |
C |
2: 111,775,270 (GRCm39) |
F177C |
probably damaging |
Het |
Or51a42 |
A |
G |
7: 103,708,612 (GRCm39) |
S66P |
probably damaging |
Het |
Pcdhb15 |
A |
T |
18: 37,608,075 (GRCm39) |
T436S |
probably benign |
Het |
Pcdhb6 |
T |
C |
18: 37,468,633 (GRCm39) |
M518T |
probably benign |
Het |
Pgm2l1 |
T |
A |
7: 99,917,319 (GRCm39) |
|
probably null |
Het |
Pih1d2 |
C |
A |
9: 50,532,379 (GRCm39) |
H162N |
probably benign |
Het |
Pitrm1 |
T |
A |
13: 6,619,327 (GRCm39) |
Y721N |
probably damaging |
Het |
Pla2r1 |
C |
A |
2: 60,288,779 (GRCm39) |
V618F |
probably damaging |
Het |
Plb1 |
T |
C |
5: 32,473,984 (GRCm39) |
S599P |
possibly damaging |
Het |
Prkg1 |
T |
C |
19: 30,556,260 (GRCm39) |
D562G |
probably damaging |
Het |
Proser1 |
T |
G |
3: 53,385,812 (GRCm39) |
S565A |
probably benign |
Het |
Prx |
T |
A |
7: 27,216,213 (GRCm39) |
V238E |
probably damaging |
Het |
Psapl1 |
T |
C |
5: 36,362,509 (GRCm39) |
I367T |
probably damaging |
Het |
Rc3h1 |
T |
C |
1: 160,767,595 (GRCm39) |
V128A |
probably damaging |
Het |
Rrm1 |
T |
A |
7: 102,091,233 (GRCm39) |
M1K |
probably null |
Het |
Rsf1 |
GCG |
GCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Rsl1 |
A |
G |
13: 67,330,892 (GRCm39) |
T447A |
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,825,823 (GRCm39) |
S552P |
probably damaging |
Het |
Sbf1 |
A |
G |
15: 89,190,896 (GRCm39) |
S225P |
possibly damaging |
Het |
Serpina3c |
T |
A |
12: 104,117,757 (GRCm39) |
I194F |
probably benign |
Het |
Setd3 |
C |
T |
12: 108,073,544 (GRCm39) |
V578M |
probably benign |
Het |
Setx |
GTGGCT |
GT |
2: 29,044,073 (GRCm39) |
1814 |
probably null |
Het |
Slc6a1 |
T |
A |
6: 114,285,632 (GRCm39) |
V356E |
probably damaging |
Het |
Slfn1 |
A |
G |
11: 83,011,992 (GRCm39) |
E36G |
possibly damaging |
Het |
Sorcs1 |
T |
C |
19: 50,218,655 (GRCm39) |
H609R |
possibly damaging |
Het |
Spag16 |
A |
G |
1: 70,764,043 (GRCm39) |
H621R |
probably benign |
Het |
Spata31d1e |
A |
G |
13: 59,890,920 (GRCm39) |
V300A |
probably benign |
Het |
Tg |
G |
A |
15: 66,553,788 (GRCm39) |
G401D |
probably benign |
Het |
Tnxb |
A |
C |
17: 34,928,391 (GRCm39) |
T2602P |
possibly damaging |
Het |
Trip11 |
T |
C |
12: 101,839,701 (GRCm39) |
N1643S |
probably benign |
Het |
Ttn |
G |
A |
2: 76,709,687 (GRCm39) |
R1581* |
probably null |
Het |
Ttn |
A |
T |
2: 76,796,155 (GRCm39) |
I590K |
probably benign |
Het |
Vmn1r225 |
A |
G |
17: 20,722,611 (GRCm39) |
I17M |
possibly damaging |
Het |
Vmn1r232 |
A |
G |
17: 21,134,465 (GRCm39) |
L45P |
probably benign |
Het |
Wdr7 |
T |
A |
18: 63,910,678 (GRCm39) |
V690E |
possibly damaging |
Het |
Xaf1 |
A |
T |
11: 72,194,228 (GRCm39) |
E36D |
possibly damaging |
Het |
Zfp131 |
A |
T |
13: 120,237,348 (GRCm39) |
F303I |
probably damaging |
Het |
Zfp513 |
T |
G |
5: 31,357,767 (GRCm39) |
K202T |
probably damaging |
Het |
Zfp788 |
A |
T |
7: 41,299,064 (GRCm39) |
I567F |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,292,861 (GRCm39) |
V2096A |
probably damaging |
Het |
|
Other mutations in Pcdhb18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01685:Pcdhb18
|
APN |
18 |
37,624,984 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02651:Pcdhb18
|
APN |
18 |
37,624,234 (GRCm39) |
nonsense |
probably null |
|
IGL02721:Pcdhb18
|
APN |
18 |
37,623,084 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02945:Pcdhb18
|
APN |
18 |
37,623,048 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03030:Pcdhb18
|
APN |
18 |
37,623,786 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03346:Pcdhb18
|
APN |
18 |
37,622,674 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R0206:Pcdhb18
|
UTSW |
18 |
37,623,240 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0208:Pcdhb18
|
UTSW |
18 |
37,623,240 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0680:Pcdhb18
|
UTSW |
18 |
37,623,347 (GRCm39) |
missense |
probably damaging |
0.98 |
R1517:Pcdhb18
|
UTSW |
18 |
37,622,673 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R1519:Pcdhb18
|
UTSW |
18 |
37,623,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Pcdhb18
|
UTSW |
18 |
37,624,820 (GRCm39) |
missense |
probably benign |
0.19 |
R1735:Pcdhb18
|
UTSW |
18 |
37,623,822 (GRCm39) |
missense |
probably benign |
0.00 |
R2089:Pcdhb18
|
UTSW |
18 |
37,623,653 (GRCm39) |
missense |
probably damaging |
0.99 |
R2091:Pcdhb18
|
UTSW |
18 |
37,623,653 (GRCm39) |
missense |
probably damaging |
0.99 |
R2091:Pcdhb18
|
UTSW |
18 |
37,623,653 (GRCm39) |
missense |
probably damaging |
0.99 |
R2206:Pcdhb18
|
UTSW |
18 |
37,624,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R4773:Pcdhb18
|
UTSW |
18 |
37,623,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Pcdhb18
|
UTSW |
18 |
37,622,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R5271:Pcdhb18
|
UTSW |
18 |
37,624,649 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5568:Pcdhb18
|
UTSW |
18 |
37,624,853 (GRCm39) |
missense |
probably benign |
0.44 |
R5647:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R5648:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R5690:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R5692:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R5812:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R5813:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R5928:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R5929:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R5930:Pcdhb18
|
UTSW |
18 |
37,624,988 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6209:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R6255:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.05 |
R6602:Pcdhb18
|
UTSW |
18 |
37,623,533 (GRCm39) |
missense |
probably damaging |
0.99 |
R6699:Pcdhb18
|
UTSW |
18 |
37,625,005 (GRCm39) |
missense |
probably benign |
0.00 |
R7055:Pcdhb18
|
UTSW |
18 |
37,623,864 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7197:Pcdhb18
|
UTSW |
18 |
37,623,436 (GRCm39) |
missense |
probably benign |
0.06 |
R7289:Pcdhb18
|
UTSW |
18 |
37,623,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R7345:Pcdhb18
|
UTSW |
18 |
37,624,976 (GRCm39) |
missense |
probably benign |
0.19 |
R7403:Pcdhb18
|
UTSW |
18 |
37,624,950 (GRCm39) |
missense |
probably benign |
0.09 |
R7541:Pcdhb18
|
UTSW |
18 |
37,624,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R7651:Pcdhb18
|
UTSW |
18 |
37,624,046 (GRCm39) |
missense |
probably benign |
0.00 |
R7670:Pcdhb18
|
UTSW |
18 |
37,624,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R7673:Pcdhb18
|
UTSW |
18 |
37,624,790 (GRCm39) |
missense |
probably benign |
0.39 |
R7783:Pcdhb18
|
UTSW |
18 |
37,622,874 (GRCm39) |
missense |
probably benign |
0.01 |
R7819:Pcdhb18
|
UTSW |
18 |
37,624,308 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7826:Pcdhb18
|
UTSW |
18 |
37,623,995 (GRCm39) |
missense |
probably damaging |
0.98 |
R7857:Pcdhb18
|
UTSW |
18 |
37,624,364 (GRCm39) |
missense |
probably benign |
|
R7866:Pcdhb18
|
UTSW |
18 |
37,623,512 (GRCm39) |
missense |
probably damaging |
0.99 |
R7895:Pcdhb18
|
UTSW |
18 |
37,623,520 (GRCm39) |
missense |
probably benign |
0.27 |
R8773:Pcdhb18
|
UTSW |
18 |
37,624,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Pcdhb18
|
UTSW |
18 |
37,623,374 (GRCm39) |
missense |
probably benign |
0.00 |
R8891:Pcdhb18
|
UTSW |
18 |
37,623,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R8938:Pcdhb18
|
UTSW |
18 |
37,623,537 (GRCm39) |
missense |
probably benign |
0.00 |
R9303:Pcdhb18
|
UTSW |
18 |
37,625,004 (GRCm39) |
missense |
probably benign |
|
R9305:Pcdhb18
|
UTSW |
18 |
37,625,004 (GRCm39) |
missense |
probably benign |
|
R9525:Pcdhb18
|
UTSW |
18 |
37,624,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Pcdhb18
|
UTSW |
18 |
37,623,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R9696:Pcdhb18
|
UTSW |
18 |
37,623,606 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0022:Pcdhb18
|
UTSW |
18 |
37,623,326 (GRCm39) |
missense |
probably benign |
0.06 |
|