Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5330417H12Rik |
T |
A |
7: 107,223,952 (GRCm39) |
|
probably benign |
Het |
A1cf |
A |
T |
19: 31,886,196 (GRCm39) |
N35I |
possibly damaging |
Het |
Abca2 |
T |
C |
2: 25,330,542 (GRCm39) |
I1106T |
possibly damaging |
Het |
Abca4 |
G |
A |
3: 121,956,577 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,581,632 (GRCm39) |
D4804G |
probably benign |
Het |
Adk |
T |
A |
14: 21,102,708 (GRCm39) |
M1K |
probably null |
Het |
Aff3 |
T |
C |
1: 38,230,364 (GRCm39) |
N1006D |
probably damaging |
Het |
Akap12 |
A |
G |
10: 4,305,475 (GRCm39) |
T762A |
probably benign |
Het |
Atosa |
C |
G |
9: 74,917,456 (GRCm39) |
S685* |
probably null |
Het |
Atp12a |
T |
A |
14: 56,623,296 (GRCm39) |
M843K |
probably damaging |
Het |
Bbx |
T |
A |
16: 50,086,633 (GRCm39) |
K169* |
probably null |
Het |
Bicra |
A |
T |
7: 15,722,284 (GRCm39) |
V411E |
possibly damaging |
Het |
Camk1d |
A |
T |
2: 5,366,836 (GRCm39) |
Y126* |
probably null |
Het |
Cel |
T |
C |
2: 28,446,338 (GRCm39) |
Y511C |
probably damaging |
Het |
Celf4 |
G |
T |
18: 25,636,140 (GRCm39) |
|
probably null |
Het |
Clasp1 |
A |
G |
1: 118,436,646 (GRCm39) |
N310S |
probably benign |
Het |
Col6a3 |
T |
C |
1: 90,709,577 (GRCm39) |
K1873R |
unknown |
Het |
Cstf1 |
A |
G |
2: 172,217,795 (GRCm39) |
D136G |
probably damaging |
Het |
Cwc22 |
T |
A |
2: 77,741,899 (GRCm39) |
E470D |
probably damaging |
Het |
Cxcr2 |
A |
T |
1: 74,197,527 (GRCm39) |
D7V |
probably benign |
Het |
Cytip |
A |
G |
2: 58,035,192 (GRCm39) |
I168T |
probably damaging |
Het |
D5Ertd579e |
A |
G |
5: 36,760,083 (GRCm39) |
L1359P |
probably benign |
Het |
Ddx25 |
A |
C |
9: 35,469,034 (GRCm39) |
V26G |
probably benign |
Het |
Dennd4a |
T |
A |
9: 64,813,327 (GRCm39) |
S1429T |
possibly damaging |
Het |
Dmd |
A |
G |
X: 83,892,306 (GRCm39) |
D2990G |
probably damaging |
Het |
Dop1a |
C |
A |
9: 86,424,785 (GRCm39) |
|
probably null |
Het |
Eps8 |
T |
C |
6: 137,499,852 (GRCm39) |
Q209R |
possibly damaging |
Het |
Fabp6 |
T |
A |
11: 43,486,992 (GRCm39) |
I112F |
probably benign |
Het |
Fbxw10 |
T |
C |
11: 62,738,418 (GRCm39) |
V104A |
possibly damaging |
Het |
Gp1ba |
C |
T |
11: 70,532,253 (GRCm39) |
P673L |
probably damaging |
Het |
Grin3a |
T |
C |
4: 49,702,804 (GRCm39) |
Y894C |
probably damaging |
Het |
Hydin |
C |
T |
8: 111,173,217 (GRCm39) |
H967Y |
probably benign |
Het |
Ip6k3 |
T |
C |
17: 27,364,242 (GRCm39) |
K269E |
possibly damaging |
Het |
Jup |
T |
C |
11: 100,274,026 (GRCm39) |
K172E |
probably damaging |
Het |
Katnal1 |
T |
C |
5: 148,841,486 (GRCm39) |
D126G |
probably benign |
Het |
Knl1 |
A |
T |
2: 118,898,788 (GRCm39) |
K163M |
probably damaging |
Het |
Krt17 |
C |
T |
11: 100,148,365 (GRCm39) |
E359K |
possibly damaging |
Het |
Lct |
T |
A |
1: 128,235,559 (GRCm39) |
I483F |
probably damaging |
Het |
Loxl2 |
G |
A |
14: 69,930,489 (GRCm39) |
G751D |
probably damaging |
Het |
Ltbp4 |
G |
A |
7: 27,006,002 (GRCm39) |
R1559C |
possibly damaging |
Het |
Man2c1 |
T |
A |
9: 57,042,503 (GRCm39) |
D183E |
probably benign |
Het |
Med17 |
T |
C |
9: 15,187,139 (GRCm39) |
|
probably null |
Het |
Mrgpra9 |
A |
C |
7: 46,885,561 (GRCm39) |
S34R |
probably benign |
Het |
Mrpl44 |
T |
A |
1: 79,755,677 (GRCm39) |
N94K |
probably damaging |
Het |
Nat8f1 |
A |
G |
6: 85,887,924 (GRCm39) |
V12A |
probably benign |
Het |
Nr2e3 |
C |
A |
9: 59,850,797 (GRCm39) |
G354V |
probably damaging |
Het |
Nrbp1 |
T |
A |
5: 31,403,157 (GRCm39) |
I210N |
probably damaging |
Het |
Nup155 |
T |
C |
15: 8,141,890 (GRCm39) |
V94A |
probably benign |
Het |
Or14a256 |
A |
T |
7: 86,265,569 (GRCm39) |
C95S |
probably damaging |
Het |
Or52h2 |
C |
T |
7: 103,839,082 (GRCm39) |
V111I |
possibly damaging |
Het |
Or5p76 |
T |
C |
7: 108,122,525 (GRCm39) |
I211V |
probably benign |
Het |
Or9q2 |
A |
T |
19: 13,772,140 (GRCm39) |
Y278* |
probably null |
Het |
Phip |
A |
C |
9: 82,797,476 (GRCm39) |
I509S |
possibly damaging |
Het |
Pkhd1 |
C |
T |
1: 20,655,381 (GRCm39) |
|
probably null |
Het |
Psme4 |
T |
G |
11: 30,802,744 (GRCm39) |
L1487R |
probably damaging |
Het |
Ptgdr2 |
A |
G |
19: 10,917,857 (GRCm39) |
S125G |
probably damaging |
Het |
Ptpro |
A |
G |
6: 137,418,114 (GRCm39) |
K126E |
probably damaging |
Het |
Rdh16f2 |
T |
A |
10: 127,712,794 (GRCm39) |
V264E |
probably benign |
Het |
Ric8b |
C |
T |
10: 84,783,535 (GRCm39) |
A131V |
possibly damaging |
Het |
Rock1 |
A |
T |
18: 10,070,233 (GRCm39) |
I1280N |
probably damaging |
Het |
Rprd2 |
A |
G |
3: 95,725,888 (GRCm39) |
V59A |
possibly damaging |
Het |
Ruvbl1 |
T |
A |
6: 88,444,551 (GRCm39) |
C49S |
probably benign |
Het |
Scn2a |
A |
G |
2: 65,514,189 (GRCm39) |
N291S |
probably benign |
Het |
Serbp1 |
T |
A |
6: 67,254,904 (GRCm39) |
H325Q |
probably damaging |
Het |
Shf |
G |
A |
2: 122,199,163 (GRCm39) |
P51S |
probably damaging |
Het |
Shisal2b |
T |
C |
13: 104,982,470 (GRCm39) |
I151V |
probably benign |
Het |
Slitrk3 |
G |
A |
3: 72,957,674 (GRCm39) |
T366I |
probably damaging |
Het |
Spryd3 |
A |
T |
15: 102,026,827 (GRCm39) |
H307Q |
possibly damaging |
Het |
Spx |
A |
T |
6: 142,364,239 (GRCm39) |
D100V |
probably benign |
Het |
Surf4 |
A |
G |
2: 26,814,476 (GRCm39) |
F142L |
probably damaging |
Het |
Syne2 |
T |
A |
12: 76,067,099 (GRCm39) |
|
probably null |
Het |
Syne2 |
T |
C |
12: 76,098,952 (GRCm39) |
M5278T |
possibly damaging |
Het |
Thap12 |
T |
C |
7: 98,365,230 (GRCm39) |
V466A |
probably benign |
Het |
Thap3 |
T |
C |
4: 152,067,673 (GRCm39) |
K135R |
possibly damaging |
Het |
Tmem131 |
G |
T |
1: 36,866,439 (GRCm39) |
D448E |
probably benign |
Het |
Tmem63b |
C |
G |
17: 45,989,904 (GRCm39) |
R88P |
possibly damaging |
Het |
Trim43a |
G |
T |
9: 88,464,146 (GRCm39) |
C19F |
probably damaging |
Het |
Trp63 |
C |
T |
16: 25,707,870 (GRCm39) |
P526L |
possibly damaging |
Het |
Ubqln3 |
T |
C |
7: 103,791,997 (GRCm39) |
D31G |
probably damaging |
Het |
Utp14b |
C |
A |
1: 78,643,162 (GRCm39) |
N353K |
probably damaging |
Het |
Vmn1r40 |
A |
G |
6: 89,691,558 (GRCm39) |
K125R |
probably damaging |
Het |
Vmn2r1 |
A |
G |
3: 64,008,734 (GRCm39) |
Y471C |
probably damaging |
Het |
Vmn2r13 |
A |
G |
5: 109,322,001 (GRCm39) |
I232T |
probably damaging |
Het |
Zfp263 |
A |
C |
16: 3,564,323 (GRCm39) |
E204D |
probably benign |
Het |
Zfp865 |
A |
T |
7: 5,032,278 (GRCm39) |
K88* |
probably null |
Het |
|
Other mutations in Pcdhb10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01151:Pcdhb10
|
APN |
18 |
37,545,248 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01383:Pcdhb10
|
APN |
18 |
37,546,328 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01765:Pcdhb10
|
APN |
18 |
37,547,072 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02240:Pcdhb10
|
APN |
18 |
37,545,455 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02548:Pcdhb10
|
APN |
18 |
37,545,743 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02563:Pcdhb10
|
APN |
18 |
37,546,126 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02598:Pcdhb10
|
APN |
18 |
37,546,834 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02711:Pcdhb10
|
APN |
18 |
37,545,779 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02813:Pcdhb10
|
APN |
18 |
37,546,815 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02893:Pcdhb10
|
APN |
18 |
37,546,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03288:Pcdhb10
|
APN |
18 |
37,546,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03310:Pcdhb10
|
APN |
18 |
37,545,374 (GRCm39) |
missense |
probably damaging |
0.97 |
R0004:Pcdhb10
|
UTSW |
18 |
37,545,012 (GRCm39) |
missense |
probably benign |
|
R0004:Pcdhb10
|
UTSW |
18 |
37,545,012 (GRCm39) |
missense |
probably benign |
|
R0211:Pcdhb10
|
UTSW |
18 |
37,547,059 (GRCm39) |
missense |
probably benign |
|
R0211:Pcdhb10
|
UTSW |
18 |
37,547,059 (GRCm39) |
missense |
probably benign |
|
R0389:Pcdhb10
|
UTSW |
18 |
37,545,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R0443:Pcdhb10
|
UTSW |
18 |
37,545,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R0480:Pcdhb10
|
UTSW |
18 |
37,546,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1218:Pcdhb10
|
UTSW |
18 |
37,546,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R1737:Pcdhb10
|
UTSW |
18 |
37,546,009 (GRCm39) |
missense |
probably benign |
0.01 |
R2092:Pcdhb10
|
UTSW |
18 |
37,547,240 (GRCm39) |
missense |
probably benign |
0.00 |
R2277:Pcdhb10
|
UTSW |
18 |
37,545,677 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2363:Pcdhb10
|
UTSW |
18 |
37,547,190 (GRCm39) |
nonsense |
probably null |
|
R3826:Pcdhb10
|
UTSW |
18 |
37,545,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R4372:Pcdhb10
|
UTSW |
18 |
37,546,366 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4412:Pcdhb10
|
UTSW |
18 |
37,547,194 (GRCm39) |
frame shift |
probably null |
|
R4760:Pcdhb10
|
UTSW |
18 |
37,544,995 (GRCm39) |
missense |
probably benign |
0.05 |
R4941:Pcdhb10
|
UTSW |
18 |
37,545,887 (GRCm39) |
missense |
probably benign |
0.29 |
R5271:Pcdhb10
|
UTSW |
18 |
37,546,222 (GRCm39) |
missense |
probably benign |
0.44 |
R5643:Pcdhb10
|
UTSW |
18 |
37,546,219 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5851:Pcdhb10
|
UTSW |
18 |
37,545,811 (GRCm39) |
missense |
probably benign |
0.00 |
R6089:Pcdhb10
|
UTSW |
18 |
37,546,679 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6125:Pcdhb10
|
UTSW |
18 |
37,546,679 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6189:Pcdhb10
|
UTSW |
18 |
37,545,456 (GRCm39) |
missense |
probably damaging |
0.99 |
R6414:Pcdhb10
|
UTSW |
18 |
37,546,898 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6731:Pcdhb10
|
UTSW |
18 |
37,546,529 (GRCm39) |
missense |
probably benign |
0.02 |
R6999:Pcdhb10
|
UTSW |
18 |
37,546,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Pcdhb10
|
UTSW |
18 |
37,546,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R7317:Pcdhb10
|
UTSW |
18 |
37,546,079 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7554:Pcdhb10
|
UTSW |
18 |
37,544,935 (GRCm39) |
missense |
probably benign |
|
R7638:Pcdhb10
|
UTSW |
18 |
37,545,365 (GRCm39) |
missense |
probably benign |
0.03 |
R7710:Pcdhb10
|
UTSW |
18 |
37,546,654 (GRCm39) |
nonsense |
probably null |
|
R7763:Pcdhb10
|
UTSW |
18 |
37,544,935 (GRCm39) |
missense |
not run |
|
R7867:Pcdhb10
|
UTSW |
18 |
37,546,619 (GRCm39) |
missense |
probably benign |
0.03 |
R8269:Pcdhb10
|
UTSW |
18 |
37,547,062 (GRCm39) |
missense |
probably benign |
0.09 |
R8355:Pcdhb10
|
UTSW |
18 |
37,545,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R9265:Pcdhb10
|
UTSW |
18 |
37,546,553 (GRCm39) |
missense |
possibly damaging |
0.82 |
X0024:Pcdhb10
|
UTSW |
18 |
37,546,051 (GRCm39) |
missense |
probably benign |
0.12 |
X0036:Pcdhb10
|
UTSW |
18 |
37,545,026 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Pcdhb10
|
UTSW |
18 |
37,546,448 (GRCm39) |
frame shift |
probably null |
|
Z1177:Pcdhb10
|
UTSW |
18 |
37,545,596 (GRCm39) |
missense |
probably damaging |
1.00 |
|