Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
T |
A |
11: 84,117,011 (GRCm39) |
I247N |
probably damaging |
Het |
Ankle1 |
G |
T |
8: 71,860,262 (GRCm39) |
S260I |
probably benign |
Het |
Aoc2 |
T |
C |
11: 101,216,018 (GRCm39) |
S34P |
probably benign |
Het |
Ap1m1 |
A |
C |
8: 73,009,966 (GRCm39) |
I397L |
possibly damaging |
Het |
Apba1 |
C |
A |
19: 23,913,925 (GRCm39) |
D649E |
probably damaging |
Het |
Aptx |
C |
T |
4: 40,697,274 (GRCm39) |
V25M |
probably benign |
Het |
Arhgef18 |
G |
A |
8: 3,489,645 (GRCm39) |
G326R |
probably damaging |
Het |
Atm |
A |
C |
9: 53,433,455 (GRCm39) |
I265S |
possibly damaging |
Het |
B3galt4 |
A |
T |
17: 34,170,187 (GRCm39) |
V17E |
probably benign |
Het |
Bcl7a |
T |
A |
5: 123,494,086 (GRCm39) |
M86K |
possibly damaging |
Het |
Calhm6 |
A |
G |
10: 34,003,896 (GRCm39) |
F4L |
probably benign |
Het |
Cela3a |
T |
A |
4: 137,129,995 (GRCm39) |
|
probably null |
Het |
Cep85 |
T |
A |
4: 133,876,039 (GRCm39) |
K456* |
probably null |
Het |
Ces1f |
C |
A |
8: 94,002,042 (GRCm39) |
A29S |
probably benign |
Het |
Chd9 |
A |
T |
8: 91,699,763 (GRCm39) |
I598F |
probably damaging |
Het |
Cntln |
T |
C |
4: 84,865,872 (GRCm39) |
L176S |
probably damaging |
Het |
Cntn3 |
A |
T |
6: 102,147,629 (GRCm39) |
N909K |
probably damaging |
Het |
Cntnap5b |
T |
C |
1: 100,003,832 (GRCm39) |
S271P |
probably damaging |
Het |
Col6a3 |
T |
A |
1: 90,701,224 (GRCm39) |
H2564L |
unknown |
Het |
Cyp2b19 |
C |
A |
7: 26,462,765 (GRCm39) |
|
probably null |
Het |
Dapk1 |
G |
T |
13: 60,866,278 (GRCm39) |
|
probably null |
Het |
Dnah7b |
T |
A |
1: 46,363,872 (GRCm39) |
Y3497* |
probably null |
Het |
Duoxa2 |
T |
C |
2: 122,129,643 (GRCm39) |
|
probably null |
Het |
Eny2 |
T |
C |
15: 44,295,874 (GRCm39) |
W42R |
probably damaging |
Het |
Epha3 |
A |
G |
16: 63,416,091 (GRCm39) |
V635A |
probably damaging |
Het |
Fam167b |
G |
C |
4: 129,472,069 (GRCm39) |
Q34E |
probably benign |
Het |
Fancm |
T |
C |
12: 65,152,430 (GRCm39) |
M962T |
probably benign |
Het |
Gimap8 |
T |
A |
6: 48,633,345 (GRCm39) |
I388N |
probably benign |
Het |
Gpaa1 |
A |
G |
15: 76,215,653 (GRCm39) |
T22A |
probably benign |
Het |
Hoxc11 |
T |
C |
15: 102,863,591 (GRCm39) |
S211P |
possibly damaging |
Het |
Hsd17b12 |
T |
C |
2: 93,863,906 (GRCm39) |
N312S |
unknown |
Het |
Idh2 |
T |
G |
7: 79,748,906 (GRCm39) |
E125A |
probably damaging |
Het |
Igdcc4 |
A |
G |
9: 65,036,077 (GRCm39) |
Y712C |
probably damaging |
Het |
Kank1 |
T |
C |
19: 25,387,668 (GRCm39) |
V447A |
possibly damaging |
Het |
Kif1b |
T |
A |
4: 149,279,958 (GRCm39) |
|
probably null |
Het |
Klc4 |
A |
T |
17: 46,947,696 (GRCm39) |
D335E |
probably damaging |
Het |
Klhl33 |
T |
A |
14: 51,130,534 (GRCm39) |
D320V |
probably benign |
Het |
Krt73 |
A |
T |
15: 101,710,482 (GRCm39) |
M84K |
possibly damaging |
Het |
Kti12 |
T |
A |
4: 108,706,055 (GRCm39) |
I323N |
probably damaging |
Het |
Kynu |
T |
C |
2: 43,569,837 (GRCm39) |
L373P |
probably damaging |
Het |
Lats1 |
T |
C |
10: 7,581,678 (GRCm39) |
M821T |
probably damaging |
Het |
Lnx1 |
A |
T |
5: 74,846,071 (GRCm39) |
H126Q |
probably benign |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Lrrc4b |
T |
A |
7: 44,110,601 (GRCm39) |
Y158N |
probably damaging |
Het |
Lrrc74b |
C |
A |
16: 17,377,617 (GRCm39) |
R87L |
probably damaging |
Het |
Meig1 |
T |
C |
2: 3,410,311 (GRCm39) |
D63G |
probably damaging |
Het |
Mrpl38 |
G |
A |
11: 116,029,255 (GRCm39) |
|
probably benign |
Het |
Mtcl2 |
T |
C |
2: 156,872,450 (GRCm39) |
T966A |
possibly damaging |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Nlrp1a |
T |
A |
11: 71,033,184 (GRCm39) |
E3D |
unknown |
Het |
Nphs2 |
T |
A |
1: 156,148,468 (GRCm39) |
D110E |
probably damaging |
Het |
Nxn |
T |
A |
11: 76,163,290 (GRCm39) |
K244N |
probably benign |
Het |
Oas3 |
A |
T |
5: 120,907,973 (GRCm39) |
F322L |
probably benign |
Het |
Obscn |
T |
A |
11: 58,994,151 (GRCm39) |
Y1577F |
probably damaging |
Het |
Or10ag57 |
G |
A |
2: 87,218,964 (GRCm39) |
R305K |
possibly damaging |
Het |
Or8b47 |
T |
A |
9: 38,435,413 (GRCm39) |
N128K |
probably benign |
Het |
Or8b50 |
G |
A |
9: 38,518,244 (GRCm39) |
G161D |
probably damaging |
Het |
Or8b52 |
A |
G |
9: 38,576,616 (GRCm39) |
Y175H |
probably benign |
Het |
Or8d2 |
T |
C |
9: 38,759,809 (GRCm39) |
M133T |
probably damaging |
Het |
Panx1 |
T |
C |
9: 14,919,079 (GRCm39) |
D260G |
probably benign |
Het |
Pik3ap1 |
C |
A |
19: 41,296,968 (GRCm39) |
V461F |
probably damaging |
Het |
Plpp3 |
G |
A |
4: 105,066,002 (GRCm39) |
|
probably null |
Het |
Prtn3 |
A |
T |
10: 79,716,375 (GRCm39) |
T61S |
probably benign |
Het |
Psen1 |
T |
A |
12: 83,771,394 (GRCm39) |
Y225N |
probably damaging |
Het |
Rab44 |
T |
A |
17: 29,359,098 (GRCm39) |
S429T |
possibly damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,809,388 (GRCm39) |
I462M |
probably benign |
Het |
Rbfox3 |
T |
C |
11: 118,396,495 (GRCm39) |
N105S |
probably damaging |
Het |
Rbm7 |
A |
C |
9: 48,401,021 (GRCm39) |
Y236D |
possibly damaging |
Het |
Samhd1 |
T |
C |
2: 156,943,652 (GRCm39) |
T621A |
probably benign |
Het |
Samt3 |
C |
A |
X: 85,090,256 (GRCm39) |
D49E |
probably benign |
Het |
Sass6 |
T |
C |
3: 116,397,122 (GRCm39) |
V26A |
possibly damaging |
Het |
Scn11a |
C |
T |
9: 119,633,478 (GRCm39) |
M418I |
possibly damaging |
Het |
Scrib |
T |
C |
15: 75,936,416 (GRCm39) |
E480G |
probably damaging |
Het |
Sec24a |
T |
G |
11: 51,586,016 (GRCm39) |
T1071P |
probably damaging |
Het |
Siglecg |
A |
C |
7: 43,058,365 (GRCm39) |
E84A |
probably benign |
Het |
Slc6a17 |
C |
T |
3: 107,381,702 (GRCm39) |
V419I |
probably damaging |
Het |
Ssr2 |
T |
C |
3: 88,488,349 (GRCm39) |
M75T |
possibly damaging |
Het |
Tbc1d22b |
A |
G |
17: 29,794,151 (GRCm39) |
T275A |
possibly damaging |
Het |
Tbx15 |
T |
A |
3: 99,259,140 (GRCm39) |
|
probably null |
Het |
Tll1 |
A |
C |
8: 64,538,585 (GRCm39) |
L353R |
possibly damaging |
Het |
Tlr4 |
C |
T |
4: 66,759,342 (GRCm39) |
P712S |
probably damaging |
Het |
Tmem145 |
T |
A |
7: 25,014,159 (GRCm39) |
F424L |
possibly damaging |
Het |
Tnrc18 |
T |
C |
5: 142,759,572 (GRCm39) |
K755E |
unknown |
Het |
Trmt44 |
A |
G |
5: 35,727,321 (GRCm39) |
I298T |
probably benign |
Het |
Vmn1r69 |
A |
G |
7: 10,314,179 (GRCm39) |
V184A |
probably benign |
Het |
Zfp84 |
T |
C |
7: 29,476,825 (GRCm39) |
C506R |
probably damaging |
Het |
|
Other mutations in Pcdhb15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00530:Pcdhb15
|
APN |
18 |
37,608,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01536:Pcdhb15
|
APN |
18 |
37,608,046 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01664:Pcdhb15
|
APN |
18 |
37,607,314 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02001:Pcdhb15
|
APN |
18 |
37,607,091 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02161:Pcdhb15
|
APN |
18 |
37,608,555 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02205:Pcdhb15
|
APN |
18 |
37,607,010 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02748:Pcdhb15
|
APN |
18 |
37,608,273 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02828:Pcdhb15
|
APN |
18 |
37,606,903 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02974:Pcdhb15
|
APN |
18 |
37,608,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03119:Pcdhb15
|
APN |
18 |
37,608,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03136:Pcdhb15
|
APN |
18 |
37,608,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03150:Pcdhb15
|
APN |
18 |
37,608,067 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Pcdhb15
|
UTSW |
18 |
37,608,724 (GRCm39) |
missense |
probably benign |
0.15 |
R0266:Pcdhb15
|
UTSW |
18 |
37,608,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R0288:Pcdhb15
|
UTSW |
18 |
37,608,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Pcdhb15
|
UTSW |
18 |
37,607,221 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0400:Pcdhb15
|
UTSW |
18 |
37,608,948 (GRCm39) |
missense |
probably benign |
|
R0554:Pcdhb15
|
UTSW |
18 |
37,607,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R0637:Pcdhb15
|
UTSW |
18 |
37,608,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0714:Pcdhb15
|
UTSW |
18 |
37,607,674 (GRCm39) |
missense |
probably damaging |
0.98 |
R1118:Pcdhb15
|
UTSW |
18 |
37,606,815 (GRCm39) |
missense |
probably benign |
0.01 |
R1423:Pcdhb15
|
UTSW |
18 |
37,606,975 (GRCm39) |
missense |
probably damaging |
0.97 |
R1672:Pcdhb15
|
UTSW |
18 |
37,607,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Pcdhb15
|
UTSW |
18 |
37,609,084 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2206:Pcdhb15
|
UTSW |
18 |
37,608,075 (GRCm39) |
missense |
probably benign |
0.05 |
R2207:Pcdhb15
|
UTSW |
18 |
37,608,075 (GRCm39) |
missense |
probably benign |
0.05 |
R2274:Pcdhb15
|
UTSW |
18 |
37,608,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R3406:Pcdhb15
|
UTSW |
18 |
37,608,442 (GRCm39) |
missense |
probably benign |
0.41 |
R3407:Pcdhb15
|
UTSW |
18 |
37,607,442 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3417:Pcdhb15
|
UTSW |
18 |
37,608,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R3752:Pcdhb15
|
UTSW |
18 |
37,606,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Pcdhb15
|
UTSW |
18 |
37,608,943 (GRCm39) |
missense |
probably benign |
0.00 |
R4432:Pcdhb15
|
UTSW |
18 |
37,608,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R4433:Pcdhb15
|
UTSW |
18 |
37,608,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R4583:Pcdhb15
|
UTSW |
18 |
37,608,628 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4612:Pcdhb15
|
UTSW |
18 |
37,608,648 (GRCm39) |
missense |
probably damaging |
0.96 |
R4988:Pcdhb15
|
UTSW |
18 |
37,608,855 (GRCm39) |
missense |
probably damaging |
0.98 |
R5635:Pcdhb15
|
UTSW |
18 |
37,606,823 (GRCm39) |
nonsense |
probably null |
|
R5692:Pcdhb15
|
UTSW |
18 |
37,607,502 (GRCm39) |
missense |
probably benign |
0.01 |
R5742:Pcdhb15
|
UTSW |
18 |
37,607,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R5913:Pcdhb15
|
UTSW |
18 |
37,607,707 (GRCm39) |
missense |
probably benign |
0.07 |
R6350:Pcdhb15
|
UTSW |
18 |
37,608,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R6522:Pcdhb15
|
UTSW |
18 |
37,607,314 (GRCm39) |
missense |
probably benign |
0.35 |
R6676:Pcdhb15
|
UTSW |
18 |
37,607,860 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6693:Pcdhb15
|
UTSW |
18 |
37,607,394 (GRCm39) |
missense |
probably benign |
0.01 |
R6905:Pcdhb15
|
UTSW |
18 |
37,607,748 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7029:Pcdhb15
|
UTSW |
18 |
37,608,621 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7335:Pcdhb15
|
UTSW |
18 |
37,607,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Pcdhb15
|
UTSW |
18 |
37,607,526 (GRCm39) |
nonsense |
probably null |
|
R7718:Pcdhb15
|
UTSW |
18 |
37,608,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Pcdhb15
|
UTSW |
18 |
37,607,788 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7967:Pcdhb15
|
UTSW |
18 |
37,607,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R8170:Pcdhb15
|
UTSW |
18 |
37,608,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R8323:Pcdhb15
|
UTSW |
18 |
37,608,715 (GRCm39) |
missense |
probably benign |
0.18 |
R8725:Pcdhb15
|
UTSW |
18 |
37,608,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R8820:Pcdhb15
|
UTSW |
18 |
37,606,971 (GRCm39) |
missense |
probably benign |
0.03 |
R9117:Pcdhb15
|
UTSW |
18 |
37,608,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R9280:Pcdhb15
|
UTSW |
18 |
37,607,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R9367:Pcdhb15
|
UTSW |
18 |
37,607,971 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9424:Pcdhb15
|
UTSW |
18 |
37,607,263 (GRCm39) |
missense |
|
|
R9432:Pcdhb15
|
UTSW |
18 |
37,608,683 (GRCm39) |
missense |
probably benign |
0.04 |
R9498:Pcdhb15
|
UTSW |
18 |
37,606,890 (GRCm39) |
nonsense |
probably null |
|
R9544:Pcdhb15
|
UTSW |
18 |
37,608,948 (GRCm39) |
missense |
probably benign |
|
X0062:Pcdhb15
|
UTSW |
18 |
37,609,068 (GRCm39) |
nonsense |
probably null |
|
X0063:Pcdhb15
|
UTSW |
18 |
37,608,137 (GRCm39) |
nonsense |
probably null |
|
|