Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
A |
G |
12: 72,960,030 (GRCm39) |
M80T |
unknown |
Het |
4930578I06Rik |
A |
G |
14: 64,223,632 (GRCm39) |
L48P |
probably damaging |
Het |
Abcc9 |
A |
G |
6: 142,625,040 (GRCm39) |
S452P |
probably benign |
Het |
Adgrb2 |
T |
C |
4: 129,907,419 (GRCm39) |
F977S |
probably damaging |
Het |
Adgrf5 |
T |
G |
17: 43,737,896 (GRCm39) |
|
probably null |
Het |
Adgrl4 |
A |
G |
3: 151,144,914 (GRCm39) |
N21S |
probably benign |
Het |
Adss2 |
A |
T |
1: 177,612,517 (GRCm39) |
Y77* |
probably null |
Het |
Ahnak |
A |
T |
19: 8,984,452 (GRCm39) |
D1912V |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,740,325 (GRCm39) |
M1249T |
possibly damaging |
Het |
Akap6 |
A |
T |
12: 53,188,958 (GRCm39) |
D2124V |
possibly damaging |
Het |
Ankrd28 |
A |
T |
14: 31,453,982 (GRCm39) |
|
probably benign |
Het |
Bbs12 |
C |
A |
3: 37,374,712 (GRCm39) |
L387I |
probably damaging |
Het |
BC023105 |
T |
C |
18: 60,575,571 (GRCm39) |
|
noncoding transcript |
Het |
Ciita |
T |
C |
16: 10,328,948 (GRCm39) |
Y411H |
probably damaging |
Het |
Ckb |
TCCACCACCA |
TCCACCA |
12: 111,636,079 (GRCm39) |
|
probably benign |
Het |
Clec9a |
G |
A |
6: 129,387,249 (GRCm39) |
V35I |
probably benign |
Het |
Cntn5 |
T |
A |
9: 9,984,082 (GRCm39) |
Q382L |
possibly damaging |
Het |
Cracdl |
T |
C |
1: 37,663,364 (GRCm39) |
K845E |
possibly damaging |
Het |
Dock2 |
A |
T |
11: 34,598,169 (GRCm39) |
I334N |
probably damaging |
Het |
Dock9 |
G |
T |
14: 121,862,617 (GRCm39) |
T833K |
probably benign |
Het |
Drd2 |
G |
A |
9: 49,313,442 (GRCm39) |
V204I |
probably benign |
Het |
Fam120a |
A |
T |
13: 49,039,342 (GRCm39) |
I938N |
possibly damaging |
Het |
Fndc1 |
T |
C |
17: 7,990,621 (GRCm39) |
E1025G |
unknown |
Het |
Fsip2 |
G |
A |
2: 82,774,504 (GRCm39) |
D64N |
probably benign |
Het |
Gm14496 |
T |
A |
2: 181,641,989 (GRCm39) |
C553* |
probably null |
Het |
Gm15587 |
C |
G |
5: 24,572,467 (GRCm39) |
|
probably benign |
Het |
Gm6020 |
C |
T |
19: 61,172,391 (GRCm39) |
H22Y |
possibly damaging |
Het |
Gvin3 |
A |
T |
7: 106,196,630 (GRCm39) |
|
noncoding transcript |
Het |
Hexa |
A |
G |
9: 59,464,586 (GRCm39) |
T159A |
probably benign |
Het |
Hmcn1 |
C |
G |
1: 150,695,251 (GRCm39) |
A218P |
possibly damaging |
Het |
Hpgds |
A |
G |
6: 65,115,217 (GRCm39) |
F22S |
probably damaging |
Het |
Il5ra |
T |
A |
6: 106,708,874 (GRCm39) |
N289Y |
probably damaging |
Het |
Ilf2 |
T |
C |
3: 90,394,767 (GRCm39) |
|
probably benign |
Het |
Irf2 |
A |
T |
8: 47,260,388 (GRCm39) |
R107* |
probably null |
Het |
Kcnk6 |
T |
C |
7: 28,925,075 (GRCm39) |
I180M |
probably benign |
Het |
Krtap5-3 |
G |
A |
7: 141,755,979 (GRCm39) |
|
probably benign |
Het |
Lrig1 |
C |
T |
6: 94,631,859 (GRCm39) |
A114T |
probably benign |
Het |
Lrrc37a |
A |
G |
11: 103,389,587 (GRCm39) |
V1946A |
probably benign |
Het |
Lrrc8b |
T |
C |
5: 105,629,217 (GRCm39) |
V521A |
probably benign |
Het |
Macf1 |
T |
G |
4: 123,348,835 (GRCm39) |
I2154L |
possibly damaging |
Het |
Macf1 |
C |
A |
4: 123,368,505 (GRCm39) |
E2085D |
probably benign |
Het |
Maml1 |
C |
T |
11: 50,157,468 (GRCm39) |
A236T |
probably benign |
Het |
Mdc1 |
C |
A |
17: 36,165,117 (GRCm39) |
T1481K |
probably benign |
Het |
Mecp2 |
C |
T |
X: 73,080,781 (GRCm39) |
A79T |
probably damaging |
Homo |
Med24 |
A |
G |
11: 98,598,108 (GRCm39) |
|
probably benign |
Het |
Mfap3l |
T |
C |
8: 61,124,424 (GRCm39) |
V222A |
possibly damaging |
Het |
Mis18bp1 |
A |
G |
12: 65,196,102 (GRCm39) |
I554T |
probably benign |
Het |
Mpped2 |
T |
C |
2: 106,529,790 (GRCm39) |
I13T |
probably benign |
Het |
Mthfd1l |
C |
A |
10: 4,056,528 (GRCm39) |
T948K |
probably damaging |
Het |
Mtus1 |
C |
T |
8: 41,537,362 (GRCm39) |
S118N |
probably damaging |
Het |
Mtx3 |
A |
G |
13: 92,984,191 (GRCm39) |
E156G |
probably benign |
Het |
Mybbp1a |
C |
T |
11: 72,336,863 (GRCm39) |
T565I |
probably benign |
Het |
Myh2 |
G |
A |
11: 67,071,676 (GRCm39) |
V498M |
probably damaging |
Het |
Myo15b |
G |
A |
11: 115,777,899 (GRCm39) |
G1049S |
probably damaging |
Het |
Myo1b |
T |
A |
1: 51,799,562 (GRCm39) |
|
probably null |
Het |
Ndufa2 |
T |
A |
18: 36,877,573 (GRCm39) |
|
probably benign |
Het |
Nipal2 |
T |
C |
15: 34,625,167 (GRCm39) |
I129M |
possibly damaging |
Het |
Nt5dc3 |
A |
G |
10: 86,669,926 (GRCm39) |
N507S |
possibly damaging |
Het |
Or4b12 |
A |
G |
2: 90,095,913 (GRCm39) |
L287P |
probably damaging |
Het |
Or8b12b |
T |
A |
9: 37,684,163 (GRCm39) |
D69E |
possibly damaging |
Het |
Pcyt2 |
A |
G |
11: 120,508,677 (GRCm39) |
M1T |
probably null |
Het |
Pear1 |
C |
A |
3: 87,717,882 (GRCm39) |
|
probably benign |
Het |
Pla2g2d |
T |
C |
4: 138,503,126 (GRCm39) |
M1T |
probably null |
Het |
Plekhg6 |
T |
C |
6: 125,340,306 (GRCm39) |
T685A |
probably damaging |
Het |
Pramel19 |
T |
A |
4: 101,798,335 (GRCm39) |
V102E |
probably damaging |
Het |
Pwwp4a |
G |
T |
X: 72,171,261 (GRCm39) |
G218C |
probably damaging |
Homo |
Pxk |
T |
C |
14: 8,151,540 (GRCm38) |
S452P |
probably damaging |
Het |
Rab42 |
A |
T |
4: 132,030,529 (GRCm39) |
D40E |
probably benign |
Het |
Rapgef6 |
A |
C |
11: 54,551,654 (GRCm39) |
T836P |
probably damaging |
Het |
Rtn1 |
A |
G |
12: 72,283,307 (GRCm39) |
|
probably benign |
Het |
Serpina3a |
A |
G |
12: 104,082,362 (GRCm39) |
D45G |
probably benign |
Het |
Slco6b1 |
A |
G |
1: 96,849,786 (GRCm39) |
|
noncoding transcript |
Het |
Smad9 |
CTTT |
CTT |
3: 54,696,600 (GRCm39) |
|
probably benign |
Het |
Sntb1 |
T |
A |
15: 55,612,745 (GRCm39) |
R278* |
probably null |
Het |
Spice1 |
T |
G |
16: 44,185,989 (GRCm39) |
S111A |
probably damaging |
Het |
Stk40 |
T |
A |
4: 126,019,538 (GRCm39) |
L90Q |
probably damaging |
Het |
Syk |
A |
G |
13: 52,794,826 (GRCm39) |
Y520C |
probably damaging |
Het |
Syngr2 |
G |
A |
11: 117,704,224 (GRCm39) |
V170M |
possibly damaging |
Het |
Tcf12 |
A |
T |
9: 71,765,816 (GRCm39) |
D541E |
possibly damaging |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Tlr4 |
T |
C |
4: 66,759,409 (GRCm39) |
V734A |
probably damaging |
Het |
Tmem132a |
T |
C |
19: 10,840,863 (GRCm39) |
E389G |
probably damaging |
Het |
Tmem150b |
A |
G |
7: 4,712,044 (GRCm39) |
I112T |
probably benign |
Het |
Tmod1 |
C |
T |
4: 46,097,069 (GRCm39) |
|
silent |
Het |
Trbc1 |
G |
A |
6: 41,512,570 (GRCm39) |
|
probably benign |
Het |
Tril |
A |
G |
6: 53,796,577 (GRCm39) |
L215P |
probably damaging |
Het |
Trim24 |
G |
T |
6: 37,934,013 (GRCm39) |
R652L |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,623,151 (GRCm39) |
P15429S |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,706,302 (GRCm39) |
|
probably benign |
Het |
Tubgcp2 |
A |
G |
7: 139,579,183 (GRCm39) |
V701A |
probably damaging |
Het |
Tubgcp2 |
A |
G |
7: 139,586,069 (GRCm39) |
F407L |
probably damaging |
Het |
Usp45 |
T |
C |
4: 21,784,811 (GRCm39) |
|
probably benign |
Het |
Vmn1r30 |
A |
C |
6: 58,412,475 (GRCm39) |
L119R |
possibly damaging |
Het |
Washc5 |
A |
C |
15: 59,231,174 (GRCm39) |
L363R |
probably damaging |
Het |
Zan |
T |
C |
5: 137,387,590 (GRCm39) |
T4874A |
unknown |
Het |
Zfp420 |
A |
T |
7: 29,573,933 (GRCm39) |
H51L |
probably damaging |
Het |
Zfp512b |
C |
A |
2: 181,230,235 (GRCm39) |
R497L |
probably damaging |
Het |
Zmat4 |
A |
G |
8: 24,505,177 (GRCm39) |
N139S |
probably damaging |
Het |
Zng1 |
A |
T |
19: 24,932,769 (GRCm39) |
V88D |
probably damaging |
Het |
|
Other mutations in Pcdhb17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00950:Pcdhb17
|
APN |
18 |
37,619,059 (GRCm39) |
splice site |
probably null |
|
IGL01367:Pcdhb17
|
APN |
18 |
37,620,548 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01923:Pcdhb17
|
APN |
18 |
37,619,790 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02060:Pcdhb17
|
APN |
18 |
37,619,469 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02494:Pcdhb17
|
APN |
18 |
37,618,347 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02654:Pcdhb17
|
APN |
18 |
37,619,614 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03168:Pcdhb17
|
APN |
18 |
37,618,825 (GRCm39) |
missense |
probably benign |
0.15 |
doughnut
|
UTSW |
18 |
37,619,989 (GRCm39) |
missense |
probably damaging |
1.00 |
miniscule
|
UTSW |
18 |
37,618,720 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4434001:Pcdhb17
|
UTSW |
18 |
37,618,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Pcdhb17
|
UTSW |
18 |
37,618,888 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1013:Pcdhb17
|
UTSW |
18 |
37,619,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R1052:Pcdhb17
|
UTSW |
18 |
37,619,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1226:Pcdhb17
|
UTSW |
18 |
37,620,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R1258:Pcdhb17
|
UTSW |
18 |
37,618,587 (GRCm39) |
missense |
probably damaging |
0.98 |
R1335:Pcdhb17
|
UTSW |
18 |
37,619,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R1443:Pcdhb17
|
UTSW |
18 |
37,619,701 (GRCm39) |
missense |
probably benign |
0.15 |
R1451:Pcdhb17
|
UTSW |
18 |
37,619,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R1505:Pcdhb17
|
UTSW |
18 |
37,619,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R1591:Pcdhb17
|
UTSW |
18 |
37,618,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R1742:Pcdhb17
|
UTSW |
18 |
37,619,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R1750:Pcdhb17
|
UTSW |
18 |
37,620,070 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1750:Pcdhb17
|
UTSW |
18 |
37,618,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R1764:Pcdhb17
|
UTSW |
18 |
37,620,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R1863:Pcdhb17
|
UTSW |
18 |
37,619,164 (GRCm39) |
missense |
probably benign |
0.00 |
R1888:Pcdhb17
|
UTSW |
18 |
37,620,438 (GRCm39) |
splice site |
probably null |
|
R2095:Pcdhb17
|
UTSW |
18 |
37,619,375 (GRCm39) |
missense |
probably benign |
0.14 |
R4565:Pcdhb17
|
UTSW |
18 |
37,619,523 (GRCm39) |
missense |
probably benign |
0.14 |
R4658:Pcdhb17
|
UTSW |
18 |
37,619,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R4669:Pcdhb17
|
UTSW |
18 |
37,619,259 (GRCm39) |
missense |
probably damaging |
0.99 |
R4816:Pcdhb17
|
UTSW |
18 |
37,620,450 (GRCm39) |
missense |
probably benign |
0.39 |
R4910:Pcdhb17
|
UTSW |
18 |
37,618,212 (GRCm39) |
start codon destroyed |
possibly damaging |
0.90 |
R5209:Pcdhb17
|
UTSW |
18 |
37,620,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R5248:Pcdhb17
|
UTSW |
18 |
37,618,939 (GRCm39) |
missense |
probably benign |
0.00 |
R5254:Pcdhb17
|
UTSW |
18 |
37,619,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R5494:Pcdhb17
|
UTSW |
18 |
37,620,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R5544:Pcdhb17
|
UTSW |
18 |
37,620,474 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5952:Pcdhb17
|
UTSW |
18 |
37,620,133 (GRCm39) |
missense |
probably benign |
0.04 |
R5977:Pcdhb17
|
UTSW |
18 |
37,618,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R6262:Pcdhb17
|
UTSW |
18 |
37,619,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R6311:Pcdhb17
|
UTSW |
18 |
37,619,316 (GRCm39) |
splice site |
probably null |
|
R6495:Pcdhb17
|
UTSW |
18 |
37,618,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R6710:Pcdhb17
|
UTSW |
18 |
37,618,452 (GRCm39) |
missense |
probably damaging |
0.96 |
R7097:Pcdhb17
|
UTSW |
18 |
37,619,566 (GRCm39) |
missense |
probably benign |
|
R7122:Pcdhb17
|
UTSW |
18 |
37,619,566 (GRCm39) |
missense |
probably benign |
|
R7130:Pcdhb17
|
UTSW |
18 |
37,618,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7437:Pcdhb17
|
UTSW |
18 |
37,619,145 (GRCm39) |
missense |
probably benign |
0.01 |
R7642:Pcdhb17
|
UTSW |
18 |
37,618,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R7703:Pcdhb17
|
UTSW |
18 |
37,619,801 (GRCm39) |
missense |
probably benign |
0.01 |
R7771:Pcdhb17
|
UTSW |
18 |
37,619,962 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7898:Pcdhb17
|
UTSW |
18 |
37,618,233 (GRCm39) |
missense |
probably benign |
0.00 |
R8028:Pcdhb17
|
UTSW |
18 |
37,620,502 (GRCm39) |
missense |
probably benign |
0.03 |
R8299:Pcdhb17
|
UTSW |
18 |
37,618,408 (GRCm39) |
missense |
probably damaging |
0.98 |
R8560:Pcdhb17
|
UTSW |
18 |
37,619,206 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8844:Pcdhb17
|
UTSW |
18 |
37,618,801 (GRCm39) |
missense |
probably benign |
0.12 |
R8925:Pcdhb17
|
UTSW |
18 |
37,620,372 (GRCm39) |
missense |
probably benign |
0.40 |
R8927:Pcdhb17
|
UTSW |
18 |
37,620,372 (GRCm39) |
missense |
probably benign |
0.40 |
R9050:Pcdhb17
|
UTSW |
18 |
37,620,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R9162:Pcdhb17
|
UTSW |
18 |
37,620,168 (GRCm39) |
missense |
probably damaging |
0.97 |
R9243:Pcdhb17
|
UTSW |
18 |
37,619,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R9286:Pcdhb17
|
UTSW |
18 |
37,619,422 (GRCm39) |
missense |
probably benign |
0.26 |
R9472:Pcdhb17
|
UTSW |
18 |
37,618,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R9617:Pcdhb17
|
UTSW |
18 |
37,618,218 (GRCm39) |
missense |
probably benign |
|
R9625:Pcdhb17
|
UTSW |
18 |
37,619,419 (GRCm39) |
nonsense |
probably null |
|
R9646:Pcdhb17
|
UTSW |
18 |
37,618,471 (GRCm39) |
missense |
possibly damaging |
0.64 |
X0062:Pcdhb17
|
UTSW |
18 |
37,619,542 (GRCm39) |
missense |
probably benign |
|
X0064:Pcdhb17
|
UTSW |
18 |
37,619,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|