Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afap1l2 |
G |
A |
19: 56,902,682 (GRCm39) |
Q720* |
probably null |
Het |
Amph |
A |
G |
13: 19,278,984 (GRCm39) |
E153G |
probably damaging |
Het |
Atad2 |
T |
C |
15: 57,985,842 (GRCm39) |
|
probably benign |
Het |
Atosa |
A |
G |
9: 74,917,450 (GRCm39) |
D683G |
probably damaging |
Het |
Cntn2 |
C |
T |
1: 132,456,678 (GRCm39) |
V123I |
probably benign |
Het |
Dhrs2 |
C |
A |
14: 55,474,775 (GRCm39) |
Q137K |
probably benign |
Het |
Fam124a |
A |
G |
14: 62,843,353 (GRCm39) |
Y287C |
probably benign |
Het |
Flg2 |
C |
T |
3: 93,110,920 (GRCm39) |
R983W |
unknown |
Het |
Gm9637 |
G |
A |
14: 19,402,173 (GRCm38) |
|
noncoding transcript |
Het |
Helz2 |
A |
G |
2: 180,871,015 (GRCm39) |
|
probably null |
Het |
Iars1 |
G |
A |
13: 49,843,923 (GRCm39) |
|
probably null |
Het |
Igll1 |
A |
T |
16: 16,680,291 (GRCm39) |
|
probably null |
Het |
Iqch |
A |
G |
9: 63,432,196 (GRCm39) |
Y361H |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,527,765 (GRCm39) |
H105Q |
probably benign |
Het |
Mapk6 |
A |
G |
9: 75,305,084 (GRCm39) |
M111T |
probably damaging |
Het |
Mrtfa |
G |
A |
15: 80,929,523 (GRCm39) |
R27W |
probably damaging |
Het |
Mt1 |
T |
A |
8: 94,906,522 (GRCm39) |
|
probably benign |
Het |
Myh7b |
A |
T |
2: 155,474,671 (GRCm39) |
D1768V |
probably damaging |
Het |
Myo6 |
A |
T |
9: 80,168,159 (GRCm39) |
Q441L |
probably benign |
Het |
Nt5c3b |
A |
T |
11: 100,327,045 (GRCm39) |
Y84N |
probably damaging |
Het |
Ntmt2 |
T |
C |
1: 163,544,692 (GRCm39) |
D97G |
probably damaging |
Het |
Or1e29 |
A |
G |
11: 73,667,289 (GRCm39) |
F288S |
probably damaging |
Het |
Paxx |
A |
G |
2: 25,350,196 (GRCm39) |
L137P |
probably damaging |
Het |
Ptprz1 |
T |
C |
6: 22,972,834 (GRCm39) |
V248A |
probably damaging |
Het |
Rif1 |
T |
A |
2: 52,002,149 (GRCm39) |
C1868S |
probably damaging |
Het |
Sec23a |
A |
T |
12: 59,032,891 (GRCm39) |
C403S |
probably benign |
Het |
Skint4 |
G |
A |
4: 111,975,432 (GRCm39) |
V131I |
probably benign |
Het |
Sugp2 |
T |
C |
8: 70,695,837 (GRCm39) |
V270A |
possibly damaging |
Het |
Tmed9 |
A |
G |
13: 55,743,321 (GRCm39) |
D151G |
possibly damaging |
Het |
Tubgcp4 |
A |
G |
2: 121,007,071 (GRCm39) |
|
probably benign |
Het |
Uaca |
A |
G |
9: 60,777,148 (GRCm39) |
R512G |
probably damaging |
Het |
Unc80 |
A |
G |
1: 66,676,169 (GRCm39) |
Y1999C |
possibly damaging |
Het |
Vwf |
T |
A |
6: 125,640,523 (GRCm39) |
C2320S |
probably damaging |
Het |
|
Other mutations in Cep152 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Cep152
|
APN |
2 |
125,405,808 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00561:Cep152
|
APN |
2 |
125,405,643 (GRCm39) |
nonsense |
probably null |
|
IGL01082:Cep152
|
APN |
2 |
125,411,465 (GRCm39) |
splice site |
probably benign |
|
IGL01420:Cep152
|
APN |
2 |
125,405,572 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01832:Cep152
|
APN |
2 |
125,460,414 (GRCm39) |
nonsense |
probably null |
|
IGL02106:Cep152
|
APN |
2 |
125,444,856 (GRCm39) |
splice site |
probably null |
|
IGL02124:Cep152
|
APN |
2 |
125,405,381 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02349:Cep152
|
APN |
2 |
125,436,876 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02541:Cep152
|
APN |
2 |
125,447,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02659:Cep152
|
APN |
2 |
125,421,469 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02711:Cep152
|
APN |
2 |
125,405,862 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02737:Cep152
|
APN |
2 |
125,428,394 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03095:Cep152
|
APN |
2 |
125,460,371 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03186:Cep152
|
APN |
2 |
125,405,895 (GRCm39) |
missense |
probably benign |
|
IGL03306:Cep152
|
APN |
2 |
125,447,328 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0034:Cep152
|
UTSW |
2 |
125,425,813 (GRCm39) |
missense |
probably benign |
0.00 |
R0034:Cep152
|
UTSW |
2 |
125,425,813 (GRCm39) |
missense |
probably benign |
0.00 |
R0079:Cep152
|
UTSW |
2 |
125,460,373 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0244:Cep152
|
UTSW |
2 |
125,406,134 (GRCm39) |
missense |
probably benign |
0.00 |
R0390:Cep152
|
UTSW |
2 |
125,418,789 (GRCm39) |
splice site |
probably benign |
|
R0462:Cep152
|
UTSW |
2 |
125,425,854 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0480:Cep152
|
UTSW |
2 |
125,423,639 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0595:Cep152
|
UTSW |
2 |
125,436,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R0973:Cep152
|
UTSW |
2 |
125,436,819 (GRCm39) |
missense |
probably benign |
0.00 |
R0973:Cep152
|
UTSW |
2 |
125,436,819 (GRCm39) |
missense |
probably benign |
0.00 |
R1634:Cep152
|
UTSW |
2 |
125,425,809 (GRCm39) |
missense |
probably benign |
0.00 |
R1664:Cep152
|
UTSW |
2 |
125,408,174 (GRCm39) |
missense |
probably benign |
0.38 |
R1693:Cep152
|
UTSW |
2 |
125,408,174 (GRCm39) |
missense |
probably benign |
0.38 |
R1887:Cep152
|
UTSW |
2 |
125,462,225 (GRCm39) |
missense |
probably benign |
0.00 |
R1930:Cep152
|
UTSW |
2 |
125,460,291 (GRCm39) |
critical splice donor site |
probably null |
|
R2178:Cep152
|
UTSW |
2 |
125,421,954 (GRCm39) |
splice site |
probably null |
|
R2225:Cep152
|
UTSW |
2 |
125,423,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R2324:Cep152
|
UTSW |
2 |
125,405,382 (GRCm39) |
missense |
probably benign |
0.38 |
R2416:Cep152
|
UTSW |
2 |
125,406,092 (GRCm39) |
nonsense |
probably null |
|
R2845:Cep152
|
UTSW |
2 |
125,429,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R3753:Cep152
|
UTSW |
2 |
125,466,972 (GRCm39) |
unclassified |
probably benign |
|
R4212:Cep152
|
UTSW |
2 |
125,461,921 (GRCm39) |
missense |
probably benign |
0.00 |
R4304:Cep152
|
UTSW |
2 |
125,405,643 (GRCm39) |
nonsense |
probably null |
|
R4371:Cep152
|
UTSW |
2 |
125,454,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R4399:Cep152
|
UTSW |
2 |
125,429,900 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4536:Cep152
|
UTSW |
2 |
125,444,867 (GRCm39) |
splice site |
probably null |
|
R4713:Cep152
|
UTSW |
2 |
125,429,868 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4777:Cep152
|
UTSW |
2 |
125,406,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4779:Cep152
|
UTSW |
2 |
125,410,812 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4785:Cep152
|
UTSW |
2 |
125,428,249 (GRCm39) |
critical splice donor site |
probably null |
|
R4816:Cep152
|
UTSW |
2 |
125,405,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R4847:Cep152
|
UTSW |
2 |
125,460,394 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4898:Cep152
|
UTSW |
2 |
125,428,301 (GRCm39) |
missense |
probably benign |
0.03 |
R4934:Cep152
|
UTSW |
2 |
125,453,016 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4997:Cep152
|
UTSW |
2 |
125,428,271 (GRCm39) |
missense |
probably benign |
0.00 |
R5068:Cep152
|
UTSW |
2 |
125,413,736 (GRCm39) |
missense |
probably benign |
0.25 |
R5183:Cep152
|
UTSW |
2 |
125,408,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R5198:Cep152
|
UTSW |
2 |
125,429,544 (GRCm39) |
missense |
probably benign |
|
R5261:Cep152
|
UTSW |
2 |
125,406,125 (GRCm39) |
missense |
probably benign |
0.06 |
R5272:Cep152
|
UTSW |
2 |
125,452,950 (GRCm39) |
missense |
probably benign |
0.27 |
R5284:Cep152
|
UTSW |
2 |
125,421,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Cep152
|
UTSW |
2 |
125,405,552 (GRCm39) |
missense |
probably benign |
0.44 |
R6155:Cep152
|
UTSW |
2 |
125,423,620 (GRCm39) |
missense |
probably benign |
|
R6239:Cep152
|
UTSW |
2 |
125,421,332 (GRCm39) |
missense |
probably benign |
0.40 |
R6590:Cep152
|
UTSW |
2 |
125,406,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R6690:Cep152
|
UTSW |
2 |
125,406,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R6754:Cep152
|
UTSW |
2 |
125,429,588 (GRCm39) |
missense |
probably damaging |
0.99 |
R6798:Cep152
|
UTSW |
2 |
125,408,447 (GRCm39) |
splice site |
probably null |
|
R6816:Cep152
|
UTSW |
2 |
125,436,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R6977:Cep152
|
UTSW |
2 |
125,410,742 (GRCm39) |
critical splice donor site |
probably null |
|
R7125:Cep152
|
UTSW |
2 |
125,408,593 (GRCm39) |
nonsense |
probably null |
|
R7146:Cep152
|
UTSW |
2 |
125,456,325 (GRCm39) |
missense |
probably benign |
0.06 |
R7588:Cep152
|
UTSW |
2 |
125,411,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R7852:Cep152
|
UTSW |
2 |
125,432,033 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7883:Cep152
|
UTSW |
2 |
125,454,978 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8047:Cep152
|
UTSW |
2 |
125,406,247 (GRCm39) |
missense |
probably benign |
0.10 |
R8082:Cep152
|
UTSW |
2 |
125,428,313 (GRCm39) |
missense |
probably benign |
|
R8680:Cep152
|
UTSW |
2 |
125,406,131 (GRCm39) |
nonsense |
probably null |
|
R8739:Cep152
|
UTSW |
2 |
125,461,975 (GRCm39) |
missense |
probably benign |
0.06 |
R8744:Cep152
|
UTSW |
2 |
125,436,791 (GRCm39) |
critical splice donor site |
probably null |
|
R8896:Cep152
|
UTSW |
2 |
125,408,155 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8924:Cep152
|
UTSW |
2 |
125,444,778 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8971:Cep152
|
UTSW |
2 |
125,421,770 (GRCm39) |
nonsense |
probably null |
|
R9004:Cep152
|
UTSW |
2 |
125,453,020 (GRCm39) |
missense |
probably benign |
0.29 |
R9149:Cep152
|
UTSW |
2 |
125,463,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9149:Cep152
|
UTSW |
2 |
125,461,803 (GRCm39) |
missense |
probably damaging |
0.99 |
R9161:Cep152
|
UTSW |
2 |
125,408,574 (GRCm39) |
nonsense |
probably null |
|
R9239:Cep152
|
UTSW |
2 |
125,425,830 (GRCm39) |
missense |
probably benign |
0.02 |
R9249:Cep152
|
UTSW |
2 |
125,405,904 (GRCm39) |
missense |
probably benign |
0.38 |
R9258:Cep152
|
UTSW |
2 |
125,421,356 (GRCm39) |
nonsense |
probably null |
|
R9619:Cep152
|
UTSW |
2 |
125,436,827 (GRCm39) |
missense |
probably benign |
0.00 |
R9643:Cep152
|
UTSW |
2 |
125,406,150 (GRCm39) |
nonsense |
probably null |
|
R9775:Cep152
|
UTSW |
2 |
125,423,660 (GRCm39) |
nonsense |
probably null |
|
X0009:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0010:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0011:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0014:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Cep152
|
UTSW |
2 |
125,461,983 (GRCm39) |
missense |
probably benign |
0.07 |
X0023:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0033:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cep152
|
UTSW |
2 |
125,425,891 (GRCm39) |
missense |
probably benign |
0.23 |
Z1177:Cep152
|
UTSW |
2 |
125,461,624 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cep152
|
UTSW |
2 |
125,456,244 (GRCm39) |
missense |
probably benign |
0.33 |
|