Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
T |
C |
5: 125,590,235 (GRCm39) |
F498S |
probably damaging |
Het |
Arhgap11a |
A |
G |
2: 113,664,601 (GRCm39) |
S561P |
probably benign |
Het |
Best3 |
T |
C |
10: 116,824,632 (GRCm39) |
Y33H |
probably damaging |
Het |
Cd209b |
T |
A |
8: 3,969,945 (GRCm39) |
|
probably benign |
Het |
Crabp2 |
A |
G |
3: 87,859,506 (GRCm39) |
Y52C |
probably damaging |
Het |
Crybg1 |
T |
C |
10: 43,868,505 (GRCm39) |
D1017G |
probably damaging |
Het |
Ctnna2 |
A |
T |
6: 76,957,744 (GRCm39) |
W137R |
probably damaging |
Het |
Cxcl9 |
T |
A |
5: 92,471,728 (GRCm39) |
H104L |
possibly damaging |
Het |
Ddr2 |
A |
G |
1: 169,811,996 (GRCm39) |
I742T |
possibly damaging |
Het |
Frem1 |
A |
G |
4: 82,877,626 (GRCm39) |
V223A |
possibly damaging |
Het |
Fzd10 |
T |
A |
5: 128,678,592 (GRCm39) |
I104N |
probably damaging |
Het |
Greb1 |
A |
G |
12: 16,761,962 (GRCm39) |
S473P |
probably damaging |
Het |
Gtf2i |
T |
C |
5: 134,271,602 (GRCm39) |
Y873C |
probably damaging |
Het |
Igsf6 |
T |
A |
7: 120,669,876 (GRCm39) |
K89* |
probably null |
Het |
Ints3 |
A |
G |
3: 90,313,636 (GRCm39) |
F331L |
probably damaging |
Het |
Kcnh3 |
A |
T |
15: 99,140,354 (GRCm39) |
H1080L |
possibly damaging |
Het |
Mettl15 |
A |
T |
2: 108,923,521 (GRCm39) |
Y300* |
probably null |
Het |
Mms19 |
A |
G |
19: 41,936,672 (GRCm39) |
F654L |
probably benign |
Het |
Myc |
A |
G |
15: 61,861,669 (GRCm39) |
H425R |
probably benign |
Het |
Ntn1 |
G |
T |
11: 68,117,445 (GRCm39) |
|
probably benign |
Het |
Ormdl2 |
C |
A |
10: 128,655,944 (GRCm39) |
G69W |
probably damaging |
Het |
Pdpr |
T |
C |
8: 111,828,704 (GRCm39) |
V69A |
possibly damaging |
Het |
Rbbp6 |
T |
C |
7: 122,587,908 (GRCm39) |
I254T |
probably damaging |
Het |
Sema6d |
A |
G |
2: 124,501,785 (GRCm39) |
R543G |
possibly damaging |
Het |
Slc18a1 |
C |
T |
8: 69,503,998 (GRCm39) |
A314T |
probably damaging |
Het |
Slc22a26 |
A |
G |
19: 7,760,201 (GRCm39) |
L514P |
probably damaging |
Het |
Slc22a28 |
A |
C |
19: 8,107,567 (GRCm39) |
S167A |
possibly damaging |
Het |
Speer1m |
A |
G |
5: 11,971,377 (GRCm39) |
S110G |
possibly damaging |
Het |
Tchh |
A |
G |
3: 93,352,606 (GRCm39) |
E682G |
unknown |
Het |
Thbs2 |
A |
T |
17: 14,889,097 (GRCm39) |
M1134K |
probably damaging |
Het |
Tmem26 |
A |
G |
10: 68,611,184 (GRCm39) |
S218G |
probably damaging |
Het |
Tmprss11c |
A |
T |
5: 86,387,254 (GRCm39) |
S208R |
probably benign |
Het |
Tnfrsf8 |
T |
C |
4: 145,019,161 (GRCm39) |
|
probably null |
Het |
Ush2a |
T |
C |
1: 188,596,875 (GRCm39) |
S3872P |
probably benign |
Het |
Vmn1r69 |
T |
C |
7: 10,313,879 (GRCm39) |
N205S |
probably benign |
Het |
Vmn2r54 |
T |
A |
7: 12,365,840 (GRCm39) |
|
probably benign |
Het |
Wwtr1 |
A |
T |
3: 57,370,942 (GRCm39) |
M328K |
possibly damaging |
Het |
Zfp64 |
G |
A |
2: 168,768,601 (GRCm39) |
S337L |
probably benign |
Het |
|
Other mutations in Cep152 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
IGL03060:Cep152
|
APN |
2 |
125,461,907 (GRCm39) |
splice site |
probably benign |
|
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 |
|