Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox4 |
T |
G |
1: 58,291,233 (GRCm39) |
S784A |
probably benign |
Het |
Ap3d1 |
T |
A |
10: 80,552,425 (GRCm39) |
H581L |
probably benign |
Het |
Atp11a |
T |
C |
8: 12,899,781 (GRCm39) |
Y915H |
probably damaging |
Het |
Atp4b |
T |
C |
8: 13,437,514 (GRCm39) |
D213G |
probably benign |
Het |
Bcl11a |
A |
G |
11: 24,113,640 (GRCm39) |
S328G |
probably benign |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Cadps2 |
T |
A |
6: 23,410,876 (GRCm39) |
Y685F |
probably damaging |
Het |
Ccdc88b |
C |
T |
19: 6,831,203 (GRCm39) |
A580T |
probably benign |
Het |
Cdc42bpa |
GACAACA |
GACA |
1: 179,958,373 (GRCm39) |
|
probably benign |
Het |
Ces1c |
T |
C |
8: 93,833,254 (GRCm39) |
I404V |
probably benign |
Het |
Cr2 |
A |
T |
1: 194,851,581 (GRCm39) |
M137K |
possibly damaging |
Het |
Cyp2d40 |
T |
C |
15: 82,644,454 (GRCm39) |
Y257C |
unknown |
Het |
Dennd1c |
T |
A |
17: 57,381,512 (GRCm39) |
D116V |
probably damaging |
Het |
Dph2 |
G |
A |
4: 117,747,575 (GRCm39) |
R270* |
probably null |
Het |
Dpp8 |
A |
C |
9: 64,985,318 (GRCm39) |
H792P |
possibly damaging |
Het |
Dusp29 |
T |
C |
14: 21,736,763 (GRCm39) |
D113G |
probably benign |
Het |
Efs |
T |
C |
14: 55,157,756 (GRCm39) |
E185G |
possibly damaging |
Het |
Eml3 |
A |
G |
19: 8,914,056 (GRCm39) |
E480G |
probably damaging |
Het |
Fam193a |
A |
G |
5: 34,583,828 (GRCm39) |
T336A |
probably benign |
Het |
Fermt1 |
C |
T |
2: 132,783,852 (GRCm39) |
|
probably benign |
Het |
Galnt4 |
T |
A |
10: 98,945,955 (GRCm39) |
V560D |
probably damaging |
Het |
Gbp2b |
C |
A |
3: 142,309,327 (GRCm39) |
T146K |
probably damaging |
Het |
Gbp5 |
C |
T |
3: 142,211,308 (GRCm39) |
T346I |
probably damaging |
Het |
Glrx |
G |
T |
13: 75,995,317 (GRCm39) |
C79F |
probably damaging |
Het |
Glt8d2 |
T |
A |
10: 82,490,616 (GRCm39) |
T225S |
probably damaging |
Het |
Grm3 |
A |
G |
5: 9,562,483 (GRCm39) |
F456L |
possibly damaging |
Het |
Gse1 |
T |
G |
8: 121,303,185 (GRCm39) |
S1109A |
unknown |
Het |
Gstp3 |
A |
T |
19: 4,108,573 (GRCm39) |
L63Q |
probably damaging |
Het |
Hapln3 |
G |
A |
7: 78,767,239 (GRCm39) |
R267W |
probably benign |
Het |
Herc4 |
T |
A |
10: 63,147,286 (GRCm39) |
I801N |
possibly damaging |
Het |
Ido1 |
G |
T |
8: 25,077,880 (GRCm39) |
D153E |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kcnj9 |
T |
A |
1: 172,153,360 (GRCm39) |
S255C |
probably damaging |
Het |
Kpna3 |
T |
C |
14: 61,629,294 (GRCm39) |
N39D |
probably benign |
Het |
Krt39 |
A |
T |
11: 99,409,095 (GRCm39) |
S269T |
probably damaging |
Het |
Lfng |
G |
A |
5: 140,598,978 (GRCm39) |
V296I |
probably benign |
Het |
Lrit3 |
T |
A |
3: 129,585,132 (GRCm39) |
I209F |
probably damaging |
Het |
Map4k5 |
T |
A |
12: 69,870,275 (GRCm39) |
D523V |
possibly damaging |
Het |
Mdn1 |
C |
T |
4: 32,678,328 (GRCm39) |
P652L |
probably benign |
Het |
Med30 |
G |
A |
15: 52,584,516 (GRCm39) |
V145I |
possibly damaging |
Het |
Megf6 |
T |
A |
4: 154,326,860 (GRCm39) |
D163E |
probably damaging |
Het |
Meltf |
T |
A |
16: 31,709,522 (GRCm39) |
|
probably benign |
Het |
Mindy4 |
T |
C |
6: 55,255,223 (GRCm39) |
L567P |
probably benign |
Het |
Mppe1 |
T |
C |
18: 67,370,472 (GRCm39) |
D75G |
probably damaging |
Het |
Muc4 |
C |
T |
16: 32,754,673 (GRCm38) |
P1516S |
probably benign |
Het |
Myo3b |
C |
A |
2: 70,069,160 (GRCm39) |
F494L |
probably damaging |
Het |
Nedd4l |
A |
G |
18: 65,298,688 (GRCm39) |
T226A |
probably benign |
Het |
Nod1 |
A |
G |
6: 54,921,277 (GRCm39) |
V347A |
probably benign |
Het |
Nup210 |
A |
T |
6: 91,019,235 (GRCm39) |
|
probably null |
Het |
Nup210l |
A |
G |
3: 90,025,932 (GRCm39) |
R185G |
probably damaging |
Het |
Oma1 |
T |
C |
4: 103,210,829 (GRCm39) |
L445S |
probably damaging |
Het |
Or13p10 |
A |
T |
4: 118,523,502 (GRCm39) |
M263L |
probably benign |
Het |
Or5ac20 |
A |
T |
16: 59,104,452 (GRCm39) |
M136K |
probably damaging |
Het |
Or8g36 |
A |
G |
9: 39,422,770 (GRCm39) |
L82P |
probably damaging |
Het |
Oxsm |
A |
T |
14: 16,242,677 (GRCm38) |
F31I |
probably benign |
Het |
Pdcd5 |
A |
T |
7: 35,346,795 (GRCm39) |
M1K |
probably null |
Het |
Pkd1l2 |
T |
C |
8: 117,740,615 (GRCm39) |
T2161A |
possibly damaging |
Het |
Pla2g3 |
A |
T |
11: 3,442,151 (GRCm39) |
S404C |
probably null |
Het |
Plec |
A |
G |
15: 76,078,560 (GRCm39) |
V60A |
unknown |
Het |
Prpsap2 |
A |
G |
11: 61,643,736 (GRCm39) |
S66P |
possibly damaging |
Het |
Rarb |
A |
G |
14: 16,436,804 (GRCm38) |
L239P |
probably damaging |
Het |
Ryr3 |
A |
T |
2: 112,583,395 (GRCm39) |
Y2845* |
probably null |
Het |
Spta1 |
T |
C |
1: 174,045,548 (GRCm39) |
C1569R |
probably damaging |
Het |
Stard13 |
G |
A |
5: 150,986,115 (GRCm39) |
S465L |
probably damaging |
Het |
Tmub1 |
A |
T |
5: 24,651,680 (GRCm39) |
S80T |
probably benign |
Het |
Trpv5 |
A |
G |
6: 41,647,847 (GRCm39) |
F322S |
probably damaging |
Het |
Vmn2r5 |
G |
A |
3: 64,411,203 (GRCm39) |
A455V |
probably benign |
Het |
Washc4 |
T |
A |
10: 83,405,882 (GRCm39) |
N459K |
probably damaging |
Het |
Wdr11 |
C |
T |
7: 129,207,437 (GRCm39) |
R300* |
probably null |
Het |
Zer1 |
A |
G |
2: 29,993,430 (GRCm39) |
F559L |
probably damaging |
Het |
Zfat |
A |
T |
15: 68,052,519 (GRCm39) |
V425D |
probably damaging |
Het |
Zfp738 |
G |
A |
13: 67,817,910 (GRCm39) |
L694F |
|
Het |
Zfp839 |
C |
T |
12: 110,835,277 (GRCm39) |
A844V |
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 |
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 |
|
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 |
|