Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930438A08Rik |
C |
A |
11: 58,182,260 (GRCm39) |
|
probably null |
Het |
Adam2 |
A |
G |
14: 66,272,165 (GRCm39) |
|
probably null |
Het |
Akt2 |
A |
T |
7: 27,317,738 (GRCm39) |
D94V |
probably benign |
Het |
Anapc7 |
C |
T |
5: 122,566,211 (GRCm39) |
S40L |
probably benign |
Het |
Ash1l |
G |
T |
3: 88,965,890 (GRCm39) |
A2431S |
possibly damaging |
Het |
Atoh1 |
A |
T |
6: 64,706,902 (GRCm39) |
Q199L |
probably damaging |
Het |
Atp10b |
T |
C |
11: 43,121,177 (GRCm39) |
C947R |
probably damaging |
Het |
Ccdc50 |
G |
A |
16: 27,255,148 (GRCm39) |
V199I |
possibly damaging |
Het |
Ccne1 |
A |
T |
7: 37,802,598 (GRCm39) |
C65S |
probably benign |
Het |
Col6a3 |
C |
G |
1: 90,695,328 (GRCm39) |
|
probably benign |
Het |
Cyp4a10 |
A |
G |
4: 115,386,667 (GRCm39) |
D438G |
probably benign |
Het |
Dgkb |
A |
G |
12: 38,488,611 (GRCm39) |
H659R |
probably damaging |
Het |
Dhx29 |
A |
G |
13: 113,089,418 (GRCm39) |
I730V |
possibly damaging |
Het |
Dync2h1 |
G |
A |
9: 7,011,220 (GRCm39) |
Q3658* |
probably null |
Het |
Eif2ak4 |
C |
A |
2: 118,261,474 (GRCm39) |
C671* |
probably null |
Het |
Eif4g3 |
AGCGGCGGCGGCGGCGGC |
AGCGGCGGCGGCGGC |
4: 137,721,372 (GRCm39) |
|
probably benign |
Het |
Ep400 |
T |
C |
5: 110,889,925 (GRCm39) |
H446R |
unknown |
Het |
Epb41l2 |
C |
T |
10: 25,317,725 (GRCm39) |
L81F |
probably damaging |
Het |
Ercc8 |
G |
A |
13: 108,320,307 (GRCm39) |
A298T |
probably benign |
Het |
Fbxo10 |
T |
C |
4: 45,043,880 (GRCm39) |
M648V |
probably benign |
Het |
G530012D18Rik |
C |
G |
1: 85,504,935 (GRCm39) |
D113E |
unknown |
Het |
Gnpda2 |
C |
T |
5: 69,735,459 (GRCm39) |
A211T |
probably damaging |
Het |
Gtf2h5 |
C |
CA |
17: 6,134,833 (GRCm39) |
|
probably null |
Het |
Hormad1 |
T |
C |
3: 95,469,926 (GRCm39) |
Y58H |
possibly damaging |
Het |
Igkv4-81 |
T |
C |
6: 68,968,046 (GRCm39) |
I18M |
possibly damaging |
Het |
Itgav |
G |
T |
2: 83,600,427 (GRCm39) |
A312S |
probably benign |
Het |
Itpr1 |
G |
T |
6: 108,354,763 (GRCm39) |
A457S |
possibly damaging |
Het |
Kcna10 |
T |
C |
3: 107,101,702 (GRCm39) |
L111P |
probably damaging |
Het |
Kcnh7 |
T |
C |
2: 63,012,433 (GRCm39) |
R92G |
possibly damaging |
Het |
Lamc2 |
G |
A |
1: 153,019,484 (GRCm39) |
P486S |
probably benign |
Het |
Lrba |
C |
T |
3: 86,211,640 (GRCm39) |
T420M |
probably benign |
Het |
Lrrc52 |
G |
A |
1: 167,294,150 (GRCm39) |
T45M |
probably benign |
Het |
Lsm8 |
C |
A |
6: 18,853,638 (GRCm39) |
A80E |
probably benign |
Het |
Ly6g |
T |
A |
15: 75,027,518 (GRCm39) |
S9T |
probably benign |
Het |
Mcc |
A |
G |
18: 44,857,639 (GRCm39) |
Y159H |
probably benign |
Het |
Megf11 |
T |
C |
9: 64,451,970 (GRCm39) |
|
probably null |
Het |
Mrpl9 |
T |
A |
3: 94,355,082 (GRCm39) |
|
probably benign |
Het |
Ndst4 |
T |
C |
3: 125,506,989 (GRCm39) |
F210L |
possibly damaging |
Het |
Or13l2 |
A |
G |
3: 97,317,597 (GRCm39) |
V300A |
probably benign |
Het |
Or5d40 |
T |
A |
2: 88,015,723 (GRCm39) |
C167* |
probably null |
Het |
Pappa2 |
A |
G |
1: 158,611,487 (GRCm39) |
V1492A |
possibly damaging |
Het |
Pcdhga2 |
A |
G |
18: 37,804,373 (GRCm39) |
H739R |
probably benign |
Het |
Pcdhga8 |
A |
G |
18: 37,860,827 (GRCm39) |
T628A |
probably damaging |
Het |
Plekhn1 |
C |
T |
4: 156,318,364 (GRCm39) |
R86H |
probably damaging |
Het |
Pofut1 |
T |
A |
2: 153,101,461 (GRCm39) |
W72R |
probably benign |
Het |
Polr3b |
C |
A |
10: 84,464,488 (GRCm39) |
|
probably benign |
Het |
Rab3b |
A |
T |
4: 108,781,184 (GRCm39) |
I104F |
probably damaging |
Het |
Rab5b |
A |
T |
10: 128,518,751 (GRCm39) |
V127D |
probably damaging |
Het |
Rnf170 |
A |
G |
8: 26,619,408 (GRCm39) |
M211V |
unknown |
Het |
Rpl7 |
T |
C |
1: 16,172,113 (GRCm39) |
T218A |
probably benign |
Het |
Serinc2 |
T |
C |
4: 130,158,988 (GRCm39) |
|
probably benign |
Het |
Socs2 |
T |
A |
10: 95,228,662 (GRCm39) |
Q196L |
|
Het |
Stab2 |
T |
C |
10: 86,805,213 (GRCm39) |
H255R |
probably benign |
Het |
Syvn1 |
G |
A |
19: 6,099,198 (GRCm39) |
G149D |
probably damaging |
Het |
Them5 |
T |
C |
3: 94,253,472 (GRCm39) |
S161P |
probably damaging |
Het |
Tlr1 |
A |
T |
5: 65,083,873 (GRCm39) |
Y235N |
possibly damaging |
Het |
Toporsl |
T |
C |
4: 52,611,967 (GRCm39) |
L620P |
probably benign |
Het |
Traf3 |
A |
T |
12: 111,228,230 (GRCm39) |
E480D |
probably benign |
Het |
Trav13n-4 |
A |
G |
14: 53,601,399 (GRCm39) |
Y56C |
probably damaging |
Het |
Trps1 |
T |
C |
15: 50,524,642 (GRCm39) |
Y1096C |
probably damaging |
Het |
Usp2 |
A |
G |
9: 43,998,510 (GRCm39) |
|
probably benign |
Het |
Usp40 |
A |
T |
1: 87,911,491 (GRCm39) |
L512Q |
probably benign |
Het |
Vmn1r175 |
T |
C |
7: 23,508,403 (GRCm39) |
T75A |
probably benign |
Het |
Zan |
A |
G |
5: 137,426,126 (GRCm39) |
V2550A |
unknown |
Het |
Zfp235 |
A |
T |
7: 23,839,924 (GRCm39) |
E114D |
possibly damaging |
Het |
Zmym1 |
A |
T |
4: 126,945,165 (GRCm39) |
D141E |
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 |
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 |
|