Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
A |
T |
18: 6,638,618 (GRCm39) |
E339V |
possibly damaging |
Het |
9230009I02Rik |
A |
T |
11: 50,982,405 (GRCm39) |
|
noncoding transcript |
Het |
9230112D13Rik |
A |
T |
14: 34,234,054 (GRCm39) |
I79K |
unknown |
Het |
Adam25 |
C |
T |
8: 41,208,987 (GRCm39) |
T751I |
probably benign |
Het |
Adgrv1 |
C |
A |
13: 81,727,015 (GRCm39) |
V446L |
probably damaging |
Het |
Afap1 |
C |
A |
5: 36,125,944 (GRCm39) |
A313D |
possibly damaging |
Het |
Akap6 |
A |
G |
12: 52,934,766 (GRCm39) |
T753A |
probably benign |
Het |
Aldh16a1 |
G |
T |
7: 44,792,262 (GRCm39) |
T730N |
probably damaging |
Het |
Amfr |
A |
T |
8: 94,725,736 (GRCm39) |
M215K |
probably damaging |
Het |
Apob |
A |
G |
12: 8,066,188 (GRCm39) |
R4386G |
possibly damaging |
Het |
Arhgap45 |
A |
T |
10: 79,857,917 (GRCm39) |
M217L |
possibly damaging |
Het |
Baiap2l2 |
C |
T |
15: 79,168,276 (GRCm39) |
E49K |
possibly damaging |
Het |
Baz1a |
C |
T |
12: 54,981,605 (GRCm39) |
E350K |
possibly damaging |
Het |
Bbx |
A |
T |
16: 50,086,647 (GRCm39) |
V83D |
probably damaging |
Het |
Btaf1 |
T |
C |
19: 36,928,586 (GRCm39) |
|
probably benign |
Het |
Cacna2d1 |
G |
A |
5: 16,567,271 (GRCm39) |
E942K |
probably benign |
Het |
Cad |
T |
C |
5: 31,219,531 (GRCm39) |
|
probably benign |
Het |
Ccdc96 |
A |
G |
5: 36,643,710 (GRCm39) |
K572R |
probably benign |
Het |
Cdc5l |
G |
A |
17: 45,726,610 (GRCm39) |
R321W |
probably damaging |
Het |
Cir1 |
A |
G |
2: 73,140,799 (GRCm39) |
|
probably null |
Het |
Crocc |
A |
G |
4: 140,757,558 (GRCm39) |
S912P |
possibly damaging |
Het |
Cwf19l2 |
T |
C |
9: 3,431,057 (GRCm39) |
L463P |
probably benign |
Het |
Cyp3a59 |
C |
T |
5: 146,033,463 (GRCm39) |
Q200* |
probably null |
Het |
Cyp4b1 |
G |
T |
4: 115,484,073 (GRCm39) |
P303T |
probably damaging |
Het |
Dcbld1 |
C |
A |
10: 52,193,173 (GRCm39) |
T306K |
probably benign |
Het |
Dgat2 |
A |
G |
7: 98,818,988 (GRCm39) |
V56A |
possibly damaging |
Het |
Dnajc16 |
A |
C |
4: 141,516,320 (GRCm39) |
L16R |
probably damaging |
Het |
Dnmt1 |
A |
C |
9: 20,829,852 (GRCm39) |
|
probably benign |
Het |
Dus3l |
A |
G |
17: 57,076,308 (GRCm39) |
I528V |
probably damaging |
Het |
Egflam |
T |
C |
15: 7,263,718 (GRCm39) |
D744G |
probably benign |
Het |
Epb41 |
A |
C |
4: 131,706,106 (GRCm39) |
|
probably benign |
Het |
Eri2 |
C |
T |
7: 119,385,206 (GRCm39) |
V432I |
probably benign |
Het |
Esyt2 |
A |
G |
12: 116,320,818 (GRCm39) |
|
probably benign |
Het |
Extl3 |
A |
T |
14: 65,315,122 (GRCm39) |
M20K |
probably benign |
Het |
Fam32a |
A |
G |
8: 72,976,063 (GRCm39) |
Y103C |
probably damaging |
Het |
Fat4 |
T |
C |
3: 39,035,870 (GRCm39) |
V3174A |
probably benign |
Het |
Fbxo40 |
T |
A |
16: 36,789,984 (GRCm39) |
E375D |
possibly damaging |
Het |
Frrs1 |
A |
G |
3: 116,676,813 (GRCm39) |
T182A |
probably benign |
Het |
Fry |
A |
G |
5: 150,357,172 (GRCm39) |
|
probably benign |
Het |
Fry |
T |
C |
5: 150,402,226 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,808,129 (GRCm39) |
I1483V |
probably benign |
Het |
Glra3 |
T |
A |
8: 56,578,111 (GRCm39) |
D389E |
probably benign |
Het |
Gpr3 |
A |
T |
4: 132,937,796 (GRCm39) |
I292N |
probably damaging |
Het |
Grina |
T |
C |
15: 76,133,045 (GRCm39) |
M230T |
probably damaging |
Het |
Igkv11-125 |
G |
A |
6: 67,890,603 (GRCm39) |
W16* |
probably null |
Het |
Il18r1 |
T |
C |
1: 40,514,061 (GRCm39) |
V89A |
probably damaging |
Het |
Ino80 |
T |
C |
2: 119,212,464 (GRCm39) |
E1286G |
possibly damaging |
Het |
Iqch |
G |
A |
9: 63,415,514 (GRCm39) |
|
probably benign |
Het |
Itpr2 |
G |
T |
6: 146,013,898 (GRCm39) |
Q2666K |
probably damaging |
Het |
Kcnh3 |
A |
G |
15: 99,130,844 (GRCm39) |
D487G |
probably damaging |
Het |
Kdm1a |
A |
G |
4: 136,288,377 (GRCm39) |
L402P |
probably damaging |
Het |
Klhl10 |
T |
G |
11: 100,337,937 (GRCm39) |
|
probably benign |
Het |
Krt39 |
T |
C |
11: 99,405,617 (GRCm39) |
T428A |
possibly damaging |
Het |
Mapk3 |
G |
A |
7: 126,362,558 (GRCm39) |
|
probably benign |
Het |
Med13l |
T |
A |
5: 118,897,188 (GRCm39) |
S2089T |
possibly damaging |
Het |
Mex3c |
G |
A |
18: 73,723,124 (GRCm39) |
D406N |
possibly damaging |
Het |
Mki67 |
G |
A |
7: 135,299,893 (GRCm39) |
R1714* |
probably null |
Het |
Mmp9 |
C |
A |
2: 164,791,740 (GRCm39) |
S211* |
probably null |
Het |
Nat8f2 |
G |
T |
6: 85,844,784 (GRCm39) |
Q193K |
probably benign |
Het |
Omt2a |
C |
A |
9: 78,220,187 (GRCm39) |
A71S |
possibly damaging |
Het |
Or10ak11 |
T |
G |
4: 118,686,897 (GRCm39) |
T247P |
probably damaging |
Het |
Or5ac22 |
T |
C |
16: 59,134,964 (GRCm39) |
K269E |
probably benign |
Het |
Pdgfra |
G |
A |
5: 75,331,434 (GRCm39) |
V315I |
probably benign |
Het |
Pdgfrb |
A |
G |
18: 61,216,337 (GRCm39) |
D1065G |
probably damaging |
Het |
Pfas |
A |
T |
11: 68,893,455 (GRCm39) |
|
probably benign |
Het |
Pramel5 |
T |
C |
4: 143,999,310 (GRCm39) |
E259G |
probably benign |
Het |
Prpf6 |
A |
G |
2: 181,264,004 (GRCm39) |
Y222C |
possibly damaging |
Het |
Rbck1 |
C |
A |
2: 152,166,250 (GRCm39) |
Q229H |
probably damaging |
Het |
Rdm1 |
T |
A |
11: 101,526,661 (GRCm39) |
C278S |
probably benign |
Het |
Sall1 |
T |
C |
8: 89,759,819 (GRCm39) |
D95G |
probably benign |
Het |
Scn1a |
T |
A |
2: 66,148,167 (GRCm39) |
D1126V |
probably damaging |
Het |
Scn4a |
C |
T |
11: 106,221,226 (GRCm39) |
G811D |
probably benign |
Het |
Sh2b1 |
A |
G |
7: 126,071,444 (GRCm39) |
I247T |
probably benign |
Het |
Shprh |
C |
A |
10: 11,038,556 (GRCm39) |
T437K |
possibly damaging |
Het |
Slc13a4 |
A |
T |
6: 35,264,339 (GRCm39) |
|
probably null |
Het |
Slc16a1 |
C |
A |
3: 104,560,734 (GRCm39) |
Y346* |
probably null |
Het |
Slc25a38 |
G |
T |
9: 119,949,772 (GRCm39) |
A163S |
probably damaging |
Het |
Slc6a12 |
G |
A |
6: 121,333,877 (GRCm39) |
V238I |
probably damaging |
Het |
Slc8b1 |
C |
A |
5: 120,657,736 (GRCm39) |
D66E |
probably damaging |
Het |
Snapin |
A |
G |
3: 90,396,893 (GRCm39) |
L106P |
probably damaging |
Het |
Tas2r122 |
G |
A |
6: 132,688,791 (GRCm39) |
S34F |
possibly damaging |
Het |
Tiam2 |
A |
G |
17: 3,471,921 (GRCm39) |
K521R |
probably damaging |
Het |
Tmem81 |
C |
G |
1: 132,435,567 (GRCm39) |
I124M |
probably damaging |
Het |
Ttc3 |
T |
C |
16: 94,188,189 (GRCm39) |
|
probably benign |
Het |
Uba1y |
T |
C |
Y: 820,911 (GRCm39) |
F31L |
probably benign |
Het |
Ucp3 |
A |
G |
7: 100,131,186 (GRCm39) |
|
probably benign |
Het |
Vcan |
T |
C |
13: 89,851,891 (GRCm39) |
E1023G |
probably damaging |
Het |
Vmn2r45 |
A |
G |
7: 8,474,820 (GRCm39) |
I736T |
probably damaging |
Het |
Vps36 |
T |
C |
8: 22,708,261 (GRCm39) |
F342L |
probably benign |
Het |
Zc3hc1 |
A |
G |
6: 30,374,929 (GRCm39) |
|
probably benign |
Het |
Zmym4 |
G |
A |
4: 126,792,194 (GRCm39) |
Q596* |
probably null |
Het |
|
Other mutations in Cep164 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00983:Cep164
|
APN |
9 |
45,686,554 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01571:Cep164
|
APN |
9 |
45,705,636 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01985:Cep164
|
APN |
9 |
45,690,904 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01989:Cep164
|
APN |
9 |
45,704,313 (GRCm39) |
splice site |
probably benign |
|
IGL02130:Cep164
|
APN |
9 |
45,691,090 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02598:Cep164
|
APN |
9 |
45,682,002 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03206:Cep164
|
APN |
9 |
45,714,023 (GRCm39) |
missense |
probably benign |
0.00 |
R0063:Cep164
|
UTSW |
9 |
45,679,916 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0109:Cep164
|
UTSW |
9 |
45,682,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R0528:Cep164
|
UTSW |
9 |
45,688,234 (GRCm39) |
unclassified |
probably benign |
|
R1445:Cep164
|
UTSW |
9 |
45,690,198 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1753:Cep164
|
UTSW |
9 |
45,704,235 (GRCm39) |
missense |
probably damaging |
0.99 |
R1824:Cep164
|
UTSW |
9 |
45,690,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Cep164
|
UTSW |
9 |
45,687,056 (GRCm39) |
splice site |
probably null |
|
R1858:Cep164
|
UTSW |
9 |
45,734,938 (GRCm39) |
splice site |
probably benign |
|
R1900:Cep164
|
UTSW |
9 |
45,721,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Cep164
|
UTSW |
9 |
45,682,104 (GRCm39) |
missense |
probably benign |
0.09 |
R2032:Cep164
|
UTSW |
9 |
45,682,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Cep164
|
UTSW |
9 |
45,714,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R2186:Cep164
|
UTSW |
9 |
45,679,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Cep164
|
UTSW |
9 |
45,686,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R4424:Cep164
|
UTSW |
9 |
45,691,002 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5126:Cep164
|
UTSW |
9 |
45,698,722 (GRCm39) |
critical splice donor site |
probably null |
|
R5997:Cep164
|
UTSW |
9 |
45,680,761 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6186:Cep164
|
UTSW |
9 |
45,705,407 (GRCm39) |
missense |
probably damaging |
0.98 |
R6357:Cep164
|
UTSW |
9 |
45,682,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R6385:Cep164
|
UTSW |
9 |
45,691,081 (GRCm39) |
missense |
probably damaging |
0.99 |
R6632:Cep164
|
UTSW |
9 |
45,691,088 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6957:Cep164
|
UTSW |
9 |
45,683,578 (GRCm39) |
critical splice donor site |
probably null |
|
R7310:Cep164
|
UTSW |
9 |
45,686,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R7420:Cep164
|
UTSW |
9 |
45,679,840 (GRCm39) |
missense |
probably benign |
0.01 |
R7651:Cep164
|
UTSW |
9 |
45,685,150 (GRCm39) |
missense |
probably benign |
0.18 |
R7918:Cep164
|
UTSW |
9 |
45,690,986 (GRCm39) |
critical splice donor site |
probably null |
|
R7982:Cep164
|
UTSW |
9 |
45,690,162 (GRCm39) |
missense |
probably benign |
0.40 |
R8010:Cep164
|
UTSW |
9 |
45,734,969 (GRCm39) |
missense |
unknown |
|
R8391:Cep164
|
UTSW |
9 |
45,718,491 (GRCm39) |
missense |
unknown |
|
R8553:Cep164
|
UTSW |
9 |
45,718,508 (GRCm39) |
unclassified |
probably benign |
|
R8700:Cep164
|
UTSW |
9 |
45,686,667 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9177:Cep164
|
UTSW |
9 |
45,691,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:Cep164
|
UTSW |
9 |
45,717,708 (GRCm39) |
missense |
unknown |
|
R9460:Cep164
|
UTSW |
9 |
45,685,282 (GRCm39) |
missense |
probably benign |
|
R9729:Cep164
|
UTSW |
9 |
45,682,897 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:Cep164
|
UTSW |
9 |
45,687,161 (GRCm39) |
critical splice donor site |
probably null |
|
X0028:Cep164
|
UTSW |
9 |
45,682,265 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Cep164
|
UTSW |
9 |
45,686,085 (GRCm39) |
missense |
probably benign |
0.03 |
|