Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310009B15Rik |
A |
G |
1: 138,779,857 (GRCm39) |
S132P |
probably damaging |
Het |
Abcb5 |
A |
G |
12: 118,871,270 (GRCm39) |
F710L |
probably damaging |
Het |
Acsm4 |
T |
G |
7: 119,310,622 (GRCm39) |
V503G |
probably damaging |
Het |
Adam26a |
T |
A |
8: 44,021,940 (GRCm39) |
M517L |
probably benign |
Het |
Adcy10 |
C |
A |
1: 165,391,854 (GRCm39) |
L1345I |
probably damaging |
Het |
Adgrv1 |
T |
C |
13: 81,715,609 (GRCm39) |
I860V |
probably benign |
Het |
Alcam |
T |
C |
16: 52,097,257 (GRCm39) |
D333G |
probably damaging |
Het |
Amt |
C |
A |
9: 108,177,032 (GRCm39) |
F213L |
possibly damaging |
Het |
Ascc3 |
A |
G |
10: 50,604,278 (GRCm39) |
T1333A |
probably damaging |
Het |
Asxl3 |
C |
A |
18: 22,655,148 (GRCm39) |
L1053I |
probably damaging |
Het |
Atxn10 |
T |
C |
15: 85,220,699 (GRCm39) |
S12P |
probably damaging |
Het |
AU021092 |
T |
C |
16: 5,030,017 (GRCm39) |
I333V |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,886,486 (GRCm39) |
I577V |
probably benign |
Het |
Cadm2 |
A |
T |
16: 66,609,726 (GRCm39) |
F132I |
probably benign |
Het |
Casp3 |
T |
A |
8: 47,087,308 (GRCm39) |
V85D |
probably damaging |
Het |
Ccdc168 |
C |
T |
1: 44,096,367 (GRCm39) |
C1577Y |
probably benign |
Het |
Ccdc85a |
A |
T |
11: 28,342,944 (GRCm39) |
|
probably benign |
Het |
Cd22 |
T |
C |
7: 30,566,999 (GRCm39) |
R760G |
possibly damaging |
Het |
Cela3a |
A |
T |
4: 137,135,441 (GRCm39) |
W41R |
probably damaging |
Het |
Cntnap5b |
A |
G |
1: 100,202,197 (GRCm39) |
E348G |
probably benign |
Het |
Ddx20 |
C |
A |
3: 105,591,626 (GRCm39) |
K181N |
probably benign |
Het |
Dnah14 |
G |
C |
1: 181,612,740 (GRCm39) |
A3846P |
possibly damaging |
Het |
Ern1 |
A |
C |
11: 106,294,365 (GRCm39) |
I813S |
probably damaging |
Het |
Fam181a |
G |
A |
12: 103,282,773 (GRCm39) |
G226D |
probably damaging |
Het |
Fam186a |
T |
A |
15: 99,844,357 (GRCm39) |
D629V |
unknown |
Het |
Gipr |
T |
A |
7: 18,898,529 (GRCm39) |
T26S |
probably benign |
Het |
Gm3159 |
A |
G |
14: 4,398,530 (GRCm38) |
R74G |
possibly damaging |
Het |
Greb1l |
G |
A |
18: 10,558,786 (GRCm39) |
V1814I |
probably benign |
Het |
Hacd1 |
A |
T |
2: 14,049,664 (GRCm39) |
V98E |
probably damaging |
Het |
Iars1 |
T |
G |
13: 49,875,637 (GRCm39) |
F775V |
probably damaging |
Het |
Il12rb2 |
G |
A |
6: 67,269,636 (GRCm39) |
L726F |
possibly damaging |
Het |
Itih4 |
T |
C |
14: 30,614,560 (GRCm39) |
V474A |
probably damaging |
Het |
Kmt2a |
A |
C |
9: 44,731,319 (GRCm39) |
|
probably benign |
Het |
Ktn1 |
T |
A |
14: 47,904,810 (GRCm39) |
L196* |
probably null |
Het |
Lipo4 |
A |
G |
19: 33,476,767 (GRCm39) |
V327A |
probably benign |
Het |
Lratd2 |
T |
C |
15: 60,694,934 (GRCm39) |
T271A |
probably benign |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Lrp4 |
C |
A |
2: 91,317,387 (GRCm39) |
T837K |
probably damaging |
Het |
Mad1l1 |
G |
T |
5: 140,051,572 (GRCm39) |
F664L |
probably damaging |
Het |
Mecr |
A |
G |
4: 131,589,172 (GRCm39) |
T247A |
probably benign |
Het |
Msi1 |
G |
A |
5: 115,583,483 (GRCm39) |
A228T |
probably benign |
Het |
Mup5 |
T |
A |
4: 61,751,273 (GRCm39) |
N125I |
probably damaging |
Het |
Mybl2 |
C |
T |
2: 162,914,728 (GRCm39) |
S282F |
possibly damaging |
Het |
Myom2 |
G |
A |
8: 15,167,741 (GRCm39) |
A1109T |
probably null |
Het |
Nalcn |
T |
C |
14: 123,744,966 (GRCm39) |
D354G |
probably damaging |
Het |
Nckap1l |
T |
C |
15: 103,399,938 (GRCm39) |
V1040A |
possibly damaging |
Het |
Nlrp12 |
T |
A |
7: 3,271,160 (GRCm39) |
D1051V |
probably damaging |
Het |
Nudt7 |
A |
G |
8: 114,860,385 (GRCm39) |
K16R |
probably benign |
Het |
Or4b1 |
G |
T |
2: 89,979,494 (GRCm39) |
Y285* |
probably null |
Het |
Or8g29-ps1 |
A |
G |
9: 39,200,577 (GRCm39) |
V203A |
unknown |
Het |
Paqr3 |
A |
T |
5: 97,256,110 (GRCm39) |
I88K |
possibly damaging |
Het |
Parp9 |
A |
G |
16: 35,768,716 (GRCm39) |
M299V |
probably benign |
Het |
Pde4dip |
A |
T |
3: 97,731,649 (GRCm39) |
|
probably null |
Het |
Pex13 |
T |
G |
11: 23,605,628 (GRCm39) |
M201L |
probably benign |
Het |
Pfas |
C |
A |
11: 68,884,709 (GRCm39) |
V498L |
probably benign |
Het |
Phka2 |
G |
A |
X: 159,316,044 (GRCm39) |
V230I |
probably damaging |
Het |
Plec |
T |
A |
15: 76,070,414 (GRCm39) |
D932V |
probably damaging |
Het |
Qng1 |
C |
A |
13: 58,529,775 (GRCm39) |
C279F |
probably damaging |
Het |
Qsox2 |
C |
T |
2: 26,107,654 (GRCm39) |
A445T |
probably benign |
Het |
Rapgef1 |
C |
A |
2: 29,623,710 (GRCm39) |
Q820K |
possibly damaging |
Het |
Samd13 |
A |
G |
3: 146,368,424 (GRCm39) |
|
probably null |
Het |
Samm50 |
G |
T |
15: 84,082,850 (GRCm39) |
D104Y |
probably damaging |
Het |
Sbk3 |
A |
T |
7: 4,970,522 (GRCm39) |
F282L |
probably benign |
Het |
Sfmbt1 |
C |
T |
14: 30,509,546 (GRCm39) |
H342Y |
probably benign |
Het |
Sgo2b |
CCATCATCATCATCATCATCAT |
CCATCATCATCATCATCAT |
8: 64,384,489 (GRCm39) |
|
probably benign |
Het |
Slc12a2 |
T |
A |
18: 58,043,344 (GRCm39) |
L596* |
probably null |
Het |
Spata31h1 |
A |
T |
10: 82,129,620 (GRCm39) |
I1130K |
probably benign |
Het |
St8sia3 |
T |
C |
18: 64,404,853 (GRCm39) |
S377P |
probably benign |
Het |
Stmnd1 |
T |
G |
13: 46,427,375 (GRCm39) |
S28A |
probably benign |
Het |
Syne3 |
A |
T |
12: 104,920,561 (GRCm39) |
L458Q |
probably damaging |
Het |
Synm |
C |
T |
7: 67,385,848 (GRCm39) |
V163I |
probably benign |
Het |
Tbc1d23 |
A |
G |
16: 57,028,686 (GRCm39) |
C161R |
probably damaging |
Het |
Tnfrsf4 |
G |
A |
4: 156,100,625 (GRCm39) |
V215I |
probably benign |
Het |
Vars2 |
T |
G |
17: 35,977,967 (GRCm39) |
K67Q |
probably benign |
Het |
Vmn2r13 |
A |
T |
5: 109,304,753 (GRCm39) |
Y559* |
probably null |
Het |
Wdpcp |
T |
C |
11: 21,671,154 (GRCm39) |
I465T |
possibly damaging |
Het |
Zwilch |
A |
C |
9: 64,069,844 (GRCm39) |
|
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 |
|
R0532:Cep164
|
UTSW |
9 |
45,721,124 (GRCm39) |
nonsense |
probably null |
|
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 |
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 |
|