Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
A |
T |
4: 144,344,398 (GRCm39) |
N58I |
probably benign |
Het |
Adgra3 |
T |
C |
5: 50,168,857 (GRCm39) |
D163G |
probably damaging |
Het |
Alcam |
C |
A |
16: 52,115,411 (GRCm39) |
E236* |
probably null |
Het |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Aplf |
G |
T |
6: 87,619,008 (GRCm39) |
|
probably null |
Het |
Arl4a |
A |
T |
12: 40,086,744 (GRCm39) |
M1K |
probably null |
Het |
Asic4 |
A |
G |
1: 75,427,870 (GRCm39) |
D132G |
probably damaging |
Het |
Bbs12 |
T |
C |
3: 37,374,422 (GRCm39) |
I290T |
probably benign |
Het |
BC024139 |
A |
G |
15: 76,008,865 (GRCm39) |
S290P |
probably benign |
Het |
Bmp6 |
G |
A |
13: 38,653,673 (GRCm39) |
A247T |
probably benign |
Het |
Cadps |
A |
G |
14: 12,457,711 (GRCm38) |
S1057P |
possibly damaging |
Het |
Caprin1 |
A |
C |
2: 103,599,778 (GRCm39) |
|
probably null |
Het |
Cdc42bpg |
G |
A |
19: 6,371,750 (GRCm39) |
R1343K |
probably benign |
Het |
Cdk18 |
A |
T |
1: 132,045,218 (GRCm39) |
|
probably null |
Het |
Cfhr1 |
A |
T |
1: 139,484,068 (GRCm39) |
|
probably null |
Het |
Chn2 |
A |
T |
6: 54,272,786 (GRCm39) |
I201F |
probably damaging |
Het |
Chrdl2 |
A |
G |
7: 99,673,129 (GRCm39) |
D175G |
probably damaging |
Het |
Disp2 |
G |
T |
2: 118,622,286 (GRCm39) |
R1006L |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,349,746 (GRCm39) |
R2399Q |
probably benign |
Het |
Dnah3 |
C |
G |
7: 119,631,861 (GRCm39) |
D1365H |
probably damaging |
Het |
Efcab8 |
T |
A |
2: 153,644,343 (GRCm39) |
Y372* |
probably null |
Het |
Eftud2 |
G |
A |
11: 102,732,011 (GRCm39) |
P768S |
probably damaging |
Het |
Ehmt1 |
A |
C |
2: 24,691,545 (GRCm39) |
S1170A |
probably benign |
Het |
Gdpd4 |
A |
C |
7: 97,664,118 (GRCm39) |
K572Q |
probably benign |
Het |
Gm7356 |
T |
C |
17: 14,221,456 (GRCm39) |
E191G |
probably damaging |
Het |
Gm8674 |
A |
T |
13: 50,055,957 (GRCm39) |
|
noncoding transcript |
Het |
Gulp1 |
T |
G |
1: 44,820,199 (GRCm39) |
H235Q |
probably benign |
Het |
Hormad1 |
T |
C |
3: 95,485,418 (GRCm39) |
V202A |
possibly damaging |
Het |
Inpp5b |
G |
A |
4: 124,645,110 (GRCm39) |
D179N |
possibly damaging |
Het |
Kcnk4 |
T |
A |
19: 6,905,069 (GRCm39) |
Y194F |
possibly damaging |
Het |
Lars1 |
A |
C |
18: 42,350,622 (GRCm39) |
S896A |
probably benign |
Het |
Lonp1 |
A |
G |
17: 56,924,793 (GRCm39) |
V538A |
probably damaging |
Het |
Map3k14 |
A |
T |
11: 103,129,972 (GRCm39) |
L315Q |
probably damaging |
Het |
Met |
T |
A |
6: 17,526,422 (GRCm39) |
Y500* |
probably null |
Het |
Mga |
T |
G |
2: 119,778,462 (GRCm39) |
I2093M |
possibly damaging |
Het |
Mpl |
T |
G |
4: 118,313,078 (GRCm39) |
I152L |
probably benign |
Het |
Mthfsd |
G |
A |
8: 121,835,058 (GRCm39) |
|
probably benign |
Het |
Mup4 |
A |
G |
4: 59,958,119 (GRCm39) |
F150L |
probably damaging |
Het |
Mybph |
T |
A |
1: 134,121,273 (GRCm39) |
V11D |
probably benign |
Het |
Or4f54 |
A |
T |
2: 111,122,946 (GRCm39) |
E111V |
probably damaging |
Het |
Or52n2c |
A |
G |
7: 104,574,933 (GRCm39) |
F13L |
probably benign |
Het |
Or5ak20 |
T |
A |
2: 85,184,142 (GRCm39) |
I43F |
probably benign |
Het |
Pde4a |
T |
C |
9: 21,114,854 (GRCm39) |
|
probably null |
Het |
Pex2 |
C |
T |
3: 5,626,428 (GRCm39) |
R127H |
probably benign |
Het |
Pgap3 |
A |
G |
11: 98,288,874 (GRCm39) |
W94R |
probably damaging |
Het |
Prl4a1 |
T |
C |
13: 28,202,467 (GRCm39) |
V14A |
probably benign |
Het |
Psg25 |
A |
T |
7: 18,260,460 (GRCm39) |
I146N |
probably benign |
Het |
Ptprn2 |
A |
G |
12: 116,822,548 (GRCm39) |
Y209C |
probably damaging |
Het |
Scart2 |
C |
A |
7: 139,877,949 (GRCm39) |
A977D |
probably benign |
Het |
Sema4c |
T |
A |
1: 36,589,407 (GRCm39) |
D573V |
probably damaging |
Het |
Setx |
A |
T |
2: 29,056,379 (GRCm39) |
I2192F |
possibly damaging |
Het |
Skic3 |
G |
A |
13: 76,295,886 (GRCm39) |
E1050K |
possibly damaging |
Het |
Sp4 |
A |
G |
12: 118,263,281 (GRCm39) |
L255P |
probably damaging |
Het |
Spaca7 |
A |
G |
8: 12,636,456 (GRCm39) |
Y94C |
probably damaging |
Het |
Stt3a |
T |
G |
9: 36,657,891 (GRCm39) |
I390L |
possibly damaging |
Het |
Tars2 |
A |
G |
3: 95,654,905 (GRCm39) |
W128R |
probably damaging |
Het |
Tll1 |
G |
A |
8: 64,504,527 (GRCm39) |
T623M |
probably damaging |
Het |
Tmem129 |
A |
T |
5: 33,812,850 (GRCm39) |
V166E |
probably damaging |
Het |
Tmem200a |
T |
A |
10: 25,870,051 (GRCm39) |
I73F |
probably benign |
Het |
Tnks1bp1 |
T |
C |
2: 84,900,976 (GRCm39) |
M1561T |
probably damaging |
Het |
Zfat |
A |
T |
15: 68,052,570 (GRCm39) |
I401N |
probably damaging |
Het |
Zfp142 |
A |
T |
1: 74,610,027 (GRCm39) |
V1153E |
probably benign |
Het |
Zwilch |
T |
C |
9: 64,060,205 (GRCm39) |
I354V |
probably benign |
Het |
|
Other mutations in Cenpf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00778:Cenpf
|
APN |
1 |
189,387,109 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01154:Cenpf
|
APN |
1 |
189,412,530 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01434:Cenpf
|
APN |
1 |
189,390,065 (GRCm39) |
nonsense |
probably null |
|
IGL01461:Cenpf
|
APN |
1 |
189,389,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01615:Cenpf
|
APN |
1 |
189,385,381 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01720:Cenpf
|
APN |
1 |
189,383,412 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01720:Cenpf
|
APN |
1 |
189,414,583 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01803:Cenpf
|
APN |
1 |
189,386,968 (GRCm39) |
nonsense |
probably null |
|
IGL02152:Cenpf
|
APN |
1 |
189,381,209 (GRCm39) |
missense |
probably benign |
|
IGL02222:Cenpf
|
APN |
1 |
189,386,641 (GRCm39) |
missense |
probably benign |
|
IGL02338:Cenpf
|
APN |
1 |
189,412,615 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02580:Cenpf
|
APN |
1 |
189,389,638 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02629:Cenpf
|
APN |
1 |
189,384,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02650:Cenpf
|
APN |
1 |
189,384,670 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02660:Cenpf
|
APN |
1 |
189,386,979 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02703:Cenpf
|
APN |
1 |
189,391,955 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02809:Cenpf
|
APN |
1 |
189,414,555 (GRCm39) |
splice site |
probably benign |
|
IGL02851:Cenpf
|
APN |
1 |
189,390,227 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02903:Cenpf
|
APN |
1 |
189,379,073 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03126:Cenpf
|
APN |
1 |
189,391,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03235:Cenpf
|
APN |
1 |
189,416,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03336:Cenpf
|
APN |
1 |
189,384,844 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03402:Cenpf
|
APN |
1 |
189,387,273 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Cenpf
|
UTSW |
1 |
189,391,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Cenpf
|
UTSW |
1 |
189,382,903 (GRCm39) |
missense |
probably benign |
0.05 |
R0129:Cenpf
|
UTSW |
1 |
189,391,847 (GRCm39) |
missense |
probably benign |
0.26 |
R0157:Cenpf
|
UTSW |
1 |
189,384,556 (GRCm39) |
missense |
probably benign |
0.07 |
R0270:Cenpf
|
UTSW |
1 |
189,382,911 (GRCm39) |
missense |
probably benign |
0.01 |
R0607:Cenpf
|
UTSW |
1 |
189,414,660 (GRCm39) |
splice site |
probably null |
|
R0621:Cenpf
|
UTSW |
1 |
189,404,825 (GRCm39) |
missense |
probably benign |
|
R0639:Cenpf
|
UTSW |
1 |
189,390,259 (GRCm39) |
missense |
probably benign |
0.01 |
R0653:Cenpf
|
UTSW |
1 |
189,392,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R0718:Cenpf
|
UTSW |
1 |
189,386,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R1157:Cenpf
|
UTSW |
1 |
189,390,650 (GRCm39) |
missense |
probably benign |
0.20 |
R1331:Cenpf
|
UTSW |
1 |
189,374,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R1463:Cenpf
|
UTSW |
1 |
189,386,936 (GRCm39) |
missense |
probably damaging |
0.97 |
R1514:Cenpf
|
UTSW |
1 |
189,411,338 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1529:Cenpf
|
UTSW |
1 |
189,392,235 (GRCm39) |
missense |
probably benign |
0.00 |
R1574:Cenpf
|
UTSW |
1 |
189,384,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Cenpf
|
UTSW |
1 |
189,384,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Cenpf
|
UTSW |
1 |
189,389,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R1671:Cenpf
|
UTSW |
1 |
189,411,341 (GRCm39) |
splice site |
probably null |
|
R1725:Cenpf
|
UTSW |
1 |
189,412,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R1743:Cenpf
|
UTSW |
1 |
189,386,460 (GRCm39) |
missense |
probably benign |
0.19 |
R1874:Cenpf
|
UTSW |
1 |
189,416,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Cenpf
|
UTSW |
1 |
189,379,046 (GRCm39) |
missense |
probably benign |
|
R1980:Cenpf
|
UTSW |
1 |
189,386,112 (GRCm39) |
missense |
probably benign |
0.04 |
R2074:Cenpf
|
UTSW |
1 |
189,389,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2096:Cenpf
|
UTSW |
1 |
189,385,656 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2109:Cenpf
|
UTSW |
1 |
189,411,264 (GRCm39) |
missense |
probably damaging |
0.99 |
R2113:Cenpf
|
UTSW |
1 |
189,411,299 (GRCm39) |
missense |
probably damaging |
0.96 |
R2134:Cenpf
|
UTSW |
1 |
189,390,839 (GRCm39) |
missense |
probably benign |
0.03 |
R2209:Cenpf
|
UTSW |
1 |
189,384,795 (GRCm39) |
missense |
probably benign |
0.04 |
R2875:Cenpf
|
UTSW |
1 |
189,390,841 (GRCm39) |
missense |
probably benign |
0.11 |
R2876:Cenpf
|
UTSW |
1 |
189,390,841 (GRCm39) |
missense |
probably benign |
0.11 |
R3433:Cenpf
|
UTSW |
1 |
189,392,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R3709:Cenpf
|
UTSW |
1 |
189,381,009 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3786:Cenpf
|
UTSW |
1 |
189,390,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R4014:Cenpf
|
UTSW |
1 |
189,385,356 (GRCm39) |
missense |
probably benign |
0.01 |
R4108:Cenpf
|
UTSW |
1 |
189,416,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Cenpf
|
UTSW |
1 |
189,385,242 (GRCm39) |
missense |
probably benign |
0.01 |
R4177:Cenpf
|
UTSW |
1 |
189,400,816 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4422:Cenpf
|
UTSW |
1 |
189,390,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R4546:Cenpf
|
UTSW |
1 |
189,386,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4592:Cenpf
|
UTSW |
1 |
189,411,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R4643:Cenpf
|
UTSW |
1 |
189,391,786 (GRCm39) |
missense |
probably benign |
0.00 |
R4650:Cenpf
|
UTSW |
1 |
189,392,235 (GRCm39) |
missense |
probably benign |
0.00 |
R4801:Cenpf
|
UTSW |
1 |
189,383,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Cenpf
|
UTSW |
1 |
189,383,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R4817:Cenpf
|
UTSW |
1 |
189,414,566 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4871:Cenpf
|
UTSW |
1 |
189,390,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R5037:Cenpf
|
UTSW |
1 |
189,416,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R5106:Cenpf
|
UTSW |
1 |
189,416,005 (GRCm39) |
missense |
probably benign |
0.00 |
R5213:Cenpf
|
UTSW |
1 |
189,387,177 (GRCm39) |
missense |
probably benign |
0.04 |
R5237:Cenpf
|
UTSW |
1 |
189,391,730 (GRCm39) |
missense |
probably benign |
0.28 |
R5255:Cenpf
|
UTSW |
1 |
189,404,824 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5378:Cenpf
|
UTSW |
1 |
189,385,663 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5468:Cenpf
|
UTSW |
1 |
189,384,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R5510:Cenpf
|
UTSW |
1 |
189,415,100 (GRCm39) |
missense |
probably benign |
0.14 |
R5616:Cenpf
|
UTSW |
1 |
189,389,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Cenpf
|
UTSW |
1 |
189,389,279 (GRCm39) |
missense |
probably damaging |
0.99 |
R5735:Cenpf
|
UTSW |
1 |
189,386,560 (GRCm39) |
missense |
probably benign |
0.10 |
R5841:Cenpf
|
UTSW |
1 |
189,389,641 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5943:Cenpf
|
UTSW |
1 |
189,392,166 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6082:Cenpf
|
UTSW |
1 |
189,390,301 (GRCm39) |
missense |
probably benign |
0.11 |
R6108:Cenpf
|
UTSW |
1 |
189,394,210 (GRCm39) |
missense |
probably benign |
0.03 |
R6269:Cenpf
|
UTSW |
1 |
189,392,117 (GRCm39) |
missense |
probably benign |
0.37 |
R6284:Cenpf
|
UTSW |
1 |
189,384,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R6425:Cenpf
|
UTSW |
1 |
189,392,095 (GRCm39) |
missense |
probably benign |
0.09 |
R6587:Cenpf
|
UTSW |
1 |
189,390,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Cenpf
|
UTSW |
1 |
189,385,051 (GRCm39) |
missense |
probably benign |
0.15 |
R6811:Cenpf
|
UTSW |
1 |
189,386,739 (GRCm39) |
missense |
probably benign |
0.06 |
R6834:Cenpf
|
UTSW |
1 |
189,391,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R6951:Cenpf
|
UTSW |
1 |
189,385,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R7095:Cenpf
|
UTSW |
1 |
189,391,373 (GRCm39) |
missense |
probably benign |
0.01 |
R7128:Cenpf
|
UTSW |
1 |
189,417,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R7185:Cenpf
|
UTSW |
1 |
189,385,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Cenpf
|
UTSW |
1 |
189,382,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R7353:Cenpf
|
UTSW |
1 |
189,386,335 (GRCm39) |
nonsense |
probably null |
|
R7402:Cenpf
|
UTSW |
1 |
189,391,575 (GRCm39) |
nonsense |
probably null |
|
R7460:Cenpf
|
UTSW |
1 |
189,386,247 (GRCm39) |
missense |
probably damaging |
0.97 |
R7484:Cenpf
|
UTSW |
1 |
189,389,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Cenpf
|
UTSW |
1 |
189,390,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7691:Cenpf
|
UTSW |
1 |
189,390,404 (GRCm39) |
nonsense |
probably null |
|
R7698:Cenpf
|
UTSW |
1 |
189,394,269 (GRCm39) |
missense |
probably benign |
0.01 |
R7901:Cenpf
|
UTSW |
1 |
189,389,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R7941:Cenpf
|
UTSW |
1 |
189,389,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R8007:Cenpf
|
UTSW |
1 |
189,379,144 (GRCm39) |
missense |
|
|
R8194:Cenpf
|
UTSW |
1 |
189,414,600 (GRCm39) |
missense |
probably benign |
0.06 |
R8420:Cenpf
|
UTSW |
1 |
189,404,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R8429:Cenpf
|
UTSW |
1 |
189,389,504 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8477:Cenpf
|
UTSW |
1 |
189,385,385 (GRCm39) |
missense |
probably benign |
|
R8492:Cenpf
|
UTSW |
1 |
189,390,926 (GRCm39) |
missense |
probably damaging |
0.99 |
R8510:Cenpf
|
UTSW |
1 |
189,382,903 (GRCm39) |
missense |
probably benign |
0.01 |
R8686:Cenpf
|
UTSW |
1 |
189,391,801 (GRCm39) |
missense |
probably benign |
0.00 |
R8696:Cenpf
|
UTSW |
1 |
189,390,194 (GRCm39) |
missense |
probably benign |
0.20 |
R8855:Cenpf
|
UTSW |
1 |
189,385,430 (GRCm39) |
missense |
probably benign |
0.11 |
R8901:Cenpf
|
UTSW |
1 |
189,394,248 (GRCm39) |
missense |
probably benign |
0.30 |
R8958:Cenpf
|
UTSW |
1 |
189,385,350 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9109:Cenpf
|
UTSW |
1 |
189,391,571 (GRCm39) |
missense |
probably benign |
0.06 |
R9135:Cenpf
|
UTSW |
1 |
189,404,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9136:Cenpf
|
UTSW |
1 |
189,403,352 (GRCm39) |
missense |
probably benign |
0.02 |
R9198:Cenpf
|
UTSW |
1 |
189,388,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R9240:Cenpf
|
UTSW |
1 |
189,389,167 (GRCm39) |
missense |
probably benign |
0.01 |
R9303:Cenpf
|
UTSW |
1 |
189,392,271 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9305:Cenpf
|
UTSW |
1 |
189,392,271 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9354:Cenpf
|
UTSW |
1 |
189,379,114 (GRCm39) |
missense |
|
|
R9502:Cenpf
|
UTSW |
1 |
189,388,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R9619:Cenpf
|
UTSW |
1 |
189,385,965 (GRCm39) |
missense |
probably benign |
0.01 |
RF006:Cenpf
|
UTSW |
1 |
189,389,583 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Cenpf
|
UTSW |
1 |
189,386,071 (GRCm39) |
missense |
possibly damaging |
0.79 |
X0066:Cenpf
|
UTSW |
1 |
189,390,126 (GRCm39) |
missense |
probably benign |
0.23 |
Z1088:Cenpf
|
UTSW |
1 |
189,385,128 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cenpf
|
UTSW |
1 |
189,391,669 (GRCm39) |
missense |
probably damaging |
1.00 |
|