Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh6a1 |
A |
G |
12: 84,483,214 (GRCm39) |
|
probably null |
Het |
Ano2 |
A |
T |
6: 125,687,592 (GRCm39) |
K32N |
probably benign |
Het |
Asic1 |
A |
G |
15: 99,569,898 (GRCm39) |
H73R |
probably benign |
Het |
B3glct |
A |
G |
5: 149,677,607 (GRCm39) |
D412G |
probably damaging |
Het |
Baz2b |
T |
C |
2: 59,733,640 (GRCm39) |
I1891V |
probably benign |
Het |
Cc2d2a |
A |
G |
5: 43,889,721 (GRCm39) |
E1278G |
probably damaging |
Het |
Ccdc116 |
T |
C |
16: 16,960,718 (GRCm39) |
E33G |
probably benign |
Het |
Celf4 |
T |
A |
18: 25,670,796 (GRCm39) |
Q129L |
probably benign |
Het |
Celf4 |
G |
T |
18: 25,670,797 (GRCm39) |
Q129K |
probably benign |
Het |
Col18a1 |
A |
G |
10: 76,909,588 (GRCm39) |
S817P |
probably damaging |
Het |
Corin |
A |
G |
5: 72,458,929 (GRCm39) |
V940A |
probably damaging |
Het |
Dlgap2 |
A |
T |
8: 14,777,525 (GRCm39) |
N257Y |
possibly damaging |
Het |
Dnah2 |
C |
A |
11: 69,349,314 (GRCm39) |
V2441L |
possibly damaging |
Het |
Evpl |
C |
T |
11: 116,112,438 (GRCm39) |
E1751K |
probably damaging |
Het |
Fat1 |
G |
A |
8: 45,403,623 (GRCm39) |
E125K |
probably damaging |
Het |
Fras1 |
A |
T |
5: 96,881,640 (GRCm39) |
|
probably benign |
Het |
Fryl |
G |
A |
5: 73,234,038 (GRCm39) |
P1496S |
probably benign |
Het |
G3bp2 |
A |
C |
5: 92,202,905 (GRCm39) |
M362R |
possibly damaging |
Het |
Grk5 |
T |
C |
19: 61,057,774 (GRCm39) |
F158S |
probably damaging |
Het |
Hmbox1 |
G |
T |
14: 65,125,048 (GRCm39) |
Q188K |
probably damaging |
Het |
Ift172 |
A |
T |
5: 31,429,348 (GRCm39) |
D604E |
probably benign |
Het |
Igkv6-32 |
T |
A |
6: 70,051,556 (GRCm39) |
T5S |
probably benign |
Het |
Impa1 |
A |
G |
3: 10,388,054 (GRCm39) |
Y123H |
probably damaging |
Het |
Itgb4 |
C |
T |
11: 115,879,550 (GRCm39) |
T612M |
probably damaging |
Het |
Med12l |
T |
A |
3: 58,944,976 (GRCm39) |
|
probably null |
Het |
Meis2 |
A |
G |
2: 115,890,002 (GRCm39) |
L160S |
probably damaging |
Het |
Micu1 |
C |
T |
10: 59,563,870 (GRCm39) |
R31* |
probably null |
Het |
Nlrp9a |
G |
T |
7: 26,256,882 (GRCm39) |
A167S |
probably damaging |
Het |
Or10j27 |
A |
G |
1: 172,958,425 (GRCm39) |
Y120H |
probably damaging |
Het |
Or4d10 |
A |
T |
19: 12,051,392 (GRCm39) |
N201K |
probably damaging |
Het |
Plpp6 |
A |
G |
19: 28,942,071 (GRCm39) |
N224S |
possibly damaging |
Het |
Sdk2 |
T |
A |
11: 113,741,810 (GRCm39) |
H803L |
probably benign |
Het |
Shld2 |
T |
C |
14: 33,967,143 (GRCm39) |
T690A |
probably benign |
Het |
Slc36a1 |
T |
A |
11: 55,119,017 (GRCm39) |
Y331N |
probably damaging |
Het |
Spata31d1c |
A |
T |
13: 65,183,009 (GRCm39) |
I184F |
possibly damaging |
Het |
Stat3 |
T |
C |
11: 100,793,582 (GRCm39) |
I338V |
possibly damaging |
Het |
Stk10 |
T |
A |
11: 32,554,143 (GRCm39) |
V610E |
possibly damaging |
Het |
Syna |
A |
G |
5: 134,587,144 (GRCm39) |
S602P |
probably benign |
Het |
Tap2 |
T |
A |
17: 34,424,399 (GRCm39) |
|
probably benign |
Het |
Tln1 |
T |
C |
4: 43,539,084 (GRCm39) |
|
probably benign |
Het |
Tra2b |
C |
A |
16: 22,073,303 (GRCm39) |
|
probably benign |
Het |
Ttc7b |
T |
C |
12: 100,339,968 (GRCm39) |
|
probably null |
Het |
Vmn2r121 |
G |
A |
X: 123,042,023 (GRCm39) |
T378I |
probably benign |
Het |
Wdr1 |
A |
T |
5: 38,690,825 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cfap251 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00487:Cfap251
|
APN |
5 |
123,412,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01090:Cfap251
|
APN |
5 |
123,418,052 (GRCm39) |
splice site |
probably benign |
|
IGL01387:Cfap251
|
APN |
5 |
123,421,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01432:Cfap251
|
APN |
5 |
123,418,015 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01642:Cfap251
|
APN |
5 |
123,426,761 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01720:Cfap251
|
APN |
5 |
123,460,557 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02104:Cfap251
|
APN |
5 |
123,440,761 (GRCm39) |
nonsense |
probably null |
|
IGL02160:Cfap251
|
APN |
5 |
123,394,081 (GRCm39) |
missense |
unknown |
|
IGL02238:Cfap251
|
APN |
5 |
123,440,486 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02820:Cfap251
|
APN |
5 |
123,392,699 (GRCm39) |
unclassified |
probably benign |
|
R0078:Cfap251
|
UTSW |
5 |
123,436,633 (GRCm39) |
missense |
probably benign |
0.04 |
R0207:Cfap251
|
UTSW |
5 |
123,421,510 (GRCm39) |
missense |
probably damaging |
0.98 |
R0411:Cfap251
|
UTSW |
5 |
123,428,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R0414:Cfap251
|
UTSW |
5 |
123,425,476 (GRCm39) |
splice site |
probably null |
|
R0722:Cfap251
|
UTSW |
5 |
123,394,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1169:Cfap251
|
UTSW |
5 |
123,392,673 (GRCm39) |
small deletion |
probably benign |
|
R1527:Cfap251
|
UTSW |
5 |
123,425,408 (GRCm39) |
missense |
probably benign |
0.19 |
R1924:Cfap251
|
UTSW |
5 |
123,440,802 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2022:Cfap251
|
UTSW |
5 |
123,411,853 (GRCm39) |
missense |
probably benign |
0.29 |
R2110:Cfap251
|
UTSW |
5 |
123,392,438 (GRCm39) |
unclassified |
probably benign |
|
R2112:Cfap251
|
UTSW |
5 |
123,392,438 (GRCm39) |
unclassified |
probably benign |
|
R2147:Cfap251
|
UTSW |
5 |
123,394,254 (GRCm39) |
missense |
probably benign |
0.01 |
R2258:Cfap251
|
UTSW |
5 |
123,421,411 (GRCm39) |
splice site |
probably null |
|
R2407:Cfap251
|
UTSW |
5 |
123,428,032 (GRCm39) |
missense |
probably benign |
0.11 |
R2418:Cfap251
|
UTSW |
5 |
123,392,331 (GRCm39) |
unclassified |
probably benign |
|
R2497:Cfap251
|
UTSW |
5 |
123,421,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2509:Cfap251
|
UTSW |
5 |
123,394,169 (GRCm39) |
missense |
probably benign |
0.00 |
R3437:Cfap251
|
UTSW |
5 |
123,392,435 (GRCm39) |
unclassified |
probably benign |
|
R3730:Cfap251
|
UTSW |
5 |
123,464,631 (GRCm39) |
missense |
possibly damaging |
0.70 |
R3800:Cfap251
|
UTSW |
5 |
123,392,784 (GRCm39) |
unclassified |
probably benign |
|
R4018:Cfap251
|
UTSW |
5 |
123,460,517 (GRCm39) |
missense |
probably benign |
0.04 |
R4181:Cfap251
|
UTSW |
5 |
123,431,873 (GRCm39) |
missense |
probably benign |
0.33 |
R4302:Cfap251
|
UTSW |
5 |
123,431,873 (GRCm39) |
missense |
probably benign |
0.33 |
R4640:Cfap251
|
UTSW |
5 |
123,440,495 (GRCm39) |
missense |
probably benign |
0.00 |
R4701:Cfap251
|
UTSW |
5 |
123,460,676 (GRCm39) |
missense |
probably benign |
0.00 |
R4799:Cfap251
|
UTSW |
5 |
123,440,835 (GRCm39) |
missense |
probably benign |
0.04 |
R4812:Cfap251
|
UTSW |
5 |
123,425,368 (GRCm39) |
missense |
probably benign |
0.01 |
R4922:Cfap251
|
UTSW |
5 |
123,394,116 (GRCm39) |
missense |
probably benign |
0.00 |
R5123:Cfap251
|
UTSW |
5 |
123,411,696 (GRCm39) |
start gained |
probably benign |
|
R5314:Cfap251
|
UTSW |
5 |
123,460,626 (GRCm39) |
missense |
probably benign |
0.01 |
R5445:Cfap251
|
UTSW |
5 |
123,425,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R5458:Cfap251
|
UTSW |
5 |
123,392,508 (GRCm39) |
unclassified |
probably benign |
|
R5462:Cfap251
|
UTSW |
5 |
123,436,695 (GRCm39) |
critical splice donor site |
probably null |
|
R5514:Cfap251
|
UTSW |
5 |
123,425,829 (GRCm39) |
critical splice donor site |
probably null |
|
R5600:Cfap251
|
UTSW |
5 |
123,426,761 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5635:Cfap251
|
UTSW |
5 |
123,460,635 (GRCm39) |
missense |
probably benign |
0.25 |
R5767:Cfap251
|
UTSW |
5 |
123,436,584 (GRCm39) |
missense |
probably benign |
0.01 |
R5943:Cfap251
|
UTSW |
5 |
123,424,420 (GRCm39) |
missense |
probably benign |
0.13 |
R6000:Cfap251
|
UTSW |
5 |
123,392,435 (GRCm39) |
unclassified |
probably benign |
|
R6030:Cfap251
|
UTSW |
5 |
123,412,267 (GRCm39) |
missense |
probably damaging |
0.97 |
R6030:Cfap251
|
UTSW |
5 |
123,412,267 (GRCm39) |
missense |
probably damaging |
0.97 |
R6293:Cfap251
|
UTSW |
5 |
123,460,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R6354:Cfap251
|
UTSW |
5 |
123,440,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R6356:Cfap251
|
UTSW |
5 |
123,392,729 (GRCm39) |
unclassified |
probably benign |
|
R6427:Cfap251
|
UTSW |
5 |
123,464,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R6896:Cfap251
|
UTSW |
5 |
123,416,421 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6909:Cfap251
|
UTSW |
5 |
123,425,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7503:Cfap251
|
UTSW |
5 |
123,435,521 (GRCm39) |
nonsense |
probably null |
|
R7707:Cfap251
|
UTSW |
5 |
123,391,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7715:Cfap251
|
UTSW |
5 |
123,400,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7809:Cfap251
|
UTSW |
5 |
123,402,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7819:Cfap251
|
UTSW |
5 |
123,392,322 (GRCm39) |
unclassified |
probably benign |
|
R7842:Cfap251
|
UTSW |
5 |
123,392,487 (GRCm39) |
missense |
unknown |
|
R7898:Cfap251
|
UTSW |
5 |
123,460,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R7967:Cfap251
|
UTSW |
5 |
123,421,579 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8004:Cfap251
|
UTSW |
5 |
123,392,513 (GRCm39) |
missense |
unknown |
|
R8068:Cfap251
|
UTSW |
5 |
123,394,229 (GRCm39) |
missense |
not run |
|
R8141:Cfap251
|
UTSW |
5 |
123,424,493 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8222:Cfap251
|
UTSW |
5 |
123,440,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R8242:Cfap251
|
UTSW |
5 |
123,411,914 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8303:Cfap251
|
UTSW |
5 |
123,460,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R8323:Cfap251
|
UTSW |
5 |
123,435,588 (GRCm39) |
missense |
probably benign |
0.16 |
R8773:Cfap251
|
UTSW |
5 |
123,411,913 (GRCm39) |
missense |
probably benign |
0.12 |
R8869:Cfap251
|
UTSW |
5 |
123,460,505 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8881:Cfap251
|
UTSW |
5 |
123,462,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R8921:Cfap251
|
UTSW |
5 |
123,424,481 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9099:Cfap251
|
UTSW |
5 |
123,418,082 (GRCm39) |
intron |
probably benign |
|
R9236:Cfap251
|
UTSW |
5 |
123,428,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R9385:Cfap251
|
UTSW |
5 |
123,426,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Cfap251
|
UTSW |
5 |
123,460,557 (GRCm39) |
missense |
probably benign |
0.07 |
R9762:Cfap251
|
UTSW |
5 |
123,460,533 (GRCm39) |
missense |
probably damaging |
1.00 |
RF007:Cfap251
|
UTSW |
5 |
123,392,317 (GRCm39) |
small insertion |
probably benign |
|
RF010:Cfap251
|
UTSW |
5 |
123,412,224 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF015:Cfap251
|
UTSW |
5 |
123,412,224 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF015:Cfap251
|
UTSW |
5 |
123,392,305 (GRCm39) |
small insertion |
probably benign |
|
RF017:Cfap251
|
UTSW |
5 |
123,391,953 (GRCm39) |
small insertion |
probably benign |
|
RF024:Cfap251
|
UTSW |
5 |
123,391,952 (GRCm39) |
small insertion |
probably benign |
|
RF024:Cfap251
|
UTSW |
5 |
123,391,951 (GRCm39) |
small insertion |
probably benign |
|
RF024:Cfap251
|
UTSW |
5 |
123,391,946 (GRCm39) |
small insertion |
probably benign |
|
X0062:Cfap251
|
UTSW |
5 |
123,412,300 (GRCm39) |
missense |
probably benign |
0.29 |
X0066:Cfap251
|
UTSW |
5 |
123,426,710 (GRCm39) |
missense |
probably benign |
0.05 |
|