Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,829,320 (GRCm39) |
I1380L |
probably benign |
Het |
Adcy3 |
T |
C |
12: 4,184,420 (GRCm39) |
V32A |
probably benign |
Het |
Ano3 |
T |
A |
2: 110,780,577 (GRCm39) |
|
probably benign |
Het |
Arhgef12 |
G |
A |
9: 42,882,399 (GRCm39) |
R1482* |
probably null |
Het |
Cd300lg |
T |
G |
11: 101,932,427 (GRCm39) |
L4R |
probably damaging |
Het |
Clasp1 |
G |
T |
1: 118,390,213 (GRCm39) |
M132I |
probably benign |
Het |
Clec18a |
T |
G |
8: 111,798,230 (GRCm39) |
D489A |
probably damaging |
Het |
Cngb1 |
A |
G |
8: 95,978,801 (GRCm39) |
S551P |
|
Het |
Efna4 |
G |
A |
3: 89,242,633 (GRCm39) |
T87M |
probably benign |
Het |
Fam229b |
T |
C |
10: 38,996,255 (GRCm39) |
R42G |
probably null |
Het |
Gm17175 |
C |
T |
14: 51,809,080 (GRCm39) |
M95I |
probably damaging |
Het |
Grk4 |
A |
G |
5: 34,833,482 (GRCm39) |
E96G |
probably benign |
Het |
Helb |
A |
C |
10: 119,925,321 (GRCm39) |
F1019V |
probably benign |
Het |
Hsd17b2 |
T |
C |
8: 118,485,440 (GRCm39) |
V301A |
possibly damaging |
Het |
Htr1b |
A |
G |
9: 81,513,582 (GRCm39) |
F342L |
probably benign |
Het |
Idua |
C |
A |
5: 108,828,441 (GRCm39) |
A265E |
possibly damaging |
Het |
Jup |
T |
G |
11: 100,277,113 (GRCm39) |
T32P |
probably damaging |
Het |
Kidins220 |
A |
G |
12: 25,107,715 (GRCm39) |
K1632E |
probably benign |
Het |
Lef1 |
G |
A |
3: 130,997,954 (GRCm39) |
|
probably null |
Het |
Lypla2 |
A |
G |
4: 135,697,112 (GRCm39) |
|
probably null |
Het |
Mall |
A |
G |
2: 127,571,785 (GRCm39) |
M1T |
probably null |
Het |
Mettl25 |
G |
T |
10: 105,661,941 (GRCm39) |
A343E |
probably benign |
Het |
Mpdz |
T |
C |
4: 81,267,324 (GRCm39) |
N940S |
probably benign |
Het |
Nsun4 |
A |
T |
4: 115,908,631 (GRCm39) |
V643D |
possibly damaging |
Het |
Nupr1 |
A |
T |
7: 126,224,109 (GRCm39) |
F70Y |
possibly damaging |
Het |
Or1e17 |
T |
A |
11: 73,831,213 (GRCm39) |
V47D |
possibly damaging |
Het |
Or52b4i |
A |
G |
7: 102,191,830 (GRCm39) |
H229R |
probably benign |
Het |
Or52e8 |
A |
T |
7: 104,624,934 (GRCm39) |
I90N |
probably damaging |
Het |
Or5ac20 |
A |
G |
16: 59,104,549 (GRCm39) |
F104L |
probably benign |
Het |
Or8g32 |
A |
T |
9: 39,305,242 (GRCm39) |
I49F |
probably damaging |
Het |
Or8k3 |
C |
G |
2: 86,058,473 (GRCm39) |
V281L |
possibly damaging |
Het |
Pabpc4 |
A |
T |
4: 123,180,508 (GRCm39) |
M77L |
probably benign |
Het |
Phactr3 |
A |
G |
2: 177,944,589 (GRCm39) |
E429G |
probably damaging |
Het |
Polr3b |
A |
G |
10: 84,549,523 (GRCm39) |
D915G |
probably damaging |
Het |
Pramel14 |
A |
T |
4: 143,718,424 (GRCm39) |
F340I |
probably benign |
Het |
Prkcg |
T |
A |
7: 3,372,037 (GRCm39) |
M501K |
probably damaging |
Het |
Prkch |
G |
A |
12: 73,747,041 (GRCm39) |
A307T |
possibly damaging |
Het |
Ptprt |
A |
G |
2: 161,769,581 (GRCm39) |
V428A |
possibly damaging |
Het |
Rnf145 |
C |
A |
11: 44,448,263 (GRCm39) |
D373E |
probably damaging |
Het |
Scfd2 |
G |
T |
5: 74,680,257 (GRCm39) |
Q299K |
probably benign |
Het |
Septin2 |
A |
G |
1: 93,433,283 (GRCm39) |
D315G |
probably benign |
Het |
Sf3a1 |
T |
A |
11: 4,125,435 (GRCm39) |
Y408* |
probably null |
Het |
Siglecf |
A |
T |
7: 43,001,214 (GRCm39) |
N61Y |
possibly damaging |
Het |
Sis |
A |
T |
3: 72,824,531 (GRCm39) |
I1334K |
probably damaging |
Het |
Slc38a6 |
A |
T |
12: 73,391,658 (GRCm39) |
T307S |
possibly damaging |
Het |
Spag9 |
T |
A |
11: 94,002,877 (GRCm39) |
F1129Y |
probably damaging |
Het |
Sra1 |
G |
A |
18: 36,808,064 (GRCm39) |
A388V |
possibly damaging |
Het |
Srpk1 |
T |
G |
17: 28,840,990 (GRCm39) |
K12T |
probably damaging |
Het |
Stam2 |
A |
T |
2: 52,596,438 (GRCm39) |
I333K |
probably damaging |
Het |
Tle1 |
GAA |
GA |
4: 72,057,216 (GRCm39) |
|
probably null |
Het |
Tmem121b |
T |
C |
6: 120,469,869 (GRCm39) |
K283E |
possibly damaging |
Het |
Tmem200a |
T |
C |
10: 25,868,850 (GRCm39) |
E473G |
probably damaging |
Het |
Tnxb |
T |
A |
17: 34,922,955 (GRCm39) |
S2513T |
probably benign |
Het |
Ttc16 |
A |
T |
2: 32,664,135 (GRCm39) |
|
probably benign |
Het |
Ttll8 |
C |
T |
15: 88,799,578 (GRCm39) |
C621Y |
probably damaging |
Het |
Ubn2 |
T |
A |
6: 38,417,475 (GRCm39) |
M171K |
probably benign |
Het |
Vmn2r19 |
T |
A |
6: 123,312,904 (GRCm39) |
V658D |
probably damaging |
Het |
Vmn2r6 |
A |
T |
3: 64,455,064 (GRCm39) |
|
probably benign |
Het |
Vwa3a |
A |
T |
7: 120,398,321 (GRCm39) |
I941L |
probably benign |
Het |
Zbtb24 |
A |
G |
10: 41,327,228 (GRCm39) |
D38G |
probably damaging |
Het |
Zfp628 |
T |
C |
7: 4,923,205 (GRCm39) |
C476R |
probably damaging |
Het |
Zfp831 |
A |
C |
2: 174,486,528 (GRCm39) |
N401T |
possibly damaging |
Het |
|
Other mutations in Cfap57 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00502:Cfap57
|
APN |
4 |
118,438,198 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00508:Cfap57
|
APN |
4 |
118,438,367 (GRCm39) |
splice site |
probably null |
|
IGL00857:Cfap57
|
APN |
4 |
118,470,120 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01147:Cfap57
|
APN |
4 |
118,446,198 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01396:Cfap57
|
APN |
4 |
118,467,792 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01420:Cfap57
|
APN |
4 |
118,470,137 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01615:Cfap57
|
APN |
4 |
118,457,993 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02154:Cfap57
|
APN |
4 |
118,470,214 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02161:Cfap57
|
APN |
4 |
118,436,569 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02481:Cfap57
|
APN |
4 |
118,438,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02483:Cfap57
|
APN |
4 |
118,438,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02503:Cfap57
|
APN |
4 |
118,426,545 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02800:Cfap57
|
APN |
4 |
118,471,947 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03083:Cfap57
|
APN |
4 |
118,441,936 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03146:Cfap57
|
APN |
4 |
118,456,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03246:Cfap57
|
APN |
4 |
118,433,842 (GRCm39) |
missense |
probably benign |
0.29 |
IGL03376:Cfap57
|
APN |
4 |
118,441,917 (GRCm39) |
missense |
probably damaging |
0.96 |
G1Funyon:Cfap57
|
UTSW |
4 |
118,450,271 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0144:Cfap57
|
UTSW |
4 |
118,441,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Cfap57
|
UTSW |
4 |
118,456,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R0415:Cfap57
|
UTSW |
4 |
118,426,628 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0515:Cfap57
|
UTSW |
4 |
118,477,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Cfap57
|
UTSW |
4 |
118,426,924 (GRCm39) |
splice site |
probably benign |
|
R0730:Cfap57
|
UTSW |
4 |
118,470,117 (GRCm39) |
splice site |
probably null |
|
R0737:Cfap57
|
UTSW |
4 |
118,438,299 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0854:Cfap57
|
UTSW |
4 |
118,419,069 (GRCm39) |
missense |
probably benign |
0.04 |
R0880:Cfap57
|
UTSW |
4 |
118,439,035 (GRCm39) |
nonsense |
probably null |
|
R1085:Cfap57
|
UTSW |
4 |
118,452,976 (GRCm39) |
missense |
probably benign |
0.20 |
R1119:Cfap57
|
UTSW |
4 |
118,463,873 (GRCm39) |
nonsense |
probably null |
|
R1217:Cfap57
|
UTSW |
4 |
118,463,849 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1294:Cfap57
|
UTSW |
4 |
118,463,731 (GRCm39) |
critical splice donor site |
probably null |
|
R1487:Cfap57
|
UTSW |
4 |
118,471,978 (GRCm39) |
missense |
probably benign |
0.01 |
R1676:Cfap57
|
UTSW |
4 |
118,453,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R1688:Cfap57
|
UTSW |
4 |
118,426,843 (GRCm39) |
missense |
probably null |
0.20 |
R1709:Cfap57
|
UTSW |
4 |
118,428,901 (GRCm39) |
missense |
probably benign |
0.00 |
R1719:Cfap57
|
UTSW |
4 |
118,463,828 (GRCm39) |
missense |
probably benign |
0.04 |
R1782:Cfap57
|
UTSW |
4 |
118,472,172 (GRCm39) |
missense |
probably damaging |
0.98 |
R1791:Cfap57
|
UTSW |
4 |
118,428,921 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1850:Cfap57
|
UTSW |
4 |
118,457,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Cfap57
|
UTSW |
4 |
118,457,124 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1912:Cfap57
|
UTSW |
4 |
118,472,207 (GRCm39) |
missense |
probably damaging |
0.96 |
R1978:Cfap57
|
UTSW |
4 |
118,450,329 (GRCm39) |
missense |
probably benign |
0.03 |
R2177:Cfap57
|
UTSW |
4 |
118,463,885 (GRCm39) |
missense |
probably benign |
0.00 |
R2322:Cfap57
|
UTSW |
4 |
118,467,922 (GRCm39) |
missense |
probably benign |
|
R3905:Cfap57
|
UTSW |
4 |
118,453,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R4013:Cfap57
|
UTSW |
4 |
118,450,340 (GRCm39) |
missense |
probably benign |
0.01 |
R4079:Cfap57
|
UTSW |
4 |
118,456,194 (GRCm39) |
missense |
probably benign |
0.34 |
R4962:Cfap57
|
UTSW |
4 |
118,470,262 (GRCm39) |
missense |
probably benign |
0.21 |
R4970:Cfap57
|
UTSW |
4 |
118,477,568 (GRCm39) |
missense |
probably damaging |
0.99 |
R4974:Cfap57
|
UTSW |
4 |
118,450,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4999:Cfap57
|
UTSW |
4 |
118,453,045 (GRCm39) |
missense |
probably benign |
0.01 |
R5482:Cfap57
|
UTSW |
4 |
118,426,838 (GRCm39) |
missense |
probably benign |
|
R5522:Cfap57
|
UTSW |
4 |
118,453,085 (GRCm39) |
missense |
probably benign |
0.41 |
R5626:Cfap57
|
UTSW |
4 |
118,471,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R5685:Cfap57
|
UTSW |
4 |
118,426,656 (GRCm39) |
missense |
probably benign |
|
R5712:Cfap57
|
UTSW |
4 |
118,471,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R5961:Cfap57
|
UTSW |
4 |
118,428,942 (GRCm39) |
missense |
probably benign |
0.00 |
R6244:Cfap57
|
UTSW |
4 |
118,436,607 (GRCm39) |
missense |
probably damaging |
0.99 |
R6268:Cfap57
|
UTSW |
4 |
118,426,648 (GRCm39) |
nonsense |
probably null |
|
R6271:Cfap57
|
UTSW |
4 |
118,452,956 (GRCm39) |
missense |
probably benign |
0.13 |
R6330:Cfap57
|
UTSW |
4 |
118,426,593 (GRCm39) |
missense |
probably benign |
|
R6439:Cfap57
|
UTSW |
4 |
118,446,172 (GRCm39) |
critical splice donor site |
probably null |
|
R6639:Cfap57
|
UTSW |
4 |
118,411,909 (GRCm39) |
missense |
probably benign |
0.13 |
R6722:Cfap57
|
UTSW |
4 |
118,441,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Cfap57
|
UTSW |
4 |
118,470,323 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7143:Cfap57
|
UTSW |
4 |
118,477,906 (GRCm39) |
unclassified |
probably benign |
|
R7162:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7174:Cfap57
|
UTSW |
4 |
118,446,264 (GRCm39) |
missense |
probably benign |
0.35 |
R7210:Cfap57
|
UTSW |
4 |
118,433,900 (GRCm39) |
nonsense |
probably null |
|
R7242:Cfap57
|
UTSW |
4 |
118,450,293 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7244:Cfap57
|
UTSW |
4 |
118,411,997 (GRCm39) |
nonsense |
probably null |
|
R7359:Cfap57
|
UTSW |
4 |
118,456,162 (GRCm39) |
missense |
probably benign |
0.01 |
R7373:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7394:Cfap57
|
UTSW |
4 |
118,450,334 (GRCm39) |
missense |
probably benign |
0.00 |
R7401:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7412:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7414:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7452:Cfap57
|
UTSW |
4 |
118,452,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R7457:Cfap57
|
UTSW |
4 |
118,446,198 (GRCm39) |
missense |
probably damaging |
0.97 |
R7559:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7642:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7741:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7744:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7745:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7842:Cfap57
|
UTSW |
4 |
118,411,952 (GRCm39) |
nonsense |
probably null |
|
R7936:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7940:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R7942:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R8301:Cfap57
|
UTSW |
4 |
118,450,271 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8411:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R8447:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R8491:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R8524:Cfap57
|
UTSW |
4 |
118,472,128 (GRCm39) |
missense |
probably benign |
|
R8670:Cfap57
|
UTSW |
4 |
118,472,122 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8707:Cfap57
|
UTSW |
4 |
118,450,203 (GRCm39) |
missense |
probably benign |
0.04 |
R8790:Cfap57
|
UTSW |
4 |
118,439,111 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8941:Cfap57
|
UTSW |
4 |
118,426,799 (GRCm39) |
missense |
probably damaging |
0.99 |
R9139:Cfap57
|
UTSW |
4 |
118,412,048 (GRCm39) |
missense |
probably benign |
0.02 |
R9212:Cfap57
|
UTSW |
4 |
118,436,649 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9442:Cfap57
|
UTSW |
4 |
118,463,731 (GRCm39) |
critical splice donor site |
probably null |
|
R9525:Cfap57
|
UTSW |
4 |
118,433,778 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Cfap57
|
UTSW |
4 |
118,471,942 (GRCm39) |
missense |
probably benign |
|
Z1088:Cfap57
|
UTSW |
4 |
118,439,079 (GRCm39) |
missense |
probably benign |
0.22 |
Z1177:Cfap57
|
UTSW |
4 |
118,456,153 (GRCm39) |
critical splice donor site |
probably null |
|
|