Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930567H17Rik |
G |
A |
X: 69,437,994 (GRCm39) |
R100W |
possibly damaging |
Het |
Acrv1 |
A |
T |
9: 36,604,608 (GRCm39) |
M1L |
probably benign |
Het |
Adam23 |
G |
A |
1: 63,624,524 (GRCm39) |
G784D |
possibly damaging |
Het |
Astl |
A |
T |
2: 127,198,479 (GRCm39) |
M365L |
probably benign |
Het |
C1ql3 |
T |
A |
2: 13,015,184 (GRCm39) |
T159S |
|
Het |
Ccser2 |
T |
G |
14: 36,601,352 (GRCm39) |
D344A |
probably damaging |
Het |
Cox11 |
A |
C |
11: 90,534,599 (GRCm39) |
I214L |
probably damaging |
Het |
Cramp1 |
C |
T |
17: 25,202,114 (GRCm39) |
G456D |
probably damaging |
Het |
Ctsq |
T |
A |
13: 61,185,502 (GRCm39) |
Y213F |
probably damaging |
Het |
Cyp2j5 |
T |
A |
4: 96,522,555 (GRCm39) |
I340F |
probably damaging |
Het |
Efcab6 |
A |
G |
15: 83,829,349 (GRCm39) |
F664L |
probably damaging |
Het |
Eif3j2 |
A |
G |
18: 43,610,276 (GRCm39) |
L179P |
probably benign |
Het |
Gabbr1 |
T |
C |
17: 37,358,436 (GRCm39) |
V58A |
probably benign |
Het |
Gabra1 |
T |
A |
11: 42,024,553 (GRCm39) |
Y374F |
probably benign |
Het |
Glt28d2 |
A |
T |
3: 85,779,359 (GRCm39) |
V38D |
possibly damaging |
Het |
Grid2 |
A |
T |
6: 63,233,923 (GRCm39) |
H28L |
probably benign |
Het |
Hat1 |
G |
A |
2: 71,269,137 (GRCm39) |
R355K |
probably damaging |
Het |
Hivep3 |
T |
C |
4: 119,953,657 (GRCm39) |
Y658H |
possibly damaging |
Het |
Hsh2d |
T |
C |
8: 72,951,690 (GRCm39) |
F108S |
probably damaging |
Het |
Il17rc |
G |
T |
6: 113,456,031 (GRCm39) |
C292F |
probably damaging |
Het |
Il31ra |
T |
C |
13: 112,660,861 (GRCm39) |
D576G |
possibly damaging |
Het |
Iqsec3 |
T |
C |
6: 121,389,515 (GRCm39) |
D652G |
probably damaging |
Het |
Kdm5a |
T |
A |
6: 120,366,624 (GRCm39) |
S420R |
probably damaging |
Het |
Klhdc7b |
A |
G |
15: 89,272,888 (GRCm39) |
T599A |
probably benign |
Het |
Lrrc8c |
A |
T |
5: 105,754,954 (GRCm39) |
E243V |
probably damaging |
Het |
Mecom |
A |
G |
3: 30,006,882 (GRCm39) |
S714P |
probably damaging |
Het |
Mindy4 |
T |
C |
6: 55,255,223 (GRCm39) |
L567P |
probably benign |
Het |
Mipep |
G |
T |
14: 61,109,506 (GRCm39) |
A628S |
probably damaging |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Mterf3 |
C |
T |
13: 67,064,676 (GRCm39) |
|
probably null |
Het |
Myh15 |
C |
A |
16: 48,959,130 (GRCm39) |
L1001I |
probably damaging |
Het |
Myom3 |
G |
A |
4: 135,541,565 (GRCm39) |
M1385I |
probably benign |
Het |
Nbea |
T |
C |
3: 55,926,784 (GRCm39) |
|
probably benign |
Het |
Nphs1 |
C |
T |
7: 30,162,080 (GRCm39) |
R270W |
probably damaging |
Het |
Nwd1 |
T |
A |
8: 73,438,484 (GRCm39) |
S1552T |
probably benign |
Het |
Or10ag60 |
A |
T |
2: 87,438,412 (GRCm39) |
I227F |
probably damaging |
Het |
Or10j5 |
G |
A |
1: 172,785,045 (GRCm39) |
V228M |
probably benign |
Het |
Or52ae9 |
G |
T |
7: 103,389,675 (GRCm39) |
F257L |
probably damaging |
Het |
Or52r1 |
A |
T |
7: 102,536,699 (GRCm39) |
Y220* |
probably null |
Het |
Pcdh7 |
A |
T |
5: 57,876,717 (GRCm39) |
I91F |
probably damaging |
Het |
Pheta2 |
G |
T |
15: 82,227,618 (GRCm39) |
V46F |
probably damaging |
Het |
Piezo1 |
T |
C |
8: 123,216,330 (GRCm39) |
R1394G |
|
Het |
Pramel28 |
G |
T |
4: 143,691,494 (GRCm39) |
Q410K |
probably benign |
Het |
Psmd1 |
G |
A |
1: 86,012,914 (GRCm39) |
R361Q |
probably damaging |
Het |
Ralb |
G |
A |
1: 119,411,246 (GRCm39) |
T31M |
probably damaging |
Het |
Rassf4 |
T |
A |
6: 116,617,305 (GRCm39) |
K233N |
probably damaging |
Het |
Rif1 |
T |
C |
2: 51,988,875 (GRCm39) |
F756S |
probably damaging |
Het |
Rpgrip1 |
G |
A |
14: 52,382,501 (GRCm39) |
D556N |
possibly damaging |
Het |
Scai |
T |
C |
2: 39,040,400 (GRCm39) |
|
probably benign |
Het |
Scfd1 |
A |
G |
12: 51,474,678 (GRCm39) |
T478A |
probably benign |
Het |
Spag17 |
T |
A |
3: 99,911,994 (GRCm39) |
I288N |
possibly damaging |
Het |
Sult1e1 |
C |
T |
5: 87,727,719 (GRCm39) |
V188I |
probably benign |
Het |
Tmco1 |
A |
G |
1: 167,143,814 (GRCm39) |
R82G |
|
Het |
Tmem109 |
T |
C |
19: 10,849,235 (GRCm39) |
S207G |
probably benign |
Het |
Vmn2r115 |
A |
G |
17: 23,578,497 (GRCm39) |
T657A |
probably damaging |
Het |
Whamm |
A |
G |
7: 81,243,640 (GRCm39) |
T621A |
probably benign |
Het |
Zbtb40 |
A |
G |
4: 136,725,897 (GRCm39) |
L554P |
probably damaging |
Het |
Zfp131 |
A |
T |
13: 120,244,338 (GRCm39) |
M114K |
probably damaging |
Het |
Zfp532 |
C |
T |
18: 65,757,404 (GRCm39) |
P446S |
probably damaging |
Het |
|
Other mutations in Fhad1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Fhad1
|
APN |
4 |
141,632,923 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01478:Fhad1
|
APN |
4 |
141,678,949 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01752:Fhad1
|
APN |
4 |
141,700,210 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01788:Fhad1
|
APN |
4 |
141,660,113 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01919:Fhad1
|
APN |
4 |
141,691,906 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02489:Fhad1
|
APN |
4 |
141,684,931 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02568:Fhad1
|
APN |
4 |
141,660,105 (GRCm39) |
missense |
probably null |
1.00 |
IGL02583:Fhad1
|
APN |
4 |
141,738,955 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02716:Fhad1
|
APN |
4 |
141,645,642 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02819:Fhad1
|
APN |
4 |
141,646,069 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02820:Fhad1
|
APN |
4 |
141,646,069 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03038:Fhad1
|
APN |
4 |
141,729,805 (GRCm39) |
missense |
probably benign |
0.38 |
IGL03167:Fhad1
|
APN |
4 |
141,700,108 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03255:Fhad1
|
APN |
4 |
141,700,191 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4466_Fhad1_343
|
UTSW |
4 |
141,684,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831_Fhad1_494
|
UTSW |
4 |
141,643,378 (GRCm39) |
splice site |
probably null |
|
R5504_Fhad1_818
|
UTSW |
4 |
141,712,846 (GRCm39) |
missense |
probably benign |
|
BB002:Fhad1
|
UTSW |
4 |
141,681,498 (GRCm39) |
missense |
probably damaging |
0.97 |
BB012:Fhad1
|
UTSW |
4 |
141,681,498 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT1430001:Fhad1
|
UTSW |
4 |
141,637,060 (GRCm39) |
missense |
probably damaging |
0.99 |
R0014:Fhad1
|
UTSW |
4 |
141,655,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Fhad1
|
UTSW |
4 |
141,667,406 (GRCm39) |
missense |
probably benign |
0.06 |
R0143:Fhad1
|
UTSW |
4 |
141,656,957 (GRCm39) |
splice site |
probably benign |
|
R0178:Fhad1
|
UTSW |
4 |
141,682,651 (GRCm39) |
missense |
probably benign |
0.31 |
R0308:Fhad1
|
UTSW |
4 |
141,712,904 (GRCm39) |
splice site |
probably benign |
|
R0384:Fhad1
|
UTSW |
4 |
141,729,737 (GRCm39) |
missense |
probably benign |
|
R0583:Fhad1
|
UTSW |
4 |
141,631,301 (GRCm39) |
missense |
probably benign |
0.37 |
R1501:Fhad1
|
UTSW |
4 |
141,691,936 (GRCm39) |
missense |
probably benign |
|
R1584:Fhad1
|
UTSW |
4 |
141,712,822 (GRCm39) |
missense |
probably benign |
0.22 |
R1615:Fhad1
|
UTSW |
4 |
141,649,634 (GRCm39) |
missense |
probably damaging |
0.99 |
R1991:Fhad1
|
UTSW |
4 |
141,709,473 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2060:Fhad1
|
UTSW |
4 |
141,626,560 (GRCm39) |
missense |
probably benign |
0.08 |
R2079:Fhad1
|
UTSW |
4 |
141,718,513 (GRCm39) |
nonsense |
probably null |
|
R2133:Fhad1
|
UTSW |
4 |
141,655,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R2337:Fhad1
|
UTSW |
4 |
141,649,655 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2843:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2844:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2845:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2846:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2866:Fhad1
|
UTSW |
4 |
141,648,099 (GRCm39) |
missense |
probably benign |
0.00 |
R3119:Fhad1
|
UTSW |
4 |
141,645,618 (GRCm39) |
frame shift |
probably null |
|
R3760:Fhad1
|
UTSW |
4 |
141,637,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R4180:Fhad1
|
UTSW |
4 |
141,712,854 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4466:Fhad1
|
UTSW |
4 |
141,684,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Fhad1
|
UTSW |
4 |
141,623,779 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4680:Fhad1
|
UTSW |
4 |
141,738,858 (GRCm39) |
nonsense |
probably null |
|
R4725:Fhad1
|
UTSW |
4 |
141,655,689 (GRCm39) |
critical splice donor site |
probably null |
|
R4755:Fhad1
|
UTSW |
4 |
141,655,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Fhad1
|
UTSW |
4 |
141,643,378 (GRCm39) |
splice site |
probably null |
|
R4909:Fhad1
|
UTSW |
4 |
141,712,822 (GRCm39) |
missense |
probably benign |
0.01 |
R4968:Fhad1
|
UTSW |
4 |
141,645,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Fhad1
|
UTSW |
4 |
141,729,910 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5036:Fhad1
|
UTSW |
4 |
141,648,052 (GRCm39) |
missense |
probably benign |
0.03 |
R5048:Fhad1
|
UTSW |
4 |
141,691,987 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5416:Fhad1
|
UTSW |
4 |
141,646,113 (GRCm39) |
missense |
probably benign |
0.39 |
R5504:Fhad1
|
UTSW |
4 |
141,712,846 (GRCm39) |
missense |
probably benign |
|
R5586:Fhad1
|
UTSW |
4 |
141,632,442 (GRCm39) |
missense |
probably benign |
0.44 |
R5692:Fhad1
|
UTSW |
4 |
141,690,768 (GRCm39) |
missense |
probably benign |
0.00 |
R5706:Fhad1
|
UTSW |
4 |
141,681,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Fhad1
|
UTSW |
4 |
141,656,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R5823:Fhad1
|
UTSW |
4 |
141,682,617 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5833:Fhad1
|
UTSW |
4 |
141,729,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Fhad1
|
UTSW |
4 |
141,618,263 (GRCm39) |
nonsense |
probably null |
|
R6286:Fhad1
|
UTSW |
4 |
141,648,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R6610:Fhad1
|
UTSW |
4 |
141,643,707 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6755:Fhad1
|
UTSW |
4 |
141,691,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7006:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7008:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7012:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7014:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7058:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7059:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7060:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7159:Fhad1
|
UTSW |
4 |
141,678,927 (GRCm39) |
missense |
probably benign |
0.01 |
R7472:Fhad1
|
UTSW |
4 |
141,691,937 (GRCm39) |
missense |
probably benign |
|
R7670:Fhad1
|
UTSW |
4 |
141,678,802 (GRCm39) |
missense |
probably benign |
0.01 |
R7694:Fhad1
|
UTSW |
4 |
141,632,375 (GRCm39) |
missense |
probably benign |
0.41 |
R7745:Fhad1
|
UTSW |
4 |
141,618,250 (GRCm39) |
missense |
probably benign |
0.00 |
R7848:Fhad1
|
UTSW |
4 |
141,632,913 (GRCm39) |
missense |
probably benign |
0.29 |
R7853:Fhad1
|
UTSW |
4 |
141,637,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R7867:Fhad1
|
UTSW |
4 |
141,632,902 (GRCm39) |
missense |
probably benign |
0.00 |
R7925:Fhad1
|
UTSW |
4 |
141,681,498 (GRCm39) |
missense |
probably damaging |
0.97 |
R8089:Fhad1
|
UTSW |
4 |
141,684,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8123:Fhad1
|
UTSW |
4 |
141,712,836 (GRCm39) |
missense |
probably benign |
0.02 |
R8711:Fhad1
|
UTSW |
4 |
141,684,924 (GRCm39) |
missense |
probably benign |
0.25 |
R8751:Fhad1
|
UTSW |
4 |
141,646,134 (GRCm39) |
missense |
probably benign |
0.04 |
R8783:Fhad1
|
UTSW |
4 |
141,636,403 (GRCm39) |
missense |
probably benign |
0.02 |
R8858:Fhad1
|
UTSW |
4 |
141,666,339 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8867:Fhad1
|
UTSW |
4 |
141,656,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R8982:Fhad1
|
UTSW |
4 |
141,729,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Fhad1
|
UTSW |
4 |
141,649,735 (GRCm39) |
splice site |
probably benign |
|
R9021:Fhad1
|
UTSW |
4 |
141,709,620 (GRCm39) |
missense |
probably damaging |
0.97 |
R9190:Fhad1
|
UTSW |
4 |
141,646,058 (GRCm39) |
critical splice donor site |
probably null |
|
R9237:Fhad1
|
UTSW |
4 |
141,632,483 (GRCm39) |
missense |
probably benign |
0.11 |
R9614:Fhad1
|
UTSW |
4 |
141,678,882 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9744:Fhad1
|
UTSW |
4 |
141,637,124 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Fhad1
|
UTSW |
4 |
141,678,927 (GRCm39) |
missense |
probably benign |
0.01 |
|