Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
A |
T |
17: 9,226,838 (GRCm39) |
Q464H |
probably damaging |
Het |
Abcc5 |
A |
T |
16: 20,224,260 (GRCm39) |
S108T |
probably damaging |
Het |
Acss3 |
T |
C |
10: 106,959,174 (GRCm39) |
S91G |
probably benign |
Het |
Adgrf4 |
T |
A |
17: 42,978,333 (GRCm39) |
I337L |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,581,648 (GRCm39) |
S4799P |
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,727,596 (GRCm39) |
D348G |
probably damaging |
Het |
Afdn |
A |
G |
17: 14,109,070 (GRCm39) |
D1546G |
probably benign |
Het |
Agr2 |
A |
T |
12: 36,045,946 (GRCm39) |
R64S |
probably benign |
Het |
Ankrd13a |
T |
A |
5: 114,927,545 (GRCm39) |
|
probably null |
Het |
Apon |
T |
A |
10: 128,090,922 (GRCm39) |
M200K |
possibly damaging |
Het |
Art4 |
T |
C |
6: 136,831,428 (GRCm39) |
S238G |
possibly damaging |
Het |
Atp2a2 |
A |
T |
5: 122,629,847 (GRCm39) |
V74D |
probably benign |
Het |
Atrnl1 |
T |
C |
19: 57,687,955 (GRCm39) |
S807P |
probably damaging |
Het |
C2cd3 |
T |
C |
7: 100,080,022 (GRCm39) |
V936A |
|
Het |
Car15 |
T |
A |
16: 17,654,652 (GRCm39) |
H122L |
probably damaging |
Het |
Cav3 |
A |
T |
6: 112,449,428 (GRCm39) |
R149W |
probably benign |
Het |
Ccdc8 |
A |
T |
7: 16,728,687 (GRCm39) |
I59F |
probably damaging |
Het |
Ccng2 |
G |
A |
5: 93,418,731 (GRCm39) |
V119I |
probably benign |
Het |
Ceacam2 |
A |
G |
7: 25,227,333 (GRCm39) |
I178T |
probably benign |
Het |
Ces2a |
A |
G |
8: 105,467,930 (GRCm39) |
D520G |
probably benign |
Het |
Cln8 |
T |
C |
8: 14,945,057 (GRCm39) |
S124P |
probably benign |
Het |
Coro2a |
T |
A |
4: 46,546,674 (GRCm39) |
D227V |
probably damaging |
Het |
Cpa4 |
A |
C |
6: 30,573,889 (GRCm39) |
R32S |
probably benign |
Het |
Creb3l4 |
G |
T |
3: 90,149,729 (GRCm39) |
D45E |
probably benign |
Het |
Crybb2 |
C |
T |
5: 113,213,759 (GRCm39) |
|
probably null |
Het |
Cul7 |
T |
A |
17: 46,965,521 (GRCm39) |
H566Q |
probably benign |
Het |
Cyp2b10 |
A |
G |
7: 25,614,204 (GRCm39) |
Y226C |
probably damaging |
Het |
Dennd2a |
A |
T |
6: 39,499,743 (GRCm39) |
V274D |
probably benign |
Het |
Dmbt1 |
G |
A |
7: 130,663,093 (GRCm39) |
|
probably null |
Het |
Drc7 |
T |
C |
8: 95,794,684 (GRCm39) |
I363T |
probably benign |
Het |
Drd3 |
G |
A |
16: 43,643,047 (GRCm39) |
V396I |
probably benign |
Het |
Dync2i1 |
A |
T |
12: 116,218,130 (GRCm39) |
|
probably null |
Het |
Eif2ak4 |
A |
G |
2: 118,280,795 (GRCm39) |
N1054S |
probably benign |
Het |
Epc1 |
A |
C |
18: 6,450,084 (GRCm39) |
V458G |
probably damaging |
Het |
Exoc1 |
T |
A |
5: 76,685,562 (GRCm39) |
D91E |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,943,485 (GRCm39) |
F793I |
probably damaging |
Het |
Galnt16 |
G |
A |
12: 80,628,084 (GRCm39) |
|
probably null |
Het |
Ganc |
A |
T |
2: 120,286,582 (GRCm39) |
T804S |
probably benign |
Het |
Gpam |
A |
T |
19: 55,070,062 (GRCm39) |
V398E |
possibly damaging |
Het |
Gpr68 |
A |
G |
12: 100,844,623 (GRCm39) |
V307A |
probably benign |
Het |
Grm7 |
C |
T |
6: 111,335,722 (GRCm39) |
S711L |
probably damaging |
Het |
Hemgn |
T |
A |
4: 46,397,034 (GRCm39) |
R67S |
probably damaging |
Het |
Hmg20b |
T |
C |
10: 81,182,493 (GRCm39) |
D281G |
possibly damaging |
Het |
Ifi211 |
A |
C |
1: 173,729,401 (GRCm39) |
F277V |
probably damaging |
Het |
Ighmbp2 |
T |
C |
19: 3,322,981 (GRCm39) |
I322V |
probably benign |
Het |
Iqce |
A |
T |
5: 140,671,830 (GRCm39) |
L265H |
probably damaging |
Het |
Itgal |
G |
T |
7: 126,898,960 (GRCm39) |
A101S |
probably benign |
Het |
Kif5a |
C |
T |
10: 127,073,248 (GRCm39) |
M647I |
probably benign |
Het |
Kirrel1 |
G |
T |
3: 87,002,988 (GRCm39) |
T135K |
probably damaging |
Het |
Klf16 |
T |
C |
10: 80,412,622 (GRCm39) |
Y138C |
probably benign |
Het |
Klhl7 |
A |
G |
5: 24,331,844 (GRCm39) |
T49A |
probably benign |
Het |
Mr1 |
T |
C |
1: 155,022,474 (GRCm39) |
|
probably benign |
Het |
Mrc1 |
A |
T |
2: 14,330,104 (GRCm39) |
I1238F |
probably damaging |
Het |
Ncoa5 |
C |
T |
2: 164,846,171 (GRCm39) |
M225I |
possibly damaging |
Het |
Nf1 |
A |
T |
11: 79,438,052 (GRCm39) |
T121S |
probably damaging |
Het |
Ngfr |
T |
C |
11: 95,465,147 (GRCm39) |
T234A |
probably benign |
Het |
Ninj1 |
T |
G |
13: 49,347,356 (GRCm39) |
F74V |
probably damaging |
Het |
Npffr1 |
T |
C |
10: 61,462,088 (GRCm39) |
V408A |
probably benign |
Het |
Nsd2 |
T |
C |
5: 34,003,570 (GRCm39) |
V240A |
probably damaging |
Het |
Obi1 |
T |
C |
14: 104,716,814 (GRCm39) |
T520A |
probably damaging |
Het |
Or12d13 |
T |
A |
17: 37,648,062 (GRCm39) |
E20D |
probably benign |
Het |
Or2z2 |
A |
G |
11: 58,345,992 (GRCm39) |
M261T |
probably damaging |
Het |
Or7a35 |
T |
A |
10: 78,853,379 (GRCm39) |
F74L |
probably benign |
Het |
Or8b44 |
G |
A |
9: 38,410,369 (GRCm39) |
V135I |
probably benign |
Het |
Or8g34 |
T |
C |
9: 39,373,173 (GRCm39) |
S146P |
possibly damaging |
Het |
Ovol1 |
T |
C |
19: 5,601,614 (GRCm39) |
H136R |
probably damaging |
Het |
Prag1 |
T |
A |
8: 36,569,760 (GRCm39) |
D114E |
possibly damaging |
Het |
Pramel17 |
T |
C |
4: 101,694,331 (GRCm39) |
N184S |
probably benign |
Het |
Prss3b |
C |
A |
6: 41,010,127 (GRCm39) |
R69L |
probably benign |
Het |
Prss57 |
T |
A |
10: 79,623,234 (GRCm39) |
H71L |
probably benign |
Het |
Ptgs2 |
T |
C |
1: 149,978,448 (GRCm39) |
F187L |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 22,959,779 (GRCm39) |
N92I |
probably damaging |
Het |
Rab23 |
A |
T |
1: 33,773,812 (GRCm39) |
T91S |
possibly damaging |
Het |
Rag1 |
A |
G |
2: 101,474,006 (GRCm39) |
S379P |
probably damaging |
Het |
Ribc2 |
G |
T |
15: 85,027,448 (GRCm39) |
D310Y |
probably damaging |
Het |
Rims1 |
A |
G |
1: 22,507,291 (GRCm39) |
Y620H |
probably damaging |
Het |
Rock1 |
A |
C |
18: 10,090,820 (GRCm39) |
V938G |
probably benign |
Het |
Rsph10b |
A |
G |
5: 143,886,244 (GRCm39) |
N314S |
possibly damaging |
Het |
Sertad1 |
A |
G |
7: 27,189,327 (GRCm39) |
D216G |
possibly damaging |
Het |
Shisal1 |
G |
A |
15: 84,290,914 (GRCm39) |
T131M |
probably benign |
Het |
Slco6d1 |
T |
A |
1: 98,425,252 (GRCm39) |
V600D |
probably damaging |
Het |
Snapc2 |
T |
C |
8: 4,305,314 (GRCm39) |
I232T |
probably damaging |
Het |
Snx13 |
A |
G |
12: 35,136,913 (GRCm39) |
S125G |
probably damaging |
Het |
Srcin1 |
C |
T |
11: 97,425,551 (GRCm39) |
R502H |
probably damaging |
Het |
Tesmin |
A |
G |
19: 3,442,218 (GRCm39) |
E167G |
possibly damaging |
Het |
Tex10 |
T |
C |
4: 48,468,787 (GRCm39) |
I129M |
possibly damaging |
Het |
Tmem235 |
A |
G |
11: 117,754,967 (GRCm39) |
S140G |
probably benign |
Het |
Trim60 |
T |
A |
8: 65,454,177 (GRCm39) |
D24V |
probably damaging |
Het |
Ttc39c |
A |
G |
18: 12,822,936 (GRCm39) |
E148G |
probably benign |
Het |
Vmn2r70 |
G |
T |
7: 85,214,243 (GRCm39) |
T303K |
probably benign |
Het |
Wdr48 |
A |
T |
9: 119,745,894 (GRCm39) |
T426S |
possibly damaging |
Het |
Xirp2 |
A |
T |
2: 67,346,326 (GRCm39) |
T2856S |
probably benign |
Het |
Zswim8 |
A |
G |
14: 20,770,001 (GRCm39) |
N1356S |
probably damaging |
Het |
|
Other mutations in Fhod1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00970:Fhod1
|
APN |
8 |
106,058,734 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01149:Fhod1
|
APN |
8 |
106,074,439 (GRCm39) |
unclassified |
probably benign |
|
IGL01325:Fhod1
|
APN |
8 |
106,058,281 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01470:Fhod1
|
APN |
8 |
106,056,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01521:Fhod1
|
APN |
8 |
106,057,055 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01861:Fhod1
|
APN |
8 |
106,057,808 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02864:Fhod1
|
APN |
8 |
106,063,796 (GRCm39) |
unclassified |
probably benign |
|
IGL02951:Fhod1
|
APN |
8 |
106,057,862 (GRCm39) |
missense |
probably damaging |
1.00 |
reactive
|
UTSW |
8 |
106,063,066 (GRCm39) |
unclassified |
probably benign |
|
treason
|
UTSW |
8 |
106,063,982 (GRCm39) |
unclassified |
probably benign |
|
R0016:Fhod1
|
UTSW |
8 |
106,058,287 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0016:Fhod1
|
UTSW |
8 |
106,058,287 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0071:Fhod1
|
UTSW |
8 |
106,063,857 (GRCm39) |
splice site |
probably null |
|
R0071:Fhod1
|
UTSW |
8 |
106,063,857 (GRCm39) |
splice site |
probably null |
|
R0498:Fhod1
|
UTSW |
8 |
106,056,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R1234:Fhod1
|
UTSW |
8 |
106,063,795 (GRCm39) |
unclassified |
probably benign |
|
R1465:Fhod1
|
UTSW |
8 |
106,065,546 (GRCm39) |
unclassified |
probably benign |
|
R1465:Fhod1
|
UTSW |
8 |
106,065,546 (GRCm39) |
unclassified |
probably benign |
|
R1485:Fhod1
|
UTSW |
8 |
106,063,430 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1585:Fhod1
|
UTSW |
8 |
106,063,957 (GRCm39) |
unclassified |
probably benign |
|
R1615:Fhod1
|
UTSW |
8 |
106,074,463 (GRCm39) |
unclassified |
probably benign |
|
R1778:Fhod1
|
UTSW |
8 |
106,056,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R1781:Fhod1
|
UTSW |
8 |
106,074,421 (GRCm39) |
unclassified |
probably benign |
|
R2291:Fhod1
|
UTSW |
8 |
106,063,596 (GRCm39) |
unclassified |
probably benign |
|
R2864:Fhod1
|
UTSW |
8 |
106,059,543 (GRCm39) |
missense |
probably null |
0.97 |
R2865:Fhod1
|
UTSW |
8 |
106,059,543 (GRCm39) |
missense |
probably null |
0.97 |
R3775:Fhod1
|
UTSW |
8 |
106,058,270 (GRCm39) |
unclassified |
probably benign |
|
R4107:Fhod1
|
UTSW |
8 |
106,064,670 (GRCm39) |
unclassified |
probably benign |
|
R4422:Fhod1
|
UTSW |
8 |
106,063,983 (GRCm39) |
unclassified |
probably benign |
|
R4423:Fhod1
|
UTSW |
8 |
106,063,983 (GRCm39) |
unclassified |
probably benign |
|
R4424:Fhod1
|
UTSW |
8 |
106,063,983 (GRCm39) |
unclassified |
probably benign |
|
R4425:Fhod1
|
UTSW |
8 |
106,063,983 (GRCm39) |
unclassified |
probably benign |
|
R4641:Fhod1
|
UTSW |
8 |
106,056,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Fhod1
|
UTSW |
8 |
106,064,493 (GRCm39) |
unclassified |
probably benign |
|
R4757:Fhod1
|
UTSW |
8 |
106,074,443 (GRCm39) |
unclassified |
probably benign |
|
R5004:Fhod1
|
UTSW |
8 |
106,063,577 (GRCm39) |
unclassified |
probably benign |
|
R5082:Fhod1
|
UTSW |
8 |
106,057,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Fhod1
|
UTSW |
8 |
106,063,066 (GRCm39) |
unclassified |
probably benign |
|
R6033:Fhod1
|
UTSW |
8 |
106,063,066 (GRCm39) |
unclassified |
probably benign |
|
R6298:Fhod1
|
UTSW |
8 |
106,063,780 (GRCm39) |
unclassified |
probably benign |
|
R6320:Fhod1
|
UTSW |
8 |
106,063,982 (GRCm39) |
unclassified |
probably benign |
|
R6362:Fhod1
|
UTSW |
8 |
106,058,273 (GRCm39) |
critical splice donor site |
probably null |
|
R6449:Fhod1
|
UTSW |
8 |
106,056,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Fhod1
|
UTSW |
8 |
106,064,522 (GRCm39) |
unclassified |
probably benign |
|
R6816:Fhod1
|
UTSW |
8 |
106,057,176 (GRCm39) |
missense |
probably benign |
0.10 |
R6955:Fhod1
|
UTSW |
8 |
106,059,639 (GRCm39) |
missense |
probably benign |
0.00 |
R7073:Fhod1
|
UTSW |
8 |
106,063,771 (GRCm39) |
missense |
unknown |
|
R7697:Fhod1
|
UTSW |
8 |
106,074,563 (GRCm39) |
unclassified |
probably benign |
|
R7789:Fhod1
|
UTSW |
8 |
106,056,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R7894:Fhod1
|
UTSW |
8 |
106,057,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R8105:Fhod1
|
UTSW |
8 |
106,063,847 (GRCm39) |
missense |
unknown |
|
R8835:Fhod1
|
UTSW |
8 |
106,065,484 (GRCm39) |
critical splice donor site |
probably null |
|
R9200:Fhod1
|
UTSW |
8 |
106,058,072 (GRCm39) |
missense |
probably benign |
0.03 |
R9266:Fhod1
|
UTSW |
8 |
106,065,531 (GRCm39) |
missense |
unknown |
|
R9426:Fhod1
|
UTSW |
8 |
106,056,490 (GRCm39) |
missense |
probably benign |
0.31 |
R9429:Fhod1
|
UTSW |
8 |
106,057,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R9507:Fhod1
|
UTSW |
8 |
106,064,694 (GRCm39) |
nonsense |
probably null |
|
R9562:Fhod1
|
UTSW |
8 |
106,074,422 (GRCm39) |
missense |
unknown |
|
R9566:Fhod1
|
UTSW |
8 |
106,064,516 (GRCm39) |
missense |
unknown |
|
R9736:Fhod1
|
UTSW |
8 |
106,059,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R9739:Fhod1
|
UTSW |
8 |
106,064,378 (GRCm39) |
missense |
unknown |
|
R9746:Fhod1
|
UTSW |
8 |
106,064,048 (GRCm39) |
missense |
unknown |
|
R9748:Fhod1
|
UTSW |
8 |
106,058,323 (GRCm39) |
missense |
probably damaging |
1.00 |
|