Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
C |
5: 9,008,431 (GRCm39) |
S1200P |
probably damaging |
Het |
Acadsb |
A |
G |
7: 131,045,382 (GRCm39) |
Y438C |
probably benign |
Het |
Acp7 |
A |
C |
7: 28,313,838 (GRCm39) |
W399G |
probably damaging |
Het |
Actr3b |
A |
G |
5: 26,027,403 (GRCm39) |
T113A |
possibly damaging |
Het |
Adgrv1 |
T |
C |
13: 81,654,259 (GRCm39) |
D2204G |
probably benign |
Het |
Ago1 |
A |
G |
4: 126,335,704 (GRCm39) |
V669A |
possibly damaging |
Het |
Ang5 |
T |
A |
14: 44,199,978 (GRCm39) |
L14Q |
probably null |
Het |
Aoc1 |
T |
C |
6: 48,883,374 (GRCm39) |
Y417H |
possibly damaging |
Het |
Arhgap32 |
T |
C |
9: 32,158,793 (GRCm39) |
I186T |
probably damaging |
Het |
Atf2 |
A |
T |
2: 73,675,855 (GRCm39) |
|
probably null |
Het |
Atg4a |
A |
G |
X: 139,890,984 (GRCm39) |
I91V |
probably benign |
Het |
Atp7b |
T |
G |
8: 22,488,282 (GRCm39) |
T1102P |
probably damaging |
Het |
Bend5 |
A |
C |
4: 111,288,207 (GRCm39) |
|
probably benign |
Het |
Camkk2 |
T |
C |
5: 122,884,398 (GRCm39) |
D341G |
probably damaging |
Het |
Cast |
T |
A |
13: 74,888,024 (GRCm39) |
I208L |
probably damaging |
Het |
Ccdc141 |
A |
T |
2: 76,962,606 (GRCm39) |
W113R |
probably damaging |
Het |
Cdk14 |
T |
A |
5: 4,938,924 (GRCm39) |
M433L |
probably benign |
Het |
Cel |
A |
G |
2: 28,451,204 (GRCm39) |
F51S |
probably damaging |
Het |
Cenpc1 |
A |
G |
5: 86,164,062 (GRCm39) |
L853S |
probably damaging |
Het |
Cep162 |
C |
A |
9: 87,088,967 (GRCm39) |
D972Y |
probably damaging |
Het |
Cimip3 |
AC |
A |
17: 47,744,348 (GRCm39) |
|
probably benign |
Het |
Clasrp |
A |
G |
7: 19,320,510 (GRCm39) |
|
probably benign |
Het |
Cntnap5c |
T |
A |
17: 58,637,310 (GRCm39) |
N1062K |
probably benign |
Het |
Col3a1 |
A |
G |
1: 45,360,792 (GRCm39) |
D74G |
unknown |
Het |
Copb1 |
T |
A |
7: 113,853,110 (GRCm39) |
D29V |
possibly damaging |
Het |
Cox6a1 |
C |
T |
5: 115,486,907 (GRCm39) |
E35K |
possibly damaging |
Het |
Cyp2b9 |
G |
A |
7: 25,873,030 (GRCm39) |
|
probably null |
Het |
Ddx46 |
A |
G |
13: 55,795,521 (GRCm39) |
K177E |
possibly damaging |
Het |
Dmbt1 |
T |
C |
7: 130,692,224 (GRCm39) |
F823L |
probably benign |
Het |
Drc7 |
A |
T |
8: 95,801,637 (GRCm39) |
H666L |
probably benign |
Het |
Fam228a |
T |
C |
12: 4,787,775 (GRCm39) |
|
probably benign |
Het |
Fam83e |
A |
T |
7: 45,378,193 (GRCm39) |
K406* |
probably null |
Het |
Fam83e |
A |
T |
7: 45,378,194 (GRCm39) |
K406M |
possibly damaging |
Het |
Fam90a1a |
T |
A |
8: 22,453,533 (GRCm39) |
L296Q |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,403,408 (GRCm39) |
Y53C |
probably damaging |
Het |
Fryl |
T |
A |
5: 73,230,187 (GRCm39) |
N1657Y |
possibly damaging |
Het |
Fsip2 |
T |
A |
2: 82,793,095 (GRCm39) |
D417E |
probably benign |
Het |
Garin5b |
T |
A |
7: 4,774,020 (GRCm39) |
M31L |
probably benign |
Het |
Greb1l |
A |
G |
18: 10,503,307 (GRCm39) |
M453V |
possibly damaging |
Het |
Gtf2b |
A |
G |
3: 142,487,185 (GRCm39) |
D207G |
probably benign |
Het |
Has3 |
C |
A |
8: 107,600,888 (GRCm39) |
L117I |
probably damaging |
Het |
Iqca1l |
C |
T |
5: 24,757,038 (GRCm39) |
|
probably benign |
Het |
Jmjd1c |
T |
A |
10: 67,061,073 (GRCm39) |
I1142N |
probably damaging |
Het |
Lipt2 |
C |
T |
7: 99,808,601 (GRCm39) |
T38I |
probably benign |
Het |
Magea2 |
A |
T |
X: 153,810,855 (GRCm39) |
L243Q |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,872,259 (GRCm39) |
C2178S |
possibly damaging |
Het |
Mctp2 |
A |
G |
7: 71,835,568 (GRCm39) |
L543P |
probably damaging |
Het |
Mmut |
A |
T |
17: 41,267,210 (GRCm39) |
I595F |
probably benign |
Het |
Mphosph9 |
C |
T |
5: 124,421,722 (GRCm39) |
V740I |
probably benign |
Het |
Mtrex |
A |
T |
13: 113,013,046 (GRCm39) |
M890K |
probably damaging |
Het |
Myo1e |
G |
A |
9: 70,285,655 (GRCm39) |
|
probably null |
Het |
Nlrc4 |
A |
G |
17: 74,752,625 (GRCm39) |
I586T |
probably damaging |
Het |
Nom1 |
T |
A |
5: 29,642,750 (GRCm39) |
V417D |
probably damaging |
Het |
Nphs1 |
A |
T |
7: 30,167,417 (GRCm39) |
I782F |
possibly damaging |
Het |
Numa1 |
A |
G |
7: 101,649,998 (GRCm39) |
E1243G |
probably damaging |
Het |
Or4a81 |
T |
C |
2: 89,618,814 (GRCm39) |
H294R |
probably benign |
Het |
Or4k42 |
T |
C |
2: 111,320,323 (GRCm39) |
Y60C |
probably damaging |
Het |
Or52e7 |
A |
G |
7: 104,685,026 (GRCm39) |
Y207C |
probably benign |
Het |
Or5g23 |
T |
A |
2: 85,438,807 (GRCm39) |
Y149F |
possibly damaging |
Het |
Or5p54 |
A |
T |
7: 107,554,244 (GRCm39) |
Y132F |
probably damaging |
Het |
Orai2 |
C |
T |
5: 136,190,454 (GRCm39) |
V52I |
probably damaging |
Het |
Osbpl5 |
A |
G |
7: 143,262,831 (GRCm39) |
C186R |
probably damaging |
Het |
Osbpl6 |
A |
G |
2: 76,414,818 (GRCm39) |
E403G |
probably damaging |
Het |
Padi4 |
G |
A |
4: 140,487,251 (GRCm39) |
T217I |
possibly damaging |
Het |
Parm1 |
C |
T |
5: 91,741,980 (GRCm39) |
T116I |
possibly damaging |
Het |
Pde4dip |
T |
A |
3: 97,625,500 (GRCm39) |
Q1366L |
probably damaging |
Het |
Phgdh |
T |
C |
3: 98,235,607 (GRCm39) |
K108E |
probably benign |
Het |
Pold1 |
T |
C |
7: 44,183,223 (GRCm39) |
|
probably null |
Het |
Ppp1r37 |
G |
T |
7: 19,295,943 (GRCm39) |
|
probably benign |
Het |
Sdk2 |
T |
C |
11: 113,721,620 (GRCm39) |
N1332S |
probably benign |
Het |
Sema6d |
A |
G |
2: 124,506,070 (GRCm39) |
D626G |
probably damaging |
Het |
Slc18b1 |
A |
G |
10: 23,686,820 (GRCm39) |
N212S |
probably benign |
Het |
Slc2a9 |
T |
C |
5: 38,610,542 (GRCm39) |
T86A |
probably damaging |
Het |
Slco1a6 |
A |
T |
6: 142,036,742 (GRCm39) |
M555K |
probably benign |
Het |
Sntg2 |
C |
T |
12: 30,286,687 (GRCm39) |
W302* |
probably null |
Het |
Spata22 |
T |
A |
11: 73,231,301 (GRCm39) |
M185K |
possibly damaging |
Het |
Stk35 |
T |
A |
2: 129,652,427 (GRCm39) |
Y309* |
probably null |
Het |
Taar8c |
A |
G |
10: 23,976,969 (GRCm39) |
V281A |
probably benign |
Het |
Thoc1 |
C |
A |
18: 9,993,466 (GRCm39) |
D608E |
possibly damaging |
Het |
Tmem121b |
A |
T |
6: 120,469,030 (GRCm39) |
Y562* |
probably null |
Het |
Tmem121b |
A |
G |
6: 120,469,032 (GRCm39) |
Y562H |
probably damaging |
Het |
Tmtc4 |
A |
T |
14: 123,178,820 (GRCm39) |
I449N |
probably benign |
Het |
Tmub1 |
C |
A |
5: 24,651,922 (GRCm39) |
G14V |
possibly damaging |
Het |
Tmub1 |
G |
A |
5: 24,652,175 (GRCm39) |
|
probably benign |
Het |
Tshz2 |
A |
G |
2: 169,728,397 (GRCm39) |
T529A |
probably damaging |
Het |
Ugdh |
A |
T |
5: 65,574,458 (GRCm39) |
|
probably benign |
Het |
Usp25 |
A |
G |
16: 76,910,682 (GRCm39) |
K913E |
probably benign |
Het |
Vgf |
A |
G |
5: 137,060,401 (GRCm39) |
|
probably benign |
Het |
Vmn2r19 |
T |
A |
6: 123,306,845 (GRCm39) |
F451Y |
probably benign |
Het |
Vmn2r59 |
A |
T |
7: 41,661,669 (GRCm39) |
C715* |
probably null |
Het |
Vps9d1 |
C |
A |
8: 123,971,860 (GRCm39) |
A582S |
probably benign |
Het |
Xbp1 |
T |
G |
11: 5,474,841 (GRCm39) |
H247Q |
probably damaging |
Het |
Zfp1008 |
A |
T |
13: 62,755,210 (GRCm39) |
I36N |
probably benign |
Het |
Zfp319 |
A |
T |
8: 96,055,129 (GRCm39) |
M358K |
possibly damaging |
Het |
Zfp438 |
A |
T |
18: 5,213,508 (GRCm39) |
N483K |
probably damaging |
Het |
Zfp518b |
T |
C |
5: 38,828,979 (GRCm39) |
N1009D |
possibly damaging |
Het |
Zfp644 |
A |
T |
5: 106,783,711 (GRCm39) |
H945Q |
probably damaging |
Het |
Zgrf1 |
T |
A |
3: 127,355,646 (GRCm39) |
S291T |
probably benign |
Het |
|
Other mutations in Fhdc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00507:Fhdc1
|
APN |
3 |
84,356,107 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00556:Fhdc1
|
APN |
3 |
84,364,549 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00951:Fhdc1
|
APN |
3 |
84,371,620 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01744:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01754:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01762:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01764:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01769:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01778:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01779:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01781:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02243:Fhdc1
|
APN |
3 |
84,381,947 (GRCm39) |
start codon destroyed |
possibly damaging |
0.89 |
IGL02260:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02261:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02266:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02271:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02284:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02292:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02296:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02301:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02347:Fhdc1
|
APN |
3 |
84,352,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02416:Fhdc1
|
APN |
3 |
84,352,535 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03189:Fhdc1
|
APN |
3 |
84,362,368 (GRCm39) |
intron |
probably benign |
|
IGL03392:Fhdc1
|
APN |
3 |
84,351,826 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0125:Fhdc1
|
UTSW |
3 |
84,352,852 (GRCm39) |
missense |
probably benign |
|
R0135:Fhdc1
|
UTSW |
3 |
84,352,925 (GRCm39) |
missense |
probably damaging |
0.97 |
R0255:Fhdc1
|
UTSW |
3 |
84,360,817 (GRCm39) |
intron |
probably benign |
|
R0401:Fhdc1
|
UTSW |
3 |
84,351,931 (GRCm39) |
missense |
probably benign |
0.02 |
R1371:Fhdc1
|
UTSW |
3 |
84,352,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Fhdc1
|
UTSW |
3 |
84,353,483 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1769:Fhdc1
|
UTSW |
3 |
84,356,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R1781:Fhdc1
|
UTSW |
3 |
84,356,111 (GRCm39) |
missense |
probably damaging |
0.99 |
R1840:Fhdc1
|
UTSW |
3 |
84,353,128 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1970:Fhdc1
|
UTSW |
3 |
84,362,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R2038:Fhdc1
|
UTSW |
3 |
84,351,868 (GRCm39) |
missense |
probably benign |
0.22 |
R2088:Fhdc1
|
UTSW |
3 |
84,382,033 (GRCm39) |
start gained |
probably benign |
|
R2939:Fhdc1
|
UTSW |
3 |
84,364,577 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3813:Fhdc1
|
UTSW |
3 |
84,371,577 (GRCm39) |
critical splice donor site |
probably null |
|
R4022:Fhdc1
|
UTSW |
3 |
84,352,409 (GRCm39) |
missense |
probably benign |
0.01 |
R4175:Fhdc1
|
UTSW |
3 |
84,364,294 (GRCm39) |
intron |
probably benign |
|
R4243:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4245:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4290:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4291:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4292:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4293:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4294:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4295:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4334:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4335:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4342:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4344:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4354:Fhdc1
|
UTSW |
3 |
84,352,133 (GRCm39) |
missense |
probably benign |
0.42 |
R4550:Fhdc1
|
UTSW |
3 |
84,352,483 (GRCm39) |
missense |
probably benign |
0.16 |
R4626:Fhdc1
|
UTSW |
3 |
84,381,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R4925:Fhdc1
|
UTSW |
3 |
84,360,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R5155:Fhdc1
|
UTSW |
3 |
84,353,457 (GRCm39) |
missense |
probably benign |
0.00 |
R5588:Fhdc1
|
UTSW |
3 |
84,372,783 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6043:Fhdc1
|
UTSW |
3 |
84,356,193 (GRCm39) |
missense |
probably damaging |
0.96 |
R6063:Fhdc1
|
UTSW |
3 |
84,353,336 (GRCm39) |
missense |
probably benign |
0.00 |
R6652:Fhdc1
|
UTSW |
3 |
84,371,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R6706:Fhdc1
|
UTSW |
3 |
84,353,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R6783:Fhdc1
|
UTSW |
3 |
84,352,834 (GRCm39) |
missense |
probably benign |
0.00 |
R6984:Fhdc1
|
UTSW |
3 |
84,351,823 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7182:Fhdc1
|
UTSW |
3 |
84,356,157 (GRCm39) |
missense |
probably damaging |
0.98 |
R7299:Fhdc1
|
UTSW |
3 |
84,351,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Fhdc1
|
UTSW |
3 |
84,353,438 (GRCm39) |
missense |
probably benign |
|
R7765:Fhdc1
|
UTSW |
3 |
84,351,906 (GRCm39) |
missense |
probably benign |
0.04 |
R8013:Fhdc1
|
UTSW |
3 |
84,381,946 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R8014:Fhdc1
|
UTSW |
3 |
84,381,946 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R8139:Fhdc1
|
UTSW |
3 |
84,358,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8264:Fhdc1
|
UTSW |
3 |
84,362,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R8384:Fhdc1
|
UTSW |
3 |
84,362,306 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8901:Fhdc1
|
UTSW |
3 |
84,352,874 (GRCm39) |
missense |
probably benign |
|
R9091:Fhdc1
|
UTSW |
3 |
84,352,290 (GRCm39) |
missense |
unknown |
|
R9270:Fhdc1
|
UTSW |
3 |
84,352,290 (GRCm39) |
missense |
unknown |
|
R9361:Fhdc1
|
UTSW |
3 |
84,356,140 (GRCm39) |
missense |
probably damaging |
1.00 |
|