Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afdn |
T |
G |
17: 14,109,144 (GRCm39) |
S1571A |
probably damaging |
Het |
Agbl1 |
C |
A |
7: 76,348,513 (GRCm39) |
A870D |
unknown |
Het |
Alpl |
C |
T |
4: 137,471,120 (GRCm39) |
G339R |
probably damaging |
Het |
Ankrd55 |
T |
C |
13: 112,504,498 (GRCm39) |
Y415H |
probably damaging |
Het |
Cd69 |
G |
A |
6: 129,247,008 (GRCm39) |
R111C |
possibly damaging |
Het |
Cdh26 |
A |
T |
2: 178,101,896 (GRCm39) |
T172S |
probably damaging |
Het |
Cflar |
T |
A |
1: 58,791,966 (GRCm39) |
V423E |
|
Het |
Cgrrf1 |
A |
C |
14: 47,091,415 (GRCm39) |
Q313P |
possibly damaging |
Het |
Chga |
G |
A |
12: 102,527,606 (GRCm39) |
A87T |
probably benign |
Het |
Chrna4 |
T |
A |
2: 180,660,386 (GRCm39) |
D102V |
|
Het |
Cpvl |
A |
T |
6: 53,909,502 (GRCm39) |
Y211* |
probably null |
Het |
Cyp26a1 |
G |
A |
19: 37,689,512 (GRCm39) |
D403N |
possibly damaging |
Het |
Dchs2 |
T |
C |
3: 83,036,789 (GRCm39) |
L512P |
probably damaging |
Het |
Dll3 |
A |
C |
7: 28,001,170 (GRCm39) |
M1R |
probably null |
Het |
Dnah12 |
A |
G |
14: 26,503,337 (GRCm39) |
T1564A |
probably damaging |
Het |
Efhb |
A |
G |
17: 53,707,836 (GRCm39) |
S776P |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,758,822 (GRCm39) |
S1831G |
probably damaging |
Het |
Fat1 |
G |
T |
8: 45,441,967 (GRCm39) |
|
probably null |
Het |
Fitm2 |
C |
T |
2: 163,311,892 (GRCm39) |
C107Y |
probably damaging |
Het |
Gdpd4 |
T |
C |
7: 97,621,146 (GRCm39) |
V153A |
probably benign |
Het |
Ggnbp2 |
A |
G |
11: 84,751,539 (GRCm39) |
V87A |
possibly damaging |
Het |
Glb1l |
G |
T |
1: 75,178,436 (GRCm39) |
A334E |
probably damaging |
Het |
Gnas |
T |
G |
2: 174,142,005 (GRCm39) |
L784R |
probably damaging |
Het |
Gtf2i |
C |
T |
5: 134,311,659 (GRCm39) |
E223K |
probably damaging |
Het |
H2-M10.5 |
T |
C |
17: 37,084,641 (GRCm39) |
Y122H |
probably damaging |
Het |
Hikeshi |
G |
A |
7: 89,579,554 (GRCm39) |
Q6* |
probably null |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Irak2 |
A |
C |
6: 113,667,859 (GRCm39) |
D528A |
probably damaging |
Het |
Lcn2 |
A |
G |
2: 32,278,042 (GRCm39) |
C17R |
unknown |
Het |
Lcp2 |
G |
T |
11: 34,000,924 (GRCm39) |
V36L |
probably benign |
Het |
Lin7c |
T |
C |
2: 109,726,617 (GRCm39) |
S89P |
probably benign |
Het |
Lrrc37a |
C |
T |
11: 103,395,204 (GRCm39) |
A74T |
probably benign |
Het |
Lrrtm3 |
T |
A |
10: 63,923,818 (GRCm39) |
M450L |
probably benign |
Het |
Lsm11 |
C |
T |
11: 45,824,768 (GRCm39) |
R253Q |
probably benign |
Het |
Map9 |
A |
T |
3: 82,266,290 (GRCm39) |
|
probably benign |
Het |
Mmp2 |
T |
A |
8: 93,558,358 (GRCm39) |
D142E |
possibly damaging |
Het |
Nrn1l |
A |
T |
8: 106,621,430 (GRCm39) |
T127S |
probably damaging |
Het |
Or14c46 |
T |
C |
7: 85,918,983 (GRCm39) |
T5A |
probably damaging |
Het |
Pelp1 |
G |
A |
11: 70,285,585 (GRCm39) |
T761I |
probably damaging |
Het |
Pmm2 |
T |
A |
16: 8,463,254 (GRCm39) |
V63E |
probably damaging |
Het |
Ptprb |
T |
A |
10: 116,208,853 (GRCm39) |
L1942H |
probably damaging |
Het |
Ptprk |
T |
A |
10: 28,465,366 (GRCm39) |
C1350S |
possibly damaging |
Het |
Rnf44 |
A |
G |
13: 54,829,841 (GRCm39) |
V381A |
probably damaging |
Het |
Robo3 |
G |
A |
9: 37,329,816 (GRCm39) |
P1167S |
probably benign |
Het |
Ryk |
A |
G |
9: 102,775,979 (GRCm39) |
E489G |
probably damaging |
Het |
Satb2 |
T |
A |
1: 56,910,683 (GRCm39) |
I321L |
probably benign |
Het |
Sh2b1 |
A |
T |
7: 126,066,929 (GRCm39) |
V655E |
probably benign |
Het |
Slc16a12 |
G |
A |
19: 34,648,035 (GRCm39) |
T486M |
probably damaging |
Het |
Slc34a1 |
G |
T |
13: 55,561,221 (GRCm39) |
R562L |
probably benign |
Het |
Slc4a9 |
A |
G |
18: 36,669,902 (GRCm39) |
E779G |
probably damaging |
Het |
Strc |
C |
A |
2: 121,207,577 (GRCm39) |
C598F |
probably damaging |
Het |
Stxbp6 |
A |
T |
12: 44,948,810 (GRCm39) |
F100I |
probably damaging |
Het |
Tap2 |
A |
G |
17: 34,424,671 (GRCm39) |
T135A |
probably benign |
Het |
Tmcc1 |
G |
A |
6: 116,110,805 (GRCm39) |
P159S |
|
Het |
Tmem106b |
T |
A |
6: 13,078,105 (GRCm39) |
M100K |
probably benign |
Het |
Ttn |
T |
A |
2: 76,578,039 (GRCm39) |
T24285S |
probably damaging |
Het |
Vmn1r116 |
G |
A |
7: 20,606,337 (GRCm39) |
V53M |
possibly damaging |
Het |
Zar1 |
A |
T |
5: 72,738,193 (GRCm39) |
S70T |
probably benign |
Het |
Zfp235 |
C |
T |
7: 23,841,525 (GRCm39) |
T648M |
probably benign |
Het |
Zfp937 |
C |
T |
2: 150,081,268 (GRCm39) |
H433Y |
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 |
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 |
R8890:Fhad1
|
UTSW |
4 |
141,656,902 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|