Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130401M01Rik |
C |
A |
15: 57,885,875 (GRCm39) |
A336S |
probably benign |
Het |
Abca8b |
A |
G |
11: 109,865,417 (GRCm39) |
S347P |
probably benign |
Het |
Acvr1 |
T |
C |
2: 58,352,983 (GRCm39) |
T326A |
possibly damaging |
Het |
Atp13a4 |
A |
G |
16: 29,275,419 (GRCm39) |
I355T |
|
Het |
Atp2a2 |
G |
A |
5: 122,607,768 (GRCm39) |
T247I |
probably damaging |
Het |
Atp2b1 |
T |
A |
10: 98,837,227 (GRCm39) |
D555E |
probably benign |
Het |
Aurkb |
G |
T |
11: 68,939,058 (GRCm39) |
G94* |
probably null |
Het |
B130006D01Rik |
A |
T |
11: 95,616,986 (GRCm39) |
H37L |
unknown |
Het |
Cabin1 |
A |
G |
10: 75,494,492 (GRCm39) |
L1629P |
probably damaging |
Het |
Ccdc168 |
G |
A |
1: 44,095,578 (GRCm39) |
T1840I |
possibly damaging |
Het |
Ccdc80 |
A |
C |
16: 44,916,186 (GRCm39) |
D314A |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,360,845 (GRCm39) |
I201N |
probably damaging |
Het |
Chd9 |
T |
C |
8: 91,761,653 (GRCm39) |
L2246P |
probably damaging |
Het |
Cpsf1 |
T |
A |
15: 76,484,511 (GRCm39) |
M657L |
probably benign |
Het |
Dmtf1 |
A |
G |
5: 9,190,453 (GRCm39) |
V87A |
probably damaging |
Het |
Dspp |
G |
A |
5: 104,326,012 (GRCm39) |
D792N |
unknown |
Het |
Fat2 |
C |
A |
11: 55,171,957 (GRCm39) |
E2919* |
probably null |
Het |
Fgf20 |
A |
G |
8: 40,732,937 (GRCm39) |
V167A |
probably damaging |
Het |
Grm5 |
T |
C |
7: 87,779,266 (GRCm39) |
V934A |
possibly damaging |
Het |
Gtf3c3 |
G |
T |
1: 54,444,198 (GRCm39) |
A730D |
possibly damaging |
Het |
H2-T24 |
A |
G |
17: 36,325,483 (GRCm39) |
V335A |
probably benign |
Het |
Havcr2 |
T |
G |
11: 46,347,384 (GRCm39) |
N120K |
probably damaging |
Het |
Hmcn2 |
T |
C |
2: 31,348,038 (GRCm39) |
F4895L |
possibly damaging |
Het |
Igsf3 |
T |
C |
3: 101,342,847 (GRCm39) |
Y475H |
probably damaging |
Het |
Lonp1 |
T |
C |
17: 56,933,620 (GRCm39) |
D85G |
probably benign |
Het |
Lrrc49 |
T |
C |
9: 60,500,975 (GRCm39) |
S657G |
probably benign |
Het |
Lrrk2 |
T |
A |
15: 91,584,816 (GRCm39) |
Y382N |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,279,391 (GRCm39) |
D3870G |
probably damaging |
Het |
Mtf1 |
T |
A |
4: 124,718,081 (GRCm39) |
C260S |
probably damaging |
Het |
Naa35 |
A |
G |
13: 59,747,598 (GRCm39) |
D110G |
probably damaging |
Het |
Npas3 |
A |
T |
12: 54,115,501 (GRCm39) |
T808S |
probably damaging |
Het |
Or5a1 |
A |
G |
19: 12,097,909 (GRCm39) |
W56R |
probably damaging |
Het |
Pax9 |
A |
T |
12: 56,746,884 (GRCm39) |
H240L |
probably benign |
Het |
Pik3c2a |
T |
C |
7: 115,993,529 (GRCm39) |
T413A |
probably benign |
Het |
Pik3r1 |
A |
G |
13: 101,846,205 (GRCm39) |
V127A |
probably benign |
Het |
Pik3r5 |
A |
G |
11: 68,381,324 (GRCm39) |
E170G |
probably damaging |
Het |
Polr1a |
T |
C |
6: 71,931,819 (GRCm39) |
I966T |
possibly damaging |
Het |
Prelid2 |
A |
G |
18: 42,045,433 (GRCm39) |
|
probably null |
Het |
Rab29 |
T |
A |
1: 131,799,923 (GRCm39) |
M166K |
probably damaging |
Het |
Rab2b |
T |
C |
14: 52,503,717 (GRCm39) |
E135G |
probably damaging |
Het |
Rnf103 |
T |
A |
6: 71,486,463 (GRCm39) |
S365T |
possibly damaging |
Het |
Rnf213 |
G |
A |
11: 119,301,687 (GRCm39) |
E387K |
|
Het |
Sh3d19 |
T |
C |
3: 86,031,038 (GRCm39) |
V734A |
probably benign |
Het |
Spata31e5 |
T |
A |
1: 28,816,689 (GRCm39) |
T448S |
possibly damaging |
Het |
Spmip3 |
T |
A |
1: 177,570,828 (GRCm39) |
I54K |
probably damaging |
Het |
Ssbp1 |
T |
G |
6: 40,454,914 (GRCm39) |
N124K |
probably damaging |
Het |
Tbc1d31 |
C |
T |
15: 57,799,494 (GRCm39) |
R227* |
probably null |
Het |
Tcerg1 |
A |
G |
18: 42,657,039 (GRCm39) |
T174A |
unknown |
Het |
Tenm2 |
T |
C |
11: 35,960,388 (GRCm39) |
S980G |
possibly damaging |
Het |
Trim30a |
T |
C |
7: 104,079,386 (GRCm39) |
I156M |
possibly damaging |
Het |
Trim39 |
T |
C |
17: 36,571,396 (GRCm39) |
D454G |
possibly damaging |
Het |
Trpc7 |
A |
T |
13: 56,921,579 (GRCm39) |
*863K |
probably null |
Het |
Tubgcp3 |
A |
G |
8: 12,707,561 (GRCm39) |
Y143H |
probably benign |
Het |
Vmn1r33 |
C |
T |
6: 66,589,357 (GRCm39) |
D66N |
probably benign |
Het |
Vmn2r8 |
A |
T |
5: 108,950,043 (GRCm39) |
I268N |
probably damaging |
Het |
Vmn2r91 |
A |
C |
17: 18,356,080 (GRCm39) |
E582D |
probably benign |
Het |
Vtcn1 |
T |
C |
3: 100,791,211 (GRCm39) |
F83S |
probably damaging |
Het |
Wdr81 |
G |
T |
11: 75,332,811 (GRCm39) |
D684E |
|
Het |
Wipi1 |
A |
G |
11: 109,470,535 (GRCm39) |
S295P |
probably damaging |
Het |
Zfp27 |
A |
T |
7: 29,593,699 (GRCm39) |
H755Q |
possibly damaging |
Het |
Zfp963 |
A |
G |
8: 70,195,533 (GRCm39) |
F307L |
possibly damaging |
Het |
|
Other mutations in Drd5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03153:Drd5
|
APN |
5 |
38,477,124 (GRCm39) |
missense |
probably benign |
0.25 |
PIT4305001:Drd5
|
UTSW |
5 |
38,477,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R0051:Drd5
|
UTSW |
5 |
38,477,957 (GRCm39) |
missense |
probably benign |
0.39 |
R0051:Drd5
|
UTSW |
5 |
38,477,957 (GRCm39) |
missense |
probably benign |
0.39 |
R0571:Drd5
|
UTSW |
5 |
38,477,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R1507:Drd5
|
UTSW |
5 |
38,478,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R1663:Drd5
|
UTSW |
5 |
38,478,198 (GRCm39) |
missense |
probably benign |
0.02 |
R1777:Drd5
|
UTSW |
5 |
38,477,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1932:Drd5
|
UTSW |
5 |
38,477,319 (GRCm39) |
missense |
probably benign |
0.14 |
R1986:Drd5
|
UTSW |
5 |
38,477,456 (GRCm39) |
missense |
probably damaging |
0.99 |
R2047:Drd5
|
UTSW |
5 |
38,477,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R3875:Drd5
|
UTSW |
5 |
38,477,157 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5033:Drd5
|
UTSW |
5 |
38,477,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R5201:Drd5
|
UTSW |
5 |
38,477,366 (GRCm39) |
missense |
probably damaging |
0.96 |
R5255:Drd5
|
UTSW |
5 |
38,477,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R5393:Drd5
|
UTSW |
5 |
38,478,248 (GRCm39) |
missense |
probably benign |
|
R5639:Drd5
|
UTSW |
5 |
38,477,178 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7241:Drd5
|
UTSW |
5 |
38,477,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R7520:Drd5
|
UTSW |
5 |
38,478,195 (GRCm39) |
missense |
probably benign |
0.00 |
R8300:Drd5
|
UTSW |
5 |
38,477,672 (GRCm39) |
missense |
probably damaging |
0.99 |
R8746:Drd5
|
UTSW |
5 |
38,477,433 (GRCm39) |
missense |
probably benign |
0.04 |
R8829:Drd5
|
UTSW |
5 |
38,477,078 (GRCm39) |
missense |
probably benign |
0.08 |
R8832:Drd5
|
UTSW |
5 |
38,477,078 (GRCm39) |
missense |
probably benign |
0.08 |
R8870:Drd5
|
UTSW |
5 |
38,477,747 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9600:Drd5
|
UTSW |
5 |
38,478,174 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9705:Drd5
|
UTSW |
5 |
38,478,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9717:Drd5
|
UTSW |
5 |
38,478,090 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Drd5
|
UTSW |
5 |
38,477,729 (GRCm39) |
missense |
possibly damaging |
0.78 |
|