Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1c |
A |
G |
2: 58,171,662 (GRCm39) |
I234T |
probably damaging |
Het |
Adam24 |
A |
G |
8: 41,132,550 (GRCm39) |
E6G |
probably damaging |
Het |
Amz1 |
A |
G |
5: 140,729,919 (GRCm39) |
D151G |
probably benign |
Het |
Arhgap24 |
T |
C |
5: 102,989,201 (GRCm39) |
L10P |
probably damaging |
Het |
Arhgap25 |
T |
G |
6: 87,509,846 (GRCm39) |
N8T |
probably benign |
Het |
Arsi |
T |
G |
18: 61,050,511 (GRCm39) |
F465V |
probably damaging |
Het |
Atp2c1 |
A |
G |
9: 105,326,024 (GRCm39) |
V293A |
probably damaging |
Het |
Bzw2 |
A |
G |
12: 36,154,350 (GRCm39) |
L340P |
probably damaging |
Het |
Camkmt |
C |
T |
17: 85,404,009 (GRCm39) |
T77I |
probably benign |
Het |
Camsap1 |
G |
T |
2: 25,825,562 (GRCm39) |
Q1375K |
probably benign |
Het |
Catsper2 |
G |
T |
2: 121,227,604 (GRCm39) |
|
probably null |
Het |
Cd163 |
T |
C |
6: 124,294,948 (GRCm39) |
C671R |
probably damaging |
Het |
Cdk7 |
T |
C |
13: 100,854,192 (GRCm39) |
|
probably null |
Het |
Cfi |
C |
T |
3: 129,666,726 (GRCm39) |
P483L |
probably damaging |
Het |
Chn2 |
C |
T |
6: 54,195,546 (GRCm39) |
L72F |
possibly damaging |
Het |
Cimip4 |
C |
T |
15: 78,270,373 (GRCm39) |
E132K |
probably benign |
Het |
Cntn2 |
C |
A |
1: 132,444,798 (GRCm39) |
E363* |
probably null |
Het |
Crebbp |
T |
C |
16: 3,911,375 (GRCm39) |
E999G |
probably damaging |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Cts3 |
A |
C |
13: 61,715,409 (GRCm39) |
I141M |
probably benign |
Het |
Cwc27 |
A |
T |
13: 104,940,861 (GRCm39) |
V166D |
probably damaging |
Het |
Defb26 |
T |
C |
2: 152,350,085 (GRCm39) |
E65G |
possibly damaging |
Het |
Dnah8 |
A |
G |
17: 31,029,327 (GRCm39) |
T4099A |
probably benign |
Het |
Eml6 |
A |
G |
11: 29,694,606 (GRCm39) |
F1953L |
probably benign |
Het |
Etl4 |
T |
A |
2: 20,344,922 (GRCm39) |
|
probably null |
Het |
Fbln1 |
A |
G |
15: 85,121,872 (GRCm39) |
E331G |
probably damaging |
Het |
Gcat |
T |
C |
15: 78,919,482 (GRCm39) |
V149A |
probably damaging |
Het |
Glp2r |
A |
T |
11: 67,612,926 (GRCm39) |
|
probably null |
Het |
Gm572 |
T |
C |
4: 148,751,302 (GRCm39) |
|
probably null |
Het |
Golgb1 |
T |
C |
16: 36,739,620 (GRCm39) |
V2653A |
probably damaging |
Het |
Grap2 |
G |
A |
15: 80,530,345 (GRCm39) |
R155Q |
possibly damaging |
Het |
Gspt1 |
T |
A |
16: 11,041,165 (GRCm39) |
I533L |
probably damaging |
Het |
Gypa |
A |
T |
8: 81,222,977 (GRCm39) |
Y27F |
unknown |
Het |
Hipk4 |
G |
A |
7: 27,228,917 (GRCm39) |
V456I |
probably benign |
Het |
Homer2 |
A |
T |
7: 81,299,311 (GRCm39) |
D51E |
probably benign |
Het |
Hspa1b |
A |
T |
17: 35,176,980 (GRCm39) |
V335E |
possibly damaging |
Het |
Ift122 |
A |
G |
6: 115,889,495 (GRCm39) |
T827A |
probably benign |
Het |
Igkv1-35 |
T |
C |
6: 69,988,119 (GRCm39) |
N58S |
probably benign |
Het |
Kat6b |
A |
T |
14: 21,669,326 (GRCm39) |
H297L |
probably damaging |
Het |
Kirrel3 |
G |
T |
9: 34,924,601 (GRCm39) |
G296W |
probably damaging |
Het |
Klhl17 |
A |
G |
4: 156,315,082 (GRCm39) |
V525A |
probably benign |
Het |
Lrrn1 |
G |
T |
6: 107,546,168 (GRCm39) |
R655S |
possibly damaging |
Het |
Ltk |
T |
C |
2: 119,583,708 (GRCm39) |
N256D |
probably damaging |
Het |
Mill2 |
G |
A |
7: 18,590,591 (GRCm39) |
G209S |
probably benign |
Het |
Mmp27 |
A |
T |
9: 7,581,369 (GRCm39) |
H544L |
probably benign |
Het |
Mphosph10 |
A |
G |
7: 64,039,344 (GRCm39) |
S209P |
probably damaging |
Het |
Mphosph8 |
A |
T |
14: 56,914,003 (GRCm39) |
K415* |
probably null |
Het |
Myb |
T |
A |
10: 21,002,137 (GRCm39) |
M616L |
probably benign |
Het |
Myo15b |
C |
T |
11: 115,776,880 (GRCm39) |
R867W |
probably damaging |
Het |
Myo18b |
A |
T |
5: 113,022,346 (GRCm39) |
|
probably benign |
Het |
Nip7 |
A |
G |
8: 107,783,589 (GRCm39) |
E8G |
possibly damaging |
Het |
Optn |
T |
A |
2: 5,050,917 (GRCm39) |
I155F |
probably benign |
Het |
Or2f1b |
T |
A |
6: 42,739,931 (GRCm39) |
L315* |
probably null |
Het |
Or4f62 |
A |
T |
2: 111,986,631 (GRCm39) |
M112L |
possibly damaging |
Het |
Or52e4 |
A |
G |
7: 104,705,689 (GRCm39) |
T79A |
possibly damaging |
Het |
Or5c1 |
T |
G |
2: 37,222,601 (GRCm39) |
F281V |
probably damaging |
Het |
Or6b6 |
T |
C |
7: 106,571,438 (GRCm39) |
I38V |
probably benign |
Het |
Papolb |
A |
T |
5: 142,514,592 (GRCm39) |
H350Q |
probably benign |
Het |
Pappa2 |
T |
A |
1: 158,666,197 (GRCm39) |
M1128L |
probably benign |
Het |
Pcdhb5 |
T |
A |
18: 37,454,170 (GRCm39) |
N183K |
probably benign |
Het |
Pde12 |
G |
T |
14: 26,390,577 (GRCm39) |
S44* |
probably null |
Het |
Peg3 |
T |
C |
7: 6,713,288 (GRCm39) |
K645E |
probably benign |
Het |
Pkd1 |
C |
T |
17: 24,792,437 (GRCm39) |
R1375C |
probably benign |
Het |
Plekha5 |
G |
A |
6: 140,525,200 (GRCm39) |
E21K |
probably damaging |
Het |
Plk2 |
C |
T |
13: 110,535,958 (GRCm39) |
P554L |
probably benign |
Het |
Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
Polg |
A |
T |
7: 79,114,353 (GRCm39) |
W203R |
probably damaging |
Het |
Ppcdc |
A |
G |
9: 57,328,446 (GRCm39) |
V65A |
possibly damaging |
Het |
Ppm1m |
T |
A |
9: 106,073,004 (GRCm39) |
Q353L |
probably benign |
Het |
Ppp1r13l |
G |
C |
7: 19,104,020 (GRCm39) |
R167P |
probably damaging |
Het |
Ppp1r9b |
T |
A |
11: 94,887,479 (GRCm39) |
V497E |
probably damaging |
Het |
Prpf6 |
T |
A |
2: 181,277,836 (GRCm39) |
H399Q |
probably benign |
Het |
Psg25 |
T |
A |
7: 18,260,461 (GRCm39) |
I146F |
possibly damaging |
Het |
Rasgef1c |
A |
T |
11: 49,851,256 (GRCm39) |
Q116L |
probably damaging |
Het |
Rbbp9 |
A |
G |
2: 144,392,676 (GRCm39) |
V8A |
possibly damaging |
Het |
Rfk |
T |
C |
19: 17,376,930 (GRCm39) |
F144S |
probably damaging |
Het |
Rfwd3 |
A |
C |
8: 112,009,385 (GRCm39) |
|
probably null |
Het |
Rhpn1 |
T |
C |
15: 75,581,109 (GRCm39) |
I117T |
probably damaging |
Het |
Sars2 |
A |
T |
7: 28,447,333 (GRCm39) |
N244Y |
probably damaging |
Het |
Scnn1b |
A |
T |
7: 121,502,110 (GRCm39) |
H256L |
probably benign |
Het |
Sgcz |
G |
A |
8: 38,006,821 (GRCm39) |
T195I |
probably damaging |
Het |
Sh3gl2 |
T |
A |
4: 85,297,494 (GRCm39) |
H157Q |
probably benign |
Het |
Spen |
T |
A |
4: 141,203,410 (GRCm39) |
Q1739L |
probably benign |
Het |
Susd1 |
G |
T |
4: 59,379,657 (GRCm39) |
S323R |
possibly damaging |
Het |
Szt2 |
T |
C |
4: 118,242,641 (GRCm39) |
E1482G |
possibly damaging |
Het |
Tex15 |
A |
T |
8: 34,061,794 (GRCm39) |
K408I |
probably damaging |
Het |
Trem1 |
T |
A |
17: 48,539,864 (GRCm39) |
F14L |
probably null |
Het |
Trim26 |
G |
T |
17: 37,161,958 (GRCm39) |
E126* |
probably null |
Het |
Trpv3 |
T |
C |
11: 73,168,660 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,746,835 (GRCm39) |
|
probably null |
Het |
Ubap1 |
C |
T |
4: 41,379,688 (GRCm39) |
L301F |
probably benign |
Het |
Uchl1 |
T |
C |
5: 66,833,780 (GRCm39) |
M12T |
probably benign |
Het |
Vill |
C |
T |
9: 118,899,093 (GRCm39) |
T253I |
possibly damaging |
Het |
Vmn2r107 |
C |
T |
17: 20,576,015 (GRCm39) |
T115I |
probably benign |
Het |
Vmn2r98 |
T |
C |
17: 19,273,815 (GRCm39) |
S21P |
probably benign |
Het |
Wapl |
A |
G |
14: 34,399,119 (GRCm39) |
K63E |
probably benign |
Het |
Wnt2 |
T |
C |
6: 18,023,125 (GRCm39) |
K175E |
possibly damaging |
Het |
Zfp592 |
T |
C |
7: 80,673,309 (GRCm39) |
L91P |
probably damaging |
Het |
Zfp74 |
T |
C |
7: 29,631,932 (GRCm39) |
|
probably null |
Het |
Zglp1 |
A |
T |
9: 20,973,957 (GRCm39) |
I243N |
probably benign |
Het |
Zranb1 |
A |
G |
7: 132,551,916 (GRCm39) |
E215G |
probably benign |
Het |
|
Other mutations in Gabra4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01111:Gabra4
|
APN |
5 |
71,790,972 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01503:Gabra4
|
APN |
5 |
71,798,429 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02028:Gabra4
|
APN |
5 |
71,790,939 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02688:Gabra4
|
APN |
5 |
71,729,510 (GRCm39) |
missense |
probably benign |
|
IGL02749:Gabra4
|
APN |
5 |
71,795,490 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03095:Gabra4
|
APN |
5 |
71,781,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03330:Gabra4
|
APN |
5 |
71,798,407 (GRCm39) |
missense |
probably null |
1.00 |
E0354:Gabra4
|
UTSW |
5 |
71,798,204 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4142001:Gabra4
|
UTSW |
5 |
71,729,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R1523:Gabra4
|
UTSW |
5 |
71,790,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R1622:Gabra4
|
UTSW |
5 |
71,729,329 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1689:Gabra4
|
UTSW |
5 |
71,790,885 (GRCm39) |
splice site |
probably null |
|
R1930:Gabra4
|
UTSW |
5 |
71,795,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R1931:Gabra4
|
UTSW |
5 |
71,795,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R1967:Gabra4
|
UTSW |
5 |
71,729,412 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2095:Gabra4
|
UTSW |
5 |
71,781,455 (GRCm39) |
missense |
probably damaging |
0.99 |
R2131:Gabra4
|
UTSW |
5 |
71,798,567 (GRCm39) |
missense |
probably benign |
0.00 |
R2698:Gabra4
|
UTSW |
5 |
71,729,421 (GRCm39) |
missense |
probably benign |
0.03 |
R3884:Gabra4
|
UTSW |
5 |
71,814,600 (GRCm39) |
missense |
probably benign |
0.33 |
R3924:Gabra4
|
UTSW |
5 |
71,799,596 (GRCm39) |
splice site |
probably benign |
|
R4029:Gabra4
|
UTSW |
5 |
71,729,532 (GRCm39) |
missense |
probably benign |
0.31 |
R4361:Gabra4
|
UTSW |
5 |
71,790,888 (GRCm39) |
critical splice donor site |
probably null |
|
R4659:Gabra4
|
UTSW |
5 |
71,798,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R4682:Gabra4
|
UTSW |
5 |
71,815,152 (GRCm39) |
start codon destroyed |
probably null |
0.74 |
R4810:Gabra4
|
UTSW |
5 |
71,781,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Gabra4
|
UTSW |
5 |
71,729,546 (GRCm39) |
missense |
probably benign |
0.01 |
R5093:Gabra4
|
UTSW |
5 |
71,798,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5889:Gabra4
|
UTSW |
5 |
71,729,234 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5906:Gabra4
|
UTSW |
5 |
71,781,253 (GRCm39) |
missense |
probably benign |
0.00 |
R6574:Gabra4
|
UTSW |
5 |
71,781,268 (GRCm39) |
missense |
probably benign |
|
R7068:Gabra4
|
UTSW |
5 |
71,729,402 (GRCm39) |
missense |
probably benign |
0.07 |
R7571:Gabra4
|
UTSW |
5 |
71,729,335 (GRCm39) |
missense |
probably benign |
|
R7815:Gabra4
|
UTSW |
5 |
71,815,152 (GRCm39) |
start codon destroyed |
possibly damaging |
0.54 |
R7817:Gabra4
|
UTSW |
5 |
71,798,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R7840:Gabra4
|
UTSW |
5 |
71,798,256 (GRCm39) |
splice site |
probably null |
|
R7899:Gabra4
|
UTSW |
5 |
71,815,338 (GRCm39) |
unclassified |
probably benign |
|
R8000:Gabra4
|
UTSW |
5 |
71,781,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R8057:Gabra4
|
UTSW |
5 |
71,781,295 (GRCm39) |
missense |
probably benign |
0.12 |
R8996:Gabra4
|
UTSW |
5 |
71,729,046 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9623:Gabra4
|
UTSW |
5 |
71,791,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R9682:Gabra4
|
UTSW |
5 |
71,798,415 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9756:Gabra4
|
UTSW |
5 |
71,729,067 (GRCm39) |
missense |
probably damaging |
0.96 |
R9762:Gabra4
|
UTSW |
5 |
71,814,463 (GRCm39) |
missense |
unknown |
|
R9787:Gabra4
|
UTSW |
5 |
71,791,004 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1176:Gabra4
|
UTSW |
5 |
71,781,238 (GRCm39) |
missense |
probably benign |
0.40 |
|