Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110018I06Rik |
G |
A |
12: 107,455,268 (GRCm39) |
R118K |
unknown |
Het |
Abcc6 |
T |
A |
7: 45,664,929 (GRCm39) |
I301F |
possibly damaging |
Het |
Akap9 |
C |
A |
5: 4,114,742 (GRCm39) |
|
probably null |
Het |
B3gat1 |
C |
T |
9: 26,668,237 (GRCm39) |
R276C |
probably damaging |
Het |
Camk1 |
A |
G |
6: 113,315,352 (GRCm39) |
Y105H |
probably damaging |
Het |
Ccdc81 |
T |
C |
7: 89,515,777 (GRCm39) |
N634S |
probably damaging |
Het |
Clcn1 |
C |
A |
6: 42,290,075 (GRCm39) |
Q837K |
probably benign |
Het |
Clec16a |
A |
G |
16: 10,506,510 (GRCm39) |
|
probably benign |
Het |
Col22a1 |
T |
C |
15: 71,753,511 (GRCm39) |
I130V |
probably benign |
Het |
Coro2b |
T |
C |
9: 62,335,263 (GRCm39) |
S308G |
probably benign |
Het |
Cpxm1 |
A |
G |
2: 130,239,423 (GRCm39) |
W2R |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,475,227 (GRCm39) |
N3364S |
probably damaging |
Het |
Dgkq |
A |
G |
5: 108,804,331 (GRCm39) |
V131A |
probably damaging |
Het |
Dnai1 |
A |
G |
4: 41,629,997 (GRCm39) |
S469G |
probably benign |
Het |
Efcab3 |
T |
G |
11: 104,601,556 (GRCm39) |
|
probably null |
Het |
Eml4 |
G |
A |
17: 83,785,489 (GRCm39) |
E885K |
probably benign |
Het |
Etfa |
A |
T |
9: 55,396,122 (GRCm39) |
I148N |
probably damaging |
Het |
Gpbar1 |
A |
G |
1: 74,318,681 (GRCm39) |
D308G |
probably benign |
Het |
Gprin3 |
T |
C |
6: 59,330,900 (GRCm39) |
E469G |
possibly damaging |
Het |
Igkv1-115 |
T |
C |
6: 68,138,667 (GRCm39) |
V90A |
probably damaging |
Het |
Ints2 |
A |
G |
11: 86,135,289 (GRCm39) |
V375A |
possibly damaging |
Het |
Mindy3 |
T |
C |
2: 12,400,993 (GRCm39) |
M242V |
possibly damaging |
Het |
Or11m3 |
A |
G |
15: 98,395,565 (GRCm39) |
I71V |
probably benign |
Het |
Or1n1b |
T |
C |
2: 36,780,698 (GRCm39) |
H54R |
probably damaging |
Het |
Or5t9 |
A |
C |
2: 86,659,281 (GRCm39) |
I62L |
probably benign |
Het |
P3h1 |
G |
A |
4: 119,095,956 (GRCm39) |
E355K |
probably benign |
Het |
Paxbp1 |
T |
C |
16: 90,820,315 (GRCm39) |
T703A |
probably benign |
Het |
Pcdh15 |
A |
T |
10: 74,046,302 (GRCm39) |
Y193F |
probably damaging |
Het |
Pdxdc1 |
A |
G |
16: 13,656,233 (GRCm39) |
V613A |
probably damaging |
Het |
Plekha5 |
T |
C |
6: 140,515,922 (GRCm39) |
|
probably benign |
Het |
Pmel |
A |
T |
10: 128,551,126 (GRCm39) |
Q123L |
possibly damaging |
Het |
Prl6a1 |
T |
C |
13: 27,502,149 (GRCm39) |
|
probably benign |
Het |
Rcan1 |
T |
C |
16: 92,190,379 (GRCm39) |
T187A |
probably damaging |
Het |
Rp1l1 |
A |
G |
14: 64,269,681 (GRCm39) |
S1756G |
probably benign |
Het |
Runx2 |
A |
T |
17: 44,919,123 (GRCm39) |
M405K |
probably damaging |
Het |
Serinc5 |
T |
C |
13: 92,797,613 (GRCm39) |
Y39H |
probably damaging |
Het |
Sgsm1 |
G |
A |
5: 113,413,740 (GRCm39) |
T676I |
probably benign |
Het |
Slc6a15 |
G |
C |
10: 103,245,657 (GRCm39) |
V547L |
probably benign |
Het |
Slk |
T |
C |
19: 47,597,432 (GRCm39) |
I80T |
probably damaging |
Het |
Spice1 |
A |
G |
16: 44,205,124 (GRCm39) |
N810S |
probably benign |
Het |
Spred2 |
A |
G |
11: 19,951,104 (GRCm39) |
|
probably benign |
Het |
Tbc1d4 |
C |
G |
14: 101,716,656 (GRCm39) |
|
probably benign |
Het |
Tdrd7 |
G |
A |
4: 46,029,762 (GRCm39) |
V1032M |
probably benign |
Het |
Tlr11 |
A |
G |
14: 50,599,793 (GRCm39) |
N593S |
probably benign |
Het |
Trpa1 |
T |
C |
1: 14,982,585 (GRCm39) |
|
probably null |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Usp25 |
T |
C |
16: 76,878,335 (GRCm39) |
|
probably benign |
Het |
Vmn2r97 |
T |
A |
17: 19,167,665 (GRCm39) |
S640T |
probably benign |
Het |
Zc3h6 |
A |
G |
2: 128,848,736 (GRCm39) |
Y321C |
probably damaging |
Het |
Zfp329 |
T |
A |
7: 12,545,395 (GRCm39) |
N43I |
probably benign |
Het |
|
Other mutations in Alg6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Alg6
|
APN |
4 |
99,641,291 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00816:Alg6
|
APN |
4 |
99,630,598 (GRCm39) |
missense |
probably null |
|
IGL01067:Alg6
|
APN |
4 |
99,629,807 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01360:Alg6
|
APN |
4 |
99,630,643 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02625:Alg6
|
APN |
4 |
99,634,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R1033:Alg6
|
UTSW |
4 |
99,650,270 (GRCm39) |
missense |
probably benign |
0.00 |
R1764:Alg6
|
UTSW |
4 |
99,629,815 (GRCm39) |
missense |
probably benign |
0.02 |
R1852:Alg6
|
UTSW |
4 |
99,634,599 (GRCm39) |
missense |
probably benign |
0.03 |
R2020:Alg6
|
UTSW |
4 |
99,626,369 (GRCm39) |
missense |
probably damaging |
0.98 |
R2248:Alg6
|
UTSW |
4 |
99,626,444 (GRCm39) |
missense |
probably damaging |
0.98 |
R4515:Alg6
|
UTSW |
4 |
99,641,023 (GRCm39) |
intron |
probably benign |
|
R4976:Alg6
|
UTSW |
4 |
99,638,965 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5207:Alg6
|
UTSW |
4 |
99,607,431 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5444:Alg6
|
UTSW |
4 |
99,629,816 (GRCm39) |
missense |
probably benign |
0.09 |
R5739:Alg6
|
UTSW |
4 |
99,632,737 (GRCm39) |
missense |
probably benign |
0.01 |
R7060:Alg6
|
UTSW |
4 |
99,650,198 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7432:Alg6
|
UTSW |
4 |
99,641,295 (GRCm39) |
missense |
probably benign |
0.01 |
R7476:Alg6
|
UTSW |
4 |
99,632,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Alg6
|
UTSW |
4 |
99,636,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7585:Alg6
|
UTSW |
4 |
99,626,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R8145:Alg6
|
UTSW |
4 |
99,634,564 (GRCm39) |
missense |
probably damaging |
0.99 |
R9621:Alg6
|
UTSW |
4 |
99,615,131 (GRCm39) |
nonsense |
probably null |
|
R9739:Alg6
|
UTSW |
4 |
99,650,195 (GRCm39) |
missense |
possibly damaging |
0.56 |
|