Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam3 |
T |
C |
8: 25,171,539 (GRCm39) |
Y764C |
probably benign |
Het |
Atxn1 |
C |
T |
13: 45,721,095 (GRCm39) |
V267M |
probably benign |
Het |
Cadps |
T |
A |
14: 12,505,793 (GRCm38) |
H759L |
possibly damaging |
Het |
Caprin2 |
A |
G |
6: 148,779,474 (GRCm39) |
L111P |
probably damaging |
Het |
Ccl8 |
A |
T |
11: 82,006,865 (GRCm39) |
D26V |
possibly damaging |
Het |
Cdh19 |
T |
C |
1: 110,882,596 (GRCm39) |
|
probably benign |
Het |
Cnga3 |
C |
A |
1: 37,283,965 (GRCm39) |
H89Q |
probably benign |
Het |
Cnga4 |
A |
T |
7: 105,056,190 (GRCm39) |
Q264L |
probably damaging |
Het |
Coil |
A |
G |
11: 88,872,673 (GRCm39) |
T345A |
probably benign |
Het |
Cyp11b2 |
A |
G |
15: 74,723,281 (GRCm39) |
L461P |
probably damaging |
Het |
Dock2 |
T |
C |
11: 34,414,922 (GRCm39) |
E151G |
probably damaging |
Het |
Dsc1 |
C |
T |
18: 20,219,701 (GRCm39) |
|
probably null |
Het |
Dync2h1 |
A |
T |
9: 7,168,743 (GRCm39) |
C357S |
probably null |
Het |
Ebf3 |
A |
C |
7: 136,826,994 (GRCm39) |
I306R |
probably damaging |
Het |
Eprs1 |
A |
G |
1: 185,128,360 (GRCm39) |
H580R |
possibly damaging |
Het |
Ermap |
A |
T |
4: 119,035,810 (GRCm39) |
F393I |
probably damaging |
Het |
Flii |
T |
C |
11: 60,613,151 (GRCm39) |
T217A |
probably benign |
Het |
Fras1 |
C |
T |
5: 96,762,732 (GRCm39) |
Q745* |
probably null |
Het |
Gja8 |
A |
G |
3: 96,826,657 (GRCm39) |
V335A |
probably benign |
Het |
Gm21560 |
A |
T |
14: 6,218,333 (GRCm38) |
N48K |
probably damaging |
Het |
Gpr158 |
C |
T |
2: 21,653,802 (GRCm39) |
T457I |
possibly damaging |
Het |
Kcnv1 |
A |
T |
15: 44,977,997 (GRCm39) |
S14T |
unknown |
Het |
Lamb2 |
T |
C |
9: 108,358,496 (GRCm39) |
Y178H |
probably damaging |
Het |
Lamc2 |
G |
A |
1: 153,012,508 (GRCm39) |
T722M |
probably benign |
Het |
Map1b |
T |
C |
13: 99,567,142 (GRCm39) |
T1860A |
unknown |
Het |
Map2k7 |
T |
C |
8: 4,294,035 (GRCm39) |
Y194H |
possibly damaging |
Het |
Map4 |
T |
A |
9: 109,881,982 (GRCm39) |
M282K |
probably benign |
Het |
Mmp10 |
A |
G |
9: 7,503,531 (GRCm39) |
I134V |
probably benign |
Het |
Mrtfa |
G |
T |
15: 80,902,649 (GRCm39) |
S220* |
probably null |
Het |
Msh5 |
A |
T |
17: 35,248,978 (GRCm39) |
L685Q |
probably damaging |
Het |
Myh1 |
T |
A |
11: 67,111,463 (GRCm39) |
I1634N |
possibly damaging |
Het |
Myh13 |
C |
T |
11: 67,217,980 (GRCm39) |
R18* |
probably null |
Het |
Myo3b |
A |
T |
2: 69,957,329 (GRCm39) |
I185L |
probably damaging |
Het |
Ninl |
G |
T |
2: 150,808,145 (GRCm39) |
H294Q |
probably benign |
Het |
Or4a79 |
G |
A |
2: 89,552,269 (GRCm39) |
A62V |
possibly damaging |
Het |
Or51b17 |
A |
T |
7: 103,542,238 (GRCm39) |
S235T |
probably benign |
Het |
Or8b44 |
T |
C |
9: 38,410,607 (GRCm39) |
I214T |
possibly damaging |
Het |
Orm3 |
T |
A |
4: 63,275,180 (GRCm39) |
L97Q |
probably damaging |
Het |
Osbpl1a |
T |
C |
18: 12,889,281 (GRCm39) |
N432S |
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,285,822 (GRCm39) |
D1020E |
probably damaging |
Het |
Pxk |
T |
A |
14: 8,122,371 (GRCm38) |
D60E |
probably benign |
Het |
Rack1 |
T |
A |
11: 48,694,752 (GRCm39) |
V198E |
probably damaging |
Het |
Ripk1 |
C |
T |
13: 34,201,100 (GRCm39) |
A271V |
probably benign |
Het |
Rsrc1 |
C |
T |
3: 66,901,982 (GRCm39) |
P44L |
unknown |
Het |
Ryr2 |
G |
T |
13: 11,669,266 (GRCm39) |
H3513N |
possibly damaging |
Het |
Scn7a |
A |
T |
2: 66,534,147 (GRCm39) |
D509E |
probably damaging |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,957,756 (GRCm39) |
|
probably benign |
Het |
Sfxn5 |
A |
G |
6: 85,233,414 (GRCm39) |
V181A |
probably benign |
Het |
Slc5a4b |
C |
T |
10: 75,925,812 (GRCm39) |
A198T |
probably damaging |
Het |
Sp2 |
C |
T |
11: 96,848,552 (GRCm39) |
R357H |
possibly damaging |
Het |
Tchh |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
3: 93,354,015 (GRCm39) |
|
probably benign |
Het |
Tnfrsf11b |
G |
A |
15: 54,115,770 (GRCm39) |
L276F |
probably damaging |
Het |
Usp37 |
A |
G |
1: 74,493,118 (GRCm39) |
V723A |
probably benign |
Het |
Usp45 |
G |
T |
4: 21,781,844 (GRCm39) |
R36I |
probably damaging |
Het |
Vcan |
T |
C |
13: 89,838,737 (GRCm39) |
D2269G |
probably damaging |
Het |
Vmn2r18 |
T |
A |
5: 151,485,338 (GRCm39) |
M719L |
possibly damaging |
Het |
Vmn2r52 |
C |
T |
7: 9,902,998 (GRCm39) |
G477R |
probably benign |
Het |
Vmn2r60 |
C |
A |
7: 41,791,716 (GRCm39) |
N546K |
probably benign |
Het |
Wnt8b |
G |
A |
19: 44,500,280 (GRCm39) |
C289Y |
probably damaging |
Het |
Zdbf2 |
T |
G |
1: 63,329,925 (GRCm39) |
M10R |
probably benign |
Het |
Zfp945 |
T |
A |
17: 23,071,543 (GRCm39) |
K140* |
probably null |
Het |
|
Other mutations in Calcoco2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03286:Calcoco2
|
APN |
11 |
95,994,098 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0671:Calcoco2
|
UTSW |
11 |
95,998,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R1668:Calcoco2
|
UTSW |
11 |
95,993,563 (GRCm39) |
missense |
probably benign |
0.33 |
R4678:Calcoco2
|
UTSW |
11 |
95,994,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R4812:Calcoco2
|
UTSW |
11 |
95,998,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R5481:Calcoco2
|
UTSW |
11 |
95,998,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5512:Calcoco2
|
UTSW |
11 |
95,994,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R6691:Calcoco2
|
UTSW |
11 |
95,990,934 (GRCm39) |
missense |
unknown |
|
R7289:Calcoco2
|
UTSW |
11 |
95,990,823 (GRCm39) |
missense |
unknown |
|
R7715:Calcoco2
|
UTSW |
11 |
95,990,862 (GRCm39) |
frame shift |
probably null |
|
R7851:Calcoco2
|
UTSW |
11 |
95,990,808 (GRCm39) |
small deletion |
probably benign |
|
R7872:Calcoco2
|
UTSW |
11 |
95,990,808 (GRCm39) |
small deletion |
probably benign |
|
R7939:Calcoco2
|
UTSW |
11 |
95,990,808 (GRCm39) |
small deletion |
probably benign |
|
R8027:Calcoco2
|
UTSW |
11 |
95,991,241 (GRCm39) |
splice site |
probably benign |
|
R8079:Calcoco2
|
UTSW |
11 |
95,998,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R8529:Calcoco2
|
UTSW |
11 |
95,990,808 (GRCm39) |
small deletion |
probably benign |
|
R8700:Calcoco2
|
UTSW |
11 |
95,994,330 (GRCm39) |
missense |
probably benign |
0.09 |
R8865:Calcoco2
|
UTSW |
11 |
95,990,808 (GRCm39) |
small deletion |
probably benign |
|
R8870:Calcoco2
|
UTSW |
11 |
95,990,808 (GRCm39) |
small deletion |
probably benign |
|
R8909:Calcoco2
|
UTSW |
11 |
95,990,808 (GRCm39) |
small deletion |
probably benign |
|
R8933:Calcoco2
|
UTSW |
11 |
95,998,252 (GRCm39) |
splice site |
probably benign |
|
R9073:Calcoco2
|
UTSW |
11 |
95,990,808 (GRCm39) |
small deletion |
probably benign |
|
R9359:Calcoco2
|
UTSW |
11 |
95,990,862 (GRCm39) |
frame shift |
probably null |
|
R9538:Calcoco2
|
UTSW |
11 |
95,990,808 (GRCm39) |
small deletion |
probably benign |
|
R9614:Calcoco2
|
UTSW |
11 |
95,991,185 (GRCm39) |
missense |
probably benign |
0.01 |
R9621:Calcoco2
|
UTSW |
11 |
95,990,862 (GRCm39) |
frame shift |
probably null |
|
R9664:Calcoco2
|
UTSW |
11 |
95,991,104 (GRCm39) |
missense |
unknown |
|
X0027:Calcoco2
|
UTSW |
11 |
95,998,385 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Calcoco2
|
UTSW |
11 |
95,994,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|