Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
G |
A |
2: 68,498,012 (GRCm39) |
E148K |
unknown |
Het |
Adgrl2 |
T |
A |
3: 148,564,852 (GRCm39) |
K243* |
probably null |
Het |
Adgrv1 |
A |
T |
13: 81,588,344 (GRCm39) |
V4414E |
possibly damaging |
Het |
Ahnak |
A |
T |
19: 8,989,383 (GRCm39) |
I3556F |
probably benign |
Het |
Akap6 |
C |
T |
12: 53,189,488 (GRCm39) |
R2301* |
probably null |
Het |
Alg6 |
A |
G |
4: 99,636,933 (GRCm39) |
T305A |
probably damaging |
Het |
Alpk1 |
C |
T |
3: 127,473,427 (GRCm39) |
A859T |
probably benign |
Het |
Apba3 |
T |
A |
10: 81,104,735 (GRCm39) |
F3I |
possibly damaging |
Het |
Birc6 |
A |
G |
17: 74,967,465 (GRCm39) |
E4151G |
probably damaging |
Het |
Bmp2k |
T |
A |
5: 97,235,978 (GRCm39) |
F1134I |
probably benign |
Het |
C6 |
A |
T |
15: 4,792,846 (GRCm39) |
H317L |
probably damaging |
Het |
Catsperg2 |
G |
A |
7: 29,416,527 (GRCm39) |
S295L |
possibly damaging |
Het |
Ccdc142 |
G |
T |
6: 83,080,212 (GRCm39) |
R385L |
possibly damaging |
Het |
Ciz1 |
A |
T |
2: 32,261,761 (GRCm39) |
M482L |
probably benign |
Het |
Crisp3 |
A |
G |
17: 40,536,693 (GRCm39) |
|
probably null |
Het |
Dcaf15 |
G |
A |
8: 84,828,392 (GRCm39) |
P233S |
probably damaging |
Het |
Def8 |
A |
G |
8: 124,174,583 (GRCm39) |
N16S |
probably damaging |
Het |
Dnah7b |
T |
G |
1: 46,364,925 (GRCm39) |
S3569A |
probably damaging |
Het |
Dok6 |
C |
T |
18: 89,787,443 (GRCm39) |
|
probably benign |
Het |
Dop1a |
A |
T |
9: 86,376,464 (GRCm39) |
T233S |
possibly damaging |
Het |
Ep300 |
T |
A |
15: 81,524,044 (GRCm39) |
V1325D |
unknown |
Het |
Fancm |
T |
A |
12: 65,146,165 (GRCm39) |
H629Q |
probably benign |
Het |
Fbxo10 |
T |
C |
4: 45,062,194 (GRCm39) |
S111G |
probably benign |
Het |
Fbxo21 |
T |
C |
5: 118,140,239 (GRCm39) |
|
probably null |
Het |
Fdx1 |
A |
C |
9: 51,859,898 (GRCm39) |
L144R |
probably damaging |
Het |
Fgfr3 |
GGACCTCTCCGTG |
GG |
5: 33,892,766 (GRCm39) |
|
probably null |
Het |
Flot2 |
G |
A |
11: 77,944,188 (GRCm39) |
|
probably null |
Het |
Fndc10 |
C |
T |
4: 155,779,195 (GRCm39) |
R80C |
probably damaging |
Het |
Fut8 |
A |
T |
12: 77,459,708 (GRCm39) |
T274S |
probably benign |
Het |
Gli2 |
T |
C |
1: 118,763,565 (GRCm39) |
M1529V |
possibly damaging |
Het |
Gm7361 |
C |
A |
5: 26,466,188 (GRCm39) |
H183Q |
probably benign |
Het |
Hdlbp |
T |
A |
1: 93,341,337 (GRCm39) |
H1007L |
probably benign |
Het |
Hmcn2 |
A |
C |
2: 31,273,487 (GRCm39) |
|
probably null |
Het |
Inhbb |
C |
T |
1: 119,345,608 (GRCm39) |
R227H |
probably damaging |
Het |
Kifc1 |
A |
G |
17: 34,102,846 (GRCm39) |
F256L |
probably benign |
Het |
Lman2 |
A |
T |
13: 55,494,790 (GRCm39) |
F326Y |
probably damaging |
Het |
Mcmdc2 |
T |
C |
1: 9,989,302 (GRCm39) |
V242A |
probably benign |
Het |
Mettl8 |
A |
C |
2: 70,795,969 (GRCm39) |
V306G |
probably damaging |
Het |
Mog |
A |
T |
17: 37,322,984 (GRCm39) |
|
probably null |
Het |
Morc2b |
G |
A |
17: 33,356,833 (GRCm39) |
A313V |
possibly damaging |
Het |
Myh3 |
A |
G |
11: 66,987,874 (GRCm39) |
N1449S |
possibly damaging |
Het |
Myh8 |
C |
A |
11: 67,174,263 (GRCm39) |
T200K |
possibly damaging |
Het |
Myo16 |
T |
A |
8: 10,450,589 (GRCm39) |
H530Q |
unknown |
Het |
Neb |
C |
T |
2: 52,148,188 (GRCm39) |
R2686H |
probably damaging |
Het |
Nudt2 |
T |
C |
4: 41,480,539 (GRCm39) |
F141L |
possibly damaging |
Het |
Obscn |
G |
A |
11: 58,973,539 (GRCm39) |
H1931Y |
probably damaging |
Het |
Odad3 |
A |
G |
9: 21,913,553 (GRCm39) |
I73T |
probably damaging |
Het |
Or10al5 |
A |
G |
17: 38,063,242 (GRCm39) |
T166A |
probably damaging |
Het |
Or2d4 |
A |
T |
7: 106,543,575 (GRCm39) |
V211D |
possibly damaging |
Het |
Or5p80 |
T |
A |
7: 108,229,623 (GRCm39) |
C141* |
probably null |
Het |
Plcb1 |
T |
A |
2: 135,104,153 (GRCm39) |
L274* |
probably null |
Het |
Plcb1 |
G |
T |
2: 135,104,154 (GRCm39) |
L274F |
probably damaging |
Het |
Potefam3d |
A |
C |
8: 69,972,475 (GRCm39) |
Y91* |
probably null |
Het |
Prc1 |
C |
T |
7: 79,962,898 (GRCm39) |
T564M |
possibly damaging |
Het |
Psd4 |
G |
A |
2: 24,296,996 (GRCm39) |
R923Q |
probably damaging |
Het |
Ptprj |
G |
A |
2: 90,266,909 (GRCm39) |
Q1300* |
probably null |
Het |
Rapgef6 |
G |
T |
11: 54,510,830 (GRCm39) |
R249L |
probably damaging |
Het |
Slain1 |
G |
A |
14: 103,893,429 (GRCm39) |
|
probably null |
Het |
Slfn9 |
A |
T |
11: 82,873,013 (GRCm39) |
I630N |
probably damaging |
Het |
Smg6 |
G |
A |
11: 74,819,932 (GRCm39) |
A68T |
probably benign |
Het |
Spata31h1 |
T |
A |
10: 82,127,113 (GRCm39) |
T1966S |
probably benign |
Het |
Spef2 |
T |
A |
15: 9,727,625 (GRCm39) |
M153L |
probably benign |
Het |
St8sia4 |
T |
A |
1: 95,519,418 (GRCm39) |
M357L |
probably benign |
Het |
Tal1 |
A |
T |
4: 114,925,879 (GRCm39) |
H316L |
possibly damaging |
Het |
Tenm4 |
A |
G |
7: 96,497,224 (GRCm39) |
E1207G |
probably damaging |
Het |
Tmem64 |
C |
A |
4: 15,266,176 (GRCm39) |
H75Q |
probably benign |
Het |
Tor4a |
A |
G |
2: 25,085,804 (GRCm39) |
V33A |
probably benign |
Het |
Traj52 |
C |
T |
14: 54,402,818 (GRCm39) |
T15I |
|
Het |
Trpm1 |
A |
T |
7: 63,858,657 (GRCm39) |
I360F |
possibly damaging |
Het |
Trpm6 |
A |
T |
19: 18,853,484 (GRCm39) |
R1835W |
probably damaging |
Het |
Ubn1 |
T |
C |
16: 4,894,969 (GRCm39) |
S672P |
probably damaging |
Het |
Ugt2a2 |
C |
T |
5: 87,622,500 (GRCm39) |
C156Y |
probably damaging |
Het |
Wnk1 |
T |
C |
6: 119,904,157 (GRCm39) |
S2223G |
unknown |
Het |
Wnt7b |
G |
T |
15: 85,427,880 (GRCm39) |
A194E |
probably damaging |
Het |
Zmpste24 |
A |
G |
4: 120,940,028 (GRCm39) |
V206A |
probably benign |
Het |
|
Other mutations in Trim50 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01357:Trim50
|
APN |
5 |
135,392,808 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01565:Trim50
|
APN |
5 |
135,396,355 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01768:Trim50
|
APN |
5 |
135,392,736 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03394:Trim50
|
APN |
5 |
135,392,807 (GRCm39) |
missense |
probably damaging |
0.97 |
BB004:Trim50
|
UTSW |
5 |
135,382,465 (GRCm39) |
missense |
probably benign |
|
BB014:Trim50
|
UTSW |
5 |
135,382,465 (GRCm39) |
missense |
probably benign |
|
PIT4498001:Trim50
|
UTSW |
5 |
135,382,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0137:Trim50
|
UTSW |
5 |
135,395,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R0694:Trim50
|
UTSW |
5 |
135,382,399 (GRCm39) |
missense |
probably benign |
|
R1797:Trim50
|
UTSW |
5 |
135,382,355 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1806:Trim50
|
UTSW |
5 |
135,387,743 (GRCm39) |
missense |
probably benign |
0.00 |
R4688:Trim50
|
UTSW |
5 |
135,395,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R5034:Trim50
|
UTSW |
5 |
135,396,147 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5334:Trim50
|
UTSW |
5 |
135,396,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Trim50
|
UTSW |
5 |
135,396,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5337:Trim50
|
UTSW |
5 |
135,396,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5689:Trim50
|
UTSW |
5 |
135,382,516 (GRCm39) |
missense |
probably damaging |
0.98 |
R6119:Trim50
|
UTSW |
5 |
135,382,274 (GRCm39) |
missense |
probably benign |
|
R6377:Trim50
|
UTSW |
5 |
135,382,454 (GRCm39) |
missense |
probably benign |
0.01 |
R7170:Trim50
|
UTSW |
5 |
135,396,365 (GRCm39) |
missense |
probably benign |
|
R7175:Trim50
|
UTSW |
5 |
135,382,151 (GRCm39) |
start codon destroyed |
probably null |
0.81 |
R7927:Trim50
|
UTSW |
5 |
135,382,465 (GRCm39) |
missense |
probably benign |
|
R7945:Trim50
|
UTSW |
5 |
135,382,156 (GRCm39) |
missense |
probably benign |
|
R8403:Trim50
|
UTSW |
5 |
135,392,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R9117:Trim50
|
UTSW |
5 |
135,382,537 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9648:Trim50
|
UTSW |
5 |
135,395,475 (GRCm39) |
missense |
probably damaging |
1.00 |
|