Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AAdacl4fm3 |
G |
T |
4: 144,430,173 (GRCm39) |
A272D |
possibly damaging |
Het |
Abr |
A |
T |
11: 76,350,038 (GRCm39) |
I347N |
probably damaging |
Het |
Acbd4 |
T |
A |
11: 102,994,985 (GRCm39) |
L50Q |
probably damaging |
Het |
Acsl5 |
T |
G |
19: 55,261,251 (GRCm39) |
Y69* |
probably null |
Het |
Agtpbp1 |
G |
A |
13: 59,652,108 (GRCm39) |
T401I |
probably damaging |
Het |
Ap3m2 |
C |
T |
8: 23,289,807 (GRCm39) |
E99K |
probably damaging |
Het |
Arhgef28 |
A |
T |
13: 98,124,769 (GRCm39) |
S504R |
possibly damaging |
Het |
Arsj |
T |
A |
3: 126,232,752 (GRCm39) |
D499E |
probably damaging |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Camk2b |
T |
C |
11: 5,939,575 (GRCm39) |
D232G |
probably damaging |
Het |
Casc3 |
C |
T |
11: 98,713,359 (GRCm39) |
P258S |
possibly damaging |
Het |
Catspere2 |
T |
A |
1: 177,845,280 (GRCm39) |
I100N |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,943,252 (GRCm39) |
N787K |
possibly damaging |
Het |
Celsr1 |
C |
A |
15: 85,789,679 (GRCm39) |
C2653F |
probably damaging |
Het |
Cep170 |
T |
C |
1: 176,584,051 (GRCm39) |
E11G |
probably damaging |
Het |
Chia1 |
A |
C |
3: 106,022,641 (GRCm39) |
N12H |
probably damaging |
Het |
Chrna4 |
T |
C |
2: 180,671,334 (GRCm39) |
T141A |
probably damaging |
Het |
Col25a1 |
T |
C |
3: 130,272,671 (GRCm39) |
|
probably null |
Het |
Dcstamp |
A |
T |
15: 39,622,929 (GRCm39) |
I417F |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,238,738 (GRCm39) |
I427V |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,333,208 (GRCm39) |
E2203G |
probably benign |
Het |
Dnmt3c |
A |
T |
2: 153,559,345 (GRCm39) |
S409C |
probably damaging |
Het |
Dock6 |
A |
T |
9: 21,724,375 (GRCm39) |
M1541K |
probably damaging |
Het |
Dzip1l |
C |
T |
9: 99,547,888 (GRCm39) |
T714I |
probably benign |
Het |
Exoc6b |
T |
C |
6: 84,825,807 (GRCm39) |
R535G |
probably damaging |
Het |
Fam83h |
A |
G |
15: 75,876,588 (GRCm39) |
S250P |
probably benign |
Het |
Fat4 |
C |
T |
3: 39,036,107 (GRCm39) |
T3253I |
probably damaging |
Het |
Fer1l6 |
T |
A |
15: 58,501,227 (GRCm39) |
F1302I |
probably damaging |
Het |
Fmnl1 |
T |
G |
11: 103,085,600 (GRCm39) |
|
probably benign |
Het |
Gckr |
C |
A |
5: 31,459,554 (GRCm39) |
F201L |
possibly damaging |
Het |
Gm10036 |
A |
G |
18: 15,966,292 (GRCm39) |
T148A |
probably benign |
Het |
Gm5142 |
G |
A |
14: 59,415,909 (GRCm39) |
S83F |
probably benign |
Het |
Gpr37 |
A |
T |
6: 25,689,004 (GRCm39) |
V31D |
possibly damaging |
Het |
Gramd2b |
A |
T |
18: 56,618,321 (GRCm39) |
Y207F |
probably damaging |
Het |
Hr |
T |
C |
14: 70,801,124 (GRCm39) |
|
probably null |
Het |
Igf2r |
A |
G |
17: 12,952,753 (GRCm39) |
L231P |
probably damaging |
Het |
Ighv1-66 |
A |
T |
12: 115,557,157 (GRCm39) |
W3R |
probably damaging |
Het |
Insyn2b |
T |
A |
11: 34,352,030 (GRCm39) |
V24E |
probably damaging |
Het |
Kcnu1 |
T |
C |
8: 26,408,491 (GRCm39) |
S101P |
probably benign |
Het |
Klhl23 |
T |
G |
2: 69,664,310 (GRCm39) |
V553G |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,388,745 (GRCm39) |
I3235V |
probably damaging |
Het |
Mb |
A |
T |
15: 76,900,256 (GRCm39) |
I57N |
probably damaging |
Het |
Micu1 |
T |
C |
10: 59,624,843 (GRCm39) |
I295T |
possibly damaging |
Het |
Mink1 |
G |
A |
11: 70,498,601 (GRCm39) |
V589I |
possibly damaging |
Het |
Mndal |
T |
C |
1: 173,703,160 (GRCm39) |
K82E |
probably damaging |
Het |
Mroh1 |
A |
C |
15: 76,321,517 (GRCm39) |
K1066T |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,396,192 (GRCm39) |
N149K |
unknown |
Het |
Myo7b |
G |
T |
18: 32,104,626 (GRCm39) |
L1404I |
probably damaging |
Het |
Nlrc4 |
A |
G |
17: 74,753,001 (GRCm39) |
S461P |
probably damaging |
Het |
Nudt12 |
A |
T |
17: 59,310,348 (GRCm39) |
D418E |
probably benign |
Het |
Or2g7 |
T |
A |
17: 38,378,948 (GRCm39) |
D295E |
probably benign |
Het |
Or5g27 |
G |
T |
2: 85,409,746 (GRCm39) |
R54S |
possibly damaging |
Het |
Pcdha1 |
A |
G |
18: 37,292,326 (GRCm39) |
H817R |
probably damaging |
Het |
Pcdha4 |
A |
G |
18: 37,087,080 (GRCm39) |
Y421C |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,306,886 (GRCm39) |
D1094G |
probably benign |
Het |
Pck2 |
A |
T |
14: 55,785,223 (GRCm39) |
D427V |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,726,421 (GRCm39) |
T1760A |
probably benign |
Het |
Pdzk1ip1 |
T |
A |
4: 114,950,188 (GRCm39) |
Y83N |
probably damaging |
Het |
Pgs1 |
T |
C |
11: 117,893,312 (GRCm39) |
I213T |
probably damaging |
Het |
Plin4 |
T |
A |
17: 56,410,969 (GRCm39) |
T1021S |
probably damaging |
Het |
Plxnb1 |
T |
A |
9: 108,941,375 (GRCm39) |
I1677N |
probably damaging |
Het |
Pm20d2 |
T |
C |
4: 33,174,752 (GRCm39) |
E378G |
possibly damaging |
Het |
Prkcq |
T |
G |
2: 11,231,661 (GRCm39) |
|
probably null |
Het |
Psmd2 |
C |
T |
16: 20,480,883 (GRCm39) |
P780L |
probably damaging |
Het |
Pvr |
A |
G |
7: 19,639,105 (GRCm39) |
S392P |
possibly damaging |
Het |
Rad51ap2 |
G |
C |
12: 11,507,432 (GRCm39) |
L451F |
possibly damaging |
Het |
Rbm20 |
A |
G |
19: 53,823,197 (GRCm39) |
E598G |
probably damaging |
Het |
Rho |
A |
T |
6: 115,912,504 (GRCm39) |
N123Y |
possibly damaging |
Het |
Rictor |
T |
C |
15: 6,737,934 (GRCm39) |
|
probably null |
Het |
Rilpl2 |
T |
G |
5: 124,606,656 (GRCm39) |
K186T |
probably damaging |
Het |
Rps6ka4 |
A |
C |
19: 6,816,992 (GRCm39) |
L61R |
probably damaging |
Het |
Sds |
C |
A |
5: 120,618,890 (GRCm39) |
Q118K |
probably benign |
Het |
Septin1 |
C |
T |
7: 126,816,157 (GRCm39) |
R91K |
probably benign |
Het |
Sf3a3 |
A |
G |
4: 124,616,673 (GRCm39) |
Y185C |
probably damaging |
Het |
Shtn1 |
T |
C |
19: 58,998,266 (GRCm39) |
M376V |
possibly damaging |
Het |
Slc6a9 |
A |
G |
4: 117,714,633 (GRCm39) |
T189A |
possibly damaging |
Het |
Slc7a6 |
T |
G |
8: 106,922,606 (GRCm39) |
V464G |
possibly damaging |
Het |
Smg8 |
T |
A |
11: 86,975,919 (GRCm39) |
D554V |
probably damaging |
Het |
Sox8 |
A |
G |
17: 25,789,082 (GRCm39) |
|
probably null |
Het |
Spata31e4 |
G |
T |
13: 50,857,019 (GRCm39) |
V886L |
possibly damaging |
Het |
Spats2l |
T |
A |
1: 57,918,689 (GRCm39) |
V41D |
probably damaging |
Het |
Sult2a3 |
A |
T |
7: 13,801,493 (GRCm39) |
F282Y |
probably damaging |
Het |
Svs3a |
T |
G |
2: 164,132,091 (GRCm39) |
Y220D |
probably damaging |
Het |
Teddm1a |
T |
A |
1: 153,768,369 (GRCm39) |
Y278N |
probably damaging |
Het |
Tlk1 |
T |
C |
2: 70,552,272 (GRCm39) |
Y526C |
probably damaging |
Het |
Tmc3 |
T |
A |
7: 83,266,025 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,596,583 (GRCm39) |
E20110V |
probably damaging |
Het |
Tulp4 |
A |
G |
17: 6,264,941 (GRCm39) |
D235G |
probably damaging |
Het |
Vmn1r224 |
T |
C |
17: 20,639,789 (GRCm39) |
L122P |
probably benign |
Het |
Vmn2r62 |
A |
G |
7: 42,438,473 (GRCm39) |
L121P |
possibly damaging |
Het |
Whrn |
G |
T |
4: 63,413,368 (GRCm39) |
|
probably benign |
Het |
Zer1 |
G |
T |
2: 30,001,033 (GRCm39) |
H129Q |
probably benign |
Het |
Zfand4 |
G |
A |
6: 116,282,618 (GRCm39) |
A64T |
probably benign |
Het |
|
Other mutations in Usp50 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01017:Usp50
|
APN |
2 |
126,551,334 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01565:Usp50
|
APN |
2 |
126,619,888 (GRCm39) |
nonsense |
probably null |
|
IGL01976:Usp50
|
APN |
2 |
126,551,386 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02192:Usp50
|
APN |
2 |
126,619,958 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02272:Usp50
|
APN |
2 |
126,611,864 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02892:Usp50
|
APN |
2 |
126,611,822 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4453001:Usp50
|
UTSW |
2 |
126,625,236 (GRCm39) |
start gained |
probably benign |
|
R0034:Usp50
|
UTSW |
2 |
126,619,895 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0382:Usp50
|
UTSW |
2 |
126,619,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Usp50
|
UTSW |
2 |
126,603,464 (GRCm39) |
missense |
probably damaging |
0.98 |
R1146:Usp50
|
UTSW |
2 |
126,551,392 (GRCm39) |
missense |
probably benign |
0.02 |
R1457:Usp50
|
UTSW |
2 |
126,603,554 (GRCm39) |
missense |
probably benign |
0.41 |
R1475:Usp50
|
UTSW |
2 |
126,611,787 (GRCm39) |
splice site |
probably null |
|
R1758:Usp50
|
UTSW |
2 |
126,617,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R1889:Usp50
|
UTSW |
2 |
126,619,818 (GRCm39) |
critical splice donor site |
probably null |
|
R1940:Usp50
|
UTSW |
2 |
126,619,943 (GRCm39) |
missense |
probably benign |
0.03 |
R1959:Usp50
|
UTSW |
2 |
126,619,881 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2698:Usp50
|
UTSW |
2 |
126,619,949 (GRCm39) |
missense |
probably damaging |
0.97 |
R4648:Usp50
|
UTSW |
2 |
126,619,953 (GRCm39) |
missense |
probably damaging |
0.98 |
R4809:Usp50
|
UTSW |
2 |
126,619,773 (GRCm39) |
intron |
probably benign |
|
R6247:Usp50
|
UTSW |
2 |
126,617,713 (GRCm39) |
missense |
probably benign |
0.33 |
R7186:Usp50
|
UTSW |
2 |
126,625,218 (GRCm39) |
start gained |
probably benign |
|
R7522:Usp50
|
UTSW |
2 |
126,625,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R8110:Usp50
|
UTSW |
2 |
126,622,250 (GRCm39) |
splice site |
probably null |
|
R8856:Usp50
|
UTSW |
2 |
126,622,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R9449:Usp50
|
UTSW |
2 |
126,619,817 (GRCm39) |
critical splice donor site |
probably null |
|
X0064:Usp50
|
UTSW |
2 |
126,603,566 (GRCm39) |
nonsense |
probably null |
|
|