Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb3 |
A |
G |
1: 25,170,350 (GRCm39) |
F983L |
probably damaging |
Het |
Cc2d1b |
T |
A |
4: 108,486,799 (GRCm39) |
M632K |
probably benign |
Het |
Cdyl2 |
G |
A |
8: 117,301,999 (GRCm39) |
R461* |
probably null |
Het |
Cfap57 |
G |
A |
4: 118,411,997 (GRCm39) |
Q1216* |
probably null |
Het |
Chd1l |
A |
T |
3: 97,505,066 (GRCm39) |
V167E |
probably damaging |
Het |
Col6a1 |
C |
A |
10: 76,553,242 (GRCm39) |
G391* |
probably null |
Het |
Ctsc |
C |
A |
7: 87,951,430 (GRCm39) |
Q226K |
probably benign |
Het |
Cyp2c54 |
A |
G |
19: 40,035,953 (GRCm39) |
V319A |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,316,303 (GRCm39) |
S3139P |
probably damaging |
Het |
Edrf1 |
T |
C |
7: 133,256,079 (GRCm39) |
S643P |
probably benign |
Het |
Fam186a |
A |
T |
15: 99,844,273 (GRCm39) |
V657D |
unknown |
Het |
Fkbp11 |
A |
G |
15: 98,626,073 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
G |
A |
2: 82,823,607 (GRCm39) |
A6447T |
possibly damaging |
Het |
H2-T9 |
C |
A |
17: 36,438,496 (GRCm39) |
|
probably null |
Het |
Hydin |
A |
G |
8: 111,276,307 (GRCm39) |
D3017G |
probably damaging |
Het |
Ifi205 |
G |
A |
1: 173,845,210 (GRCm39) |
Q191* |
probably null |
Het |
Mbd4 |
C |
T |
6: 115,821,564 (GRCm39) |
D484N |
probably benign |
Het |
Med24 |
C |
T |
11: 98,605,223 (GRCm39) |
|
probably null |
Het |
Mis18bp1 |
T |
C |
12: 65,208,404 (GRCm39) |
N103S |
probably damaging |
Het |
Mmd2 |
T |
C |
5: 142,550,587 (GRCm39) |
H217R |
probably damaging |
Het |
Mn1 |
C |
T |
5: 111,566,699 (GRCm39) |
T223M |
possibly damaging |
Het |
Ms4a4a |
A |
G |
19: 11,358,794 (GRCm39) |
Y84C |
probably damaging |
Het |
Mybl2 |
C |
T |
2: 162,924,605 (GRCm39) |
P658S |
probably benign |
Het |
Mycbp2 |
C |
A |
14: 103,446,345 (GRCm39) |
V1828L |
probably damaging |
Het |
Myh15 |
T |
C |
16: 49,017,149 (GRCm39) |
Y1887H |
probably damaging |
Het |
Nadk2 |
A |
G |
15: 9,083,271 (GRCm39) |
|
probably null |
Het |
Nsd3 |
A |
G |
8: 26,156,055 (GRCm39) |
N541D |
probably damaging |
Het |
Or52e8b |
A |
G |
7: 104,674,148 (GRCm39) |
V13A |
probably benign |
Het |
Or52i2 |
G |
T |
7: 102,319,046 (GRCm39) |
|
probably benign |
Het |
Oxa1l |
A |
T |
14: 54,598,312 (GRCm39) |
M1L |
probably benign |
Het |
Pcdha11 |
A |
T |
18: 37,144,421 (GRCm39) |
R171* |
probably null |
Het |
Pkd1l1 |
A |
T |
11: 8,821,771 (GRCm39) |
V1641E |
|
Het |
Pramel28 |
A |
T |
4: 143,692,455 (GRCm39) |
M182K |
probably benign |
Het |
Prom1 |
T |
A |
5: 44,178,242 (GRCm39) |
I497L |
probably benign |
Het |
Rasgef1b |
T |
C |
5: 99,706,753 (GRCm39) |
K41E |
possibly damaging |
Het |
Rasgrf1 |
T |
C |
9: 89,876,810 (GRCm39) |
F725S |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,612,032 (GRCm39) |
S3962C |
probably damaging |
Het |
Sema5b |
A |
T |
16: 35,480,915 (GRCm39) |
T829S |
probably benign |
Het |
Tdp2 |
A |
G |
13: 25,025,284 (GRCm39) |
D351G |
probably benign |
Het |
Tet3 |
A |
T |
6: 83,347,603 (GRCm39) |
D1130E |
probably damaging |
Het |
Tg |
T |
C |
15: 66,612,563 (GRCm39) |
C1993R |
probably damaging |
Het |
Tll1 |
T |
C |
8: 64,478,222 (GRCm39) |
I844V |
probably benign |
Het |
Ttll13 |
A |
C |
7: 79,903,911 (GRCm39) |
K280Q |
probably damaging |
Het |
Vmn2r109 |
A |
G |
17: 20,760,945 (GRCm39) |
V804A |
possibly damaging |
Het |
Vps13c |
T |
C |
9: 67,797,086 (GRCm39) |
V491A |
probably benign |
Het |
Xpo5 |
G |
T |
17: 46,525,551 (GRCm39) |
G233C |
probably damaging |
Het |
|
Other mutations in Mup5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0167:Mup5
|
UTSW |
4 |
61,752,019 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0485:Mup5
|
UTSW |
4 |
61,751,229 (GRCm39) |
splice site |
probably null |
|
R0547:Mup5
|
UTSW |
4 |
61,751,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1054:Mup5
|
UTSW |
4 |
61,750,871 (GRCm39) |
missense |
probably benign |
0.07 |
R1597:Mup5
|
UTSW |
4 |
61,753,317 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1721:Mup5
|
UTSW |
4 |
61,750,607 (GRCm39) |
nonsense |
probably null |
|
R1772:Mup5
|
UTSW |
4 |
61,750,578 (GRCm39) |
critical splice donor site |
probably null |
|
R1881:Mup5
|
UTSW |
4 |
61,752,868 (GRCm39) |
nonsense |
probably null |
|
R2104:Mup5
|
UTSW |
4 |
61,751,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R2384:Mup5
|
UTSW |
4 |
61,753,261 (GRCm39) |
splice site |
probably null |
|
R4971:Mup5
|
UTSW |
4 |
61,751,297 (GRCm39) |
missense |
probably benign |
0.32 |
R5246:Mup5
|
UTSW |
4 |
61,752,874 (GRCm39) |
missense |
probably benign |
0.04 |
R5926:Mup5
|
UTSW |
4 |
61,751,286 (GRCm39) |
missense |
probably benign |
0.03 |
R6905:Mup5
|
UTSW |
4 |
61,751,340 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6912:Mup5
|
UTSW |
4 |
61,752,806 (GRCm39) |
missense |
probably benign |
0.03 |
R6957:Mup5
|
UTSW |
4 |
61,751,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Mup5
|
UTSW |
4 |
61,751,992 (GRCm39) |
missense |
probably damaging |
0.96 |
R7224:Mup5
|
UTSW |
4 |
61,750,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7570:Mup5
|
UTSW |
4 |
61,752,911 (GRCm39) |
nonsense |
probably null |
|
R8253:Mup5
|
UTSW |
4 |
61,752,811 (GRCm39) |
missense |
probably benign |
0.00 |
R8465:Mup5
|
UTSW |
4 |
61,752,015 (GRCm39) |
missense |
probably benign |
|
R9048:Mup5
|
UTSW |
4 |
61,750,612 (GRCm39) |
missense |
probably benign |
0.20 |
R9571:Mup5
|
UTSW |
4 |
61,750,787 (GRCm39) |
critical splice donor site |
probably null |
|
|