Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
C |
A |
11: 84,161,213 (GRCm39) |
Y1026* |
probably null |
Het |
Acaca |
T |
G |
11: 84,191,297 (GRCm39) |
|
probably benign |
Het |
Adcy8 |
C |
T |
15: 64,678,503 (GRCm39) |
M483I |
probably damaging |
Het |
Adgrb2 |
G |
A |
4: 129,904,078 (GRCm39) |
G735S |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,100,173 (GRCm39) |
T2612A |
probably benign |
Het |
Armc1 |
A |
T |
3: 19,189,060 (GRCm39) |
S202T |
possibly damaging |
Het |
Arsj |
T |
C |
3: 126,232,486 (GRCm39) |
S411P |
probably damaging |
Het |
Ash1l |
T |
C |
3: 88,888,862 (GRCm39) |
V247A |
probably benign |
Het |
Camta2 |
T |
C |
11: 70,562,842 (GRCm39) |
D935G |
probably benign |
Het |
Cc2d2a |
G |
T |
5: 43,898,170 (GRCm39) |
V1626F |
probably damaging |
Het |
Cpne3 |
T |
A |
4: 19,535,266 (GRCm39) |
R255S |
probably benign |
Het |
Cramp1 |
A |
G |
17: 25,196,656 (GRCm39) |
|
probably benign |
Het |
Csf2rb2 |
C |
T |
15: 78,176,735 (GRCm39) |
|
probably null |
Het |
Cstf3 |
A |
T |
2: 104,484,563 (GRCm39) |
M396L |
probably benign |
Het |
Ctnnd2 |
A |
G |
15: 31,005,227 (GRCm39) |
|
probably benign |
Het |
Cul7 |
A |
T |
17: 46,962,888 (GRCm39) |
Y173F |
probably damaging |
Het |
Dach1 |
A |
T |
14: 98,138,832 (GRCm39) |
M537K |
probably benign |
Het |
Ddhd2 |
T |
C |
8: 26,217,727 (GRCm39) |
I717V |
probably damaging |
Het |
Dnm1 |
C |
T |
2: 32,213,742 (GRCm39) |
V475I |
probably damaging |
Het |
Dnm3 |
C |
T |
1: 162,305,517 (GRCm39) |
|
probably benign |
Het |
Dsg1c |
T |
A |
18: 20,405,597 (GRCm39) |
|
probably benign |
Het |
Eaf2 |
A |
T |
16: 36,620,941 (GRCm39) |
|
probably benign |
Het |
En1 |
T |
A |
1: 120,530,904 (GRCm39) |
V48E |
unknown |
Het |
Eral1 |
T |
A |
11: 77,966,875 (GRCm39) |
H180L |
possibly damaging |
Het |
Fry |
T |
A |
5: 150,401,511 (GRCm39) |
C2760S |
probably damaging |
Het |
Gtf2h3 |
C |
T |
5: 124,722,336 (GRCm39) |
A113V |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,514,651 (GRCm39) |
V3574M |
probably benign |
Het |
Ifnl2 |
T |
A |
7: 28,209,112 (GRCm39) |
R68W |
probably damaging |
Het |
Il6st |
A |
G |
13: 112,640,947 (GRCm39) |
T908A |
probably damaging |
Het |
Krtap4-1 |
C |
T |
11: 99,518,990 (GRCm39) |
G7S |
probably null |
Het |
Ly75 |
T |
C |
2: 60,180,284 (GRCm39) |
E631G |
probably benign |
Het |
Myh15 |
A |
G |
16: 48,891,446 (GRCm39) |
I189V |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,688,420 (GRCm39) |
Q619L |
probably damaging |
Het |
Or14a257 |
T |
C |
7: 86,138,646 (GRCm39) |
M38V |
probably benign |
Het |
Or1p1 |
A |
T |
11: 74,179,492 (GRCm39) |
T7S |
probably benign |
Het |
Or4n4b |
A |
G |
14: 50,536,472 (GRCm39) |
I98T |
probably damaging |
Het |
Or5e1 |
T |
C |
7: 108,354,335 (GRCm39) |
S91P |
probably damaging |
Het |
Pam |
T |
C |
1: 97,850,876 (GRCm39) |
T161A |
probably benign |
Het |
Phf8-ps |
T |
A |
17: 33,284,258 (GRCm39) |
D848V |
probably damaging |
Het |
Pigs |
T |
C |
11: 78,232,582 (GRCm39) |
V472A |
probably benign |
Het |
Plek |
A |
T |
11: 16,940,111 (GRCm39) |
N176K |
probably benign |
Het |
Poc5 |
A |
G |
13: 96,535,239 (GRCm39) |
N168S |
probably benign |
Het |
Pomt2 |
G |
T |
12: 87,182,370 (GRCm39) |
A219D |
probably damaging |
Het |
Rttn |
T |
A |
18: 89,033,336 (GRCm39) |
S716T |
probably damaging |
Het |
Sema4b |
A |
T |
7: 79,866,540 (GRCm39) |
S207C |
probably damaging |
Het |
Slc25a20 |
G |
A |
9: 108,557,408 (GRCm39) |
|
probably null |
Het |
Slc5a6 |
A |
T |
5: 31,194,155 (GRCm39) |
L634Q |
probably damaging |
Het |
Slfn3 |
A |
G |
11: 83,104,202 (GRCm39) |
I235V |
possibly damaging |
Het |
Smarcc1 |
T |
A |
9: 110,004,167 (GRCm39) |
L407Q |
probably damaging |
Het |
Spata32 |
T |
C |
11: 103,101,561 (GRCm39) |
|
probably benign |
Het |
Tdrd3 |
A |
G |
14: 87,723,783 (GRCm39) |
|
probably null |
Het |
Thada |
A |
G |
17: 84,744,130 (GRCm39) |
V726A |
probably benign |
Het |
Tmed7 |
A |
T |
18: 46,721,622 (GRCm39) |
|
probably null |
Het |
Tmem161a |
G |
A |
8: 70,633,435 (GRCm39) |
G94S |
probably null |
Het |
Tmem81 |
T |
A |
1: 132,435,948 (GRCm39) |
|
probably benign |
Het |
Trim63 |
C |
A |
4: 134,043,702 (GRCm39) |
A55E |
probably damaging |
Het |
Trmt1 |
A |
C |
8: 85,415,896 (GRCm39) |
|
probably benign |
Het |
Trpv4 |
C |
T |
5: 114,761,687 (GRCm39) |
V814M |
probably benign |
Het |
Tshz3 |
T |
C |
7: 36,471,079 (GRCm39) |
S1023P |
possibly damaging |
Het |
Upk3bl |
G |
A |
5: 136,086,157 (GRCm39) |
R31Q |
probably benign |
Het |
Usp40 |
T |
C |
1: 87,921,993 (GRCm39) |
D290G |
probably benign |
Het |
Vmn1r192 |
G |
T |
13: 22,371,764 (GRCm39) |
A152E |
probably benign |
Het |
Vmn1r26 |
T |
A |
6: 57,985,650 (GRCm39) |
T180S |
probably benign |
Het |
Wdr48 |
G |
T |
9: 119,738,606 (GRCm39) |
V89L |
probably benign |
Het |
Wdr6 |
G |
T |
9: 108,450,378 (GRCm39) |
|
probably null |
Het |
Zfp345 |
A |
G |
2: 150,314,275 (GRCm39) |
Y421H |
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 |
|
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 |
R7244:Mup5
|
UTSW |
4 |
61,749,818 (GRCm39) |
splice site |
probably null |
|
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 |
|
|