Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aga |
T |
C |
8: 53,964,861 (GRCm39) |
S8P |
probably benign |
Het |
Ankrd34c |
C |
T |
9: 89,612,337 (GRCm39) |
M1I |
probably null |
Het |
Ankrd44 |
T |
C |
1: 54,805,968 (GRCm39) |
H146R |
probably damaging |
Het |
Bst1 |
A |
G |
5: 43,983,604 (GRCm39) |
|
probably null |
Het |
Btbd8 |
T |
G |
5: 107,639,464 (GRCm39) |
|
probably null |
Het |
Cdh12 |
A |
T |
15: 21,480,416 (GRCm39) |
I211F |
probably damaging |
Het |
Cenpj |
G |
T |
14: 56,764,406 (GRCm39) |
D1335E |
probably benign |
Het |
Clpx |
G |
A |
9: 65,230,057 (GRCm39) |
V502I |
possibly damaging |
Het |
Cntnap4 |
T |
C |
8: 113,500,222 (GRCm39) |
S505P |
probably benign |
Het |
Cog2 |
T |
C |
8: 125,262,131 (GRCm39) |
|
probably benign |
Het |
Cped1 |
A |
G |
6: 22,233,601 (GRCm39) |
Q819R |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,805,759 (GRCm39) |
E2190G |
possibly damaging |
Het |
Ctsa |
G |
A |
2: 164,679,368 (GRCm39) |
R359Q |
probably damaging |
Het |
Cul9 |
A |
G |
17: 46,813,623 (GRCm39) |
|
probably benign |
Het |
Dab1 |
G |
T |
4: 104,584,777 (GRCm39) |
V306F |
probably damaging |
Het |
Dysf |
A |
G |
6: 84,050,876 (GRCm39) |
I438V |
probably benign |
Het |
Eif4g3 |
G |
T |
4: 137,847,699 (GRCm39) |
G380W |
probably damaging |
Het |
Exd1 |
T |
A |
2: 119,350,862 (GRCm39) |
K466N |
probably benign |
Het |
Eya3 |
A |
C |
4: 132,434,294 (GRCm39) |
D325A |
probably damaging |
Het |
Fmn1 |
A |
G |
2: 113,195,445 (GRCm39) |
T382A |
unknown |
Het |
Fry |
T |
A |
5: 150,269,021 (GRCm39) |
D106E |
possibly damaging |
Het |
Gm21957 |
T |
A |
7: 124,818,733 (GRCm39) |
|
noncoding transcript |
Het |
Gm44511 |
A |
G |
6: 128,761,059 (GRCm39) |
|
probably benign |
Het |
Itga4 |
A |
G |
2: 79,155,982 (GRCm39) |
I983V |
probably benign |
Het |
Lrpprc |
A |
T |
17: 85,058,675 (GRCm39) |
D5E |
probably benign |
Het |
Lrrc37 |
T |
C |
11: 103,511,293 (GRCm39) |
E225G |
unknown |
Het |
Ltbp4 |
G |
T |
7: 27,023,789 (GRCm39) |
N747K |
probably damaging |
Het |
Minar1 |
A |
G |
9: 89,478,731 (GRCm39) |
Y772H |
probably damaging |
Het |
Mlh3 |
T |
C |
12: 85,287,625 (GRCm39) |
Q1308R |
probably benign |
Het |
Mtfr2 |
T |
A |
10: 20,229,185 (GRCm39) |
C63S |
possibly damaging |
Het |
Myh11 |
T |
A |
16: 14,022,617 (GRCm39) |
M1661L |
probably benign |
Het |
Myo1c |
T |
C |
11: 75,549,240 (GRCm39) |
M137T |
probably benign |
Het |
Myocd |
A |
C |
11: 65,078,392 (GRCm39) |
L340V |
probably damaging |
Het |
Napsa |
A |
T |
7: 44,235,220 (GRCm39) |
Q335L |
possibly damaging |
Het |
Nlrp4b |
C |
A |
7: 10,448,516 (GRCm39) |
Q240K |
probably benign |
Het |
Npepps |
A |
C |
11: 97,128,984 (GRCm39) |
F400C |
probably damaging |
Het |
Nxpe4 |
A |
T |
9: 48,304,738 (GRCm39) |
E275V |
probably benign |
Het |
Ofd1 |
T |
C |
X: 165,192,530 (GRCm39) |
D501G |
probably benign |
Het |
Or13a19 |
T |
C |
7: 139,903,445 (GRCm39) |
Y278H |
probably damaging |
Het |
Or4f6 |
A |
G |
2: 111,838,868 (GRCm39) |
I221T |
possibly damaging |
Het |
Or5p79 |
T |
G |
7: 108,221,490 (GRCm39) |
L157R |
probably damaging |
Het |
Or8k41 |
A |
T |
2: 86,313,678 (GRCm39) |
M136K |
probably damaging |
Het |
P2ry1 |
A |
T |
3: 60,910,947 (GRCm39) |
T29S |
probably benign |
Het |
Papss1 |
T |
C |
3: 131,290,860 (GRCm39) |
V201A |
possibly damaging |
Het |
Paxip1 |
A |
G |
5: 27,957,764 (GRCm39) |
V864A |
probably benign |
Het |
Pcdhgc5 |
T |
A |
18: 37,954,887 (GRCm39) |
H720Q |
probably benign |
Het |
Pdxdc1 |
T |
C |
16: 13,694,023 (GRCm39) |
N133S |
possibly damaging |
Het |
Prkar1a |
T |
C |
11: 109,544,690 (GRCm39) |
I27T |
probably damaging |
Het |
Scn9a |
A |
G |
2: 66,392,855 (GRCm39) |
S246P |
probably damaging |
Het |
Sertad2 |
G |
T |
11: 20,597,798 (GRCm39) |
|
probably benign |
Het |
Slc22a27 |
A |
G |
19: 7,887,067 (GRCm39) |
I274T |
possibly damaging |
Het |
Slc22a5 |
A |
T |
11: 53,782,058 (GRCm39) |
V103E |
probably damaging |
Het |
Slc5a9 |
A |
T |
4: 111,748,138 (GRCm39) |
F225I |
probably benign |
Het |
Slc6a3 |
G |
A |
13: 73,706,404 (GRCm39) |
|
probably null |
Het |
Smcr8 |
A |
G |
11: 60,669,287 (GRCm39) |
E145G |
probably damaging |
Het |
Spen |
A |
T |
4: 141,203,448 (GRCm39) |
D1726E |
possibly damaging |
Het |
Sphkap |
A |
T |
1: 83,254,552 (GRCm39) |
S779T |
probably damaging |
Het |
Stag1 |
A |
T |
9: 100,658,844 (GRCm39) |
N144Y |
probably damaging |
Het |
Strada |
T |
C |
11: 106,061,783 (GRCm39) |
H156R |
probably damaging |
Het |
Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
Tas2r138 |
A |
C |
6: 40,590,116 (GRCm39) |
D43E |
probably damaging |
Het |
Tdpoz3 |
A |
T |
3: 93,733,642 (GRCm39) |
K106* |
probably null |
Het |
Trbv13-1 |
A |
G |
6: 41,093,229 (GRCm39) |
D54G |
probably damaging |
Het |
Ttc39b |
A |
G |
4: 83,165,932 (GRCm39) |
V218A |
probably benign |
Het |
Ttn |
G |
A |
2: 76,611,203 (GRCm39) |
T15697I |
probably damaging |
Het |
Ugt2b38 |
G |
A |
5: 87,560,282 (GRCm39) |
T344I |
probably benign |
Het |
Vmn2r94 |
T |
C |
17: 18,477,908 (GRCm39) |
M168V |
probably benign |
Het |
Wdr11 |
T |
C |
7: 129,208,715 (GRCm39) |
|
probably benign |
Het |
Wipf2 |
T |
C |
11: 98,783,554 (GRCm39) |
|
probably benign |
Het |
Zranb2 |
T |
A |
3: 157,252,302 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Rnf10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01014:Rnf10
|
APN |
5 |
115,395,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01995:Rnf10
|
APN |
5 |
115,389,161 (GRCm39) |
nonsense |
probably null |
|
IGL02291:Rnf10
|
APN |
5 |
115,398,255 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02751:Rnf10
|
APN |
5 |
115,380,725 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02897:Rnf10
|
APN |
5 |
115,386,700 (GRCm39) |
missense |
probably benign |
|
IGL02968:Rnf10
|
APN |
5 |
115,383,947 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03098:Rnf10
|
UTSW |
5 |
115,410,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R0409:Rnf10
|
UTSW |
5 |
115,393,506 (GRCm39) |
splice site |
probably benign |
|
R1083:Rnf10
|
UTSW |
5 |
115,398,163 (GRCm39) |
splice site |
probably benign |
|
R1754:Rnf10
|
UTSW |
5 |
115,383,924 (GRCm39) |
missense |
probably damaging |
0.99 |
R1957:Rnf10
|
UTSW |
5 |
115,398,381 (GRCm39) |
splice site |
probably benign |
|
R2398:Rnf10
|
UTSW |
5 |
115,385,332 (GRCm39) |
missense |
probably benign |
0.33 |
R2848:Rnf10
|
UTSW |
5 |
115,387,171 (GRCm39) |
missense |
probably benign |
|
R2849:Rnf10
|
UTSW |
5 |
115,387,171 (GRCm39) |
missense |
probably benign |
|
R4527:Rnf10
|
UTSW |
5 |
115,398,210 (GRCm39) |
missense |
probably damaging |
0.96 |
R4617:Rnf10
|
UTSW |
5 |
115,386,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R4673:Rnf10
|
UTSW |
5 |
115,389,148 (GRCm39) |
missense |
probably damaging |
0.99 |
R4823:Rnf10
|
UTSW |
5 |
115,393,501 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5560:Rnf10
|
UTSW |
5 |
115,388,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R5805:Rnf10
|
UTSW |
5 |
115,382,127 (GRCm39) |
missense |
probably benign |
|
R6192:Rnf10
|
UTSW |
5 |
115,395,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R7061:Rnf10
|
UTSW |
5 |
115,395,149 (GRCm39) |
missense |
probably damaging |
0.98 |
R7206:Rnf10
|
UTSW |
5 |
115,382,180 (GRCm39) |
missense |
probably benign |
0.04 |
R7213:Rnf10
|
UTSW |
5 |
115,380,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R7213:Rnf10
|
UTSW |
5 |
115,380,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7429:Rnf10
|
UTSW |
5 |
115,386,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R8098:Rnf10
|
UTSW |
5 |
115,389,438 (GRCm39) |
missense |
probably damaging |
0.98 |
R8179:Rnf10
|
UTSW |
5 |
115,398,176 (GRCm39) |
frame shift |
probably null |
|
R8252:Rnf10
|
UTSW |
5 |
115,398,373 (GRCm39) |
missense |
probably benign |
0.03 |
R8357:Rnf10
|
UTSW |
5 |
115,410,320 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8457:Rnf10
|
UTSW |
5 |
115,410,320 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9160:Rnf10
|
UTSW |
5 |
115,398,249 (GRCm39) |
missense |
probably benign |
0.06 |
R9274:Rnf10
|
UTSW |
5 |
115,385,322 (GRCm39) |
nonsense |
probably null |
|
|