Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,429,234 (GRCm39) |
I774F |
probably benign |
Het |
3425401B19Rik |
A |
T |
14: 32,383,626 (GRCm39) |
C780S |
possibly damaging |
Het |
Abca12 |
T |
C |
1: 71,380,690 (GRCm39) |
D306G |
probably benign |
Het |
Adgrl2 |
T |
C |
3: 148,558,163 (GRCm39) |
|
probably benign |
Het |
Agt |
T |
C |
8: 125,291,184 (GRCm39) |
Y41C |
probably benign |
Het |
Alx3 |
G |
T |
3: 107,511,603 (GRCm39) |
R204L |
probably damaging |
Het |
Arih2 |
C |
G |
9: 108,488,938 (GRCm39) |
R260P |
probably damaging |
Het |
Bcl11a |
C |
T |
11: 24,114,763 (GRCm39) |
P702L |
probably damaging |
Het |
Bpifa2 |
A |
G |
2: 153,851,090 (GRCm39) |
N17S |
probably benign |
Het |
Cabcoco1 |
T |
C |
10: 68,377,584 (GRCm39) |
D35G |
probably benign |
Het |
Cd69 |
T |
C |
6: 129,252,187 (GRCm39) |
K21R |
probably benign |
Het |
Cdhr18 |
T |
C |
14: 13,823,796 (GRCm38) |
|
probably null |
Het |
Cntn4 |
T |
C |
6: 106,330,743 (GRCm39) |
|
probably null |
Het |
Cntnap5c |
A |
C |
17: 58,506,043 (GRCm39) |
N689T |
probably damaging |
Het |
Cog5 |
A |
G |
12: 31,883,238 (GRCm39) |
Y389C |
probably damaging |
Het |
Col5a1 |
T |
C |
2: 27,887,630 (GRCm39) |
|
probably null |
Het |
Coro1b |
G |
A |
19: 4,200,803 (GRCm39) |
R245Q |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,748,019 (GRCm39) |
D244G |
probably damaging |
Het |
Ctcfl |
C |
T |
2: 172,937,121 (GRCm39) |
|
probably null |
Het |
Dpy19l4 |
G |
A |
4: 11,317,078 (GRCm39) |
P40L |
possibly damaging |
Het |
Dsg4 |
C |
A |
18: 20,584,929 (GRCm39) |
Y214* |
probably null |
Het |
Eapp |
A |
T |
12: 54,739,440 (GRCm39) |
|
probably benign |
Het |
Fmo6 |
T |
C |
1: 162,748,114 (GRCm39) |
T317A |
possibly damaging |
Het |
Gm11595 |
A |
G |
11: 99,663,564 (GRCm39) |
C39R |
unknown |
Het |
Golim4 |
T |
C |
3: 75,813,703 (GRCm39) |
|
probably benign |
Het |
Greb1 |
G |
A |
12: 16,740,903 (GRCm39) |
S1393L |
possibly damaging |
Het |
Guca1b |
A |
G |
17: 47,700,044 (GRCm39) |
I73V |
probably benign |
Het |
Hdac7 |
C |
T |
15: 97,694,789 (GRCm39) |
V796I |
possibly damaging |
Het |
Hectd1 |
A |
G |
12: 51,795,616 (GRCm39) |
I2271T |
probably damaging |
Het |
Heg1 |
T |
G |
16: 33,558,627 (GRCm39) |
Y1066* |
probably null |
Het |
Helz2 |
C |
A |
2: 180,880,173 (GRCm39) |
K514N |
|
Het |
Ice1 |
C |
T |
13: 70,740,787 (GRCm39) |
R70Q |
|
Het |
Il18rap |
C |
T |
1: 40,582,177 (GRCm39) |
T366M |
probably benign |
Het |
Itgae |
A |
G |
11: 73,004,447 (GRCm39) |
T245A |
probably damaging |
Het |
Jhy |
G |
A |
9: 40,822,453 (GRCm39) |
Q562* |
probably null |
Het |
Khnyn |
A |
G |
14: 56,124,735 (GRCm39) |
R330G |
probably benign |
Het |
Lamc2 |
A |
T |
1: 153,027,873 (GRCm39) |
C184S |
probably damaging |
Het |
Lhx5 |
T |
A |
5: 120,574,509 (GRCm39) |
L271* |
probably null |
Het |
Magel2 |
G |
A |
7: 62,029,537 (GRCm39) |
V814M |
unknown |
Het |
Manf |
A |
G |
9: 106,767,461 (GRCm39) |
I85T |
possibly damaging |
Het |
Mgmt |
A |
G |
7: 136,729,794 (GRCm39) |
T203A |
probably benign |
Het |
Mmp9 |
C |
T |
2: 164,794,568 (GRCm39) |
S520F |
possibly damaging |
Het |
Myrip |
A |
G |
9: 120,270,484 (GRCm39) |
E578G |
possibly damaging |
Het |
Naaladl2 |
A |
G |
3: 23,900,757 (GRCm39) |
M691T |
probably damaging |
Het |
Ncln |
C |
T |
10: 81,323,519 (GRCm39) |
V51I |
probably benign |
Het |
Or2n1d |
A |
T |
17: 38,646,320 (GRCm39) |
T91S |
possibly damaging |
Het |
Or4c112 |
T |
C |
2: 88,854,294 (GRCm39) |
N18D |
probably benign |
Het |
Or4c117 |
T |
C |
2: 88,955,608 (GRCm39) |
I156V |
probably benign |
Het |
Pcdhga12 |
A |
T |
18: 37,900,118 (GRCm39) |
M317L |
possibly damaging |
Het |
Pcnt |
T |
G |
10: 76,223,359 (GRCm39) |
K1941T |
probably damaging |
Het |
Pde4dip |
A |
T |
3: 97,650,917 (GRCm39) |
M896K |
probably benign |
Het |
Pfkfb3 |
A |
T |
2: 11,487,254 (GRCm39) |
|
probably null |
Het |
Pik3cb |
A |
G |
9: 98,946,201 (GRCm39) |
S542P |
probably benign |
Het |
Pik3cg |
A |
G |
12: 32,247,257 (GRCm39) |
V822A |
probably benign |
Het |
Plcl2 |
G |
T |
17: 50,915,141 (GRCm39) |
G717C |
probably damaging |
Het |
Ptprs |
C |
T |
17: 56,730,320 (GRCm39) |
A1185T |
probably benign |
Het |
Ptpru |
T |
A |
4: 131,503,560 (GRCm39) |
I1157F |
probably damaging |
Het |
Rbbp6 |
A |
G |
7: 122,591,268 (GRCm39) |
T457A |
possibly damaging |
Het |
Rdh16f2 |
A |
G |
10: 127,712,812 (GRCm39) |
E270G |
probably damaging |
Het |
Rrp15 |
C |
T |
1: 186,453,641 (GRCm39) |
E269K |
unknown |
Het |
Sec23b |
T |
C |
2: 144,401,316 (GRCm39) |
V59A |
probably benign |
Het |
Slc22a21 |
A |
T |
11: 53,846,809 (GRCm39) |
|
probably null |
Het |
Sp5 |
C |
A |
2: 70,306,962 (GRCm39) |
P216T |
probably benign |
Het |
Synj1 |
A |
T |
16: 90,775,622 (GRCm39) |
D385E |
probably damaging |
Het |
Trim37 |
C |
T |
11: 87,097,629 (GRCm39) |
S808F |
possibly damaging |
Het |
Tsks |
A |
T |
7: 44,592,694 (GRCm39) |
|
probably benign |
Het |
Upf1 |
A |
T |
8: 70,791,087 (GRCm39) |
S563T |
possibly damaging |
Het |
Usp14 |
A |
G |
18: 9,996,194 (GRCm39) |
I462T |
probably damaging |
Het |
Usp48 |
G |
A |
4: 137,340,996 (GRCm39) |
G332E |
probably benign |
Het |
Vmn1r184 |
C |
G |
7: 25,966,310 (GRCm39) |
Q19E |
possibly damaging |
Het |
Vps50 |
C |
A |
6: 3,516,710 (GRCm39) |
A64E |
probably benign |
Het |
Zc3h11a |
T |
A |
1: 133,566,339 (GRCm39) |
N211I |
probably damaging |
Het |
Zfp518a |
A |
C |
19: 40,901,870 (GRCm39) |
K600Q |
possibly damaging |
Het |
Zfp729a |
A |
T |
13: 67,768,061 (GRCm39) |
S723T |
probably benign |
Het |
Zmynd12 |
A |
T |
4: 119,294,286 (GRCm39) |
I88F |
probably damaging |
Het |
|
Other mutations in Upf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Upf2
|
APN |
2 |
5,966,111 (GRCm39) |
missense |
unknown |
|
IGL01394:Upf2
|
APN |
2 |
6,045,024 (GRCm39) |
splice site |
probably null |
|
IGL01571:Upf2
|
APN |
2 |
6,023,750 (GRCm39) |
unclassified |
probably benign |
|
IGL01624:Upf2
|
APN |
2 |
6,038,990 (GRCm39) |
missense |
probably benign |
|
IGL02121:Upf2
|
APN |
2 |
6,031,134 (GRCm39) |
splice site |
probably benign |
|
IGL02485:Upf2
|
APN |
2 |
6,032,102 (GRCm39) |
missense |
unknown |
|
IGL02491:Upf2
|
APN |
2 |
6,030,975 (GRCm39) |
missense |
unknown |
|
Balderdash
|
UTSW |
2 |
5,978,347 (GRCm39) |
missense |
unknown |
|
nonsense
|
UTSW |
2 |
6,051,845 (GRCm39) |
missense |
unknown |
|
R0265:Upf2
|
UTSW |
2 |
6,032,015 (GRCm39) |
splice site |
probably benign |
|
R0390:Upf2
|
UTSW |
2 |
6,023,705 (GRCm39) |
unclassified |
probably benign |
|
R0480:Upf2
|
UTSW |
2 |
5,962,445 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0513:Upf2
|
UTSW |
2 |
5,962,478 (GRCm39) |
missense |
unknown |
|
R0579:Upf2
|
UTSW |
2 |
5,993,240 (GRCm39) |
missense |
unknown |
|
R0612:Upf2
|
UTSW |
2 |
6,038,909 (GRCm39) |
splice site |
probably benign |
|
R0856:Upf2
|
UTSW |
2 |
5,962,463 (GRCm39) |
missense |
unknown |
|
R1103:Upf2
|
UTSW |
2 |
6,030,986 (GRCm39) |
missense |
unknown |
|
R1384:Upf2
|
UTSW |
2 |
5,965,800 (GRCm39) |
missense |
unknown |
|
R1672:Upf2
|
UTSW |
2 |
6,044,908 (GRCm39) |
splice site |
probably null |
|
R1728:Upf2
|
UTSW |
2 |
6,032,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Upf2
|
UTSW |
2 |
6,032,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Upf2
|
UTSW |
2 |
6,055,135 (GRCm39) |
splice site |
probably null |
|
R2252:Upf2
|
UTSW |
2 |
5,966,271 (GRCm39) |
missense |
unknown |
|
R2339:Upf2
|
UTSW |
2 |
6,044,913 (GRCm39) |
splice site |
probably benign |
|
R3015:Upf2
|
UTSW |
2 |
5,980,890 (GRCm39) |
missense |
unknown |
|
R3931:Upf2
|
UTSW |
2 |
6,051,821 (GRCm39) |
missense |
unknown |
|
R4151:Upf2
|
UTSW |
2 |
5,966,516 (GRCm39) |
missense |
unknown |
|
R4283:Upf2
|
UTSW |
2 |
5,978,369 (GRCm39) |
missense |
unknown |
|
R4558:Upf2
|
UTSW |
2 |
5,978,404 (GRCm39) |
missense |
unknown |
|
R4564:Upf2
|
UTSW |
2 |
6,032,123 (GRCm39) |
missense |
unknown |
|
R5630:Upf2
|
UTSW |
2 |
6,032,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R6370:Upf2
|
UTSW |
2 |
5,980,821 (GRCm39) |
missense |
unknown |
|
R6418:Upf2
|
UTSW |
2 |
6,032,150 (GRCm39) |
missense |
unknown |
|
R6432:Upf2
|
UTSW |
2 |
5,984,588 (GRCm39) |
missense |
unknown |
|
R7184:Upf2
|
UTSW |
2 |
6,028,131 (GRCm39) |
missense |
unknown |
|
R7308:Upf2
|
UTSW |
2 |
5,978,329 (GRCm39) |
missense |
unknown |
|
R7371:Upf2
|
UTSW |
2 |
5,965,851 (GRCm39) |
missense |
unknown |
|
R7404:Upf2
|
UTSW |
2 |
6,045,014 (GRCm39) |
missense |
unknown |
|
R7439:Upf2
|
UTSW |
2 |
6,023,743 (GRCm39) |
missense |
unknown |
|
R7441:Upf2
|
UTSW |
2 |
6,023,743 (GRCm39) |
missense |
unknown |
|
R7461:Upf2
|
UTSW |
2 |
5,978,347 (GRCm39) |
missense |
unknown |
|
R7483:Upf2
|
UTSW |
2 |
6,032,219 (GRCm39) |
missense |
unknown |
|
R7613:Upf2
|
UTSW |
2 |
5,978,347 (GRCm39) |
missense |
unknown |
|
R7976:Upf2
|
UTSW |
2 |
6,030,926 (GRCm39) |
missense |
unknown |
|
R8044:Upf2
|
UTSW |
2 |
6,034,249 (GRCm39) |
missense |
unknown |
|
R8516:Upf2
|
UTSW |
2 |
6,023,782 (GRCm39) |
missense |
unknown |
|
R8880:Upf2
|
UTSW |
2 |
6,030,983 (GRCm39) |
missense |
unknown |
|
R9138:Upf2
|
UTSW |
2 |
6,028,132 (GRCm39) |
missense |
unknown |
|
R9226:Upf2
|
UTSW |
2 |
6,051,845 (GRCm39) |
missense |
unknown |
|
R9444:Upf2
|
UTSW |
2 |
6,023,755 (GRCm39) |
missense |
unknown |
|
R9484:Upf2
|
UTSW |
2 |
5,966,078 (GRCm39) |
missense |
unknown |
|
R9665:Upf2
|
UTSW |
2 |
6,051,715 (GRCm39) |
missense |
unknown |
|
R9691:Upf2
|
UTSW |
2 |
6,032,024 (GRCm39) |
missense |
unknown |
|
Z1176:Upf2
|
UTSW |
2 |
6,028,199 (GRCm39) |
missense |
unknown |
|
|