Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921513D11Rik |
G |
T |
17: 79,935,180 (GRCm39) |
A98S |
probably benign |
Het |
Acp2 |
A |
G |
2: 91,038,767 (GRCm39) |
|
probably null |
Het |
Akap13 |
T |
G |
7: 75,261,125 (GRCm39) |
S447A |
possibly damaging |
Het |
Alk |
G |
A |
17: 72,291,740 (GRCm39) |
|
probably benign |
Het |
Ankrd55 |
A |
G |
13: 112,517,767 (GRCm39) |
|
probably benign |
Het |
Arhgef39 |
T |
C |
4: 43,496,834 (GRCm39) |
T327A |
probably benign |
Het |
Calhm5 |
T |
G |
10: 33,972,013 (GRCm39) |
I141L |
probably benign |
Het |
Cdan1 |
G |
A |
2: 120,551,083 (GRCm39) |
A1103V |
probably damaging |
Het |
Cdk17 |
T |
A |
10: 93,074,895 (GRCm39) |
Y3* |
probably null |
Het |
Cdon |
T |
C |
9: 35,367,733 (GRCm39) |
|
probably benign |
Het |
Cntn3 |
T |
A |
6: 102,222,119 (GRCm39) |
N460I |
probably benign |
Het |
Cntrl |
T |
A |
2: 35,050,639 (GRCm39) |
C985S |
possibly damaging |
Het |
Col6a2 |
T |
C |
10: 76,443,574 (GRCm39) |
E497G |
probably benign |
Het |
Crybg1 |
A |
G |
10: 43,875,089 (GRCm39) |
M673T |
possibly damaging |
Het |
Csmd1 |
A |
C |
8: 15,971,174 (GRCm39) |
I3047S |
probably benign |
Het |
Cyp2u1 |
A |
G |
3: 131,087,258 (GRCm39) |
I441T |
possibly damaging |
Het |
Disp2 |
T |
C |
2: 118,620,920 (GRCm39) |
S551P |
probably damaging |
Het |
Dstyk |
A |
G |
1: 132,381,063 (GRCm39) |
|
probably benign |
Het |
Frem1 |
T |
C |
4: 82,868,557 (GRCm39) |
S1457G |
probably damaging |
Het |
Gabbr2 |
C |
T |
4: 46,718,838 (GRCm39) |
C613Y |
probably damaging |
Het |
Gdf7 |
C |
A |
12: 8,351,555 (GRCm39) |
|
probably benign |
Het |
Ift70a1 |
A |
T |
2: 75,810,320 (GRCm39) |
C588S |
probably damaging |
Het |
Iqcf4 |
T |
C |
9: 106,445,860 (GRCm39) |
I96V |
probably benign |
Het |
Iqck |
G |
A |
7: 118,498,880 (GRCm39) |
D173N |
possibly damaging |
Het |
Itpr3 |
C |
T |
17: 27,329,529 (GRCm39) |
H1518Y |
probably benign |
Het |
Kdm5d |
T |
A |
Y: 910,539 (GRCm39) |
L250H |
probably damaging |
Het |
Kntc1 |
C |
T |
5: 123,937,965 (GRCm39) |
|
probably benign |
Het |
Lmtk3 |
T |
A |
7: 45,444,427 (GRCm39) |
|
probably benign |
Het |
Lpin3 |
A |
G |
2: 160,735,999 (GRCm39) |
D93G |
probably benign |
Het |
Ncoa6 |
A |
T |
2: 155,253,440 (GRCm39) |
|
probably benign |
Het |
Nudt7 |
G |
A |
8: 114,862,111 (GRCm39) |
|
probably benign |
Het |
Nup160 |
A |
G |
2: 90,563,563 (GRCm39) |
|
probably benign |
Het |
Oit3 |
G |
A |
10: 59,264,016 (GRCm39) |
R373C |
probably damaging |
Het |
Olfml2a |
A |
T |
2: 38,849,765 (GRCm39) |
I494L |
probably damaging |
Het |
Opa3 |
A |
G |
7: 18,962,524 (GRCm39) |
|
probably benign |
Het |
Or51e2 |
A |
G |
7: 102,392,214 (GRCm39) |
|
probably benign |
Het |
Or5ac15 |
A |
T |
16: 58,940,187 (GRCm39) |
V82D |
probably damaging |
Het |
Or9r7 |
A |
G |
10: 129,962,522 (GRCm39) |
Y135H |
probably damaging |
Het |
Pak3 |
TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
X: 142,526,889 (GRCm39) |
|
probably benign |
Het |
Parp6 |
G |
T |
9: 59,556,847 (GRCm39) |
C584F |
probably damaging |
Het |
Pcgf2 |
A |
G |
11: 97,582,676 (GRCm39) |
|
probably benign |
Het |
Pde3a |
T |
C |
6: 141,405,042 (GRCm39) |
|
probably benign |
Het |
Pitrm1 |
A |
G |
13: 6,608,280 (GRCm39) |
D335G |
probably benign |
Het |
Pkhd1 |
A |
T |
1: 20,187,708 (GRCm39) |
N3533K |
probably benign |
Het |
Pkp4 |
T |
C |
2: 59,169,109 (GRCm39) |
L752P |
probably damaging |
Het |
Plcb3 |
C |
A |
19: 6,939,281 (GRCm39) |
E566* |
probably null |
Het |
Ppef2 |
T |
C |
5: 92,392,689 (GRCm39) |
K261R |
probably benign |
Het |
Prdm14 |
A |
G |
1: 13,184,585 (GRCm39) |
S529P |
probably damaging |
Het |
Prune2 |
T |
C |
19: 17,102,586 (GRCm39) |
S2582P |
probably benign |
Het |
Sardh |
G |
A |
2: 27,081,931 (GRCm39) |
T865I |
possibly damaging |
Het |
Slc26a3 |
A |
T |
12: 31,515,812 (GRCm39) |
I571F |
possibly damaging |
Het |
Slc5a5 |
A |
T |
8: 71,342,864 (GRCm39) |
M232K |
probably benign |
Het |
Slc9a1 |
T |
A |
4: 133,097,859 (GRCm39) |
M2K |
probably benign |
Het |
Spata31e3 |
A |
T |
13: 50,402,296 (GRCm39) |
D83E |
possibly damaging |
Het |
Ss18l1 |
G |
A |
2: 179,697,647 (GRCm39) |
S177N |
possibly damaging |
Het |
Svs5 |
A |
T |
2: 164,175,507 (GRCm39) |
I120L |
probably benign |
Het |
Tcl1b1 |
G |
T |
12: 105,126,074 (GRCm39) |
V19F |
probably damaging |
Het |
Tmem108 |
C |
T |
9: 103,361,889 (GRCm39) |
V566M |
probably damaging |
Het |
Trmu |
C |
A |
15: 85,763,604 (GRCm39) |
C9* |
probably null |
Het |
Vnn1 |
A |
T |
10: 23,775,499 (GRCm39) |
I250F |
possibly damaging |
Het |
Vps13c |
T |
A |
9: 67,879,285 (GRCm39) |
Y3409N |
probably damaging |
Het |
Xrn1 |
T |
A |
9: 95,873,322 (GRCm39) |
N695K |
probably benign |
Het |
Zfp84 |
T |
A |
7: 29,470,797 (GRCm39) |
M1K |
probably null |
Het |
Zfyve26 |
G |
A |
12: 79,326,841 (GRCm39) |
R761C |
probably damaging |
Het |
Zp3r |
A |
G |
1: 130,505,621 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Hnrnpul2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01989:Hnrnpul2
|
APN |
19 |
8,800,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R0136:Hnrnpul2
|
UTSW |
19 |
8,804,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Hnrnpul2
|
UTSW |
19 |
8,801,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R0784:Hnrnpul2
|
UTSW |
19 |
8,802,416 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1110:Hnrnpul2
|
UTSW |
19 |
8,804,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R1227:Hnrnpul2
|
UTSW |
19 |
8,800,601 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1589:Hnrnpul2
|
UTSW |
19 |
8,808,696 (GRCm39) |
missense |
probably benign |
0.00 |
R2126:Hnrnpul2
|
UTSW |
19 |
8,801,802 (GRCm39) |
nonsense |
probably null |
|
R2226:Hnrnpul2
|
UTSW |
19 |
8,802,349 (GRCm39) |
missense |
probably damaging |
0.96 |
R2243:Hnrnpul2
|
UTSW |
19 |
8,798,001 (GRCm39) |
missense |
probably benign |
|
R3703:Hnrnpul2
|
UTSW |
19 |
8,801,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R4038:Hnrnpul2
|
UTSW |
19 |
8,800,591 (GRCm39) |
unclassified |
probably benign |
|
R4856:Hnrnpul2
|
UTSW |
19 |
8,807,191 (GRCm39) |
missense |
probably benign |
0.20 |
R4886:Hnrnpul2
|
UTSW |
19 |
8,807,191 (GRCm39) |
missense |
probably benign |
0.20 |
R5016:Hnrnpul2
|
UTSW |
19 |
8,800,189 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5365:Hnrnpul2
|
UTSW |
19 |
8,798,080 (GRCm39) |
missense |
probably benign |
|
R5435:Hnrnpul2
|
UTSW |
19 |
8,797,682 (GRCm39) |
missense |
probably benign |
0.32 |
R5951:Hnrnpul2
|
UTSW |
19 |
8,802,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Hnrnpul2
|
UTSW |
19 |
8,800,596 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6824:Hnrnpul2
|
UTSW |
19 |
8,804,081 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6924:Hnrnpul2
|
UTSW |
19 |
8,808,873 (GRCm39) |
missense |
unknown |
|
R6978:Hnrnpul2
|
UTSW |
19 |
8,801,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R7602:Hnrnpul2
|
UTSW |
19 |
8,808,673 (GRCm39) |
missense |
probably damaging |
0.99 |
R7688:Hnrnpul2
|
UTSW |
19 |
8,797,994 (GRCm39) |
missense |
probably benign |
|
R7726:Hnrnpul2
|
UTSW |
19 |
8,808,644 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7749:Hnrnpul2
|
UTSW |
19 |
8,797,788 (GRCm39) |
missense |
probably benign |
|
R7753:Hnrnpul2
|
UTSW |
19 |
8,802,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R8007:Hnrnpul2
|
UTSW |
19 |
8,798,179 (GRCm39) |
critical splice donor site |
probably null |
|
R8725:Hnrnpul2
|
UTSW |
19 |
8,798,064 (GRCm39) |
missense |
probably benign |
0.00 |
R8727:Hnrnpul2
|
UTSW |
19 |
8,798,064 (GRCm39) |
missense |
probably benign |
0.00 |
R8901:Hnrnpul2
|
UTSW |
19 |
8,801,809 (GRCm39) |
missense |
probably damaging |
0.98 |
R8994:Hnrnpul2
|
UTSW |
19 |
8,802,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R9012:Hnrnpul2
|
UTSW |
19 |
8,801,829 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9187:Hnrnpul2
|
UTSW |
19 |
8,808,319 (GRCm39) |
missense |
probably benign |
0.28 |
R9347:Hnrnpul2
|
UTSW |
19 |
8,798,080 (GRCm39) |
missense |
probably benign |
|
|