Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb1 |
G |
A |
15: 74,410,219 (GRCm39) |
R286H |
possibly damaging |
Het |
Ank3 |
A |
T |
10: 69,828,774 (GRCm39) |
|
probably benign |
Het |
Arhgap24 |
G |
A |
5: 102,700,025 (GRCm39) |
|
probably null |
Het |
Arhgef2 |
T |
C |
3: 88,543,176 (GRCm39) |
Y396H |
probably benign |
Het |
Asap3 |
G |
T |
4: 135,968,720 (GRCm39) |
G722C |
probably benign |
Het |
Birc2 |
A |
C |
9: 7,857,343 (GRCm39) |
*377E |
probably null |
Het |
Cdc123 |
G |
T |
2: 5,803,174 (GRCm39) |
Q282K |
possibly damaging |
Het |
Cdkl4 |
C |
T |
17: 80,855,120 (GRCm39) |
|
probably null |
Het |
Cep97 |
T |
C |
16: 55,725,820 (GRCm39) |
N689S |
probably benign |
Het |
Cfap97 |
T |
G |
8: 46,634,895 (GRCm39) |
S407A |
probably damaging |
Het |
Cfh |
A |
T |
1: 140,063,967 (GRCm39) |
N436K |
probably benign |
Het |
Chpf2 |
A |
T |
5: 24,797,421 (GRCm39) |
|
probably benign |
Het |
Cnnm2 |
A |
G |
19: 46,751,616 (GRCm39) |
T469A |
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,703,922 (GRCm39) |
I2275F |
unknown |
Het |
Ctdspl2 |
A |
T |
2: 121,809,414 (GRCm39) |
N122Y |
probably damaging |
Het |
Dcaf6 |
A |
T |
1: 165,178,724 (GRCm39) |
C602S |
probably benign |
Het |
Dda1 |
T |
A |
8: 71,927,294 (GRCm39) |
|
probably benign |
Het |
Dixdc1 |
T |
C |
9: 50,609,888 (GRCm39) |
|
probably benign |
Het |
Dnah2 |
C |
T |
11: 69,349,746 (GRCm39) |
R2399Q |
probably benign |
Het |
Emilin3 |
T |
A |
2: 160,750,990 (GRCm39) |
N253I |
probably damaging |
Het |
Epg5 |
T |
A |
18: 78,002,847 (GRCm39) |
|
probably null |
Het |
Fam204a |
A |
T |
19: 60,209,525 (GRCm39) |
Y68* |
probably null |
Het |
Fbln5 |
T |
G |
12: 101,727,002 (GRCm39) |
D329A |
possibly damaging |
Het |
Fkbp15 |
T |
A |
4: 62,246,047 (GRCm39) |
|
probably null |
Het |
Fnbp4 |
C |
G |
2: 90,605,137 (GRCm39) |
|
probably benign |
Het |
Foxn2 |
C |
A |
17: 88,770,138 (GRCm39) |
|
probably null |
Het |
Frem1 |
T |
C |
4: 82,920,012 (GRCm39) |
D448G |
probably damaging |
Het |
Fzd9 |
T |
C |
5: 135,278,199 (GRCm39) |
Y562C |
probably benign |
Het |
Gcn1 |
A |
G |
5: 115,748,194 (GRCm39) |
|
silent |
Het |
Gm6003 |
A |
G |
7: 32,864,691 (GRCm39) |
|
noncoding transcript |
Het |
Gnl3 |
C |
A |
14: 30,738,853 (GRCm39) |
E65D |
possibly damaging |
Het |
Hax1 |
GTCATCATCATCATCATC |
GTCATCATCATCATCATCATC |
3: 89,905,247 (GRCm39) |
|
probably benign |
Het |
Hk2 |
C |
T |
6: 82,713,615 (GRCm39) |
R461K |
probably benign |
Het |
Ice1 |
A |
G |
13: 70,754,496 (GRCm39) |
F530S |
possibly damaging |
Het |
Ing3 |
T |
A |
6: 21,968,904 (GRCm39) |
S129T |
probably benign |
Het |
Ino80 |
G |
A |
2: 119,288,697 (GRCm39) |
S3L |
probably damaging |
Het |
Ints2 |
T |
A |
11: 86,113,000 (GRCm39) |
Q839H |
probably benign |
Het |
Kcnrg |
T |
C |
14: 61,849,280 (GRCm39) |
M247T |
probably benign |
Het |
Krtap28-13 |
T |
A |
1: 83,039,044 (GRCm39) |
|
probably benign |
Het |
Lgr4 |
T |
A |
2: 109,748,617 (GRCm39) |
V51E |
possibly damaging |
Het |
Map3k5 |
A |
C |
10: 19,980,001 (GRCm39) |
E836D |
probably benign |
Het |
Mapk11 |
T |
C |
15: 89,030,038 (GRCm39) |
I193V |
probably benign |
Het |
Marchf10 |
A |
T |
11: 105,276,308 (GRCm39) |
V660E |
probably damaging |
Het |
Matn4 |
T |
C |
2: 164,235,144 (GRCm39) |
E435G |
probably damaging |
Het |
Mre11a |
G |
T |
9: 14,723,232 (GRCm39) |
R402M |
probably damaging |
Het |
Msr1 |
C |
T |
8: 40,034,868 (GRCm39) |
G428R |
probably damaging |
Het |
Ndufv3 |
C |
T |
17: 31,750,206 (GRCm39) |
R99* |
probably null |
Het |
Nkx6-1 |
C |
T |
5: 101,811,847 (GRCm39) |
S85N |
unknown |
Het |
Nop2 |
A |
T |
6: 125,111,691 (GRCm39) |
E141D |
probably benign |
Het |
Or5b3 |
A |
G |
19: 13,388,326 (GRCm39) |
H131R |
probably benign |
Het |
Or8b1 |
G |
C |
9: 38,399,657 (GRCm39) |
E111Q |
probably damaging |
Het |
Paox |
T |
C |
7: 139,709,101 (GRCm39) |
S205P |
probably damaging |
Het |
Pcdh15 |
T |
C |
10: 74,466,768 (GRCm39) |
V995A |
probably benign |
Het |
Pdcd1 |
T |
A |
1: 93,968,550 (GRCm39) |
K161N |
probably benign |
Het |
Pfkfb2 |
C |
A |
1: 130,627,832 (GRCm39) |
V372L |
probably damaging |
Het |
Phldb1 |
G |
A |
9: 44,622,948 (GRCm39) |
T19I |
probably damaging |
Het |
Pik3c2g |
G |
T |
6: 139,599,477 (GRCm39) |
V198L |
probably benign |
Het |
Pnpla8 |
T |
A |
12: 44,342,753 (GRCm39) |
L41* |
probably null |
Het |
Postn |
C |
T |
3: 54,281,221 (GRCm39) |
Q449* |
probably null |
Het |
Ppp1r3a |
C |
T |
6: 14,718,988 (GRCm39) |
S642N |
probably benign |
Het |
Ptpn23 |
G |
A |
9: 110,214,511 (GRCm39) |
|
probably benign |
Het |
Ptprj |
T |
C |
2: 90,283,684 (GRCm39) |
N923S |
possibly damaging |
Het |
Rai1 |
T |
C |
11: 60,078,630 (GRCm39) |
V898A |
probably benign |
Het |
Rasgef1a |
A |
T |
6: 118,057,515 (GRCm39) |
Y72F |
possibly damaging |
Het |
Serpinb7 |
T |
C |
1: 107,379,580 (GRCm39) |
V329A |
probably damaging |
Het |
Slc24a4 |
T |
A |
12: 102,201,049 (GRCm39) |
I311N |
probably damaging |
Het |
Slc45a1 |
C |
A |
4: 150,713,997 (GRCm39) |
L749F |
possibly damaging |
Het |
Spon1 |
G |
A |
7: 113,630,056 (GRCm39) |
D428N |
probably damaging |
Het |
Tcf7l2 |
G |
A |
19: 55,886,992 (GRCm39) |
E2K |
probably benign |
Het |
Thoc5 |
A |
G |
11: 4,870,416 (GRCm39) |
M472V |
possibly damaging |
Het |
Tm6sf2 |
T |
C |
8: 70,528,213 (GRCm39) |
Y121H |
probably damaging |
Het |
Tmc4 |
T |
A |
7: 3,675,008 (GRCm39) |
D221V |
probably benign |
Het |
Trim30b |
A |
T |
7: 104,006,572 (GRCm39) |
S95T |
probably damaging |
Het |
Trip12 |
T |
C |
1: 84,741,179 (GRCm39) |
E571G |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,781,656 (GRCm39) |
|
probably null |
Het |
Ubp1 |
A |
T |
9: 113,785,807 (GRCm39) |
R161W |
probably benign |
Het |
Usp21 |
G |
A |
1: 171,109,745 (GRCm39) |
|
probably benign |
Het |
Vmn1r61 |
T |
A |
7: 5,613,529 (GRCm39) |
R262W |
probably damaging |
Het |
Vmn2r67 |
A |
T |
7: 84,801,044 (GRCm39) |
D297E |
probably damaging |
Het |
Vwa5a |
T |
C |
9: 38,653,038 (GRCm39) |
L784S |
probably benign |
Het |
Vwc2 |
G |
A |
11: 11,104,244 (GRCm39) |
V259M |
probably damaging |
Het |
Zeb2 |
T |
C |
2: 44,887,064 (GRCm39) |
I596M |
probably benign |
Het |
Zgrf1 |
T |
A |
3: 127,354,672 (GRCm39) |
L97H |
probably damaging |
Het |
|
Other mutations in Kpna6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01088:Kpna6
|
APN |
4 |
129,549,276 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02750:Kpna6
|
APN |
4 |
129,555,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02904:Kpna6
|
APN |
4 |
129,544,480 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02998:Kpna6
|
APN |
4 |
129,549,297 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03370:Kpna6
|
APN |
4 |
129,549,314 (GRCm39) |
missense |
probably damaging |
1.00 |
krazy_eight
|
UTSW |
4 |
129,549,221 (GRCm39) |
critical splice donor site |
probably null |
|
magnificent_seven
|
UTSW |
4 |
129,543,099 (GRCm39) |
nonsense |
probably null |
|
R0054:Kpna6
|
UTSW |
4 |
129,551,251 (GRCm39) |
missense |
probably benign |
0.01 |
R0054:Kpna6
|
UTSW |
4 |
129,551,251 (GRCm39) |
missense |
probably benign |
0.01 |
R0305:Kpna6
|
UTSW |
4 |
129,543,042 (GRCm39) |
missense |
probably benign |
0.00 |
R0390:Kpna6
|
UTSW |
4 |
129,551,597 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0623:Kpna6
|
UTSW |
4 |
129,549,209 (GRCm39) |
unclassified |
probably benign |
|
R0646:Kpna6
|
UTSW |
4 |
129,544,583 (GRCm39) |
missense |
probably benign |
0.43 |
R1067:Kpna6
|
UTSW |
4 |
129,541,896 (GRCm39) |
missense |
probably benign |
0.39 |
R1348:Kpna6
|
UTSW |
4 |
129,555,152 (GRCm39) |
nonsense |
probably null |
|
R1661:Kpna6
|
UTSW |
4 |
129,551,264 (GRCm39) |
missense |
probably benign |
0.10 |
R1665:Kpna6
|
UTSW |
4 |
129,551,264 (GRCm39) |
missense |
probably benign |
0.10 |
R1766:Kpna6
|
UTSW |
4 |
129,551,235 (GRCm39) |
missense |
probably benign |
0.33 |
R4833:Kpna6
|
UTSW |
4 |
129,551,572 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4941:Kpna6
|
UTSW |
4 |
129,541,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Kpna6
|
UTSW |
4 |
129,550,198 (GRCm39) |
splice site |
probably null |
|
R5244:Kpna6
|
UTSW |
4 |
129,549,221 (GRCm39) |
critical splice donor site |
probably null |
|
R6148:Kpna6
|
UTSW |
4 |
129,543,099 (GRCm39) |
nonsense |
probably null |
|
R6713:Kpna6
|
UTSW |
4 |
129,547,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R6799:Kpna6
|
UTSW |
4 |
129,551,247 (GRCm39) |
missense |
probably damaging |
0.99 |
R6942:Kpna6
|
UTSW |
4 |
129,545,514 (GRCm39) |
splice site |
probably null |
|
R7073:Kpna6
|
UTSW |
4 |
129,548,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Kpna6
|
UTSW |
4 |
129,541,844 (GRCm39) |
missense |
probably benign |
|
R7815:Kpna6
|
UTSW |
4 |
129,551,590 (GRCm39) |
missense |
probably benign |
|
R8290:Kpna6
|
UTSW |
4 |
129,555,097 (GRCm39) |
critical splice donor site |
probably null |
|
R9360:Kpna6
|
UTSW |
4 |
129,547,635 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Kpna6
|
UTSW |
4 |
129,549,341 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kpna6
|
UTSW |
4 |
129,541,871 (GRCm39) |
missense |
possibly damaging |
0.92 |
|