Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
A |
T |
5: 36,006,860 (GRCm39) |
D425V |
probably damaging |
Het |
Afdn |
G |
T |
17: 14,072,728 (GRCm39) |
|
probably benign |
Het |
Afg2a |
A |
G |
3: 37,490,814 (GRCm39) |
D453G |
probably damaging |
Het |
Ap2a2 |
C |
T |
7: 141,209,136 (GRCm39) |
T776I |
probably benign |
Het |
Apcdd1 |
T |
C |
18: 63,084,891 (GRCm39) |
|
probably benign |
Het |
Bdp1 |
A |
T |
13: 100,188,047 (GRCm39) |
Y1513N |
probably benign |
Het |
Btaf1 |
T |
C |
19: 36,955,828 (GRCm39) |
|
probably benign |
Het |
C2cd3 |
A |
T |
7: 100,068,922 (GRCm39) |
M917L |
possibly damaging |
Het |
Cmtm6 |
T |
C |
9: 114,575,613 (GRCm39) |
V174A |
probably benign |
Het |
Cyp2d12 |
T |
A |
15: 82,443,535 (GRCm39) |
I448K |
probably benign |
Het |
Ddb1 |
A |
G |
19: 10,585,247 (GRCm39) |
I101V |
probably benign |
Het |
Dicer1 |
A |
G |
12: 104,671,388 (GRCm39) |
Y961H |
probably damaging |
Het |
Dnaaf1 |
T |
G |
8: 120,309,260 (GRCm39) |
I116S |
probably damaging |
Het |
Ecscr |
T |
A |
18: 35,854,451 (GRCm39) |
I5F |
possibly damaging |
Het |
Eftud2 |
T |
C |
11: 102,732,538 (GRCm39) |
E691G |
probably damaging |
Het |
Fat2 |
A |
G |
11: 55,201,922 (GRCm39) |
V384A |
probably damaging |
Het |
Ftcd |
T |
C |
10: 76,420,439 (GRCm39) |
M391T |
probably damaging |
Het |
Gab2 |
T |
G |
7: 96,953,389 (GRCm39) |
S587R |
probably damaging |
Het |
Gm18856 |
G |
A |
13: 14,139,809 (GRCm39) |
|
probably benign |
Het |
Herc2 |
A |
T |
7: 55,785,426 (GRCm39) |
R1559* |
probably null |
Het |
Inpp5f |
G |
A |
7: 128,265,738 (GRCm39) |
R161H |
probably damaging |
Het |
Iws1 |
A |
T |
18: 32,203,217 (GRCm39) |
D31V |
possibly damaging |
Het |
Klhl2 |
A |
T |
8: 65,205,801 (GRCm39) |
Y373* |
probably null |
Het |
Lce6a |
A |
T |
3: 92,527,607 (GRCm39) |
C67S |
possibly damaging |
Het |
Lrba |
A |
G |
3: 86,233,038 (GRCm39) |
I800V |
possibly damaging |
Het |
Mis18bp1 |
A |
C |
12: 65,200,654 (GRCm39) |
Y407* |
probably null |
Het |
Mllt3 |
A |
C |
4: 87,949,860 (GRCm39) |
W29G |
probably damaging |
Het |
Mon2 |
A |
G |
10: 122,845,401 (GRCm39) |
|
probably benign |
Het |
Mtbp |
C |
T |
15: 55,483,039 (GRCm39) |
T372M |
probably benign |
Het |
Nefm |
A |
T |
14: 68,357,664 (GRCm39) |
|
probably benign |
Het |
Nf1 |
A |
T |
11: 79,335,424 (GRCm39) |
|
probably null |
Het |
Nf1 |
G |
A |
11: 79,335,425 (GRCm39) |
|
probably null |
Het |
Ntn1 |
T |
A |
11: 68,276,295 (GRCm39) |
I218F |
probably benign |
Het |
Or14a259 |
C |
T |
7: 86,012,811 (GRCm39) |
V245I |
possibly damaging |
Het |
Pcsk5 |
A |
T |
19: 17,434,134 (GRCm39) |
D1411E |
probably damaging |
Het |
Prl2b1 |
G |
T |
13: 27,569,225 (GRCm39) |
N124K |
possibly damaging |
Het |
Rab15 |
T |
C |
12: 76,851,225 (GRCm39) |
I30M |
possibly damaging |
Het |
Rnf215 |
G |
T |
11: 4,090,307 (GRCm39) |
V342L |
probably damaging |
Het |
Saxo4 |
A |
T |
19: 10,459,655 (GRCm39) |
S17R |
probably damaging |
Het |
Togaram2 |
T |
A |
17: 72,036,234 (GRCm39) |
I908N |
probably damaging |
Het |
Trim54 |
A |
G |
5: 31,293,391 (GRCm39) |
N205S |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,697,795 (GRCm39) |
T80I |
possibly damaging |
Het |
Vmn2r106 |
G |
A |
17: 20,488,344 (GRCm39) |
T685I |
possibly damaging |
Het |
Vwa5b2 |
T |
C |
16: 20,414,063 (GRCm39) |
|
probably benign |
Het |
Zfat |
A |
T |
15: 68,052,570 (GRCm39) |
I401N |
probably damaging |
Het |
Zfp40 |
G |
A |
17: 23,395,960 (GRCm39) |
S209F |
probably benign |
Het |
|
Other mutations in Numa1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00509:Numa1
|
APN |
7 |
101,662,493 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00819:Numa1
|
APN |
7 |
101,641,917 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01103:Numa1
|
APN |
7 |
101,650,778 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01153:Numa1
|
APN |
7 |
101,643,951 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01954:Numa1
|
APN |
7 |
101,645,300 (GRCm39) |
nonsense |
probably null |
|
IGL02114:Numa1
|
APN |
7 |
101,661,083 (GRCm39) |
unclassified |
probably benign |
|
IGL02245:Numa1
|
APN |
7 |
101,649,601 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02259:Numa1
|
APN |
7 |
101,636,955 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02313:Numa1
|
APN |
7 |
101,649,439 (GRCm39) |
nonsense |
probably null |
|
IGL02316:Numa1
|
APN |
7 |
101,650,577 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02386:Numa1
|
APN |
7 |
101,656,739 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02517:Numa1
|
APN |
7 |
101,661,216 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02529:Numa1
|
APN |
7 |
101,649,160 (GRCm39) |
splice site |
probably null |
|
IGL02721:Numa1
|
APN |
7 |
101,649,118 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02816:Numa1
|
APN |
7 |
101,645,307 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03126:Numa1
|
APN |
7 |
101,649,874 (GRCm39) |
nonsense |
probably null |
|
meltdown
|
UTSW |
7 |
101,639,778 (GRCm39) |
critical splice acceptor site |
probably null |
|
1mM(1):Numa1
|
UTSW |
7 |
101,643,922 (GRCm39) |
missense |
probably benign |
0.06 |
PIT4651001:Numa1
|
UTSW |
7 |
101,663,141 (GRCm39) |
missense |
probably damaging |
0.97 |
R0047:Numa1
|
UTSW |
7 |
101,658,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Numa1
|
UTSW |
7 |
101,658,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R0548:Numa1
|
UTSW |
7 |
101,644,731 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0554:Numa1
|
UTSW |
7 |
101,644,731 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0592:Numa1
|
UTSW |
7 |
101,663,104 (GRCm39) |
missense |
probably benign |
|
R0669:Numa1
|
UTSW |
7 |
101,648,884 (GRCm39) |
missense |
probably benign |
|
R0856:Numa1
|
UTSW |
7 |
101,648,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R1072:Numa1
|
UTSW |
7 |
101,650,357 (GRCm39) |
splice site |
probably null |
|
R1776:Numa1
|
UTSW |
7 |
101,660,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R1898:Numa1
|
UTSW |
7 |
101,641,927 (GRCm39) |
critical splice donor site |
probably null |
|
R1969:Numa1
|
UTSW |
7 |
101,658,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R1970:Numa1
|
UTSW |
7 |
101,658,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R1971:Numa1
|
UTSW |
7 |
101,658,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R2180:Numa1
|
UTSW |
7 |
101,649,197 (GRCm39) |
missense |
probably benign |
0.00 |
R2256:Numa1
|
UTSW |
7 |
101,649,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R2257:Numa1
|
UTSW |
7 |
101,649,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Numa1
|
UTSW |
7 |
101,644,731 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2958:Numa1
|
UTSW |
7 |
101,658,702 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4210:Numa1
|
UTSW |
7 |
101,658,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R4211:Numa1
|
UTSW |
7 |
101,658,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R4643:Numa1
|
UTSW |
7 |
101,649,872 (GRCm39) |
splice site |
probably null |
|
R4783:Numa1
|
UTSW |
7 |
101,662,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Numa1
|
UTSW |
7 |
101,645,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Numa1
|
UTSW |
7 |
101,662,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Numa1
|
UTSW |
7 |
101,660,064 (GRCm39) |
missense |
probably benign |
0.32 |
R4981:Numa1
|
UTSW |
7 |
101,641,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R5120:Numa1
|
UTSW |
7 |
101,626,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R5122:Numa1
|
UTSW |
7 |
101,662,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R5210:Numa1
|
UTSW |
7 |
101,649,188 (GRCm39) |
missense |
probably benign |
0.03 |
R5230:Numa1
|
UTSW |
7 |
101,644,731 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5547:Numa1
|
UTSW |
7 |
101,663,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R5861:Numa1
|
UTSW |
7 |
101,658,494 (GRCm39) |
splice site |
probably null |
|
R6006:Numa1
|
UTSW |
7 |
101,641,926 (GRCm39) |
critical splice donor site |
probably null |
|
R6031:Numa1
|
UTSW |
7 |
101,661,219 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6031:Numa1
|
UTSW |
7 |
101,661,219 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6295:Numa1
|
UTSW |
7 |
101,649,974 (GRCm39) |
missense |
probably benign |
0.03 |
R6322:Numa1
|
UTSW |
7 |
101,650,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R6413:Numa1
|
UTSW |
7 |
101,639,778 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6786:Numa1
|
UTSW |
7 |
101,641,845 (GRCm39) |
missense |
probably benign |
0.05 |
R7218:Numa1
|
UTSW |
7 |
101,650,117 (GRCm39) |
missense |
probably benign |
0.02 |
R7312:Numa1
|
UTSW |
7 |
101,639,806 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7374:Numa1
|
UTSW |
7 |
101,658,335 (GRCm39) |
missense |
probably benign |
0.00 |
R7626:Numa1
|
UTSW |
7 |
101,648,630 (GRCm39) |
missense |
probably benign |
0.42 |
R7769:Numa1
|
UTSW |
7 |
101,648,207 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7830:Numa1
|
UTSW |
7 |
101,648,492 (GRCm39) |
missense |
probably benign |
0.03 |
R7886:Numa1
|
UTSW |
7 |
101,663,072 (GRCm39) |
missense |
probably benign |
0.27 |
R7935:Numa1
|
UTSW |
7 |
101,651,538 (GRCm39) |
missense |
probably damaging |
0.96 |
R8134:Numa1
|
UTSW |
7 |
101,650,834 (GRCm39) |
missense |
probably benign |
0.14 |
R8143:Numa1
|
UTSW |
7 |
101,648,891 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8217:Numa1
|
UTSW |
7 |
101,641,876 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8263:Numa1
|
UTSW |
7 |
101,648,491 (GRCm39) |
missense |
probably benign |
0.03 |
R8536:Numa1
|
UTSW |
7 |
101,650,787 (GRCm39) |
missense |
probably damaging |
0.96 |
R8677:Numa1
|
UTSW |
7 |
101,650,148 (GRCm39) |
missense |
probably damaging |
0.99 |
R8683:Numa1
|
UTSW |
7 |
101,626,617 (GRCm39) |
start codon destroyed |
probably null |
0.09 |
R8786:Numa1
|
UTSW |
7 |
101,647,616 (GRCm39) |
missense |
probably benign |
0.45 |
R8855:Numa1
|
UTSW |
7 |
101,639,835 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8881:Numa1
|
UTSW |
7 |
101,650,684 (GRCm39) |
missense |
probably benign |
0.01 |
R9127:Numa1
|
UTSW |
7 |
101,641,869 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9153:Numa1
|
UTSW |
7 |
101,649,118 (GRCm39) |
missense |
probably benign |
0.01 |
R9214:Numa1
|
UTSW |
7 |
101,650,139 (GRCm39) |
missense |
probably damaging |
0.99 |
R9294:Numa1
|
UTSW |
7 |
101,662,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R9294:Numa1
|
UTSW |
7 |
101,644,623 (GRCm39) |
missense |
possibly damaging |
0.77 |
RF013:Numa1
|
UTSW |
7 |
101,648,987 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Numa1
|
UTSW |
7 |
101,647,609 (GRCm39) |
missense |
probably benign |
0.27 |
Z1088:Numa1
|
UTSW |
7 |
101,647,538 (GRCm39) |
missense |
probably damaging |
0.99 |
|