Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
A |
C |
12: 118,838,379 (GRCm39) |
V1061G |
probably damaging |
Het |
Acap1 |
A |
G |
11: 69,781,413 (GRCm39) |
|
probably null |
Het |
Apbb1 |
A |
G |
7: 105,215,902 (GRCm39) |
F112L |
probably benign |
Het |
Atg9a |
A |
G |
1: 75,161,702 (GRCm39) |
S615P |
probably benign |
Het |
Atp8a2 |
G |
A |
14: 60,249,848 (GRCm39) |
R548* |
probably null |
Het |
Bbof1 |
A |
T |
12: 84,457,942 (GRCm39) |
N69I |
possibly damaging |
Het |
Bcl2l14 |
T |
A |
6: 134,404,370 (GRCm39) |
V186D |
probably benign |
Het |
Bmp1 |
T |
G |
14: 70,728,823 (GRCm39) |
Y583S |
possibly damaging |
Het |
Boc |
A |
C |
16: 44,312,711 (GRCm39) |
S586R |
probably benign |
Het |
Btbd9 |
A |
T |
17: 30,518,710 (GRCm39) |
|
probably null |
Het |
Cacna1e |
T |
C |
1: 154,317,919 (GRCm39) |
M1180V |
probably damaging |
Het |
Ciao1 |
T |
C |
2: 127,088,376 (GRCm39) |
H149R |
probably damaging |
Het |
Cops5 |
T |
C |
1: 10,100,920 (GRCm39) |
|
probably benign |
Het |
Doc2b |
C |
T |
11: 75,671,093 (GRCm39) |
R209Q |
probably damaging |
Het |
Doc2b |
T |
C |
11: 75,686,451 (GRCm39) |
Y90C |
probably benign |
Het |
Ep400 |
A |
G |
5: 110,901,675 (GRCm39) |
F481L |
probably benign |
Het |
Fat4 |
T |
A |
3: 39,061,229 (GRCm39) |
|
probably null |
Het |
Fbxw16 |
T |
A |
9: 109,277,837 (GRCm39) |
|
probably benign |
Het |
Fbxw27 |
T |
C |
9: 109,601,154 (GRCm39) |
E17G |
possibly damaging |
Het |
Gm29735 |
G |
A |
7: 141,710,367 (GRCm39) |
P162S |
unknown |
Het |
Gypa |
T |
G |
8: 81,222,969 (GRCm39) |
S24R |
unknown |
Het |
Hdhd5 |
T |
C |
6: 120,495,485 (GRCm39) |
N153D |
probably benign |
Het |
Ibsp |
C |
A |
5: 104,449,987 (GRCm39) |
|
probably null |
Het |
Klhdc3 |
C |
T |
17: 46,988,972 (GRCm39) |
V73I |
probably benign |
Het |
Lrrc37a |
T |
C |
11: 103,388,459 (GRCm39) |
E2322G |
unknown |
Het |
Lrrtm3 |
T |
C |
10: 63,765,913 (GRCm39) |
H558R |
probably benign |
Het |
Mbtd1 |
C |
T |
11: 93,823,058 (GRCm39) |
H493Y |
possibly damaging |
Het |
Mphosph9 |
A |
G |
5: 124,458,978 (GRCm39) |
V64A |
possibly damaging |
Het |
Nthl1 |
C |
T |
17: 24,857,475 (GRCm39) |
R251C |
probably damaging |
Het |
Opn1sw |
T |
A |
6: 29,379,413 (GRCm39) |
Y197F |
possibly damaging |
Het |
Or10a3m |
T |
C |
7: 108,312,845 (GRCm39) |
V95A |
probably damaging |
Het |
Pcca |
A |
T |
14: 122,896,187 (GRCm39) |
I268F |
probably benign |
Het |
Per2 |
A |
T |
1: 91,377,594 (GRCm39) |
D76E |
unknown |
Het |
Pfas |
T |
C |
11: 68,888,825 (GRCm39) |
N374S |
probably benign |
Het |
Pomk |
C |
A |
8: 26,472,955 (GRCm39) |
V333F |
probably damaging |
Het |
Ptgfr |
T |
C |
3: 151,540,926 (GRCm39) |
E194G |
probably benign |
Het |
Ptpn14 |
C |
T |
1: 189,582,997 (GRCm39) |
P615S |
probably damaging |
Het |
Pyroxd1 |
T |
C |
6: 142,300,479 (GRCm39) |
I203T |
probably benign |
Het |
Rgs22 |
T |
C |
15: 36,087,520 (GRCm39) |
N466S |
probably benign |
Het |
Rpl3l |
G |
A |
17: 24,952,966 (GRCm39) |
V309I |
probably benign |
Het |
Rtkn2 |
C |
T |
10: 67,815,529 (GRCm39) |
|
probably benign |
Het |
Sec16a |
C |
T |
2: 26,318,253 (GRCm39) |
A1613T |
probably damaging |
Het |
Sis |
T |
A |
3: 72,874,103 (GRCm39) |
T33S |
probably damaging |
Het |
Slc22a4 |
C |
A |
11: 53,898,634 (GRCm39) |
V153F |
possibly damaging |
Het |
Stxbp1 |
C |
G |
2: 32,684,621 (GRCm39) |
E603Q |
probably damaging |
Het |
Tiam2 |
A |
G |
17: 3,559,831 (GRCm39) |
S1291G |
probably damaging |
Het |
Tmem94 |
T |
A |
11: 115,687,572 (GRCm39) |
L1144M |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,579,673 (GRCm39) |
T23740M |
probably damaging |
Het |
Vmn1r201 |
T |
C |
13: 22,659,533 (GRCm39) |
V249A |
probably benign |
Het |
Wdr7 |
T |
A |
18: 63,888,182 (GRCm39) |
C552S |
probably damaging |
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 |
|
IGL02664:Numa1
|
APN |
7 |
101,648,109 (GRCm39) |
missense |
possibly damaging |
0.83 |
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 |
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 |
|