Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
T |
C |
2: 19,558,581 (GRCm39) |
|
probably null |
Het |
Abca4 |
T |
A |
3: 121,930,743 (GRCm39) |
Y205* |
probably null |
Het |
Adgrf1 |
A |
G |
17: 43,621,164 (GRCm39) |
D467G |
probably benign |
Het |
Atp7b |
T |
C |
8: 22,510,841 (GRCm39) |
D550G |
possibly damaging |
Het |
Bicd1 |
T |
A |
6: 149,414,674 (GRCm39) |
Y462* |
probably null |
Het |
Cfap97 |
T |
C |
8: 46,644,769 (GRCm39) |
|
probably null |
Het |
Csf1r |
T |
A |
18: 61,258,900 (GRCm39) |
Y706* |
probably null |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dst |
A |
G |
1: 34,233,621 (GRCm39) |
D3443G |
probably benign |
Het |
Fktn |
C |
T |
4: 53,731,136 (GRCm39) |
A96V |
probably benign |
Het |
Inppl1 |
G |
A |
7: 101,473,506 (GRCm39) |
T1048M |
possibly damaging |
Het |
Itga2 |
T |
C |
13: 114,976,097 (GRCm39) |
T1092A |
probably benign |
Het |
Lactbl1 |
C |
A |
4: 136,365,229 (GRCm39) |
A527E |
probably benign |
Het |
Miga1 |
C |
T |
3: 151,984,586 (GRCm39) |
A510T |
probably benign |
Het |
Mip |
T |
A |
10: 128,061,875 (GRCm39) |
L42* |
probably null |
Het |
Or51f5 |
A |
T |
7: 102,423,883 (GRCm39) |
I51F |
probably damaging |
Het |
Or52l1 |
T |
C |
7: 104,829,917 (GRCm39) |
Y216C |
probably damaging |
Het |
Or6c69 |
T |
A |
10: 129,747,536 (GRCm39) |
T204S |
probably damaging |
Het |
Pcm1 |
T |
A |
8: 41,783,862 (GRCm39) |
M1986K |
probably damaging |
Het |
Pex6 |
T |
A |
17: 47,023,034 (GRCm39) |
D203E |
probably benign |
Het |
Rlbp1 |
T |
C |
7: 79,029,876 (GRCm39) |
N119S |
probably benign |
Het |
Rptn |
C |
G |
3: 93,305,437 (GRCm39) |
H923Q |
possibly damaging |
Het |
Rusc1 |
T |
A |
3: 88,999,048 (GRCm39) |
T245S |
probably benign |
Het |
Slc26a5 |
A |
T |
5: 22,026,095 (GRCm39) |
C378S |
probably damaging |
Het |
Smtn |
A |
G |
11: 3,477,624 (GRCm39) |
|
probably benign |
Het |
Tes3-ps |
T |
C |
13: 49,647,516 (GRCm39) |
C131R |
probably damaging |
Het |
Thbs4 |
T |
C |
13: 92,911,190 (GRCm39) |
E331G |
probably null |
Het |
Tlr4 |
T |
C |
4: 66,758,832 (GRCm39) |
Y542H |
probably benign |
Het |
Trf |
G |
A |
9: 103,107,504 (GRCm39) |
|
probably benign |
Het |
Trim75 |
T |
A |
8: 65,435,748 (GRCm39) |
H234L |
probably benign |
Het |
Zan |
T |
G |
5: 137,466,605 (GRCm39) |
R417S |
probably damaging |
Het |
Zfp213 |
T |
C |
17: 23,776,996 (GRCm39) |
T349A |
probably benign |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Naca |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00909:Naca
|
APN |
10 |
127,877,551 (GRCm39) |
intron |
probably benign |
|
IGL00990:Naca
|
APN |
10 |
127,879,669 (GRCm39) |
intron |
probably benign |
|
IGL01093:Naca
|
APN |
10 |
127,883,982 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01356:Naca
|
APN |
10 |
127,877,584 (GRCm39) |
intron |
probably benign |
|
IGL01548:Naca
|
APN |
10 |
127,876,773 (GRCm39) |
intron |
probably benign |
|
IGL02089:Naca
|
APN |
10 |
127,872,358 (GRCm39) |
splice site |
probably benign |
|
IGL02148:Naca
|
APN |
10 |
127,879,753 (GRCm39) |
intron |
probably benign |
|
IGL02494:Naca
|
APN |
10 |
127,877,179 (GRCm39) |
intron |
probably benign |
|
IGL02672:Naca
|
APN |
10 |
127,876,152 (GRCm39) |
intron |
probably benign |
|
IGL02822:Naca
|
APN |
10 |
127,875,214 (GRCm39) |
intron |
probably benign |
|
IGL02904:Naca
|
APN |
10 |
127,879,159 (GRCm39) |
intron |
probably benign |
|
IGL02931:Naca
|
APN |
10 |
127,883,551 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02971:Naca
|
APN |
10 |
127,877,437 (GRCm39) |
intron |
probably benign |
|
IGL03104:Naca
|
APN |
10 |
127,876,233 (GRCm39) |
intron |
probably benign |
|
Sinewy
|
UTSW |
10 |
127,884,227 (GRCm39) |
missense |
probably damaging |
1.00 |
D4216:Naca
|
UTSW |
10 |
127,880,109 (GRCm39) |
missense |
possibly damaging |
0.73 |
P0042:Naca
|
UTSW |
10 |
127,877,422 (GRCm39) |
intron |
probably benign |
|
R0110:Naca
|
UTSW |
10 |
127,880,659 (GRCm39) |
missense |
probably benign |
0.13 |
R0220:Naca
|
UTSW |
10 |
127,879,255 (GRCm39) |
intron |
probably benign |
|
R0469:Naca
|
UTSW |
10 |
127,880,659 (GRCm39) |
missense |
probably benign |
0.13 |
R0528:Naca
|
UTSW |
10 |
127,879,162 (GRCm39) |
missense |
probably benign |
0.23 |
R0594:Naca
|
UTSW |
10 |
127,876,224 (GRCm39) |
intron |
probably benign |
|
R0626:Naca
|
UTSW |
10 |
127,877,031 (GRCm39) |
intron |
probably benign |
|
R0885:Naca
|
UTSW |
10 |
127,876,048 (GRCm39) |
nonsense |
probably null |
|
R1129:Naca
|
UTSW |
10 |
127,876,071 (GRCm39) |
intron |
probably benign |
|
R1437:Naca
|
UTSW |
10 |
127,878,048 (GRCm39) |
intron |
probably benign |
|
R1464:Naca
|
UTSW |
10 |
127,884,157 (GRCm39) |
missense |
probably damaging |
0.96 |
R1464:Naca
|
UTSW |
10 |
127,884,157 (GRCm39) |
missense |
probably damaging |
0.96 |
R1509:Naca
|
UTSW |
10 |
127,879,266 (GRCm39) |
intron |
probably benign |
|
R1561:Naca
|
UTSW |
10 |
127,876,267 (GRCm39) |
intron |
probably benign |
|
R1574:Naca
|
UTSW |
10 |
127,876,267 (GRCm39) |
intron |
probably benign |
|
R1678:Naca
|
UTSW |
10 |
127,879,395 (GRCm39) |
intron |
probably benign |
|
R1901:Naca
|
UTSW |
10 |
127,879,590 (GRCm39) |
intron |
probably benign |
|
R2884:Naca
|
UTSW |
10 |
127,877,547 (GRCm39) |
intron |
probably benign |
|
R2886:Naca
|
UTSW |
10 |
127,877,547 (GRCm39) |
intron |
probably benign |
|
R3176:Naca
|
UTSW |
10 |
127,876,530 (GRCm39) |
intron |
probably benign |
|
R3276:Naca
|
UTSW |
10 |
127,876,530 (GRCm39) |
intron |
probably benign |
|
R4227:Naca
|
UTSW |
10 |
127,877,530 (GRCm39) |
intron |
probably benign |
|
R4388:Naca
|
UTSW |
10 |
127,880,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R4402:Naca
|
UTSW |
10 |
127,879,341 (GRCm39) |
intron |
probably benign |
|
R4798:Naca
|
UTSW |
10 |
127,883,672 (GRCm39) |
missense |
probably null |
0.99 |
R4955:Naca
|
UTSW |
10 |
127,878,084 (GRCm39) |
intron |
probably benign |
|
R4996:Naca
|
UTSW |
10 |
127,878,298 (GRCm39) |
intron |
probably benign |
|
R5027:Naca
|
UTSW |
10 |
127,883,990 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5580:Naca
|
UTSW |
10 |
127,876,462 (GRCm39) |
intron |
probably benign |
|
R5752:Naca
|
UTSW |
10 |
127,877,797 (GRCm39) |
intron |
probably benign |
|
R5788:Naca
|
UTSW |
10 |
127,876,011 (GRCm39) |
intron |
probably benign |
|
R6156:Naca
|
UTSW |
10 |
127,875,160 (GRCm39) |
intron |
probably benign |
|
R6317:Naca
|
UTSW |
10 |
127,879,993 (GRCm39) |
missense |
probably benign |
0.33 |
R6665:Naca
|
UTSW |
10 |
127,884,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R7170:Naca
|
UTSW |
10 |
127,875,990 (GRCm39) |
missense |
unknown |
|
R7247:Naca
|
UTSW |
10 |
127,878,467 (GRCm39) |
missense |
unknown |
|
R7632:Naca
|
UTSW |
10 |
127,876,375 (GRCm39) |
missense |
unknown |
|
R7826:Naca
|
UTSW |
10 |
127,879,479 (GRCm39) |
intron |
probably benign |
|
R7921:Naca
|
UTSW |
10 |
127,878,918 (GRCm39) |
missense |
unknown |
|
R8059:Naca
|
UTSW |
10 |
127,876,372 (GRCm39) |
missense |
unknown |
|
R8084:Naca
|
UTSW |
10 |
127,877,400 (GRCm39) |
missense |
unknown |
|
R8385:Naca
|
UTSW |
10 |
127,878,307 (GRCm39) |
missense |
unknown |
|
R8515:Naca
|
UTSW |
10 |
127,880,112 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8708:Naca
|
UTSW |
10 |
127,883,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R9629:Naca
|
UTSW |
10 |
127,878,226 (GRCm39) |
missense |
unknown |
|
X0053:Naca
|
UTSW |
10 |
127,884,124 (GRCm39) |
missense |
probably damaging |
0.98 |
|