Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adap1 |
C |
A |
5: 139,265,295 (GRCm39) |
R206L |
probably damaging |
Het |
Adcy3 |
A |
G |
12: 4,248,440 (GRCm39) |
K501E |
probably benign |
Het |
Agl |
T |
C |
3: 116,545,764 (GRCm39) |
D679G |
|
Het |
Ankrd10 |
A |
T |
8: 11,662,548 (GRCm39) |
V395D |
probably damaging |
Het |
Ano5 |
A |
G |
7: 51,224,636 (GRCm39) |
I531V |
probably damaging |
Het |
Apol9a |
T |
A |
15: 77,288,761 (GRCm39) |
H202L |
possibly damaging |
Het |
Atp6v1c2 |
A |
C |
12: 17,351,215 (GRCm39) |
I105M |
probably benign |
Het |
Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
Coro1b |
T |
C |
19: 4,200,220 (GRCm39) |
|
probably null |
Het |
D930020B18Rik |
A |
G |
10: 121,492,131 (GRCm39) |
|
probably benign |
Het |
Dcst2 |
T |
C |
3: 89,276,021 (GRCm39) |
F384S |
possibly damaging |
Het |
Ddx39a |
T |
A |
8: 84,447,595 (GRCm39) |
F147I |
possibly damaging |
Het |
Drosha |
A |
G |
15: 12,842,508 (GRCm39) |
E393G |
probably damaging |
Het |
Etfdh |
T |
C |
3: 79,530,886 (GRCm39) |
Y45C |
probably damaging |
Het |
Fam20c |
G |
T |
5: 138,778,954 (GRCm39) |
E287D |
possibly damaging |
Het |
Flnc |
T |
A |
6: 29,459,009 (GRCm39) |
D2463E |
probably damaging |
Het |
Flt4 |
A |
T |
11: 49,535,198 (GRCm39) |
I1209F |
possibly damaging |
Het |
Foxp1 |
T |
C |
6: 98,922,521 (GRCm39) |
D437G |
unknown |
Het |
Fras1 |
T |
C |
5: 96,888,713 (GRCm39) |
V2753A |
possibly damaging |
Het |
Ftsj3 |
T |
C |
11: 106,143,813 (GRCm39) |
D277G |
possibly damaging |
Het |
Gad1 |
T |
C |
2: 70,394,256 (GRCm39) |
|
probably null |
Het |
Gal3st2c |
A |
G |
1: 93,937,075 (GRCm39) |
Y340C |
probably damaging |
Het |
Gbp9 |
A |
G |
5: 105,232,975 (GRCm39) |
F226L |
probably damaging |
Het |
Gm11992 |
C |
T |
11: 9,002,747 (GRCm39) |
P37S |
possibly damaging |
Het |
Gm19668 |
G |
T |
10: 77,634,572 (GRCm39) |
C132* |
probably null |
Het |
Hdac3 |
A |
T |
18: 38,078,569 (GRCm39) |
F139I |
possibly damaging |
Het |
Hectd4 |
A |
G |
5: 121,453,573 (GRCm39) |
|
probably null |
Het |
Helz |
T |
A |
11: 107,491,104 (GRCm39) |
S162T |
possibly damaging |
Het |
Hspb6 |
C |
A |
7: 30,253,712 (GRCm39) |
S75Y |
probably damaging |
Het |
Il17rb |
T |
A |
14: 29,719,000 (GRCm39) |
I361F |
probably damaging |
Het |
Iqsec3 |
A |
T |
6: 121,364,739 (GRCm39) |
V850D |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,924,487 (GRCm39) |
E1840G |
possibly damaging |
Het |
Lamc3 |
A |
G |
2: 31,812,380 (GRCm39) |
K939R |
probably benign |
Het |
Lmo7 |
C |
T |
14: 102,124,662 (GRCm39) |
R496* |
probably null |
Het |
Lsm14a |
A |
T |
7: 34,052,826 (GRCm39) |
C374* |
probably null |
Het |
Luc7l |
T |
C |
17: 26,474,089 (GRCm39) |
L49P |
probably damaging |
Het |
Mdga2 |
A |
C |
12: 66,520,003 (GRCm39) |
C988G |
probably damaging |
Het |
Mtf1 |
T |
C |
4: 124,713,999 (GRCm39) |
V136A |
probably damaging |
Het |
Myo7b |
T |
A |
18: 32,116,413 (GRCm39) |
I1016F |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,356,204 (GRCm39) |
Q1137R |
probably benign |
Het |
Naip5 |
G |
T |
13: 100,356,205 (GRCm39) |
Q1137K |
not run |
Het |
Nr4a1 |
T |
C |
15: 101,168,780 (GRCm39) |
V272A |
probably damaging |
Het |
Opcml |
A |
T |
9: 28,814,620 (GRCm39) |
T291S |
probably benign |
Het |
Or13a24 |
T |
A |
7: 140,154,356 (GRCm39) |
C97S |
probably damaging |
Het |
Or52u1 |
C |
A |
7: 104,237,087 (GRCm39) |
H25Q |
probably damaging |
Het |
Or56b1b |
C |
T |
7: 108,164,763 (GRCm39) |
A80T |
probably damaging |
Het |
Osbp2 |
C |
G |
11: 3,662,493 (GRCm39) |
K196N |
probably damaging |
Het |
Otoa |
T |
C |
7: 120,743,149 (GRCm39) |
V792A |
probably damaging |
Het |
Pcmtd1 |
A |
G |
1: 7,239,766 (GRCm39) |
D245G |
probably damaging |
Het |
Pcnx1 |
T |
C |
12: 82,039,896 (GRCm39) |
V1428A |
unknown |
Het |
Pik3r4 |
A |
G |
9: 105,555,352 (GRCm39) |
H1103R |
probably benign |
Het |
Pjvk |
C |
T |
2: 76,486,154 (GRCm39) |
H185Y |
probably benign |
Het |
Pkd1l3 |
T |
C |
8: 110,351,072 (GRCm39) |
V639A |
probably benign |
Het |
Pklr |
T |
C |
3: 89,050,365 (GRCm39) |
S405P |
probably damaging |
Het |
Pla2g12a |
T |
A |
3: 129,672,569 (GRCm39) |
Y68N |
probably damaging |
Het |
Proz |
A |
G |
8: 13,113,455 (GRCm39) |
H92R |
probably benign |
Het |
Sec23ip |
G |
T |
7: 128,379,074 (GRCm39) |
V844F |
possibly damaging |
Het |
Sema3f |
A |
G |
9: 107,561,777 (GRCm39) |
V520A |
possibly damaging |
Het |
Serpinb12 |
A |
G |
1: 106,881,453 (GRCm39) |
I197V |
probably damaging |
Het |
Sim2 |
A |
T |
16: 93,910,218 (GRCm39) |
I207F |
possibly damaging |
Het |
Slc15a2 |
C |
T |
16: 36,572,259 (GRCm39) |
V702I |
probably benign |
Het |
Slc35f4 |
T |
C |
14: 49,541,732 (GRCm39) |
I341V |
probably benign |
Het |
Spam1 |
A |
G |
6: 24,800,452 (GRCm39) |
Y397C |
probably damaging |
Het |
Spire1 |
A |
T |
18: 67,634,187 (GRCm39) |
M417K |
probably benign |
Het |
Srcap |
T |
C |
7: 127,129,722 (GRCm39) |
S515P |
unknown |
Het |
Tfrc |
T |
A |
16: 32,440,235 (GRCm39) |
|
probably null |
Het |
Topors |
A |
G |
4: 40,261,401 (GRCm39) |
S628P |
unknown |
Het |
Trim71 |
T |
C |
9: 114,342,110 (GRCm39) |
Y724C |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,623,199 (GRCm39) |
V15413I |
probably damaging |
Het |
Vmn1r21 |
A |
T |
6: 57,821,227 (GRCm39) |
N72K |
probably damaging |
Het |
Vmn2r80 |
A |
T |
10: 79,030,459 (GRCm39) |
M762L |
probably benign |
Het |
Wdr62 |
A |
G |
7: 29,970,198 (GRCm39) |
I203T |
probably damaging |
Het |
|
Other mutations in Nadsyn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Nadsyn1
|
APN |
7 |
143,366,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01359:Nadsyn1
|
APN |
7 |
143,374,967 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL01412:Nadsyn1
|
APN |
7 |
143,362,527 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01481:Nadsyn1
|
APN |
7 |
143,366,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01642:Nadsyn1
|
APN |
7 |
143,351,615 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Nadsyn1
|
APN |
7 |
143,367,164 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02126:Nadsyn1
|
APN |
7 |
143,357,753 (GRCm39) |
nonsense |
probably null |
|
IGL02173:Nadsyn1
|
APN |
7 |
143,357,743 (GRCm39) |
splice site |
probably benign |
|
IGL02351:Nadsyn1
|
APN |
7 |
143,353,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02358:Nadsyn1
|
APN |
7 |
143,353,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03216:Nadsyn1
|
APN |
7 |
143,351,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0029:Nadsyn1
|
UTSW |
7 |
143,359,815 (GRCm39) |
missense |
probably benign |
0.01 |
R0036:Nadsyn1
|
UTSW |
7 |
143,365,028 (GRCm39) |
missense |
probably benign |
0.23 |
R0968:Nadsyn1
|
UTSW |
7 |
143,359,770 (GRCm39) |
missense |
probably benign |
0.30 |
R1487:Nadsyn1
|
UTSW |
7 |
143,360,662 (GRCm39) |
missense |
probably benign |
0.31 |
R1694:Nadsyn1
|
UTSW |
7 |
143,361,749 (GRCm39) |
missense |
probably benign |
0.00 |
R1874:Nadsyn1
|
UTSW |
7 |
143,351,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4540:Nadsyn1
|
UTSW |
7 |
143,356,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R4742:Nadsyn1
|
UTSW |
7 |
143,352,367 (GRCm39) |
intron |
probably benign |
|
R4755:Nadsyn1
|
UTSW |
7 |
143,360,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Nadsyn1
|
UTSW |
7 |
143,360,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R5288:Nadsyn1
|
UTSW |
7 |
143,357,023 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5326:Nadsyn1
|
UTSW |
7 |
143,362,567 (GRCm39) |
missense |
probably benign |
0.42 |
R5666:Nadsyn1
|
UTSW |
7 |
143,361,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R5669:Nadsyn1
|
UTSW |
7 |
143,361,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R5691:Nadsyn1
|
UTSW |
7 |
143,366,316 (GRCm39) |
splice site |
probably null |
|
R5861:Nadsyn1
|
UTSW |
7 |
143,364,964 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6213:Nadsyn1
|
UTSW |
7 |
143,353,549 (GRCm39) |
missense |
probably benign |
0.05 |
R6624:Nadsyn1
|
UTSW |
7 |
143,359,710 (GRCm39) |
missense |
probably benign |
0.02 |
R6652:Nadsyn1
|
UTSW |
7 |
143,364,955 (GRCm39) |
missense |
probably benign |
0.03 |
R6791:Nadsyn1
|
UTSW |
7 |
143,372,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Nadsyn1
|
UTSW |
7 |
143,364,952 (GRCm39) |
missense |
probably damaging |
0.99 |
R7770:Nadsyn1
|
UTSW |
7 |
143,359,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R7802:Nadsyn1
|
UTSW |
7 |
143,359,763 (GRCm39) |
missense |
probably benign |
|
R7871:Nadsyn1
|
UTSW |
7 |
143,352,233 (GRCm39) |
nonsense |
probably null |
|
R9266:Nadsyn1
|
UTSW |
7 |
143,369,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R9550:Nadsyn1
|
UTSW |
7 |
143,353,615 (GRCm39) |
missense |
probably damaging |
0.97 |
|