Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam22 |
A |
T |
5: 8,186,804 (GRCm39) |
|
probably null |
Het |
Ahnak |
A |
T |
19: 8,988,796 (GRCm39) |
D3360V |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,100,381 (GRCm39) |
L2681P |
probably benign |
Het |
Ankrd52 |
C |
A |
10: 128,217,857 (GRCm39) |
A279E |
probably damaging |
Het |
Arhgef4 |
T |
C |
1: 34,760,978 (GRCm39) |
L78P |
unknown |
Het |
Cfap300 |
T |
A |
9: 8,027,111 (GRCm39) |
E142D |
possibly damaging |
Het |
Chpf |
A |
T |
1: 75,453,904 (GRCm39) |
C291* |
probably null |
Het |
Cr1l |
T |
C |
1: 194,800,030 (GRCm39) |
T215A |
probably damaging |
Het |
Ctc1 |
A |
T |
11: 68,918,209 (GRCm39) |
K444* |
probably null |
Het |
Dscaml1 |
T |
C |
9: 45,595,029 (GRCm39) |
S711P |
probably damaging |
Het |
Elavl4 |
A |
T |
4: 110,068,845 (GRCm39) |
V176D |
probably benign |
Het |
Faim2 |
A |
G |
15: 99,408,515 (GRCm39) |
V251A |
possibly damaging |
Het |
Fancg |
A |
G |
4: 43,004,963 (GRCm39) |
I410T |
probably damaging |
Het |
Frmd3 |
G |
A |
4: 74,071,852 (GRCm39) |
V245I |
probably damaging |
Het |
Gls |
T |
C |
1: 52,230,271 (GRCm39) |
H480R |
probably damaging |
Het |
Gm30191 |
A |
G |
4: 133,977,223 (GRCm39) |
D145G |
possibly damaging |
Het |
Grik2 |
T |
C |
10: 49,280,438 (GRCm39) |
I438V |
probably benign |
Het |
Klhl3 |
G |
T |
13: 58,211,611 (GRCm39) |
Q197K |
probably benign |
Het |
Krt42 |
G |
C |
11: 100,155,865 (GRCm39) |
R294G |
possibly damaging |
Het |
Mmp23 |
G |
A |
4: 155,736,462 (GRCm39) |
T193I |
possibly damaging |
Het |
Mmrn1 |
T |
C |
6: 60,952,961 (GRCm39) |
V414A |
probably damaging |
Het |
Mmrn2 |
C |
T |
14: 34,118,138 (GRCm39) |
Q61* |
probably null |
Het |
Mprip |
G |
A |
11: 59,657,682 (GRCm39) |
R852H |
probably damaging |
Het |
Nomo1 |
A |
G |
7: 45,690,986 (GRCm39) |
N124S |
probably null |
Het |
Or1e17 |
G |
T |
11: 73,831,401 (GRCm39) |
V110F |
probably benign |
Het |
Or1j17 |
A |
G |
2: 36,578,106 (GRCm39) |
I31V |
probably benign |
Het |
Peak1 |
T |
A |
9: 56,114,676 (GRCm39) |
N1422Y |
possibly damaging |
Het |
Perm1 |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
4: 156,302,525 (GRCm39) |
|
probably benign |
Het |
Pfkm |
G |
A |
15: 98,026,117 (GRCm39) |
E571K |
probably damaging |
Het |
Ptpn2 |
A |
T |
18: 67,814,641 (GRCm39) |
C123S |
possibly damaging |
Het |
Raph1 |
G |
A |
1: 60,565,148 (GRCm39) |
T113I |
probably benign |
Het |
Rsf1 |
A |
G |
7: 97,334,920 (GRCm39) |
E1351G |
|
Het |
Serinc4 |
C |
T |
2: 121,285,793 (GRCm39) |
V163I |
probably benign |
Het |
Slc7a2 |
G |
T |
8: 41,357,541 (GRCm39) |
G270C |
probably damaging |
Het |
Smc2 |
G |
A |
4: 52,450,857 (GRCm39) |
R225Q |
probably damaging |
Het |
Tas2r140 |
T |
C |
6: 40,468,601 (GRCm39) |
S144P |
probably damaging |
Het |
Tcl1b4 |
A |
T |
12: 105,168,865 (GRCm39) |
H43L |
probably benign |
Het |
Tmem156 |
T |
C |
5: 65,237,352 (GRCm39) |
T103A |
possibly damaging |
Het |
Tns3 |
A |
T |
11: 8,442,701 (GRCm39) |
M554K |
probably benign |
Het |
Tpp2 |
A |
T |
1: 43,979,297 (GRCm39) |
I65F |
probably benign |
Het |
Trank1 |
T |
A |
9: 111,206,967 (GRCm39) |
M1700K |
probably benign |
Het |
Ttc39c |
T |
A |
18: 12,866,022 (GRCm39) |
H473Q |
probably benign |
Het |
Vmn2r68 |
A |
C |
7: 84,883,625 (GRCm39) |
|
probably null |
Het |
Wnk1 |
T |
C |
6: 120,014,409 (GRCm39) |
D62G |
probably damaging |
Het |
Wnk2 |
A |
T |
13: 49,248,884 (GRCm39) |
M389K |
probably damaging |
Het |
Zfp292 |
G |
A |
4: 34,809,198 (GRCm39) |
T1287M |
probably benign |
Het |
Zfp451 |
G |
A |
1: 33,821,219 (GRCm39) |
S211L |
probably benign |
Het |
Zfp710 |
T |
C |
7: 79,738,327 (GRCm39) |
S626P |
unknown |
Het |
Zfp787 |
C |
T |
7: 6,146,094 (GRCm39) |
E16K |
probably damaging |
Het |
Zfp788 |
G |
T |
7: 41,284,324 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Nars2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00796:Nars2
|
APN |
7 |
96,680,787 (GRCm39) |
missense |
probably benign |
0.40 |
IGL00796:Nars2
|
APN |
7 |
96,680,786 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00990:Nars2
|
APN |
7 |
96,651,997 (GRCm39) |
splice site |
probably benign |
|
IGL02954:Nars2
|
APN |
7 |
96,689,100 (GRCm39) |
splice site |
probably null |
|
IGL03256:Nars2
|
APN |
7 |
96,689,117 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03394:Nars2
|
APN |
7 |
96,689,220 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0600:Nars2
|
UTSW |
7 |
96,689,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0943:Nars2
|
UTSW |
7 |
96,605,138 (GRCm39) |
splice site |
probably benign |
|
R1389:Nars2
|
UTSW |
7 |
96,652,036 (GRCm39) |
missense |
probably benign |
|
R4076:Nars2
|
UTSW |
7 |
96,607,301 (GRCm39) |
missense |
probably damaging |
0.99 |
R4397:Nars2
|
UTSW |
7 |
96,622,771 (GRCm39) |
critical splice donor site |
probably null |
|
R4758:Nars2
|
UTSW |
7 |
96,622,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Nars2
|
UTSW |
7 |
96,684,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Nars2
|
UTSW |
7 |
96,672,948 (GRCm39) |
missense |
probably benign |
0.07 |
R5162:Nars2
|
UTSW |
7 |
96,709,027 (GRCm39) |
utr 3 prime |
probably benign |
|
R6209:Nars2
|
UTSW |
7 |
96,706,728 (GRCm39) |
missense |
probably benign |
0.00 |
R7464:Nars2
|
UTSW |
7 |
96,689,137 (GRCm39) |
missense |
probably benign |
0.40 |
R8284:Nars2
|
UTSW |
7 |
96,600,845 (GRCm39) |
utr 5 prime |
probably benign |
|
R8885:Nars2
|
UTSW |
7 |
96,652,095 (GRCm39) |
missense |
probably damaging |
0.98 |
R9614:Nars2
|
UTSW |
7 |
96,689,125 (GRCm39) |
missense |
probably damaging |
0.99 |
R9658:Nars2
|
UTSW |
7 |
96,689,178 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Nars2
|
UTSW |
7 |
96,601,104 (GRCm39) |
missense |
probably benign |
0.04 |
|