Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre4 |
A |
G |
17: 56,092,121 (GRCm39) |
Y127C |
probably damaging |
Het |
Aif1l |
A |
T |
2: 31,852,251 (GRCm39) |
S40C |
probably damaging |
Het |
Alkal1 |
A |
G |
1: 6,458,839 (GRCm39) |
K76R |
probably damaging |
Het |
Atm |
T |
C |
9: 53,391,969 (GRCm39) |
S1807G |
probably benign |
Het |
Bhmt-ps1 |
T |
A |
4: 26,369,352 (GRCm39) |
|
noncoding transcript |
Het |
Brd10 |
A |
T |
19: 29,696,149 (GRCm39) |
S1115T |
probably benign |
Het |
Cyp3a11 |
A |
T |
5: 145,797,276 (GRCm39) |
Y368N |
probably damaging |
Het |
Gar1 |
A |
T |
3: 129,624,455 (GRCm39) |
|
probably benign |
Het |
Gm5265 |
A |
T |
1: 169,281,370 (GRCm39) |
|
noncoding transcript |
Het |
Grin1 |
T |
C |
2: 25,187,332 (GRCm39) |
|
probably benign |
Het |
H1f5 |
A |
T |
13: 21,964,147 (GRCm39) |
|
probably benign |
Het |
Hapln4 |
T |
A |
8: 70,539,610 (GRCm39) |
W214R |
probably damaging |
Het |
Ift56 |
A |
G |
6: 38,372,010 (GRCm39) |
Y200C |
probably damaging |
Het |
Irgq |
C |
A |
7: 24,233,050 (GRCm39) |
A297D |
possibly damaging |
Het |
Kri1 |
T |
C |
9: 21,192,359 (GRCm39) |
E145G |
probably benign |
Het |
Lama3 |
T |
C |
18: 12,583,460 (GRCm39) |
C683R |
probably damaging |
Het |
Mrpl22 |
T |
A |
11: 58,062,693 (GRCm39) |
|
probably benign |
Het |
Myo7a |
T |
A |
7: 97,722,436 (GRCm39) |
Q1163L |
possibly damaging |
Het |
Nipsnap3a |
T |
A |
4: 52,997,251 (GRCm39) |
D172E |
probably benign |
Het |
Nrxn3 |
G |
T |
12: 89,499,762 (GRCm39) |
G718* |
probably null |
Het |
Olfm3 |
C |
T |
3: 114,883,820 (GRCm39) |
Q41* |
probably null |
Het |
Or52z12 |
A |
G |
7: 103,233,966 (GRCm39) |
T246A |
probably damaging |
Het |
Or8u8 |
G |
T |
2: 86,012,341 (GRCm39) |
T38K |
probably damaging |
Het |
Parm1 |
G |
A |
5: 91,741,726 (GRCm39) |
M31I |
probably benign |
Het |
Phc3 |
A |
T |
3: 30,990,968 (GRCm39) |
S383R |
probably damaging |
Het |
Pkn2 |
A |
T |
3: 142,499,627 (GRCm39) |
L950* |
probably null |
Het |
Plec |
C |
T |
15: 76,061,519 (GRCm39) |
R2671H |
probably damaging |
Het |
Ptbp1 |
T |
C |
10: 79,695,047 (GRCm39) |
I125T |
probably benign |
Het |
Ptch1 |
C |
T |
13: 63,682,143 (GRCm39) |
R537H |
probably damaging |
Het |
Ptk7 |
A |
T |
17: 46,885,389 (GRCm39) |
M679K |
probably benign |
Het |
Ptx3 |
C |
T |
3: 66,132,127 (GRCm39) |
T216I |
probably damaging |
Het |
Rrp8 |
T |
C |
7: 105,383,229 (GRCm39) |
I346V |
possibly damaging |
Het |
Rsrc1 |
A |
G |
3: 66,901,900 (GRCm39) |
K17E |
unknown |
Het |
Ryr2 |
T |
A |
13: 11,752,759 (GRCm39) |
E1854V |
possibly damaging |
Het |
Semp2l2a |
T |
C |
8: 13,888,061 (GRCm39) |
E10G |
probably benign |
Het |
Slc25a45 |
A |
T |
19: 5,930,146 (GRCm39) |
I39F |
probably damaging |
Het |
Spag5 |
G |
A |
11: 78,195,337 (GRCm39) |
V215I |
probably damaging |
Het |
Ston1 |
A |
G |
17: 88,944,199 (GRCm39) |
Y535C |
probably damaging |
Het |
Tbc1d14 |
A |
T |
5: 36,650,452 (GRCm39) |
S395T |
probably benign |
Het |
Tlr11 |
C |
T |
14: 50,599,306 (GRCm39) |
P431S |
probably damaging |
Het |
Trerf1 |
G |
T |
17: 47,625,727 (GRCm39) |
|
noncoding transcript |
Het |
Trim43b |
T |
A |
9: 88,972,692 (GRCm39) |
Q154L |
probably benign |
Het |
Vmn1r49 |
A |
G |
6: 90,049,228 (GRCm39) |
F258S |
probably benign |
Het |
Vmn1r-ps103 |
C |
A |
13: 22,626,198 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r14 |
A |
G |
5: 109,364,149 (GRCm39) |
M589T |
probably benign |
Het |
Vmn2r60 |
A |
T |
7: 41,765,952 (GRCm39) |
T20S |
probably benign |
Het |
Zbtb5 |
A |
G |
4: 44,993,855 (GRCm39) |
|
probably null |
Het |
Zfp35 |
T |
G |
18: 24,136,246 (GRCm39) |
F197V |
possibly damaging |
Het |
|
Other mutations in Gm7964 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01665:Gm7964
|
APN |
7 |
83,406,341 (GRCm39) |
exon |
noncoding transcript |
|
IGL01691:Gm7964
|
APN |
7 |
83,405,344 (GRCm39) |
exon |
noncoding transcript |
|
IGL02232:Gm7964
|
APN |
7 |
83,405,515 (GRCm39) |
exon |
noncoding transcript |
|
IGL02525:Gm7964
|
APN |
7 |
83,405,250 (GRCm39) |
exon |
noncoding transcript |
|
R0512:Gm7964
|
UTSW |
7 |
83,405,158 (GRCm39) |
exon |
noncoding transcript |
|
R0543:Gm7964
|
UTSW |
7 |
83,405,602 (GRCm39) |
exon |
noncoding transcript |
|
R0723:Gm7964
|
UTSW |
7 |
83,405,374 (GRCm39) |
exon |
noncoding transcript |
|
R1977:Gm7964
|
UTSW |
7 |
83,406,560 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2397:Gm7964
|
UTSW |
7 |
83,406,321 (GRCm39) |
exon |
noncoding transcript |
|
R3623:Gm7964
|
UTSW |
7 |
83,405,629 (GRCm39) |
missense |
probably benign |
0.02 |
R3769:Gm7964
|
UTSW |
7 |
83,405,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R4224:Gm7964
|
UTSW |
7 |
83,406,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Gm7964
|
UTSW |
7 |
83,405,109 (GRCm39) |
splice site |
probably null |
|
R4869:Gm7964
|
UTSW |
7 |
83,405,350 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5086:Gm7964
|
UTSW |
7 |
83,406,560 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5944:Gm7964
|
UTSW |
7 |
83,405,743 (GRCm39) |
missense |
probably benign |
0.00 |
|