Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam29 |
T |
A |
8: 56,325,933 (GRCm39) |
M174L |
probably benign |
Het |
Adamtsl1 |
C |
T |
4: 86,117,594 (GRCm39) |
R186W |
probably damaging |
Het |
Agtpbp1 |
C |
T |
13: 59,622,383 (GRCm39) |
V948I |
probably benign |
Het |
Atp13a2 |
A |
G |
4: 140,730,466 (GRCm39) |
T787A |
probably benign |
Het |
Capn11 |
T |
A |
17: 45,964,147 (GRCm39) |
N139I |
probably damaging |
Het |
Cars1 |
T |
C |
7: 143,146,244 (GRCm39) |
D60G |
possibly damaging |
Het |
Cers1 |
A |
T |
8: 70,774,186 (GRCm39) |
I148F |
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,201,835 (GRCm39) |
I41T |
unknown |
Het |
Cyp2d26 |
C |
T |
15: 82,678,236 (GRCm39) |
G47R |
probably damaging |
Het |
Dhx36 |
A |
T |
3: 62,405,518 (GRCm39) |
M205K |
probably benign |
Het |
Dyrk2 |
T |
A |
10: 118,697,273 (GRCm39) |
|
probably benign |
Het |
Echs1 |
T |
C |
7: 139,692,390 (GRCm39) |
H119R |
possibly damaging |
Het |
Ehf |
T |
A |
2: 103,107,164 (GRCm39) |
D120V |
probably damaging |
Het |
Esrra |
A |
G |
19: 6,897,544 (GRCm39) |
L71P |
probably damaging |
Het |
Fam228a |
A |
T |
12: 4,768,718 (GRCm39) |
S200R |
probably benign |
Het |
Fibcd1 |
A |
T |
2: 31,724,435 (GRCm39) |
M191K |
probably benign |
Het |
Foxn4 |
A |
G |
5: 114,393,556 (GRCm39) |
L521P |
probably damaging |
Het |
Fscn2 |
T |
C |
11: 120,252,995 (GRCm39) |
L154P |
probably damaging |
Het |
Golga3 |
T |
C |
5: 110,353,743 (GRCm39) |
|
probably benign |
Het |
Gria4 |
A |
G |
9: 4,537,717 (GRCm39) |
L197P |
probably damaging |
Het |
Heg1 |
T |
A |
16: 33,562,849 (GRCm39) |
M913K |
probably damaging |
Het |
Ifi205 |
T |
C |
1: 173,845,141 (GRCm39) |
T214A |
possibly damaging |
Het |
Ift140 |
T |
G |
17: 25,239,710 (GRCm39) |
D122E |
probably damaging |
Het |
Jakmip1 |
T |
A |
5: 37,258,087 (GRCm39) |
D244E |
probably damaging |
Het |
Krt84 |
A |
G |
15: 101,438,689 (GRCm39) |
V266A |
probably benign |
Het |
Mc2r |
T |
A |
18: 68,541,224 (GRCm39) |
D23V |
probably benign |
Het |
Ncr1 |
T |
A |
7: 4,341,260 (GRCm39) |
F47I |
probably benign |
Het |
Nr1h3 |
G |
A |
2: 91,022,202 (GRCm39) |
T142I |
possibly damaging |
Het |
Obox2 |
C |
T |
7: 15,130,971 (GRCm39) |
P68S |
probably benign |
Het |
Pacs2 |
G |
A |
12: 113,026,987 (GRCm39) |
D605N |
probably damaging |
Het |
Parn |
A |
G |
16: 13,384,518 (GRCm39) |
V515A |
probably benign |
Het |
Ptdss2 |
T |
A |
7: 140,727,005 (GRCm39) |
F105I |
probably benign |
Het |
Ruvbl1 |
A |
C |
6: 88,442,534 (GRCm39) |
T9P |
possibly damaging |
Het |
Slc15a3 |
A |
G |
19: 10,820,407 (GRCm39) |
E8G |
probably benign |
Het |
Slf1 |
G |
T |
13: 77,251,702 (GRCm39) |
Y303* |
probably null |
Het |
Socs5 |
T |
C |
17: 87,442,377 (GRCm39) |
F439S |
probably damaging |
Het |
Tcp10c |
C |
A |
17: 13,590,473 (GRCm39) |
A357E |
probably damaging |
Het |
Tmem200c |
T |
C |
17: 69,147,942 (GRCm39) |
V175A |
probably damaging |
Het |
Vmn2r124 |
T |
A |
17: 18,269,859 (GRCm39) |
H38Q |
possibly damaging |
Het |
Vmn2r54 |
T |
G |
7: 12,349,578 (GRCm39) |
Q668P |
probably damaging |
Het |
Xrcc2 |
T |
C |
5: 25,910,708 (GRCm39) |
S3G |
probably null |
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 |
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 |
R4222:Gm7964
|
UTSW |
7 |
83,406,030 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|