Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700102P08Rik |
A |
T |
9: 108,270,676 (GRCm39) |
H80L |
possibly damaging |
Het |
A1bg |
A |
T |
15: 60,791,484 (GRCm39) |
|
probably null |
Het |
Aco2 |
C |
T |
15: 81,779,394 (GRCm39) |
S33L |
probably damaging |
Het |
Agrn |
T |
A |
4: 156,256,756 (GRCm39) |
Y1283F |
probably benign |
Het |
Akap6 |
T |
C |
12: 52,842,973 (GRCm39) |
V107A |
probably damaging |
Het |
Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
Btnl9 |
A |
T |
11: 49,071,574 (GRCm39) |
V83E |
probably damaging |
Het |
Camk2a |
T |
A |
18: 61,085,396 (GRCm39) |
C131* |
probably null |
Het |
Ccdc14 |
C |
T |
16: 34,544,198 (GRCm39) |
T852M |
probably damaging |
Het |
Cntn4 |
T |
C |
6: 106,330,558 (GRCm39) |
|
probably benign |
Het |
Cp |
T |
G |
3: 20,031,316 (GRCm39) |
S585R |
probably damaging |
Het |
Cpt1b |
G |
A |
15: 89,303,213 (GRCm39) |
A614V |
probably benign |
Het |
Crygn |
T |
C |
5: 24,956,146 (GRCm39) |
Y153C |
probably damaging |
Het |
Dennd1a |
A |
T |
2: 37,851,728 (GRCm39) |
D53E |
probably damaging |
Het |
Deptor |
T |
C |
15: 55,115,406 (GRCm39) |
C357R |
probably benign |
Het |
Dnajc28 |
C |
A |
16: 91,415,530 (GRCm39) |
|
probably benign |
Het |
Eml6 |
G |
A |
11: 29,705,044 (GRCm39) |
A1500V |
possibly damaging |
Het |
Fgd5 |
T |
A |
6: 91,963,959 (GRCm39) |
L64Q |
possibly damaging |
Het |
Fgfbp1 |
A |
G |
5: 44,136,939 (GRCm39) |
Y118H |
probably damaging |
Het |
Ftcd |
G |
A |
10: 76,415,653 (GRCm39) |
R135H |
probably damaging |
Het |
Gpr37l1 |
A |
T |
1: 135,094,710 (GRCm39) |
L178Q |
probably damaging |
Het |
Gtf2ird1 |
A |
G |
5: 134,439,918 (GRCm39) |
V104A |
possibly damaging |
Het |
Irs1 |
T |
A |
1: 82,267,347 (GRCm39) |
S290C |
probably damaging |
Het |
Kel |
C |
T |
6: 41,665,525 (GRCm39) |
V532I |
possibly damaging |
Het |
Kif1c |
A |
G |
11: 70,599,427 (GRCm39) |
E442G |
possibly damaging |
Het |
Klhdc10 |
T |
A |
6: 30,449,493 (GRCm39) |
V185D |
probably damaging |
Het |
Lpp |
C |
T |
16: 24,500,610 (GRCm39) |
R141C |
probably damaging |
Het |
Or52a5 |
A |
T |
7: 103,427,192 (GRCm39) |
M120K |
probably damaging |
Het |
Or5m13 |
A |
G |
2: 85,748,379 (GRCm39) |
I37V |
probably benign |
Het |
Pcnx2 |
G |
T |
8: 126,614,053 (GRCm39) |
P466H |
possibly damaging |
Het |
Pcsk1 |
A |
T |
13: 75,244,532 (GRCm39) |
|
probably benign |
Het |
Pkd2l2 |
T |
C |
18: 34,571,269 (GRCm39) |
|
probably null |
Het |
Pomt1 |
A |
G |
2: 32,140,504 (GRCm39) |
N454S |
probably benign |
Het |
Samhd1 |
A |
T |
2: 156,951,381 (GRCm39) |
I452N |
probably damaging |
Het |
Sez6 |
A |
G |
11: 77,844,711 (GRCm39) |
Q178R |
probably benign |
Het |
Slc25a44 |
A |
G |
3: 88,328,293 (GRCm39) |
V66A |
probably damaging |
Het |
Slc46a2 |
T |
C |
4: 59,914,189 (GRCm39) |
T245A |
probably benign |
Het |
Slc4a4 |
G |
A |
5: 89,363,653 (GRCm39) |
|
probably null |
Het |
Spata6 |
T |
A |
4: 111,656,342 (GRCm39) |
C329S |
possibly damaging |
Het |
Srrm2 |
A |
T |
17: 24,036,725 (GRCm39) |
|
probably benign |
Het |
Stard9 |
C |
A |
2: 120,504,117 (GRCm39) |
S221R |
probably damaging |
Het |
Svil |
T |
A |
18: 5,059,217 (GRCm39) |
|
probably benign |
Het |
Tenm3 |
G |
T |
8: 48,688,617 (GRCm39) |
S2323R |
probably damaging |
Het |
Tsc1 |
G |
A |
2: 28,555,638 (GRCm39) |
R245Q |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,739,100 (GRCm39) |
V3813A |
probably benign |
Het |
Ttn |
G |
A |
2: 76,780,388 (GRCm39) |
T1121M |
possibly damaging |
Het |
Ush2a |
G |
A |
1: 188,491,992 (GRCm39) |
V3094I |
probably benign |
Het |
Vcan |
A |
G |
13: 89,827,913 (GRCm39) |
|
probably null |
Het |
Vmn1r189 |
A |
T |
13: 22,286,828 (GRCm39) |
L3Q |
probably damaging |
Het |
Vmn1r60 |
A |
C |
7: 5,547,971 (GRCm39) |
V43G |
probably damaging |
Het |
Vmn2r110 |
A |
G |
17: 20,803,525 (GRCm39) |
I350T |
probably benign |
Het |
Vmn2r86 |
T |
A |
10: 130,284,443 (GRCm39) |
|
probably benign |
Het |
Xrn1 |
A |
G |
9: 95,863,814 (GRCm39) |
|
probably benign |
Het |
Zfp251 |
C |
T |
15: 76,738,436 (GRCm39) |
R219Q |
possibly damaging |
Het |
|
Other mutations in Gm5174 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
Laco
|
UTSW |
10 |
86,491,972 (GRCm39) |
unclassified |
noncoding transcript |
|
R1083:Gm5174
|
UTSW |
10 |
86,491,972 (GRCm39) |
unclassified |
noncoding transcript |
|
R1296:Gm5174
|
UTSW |
10 |
86,492,866 (GRCm39) |
unclassified |
noncoding transcript |
|
R1715:Gm5174
|
UTSW |
10 |
86,492,776 (GRCm39) |
unclassified |
noncoding transcript |
|
R1957:Gm5174
|
UTSW |
10 |
86,492,617 (GRCm39) |
unclassified |
noncoding transcript |
|
R2221:Gm5174
|
UTSW |
10 |
86,492,372 (GRCm39) |
unclassified |
noncoding transcript |
|
R2223:Gm5174
|
UTSW |
10 |
86,492,372 (GRCm39) |
unclassified |
noncoding transcript |
|
R3104:Gm5174
|
UTSW |
10 |
86,492,519 (GRCm39) |
unclassified |
noncoding transcript |
|
R4165:Gm5174
|
UTSW |
10 |
86,492,797 (GRCm39) |
unclassified |
noncoding transcript |
|
R4166:Gm5174
|
UTSW |
10 |
86,492,797 (GRCm39) |
unclassified |
noncoding transcript |
|
R4243:Gm5174
|
UTSW |
10 |
86,492,144 (GRCm39) |
unclassified |
noncoding transcript |
|
R4244:Gm5174
|
UTSW |
10 |
86,492,144 (GRCm39) |
unclassified |
noncoding transcript |
|
R5024:Gm5174
|
UTSW |
10 |
86,492,451 (GRCm39) |
unclassified |
noncoding transcript |
|
R5292:Gm5174
|
UTSW |
10 |
86,492,562 (GRCm39) |
unclassified |
noncoding transcript |
|
R5586:Gm5174
|
UTSW |
10 |
86,492,409 (GRCm39) |
unclassified |
noncoding transcript |
|
R5864:Gm5174
|
UTSW |
10 |
86,493,045 (GRCm39) |
unclassified |
noncoding transcript |
|
|