Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apcdd1 |
A |
G |
18: 63,085,095 (GRCm39) |
T431A |
probably benign |
Het |
Bcan |
T |
A |
3: 87,896,534 (GRCm39) |
I721F |
probably damaging |
Het |
Card10 |
T |
C |
15: 78,686,643 (GRCm39) |
D58G |
possibly damaging |
Het |
Cd200r2 |
A |
G |
16: 44,729,969 (GRCm39) |
N171S |
probably damaging |
Het |
Celsr1 |
T |
C |
15: 85,916,248 (GRCm39) |
D575G |
probably damaging |
Het |
Ces1f |
A |
G |
8: 93,993,870 (GRCm39) |
|
probably benign |
Het |
Cped1 |
A |
T |
6: 22,237,698 (GRCm39) |
H938L |
probably benign |
Het |
Creld1 |
A |
G |
6: 113,468,656 (GRCm39) |
D259G |
probably benign |
Het |
Cubn |
T |
C |
2: 13,341,053 (GRCm39) |
I2223V |
possibly damaging |
Het |
Dop1a |
A |
G |
9: 86,397,459 (GRCm39) |
D921G |
probably damaging |
Het |
Dusp7 |
T |
C |
9: 106,250,849 (GRCm39) |
S325P |
possibly damaging |
Het |
Fat4 |
A |
T |
3: 39,037,091 (GRCm39) |
D3581V |
possibly damaging |
Het |
Fhl3 |
T |
C |
4: 124,599,584 (GRCm39) |
|
probably null |
Het |
Gap43 |
T |
C |
16: 42,112,167 (GRCm39) |
E198G |
probably benign |
Het |
Grina |
T |
C |
15: 76,132,779 (GRCm39) |
F182S |
probably damaging |
Het |
Gsk3b |
T |
C |
16: 38,028,346 (GRCm39) |
|
probably benign |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Haus6 |
A |
G |
4: 86,503,563 (GRCm39) |
|
probably null |
Het |
Hmcn1 |
C |
T |
1: 150,494,679 (GRCm39) |
A4137T |
possibly damaging |
Het |
Itih4 |
C |
A |
14: 30,618,124 (GRCm39) |
|
probably benign |
Het |
Itprid1 |
T |
C |
6: 55,866,155 (GRCm39) |
F183L |
probably damaging |
Het |
Kif22 |
A |
G |
7: 126,631,916 (GRCm39) |
S384P |
probably benign |
Het |
Lbr |
A |
C |
1: 181,648,233 (GRCm39) |
|
probably benign |
Het |
Mei1 |
G |
A |
15: 82,000,068 (GRCm39) |
|
probably benign |
Het |
Misp |
T |
C |
10: 79,662,969 (GRCm39) |
V462A |
probably benign |
Het |
Mrgpra3 |
A |
C |
7: 47,239,039 (GRCm39) |
L296V |
possibly damaging |
Het |
Ndufa9 |
A |
T |
6: 126,799,031 (GRCm39) |
L362Q |
probably damaging |
Het |
Nlrp9c |
A |
T |
7: 26,083,862 (GRCm39) |
D572E |
probably benign |
Het |
Or4f14 |
T |
A |
2: 111,743,222 (GRCm39) |
T18S |
probably benign |
Het |
Otud4 |
C |
T |
8: 80,379,980 (GRCm39) |
|
probably benign |
Het |
P4ha3 |
T |
C |
7: 99,962,535 (GRCm39) |
I431T |
probably damaging |
Het |
Pcdhb15 |
T |
A |
18: 37,606,815 (GRCm39) |
F16I |
probably benign |
Het |
Pcnp |
A |
G |
16: 55,844,754 (GRCm39) |
S49P |
probably damaging |
Het |
Pdxdc1 |
T |
A |
16: 13,697,278 (GRCm39) |
|
probably benign |
Het |
Pgc |
T |
A |
17: 48,039,828 (GRCm39) |
|
probably null |
Het |
Phf11a |
T |
C |
14: 59,521,778 (GRCm39) |
D131G |
probably benign |
Het |
Prdm2 |
G |
A |
4: 142,858,953 (GRCm39) |
H1446Y |
possibly damaging |
Het |
Rad54b |
T |
C |
4: 11,563,352 (GRCm39) |
S4P |
probably damaging |
Het |
Slc52a2 |
T |
C |
15: 76,423,808 (GRCm39) |
|
probably benign |
Het |
Slc9a4 |
G |
A |
1: 40,623,490 (GRCm39) |
|
probably benign |
Het |
Smad4 |
T |
C |
18: 73,773,333 (GRCm39) |
D551G |
probably benign |
Het |
Smg7 |
A |
T |
1: 152,742,326 (GRCm39) |
|
probably benign |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Sspo |
A |
G |
6: 48,436,352 (GRCm39) |
Y1234C |
probably damaging |
Het |
Stab2 |
A |
T |
10: 86,721,582 (GRCm39) |
|
probably null |
Het |
Stk36 |
A |
G |
1: 74,671,925 (GRCm39) |
E875G |
probably benign |
Het |
Stmn4 |
T |
G |
14: 66,591,844 (GRCm39) |
|
probably benign |
Het |
Tagln3 |
C |
A |
16: 45,544,635 (GRCm39) |
R12L |
probably damaging |
Het |
Tex14 |
A |
T |
11: 87,413,343 (GRCm39) |
R1031S |
probably benign |
Het |
Tia1 |
G |
A |
6: 86,396,091 (GRCm39) |
V96I |
probably benign |
Het |
Ticrr |
C |
T |
7: 79,343,701 (GRCm39) |
P1189S |
probably benign |
Het |
Tnxb |
G |
A |
17: 34,904,017 (GRCm39) |
V1053M |
probably damaging |
Het |
Tpp2 |
T |
C |
1: 44,031,556 (GRCm39) |
|
probably null |
Het |
Trpm7 |
A |
G |
2: 126,664,406 (GRCm39) |
M991T |
possibly damaging |
Het |
Ttc3 |
T |
A |
16: 94,217,127 (GRCm39) |
|
probably benign |
Het |
Vcan |
G |
A |
13: 89,853,782 (GRCm39) |
P393S |
probably damaging |
Het |
Vmn2r107 |
G |
A |
17: 20,576,860 (GRCm39) |
R286Q |
probably benign |
Het |
Wdr87-ps |
G |
A |
7: 29,233,669 (GRCm39) |
|
noncoding transcript |
Het |
Wrap73 |
A |
T |
4: 154,236,884 (GRCm39) |
|
probably null |
Het |
Zfp958 |
A |
T |
8: 4,676,169 (GRCm39) |
N46Y |
possibly damaging |
Het |
|
Other mutations in Garin4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Garin4
|
APN |
1 |
190,895,224 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01541:Garin4
|
APN |
1 |
190,896,606 (GRCm39) |
nonsense |
probably null |
|
IGL02364:Garin4
|
APN |
1 |
190,895,713 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02573:Garin4
|
APN |
1 |
190,896,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02705:Garin4
|
APN |
1 |
190,896,499 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03057:Garin4
|
APN |
1 |
190,895,141 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03283:Garin4
|
APN |
1 |
190,895,029 (GRCm39) |
missense |
probably benign |
0.08 |
R0234:Garin4
|
UTSW |
1 |
190,895,105 (GRCm39) |
missense |
probably benign |
0.00 |
R0234:Garin4
|
UTSW |
1 |
190,895,105 (GRCm39) |
missense |
probably benign |
0.00 |
R0402:Garin4
|
UTSW |
1 |
190,896,637 (GRCm39) |
missense |
probably benign |
0.03 |
R0635:Garin4
|
UTSW |
1 |
190,895,924 (GRCm39) |
missense |
probably benign |
|
R0750:Garin4
|
UTSW |
1 |
190,896,682 (GRCm39) |
start gained |
probably benign |
|
R1521:Garin4
|
UTSW |
1 |
190,896,219 (GRCm39) |
missense |
probably benign |
0.00 |
R1573:Garin4
|
UTSW |
1 |
190,896,682 (GRCm39) |
start gained |
probably benign |
|
R1654:Garin4
|
UTSW |
1 |
190,895,678 (GRCm39) |
missense |
probably benign |
0.00 |
R1699:Garin4
|
UTSW |
1 |
190,896,018 (GRCm39) |
missense |
probably benign |
0.01 |
R1900:Garin4
|
UTSW |
1 |
190,896,631 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2912:Garin4
|
UTSW |
1 |
190,895,425 (GRCm39) |
missense |
probably benign |
0.00 |
R2939:Garin4
|
UTSW |
1 |
190,896,103 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3747:Garin4
|
UTSW |
1 |
190,896,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Garin4
|
UTSW |
1 |
190,895,205 (GRCm39) |
missense |
probably benign |
0.05 |
R6038:Garin4
|
UTSW |
1 |
190,894,919 (GRCm39) |
missense |
probably damaging |
0.98 |
R6038:Garin4
|
UTSW |
1 |
190,894,919 (GRCm39) |
missense |
probably damaging |
0.98 |
R7179:Garin4
|
UTSW |
1 |
190,896,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R7182:Garin4
|
UTSW |
1 |
190,895,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R7261:Garin4
|
UTSW |
1 |
190,896,308 (GRCm39) |
missense |
unknown |
|
R7326:Garin4
|
UTSW |
1 |
190,896,550 (GRCm39) |
missense |
probably benign |
0.00 |
R7363:Garin4
|
UTSW |
1 |
190,895,910 (GRCm39) |
missense |
probably damaging |
0.99 |
R7960:Garin4
|
UTSW |
1 |
190,895,645 (GRCm39) |
missense |
probably benign |
0.02 |
R8120:Garin4
|
UTSW |
1 |
190,895,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R8916:Garin4
|
UTSW |
1 |
190,895,857 (GRCm39) |
missense |
probably benign |
0.00 |
R9011:Garin4
|
UTSW |
1 |
190,895,258 (GRCm39) |
missense |
probably benign |
0.08 |
R9090:Garin4
|
UTSW |
1 |
190,895,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R9165:Garin4
|
UTSW |
1 |
190,895,258 (GRCm39) |
missense |
probably benign |
0.04 |
R9189:Garin4
|
UTSW |
1 |
190,894,900 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9271:Garin4
|
UTSW |
1 |
190,895,153 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Garin4
|
UTSW |
1 |
190,895,942 (GRCm39) |
missense |
probably benign |
0.03 |
|