Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
A |
G |
13: 119,622,349 (GRCm39) |
T606A |
probably benign |
Het |
Adtrp |
T |
A |
13: 41,920,905 (GRCm39) |
S221C |
possibly damaging |
Het |
Ap1g2 |
T |
A |
14: 55,336,797 (GRCm39) |
|
probably null |
Het |
Arhgef5 |
A |
T |
6: 43,251,354 (GRCm39) |
M702L |
probably benign |
Het |
Axdnd1 |
A |
G |
1: 156,245,879 (GRCm39) |
V34A |
probably damaging |
Het |
Ccdc154 |
T |
A |
17: 25,389,897 (GRCm39) |
V509E |
probably damaging |
Het |
Cttnbp2 |
C |
T |
6: 18,426,096 (GRCm39) |
D761N |
probably benign |
Het |
Ddx18 |
A |
T |
1: 121,486,138 (GRCm39) |
|
probably null |
Het |
Dipk1a |
A |
T |
5: 108,057,325 (GRCm39) |
L411* |
probably null |
Het |
Fam241b |
A |
T |
10: 61,945,745 (GRCm39) |
I4N |
probably damaging |
Het |
Hemgn |
T |
A |
4: 46,396,417 (GRCm39) |
H273L |
possibly damaging |
Het |
Hsp90aa1 |
A |
G |
12: 110,659,168 (GRCm39) |
V543A |
probably damaging |
Het |
Hspa1l |
A |
G |
17: 35,196,299 (GRCm39) |
K113E |
probably benign |
Het |
Hspb2 |
A |
G |
9: 50,663,015 (GRCm39) |
I38T |
probably damaging |
Het |
Htt |
A |
T |
5: 35,034,819 (GRCm39) |
E2021D |
probably benign |
Het |
Lrpprc |
C |
T |
17: 85,077,505 (GRCm39) |
R394Q |
probably benign |
Het |
Lrrc8b |
T |
C |
5: 105,629,753 (GRCm39) |
Y700H |
probably damaging |
Het |
Mefv |
A |
G |
16: 3,528,752 (GRCm39) |
V593A |
probably benign |
Het |
Mrgprh |
C |
T |
17: 13,095,856 (GRCm39) |
T32M |
probably benign |
Het |
Mrpl18 |
A |
G |
17: 13,132,655 (GRCm39) |
|
probably null |
Het |
Muc1 |
A |
G |
3: 89,138,903 (GRCm39) |
E504G |
probably damaging |
Het |
Ndufa13 |
G |
A |
8: 70,347,169 (GRCm39) |
A77V |
probably damaging |
Het |
Or8g33 |
A |
G |
9: 39,337,654 (GRCm39) |
F238L |
possibly damaging |
Het |
Pgbd5 |
T |
A |
8: 125,111,363 (GRCm39) |
|
probably null |
Het |
Pgm5 |
T |
A |
19: 24,812,179 (GRCm39) |
I118F |
probably damaging |
Het |
Phyhip |
T |
C |
14: 70,704,572 (GRCm39) |
F264L |
possibly damaging |
Het |
Polr3e |
C |
T |
7: 120,531,360 (GRCm39) |
R176W |
probably damaging |
Het |
Prkacb |
C |
T |
3: 146,452,438 (GRCm39) |
|
probably null |
Het |
Rab19 |
T |
G |
6: 39,360,975 (GRCm39) |
V41G |
possibly damaging |
Het |
Rapgef5 |
A |
G |
12: 117,679,130 (GRCm39) |
Y234C |
probably benign |
Het |
Slc26a5 |
T |
C |
5: 22,018,863 (GRCm39) |
T659A |
probably damaging |
Het |
Slc6a2 |
G |
A |
8: 93,720,729 (GRCm39) |
V449I |
probably benign |
Het |
Stab2 |
A |
G |
10: 86,723,726 (GRCm39) |
S1490P |
probably damaging |
Het |
Tln1 |
T |
C |
4: 43,548,005 (GRCm39) |
T713A |
probably damaging |
Het |
Tmc6 |
A |
T |
11: 117,659,932 (GRCm39) |
L732Q |
probably damaging |
Het |
Unc80 |
C |
T |
1: 66,560,740 (GRCm39) |
H823Y |
possibly damaging |
Het |
Vmn1r203 |
A |
T |
13: 22,708,905 (GRCm39) |
K229* |
probably null |
Het |
Xylt1 |
G |
A |
7: 117,266,660 (GRCm39) |
G893R |
probably damaging |
Het |
Ythdf1 |
A |
T |
2: 180,553,907 (GRCm39) |
S69T |
probably damaging |
Het |
Zfp114 |
C |
T |
7: 23,880,509 (GRCm39) |
T285I |
probably benign |
Het |
Zfp458 |
T |
C |
13: 67,405,113 (GRCm39) |
E439G |
probably damaging |
Het |
Zfp65 |
G |
A |
13: 67,858,499 (GRCm39) |
T55I |
probably damaging |
Het |
Zmym1 |
C |
T |
4: 126,947,996 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Gm5800 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00958:Gm5800
|
APN |
14 |
51,951,269 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL03325:Gm5800
|
APN |
14 |
51,951,983 (GRCm39) |
missense |
probably benign |
|
R0037:Gm5800
|
UTSW |
14 |
51,953,605 (GRCm39) |
splice site |
probably benign |
|
R0597:Gm5800
|
UTSW |
14 |
51,953,461 (GRCm39) |
missense |
probably benign |
|
R1577:Gm5800
|
UTSW |
14 |
51,952,016 (GRCm39) |
missense |
probably benign |
0.05 |
R1834:Gm5800
|
UTSW |
14 |
51,953,549 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1934:Gm5800
|
UTSW |
14 |
51,949,396 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2180:Gm5800
|
UTSW |
14 |
51,953,451 (GRCm39) |
nonsense |
probably null |
|
R4861:Gm5800
|
UTSW |
14 |
51,953,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R4861:Gm5800
|
UTSW |
14 |
51,953,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R5267:Gm5800
|
UTSW |
14 |
51,951,294 (GRCm39) |
splice site |
probably null |
|
R6545:Gm5800
|
UTSW |
14 |
51,949,419 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6634:Gm5800
|
UTSW |
14 |
51,953,595 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6925:Gm5800
|
UTSW |
14 |
51,951,157 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7632:Gm5800
|
UTSW |
14 |
51,953,905 (GRCm39) |
splice site |
probably null |
|
R9067:Gm5800
|
UTSW |
14 |
51,951,995 (GRCm39) |
missense |
possibly damaging |
0.92 |
|