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 |
Gm5800 |
T |
C |
14: 51,951,135 (GRCm39) |
K155E |
possibly 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 |
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 Rab19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Rab19
|
APN |
6 |
39,365,132 (GRCm39) |
splice site |
probably benign |
|
IGL02188:Rab19
|
APN |
6 |
39,360,968 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02452:Rab19
|
APN |
6 |
39,366,732 (GRCm39) |
missense |
probably benign |
|
IGL03027:Rab19
|
APN |
6 |
39,360,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Rab19
|
UTSW |
6 |
39,366,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Rab19
|
UTSW |
6 |
39,361,023 (GRCm39) |
missense |
probably benign |
0.02 |
R0726:Rab19
|
UTSW |
6 |
39,360,893 (GRCm39) |
missense |
probably benign |
0.00 |
R1727:Rab19
|
UTSW |
6 |
39,365,095 (GRCm39) |
nonsense |
probably null |
|
R1954:Rab19
|
UTSW |
6 |
39,361,016 (GRCm39) |
missense |
probably benign |
0.06 |
R3796:Rab19
|
UTSW |
6 |
39,360,975 (GRCm39) |
missense |
probably benign |
0.01 |
R4465:Rab19
|
UTSW |
6 |
39,365,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R5977:Rab19
|
UTSW |
6 |
39,360,860 (GRCm39) |
missense |
probably benign |
0.07 |
R6619:Rab19
|
UTSW |
6 |
39,365,060 (GRCm39) |
missense |
probably damaging |
0.99 |
R7489:Rab19
|
UTSW |
6 |
39,365,039 (GRCm39) |
missense |
probably benign |
0.09 |
R8385:Rab19
|
UTSW |
6 |
39,360,892 (GRCm39) |
missense |
probably benign |
0.00 |
R9414:Rab19
|
UTSW |
6 |
39,360,855 (GRCm39) |
start codon destroyed |
probably null |
0.43 |
|