Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,225,092 (GRCm39) |
S524G |
probably benign |
Het |
Abca8b |
A |
T |
11: 109,857,937 (GRCm39) |
I546N |
possibly damaging |
Het |
Abcd4 |
C |
T |
12: 84,650,752 (GRCm39) |
R532H |
probably damaging |
Het |
Acsf2 |
A |
T |
11: 94,460,786 (GRCm39) |
D373E |
probably damaging |
Het |
Acsm1 |
A |
G |
7: 119,259,880 (GRCm39) |
T510A |
probably damaging |
Het |
Adam21 |
C |
T |
12: 81,607,550 (GRCm39) |
V71I |
probably benign |
Het |
Adgra3 |
T |
C |
5: 50,147,621 (GRCm39) |
D473G |
probably damaging |
Het |
Agbl2 |
G |
A |
2: 90,631,499 (GRCm39) |
V286I |
possibly damaging |
Het |
Alkbh8 |
A |
G |
9: 3,344,642 (GRCm39) |
E141G |
probably null |
Het |
Arhgap21 |
T |
C |
2: 20,865,236 (GRCm39) |
D952G |
probably damaging |
Het |
Asb4 |
A |
T |
6: 5,390,653 (GRCm39) |
K15N |
possibly damaging |
Het |
Cert1 |
T |
C |
13: 96,770,690 (GRCm39) |
V533A |
probably damaging |
Het |
Clip1 |
G |
T |
5: 123,752,770 (GRCm39) |
|
probably benign |
Het |
Clip4 |
T |
C |
17: 72,170,839 (GRCm39) |
|
probably benign |
Het |
Cyp2b10 |
T |
C |
7: 25,614,306 (GRCm39) |
V260A |
probably benign |
Het |
Dnm1 |
C |
T |
2: 32,224,739 (GRCm39) |
M430I |
probably benign |
Het |
Dspp |
A |
G |
5: 104,321,883 (GRCm39) |
|
probably benign |
Het |
Ephb1 |
A |
C |
9: 101,841,164 (GRCm39) |
D730E |
probably benign |
Het |
Fancf |
A |
G |
7: 51,511,632 (GRCm39) |
V124A |
probably benign |
Het |
Fgfr2 |
G |
A |
7: 129,765,745 (GRCm39) |
P692S |
possibly damaging |
Het |
Fkbp15 |
G |
A |
4: 62,230,521 (GRCm39) |
R731* |
probably null |
Het |
Fos |
T |
C |
12: 85,522,805 (GRCm39) |
F239S |
probably benign |
Het |
Fuz |
T |
C |
7: 44,548,092 (GRCm39) |
Y107H |
probably damaging |
Het |
Gm3159 |
A |
C |
14: 4,400,520 (GRCm38) |
N193T |
probably damaging |
Het |
Helz2 |
T |
A |
2: 180,871,124 (GRCm39) |
D2771V |
probably damaging |
Het |
Ighv1-18 |
T |
A |
12: 114,646,325 (GRCm39) |
K92M |
probably damaging |
Het |
Kcnh3 |
A |
G |
15: 99,136,091 (GRCm39) |
Y696C |
probably damaging |
Het |
Klf15 |
T |
A |
6: 90,444,160 (GRCm39) |
V245D |
probably damaging |
Het |
L1td1 |
C |
T |
4: 98,625,911 (GRCm39) |
A702V |
probably damaging |
Het |
Lamc2 |
A |
G |
1: 153,034,637 (GRCm39) |
M122T |
probably benign |
Het |
Lrp1b |
A |
G |
2: 41,618,702 (GRCm39) |
L124P |
probably damaging |
Het |
Mcrs1 |
G |
T |
15: 99,146,349 (GRCm39) |
Y85* |
probably null |
Het |
Mgst1 |
A |
T |
6: 138,120,026 (GRCm39) |
I29L |
probably benign |
Het |
Miga1 |
C |
T |
3: 151,982,390 (GRCm39) |
R562H |
probably damaging |
Het |
Mybpc3 |
T |
C |
2: 90,959,117 (GRCm39) |
W687R |
probably damaging |
Het |
Myh11 |
G |
T |
16: 14,022,532 (GRCm39) |
A1682D |
possibly damaging |
Het |
Nes |
T |
C |
3: 87,887,320 (GRCm39) |
S1816P |
probably damaging |
Het |
Or52p1 |
T |
C |
7: 104,267,069 (GRCm39) |
V69A |
possibly damaging |
Het |
Or5c1 |
T |
G |
2: 37,222,662 (GRCm39) |
V301G |
probably damaging |
Het |
Pkhd1l1 |
T |
G |
15: 44,410,812 (GRCm39) |
F2773C |
probably damaging |
Het |
Pkp1 |
C |
G |
1: 135,846,714 (GRCm39) |
E13Q |
probably damaging |
Het |
Ppp2r2b |
T |
C |
18: 43,031,869 (GRCm39) |
D4G |
probably benign |
Het |
Ppp6r3 |
G |
A |
19: 3,537,072 (GRCm39) |
H455Y |
probably benign |
Het |
R3hdm1 |
A |
G |
1: 128,106,657 (GRCm39) |
R202G |
probably benign |
Het |
Sgcz |
T |
G |
8: 38,190,207 (GRCm39) |
K106N |
probably benign |
Het |
Slc13a4 |
T |
C |
6: 35,247,304 (GRCm39) |
Y572C |
probably damaging |
Het |
Syne2 |
C |
T |
12: 76,088,881 (GRCm39) |
Q5080* |
probably null |
Het |
Tpst2 |
C |
T |
5: 112,456,171 (GRCm39) |
Q5* |
probably null |
Het |
Ttn |
T |
A |
2: 76,561,877 (GRCm39) |
T28908S |
possibly damaging |
Het |
Vmn1r120 |
C |
T |
7: 20,787,027 (GRCm39) |
R228H |
probably benign |
Het |
Vmn2r3 |
T |
C |
3: 64,186,370 (GRCm39) |
N105S |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,979,829 (GRCm39) |
T195A |
probably damaging |
Het |
Zfp616 |
T |
A |
11: 73,974,909 (GRCm39) |
S484T |
probably benign |
Het |
|
Other mutations in Dpp7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01637:Dpp7
|
APN |
2 |
25,244,625 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02897:Dpp7
|
APN |
2 |
25,243,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02992:Dpp7
|
APN |
2 |
25,244,589 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03069:Dpp7
|
APN |
2 |
25,245,735 (GRCm39) |
critical splice acceptor site |
probably null |
|
1mM(1):Dpp7
|
UTSW |
2 |
25,246,152 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4519001:Dpp7
|
UTSW |
2 |
25,242,460 (GRCm39) |
missense |
probably damaging |
0.97 |
R0051:Dpp7
|
UTSW |
2 |
25,246,107 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0051:Dpp7
|
UTSW |
2 |
25,246,107 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0900:Dpp7
|
UTSW |
2 |
25,246,311 (GRCm39) |
missense |
probably damaging |
0.99 |
R1889:Dpp7
|
UTSW |
2 |
25,243,691 (GRCm39) |
splice site |
probably null |
|
R1895:Dpp7
|
UTSW |
2 |
25,243,691 (GRCm39) |
splice site |
probably null |
|
R2055:Dpp7
|
UTSW |
2 |
25,244,490 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4697:Dpp7
|
UTSW |
2 |
25,244,931 (GRCm39) |
missense |
probably benign |
0.00 |
R4832:Dpp7
|
UTSW |
2 |
25,242,398 (GRCm39) |
unclassified |
probably benign |
|
R4887:Dpp7
|
UTSW |
2 |
25,242,770 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5114:Dpp7
|
UTSW |
2 |
25,242,749 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6976:Dpp7
|
UTSW |
2 |
25,244,836 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7577:Dpp7
|
UTSW |
2 |
25,245,603 (GRCm39) |
missense |
probably benign |
|
R8459:Dpp7
|
UTSW |
2 |
25,242,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R8672:Dpp7
|
UTSW |
2 |
25,246,133 (GRCm39) |
missense |
probably benign |
0.00 |
R8690:Dpp7
|
UTSW |
2 |
25,245,645 (GRCm39) |
missense |
probably damaging |
1.00 |
X0058:Dpp7
|
UTSW |
2 |
25,244,764 (GRCm39) |
missense |
probably benign |
0.05 |
|