Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,775,632 (GRCm39) |
L1607P |
probably damaging |
Het |
1700016H13Rik |
T |
C |
5: 103,796,687 (GRCm39) |
*118W |
probably null |
Het |
Abcc2 |
A |
T |
19: 43,815,053 (GRCm39) |
R1147* |
probably null |
Het |
Acsbg3 |
A |
T |
17: 57,190,835 (GRCm39) |
N468Y |
probably benign |
Het |
Agap2 |
A |
G |
10: 126,927,571 (GRCm39) |
T1131A |
possibly damaging |
Het |
Aldh9a1 |
A |
G |
1: 167,189,416 (GRCm39) |
D388G |
probably damaging |
Het |
Ap3d1 |
G |
T |
10: 80,565,876 (GRCm39) |
A97E |
probably damaging |
Het |
Arhgef10 |
T |
A |
8: 15,012,636 (GRCm39) |
V320E |
probably damaging |
Het |
Baiap2l1 |
C |
A |
5: 144,202,820 (GRCm39) |
V498L |
probably damaging |
Het |
Bltp2 |
A |
C |
11: 78,160,530 (GRCm39) |
|
probably benign |
Het |
Cdh2 |
T |
C |
18: 16,762,633 (GRCm39) |
N437S |
probably benign |
Het |
Cert1 |
T |
A |
13: 96,685,795 (GRCm39) |
Y63N |
probably benign |
Het |
Cfap119 |
T |
C |
7: 127,184,034 (GRCm39) |
E261G |
probably damaging |
Het |
Cfap20dc |
C |
T |
14: 8,518,695 (GRCm38) |
G254R |
probably damaging |
Het |
Chd1 |
C |
A |
17: 15,945,693 (GRCm39) |
N72K |
probably benign |
Het |
Cstf2t |
A |
T |
19: 31,062,026 (GRCm39) |
M521L |
probably benign |
Het |
Dlx5 |
T |
C |
6: 6,881,619 (GRCm39) |
K90E |
possibly damaging |
Het |
Espnl |
T |
G |
1: 91,272,211 (GRCm39) |
Y524D |
probably damaging |
Het |
Fam20c |
T |
C |
5: 138,741,479 (GRCm39) |
L30P |
probably damaging |
Het |
Fat1 |
G |
T |
8: 45,479,590 (GRCm39) |
A2879S |
probably benign |
Het |
Gabrg1 |
A |
T |
5: 70,931,732 (GRCm39) |
V337D |
probably damaging |
Het |
Gart |
C |
A |
16: 91,420,291 (GRCm39) |
D851Y |
possibly damaging |
Het |
Gcc1 |
T |
C |
6: 28,420,615 (GRCm39) |
H234R |
probably damaging |
Het |
Gemin6 |
T |
A |
17: 80,535,524 (GRCm39) |
H161Q |
probably damaging |
Het |
Glt6d1 |
A |
G |
2: 25,684,082 (GRCm39) |
I308T |
probably benign |
Het |
Gm10320 |
T |
C |
13: 98,628,491 (GRCm39) |
T7A |
probably benign |
Het |
Gm10912 |
T |
C |
2: 103,896,875 (GRCm39) |
S5P |
probably benign |
Het |
Gmpr2 |
T |
A |
14: 55,910,192 (GRCm39) |
D7E |
possibly damaging |
Het |
Hc |
A |
G |
2: 34,874,762 (GRCm39) |
Y1620H |
probably damaging |
Het |
Hoxa3 |
T |
C |
6: 52,147,123 (GRCm39) |
|
probably benign |
Het |
Ift140 |
A |
G |
17: 25,309,907 (GRCm39) |
T1105A |
probably benign |
Het |
Kdr |
G |
T |
5: 76,129,082 (GRCm39) |
T188N |
possibly damaging |
Het |
Lepr |
A |
T |
4: 101,609,349 (GRCm39) |
D312V |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,880,329 (GRCm39) |
V501A |
probably damaging |
Het |
Mcur1 |
T |
C |
13: 43,699,216 (GRCm39) |
Y267C |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,197,864 (GRCm39) |
T736S |
probably benign |
Het |
Med13l |
T |
C |
5: 118,809,067 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
G |
C |
1: 88,173,764 (GRCm39) |
A871P |
probably damaging |
Het |
Ndrg2 |
T |
A |
14: 52,144,460 (GRCm39) |
|
probably benign |
Het |
Oas3 |
G |
A |
5: 120,894,210 (GRCm39) |
R39C |
probably damaging |
Het |
Onecut2 |
T |
A |
18: 64,474,543 (GRCm39) |
S365T |
possibly damaging |
Het |
Or13c25 |
G |
A |
4: 52,910,849 (GRCm39) |
T315M |
probably benign |
Het |
Or4c10 |
A |
G |
2: 89,760,545 (GRCm39) |
T131A |
probably benign |
Het |
Or4k48 |
C |
T |
2: 111,476,136 (GRCm39) |
V69I |
probably benign |
Het |
Or51e1 |
T |
A |
7: 102,359,202 (GRCm39) |
H245Q |
probably damaging |
Het |
Pds5b |
C |
A |
5: 150,677,896 (GRCm39) |
Q505K |
probably benign |
Het |
Pramel22 |
C |
T |
4: 143,383,010 (GRCm39) |
E70K |
possibly damaging |
Het |
Rfx2 |
T |
C |
17: 57,110,722 (GRCm39) |
Y88C |
probably damaging |
Het |
Rpl6 |
T |
C |
5: 121,346,541 (GRCm39) |
V214A |
probably benign |
Het |
Samd3 |
T |
A |
10: 26,147,752 (GRCm39) |
C476S |
possibly damaging |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Shank1 |
C |
T |
7: 44,001,718 (GRCm39) |
R1146W |
unknown |
Het |
Smcr8 |
T |
C |
11: 60,668,941 (GRCm39) |
Y30H |
probably damaging |
Het |
Smpd4 |
T |
A |
16: 17,459,461 (GRCm39) |
|
probably null |
Het |
Strip1 |
C |
A |
3: 107,521,929 (GRCm39) |
D750Y |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,070,851 (GRCm39) |
K2312E |
possibly damaging |
Het |
Taf1c |
A |
T |
8: 120,326,722 (GRCm39) |
I438N |
probably damaging |
Het |
Tnfaip1 |
A |
T |
11: 78,420,840 (GRCm39) |
|
probably benign |
Het |
Unc45b |
T |
A |
11: 82,831,031 (GRCm39) |
L797Q |
possibly damaging |
Het |
Usp24 |
T |
A |
4: 106,264,330 (GRCm39) |
W1754R |
probably damaging |
Het |
Utp20 |
G |
A |
10: 88,613,378 (GRCm39) |
P1301L |
probably benign |
Het |
Vmn2r115 |
T |
A |
17: 23,578,755 (GRCm39) |
S743T |
probably damaging |
Het |
Vps41 |
T |
G |
13: 19,038,833 (GRCm39) |
|
probably null |
Het |
Vps72 |
G |
T |
3: 95,029,894 (GRCm39) |
L304F |
probably damaging |
Het |
Wiz |
A |
T |
17: 32,575,415 (GRCm39) |
I907N |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,978,119 (GRCm39) |
T765A |
probably benign |
Het |
Zfp616 |
A |
T |
11: 73,976,500 (GRCm39) |
H923L |
probably damaging |
Het |
Zp2 |
A |
T |
7: 119,742,799 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Dmp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00498:Dmp1
|
APN |
5 |
104,358,021 (GRCm39) |
splice site |
probably benign |
|
IGL01063:Dmp1
|
APN |
5 |
104,354,965 (GRCm39) |
start codon destroyed |
probably null |
0.73 |
IGL01599:Dmp1
|
APN |
5 |
104,360,328 (GRCm39) |
nonsense |
probably null |
|
IGL01631:Dmp1
|
APN |
5 |
104,360,734 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01646:Dmp1
|
APN |
5 |
104,359,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02611:Dmp1
|
APN |
5 |
104,360,380 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02642:Dmp1
|
APN |
5 |
104,359,536 (GRCm39) |
missense |
probably damaging |
0.97 |
choppers
|
UTSW |
5 |
104,354,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Dmp1
|
UTSW |
5 |
104,360,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R0529:Dmp1
|
UTSW |
5 |
104,360,092 (GRCm39) |
missense |
probably benign |
0.03 |
R0850:Dmp1
|
UTSW |
5 |
104,360,653 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0883:Dmp1
|
UTSW |
5 |
104,355,496 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1858:Dmp1
|
UTSW |
5 |
104,355,496 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1869:Dmp1
|
UTSW |
5 |
104,359,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R1995:Dmp1
|
UTSW |
5 |
104,357,779 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2004:Dmp1
|
UTSW |
5 |
104,359,790 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2009:Dmp1
|
UTSW |
5 |
104,360,706 (GRCm39) |
missense |
probably damaging |
0.97 |
R2870:Dmp1
|
UTSW |
5 |
104,359,974 (GRCm39) |
missense |
probably benign |
0.05 |
R2870:Dmp1
|
UTSW |
5 |
104,359,974 (GRCm39) |
missense |
probably benign |
0.05 |
R4716:Dmp1
|
UTSW |
5 |
104,360,427 (GRCm39) |
missense |
probably damaging |
0.99 |
R5687:Dmp1
|
UTSW |
5 |
104,354,952 (GRCm39) |
start gained |
probably benign |
|
R6331:Dmp1
|
UTSW |
5 |
104,354,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R6389:Dmp1
|
UTSW |
5 |
104,360,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7006:Dmp1
|
UTSW |
5 |
104,360,188 (GRCm39) |
missense |
probably benign |
0.02 |
R7103:Dmp1
|
UTSW |
5 |
104,359,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Dmp1
|
UTSW |
5 |
104,359,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R8181:Dmp1
|
UTSW |
5 |
104,359,380 (GRCm39) |
splice site |
probably null |
|
R8350:Dmp1
|
UTSW |
5 |
104,360,765 (GRCm39) |
missense |
probably damaging |
0.99 |
R8379:Dmp1
|
UTSW |
5 |
104,359,571 (GRCm39) |
nonsense |
probably null |
|
R8450:Dmp1
|
UTSW |
5 |
104,360,765 (GRCm39) |
missense |
probably damaging |
0.99 |
R8531:Dmp1
|
UTSW |
5 |
104,360,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R9316:Dmp1
|
UTSW |
5 |
104,357,767 (GRCm39) |
missense |
probably benign |
0.45 |
Z1177:Dmp1
|
UTSW |
5 |
104,359,518 (GRCm39) |
missense |
probably benign |
0.04 |
|