Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
C |
T |
17: 9,226,839 (GRCm39) |
R465* |
probably null |
Het |
Abcg3 |
A |
T |
5: 105,114,649 (GRCm39) |
D289E |
probably damaging |
Het |
Ablim2 |
G |
T |
5: 36,024,115 (GRCm39) |
|
probably null |
Het |
Acp1 |
A |
T |
12: 30,955,078 (GRCm39) |
V36D |
probably benign |
Het |
Adgrb1 |
T |
A |
15: 74,449,348 (GRCm39) |
|
probably benign |
Het |
Akap6 |
G |
A |
12: 52,933,329 (GRCm39) |
V274I |
probably damaging |
Het |
Arhgap39 |
T |
C |
15: 76,609,715 (GRCm39) |
|
probably benign |
Het |
Bmp1 |
G |
A |
14: 70,717,605 (GRCm39) |
R789W |
probably damaging |
Het |
Catspere2 |
A |
T |
1: 177,976,474 (GRCm39) |
|
probably benign |
Het |
Cfhr2 |
T |
A |
1: 139,749,520 (GRCm39) |
Y154F |
possibly damaging |
Het |
Cilp2 |
T |
C |
8: 70,336,015 (GRCm39) |
Y358C |
probably damaging |
Het |
Cyp1a2 |
T |
A |
9: 57,584,516 (GRCm39) |
K513* |
probably null |
Het |
Dlg1 |
T |
A |
16: 31,655,085 (GRCm39) |
S542T |
probably benign |
Het |
Dmbt1 |
A |
T |
7: 130,696,465 (GRCm39) |
I893F |
possibly damaging |
Het |
Dnhd1 |
A |
T |
7: 105,353,130 (GRCm39) |
E2761V |
possibly damaging |
Het |
F11 |
T |
C |
8: 45,708,341 (GRCm39) |
T40A |
probably benign |
Het |
Fam227a |
T |
C |
15: 79,520,936 (GRCm39) |
D296G |
possibly damaging |
Het |
Fance |
C |
T |
17: 28,534,589 (GRCm39) |
|
probably benign |
Het |
Gaa |
A |
G |
11: 119,167,669 (GRCm39) |
D149G |
probably damaging |
Het |
Gapt |
A |
G |
13: 110,490,522 (GRCm39) |
M47T |
possibly damaging |
Het |
Gm1110 |
T |
C |
9: 26,813,774 (GRCm39) |
N202D |
probably damaging |
Het |
Gm7535 |
T |
C |
17: 18,131,809 (GRCm39) |
|
probably benign |
Het |
Gm973 |
T |
A |
1: 59,601,859 (GRCm39) |
M491K |
probably benign |
Het |
Gmnc |
A |
G |
16: 26,782,695 (GRCm39) |
V27A |
probably benign |
Het |
Kif27 |
T |
C |
13: 58,440,915 (GRCm39) |
T1167A |
possibly damaging |
Het |
Klrg1 |
T |
A |
6: 122,248,331 (GRCm39) |
*189C |
probably null |
Het |
Lime1 |
T |
A |
2: 181,024,640 (GRCm39) |
M98K |
probably benign |
Het |
Lrp1 |
C |
A |
10: 127,391,965 (GRCm39) |
A2867S |
probably benign |
Het |
Lrrd1 |
G |
A |
5: 3,908,735 (GRCm39) |
S669N |
probably benign |
Het |
Mmel1 |
A |
G |
4: 154,976,456 (GRCm39) |
N520S |
probably damaging |
Het |
Mrpl48 |
A |
C |
7: 100,198,535 (GRCm39) |
L206V |
probably damaging |
Het |
Nagpa |
C |
T |
16: 5,021,596 (GRCm39) |
A52T |
probably benign |
Het |
Or1o3 |
A |
G |
17: 37,573,919 (GRCm39) |
V212A |
probably benign |
Het |
Or4c3 |
T |
G |
2: 89,851,528 (GRCm39) |
D294A |
probably benign |
Het |
Orai2 |
A |
G |
5: 136,190,355 (GRCm39) |
S71P |
probably damaging |
Het |
Pcbp1 |
A |
T |
6: 86,502,209 (GRCm39) |
I230N |
probably damaging |
Het |
Pcdh15 |
T |
C |
10: 74,138,986 (GRCm39) |
L349P |
probably damaging |
Het |
Pcdhb16 |
T |
C |
18: 37,613,011 (GRCm39) |
V657A |
probably benign |
Het |
Prdm15 |
G |
T |
16: 97,609,875 (GRCm39) |
H590N |
probably damaging |
Het |
Psg18 |
T |
C |
7: 18,079,874 (GRCm39) |
I442M |
probably damaging |
Het |
Pygm |
C |
A |
19: 6,439,494 (GRCm39) |
D279E |
probably benign |
Het |
Rrn3 |
T |
A |
16: 13,610,798 (GRCm39) |
|
probably null |
Het |
Sass6 |
T |
C |
3: 116,407,702 (GRCm39) |
S273P |
possibly damaging |
Het |
Schip1 |
A |
G |
3: 68,402,270 (GRCm39) |
M116V |
probably benign |
Het |
Sdc3 |
G |
A |
4: 130,546,087 (GRCm39) |
V55I |
unknown |
Het |
Serpinb8 |
T |
A |
1: 107,525,201 (GRCm39) |
M1K |
probably null |
Het |
Slc24a5 |
T |
C |
2: 124,927,739 (GRCm39) |
I346T |
probably damaging |
Het |
Slc35f3 |
T |
A |
8: 127,117,846 (GRCm39) |
I335N |
probably damaging |
Het |
Snapc2 |
T |
A |
8: 4,305,299 (GRCm39) |
V147E |
probably damaging |
Het |
Snx2 |
T |
C |
18: 53,322,784 (GRCm39) |
S56P |
possibly damaging |
Het |
Sptbn5 |
A |
G |
2: 119,915,812 (GRCm39) |
|
probably benign |
Het |
Stk19 |
A |
T |
17: 35,040,400 (GRCm39) |
|
probably benign |
Het |
Sulf1 |
A |
G |
1: 12,911,702 (GRCm39) |
E692G |
probably benign |
Het |
Tet1 |
C |
T |
10: 62,674,450 (GRCm39) |
V1209I |
probably damaging |
Het |
Tln1 |
T |
C |
4: 43,539,406 (GRCm39) |
T1639A |
probably benign |
Het |
Tmem135 |
G |
T |
7: 88,845,335 (GRCm39) |
Y165* |
probably null |
Het |
Tmprss6 |
T |
C |
15: 78,336,707 (GRCm39) |
T398A |
probably damaging |
Het |
Ube4a |
C |
T |
9: 44,851,258 (GRCm39) |
|
probably null |
Het |
Vmn1r227 |
T |
C |
17: 20,955,499 (GRCm39) |
|
noncoding transcript |
Het |
Wdhd1 |
T |
C |
14: 47,488,273 (GRCm39) |
S745G |
probably benign |
Het |
Xylt1 |
A |
G |
7: 117,191,263 (GRCm39) |
H353R |
probably damaging |
Het |
Zfp788 |
A |
G |
7: 41,298,980 (GRCm39) |
T539A |
probably benign |
Het |
Zfp866 |
A |
T |
8: 70,218,091 (GRCm39) |
F510I |
possibly damaging |
Het |
|
Other mutations in Dennd4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Dennd4a
|
APN |
9 |
64,819,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01610:Dennd4a
|
APN |
9 |
64,814,166 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01788:Dennd4a
|
APN |
9 |
64,749,903 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01827:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL01828:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL01829:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL01979:Dennd4a
|
APN |
9 |
64,801,691 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02100:Dennd4a
|
APN |
9 |
64,816,988 (GRCm39) |
splice site |
probably benign |
|
IGL02339:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL02341:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL02584:Dennd4a
|
APN |
9 |
64,758,580 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02607:Dennd4a
|
APN |
9 |
64,769,609 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02654:Dennd4a
|
APN |
9 |
64,817,473 (GRCm39) |
splice site |
probably benign |
|
IGL02701:Dennd4a
|
APN |
9 |
64,804,635 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03051:Dennd4a
|
APN |
9 |
64,769,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03257:Dennd4a
|
APN |
9 |
64,779,156 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03346:Dennd4a
|
APN |
9 |
64,795,808 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03349:Dennd4a
|
APN |
9 |
64,796,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03398:Dennd4a
|
APN |
9 |
64,779,164 (GRCm39) |
missense |
probably benign |
0.32 |
R0010:Dennd4a
|
UTSW |
9 |
64,803,997 (GRCm39) |
missense |
probably benign |
0.00 |
R0010:Dennd4a
|
UTSW |
9 |
64,803,997 (GRCm39) |
missense |
probably benign |
0.00 |
R0129:Dennd4a
|
UTSW |
9 |
64,800,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R0220:Dennd4a
|
UTSW |
9 |
64,759,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Dennd4a
|
UTSW |
9 |
64,769,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R0881:Dennd4a
|
UTSW |
9 |
64,758,665 (GRCm39) |
critical splice donor site |
probably null |
|
R1225:Dennd4a
|
UTSW |
9 |
64,818,957 (GRCm39) |
missense |
probably benign |
0.03 |
R1311:Dennd4a
|
UTSW |
9 |
64,817,286 (GRCm39) |
missense |
probably benign |
0.34 |
R1448:Dennd4a
|
UTSW |
9 |
64,813,327 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1450:Dennd4a
|
UTSW |
9 |
64,818,947 (GRCm39) |
missense |
probably benign |
0.03 |
R1630:Dennd4a
|
UTSW |
9 |
64,779,164 (GRCm39) |
missense |
probably benign |
0.32 |
R1709:Dennd4a
|
UTSW |
9 |
64,796,887 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1824:Dennd4a
|
UTSW |
9 |
64,766,640 (GRCm39) |
critical splice donor site |
probably null |
|
R1851:Dennd4a
|
UTSW |
9 |
64,769,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R1870:Dennd4a
|
UTSW |
9 |
64,804,516 (GRCm39) |
missense |
probably benign |
0.00 |
R1900:Dennd4a
|
UTSW |
9 |
64,804,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R1911:Dennd4a
|
UTSW |
9 |
64,796,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Dennd4a
|
UTSW |
9 |
64,749,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Dennd4a
|
UTSW |
9 |
64,759,749 (GRCm39) |
missense |
probably benign |
0.02 |
R1955:Dennd4a
|
UTSW |
9 |
64,759,749 (GRCm39) |
missense |
probably benign |
0.02 |
R2049:Dennd4a
|
UTSW |
9 |
64,796,887 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2129:Dennd4a
|
UTSW |
9 |
64,813,256 (GRCm39) |
splice site |
probably null |
|
R2138:Dennd4a
|
UTSW |
9 |
64,796,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R2929:Dennd4a
|
UTSW |
9 |
64,759,699 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3083:Dennd4a
|
UTSW |
9 |
64,813,363 (GRCm39) |
missense |
probably benign |
0.03 |
R3108:Dennd4a
|
UTSW |
9 |
64,819,669 (GRCm39) |
missense |
probably benign |
0.23 |
R3176:Dennd4a
|
UTSW |
9 |
64,796,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3177:Dennd4a
|
UTSW |
9 |
64,796,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3276:Dennd4a
|
UTSW |
9 |
64,796,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3277:Dennd4a
|
UTSW |
9 |
64,796,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3890:Dennd4a
|
UTSW |
9 |
64,779,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R3953:Dennd4a
|
UTSW |
9 |
64,759,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R3963:Dennd4a
|
UTSW |
9 |
64,769,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4059:Dennd4a
|
UTSW |
9 |
64,819,174 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4499:Dennd4a
|
UTSW |
9 |
64,817,405 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4500:Dennd4a
|
UTSW |
9 |
64,817,405 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4501:Dennd4a
|
UTSW |
9 |
64,817,405 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4671:Dennd4a
|
UTSW |
9 |
64,801,689 (GRCm39) |
missense |
probably benign |
|
R4701:Dennd4a
|
UTSW |
9 |
64,804,639 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4821:Dennd4a
|
UTSW |
9 |
64,804,531 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4829:Dennd4a
|
UTSW |
9 |
64,796,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R4876:Dennd4a
|
UTSW |
9 |
64,803,872 (GRCm39) |
missense |
probably benign |
|
R4881:Dennd4a
|
UTSW |
9 |
64,746,126 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4962:Dennd4a
|
UTSW |
9 |
64,813,285 (GRCm39) |
missense |
probably benign |
0.00 |
R5557:Dennd4a
|
UTSW |
9 |
64,811,509 (GRCm39) |
missense |
probably benign |
0.07 |
R5649:Dennd4a
|
UTSW |
9 |
64,758,491 (GRCm39) |
splice site |
probably null |
|
R5868:Dennd4a
|
UTSW |
9 |
64,804,011 (GRCm39) |
missense |
probably benign |
0.02 |
R5876:Dennd4a
|
UTSW |
9 |
64,819,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6052:Dennd4a
|
UTSW |
9 |
64,794,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6411:Dennd4a
|
UTSW |
9 |
64,779,181 (GRCm39) |
missense |
probably benign |
0.04 |
R6596:Dennd4a
|
UTSW |
9 |
64,759,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R6668:Dennd4a
|
UTSW |
9 |
64,794,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Dennd4a
|
UTSW |
9 |
64,759,771 (GRCm39) |
nonsense |
probably null |
|
R7056:Dennd4a
|
UTSW |
9 |
64,814,205 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7107:Dennd4a
|
UTSW |
9 |
64,801,681 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7203:Dennd4a
|
UTSW |
9 |
64,803,756 (GRCm39) |
missense |
probably benign |
0.05 |
R7238:Dennd4a
|
UTSW |
9 |
64,769,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R7373:Dennd4a
|
UTSW |
9 |
64,804,551 (GRCm39) |
missense |
probably benign |
0.01 |
R7454:Dennd4a
|
UTSW |
9 |
64,759,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R7546:Dennd4a
|
UTSW |
9 |
64,780,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R7590:Dennd4a
|
UTSW |
9 |
64,795,869 (GRCm39) |
missense |
probably benign |
0.01 |
R7662:Dennd4a
|
UTSW |
9 |
64,759,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Dennd4a
|
UTSW |
9 |
64,814,202 (GRCm39) |
missense |
probably damaging |
0.98 |
R7909:Dennd4a
|
UTSW |
9 |
64,780,275 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7976:Dennd4a
|
UTSW |
9 |
64,759,794 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8026:Dennd4a
|
UTSW |
9 |
64,780,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R8034:Dennd4a
|
UTSW |
9 |
64,795,850 (GRCm39) |
missense |
probably benign |
0.01 |
R8089:Dennd4a
|
UTSW |
9 |
64,756,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R8298:Dennd4a
|
UTSW |
9 |
64,814,157 (GRCm39) |
missense |
probably benign |
0.00 |
R8397:Dennd4a
|
UTSW |
9 |
64,796,391 (GRCm39) |
missense |
probably benign |
|
R8425:Dennd4a
|
UTSW |
9 |
64,746,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R8495:Dennd4a
|
UTSW |
9 |
64,794,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R8855:Dennd4a
|
UTSW |
9 |
64,819,672 (GRCm39) |
missense |
probably benign |
|
R9219:Dennd4a
|
UTSW |
9 |
64,796,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R9275:Dennd4a
|
UTSW |
9 |
64,749,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R9376:Dennd4a
|
UTSW |
9 |
64,819,974 (GRCm39) |
missense |
probably benign |
0.00 |
R9485:Dennd4a
|
UTSW |
9 |
64,814,388 (GRCm39) |
nonsense |
probably null |
|
R9672:Dennd4a
|
UTSW |
9 |
64,800,640 (GRCm39) |
missense |
probably benign |
|
R9746:Dennd4a
|
UTSW |
9 |
64,801,793 (GRCm39) |
missense |
probably benign |
|
X0026:Dennd4a
|
UTSW |
9 |
64,804,602 (GRCm39) |
missense |
possibly damaging |
0.67 |
Z1088:Dennd4a
|
UTSW |
9 |
64,779,304 (GRCm39) |
missense |
probably damaging |
1.00 |
|