Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
C |
6: 128,547,057 (GRCm39) |
|
probably benign |
Het |
Atp6v1h |
A |
T |
1: 5,154,677 (GRCm39) |
T2S |
probably benign |
Het |
Bcl11b |
G |
A |
12: 107,932,036 (GRCm39) |
P179S |
probably benign |
Het |
Cacna1a |
C |
T |
8: 85,306,687 (GRCm39) |
|
probably benign |
Het |
Ccdc146 |
C |
T |
5: 21,502,004 (GRCm39) |
|
probably null |
Het |
Ccdc61 |
T |
C |
7: 18,626,461 (GRCm39) |
D128G |
probably damaging |
Het |
Cd55 |
A |
G |
1: 130,387,313 (GRCm39) |
|
probably benign |
Het |
Cdk7 |
C |
A |
13: 100,855,812 (GRCm39) |
E99* |
probably null |
Het |
Cfap96 |
A |
T |
8: 46,421,198 (GRCm39) |
S108R |
probably damaging |
Het |
Cox8a |
A |
T |
19: 7,194,874 (GRCm39) |
S2T |
probably damaging |
Het |
Cracdl |
A |
C |
1: 37,663,337 (GRCm39) |
S854A |
probably benign |
Het |
Dop1a |
A |
C |
9: 86,394,705 (GRCm39) |
E602A |
probably benign |
Het |
Ephx4 |
T |
C |
5: 107,560,944 (GRCm39) |
L32S |
probably damaging |
Het |
Fbxo21 |
T |
A |
5: 118,138,555 (GRCm39) |
D493E |
probably benign |
Het |
Frmd4b |
A |
T |
6: 97,300,610 (GRCm39) |
|
probably benign |
Het |
Fzd1 |
A |
T |
5: 4,806,037 (GRCm39) |
M515K |
possibly damaging |
Het |
Gli2 |
A |
G |
1: 118,818,138 (GRCm39) |
|
probably benign |
Het |
Gm12887 |
T |
A |
4: 121,473,666 (GRCm39) |
K61N |
probably damaging |
Het |
Grin2a |
A |
T |
16: 9,487,671 (GRCm39) |
V409D |
probably damaging |
Het |
Grin2b |
T |
C |
6: 135,900,201 (GRCm39) |
I227V |
probably benign |
Het |
Helz2 |
T |
G |
2: 180,870,614 (GRCm39) |
D2879A |
possibly damaging |
Het |
Itpr2 |
T |
C |
6: 146,224,631 (GRCm39) |
N1453S |
probably benign |
Het |
Itpr3 |
C |
A |
17: 27,317,296 (GRCm39) |
S817Y |
probably damaging |
Het |
Lin7c |
T |
A |
2: 109,726,798 (GRCm39) |
|
probably benign |
Het |
Ly75 |
T |
C |
2: 60,152,262 (GRCm39) |
E1097G |
probably benign |
Het |
Mcm10 |
T |
C |
2: 4,996,218 (GRCm39) |
N882D |
probably damaging |
Het |
Mettl13 |
A |
T |
1: 162,373,750 (GRCm39) |
L167Q |
probably damaging |
Het |
Morn2 |
A |
T |
17: 80,602,942 (GRCm39) |
M1L |
probably benign |
Het |
Mybph |
G |
T |
1: 134,121,590 (GRCm39) |
V88L |
probably damaging |
Het |
Nefm |
T |
A |
14: 68,358,648 (GRCm39) |
|
probably benign |
Het |
Nf1 |
A |
G |
11: 79,362,377 (GRCm39) |
E1497G |
probably damaging |
Het |
Or2j3 |
T |
C |
17: 38,615,702 (GRCm39) |
S217G |
possibly damaging |
Het |
Or4k37 |
T |
A |
2: 111,158,870 (GRCm39) |
Y35* |
probably null |
Het |
Or51ah3 |
A |
G |
7: 103,210,244 (GRCm39) |
K187E |
probably damaging |
Het |
Or52e18 |
T |
A |
7: 104,609,703 (GRCm39) |
T79S |
possibly damaging |
Het |
Phf8-ps |
A |
T |
17: 33,285,696 (GRCm39) |
W369R |
probably damaging |
Het |
Plcd3 |
C |
G |
11: 102,968,411 (GRCm39) |
W382S |
probably damaging |
Het |
Plxna1 |
T |
A |
6: 89,306,721 (GRCm39) |
I1370F |
possibly damaging |
Het |
Qng1 |
T |
C |
13: 58,531,980 (GRCm39) |
D192G |
probably damaging |
Het |
Rarb |
G |
A |
14: 16,509,066 (GRCm38) |
R106C |
probably damaging |
Het |
Rps6ka5 |
G |
A |
12: 100,644,839 (GRCm39) |
T37I |
probably damaging |
Het |
Runx1 |
G |
T |
16: 92,441,029 (GRCm39) |
|
probably benign |
Het |
Scube1 |
A |
G |
15: 83,518,937 (GRCm39) |
V301A |
probably damaging |
Het |
Sema3a |
A |
T |
5: 13,450,004 (GRCm39) |
N27I |
possibly damaging |
Het |
Slc15a3 |
G |
T |
19: 10,820,406 (GRCm39) |
E8* |
probably null |
Het |
Slc22a5 |
T |
C |
11: 53,782,032 (GRCm39) |
S112G |
probably benign |
Het |
Slc25a45 |
T |
C |
19: 5,930,495 (GRCm39) |
F3L |
probably damaging |
Het |
Slc4a4 |
A |
C |
5: 89,304,195 (GRCm39) |
H502P |
possibly damaging |
Het |
Slfn10-ps |
A |
G |
11: 82,921,126 (GRCm39) |
|
noncoding transcript |
Het |
Slit2 |
C |
A |
5: 48,439,068 (GRCm39) |
C1077* |
probably null |
Het |
Spn |
A |
G |
7: 126,735,494 (GRCm39) |
F82L |
possibly damaging |
Het |
Tbccd1 |
A |
G |
16: 22,660,655 (GRCm39) |
W54R |
probably damaging |
Het |
Ucp1 |
G |
T |
8: 84,017,233 (GRCm39) |
E8* |
probably null |
Het |
Unc80 |
A |
T |
1: 66,545,782 (GRCm39) |
|
probably benign |
Het |
Vsnl1 |
A |
T |
12: 11,436,987 (GRCm39) |
|
probably null |
Het |
Zdhhc11 |
C |
T |
13: 74,130,805 (GRCm39) |
Q295* |
probably null |
Het |
Zfp457 |
T |
A |
13: 67,442,098 (GRCm39) |
H63L |
probably damaging |
Het |
|
Other mutations in Dennd5a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00661:Dennd5a
|
APN |
7 |
109,507,579 (GRCm39) |
missense |
probably benign |
|
IGL01338:Dennd5a
|
APN |
7 |
109,518,611 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01618:Dennd5a
|
APN |
7 |
109,533,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02047:Dennd5a
|
APN |
7 |
109,533,991 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02277:Dennd5a
|
APN |
7 |
109,497,176 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02492:Dennd5a
|
APN |
7 |
109,532,844 (GRCm39) |
missense |
probably benign |
|
IGL02697:Dennd5a
|
APN |
7 |
109,493,988 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02935:Dennd5a
|
APN |
7 |
109,520,514 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02986:Dennd5a
|
APN |
7 |
109,534,731 (GRCm39) |
missense |
probably benign |
|
IGL03088:Dennd5a
|
APN |
7 |
109,507,588 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03156:Dennd5a
|
APN |
7 |
109,518,462 (GRCm39) |
splice site |
probably benign |
|
IGL03181:Dennd5a
|
APN |
7 |
109,532,865 (GRCm39) |
missense |
probably damaging |
1.00 |
big_pal
|
UTSW |
7 |
109,518,630 (GRCm39) |
nonsense |
probably null |
|
Celestial
|
UTSW |
7 |
109,500,296 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4434001:Dennd5a
|
UTSW |
7 |
109,532,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Dennd5a
|
UTSW |
7 |
109,498,998 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0092:Dennd5a
|
UTSW |
7 |
109,499,013 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0111:Dennd5a
|
UTSW |
7 |
109,533,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0517:Dennd5a
|
UTSW |
7 |
109,533,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Dennd5a
|
UTSW |
7 |
109,520,633 (GRCm39) |
missense |
probably benign |
0.01 |
R0811:Dennd5a
|
UTSW |
7 |
109,532,820 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0812:Dennd5a
|
UTSW |
7 |
109,532,820 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0827:Dennd5a
|
UTSW |
7 |
109,498,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0831:Dennd5a
|
UTSW |
7 |
109,533,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R1075:Dennd5a
|
UTSW |
7 |
109,517,808 (GRCm39) |
missense |
probably benign |
|
R1115:Dennd5a
|
UTSW |
7 |
109,517,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R1128:Dennd5a
|
UTSW |
7 |
109,520,541 (GRCm39) |
nonsense |
probably null |
|
R1300:Dennd5a
|
UTSW |
7 |
109,518,614 (GRCm39) |
missense |
probably benign |
|
R1698:Dennd5a
|
UTSW |
7 |
109,516,587 (GRCm39) |
splice site |
probably null |
|
R1711:Dennd5a
|
UTSW |
7 |
109,517,919 (GRCm39) |
missense |
probably benign |
0.00 |
R1771:Dennd5a
|
UTSW |
7 |
109,517,893 (GRCm39) |
missense |
probably damaging |
0.98 |
R1803:Dennd5a
|
UTSW |
7 |
109,497,820 (GRCm39) |
missense |
probably benign |
0.00 |
R2064:Dennd5a
|
UTSW |
7 |
109,497,900 (GRCm39) |
splice site |
probably benign |
|
R2176:Dennd5a
|
UTSW |
7 |
109,504,327 (GRCm39) |
splice site |
probably null |
|
R2182:Dennd5a
|
UTSW |
7 |
109,533,201 (GRCm39) |
missense |
probably benign |
0.03 |
R2852:Dennd5a
|
UTSW |
7 |
109,532,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R2853:Dennd5a
|
UTSW |
7 |
109,532,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R3035:Dennd5a
|
UTSW |
7 |
109,520,559 (GRCm39) |
missense |
probably benign |
0.00 |
R3835:Dennd5a
|
UTSW |
7 |
109,533,449 (GRCm39) |
missense |
probably benign |
0.00 |
R3953:Dennd5a
|
UTSW |
7 |
109,504,906 (GRCm39) |
missense |
probably benign |
0.44 |
R3954:Dennd5a
|
UTSW |
7 |
109,504,906 (GRCm39) |
missense |
probably benign |
0.44 |
R3955:Dennd5a
|
UTSW |
7 |
109,504,906 (GRCm39) |
missense |
probably benign |
0.44 |
R3957:Dennd5a
|
UTSW |
7 |
109,504,906 (GRCm39) |
missense |
probably benign |
0.44 |
R4014:Dennd5a
|
UTSW |
7 |
109,534,688 (GRCm39) |
critical splice donor site |
probably null |
|
R4166:Dennd5a
|
UTSW |
7 |
109,526,032 (GRCm39) |
critical splice donor site |
probably null |
|
R4362:Dennd5a
|
UTSW |
7 |
109,495,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R4567:Dennd5a
|
UTSW |
7 |
109,498,942 (GRCm39) |
missense |
probably benign |
0.06 |
R4700:Dennd5a
|
UTSW |
7 |
109,520,405 (GRCm39) |
missense |
probably benign |
0.01 |
R4734:Dennd5a
|
UTSW |
7 |
109,495,543 (GRCm39) |
missense |
probably damaging |
0.96 |
R4914:Dennd5a
|
UTSW |
7 |
109,500,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Dennd5a
|
UTSW |
7 |
109,500,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R4918:Dennd5a
|
UTSW |
7 |
109,500,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Dennd5a
|
UTSW |
7 |
109,493,919 (GRCm39) |
missense |
probably damaging |
0.98 |
R5011:Dennd5a
|
UTSW |
7 |
109,513,983 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5013:Dennd5a
|
UTSW |
7 |
109,513,983 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5034:Dennd5a
|
UTSW |
7 |
109,499,004 (GRCm39) |
missense |
probably damaging |
0.98 |
R5194:Dennd5a
|
UTSW |
7 |
109,532,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R5359:Dennd5a
|
UTSW |
7 |
109,497,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R5430:Dennd5a
|
UTSW |
7 |
109,533,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Dennd5a
|
UTSW |
7 |
109,504,928 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5607:Dennd5a
|
UTSW |
7 |
109,518,630 (GRCm39) |
nonsense |
probably null |
|
R5608:Dennd5a
|
UTSW |
7 |
109,518,630 (GRCm39) |
nonsense |
probably null |
|
R5783:Dennd5a
|
UTSW |
7 |
109,493,843 (GRCm39) |
missense |
probably damaging |
0.97 |
R5866:Dennd5a
|
UTSW |
7 |
109,518,567 (GRCm39) |
missense |
probably benign |
0.00 |
R5890:Dennd5a
|
UTSW |
7 |
109,533,428 (GRCm39) |
missense |
probably benign |
0.00 |
R6053:Dennd5a
|
UTSW |
7 |
109,532,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Dennd5a
|
UTSW |
7 |
109,497,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R6362:Dennd5a
|
UTSW |
7 |
109,533,472 (GRCm39) |
nonsense |
probably null |
|
R6446:Dennd5a
|
UTSW |
7 |
109,493,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R6894:Dennd5a
|
UTSW |
7 |
109,500,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R7061:Dennd5a
|
UTSW |
7 |
109,504,386 (GRCm39) |
missense |
probably benign |
0.19 |
R7115:Dennd5a
|
UTSW |
7 |
109,493,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Dennd5a
|
UTSW |
7 |
109,495,449 (GRCm39) |
critical splice donor site |
probably null |
|
R7302:Dennd5a
|
UTSW |
7 |
109,504,906 (GRCm39) |
missense |
probably damaging |
0.98 |
R7339:Dennd5a
|
UTSW |
7 |
109,500,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R7704:Dennd5a
|
UTSW |
7 |
109,496,174 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7756:Dennd5a
|
UTSW |
7 |
109,520,714 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7838:Dennd5a
|
UTSW |
7 |
109,533,196 (GRCm39) |
missense |
probably benign |
|
R7873:Dennd5a
|
UTSW |
7 |
109,526,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Dennd5a
|
UTSW |
7 |
109,497,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R8309:Dennd5a
|
UTSW |
7 |
109,500,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R8345:Dennd5a
|
UTSW |
7 |
109,504,477 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8560:Dennd5a
|
UTSW |
7 |
109,533,898 (GRCm39) |
critical splice donor site |
probably null |
|
R9104:Dennd5a
|
UTSW |
7 |
109,497,713 (GRCm39) |
critical splice donor site |
probably null |
|
R9218:Dennd5a
|
UTSW |
7 |
109,507,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:Dennd5a
|
UTSW |
7 |
109,498,942 (GRCm39) |
missense |
probably benign |
0.00 |
R9348:Dennd5a
|
UTSW |
7 |
109,498,930 (GRCm39) |
critical splice donor site |
probably null |
|
R9566:Dennd5a
|
UTSW |
7 |
109,533,254 (GRCm39) |
missense |
probably benign |
0.01 |
R9608:Dennd5a
|
UTSW |
7 |
109,520,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9756:Dennd5a
|
UTSW |
7 |
109,496,174 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9800:Dennd5a
|
UTSW |
7 |
109,500,374 (GRCm39) |
missense |
probably benign |
0.40 |
Z1088:Dennd5a
|
UTSW |
7 |
109,504,480 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dennd5a
|
UTSW |
7 |
109,493,954 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Dennd5a
|
UTSW |
7 |
109,533,231 (GRCm39) |
missense |
probably benign |
|
|