Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd16b |
A |
G |
2: 181,135,578 (GRCm39) |
D160G |
probably damaging |
Het |
Acap1 |
A |
G |
11: 69,780,505 (GRCm39) |
F15S |
probably damaging |
Het |
Adam30 |
A |
T |
3: 98,068,625 (GRCm39) |
S153C |
probably damaging |
Het |
Afp |
A |
T |
5: 90,652,269 (GRCm39) |
D420V |
possibly damaging |
Het |
Ak9 |
T |
A |
10: 41,246,095 (GRCm39) |
H729Q |
unknown |
Het |
Armh3 |
T |
C |
19: 45,834,554 (GRCm39) |
E618G |
possibly damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Bcr |
A |
G |
10: 74,898,124 (GRCm39) |
T423A |
probably benign |
Het |
Cc2d1b |
C |
T |
4: 108,490,422 (GRCm39) |
R825W |
probably damaging |
Het |
Ctns |
T |
C |
11: 73,083,954 (GRCm39) |
T23A |
probably benign |
Het |
Dysf |
T |
A |
6: 84,126,727 (GRCm39) |
I1344N |
probably damaging |
Het |
Elovl3 |
A |
T |
19: 46,122,939 (GRCm39) |
M172L |
probably benign |
Het |
Fbxo6 |
A |
T |
4: 148,233,979 (GRCm39) |
I39N |
probably damaging |
Het |
Filip1l |
T |
A |
16: 57,390,352 (GRCm39) |
N313K |
probably benign |
Het |
Foxp2 |
C |
A |
6: 15,437,947 (GRCm39) |
T716K |
probably damaging |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gm10645 |
A |
G |
8: 83,892,386 (GRCm39) |
|
probably benign |
Het |
Gm10735 |
T |
C |
13: 113,178,030 (GRCm39) |
|
probably benign |
Het |
Gm4847 |
A |
T |
1: 166,462,541 (GRCm39) |
D316E |
probably damaging |
Het |
Gorasp2 |
T |
C |
2: 70,521,134 (GRCm39) |
L388P |
probably damaging |
Het |
Heatr5b |
A |
G |
17: 79,081,106 (GRCm39) |
L1382P |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,341,070 (GRCm39) |
Y1729C |
probably damaging |
Het |
Ifi207 |
A |
T |
1: 173,557,112 (GRCm39) |
L542H |
probably damaging |
Het |
Ighv3-5 |
T |
A |
12: 114,226,338 (GRCm39) |
N96I |
probably damaging |
Het |
Isl1 |
T |
C |
13: 116,439,803 (GRCm39) |
T182A |
probably benign |
Het |
Jph4 |
T |
C |
14: 55,347,542 (GRCm39) |
E421G |
probably benign |
Het |
Lrrc45 |
T |
C |
11: 120,610,353 (GRCm39) |
I488T |
probably benign |
Het |
Mroh8 |
A |
G |
2: 157,075,083 (GRCm39) |
I471T |
probably benign |
Het |
Ms4a2 |
A |
T |
19: 11,594,927 (GRCm39) |
D96E |
probably damaging |
Het |
Mst1r |
T |
A |
9: 107,784,547 (GRCm39) |
N68K |
probably benign |
Het |
Myo18b |
A |
G |
5: 112,905,373 (GRCm39) |
M2075T |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,160,984 (GRCm39) |
K2229R |
probably null |
Het |
Nkx6-3 |
T |
A |
8: 23,643,987 (GRCm39) |
|
probably null |
Het |
Nlrp1a |
C |
A |
11: 71,033,164 (GRCm39) |
S10I |
probably benign |
Het |
Npas2 |
A |
T |
1: 39,375,142 (GRCm39) |
T487S |
probably benign |
Het |
Nrxn1 |
G |
C |
17: 91,395,904 (GRCm39) |
T84R |
probably benign |
Het |
Or4k2 |
C |
A |
14: 50,424,135 (GRCm39) |
D180Y |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pcdh18 |
A |
G |
3: 49,699,700 (GRCm39) |
C921R |
probably damaging |
Het |
Pcdha9 |
A |
G |
18: 37,131,531 (GRCm39) |
Y200C |
probably damaging |
Het |
Pknox1 |
A |
T |
17: 31,822,177 (GRCm39) |
R315* |
probably null |
Het |
Rasgrp1 |
C |
T |
2: 117,115,410 (GRCm39) |
W726* |
probably null |
Het |
Rassf8 |
G |
A |
6: 145,762,859 (GRCm39) |
R402H |
probably damaging |
Het |
Rev3l |
T |
A |
10: 39,698,775 (GRCm39) |
Y1091N |
probably damaging |
Het |
Riok3 |
T |
G |
18: 12,282,608 (GRCm39) |
V349G |
probably damaging |
Het |
Rps18 |
A |
T |
17: 34,174,110 (GRCm39) |
V15E |
probably damaging |
Het |
Rptor |
A |
T |
11: 119,788,268 (GRCm39) |
Y1323F |
possibly damaging |
Het |
Rspry1 |
T |
C |
8: 95,385,378 (GRCm39) |
C437R |
probably damaging |
Het |
Sema5a |
T |
A |
15: 32,686,875 (GRCm39) |
Y996N |
probably damaging |
Het |
Smarcad1 |
A |
G |
6: 65,091,313 (GRCm39) |
I1011M |
probably benign |
Het |
Supv3l1 |
A |
T |
10: 62,274,800 (GRCm39) |
M295K |
possibly damaging |
Het |
Sv2c |
T |
C |
13: 96,113,134 (GRCm39) |
D605G |
probably damaging |
Het |
Teddm1b |
G |
A |
1: 153,750,947 (GRCm39) |
W252* |
probably null |
Het |
Tes |
T |
A |
6: 17,086,195 (GRCm39) |
C29* |
probably null |
Het |
Thsd4 |
A |
G |
9: 59,890,030 (GRCm39) |
W856R |
probably damaging |
Het |
Treml4 |
A |
T |
17: 48,571,876 (GRCm39) |
D93V |
possibly damaging |
Het |
Trim66 |
T |
C |
7: 109,082,300 (GRCm39) |
T218A |
probably damaging |
Het |
Tssk5 |
T |
C |
15: 76,257,973 (GRCm39) |
D128G |
probably damaging |
Het |
Ubr3 |
T |
A |
2: 69,850,819 (GRCm39) |
W1746R |
probably damaging |
Het |
Vmn2r11 |
T |
C |
5: 109,201,434 (GRCm39) |
I357V |
probably benign |
Het |
Vmn2r87 |
A |
T |
10: 130,315,807 (GRCm39) |
D86E |
probably benign |
Het |
Zfp184 |
T |
G |
13: 22,144,377 (GRCm39) |
H694Q |
probably damaging |
Het |
Zranb3 |
A |
C |
1: 127,927,141 (GRCm39) |
F341L |
probably benign |
Het |
|
Other mutations in Ddx54 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00922:Ddx54
|
APN |
5 |
120,761,875 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01324:Ddx54
|
APN |
5 |
120,761,703 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01399:Ddx54
|
APN |
5 |
120,761,968 (GRCm39) |
nonsense |
probably null |
|
IGL02052:Ddx54
|
APN |
5 |
120,763,783 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02095:Ddx54
|
APN |
5 |
120,761,856 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02370:Ddx54
|
APN |
5 |
120,757,852 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02861:Ddx54
|
APN |
5 |
120,756,195 (GRCm39) |
splice site |
probably benign |
|
R0521:Ddx54
|
UTSW |
5 |
120,764,927 (GRCm39) |
missense |
probably benign |
0.00 |
R0556:Ddx54
|
UTSW |
5 |
120,757,719 (GRCm39) |
splice site |
probably benign |
|
R0723:Ddx54
|
UTSW |
5 |
120,761,703 (GRCm39) |
missense |
probably benign |
0.00 |
R2968:Ddx54
|
UTSW |
5 |
120,756,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R4622:Ddx54
|
UTSW |
5 |
120,764,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R4853:Ddx54
|
UTSW |
5 |
120,761,694 (GRCm39) |
missense |
probably benign |
0.12 |
R5168:Ddx54
|
UTSW |
5 |
120,755,097 (GRCm39) |
missense |
probably benign |
0.00 |
R5169:Ddx54
|
UTSW |
5 |
120,761,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R5424:Ddx54
|
UTSW |
5 |
120,757,926 (GRCm39) |
critical splice donor site |
probably null |
|
R5489:Ddx54
|
UTSW |
5 |
120,762,786 (GRCm39) |
missense |
probably benign |
|
R5956:Ddx54
|
UTSW |
5 |
120,764,432 (GRCm39) |
unclassified |
probably benign |
|
R5999:Ddx54
|
UTSW |
5 |
120,761,645 (GRCm39) |
missense |
probably benign |
0.00 |
R6413:Ddx54
|
UTSW |
5 |
120,765,127 (GRCm39) |
missense |
probably benign |
|
R6477:Ddx54
|
UTSW |
5 |
120,759,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R6702:Ddx54
|
UTSW |
5 |
120,764,568 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6783:Ddx54
|
UTSW |
5 |
120,756,779 (GRCm39) |
nonsense |
probably null |
|
R6865:Ddx54
|
UTSW |
5 |
120,759,892 (GRCm39) |
critical splice donor site |
probably null |
|
R7258:Ddx54
|
UTSW |
5 |
120,758,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Ddx54
|
UTSW |
5 |
120,764,985 (GRCm39) |
missense |
probably benign |
0.21 |
R7488:Ddx54
|
UTSW |
5 |
120,762,789 (GRCm39) |
missense |
probably benign |
|
R7887:Ddx54
|
UTSW |
5 |
120,765,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R8179:Ddx54
|
UTSW |
5 |
120,765,167 (GRCm39) |
missense |
probably benign |
|
R8303:Ddx54
|
UTSW |
5 |
120,759,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R8781:Ddx54
|
UTSW |
5 |
120,751,217 (GRCm39) |
missense |
probably benign |
0.37 |
R9451:Ddx54
|
UTSW |
5 |
120,765,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R9731:Ddx54
|
UTSW |
5 |
120,758,807 (GRCm39) |
missense |
probably benign |
0.00 |
R9732:Ddx54
|
UTSW |
5 |
120,763,911 (GRCm39) |
critical splice donor site |
probably null |
|
R9760:Ddx54
|
UTSW |
5 |
120,761,672 (GRCm39) |
missense |
probably benign |
0.05 |
|