Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adarb1 |
A |
G |
10: 77,149,237 (GRCm39) |
|
probably null |
Het |
Ap1b1 |
T |
A |
11: 4,981,641 (GRCm39) |
N516K |
probably damaging |
Het |
Atp1a4 |
A |
G |
1: 172,062,044 (GRCm39) |
Y694H |
probably benign |
Het |
Bhlha9 |
T |
C |
11: 76,563,433 (GRCm39) |
V20A |
probably benign |
Het |
Ccl28 |
C |
A |
13: 120,112,398 (GRCm39) |
|
probably null |
Het |
Cdk14 |
T |
C |
5: 5,299,051 (GRCm39) |
I55V |
probably benign |
Het |
Cit |
C |
A |
5: 116,119,735 (GRCm39) |
D1246E |
probably benign |
Het |
Clp1 |
A |
G |
2: 84,554,488 (GRCm39) |
V227A |
possibly damaging |
Het |
Lima1 |
C |
T |
15: 99,699,991 (GRCm39) |
|
probably null |
Het |
Lyst |
A |
G |
13: 13,844,458 (GRCm39) |
I1883V |
probably benign |
Het |
Myh1 |
C |
T |
11: 67,111,522 (GRCm39) |
Q1654* |
probably null |
Het |
Or5d46 |
T |
C |
2: 88,170,827 (GRCm39) |
I306T |
probably benign |
Het |
Pbx3 |
G |
T |
2: 34,062,933 (GRCm39) |
T422K |
probably damaging |
Het |
Plekhg4 |
T |
C |
8: 106,107,493 (GRCm39) |
L1008P |
probably damaging |
Het |
Rbm26 |
T |
A |
14: 105,380,270 (GRCm39) |
T516S |
probably benign |
Het |
Slc25a40 |
C |
T |
5: 8,477,505 (GRCm39) |
T30I |
probably damaging |
Het |
Spata31d1c |
A |
T |
13: 65,181,005 (GRCm39) |
I35F |
possibly damaging |
Het |
Tmem18 |
A |
T |
12: 30,637,252 (GRCm39) |
R78* |
probably null |
Het |
Uggt2 |
C |
T |
14: 119,256,919 (GRCm39) |
S1105N |
probably benign |
Het |
Zfp53 |
C |
A |
17: 21,728,736 (GRCm39) |
C256* |
probably null |
Het |
|
Other mutations in Dhx29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Dhx29
|
APN |
13 |
113,101,137 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00434:Dhx29
|
APN |
13 |
113,091,759 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00659:Dhx29
|
APN |
13 |
113,103,169 (GRCm39) |
splice site |
probably benign |
|
IGL01618:Dhx29
|
APN |
13 |
113,101,756 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01777:Dhx29
|
APN |
13 |
113,067,406 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02010:Dhx29
|
APN |
13 |
113,103,168 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02125:Dhx29
|
APN |
13 |
113,091,834 (GRCm39) |
splice site |
probably benign |
|
IGL02324:Dhx29
|
APN |
13 |
113,064,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02801:Dhx29
|
APN |
13 |
113,101,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R0001:Dhx29
|
UTSW |
13 |
113,101,090 (GRCm39) |
missense |
probably damaging |
0.99 |
R0362:Dhx29
|
UTSW |
13 |
113,099,393 (GRCm39) |
missense |
probably benign |
|
R0468:Dhx29
|
UTSW |
13 |
113,099,811 (GRCm39) |
missense |
probably benign |
|
R0569:Dhx29
|
UTSW |
13 |
113,084,748 (GRCm39) |
missense |
probably benign |
0.01 |
R0714:Dhx29
|
UTSW |
13 |
113,064,499 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1460:Dhx29
|
UTSW |
13 |
113,101,744 (GRCm39) |
splice site |
probably benign |
|
R1579:Dhx29
|
UTSW |
13 |
113,072,132 (GRCm39) |
critical splice donor site |
probably null |
|
R1657:Dhx29
|
UTSW |
13 |
113,089,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R1735:Dhx29
|
UTSW |
13 |
113,081,620 (GRCm39) |
missense |
probably benign |
0.00 |
R1768:Dhx29
|
UTSW |
13 |
113,084,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Dhx29
|
UTSW |
13 |
113,084,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Dhx29
|
UTSW |
13 |
113,101,864 (GRCm39) |
missense |
probably benign |
0.06 |
R2180:Dhx29
|
UTSW |
13 |
113,099,406 (GRCm39) |
critical splice donor site |
probably null |
|
R2219:Dhx29
|
UTSW |
13 |
113,089,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R2442:Dhx29
|
UTSW |
13 |
113,083,508 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2679:Dhx29
|
UTSW |
13 |
113,083,910 (GRCm39) |
critical splice donor site |
probably null |
|
R2912:Dhx29
|
UTSW |
13 |
113,072,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R3414:Dhx29
|
UTSW |
13 |
113,083,807 (GRCm39) |
missense |
probably damaging |
0.99 |
R3931:Dhx29
|
UTSW |
13 |
113,095,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R3957:Dhx29
|
UTSW |
13 |
113,067,455 (GRCm39) |
missense |
probably benign |
|
R4065:Dhx29
|
UTSW |
13 |
113,101,276 (GRCm39) |
critical splice donor site |
probably null |
|
R4207:Dhx29
|
UTSW |
13 |
113,064,483 (GRCm39) |
missense |
probably benign |
0.01 |
R4422:Dhx29
|
UTSW |
13 |
113,083,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Dhx29
|
UTSW |
13 |
113,083,469 (GRCm39) |
missense |
unknown |
|
R4718:Dhx29
|
UTSW |
13 |
113,083,469 (GRCm39) |
missense |
unknown |
|
R5125:Dhx29
|
UTSW |
13 |
113,069,134 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5178:Dhx29
|
UTSW |
13 |
113,069,134 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5263:Dhx29
|
UTSW |
13 |
113,084,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5458:Dhx29
|
UTSW |
13 |
113,103,155 (GRCm39) |
missense |
probably benign |
0.00 |
R5469:Dhx29
|
UTSW |
13 |
113,081,073 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5541:Dhx29
|
UTSW |
13 |
113,076,908 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5573:Dhx29
|
UTSW |
13 |
113,069,749 (GRCm39) |
missense |
probably benign |
0.07 |
R5664:Dhx29
|
UTSW |
13 |
113,083,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5682:Dhx29
|
UTSW |
13 |
113,067,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Dhx29
|
UTSW |
13 |
113,090,251 (GRCm39) |
missense |
probably damaging |
0.99 |
R5917:Dhx29
|
UTSW |
13 |
113,099,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R5928:Dhx29
|
UTSW |
13 |
113,101,002 (GRCm39) |
missense |
probably benign |
0.00 |
R6115:Dhx29
|
UTSW |
13 |
113,089,335 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6144:Dhx29
|
UTSW |
13 |
113,101,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Dhx29
|
UTSW |
13 |
113,101,071 (GRCm39) |
missense |
probably benign |
0.08 |
R6233:Dhx29
|
UTSW |
13 |
113,101,071 (GRCm39) |
missense |
probably benign |
0.08 |
R6430:Dhx29
|
UTSW |
13 |
113,081,153 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6480:Dhx29
|
UTSW |
13 |
113,090,322 (GRCm39) |
nonsense |
probably null |
|
R6527:Dhx29
|
UTSW |
13 |
113,069,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R6856:Dhx29
|
UTSW |
13 |
113,089,395 (GRCm39) |
missense |
probably benign |
0.43 |
R7391:Dhx29
|
UTSW |
13 |
113,099,393 (GRCm39) |
missense |
probably benign |
|
R7555:Dhx29
|
UTSW |
13 |
113,064,176 (GRCm39) |
start gained |
probably benign |
|
R7602:Dhx29
|
UTSW |
13 |
113,081,093 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8744:Dhx29
|
UTSW |
13 |
113,089,418 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9281:Dhx29
|
UTSW |
13 |
113,078,240 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9450:Dhx29
|
UTSW |
13 |
113,083,862 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9496:Dhx29
|
UTSW |
13 |
113,089,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R9716:Dhx29
|
UTSW |
13 |
113,081,612 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Dhx29
|
UTSW |
13 |
113,092,051 (GRCm39) |
missense |
probably null |
1.00 |
|