Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actg1 |
A |
G |
11: 120,238,517 (GRCm39) |
V160A |
possibly damaging |
Het |
Anapc5 |
A |
G |
5: 122,956,033 (GRCm39) |
*96Q |
probably null |
Het |
Ano2 |
A |
G |
6: 125,957,133 (GRCm39) |
Y634C |
probably damaging |
Het |
Appl2 |
T |
C |
10: 83,446,866 (GRCm39) |
K406R |
probably benign |
Het |
Arhgef15 |
T |
A |
11: 68,838,496 (GRCm39) |
|
probably null |
Het |
Atp13a4 |
C |
A |
16: 29,236,654 (GRCm39) |
E868D |
possibly damaging |
Het |
BC005624 |
T |
C |
2: 30,871,857 (GRCm39) |
K6E |
possibly damaging |
Het |
Cd200l2 |
A |
G |
16: 45,348,834 (GRCm39) |
Y113H |
probably damaging |
Het |
Cenpe |
T |
A |
3: 134,965,002 (GRCm39) |
I2024N |
probably damaging |
Het |
Clint1 |
T |
G |
11: 45,781,457 (GRCm39) |
Y176D |
probably damaging |
Het |
Crxos |
T |
C |
7: 15,637,625 (GRCm39) |
S65P |
possibly damaging |
Het |
Cyp4f15 |
A |
G |
17: 32,920,948 (GRCm39) |
T408A |
probably benign |
Het |
Depdc1a |
A |
G |
3: 159,229,512 (GRCm39) |
M615V |
probably damaging |
Het |
Dpysl2 |
T |
C |
14: 67,066,850 (GRCm39) |
I194M |
possibly damaging |
Het |
Dsg2 |
A |
G |
18: 20,734,431 (GRCm39) |
Y803C |
probably damaging |
Het |
Gabrb2 |
A |
T |
11: 42,517,491 (GRCm39) |
S438C |
possibly damaging |
Het |
Gjb5 |
C |
A |
4: 127,250,078 (GRCm39) |
R22L |
probably damaging |
Het |
Gls |
A |
G |
1: 52,239,012 (GRCm39) |
|
probably null |
Het |
Gm10800 |
AAGAAAACTGAAAATCAT |
A |
2: 98,497,379 (GRCm39) |
|
probably benign |
Het |
Gstt2 |
T |
A |
10: 75,667,823 (GRCm39) |
S211C |
possibly damaging |
Het |
Hck |
A |
G |
2: 152,966,130 (GRCm39) |
K35E |
probably benign |
Het |
Idh2 |
GGTCCCAG |
GG |
7: 79,748,077 (GRCm39) |
|
probably benign |
Het |
Igsf10 |
C |
T |
3: 59,227,431 (GRCm39) |
G2081R |
probably damaging |
Het |
Lrp1 |
C |
T |
10: 127,396,356 (GRCm39) |
E2403K |
probably damaging |
Het |
Or3a1 |
C |
T |
11: 74,225,932 (GRCm39) |
V42I |
probably benign |
Het |
Or6c3b |
T |
A |
10: 129,527,343 (GRCm39) |
D189V |
probably damaging |
Het |
Phlpp2 |
A |
T |
8: 110,640,202 (GRCm39) |
M456L |
probably benign |
Het |
Pnp2 |
A |
G |
14: 51,201,836 (GRCm39) |
E274G |
possibly damaging |
Het |
Pold3 |
T |
C |
7: 99,738,938 (GRCm39) |
Y303C |
probably benign |
Het |
Prr5 |
C |
T |
15: 84,578,005 (GRCm39) |
R96C |
probably damaging |
Het |
Repin1 |
A |
T |
6: 48,570,952 (GRCm39) |
D2V |
probably damaging |
Het |
Sec23b |
T |
A |
2: 144,423,983 (GRCm39) |
V544E |
probably damaging |
Het |
Slc6a17 |
A |
G |
3: 107,384,574 (GRCm39) |
F342S |
possibly damaging |
Het |
Slco4c1 |
T |
C |
1: 96,759,736 (GRCm39) |
N532S |
probably benign |
Het |
Slitrk3 |
T |
G |
3: 72,958,520 (GRCm39) |
Y84S |
probably benign |
Het |
Srcin1 |
T |
C |
11: 97,416,686 (GRCm39) |
|
probably null |
Het |
Syne2 |
C |
T |
12: 76,012,546 (GRCm39) |
A2580V |
probably benign |
Het |
Tex48 |
C |
T |
4: 63,530,160 (GRCm39) |
E20K |
probably benign |
Het |
Trip13 |
A |
T |
13: 74,081,032 (GRCm39) |
N111K |
probably benign |
Het |
Ugcg |
T |
A |
4: 59,213,896 (GRCm39) |
N159K |
probably benign |
Het |
|
Other mutations in Dtd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02182:Dtd2
|
APN |
12 |
52,046,492 (GRCm39) |
missense |
probably benign |
|
IGL02626:Dtd2
|
APN |
12 |
52,051,708 (GRCm39) |
nonsense |
probably null |
|
PIT4366001:Dtd2
|
UTSW |
12 |
52,046,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0519:Dtd2
|
UTSW |
12 |
52,051,742 (GRCm39) |
splice site |
probably benign |
|
R0741:Dtd2
|
UTSW |
12 |
52,046,455 (GRCm39) |
missense |
probably benign |
0.07 |
R2421:Dtd2
|
UTSW |
12 |
52,046,638 (GRCm39) |
missense |
probably benign |
0.25 |
R3922:Dtd2
|
UTSW |
12 |
52,051,734 (GRCm39) |
splice site |
probably null |
|
R3923:Dtd2
|
UTSW |
12 |
52,051,734 (GRCm39) |
splice site |
probably null |
|
R3924:Dtd2
|
UTSW |
12 |
52,051,734 (GRCm39) |
splice site |
probably null |
|
R5666:Dtd2
|
UTSW |
12 |
52,046,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R5670:Dtd2
|
UTSW |
12 |
52,046,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R8142:Dtd2
|
UTSW |
12 |
52,046,593 (GRCm39) |
missense |
probably damaging |
0.99 |
|