Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
A |
G |
10: 14,343,336 (GRCm39) |
Y204H |
probably damaging |
Het |
Akap13 |
C |
A |
7: 75,316,293 (GRCm39) |
T583K |
probably benign |
Het |
Alms1 |
C |
A |
6: 85,628,385 (GRCm39) |
Q2948K |
possibly damaging |
Het |
Auts2 |
C |
T |
5: 131,499,259 (GRCm39) |
R327Q |
probably damaging |
Het |
Card14 |
A |
C |
11: 119,235,530 (GRCm39) |
E988A |
probably damaging |
Het |
Ccl25 |
T |
C |
8: 4,398,700 (GRCm39) |
|
probably benign |
Het |
Cttnbp2nl |
A |
C |
3: 104,918,582 (GRCm39) |
V86G |
probably damaging |
Het |
Cyb5r2 |
G |
A |
7: 107,350,394 (GRCm39) |
T213I |
probably damaging |
Het |
Ear6 |
A |
G |
14: 52,091,903 (GRCm39) |
H150R |
probably damaging |
Het |
Ecm2 |
T |
C |
13: 49,671,846 (GRCm39) |
C116R |
probably damaging |
Het |
Gabrr2 |
G |
T |
4: 33,095,340 (GRCm39) |
E385* |
probably null |
Het |
Hyal5 |
T |
A |
6: 24,876,961 (GRCm39) |
V278D |
probably damaging |
Het |
Mboat1 |
T |
C |
13: 30,408,380 (GRCm39) |
L181P |
probably benign |
Het |
Mdm1 |
A |
G |
10: 117,982,523 (GRCm39) |
I53V |
probably damaging |
Het |
Mfrp |
T |
C |
9: 44,015,986 (GRCm39) |
Y368H |
probably benign |
Het |
Myo1b |
A |
G |
1: 51,833,496 (GRCm39) |
V365A |
probably damaging |
Het |
Nexmif |
G |
T |
X: 103,126,817 (GRCm39) |
H1509Q |
probably benign |
Het |
Nlrp4a |
G |
T |
7: 26,148,703 (GRCm39) |
K103N |
possibly damaging |
Het |
Optc |
T |
A |
1: 133,828,914 (GRCm39) |
I178F |
probably damaging |
Het |
Or4p22 |
T |
A |
2: 88,317,346 (GRCm39) |
I90N |
probably damaging |
Het |
Or56a42-ps1 |
G |
T |
7: 104,776,254 (GRCm39) |
L85I |
probably benign |
Het |
Pcdh15 |
T |
A |
10: 74,466,700 (GRCm39) |
N1535K |
probably benign |
Het |
Pcdhb19 |
A |
T |
18: 37,631,597 (GRCm39) |
N464I |
probably damaging |
Het |
Pcsk5 |
C |
T |
19: 17,416,406 (GRCm39) |
V1681I |
probably benign |
Het |
Phf8-ps |
T |
C |
17: 33,285,104 (GRCm39) |
E566G |
probably damaging |
Het |
Pknox1 |
T |
A |
17: 31,822,339 (GRCm39) |
|
probably benign |
Het |
Ppa2 |
T |
C |
3: 133,083,623 (GRCm39) |
F327S |
probably damaging |
Het |
Rab39b |
G |
T |
X: 74,618,309 (GRCm39) |
L174M |
probably damaging |
Het |
Reep5 |
A |
T |
18: 34,505,526 (GRCm39) |
Y48* |
probably null |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Sar1a |
T |
A |
10: 61,520,673 (GRCm39) |
|
probably benign |
Het |
Satb1 |
T |
A |
17: 52,047,095 (GRCm39) |
D740V |
probably damaging |
Het |
Sema3f |
G |
A |
9: 107,569,440 (GRCm39) |
T128I |
probably damaging |
Het |
Snx1 |
A |
T |
9: 66,005,731 (GRCm39) |
S129R |
probably damaging |
Het |
Sptb |
T |
A |
12: 76,652,313 (GRCm39) |
K1641N |
possibly damaging |
Het |
Sptbn1 |
T |
C |
11: 30,095,979 (GRCm39) |
E305G |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Taar7d |
A |
T |
10: 23,904,152 (GRCm39) |
I345F |
probably benign |
Het |
Tes |
T |
C |
6: 17,099,779 (GRCm39) |
L258P |
probably damaging |
Het |
Trav9-4 |
A |
T |
14: 53,913,817 (GRCm39) |
T24S |
possibly damaging |
Het |
Utp20 |
A |
G |
10: 88,657,739 (GRCm39) |
|
probably benign |
Het |
Vcam1 |
T |
A |
3: 115,919,646 (GRCm39) |
T207S |
probably benign |
Het |
Xkrx |
T |
C |
X: 133,051,311 (GRCm39) |
S447G |
probably benign |
Het |
Zfp318 |
T |
C |
17: 46,707,644 (GRCm39) |
L234P |
probably damaging |
Het |
|
Other mutations in Obox6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00705:Obox6
|
APN |
7 |
15,567,662 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01981:Obox6
|
APN |
7 |
15,568,846 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02066:Obox6
|
APN |
7 |
15,568,628 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02450:Obox6
|
APN |
7 |
15,567,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R0091:Obox6
|
UTSW |
7 |
15,568,364 (GRCm39) |
missense |
probably benign |
0.38 |
R0512:Obox6
|
UTSW |
7 |
15,567,874 (GRCm39) |
missense |
probably benign |
0.42 |
R1686:Obox6
|
UTSW |
7 |
15,567,750 (GRCm39) |
missense |
probably damaging |
0.99 |
R1727:Obox6
|
UTSW |
7 |
15,568,502 (GRCm39) |
missense |
probably benign |
0.04 |
R1755:Obox6
|
UTSW |
7 |
15,568,445 (GRCm39) |
missense |
probably damaging |
0.98 |
R1813:Obox6
|
UTSW |
7 |
15,568,770 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1896:Obox6
|
UTSW |
7 |
15,568,770 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2086:Obox6
|
UTSW |
7 |
15,567,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R4730:Obox6
|
UTSW |
7 |
15,568,738 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4732:Obox6
|
UTSW |
7 |
15,568,697 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4733:Obox6
|
UTSW |
7 |
15,568,697 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4790:Obox6
|
UTSW |
7 |
15,568,502 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5830:Obox6
|
UTSW |
7 |
15,568,382 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6838:Obox6
|
UTSW |
7 |
15,567,664 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7275:Obox6
|
UTSW |
7 |
15,567,805 (GRCm39) |
missense |
probably benign |
0.19 |
R7347:Obox6
|
UTSW |
7 |
15,568,571 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7485:Obox6
|
UTSW |
7 |
15,567,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R8326:Obox6
|
UTSW |
7 |
15,567,481 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8438:Obox6
|
UTSW |
7 |
15,567,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8802:Obox6
|
UTSW |
7 |
15,567,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R9274:Obox6
|
UTSW |
7 |
15,567,766 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9340:Obox6
|
UTSW |
7 |
15,567,722 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9566:Obox6
|
UTSW |
7 |
15,568,352 (GRCm39) |
missense |
|
|
R9641:Obox6
|
UTSW |
7 |
15,568,742 (GRCm39) |
nonsense |
probably null |
|
R9722:Obox6
|
UTSW |
7 |
15,568,831 (GRCm39) |
missense |
probably benign |
0.01 |
|