Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
T |
A |
15: 11,241,574 (GRCm39) |
I382N |
probably damaging |
Het |
Adamts5 |
T |
C |
16: 85,659,902 (GRCm39) |
T797A |
probably damaging |
Het |
Ahr |
A |
T |
12: 35,554,325 (GRCm39) |
V598E |
possibly damaging |
Het |
Akap10 |
A |
G |
11: 61,806,099 (GRCm39) |
S210P |
probably benign |
Het |
Asb5 |
G |
T |
8: 55,036,582 (GRCm39) |
|
probably benign |
Het |
AU041133 |
T |
C |
10: 81,974,178 (GRCm39) |
V31A |
probably damaging |
Het |
Bcar3 |
T |
C |
3: 122,306,618 (GRCm39) |
V197A |
probably benign |
Het |
Bptf |
A |
G |
11: 106,990,559 (GRCm39) |
V510A |
possibly damaging |
Het |
Ccar2 |
A |
T |
14: 70,377,517 (GRCm39) |
D712E |
probably damaging |
Het |
Cenpt |
G |
A |
8: 106,576,297 (GRCm39) |
Q85* |
probably null |
Het |
Ciita |
C |
A |
16: 10,321,736 (GRCm39) |
H98N |
probably damaging |
Het |
Cplane1 |
A |
C |
15: 8,230,826 (GRCm39) |
K1034N |
probably damaging |
Het |
Csn1s1 |
T |
A |
5: 87,815,152 (GRCm39) |
M16K |
probably benign |
Het |
Fah |
A |
G |
7: 84,242,417 (GRCm39) |
I297T |
probably damaging |
Het |
Fbxo25 |
A |
G |
8: 13,979,423 (GRCm39) |
N214D |
probably benign |
Het |
Frem3 |
A |
C |
8: 81,337,719 (GRCm39) |
D4A |
probably benign |
Het |
Gm3409 |
A |
G |
5: 146,476,334 (GRCm39) |
K162E |
probably benign |
Het |
Gxylt1 |
T |
C |
15: 93,159,656 (GRCm39) |
D148G |
possibly damaging |
Het |
Hoxd4 |
A |
T |
2: 74,558,681 (GRCm39) |
E168V |
possibly damaging |
Het |
Iqck |
T |
A |
7: 118,475,494 (GRCm39) |
H97Q |
probably benign |
Het |
Kif16b |
T |
A |
2: 142,553,789 (GRCm39) |
E1003V |
probably damaging |
Het |
Lrp1b |
G |
A |
2: 40,592,836 (GRCm39) |
P3761L |
probably benign |
Het |
Mc4r |
C |
T |
18: 66,992,597 (GRCm39) |
C172Y |
possibly damaging |
Het |
Oosp1 |
T |
A |
19: 11,664,744 (GRCm39) |
N104I |
probably damaging |
Het |
Or2z9 |
A |
G |
8: 72,854,341 (GRCm39) |
T246A |
probably benign |
Het |
Pram1 |
A |
T |
17: 33,861,117 (GRCm39) |
I513F |
probably damaging |
Het |
Pramel18 |
T |
C |
4: 101,767,125 (GRCm39) |
S125P |
probably benign |
Het |
Rasef |
A |
G |
4: 73,652,771 (GRCm39) |
S577P |
probably damaging |
Het |
Rfx8 |
T |
C |
1: 39,729,333 (GRCm39) |
D144G |
possibly damaging |
Het |
Rreb1 |
A |
C |
13: 38,113,550 (GRCm39) |
N303T |
possibly damaging |
Het |
Rrn3 |
A |
T |
16: 13,617,809 (GRCm39) |
K351* |
probably null |
Het |
Sox30 |
A |
T |
11: 45,908,035 (GRCm39) |
E734V |
probably damaging |
Het |
Spns1 |
C |
T |
7: 125,970,708 (GRCm39) |
|
probably null |
Het |
Tgfbr2 |
T |
A |
9: 115,939,370 (GRCm39) |
E177D |
probably benign |
Het |
Tnfaip8l3 |
A |
G |
9: 53,934,741 (GRCm39) |
M78T |
possibly damaging |
Het |
Vmn2r92 |
C |
T |
17: 18,387,114 (GRCm39) |
T151I |
probably damaging |
Het |
Wwc1 |
A |
G |
11: 35,806,111 (GRCm39) |
Y41H |
possibly damaging |
Het |
Zfp407 |
A |
T |
18: 84,578,922 (GRCm39) |
N730K |
probably damaging |
Het |
|
Other mutations in Ifna6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0336:Ifna6
|
UTSW |
4 |
88,746,178 (GRCm39) |
missense |
probably damaging |
0.97 |
R0521:Ifna6
|
UTSW |
4 |
88,745,887 (GRCm39) |
missense |
probably benign |
0.30 |
R2863:Ifna6
|
UTSW |
4 |
88,746,086 (GRCm39) |
missense |
probably benign |
|
R2863:Ifna6
|
UTSW |
4 |
88,746,099 (GRCm39) |
missense |
probably benign |
0.36 |
R2865:Ifna6
|
UTSW |
4 |
88,746,086 (GRCm39) |
missense |
probably benign |
|
R2865:Ifna6
|
UTSW |
4 |
88,746,099 (GRCm39) |
missense |
probably benign |
0.36 |
R4171:Ifna6
|
UTSW |
4 |
88,746,038 (GRCm39) |
missense |
probably benign |
0.06 |
R4534:Ifna6
|
UTSW |
4 |
88,746,099 (GRCm39) |
missense |
probably benign |
0.36 |
R4534:Ifna6
|
UTSW |
4 |
88,746,086 (GRCm39) |
missense |
probably benign |
|
R4992:Ifna6
|
UTSW |
4 |
88,745,777 (GRCm39) |
missense |
probably benign |
0.00 |
R5667:Ifna6
|
UTSW |
4 |
88,745,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Ifna6
|
UTSW |
4 |
88,745,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Ifna6
|
UTSW |
4 |
88,745,956 (GRCm39) |
missense |
probably benign |
0.00 |
R6487:Ifna6
|
UTSW |
4 |
88,745,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R6751:Ifna6
|
UTSW |
4 |
88,745,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R7424:Ifna6
|
UTSW |
4 |
88,746,044 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7711:Ifna6
|
UTSW |
4 |
88,745,971 (GRCm39) |
missense |
probably benign |
0.06 |
R8850:Ifna6
|
UTSW |
4 |
88,746,222 (GRCm39) |
makesense |
probably null |
|
|