Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accs |
T |
G |
2: 93,676,121 (GRCm39) |
K85Q |
probably damaging |
Het |
Acmsd |
A |
T |
1: 127,676,822 (GRCm39) |
T116S |
possibly damaging |
Het |
Agrn |
T |
A |
4: 156,257,264 (GRCm39) |
K1189* |
probably null |
Het |
Alk |
T |
C |
17: 72,292,455 (GRCm39) |
R508G |
probably benign |
Het |
Arhgap23 |
T |
A |
11: 97,382,005 (GRCm39) |
Y1123N |
probably damaging |
Het |
Arl6ip5 |
G |
T |
6: 97,209,365 (GRCm39) |
M133I |
probably benign |
Het |
Axin2 |
G |
A |
11: 108,833,772 (GRCm39) |
G573D |
possibly damaging |
Het |
B4galt2 |
A |
G |
4: 117,734,075 (GRCm39) |
|
probably null |
Het |
Baz2b |
G |
T |
2: 59,807,718 (GRCm39) |
D180E |
possibly damaging |
Het |
Cct7 |
A |
T |
6: 85,436,131 (GRCm39) |
D14V |
probably damaging |
Het |
Cd55 |
T |
A |
1: 130,377,149 (GRCm39) |
|
probably benign |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cdh2 |
C |
T |
18: 16,762,537 (GRCm39) |
R526Q |
probably benign |
Het |
Chi3l1 |
A |
C |
1: 134,116,981 (GRCm39) |
E315A |
probably damaging |
Het |
Cmya5 |
A |
G |
13: 93,233,163 (GRCm39) |
S642P |
probably benign |
Het |
Cpm |
C |
A |
10: 117,465,756 (GRCm39) |
T43K |
probably damaging |
Het |
Cracd |
T |
C |
5: 77,006,306 (GRCm39) |
V889A |
unknown |
Het |
Cyp8b1 |
A |
T |
9: 121,744,453 (GRCm39) |
V293D |
probably benign |
Het |
Dock1 |
T |
G |
7: 134,765,082 (GRCm39) |
D1691E |
probably benign |
Het |
Fasn |
T |
C |
11: 120,700,659 (GRCm39) |
D2120G |
probably benign |
Het |
Gal3st4 |
T |
C |
5: 138,263,679 (GRCm39) |
K440R |
probably benign |
Het |
Gfpt1 |
A |
T |
6: 87,033,164 (GRCm39) |
K130* |
probably null |
Het |
Gpr26 |
T |
C |
7: 131,576,121 (GRCm39) |
|
probably null |
Het |
Htr2a |
A |
T |
14: 74,882,502 (GRCm39) |
I163F |
probably damaging |
Het |
Ift70a2 |
T |
C |
2: 75,806,682 (GRCm39) |
E610G |
probably benign |
Het |
Insrr |
A |
G |
3: 87,716,879 (GRCm39) |
D673G |
probably benign |
Het |
Ipo8 |
G |
T |
6: 148,692,979 (GRCm39) |
C636* |
probably null |
Het |
Kirrel1 |
C |
A |
3: 86,997,780 (GRCm39) |
E248* |
probably null |
Het |
Lrp6 |
A |
G |
6: 134,461,228 (GRCm39) |
V743A |
probably damaging |
Het |
Lrrc45 |
C |
A |
11: 120,609,144 (GRCm39) |
S374R |
probably benign |
Het |
Map3k9 |
G |
A |
12: 81,771,516 (GRCm39) |
P714S |
probably benign |
Het |
Mrgprb8 |
T |
A |
7: 48,039,121 (GRCm39) |
L264Q |
possibly damaging |
Het |
Mroh4 |
C |
A |
15: 74,478,000 (GRCm39) |
W902L |
probably benign |
Het |
Nfat5 |
T |
A |
8: 108,085,367 (GRCm39) |
D535E |
probably damaging |
Het |
Nfatc3 |
T |
C |
8: 106,834,817 (GRCm39) |
V713A |
probably benign |
Het |
Npc1l1 |
C |
T |
11: 6,164,684 (GRCm39) |
V1122M |
possibly damaging |
Het |
Nsg2 |
A |
G |
11: 32,005,011 (GRCm39) |
|
probably null |
Het |
Or4c15 |
C |
A |
2: 88,759,792 (GRCm39) |
R289L |
probably damaging |
Het |
Or8s10 |
T |
A |
15: 98,335,660 (GRCm39) |
F103L |
probably benign |
Het |
Pax9 |
A |
T |
12: 56,756,604 (GRCm39) |
H314L |
possibly damaging |
Het |
Phf21a |
A |
T |
2: 92,190,592 (GRCm39) |
I584F |
probably damaging |
Het |
Pip5k1c |
A |
G |
10: 81,149,296 (GRCm39) |
E536G |
probably benign |
Het |
Plekhm3 |
A |
G |
1: 64,834,276 (GRCm39) |
S736P |
probably damaging |
Het |
Ppp3cb |
T |
A |
14: 20,573,645 (GRCm39) |
|
probably null |
Het |
Prdm9 |
A |
T |
17: 15,783,522 (GRCm39) |
S14R |
probably benign |
Het |
Proc |
A |
G |
18: 32,267,925 (GRCm39) |
I71T |
probably damaging |
Het |
Prom2 |
T |
A |
2: 127,380,577 (GRCm39) |
|
probably benign |
Het |
Psd |
T |
C |
19: 46,307,984 (GRCm39) |
T675A |
probably benign |
Het |
Rnf215 |
G |
T |
11: 4,090,305 (GRCm39) |
R341L |
probably damaging |
Het |
Ryr3 |
A |
G |
2: 112,732,921 (GRCm39) |
|
probably null |
Het |
Sh2d7 |
C |
A |
9: 54,448,105 (GRCm39) |
T42N |
probably benign |
Het |
Sh3glb2 |
C |
T |
2: 30,236,368 (GRCm39) |
G279D |
probably benign |
Het |
Slc25a46 |
A |
G |
18: 31,738,868 (GRCm39) |
|
probably benign |
Het |
Snx17 |
T |
C |
5: 31,354,390 (GRCm39) |
S167P |
probably damaging |
Het |
Snx19 |
A |
G |
9: 30,343,556 (GRCm39) |
N572S |
possibly damaging |
Het |
Sptbn4 |
G |
A |
7: 27,067,104 (GRCm39) |
R1937C |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Srsf11 |
T |
C |
3: 157,722,068 (GRCm39) |
|
probably benign |
Het |
Taar7b |
A |
T |
10: 23,876,581 (GRCm39) |
M249L |
probably benign |
Het |
Tle6 |
G |
A |
10: 81,435,898 (GRCm39) |
Q6* |
probably null |
Het |
Twnk |
G |
T |
19: 44,996,557 (GRCm39) |
R330L |
probably damaging |
Het |
Unc13a |
C |
A |
8: 72,108,949 (GRCm39) |
|
probably benign |
Het |
Vmn2r107 |
A |
G |
17: 20,577,006 (GRCm39) |
T335A |
possibly damaging |
Het |
Wdtc1 |
A |
T |
4: 133,024,789 (GRCm39) |
S469R |
possibly damaging |
Het |
Ypel1 |
A |
G |
16: 16,921,466 (GRCm39) |
Y73H |
probably benign |
Het |
Zfp382 |
A |
T |
7: 29,833,162 (GRCm39) |
Y271F |
probably benign |
Het |
|
Other mutations in Btnl6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02127:Btnl6
|
APN |
17 |
34,733,017 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02501:Btnl6
|
APN |
17 |
34,734,648 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02539:Btnl6
|
APN |
17 |
34,727,288 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02629:Btnl6
|
APN |
17 |
34,733,442 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03366:Btnl6
|
APN |
17 |
34,727,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Btnl6
|
UTSW |
17 |
34,734,505 (GRCm39) |
nonsense |
probably null |
|
R0025:Btnl6
|
UTSW |
17 |
34,733,273 (GRCm39) |
missense |
probably benign |
0.02 |
R0144:Btnl6
|
UTSW |
17 |
34,732,994 (GRCm39) |
missense |
probably benign |
0.29 |
R0255:Btnl6
|
UTSW |
17 |
34,727,477 (GRCm39) |
missense |
probably benign |
0.01 |
R1474:Btnl6
|
UTSW |
17 |
34,732,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1757:Btnl6
|
UTSW |
17 |
34,733,062 (GRCm39) |
missense |
probably benign |
0.09 |
R1838:Btnl6
|
UTSW |
17 |
34,734,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R2149:Btnl6
|
UTSW |
17 |
34,733,321 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2994:Btnl6
|
UTSW |
17 |
34,734,498 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3441:Btnl6
|
UTSW |
17 |
34,727,292 (GRCm39) |
missense |
probably benign |
0.06 |
R3809:Btnl6
|
UTSW |
17 |
34,727,202 (GRCm39) |
missense |
probably benign |
0.00 |
R3936:Btnl6
|
UTSW |
17 |
34,736,316 (GRCm39) |
missense |
probably benign |
|
R4462:Btnl6
|
UTSW |
17 |
34,727,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R4604:Btnl6
|
UTSW |
17 |
34,727,435 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4618:Btnl6
|
UTSW |
17 |
34,733,120 (GRCm39) |
missense |
probably damaging |
0.98 |
R4832:Btnl6
|
UTSW |
17 |
34,732,966 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5369:Btnl6
|
UTSW |
17 |
34,726,959 (GRCm39) |
nonsense |
probably null |
|
R5422:Btnl6
|
UTSW |
17 |
34,733,081 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6046:Btnl6
|
UTSW |
17 |
34,727,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Btnl6
|
UTSW |
17 |
34,734,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R6385:Btnl6
|
UTSW |
17 |
34,727,343 (GRCm39) |
missense |
probably benign |
0.01 |
R8213:Btnl6
|
UTSW |
17 |
34,727,857 (GRCm39) |
splice site |
probably null |
|
R8676:Btnl6
|
UTSW |
17 |
34,727,043 (GRCm39) |
missense |
probably benign |
0.00 |
R8895:Btnl6
|
UTSW |
17 |
34,734,391 (GRCm39) |
missense |
probably benign |
0.01 |
R9654:Btnl6
|
UTSW |
17 |
34,733,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Btnl6
|
UTSW |
17 |
34,732,635 (GRCm39) |
missense |
probably benign |
|
|