Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
T |
A |
14: 118,771,556 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
GTT |
GT |
13: 81,553,457 (GRCm39) |
|
probably null |
Het |
Ank2 |
A |
T |
3: 126,723,471 (GRCm39) |
M952K |
probably benign |
Het |
Ccser2 |
A |
T |
14: 36,662,076 (GRCm39) |
N369K |
probably benign |
Het |
Cd300e |
A |
T |
11: 114,946,348 (GRCm39) |
Y38N |
probably damaging |
Het |
Crat |
G |
T |
2: 30,297,887 (GRCm39) |
F212L |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 31,009,807 (GRCm39) |
S3733T |
probably benign |
Het |
Fam135a |
C |
T |
1: 24,067,621 (GRCm39) |
D1083N |
probably damaging |
Het |
Fam174a |
C |
A |
1: 95,241,689 (GRCm39) |
P50T |
possibly damaging |
Het |
Fars2 |
T |
A |
13: 36,388,849 (GRCm39) |
Y113N |
probably damaging |
Het |
Fpr3 |
T |
C |
17: 18,191,341 (GRCm39) |
I204T |
possibly damaging |
Het |
Frmd3 |
T |
C |
4: 74,088,985 (GRCm39) |
V394A |
probably benign |
Het |
Garin5a |
G |
T |
7: 44,146,342 (GRCm39) |
R16L |
probably benign |
Het |
Gpbp1 |
C |
A |
13: 111,603,384 (GRCm39) |
|
probably null |
Het |
Hectd4 |
T |
A |
5: 121,441,629 (GRCm39) |
F1197Y |
probably benign |
Het |
Herc3 |
A |
G |
6: 58,851,328 (GRCm39) |
T526A |
probably benign |
Het |
Hnrnpul2 |
T |
C |
19: 8,802,350 (GRCm39) |
C406R |
probably damaging |
Het |
Hsd17b3 |
T |
C |
13: 64,210,695 (GRCm39) |
Q220R |
probably damaging |
Het |
Igf2r |
T |
A |
17: 12,935,537 (GRCm39) |
Y651F |
possibly damaging |
Het |
Kcng1 |
C |
T |
2: 168,110,768 (GRCm39) |
R132Q |
probably benign |
Het |
Kif1a |
G |
A |
1: 92,983,457 (GRCm39) |
S680F |
possibly damaging |
Het |
Kif1b |
T |
C |
4: 149,279,939 (GRCm39) |
D27G |
|
Het |
Klk12 |
A |
T |
7: 43,421,485 (GRCm39) |
T180S |
probably damaging |
Het |
Klk1b27 |
A |
G |
7: 43,705,136 (GRCm39) |
H101R |
probably damaging |
Het |
Lrp6 |
C |
A |
6: 134,518,656 (GRCm39) |
E136D |
probably benign |
Het |
Mcm9 |
T |
C |
10: 53,424,620 (GRCm39) |
I657V |
probably benign |
Het |
Med13l |
A |
C |
5: 118,866,226 (GRCm39) |
K427Q |
possibly damaging |
Het |
Nol10 |
A |
T |
12: 17,402,717 (GRCm39) |
D63V |
probably damaging |
Het |
Nudcd2 |
A |
G |
11: 40,624,862 (GRCm39) |
T24A |
probably damaging |
Het |
Nup155 |
T |
C |
15: 8,172,645 (GRCm39) |
|
probably null |
Het |
Or10al7 |
T |
C |
17: 38,366,220 (GRCm39) |
Y79C |
possibly damaging |
Het |
Or10p1 |
A |
T |
10: 129,444,005 (GRCm39) |
L115H |
probably damaging |
Het |
Or51af1 |
A |
T |
7: 103,141,800 (GRCm39) |
M95K |
probably benign |
Het |
Or5p81 |
G |
A |
7: 108,267,169 (GRCm39) |
C182Y |
probably damaging |
Het |
Or8c19-ps1 |
A |
T |
9: 38,220,581 (GRCm39) |
*163Y |
probably null |
Het |
Piezo1 |
T |
C |
8: 123,209,829 (GRCm39) |
D2314G |
unknown |
Het |
Pkhd1l1 |
T |
C |
15: 44,410,499 (GRCm39) |
F2669L |
probably damaging |
Het |
Plpp4 |
A |
G |
7: 128,981,157 (GRCm39) |
R178G |
probably damaging |
Het |
Ppp1r13l |
G |
T |
7: 19,102,695 (GRCm39) |
A37S |
possibly damaging |
Het |
Prl6a1 |
A |
G |
13: 27,499,417 (GRCm39) |
T62A |
probably benign |
Het |
Ranbp2 |
C |
A |
10: 58,315,891 (GRCm39) |
Q2204K |
possibly damaging |
Het |
Rbm48 |
T |
A |
5: 3,640,795 (GRCm39) |
M195L |
probably benign |
Het |
Rigi |
C |
A |
4: 40,205,941 (GRCm39) |
E884* |
probably null |
Het |
Shank3 |
T |
A |
15: 89,417,416 (GRCm39) |
F4L |
probably benign |
Het |
Slain2 |
T |
A |
5: 73,114,984 (GRCm39) |
V405D |
probably damaging |
Het |
Slitrk5 |
A |
C |
14: 111,918,227 (GRCm39) |
D617A |
probably benign |
Het |
Sp140 |
T |
A |
1: 85,549,603 (GRCm39) |
|
probably null |
Het |
Stk32a |
A |
G |
18: 43,443,542 (GRCm39) |
T240A |
probably benign |
Het |
Timm21 |
T |
C |
18: 84,969,489 (GRCm39) |
|
probably benign |
Het |
Tmem131 |
T |
C |
1: 36,854,538 (GRCm39) |
S904G |
probably benign |
Het |
Wdr33 |
T |
C |
18: 31,960,459 (GRCm39) |
L41P |
probably benign |
Het |
Zfp112 |
A |
C |
7: 23,825,490 (GRCm39) |
H490P |
probably benign |
Het |
Zfp455 |
T |
C |
13: 67,355,478 (GRCm39) |
Y184H |
probably damaging |
Het |
|
Other mutations in Tmem86b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00793:Tmem86b
|
APN |
7 |
4,631,756 (GRCm39) |
splice site |
probably benign |
|
IGL02055:Tmem86b
|
APN |
7 |
4,631,762 (GRCm39) |
splice site |
probably benign |
|
R1875:Tmem86b
|
UTSW |
7 |
4,632,698 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1956:Tmem86b
|
UTSW |
7 |
4,631,706 (GRCm39) |
missense |
probably benign |
0.39 |
R3756:Tmem86b
|
UTSW |
7 |
4,631,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Tmem86b
|
UTSW |
7 |
4,631,465 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6362:Tmem86b
|
UTSW |
7 |
4,632,835 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R6518:Tmem86b
|
UTSW |
7 |
4,632,608 (GRCm39) |
nonsense |
probably null |
|
R7890:Tmem86b
|
UTSW |
7 |
4,631,404 (GRCm39) |
nonsense |
probably null |
|
R8143:Tmem86b
|
UTSW |
7 |
4,631,484 (GRCm39) |
missense |
probably damaging |
0.99 |
R9186:Tmem86b
|
UTSW |
7 |
4,632,725 (GRCm39) |
missense |
probably damaging |
1.00 |
|