Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adipor1 |
A |
G |
1: 134,358,923 (GRCm39) |
T312A |
probably benign |
Het |
Begain |
T |
G |
12: 109,000,235 (GRCm39) |
K384Q |
possibly damaging |
Het |
C2cd6 |
T |
C |
1: 59,099,763 (GRCm39) |
I393V |
probably benign |
Het |
Catsperz |
A |
G |
19: 6,902,664 (GRCm39) |
V5A |
probably benign |
Het |
Cbx1 |
T |
A |
11: 96,692,315 (GRCm39) |
F67L |
probably damaging |
Het |
Ccn2 |
A |
G |
10: 24,472,307 (GRCm39) |
S117G |
probably damaging |
Het |
Ccn3 |
T |
C |
15: 54,611,330 (GRCm39) |
V155A |
probably damaging |
Het |
Cerkl |
T |
C |
2: 79,171,630 (GRCm39) |
|
probably benign |
Het |
Cubn |
G |
T |
2: 13,292,405 (GRCm39) |
D3259E |
probably damaging |
Het |
Cyp2u1 |
A |
G |
3: 131,091,600 (GRCm39) |
Y307H |
probably damaging |
Het |
Dcaf6 |
A |
C |
1: 165,251,910 (GRCm39) |
D71E |
probably damaging |
Het |
Dclk3 |
A |
T |
9: 111,296,911 (GRCm39) |
K152* |
probably null |
Het |
Fcgbp |
G |
A |
7: 27,774,629 (GRCm39) |
D68N |
probably damaging |
Het |
Gm6576 |
A |
G |
15: 27,025,952 (GRCm39) |
|
noncoding transcript |
Het |
Has2 |
T |
C |
15: 56,531,567 (GRCm39) |
T383A |
probably damaging |
Het |
Htr1f |
T |
A |
16: 64,746,684 (GRCm39) |
K203* |
probably null |
Het |
Il36g |
A |
T |
2: 24,082,797 (GRCm39) |
I191L |
probably benign |
Het |
Iqgap3 |
T |
C |
3: 87,994,649 (GRCm39) |
I116T |
possibly damaging |
Het |
Itga1 |
C |
T |
13: 115,126,591 (GRCm39) |
|
probably null |
Het |
Kif5b |
T |
C |
18: 6,209,089 (GRCm39) |
D891G |
possibly damaging |
Het |
Krt74 |
T |
C |
15: 101,665,229 (GRCm39) |
|
noncoding transcript |
Het |
Lama3 |
A |
G |
18: 12,649,570 (GRCm39) |
K1776E |
probably damaging |
Het |
Lats1 |
T |
C |
10: 7,588,712 (GRCm39) |
S1110P |
probably benign |
Het |
Lipo3 |
T |
A |
19: 33,557,919 (GRCm39) |
K158* |
probably null |
Het |
Lrrc9 |
T |
A |
12: 72,517,108 (GRCm39) |
|
probably benign |
Het |
Met |
A |
G |
6: 17,563,726 (GRCm39) |
|
probably benign |
Het |
Mmp13 |
A |
G |
9: 7,272,955 (GRCm39) |
Y105C |
probably damaging |
Het |
Mtus1 |
T |
C |
8: 41,446,638 (GRCm39) |
E1151G |
probably damaging |
Het |
Nptx1 |
T |
C |
11: 119,435,422 (GRCm39) |
D298G |
possibly damaging |
Het |
Odad4 |
C |
T |
11: 100,460,728 (GRCm39) |
T495M |
probably damaging |
Het |
Pdlim1 |
T |
C |
19: 40,231,910 (GRCm39) |
N156S |
probably benign |
Het |
Pdzk1 |
A |
G |
3: 96,761,989 (GRCm39) |
|
probably benign |
Het |
Pex5 |
A |
G |
6: 124,375,847 (GRCm39) |
S448P |
probably benign |
Het |
Polr3e |
G |
T |
7: 120,530,186 (GRCm39) |
R124L |
probably damaging |
Het |
Ppp2r2c |
C |
T |
5: 37,109,816 (GRCm39) |
R392C |
probably damaging |
Het |
Prpf4b |
T |
C |
13: 35,073,554 (GRCm39) |
I543T |
probably benign |
Het |
Prr27 |
A |
G |
5: 87,991,302 (GRCm39) |
S305G |
possibly damaging |
Het |
Repin1 |
A |
G |
6: 48,573,407 (GRCm39) |
H56R |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,611,998 (GRCm39) |
L408H |
probably damaging |
Het |
Sbf2 |
T |
A |
7: 110,060,348 (GRCm39) |
Q205H |
probably damaging |
Het |
Sgo2b |
G |
A |
8: 64,379,863 (GRCm39) |
P990S |
probably benign |
Het |
Slc33a1 |
G |
T |
3: 63,855,562 (GRCm39) |
P361Q |
probably damaging |
Het |
Vmn1r16 |
T |
C |
6: 57,300,044 (GRCm39) |
T193A |
possibly damaging |
Het |
Vmn1r5 |
T |
A |
6: 56,962,640 (GRCm39) |
I105K |
probably damaging |
Het |
Zfp473 |
A |
T |
7: 44,387,462 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tmem98 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R2130:Tmem98
|
UTSW |
11 |
80,708,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Tmem98
|
UTSW |
11 |
80,705,158 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2365:Tmem98
|
UTSW |
11 |
80,706,511 (GRCm39) |
missense |
probably damaging |
0.98 |
R3441:Tmem98
|
UTSW |
11 |
80,705,125 (GRCm39) |
missense |
probably damaging |
0.98 |
R5181:Tmem98
|
UTSW |
11 |
80,710,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R6226:Tmem98
|
UTSW |
11 |
80,712,220 (GRCm39) |
missense |
probably benign |
0.00 |
R6502:Tmem98
|
UTSW |
11 |
80,703,461 (GRCm39) |
missense |
probably benign |
0.22 |
R7026:Tmem98
|
UTSW |
11 |
80,712,214 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7467:Tmem98
|
UTSW |
11 |
80,711,011 (GRCm39) |
splice site |
probably null |
|
R7525:Tmem98
|
UTSW |
11 |
80,708,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R7753:Tmem98
|
UTSW |
11 |
80,705,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:Tmem98
|
UTSW |
11 |
80,710,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Tmem98
|
UTSW |
11 |
80,712,135 (GRCm39) |
missense |
probably benign |
0.21 |
R9300:Tmem98
|
UTSW |
11 |
80,708,432 (GRCm39) |
missense |
probably damaging |
1.00 |
|