Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414J04Rik |
A |
T |
11: 21,457,249 (GRCm39) |
|
noncoding transcript |
Het |
4933416I08Rik |
TCC |
TCCC |
X: 52,692,862 (GRCm39) |
|
noncoding transcript |
Het |
Afdn |
C |
T |
17: 14,066,548 (GRCm39) |
T580I |
probably benign |
Het |
Ankfy1 |
G |
T |
11: 72,603,011 (GRCm39) |
L13F |
probably damaging |
Het |
Arhgap12 |
T |
C |
18: 6,111,936 (GRCm39) |
T143A |
probably benign |
Het |
Arsi |
T |
G |
18: 61,050,424 (GRCm39) |
W436G |
probably damaging |
Het |
Bcl2l10 |
C |
T |
9: 75,255,480 (GRCm39) |
T99M |
probably damaging |
Het |
Cacna1a |
A |
G |
8: 85,285,716 (GRCm39) |
Q740R |
probably damaging |
Het |
Cacna1g |
A |
G |
11: 94,350,651 (GRCm39) |
F398S |
probably damaging |
Het |
Ccrl2 |
A |
C |
9: 110,884,725 (GRCm39) |
Y258D |
probably damaging |
Het |
Cemip |
T |
A |
7: 83,648,445 (GRCm39) |
D38V |
probably damaging |
Het |
Chd6 |
C |
G |
2: 160,807,403 (GRCm39) |
C1937S |
possibly damaging |
Het |
Cilp |
TGGG |
TGG |
9: 65,187,412 (GRCm39) |
|
probably null |
Het |
Col1a2 |
T |
G |
6: 4,521,387 (GRCm39) |
|
probably benign |
Het |
Col4a1 |
T |
C |
8: 11,290,069 (GRCm39) |
|
probably null |
Het |
Cops7b |
T |
A |
1: 86,520,056 (GRCm39) |
L69Q |
probably damaging |
Het |
Crb1 |
CG |
C |
1: 139,164,824 (GRCm39) |
|
probably null |
Het |
Ddx3y |
T |
A |
Y: 1,278,949 (GRCm39) |
D163V |
possibly damaging |
Het |
Dnajc19 |
A |
G |
3: 34,132,884 (GRCm39) |
|
probably benign |
Het |
Fhip2b |
T |
C |
14: 70,826,149 (GRCm39) |
T288A |
possibly damaging |
Het |
G2e3 |
T |
A |
12: 51,410,813 (GRCm39) |
|
probably benign |
Het |
Gkap1 |
G |
A |
13: 58,411,746 (GRCm39) |
|
probably benign |
Het |
Gm3404 |
G |
A |
5: 146,463,706 (GRCm39) |
R117Q |
probably benign |
Het |
Herc1 |
T |
TN |
9: 66,341,345 (GRCm39) |
|
probably benign |
Homo |
Homer3 |
T |
C |
8: 70,738,985 (GRCm39) |
Y115H |
probably benign |
Het |
Ighv10-1 |
T |
A |
12: 114,442,689 (GRCm39) |
M99L |
probably benign |
Het |
Kdm2b |
A |
C |
5: 123,070,737 (GRCm39) |
S398R |
probably damaging |
Het |
Lyl1 |
C |
T |
8: 85,429,300 (GRCm39) |
P3L |
possibly damaging |
Het |
Mettl25 |
G |
A |
10: 105,661,888 (GRCm39) |
Q361* |
probably null |
Het |
Mkrn2 |
T |
A |
6: 115,590,496 (GRCm39) |
I284N |
probably damaging |
Het |
Mmp14 |
T |
A |
14: 54,676,563 (GRCm39) |
N369K |
probably damaging |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Myo6 |
C |
G |
9: 80,199,749 (GRCm39) |
N1019K |
probably damaging |
Het |
Myo7a |
C |
T |
7: 97,705,974 (GRCm39) |
V1857I |
probably damaging |
Het |
Nhsl3 |
A |
G |
4: 129,116,280 (GRCm39) |
S783P |
possibly damaging |
Het |
Nktr |
T |
C |
9: 121,575,532 (GRCm39) |
S347P |
probably damaging |
Het |
Nup210 |
T |
G |
6: 91,007,172 (GRCm39) |
D548A |
probably damaging |
Het |
Nup210l |
A |
G |
3: 90,098,194 (GRCm39) |
Y1382C |
possibly damaging |
Het |
Or14c41 |
G |
A |
7: 86,235,220 (GRCm39) |
V246M |
probably damaging |
Het |
Or1e23 |
T |
A |
11: 73,407,941 (GRCm39) |
Y28F |
probably benign |
Het |
Pax8 |
T |
C |
2: 24,311,403 (GRCm39) |
|
probably benign |
Het |
Pcdhgb7 |
A |
G |
18: 37,884,935 (GRCm39) |
Y35C |
probably damaging |
Het |
Pld1 |
A |
T |
3: 28,083,316 (GRCm39) |
R145S |
probably benign |
Het |
Pom121 |
G |
A |
5: 135,410,935 (GRCm39) |
P741S |
unknown |
Het |
Rarb |
T |
C |
14: 16,436,910 (GRCm38) |
N204D |
probably damaging |
Het |
Sdc3 |
A |
G |
4: 130,548,815 (GRCm39) |
E337G |
probably benign |
Het |
Serpina9 |
T |
C |
12: 103,967,696 (GRCm39) |
K233R |
probably null |
Het |
Speer4c1 |
A |
C |
5: 15,919,214 (GRCm39) |
|
probably benign |
Het |
Sspo |
T |
A |
6: 48,427,999 (GRCm39) |
M159K |
probably benign |
Het |
Stxbp4 |
C |
A |
11: 90,498,010 (GRCm39) |
R96S |
probably damaging |
Het |
Tg |
A |
C |
15: 66,612,567 (GRCm39) |
E375A |
probably damaging |
Het |
Tmem176b |
A |
G |
6: 48,815,287 (GRCm39) |
V2A |
probably benign |
Het |
Toporsl |
G |
A |
4: 52,610,281 (GRCm39) |
C58Y |
probably damaging |
Het |
Ugt1a1 |
AT |
A |
1: 88,140,093 (GRCm39) |
|
probably null |
Het |
Vav3 |
T |
C |
3: 109,470,410 (GRCm39) |
|
probably benign |
Het |
Zfp180 |
T |
A |
7: 23,804,170 (GRCm39) |
D196E |
possibly damaging |
Het |
Zfp407 |
C |
T |
18: 84,228,080 (GRCm39) |
S1843N |
probably damaging |
Het |
|
Other mutations in Gimap7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00584:Gimap7
|
APN |
6 |
48,700,667 (GRCm39) |
nonsense |
probably null |
|
IGL01508:Gimap7
|
APN |
6 |
48,701,230 (GRCm39) |
missense |
probably damaging |
0.98 |
R0848:Gimap7
|
UTSW |
6 |
48,700,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R1590:Gimap7
|
UTSW |
6 |
48,700,953 (GRCm39) |
missense |
probably damaging |
0.96 |
R1603:Gimap7
|
UTSW |
6 |
48,700,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Gimap7
|
UTSW |
6 |
48,700,449 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1982:Gimap7
|
UTSW |
6 |
48,701,175 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2471:Gimap7
|
UTSW |
6 |
48,700,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R3888:Gimap7
|
UTSW |
6 |
48,700,779 (GRCm39) |
missense |
probably benign |
0.05 |
R5512:Gimap7
|
UTSW |
6 |
48,700,530 (GRCm39) |
missense |
probably benign |
0.07 |
R6378:Gimap7
|
UTSW |
6 |
48,701,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Gimap7
|
UTSW |
6 |
48,700,791 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7700:Gimap7
|
UTSW |
6 |
48,700,791 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9172:Gimap7
|
UTSW |
6 |
48,700,761 (GRCm39) |
nonsense |
probably null |
|
R9320:Gimap7
|
UTSW |
6 |
48,701,260 (GRCm39) |
missense |
probably benign |
0.16 |
R9627:Gimap7
|
UTSW |
6 |
48,700,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R9789:Gimap7
|
UTSW |
6 |
48,700,470 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Gimap7
|
UTSW |
6 |
48,701,087 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Gimap7
|
UTSW |
6 |
48,701,255 (GRCm39) |
frame shift |
probably null |
|
|