Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430033K04Rik |
T |
A |
5: 138,644,784 (GRCm39) |
M223K |
probably benign |
Het |
Abce1 |
T |
C |
8: 80,412,678 (GRCm39) |
T550A |
probably benign |
Het |
Acoxl |
C |
T |
2: 127,696,835 (GRCm39) |
Q28* |
probably null |
Het |
Adam8 |
T |
C |
7: 139,559,412 (GRCm39) |
K820R |
possibly damaging |
Het |
Adamts3 |
G |
T |
5: 90,009,354 (GRCm39) |
A103D |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,386,696 (GRCm39) |
V441D |
probably damaging |
Het |
Arap2 |
A |
G |
5: 62,833,293 (GRCm39) |
|
probably null |
Het |
Arhgef10l |
T |
A |
4: 140,308,222 (GRCm39) |
M44L |
probably benign |
Het |
Asb4 |
T |
C |
6: 5,398,499 (GRCm39) |
C155R |
probably damaging |
Het |
Bpifb6 |
A |
T |
2: 153,748,810 (GRCm39) |
K269* |
probably null |
Het |
Cc2d2a |
A |
T |
5: 43,840,481 (GRCm39) |
T161S |
probably benign |
Het |
Ccdc15 |
T |
A |
9: 37,255,256 (GRCm39) |
Q98L |
probably damaging |
Het |
Col19a1 |
A |
G |
1: 24,565,555 (GRCm39) |
S259P |
unknown |
Het |
Col5a2 |
A |
T |
1: 45,419,227 (GRCm39) |
D1284E |
possibly damaging |
Het |
Cyp2c70 |
T |
C |
19: 40,168,931 (GRCm39) |
T119A |
probably benign |
Het |
Dennd6b |
C |
T |
15: 89,072,890 (GRCm39) |
C188Y |
probably damaging |
Het |
Dhx8 |
T |
A |
11: 101,628,594 (GRCm39) |
|
probably null |
Het |
Dhx9 |
T |
C |
1: 153,340,768 (GRCm39) |
K624R |
probably benign |
Het |
Dpys |
C |
T |
15: 39,656,727 (GRCm39) |
V447M |
probably damaging |
Het |
E130308A19Rik |
T |
C |
4: 59,753,004 (GRCm39) |
S706P |
possibly damaging |
Het |
Esrrb |
A |
G |
12: 86,517,189 (GRCm39) |
D107G |
probably benign |
Het |
Frmd4a |
T |
C |
2: 4,577,244 (GRCm39) |
S367P |
probably damaging |
Het |
Gdi1 |
G |
A |
X: 73,350,461 (GRCm39) |
R55H |
probably benign |
Het |
Gm136 |
T |
C |
4: 34,746,628 (GRCm39) |
I128V |
probably benign |
Het |
Gm6525 |
T |
A |
3: 84,082,309 (GRCm39) |
C77S |
possibly damaging |
Het |
Grid2ip |
T |
C |
5: 143,343,346 (GRCm39) |
F14S |
probably damaging |
Het |
Hdhd3 |
C |
T |
4: 62,418,152 (GRCm39) |
R8H |
probably damaging |
Het |
Kdelr1 |
C |
A |
7: 45,523,480 (GRCm39) |
A69D |
possibly damaging |
Het |
Krtap16-3 |
T |
A |
16: 88,759,560 (GRCm39) |
Y51F |
unknown |
Het |
Lrrc40 |
T |
A |
3: 157,747,276 (GRCm39) |
N129K |
probably benign |
Het |
Man1b1 |
T |
A |
2: 25,228,196 (GRCm39) |
D155E |
probably damaging |
Het |
Mcm5 |
T |
C |
8: 75,847,529 (GRCm39) |
V442A |
probably damaging |
Het |
Mfsd14a |
C |
T |
3: 116,435,361 (GRCm39) |
A235T |
probably benign |
Het |
Mmp1a |
C |
A |
9: 7,475,938 (GRCm39) |
T401K |
probably benign |
Het |
Mpig6b |
C |
T |
17: 35,283,320 (GRCm39) |
R196Q |
unknown |
Het |
Mroh1 |
C |
T |
15: 76,292,657 (GRCm39) |
Q262* |
probably null |
Het |
Msh3 |
A |
T |
13: 92,410,619 (GRCm39) |
D656E |
possibly damaging |
Het |
Muc4 |
A |
T |
16: 32,577,465 (GRCm39) |
T252S |
|
Het |
Myh15 |
C |
T |
16: 48,997,420 (GRCm39) |
A1746V |
possibly damaging |
Het |
Myh8 |
C |
A |
11: 67,169,879 (GRCm39) |
T66K |
probably benign |
Het |
Nemf |
A |
T |
12: 69,359,241 (GRCm39) |
Y999N |
probably damaging |
Het |
Neurod1 |
T |
C |
2: 79,285,029 (GRCm39) |
N118S |
probably damaging |
Het |
Nlrp1b |
T |
A |
11: 71,109,100 (GRCm39) |
I134L |
possibly damaging |
Het |
Nsun7 |
A |
T |
5: 66,418,326 (GRCm39) |
I19F |
probably damaging |
Het |
Ofcc1 |
A |
G |
13: 40,157,442 (GRCm39) |
|
probably null |
Het |
P2rx7 |
A |
G |
5: 122,811,856 (GRCm39) |
E389G |
probably damaging |
Het |
Pam |
C |
T |
1: 97,826,072 (GRCm39) |
R194H |
probably benign |
Het |
Pcnt |
A |
G |
10: 76,220,673 (GRCm39) |
S2052P |
probably benign |
Het |
Pfkfb4 |
T |
A |
9: 108,828,222 (GRCm39) |
Y86N |
probably benign |
Het |
Plcd3 |
T |
A |
11: 102,968,689 (GRCm39) |
D334V |
probably damaging |
Het |
Ppard |
T |
C |
17: 28,517,787 (GRCm39) |
V285A |
possibly damaging |
Het |
Prune2 |
A |
G |
19: 17,097,966 (GRCm39) |
S1157G |
probably benign |
Het |
Psg21 |
A |
T |
7: 18,386,470 (GRCm39) |
L172H |
probably damaging |
Het |
Psme4 |
C |
A |
11: 30,800,661 (GRCm39) |
T1417K |
probably damaging |
Het |
Ptprc |
T |
C |
1: 138,027,423 (GRCm39) |
D336G |
probably benign |
Het |
Ralgapa1 |
A |
T |
12: 55,837,095 (GRCm39) |
|
probably null |
Het |
Rap1gap |
C |
A |
4: 137,443,393 (GRCm39) |
|
probably null |
Het |
Scap |
T |
C |
9: 110,201,310 (GRCm39) |
S100P |
possibly damaging |
Het |
Scpep1 |
T |
C |
11: 88,820,011 (GRCm39) |
I426V |
possibly damaging |
Het |
Sdk1 |
T |
C |
5: 142,082,625 (GRCm39) |
I1341T |
probably damaging |
Het |
Sfmbt2 |
T |
A |
2: 10,584,000 (GRCm39) |
Y786N |
probably benign |
Het |
Sh3tc1 |
A |
T |
5: 35,859,358 (GRCm39) |
|
probably null |
Het |
Slc5a5 |
T |
A |
8: 71,341,182 (GRCm39) |
I386F |
probably damaging |
Het |
Smarca4 |
T |
G |
9: 21,546,116 (GRCm39) |
M98R |
probably benign |
Het |
St18 |
G |
A |
1: 6,898,066 (GRCm39) |
D623N |
probably damaging |
Het |
Sult2a1 |
A |
T |
7: 13,549,978 (GRCm39) |
|
probably null |
Het |
Tgfb2 |
C |
T |
1: 186,362,834 (GRCm39) |
R330H |
probably damaging |
Het |
Thoc3 |
A |
G |
13: 54,614,119 (GRCm39) |
I168T |
probably damaging |
Het |
Tmem126a |
C |
T |
7: 90,100,062 (GRCm39) |
M160I |
possibly damaging |
Het |
Tmem200b |
C |
T |
4: 131,649,704 (GRCm39) |
P208L |
probably benign |
Het |
Tnrc6c |
T |
C |
11: 117,604,952 (GRCm39) |
V29A |
probably benign |
Het |
Tsc1 |
C |
T |
2: 28,565,744 (GRCm39) |
S465F |
probably benign |
Het |
Ttll5 |
A |
G |
12: 85,964,447 (GRCm39) |
|
probably null |
Het |
Unc13d |
G |
T |
11: 115,954,552 (GRCm39) |
L1019I |
probably damaging |
Het |
Vmn2r102 |
A |
T |
17: 19,914,670 (GRCm39) |
H745L |
probably damaging |
Het |
Wars2 |
T |
G |
3: 99,123,957 (GRCm39) |
S273A |
probably damaging |
Het |
Xrcc6 |
C |
A |
15: 81,919,955 (GRCm39) |
S498* |
probably null |
Het |
Ybx1 |
A |
T |
4: 119,140,050 (GRCm39) |
N92K |
possibly damaging |
Het |
|
Other mutations in Garin2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02123:Garin2
|
APN |
12 |
78,780,981 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02738:Garin2
|
APN |
12 |
78,780,989 (GRCm39) |
splice site |
probably benign |
|
R0760:Garin2
|
UTSW |
12 |
78,761,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R1832:Garin2
|
UTSW |
12 |
78,762,280 (GRCm39) |
unclassified |
probably benign |
|
R1833:Garin2
|
UTSW |
12 |
78,762,280 (GRCm39) |
unclassified |
probably benign |
|
R4335:Garin2
|
UTSW |
12 |
78,759,006 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4437:Garin2
|
UTSW |
12 |
78,761,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Garin2
|
UTSW |
12 |
78,761,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R5234:Garin2
|
UTSW |
12 |
78,762,045 (GRCm39) |
nonsense |
probably null |
|
R5445:Garin2
|
UTSW |
12 |
78,761,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R5587:Garin2
|
UTSW |
12 |
78,761,849 (GRCm39) |
missense |
probably damaging |
0.99 |
R5965:Garin2
|
UTSW |
12 |
78,757,080 (GRCm39) |
missense |
unknown |
|
R5993:Garin2
|
UTSW |
12 |
78,762,210 (GRCm39) |
missense |
probably damaging |
0.98 |
R6644:Garin2
|
UTSW |
12 |
78,762,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R6660:Garin2
|
UTSW |
12 |
78,762,131 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7052:Garin2
|
UTSW |
12 |
78,766,176 (GRCm39) |
missense |
probably benign |
0.00 |
R7189:Garin2
|
UTSW |
12 |
78,758,982 (GRCm39) |
missense |
probably benign |
0.22 |
R7305:Garin2
|
UTSW |
12 |
78,761,809 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7578:Garin2
|
UTSW |
12 |
78,762,275 (GRCm39) |
critical splice donor site |
probably null |
|
R7604:Garin2
|
UTSW |
12 |
78,761,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7720:Garin2
|
UTSW |
12 |
78,758,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R7786:Garin2
|
UTSW |
12 |
78,766,403 (GRCm39) |
missense |
probably benign |
0.18 |
R8008:Garin2
|
UTSW |
12 |
78,761,817 (GRCm39) |
missense |
probably benign |
0.33 |
R8680:Garin2
|
UTSW |
12 |
78,762,057 (GRCm39) |
unclassified |
probably benign |
|
R8683:Garin2
|
UTSW |
12 |
78,762,057 (GRCm39) |
unclassified |
probably benign |
|
R8792:Garin2
|
UTSW |
12 |
78,761,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R9026:Garin2
|
UTSW |
12 |
78,757,097 (GRCm39) |
missense |
probably benign |
0.00 |
R9112:Garin2
|
UTSW |
12 |
78,757,202 (GRCm39) |
critical splice donor site |
probably null |
|
R9290:Garin2
|
UTSW |
12 |
78,759,028 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9620:Garin2
|
UTSW |
12 |
78,762,077 (GRCm39) |
missense |
probably damaging |
1.00 |
U24488:Garin2
|
UTSW |
12 |
78,761,811 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1190:Garin2
|
UTSW |
12 |
78,758,994 (GRCm39) |
missense |
possibly damaging |
0.67 |
|