Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,073,708 (GRCm39) |
T1448A |
probably damaging |
Het |
Aldoart2 |
G |
T |
12: 55,612,233 (GRCm39) |
E53* |
probably null |
Het |
Ankra2 |
C |
T |
13: 98,409,891 (GRCm39) |
Q137* |
probably null |
Het |
Arpc1a |
C |
T |
5: 145,028,054 (GRCm39) |
T21I |
possibly damaging |
Het |
Arvcf |
T |
C |
16: 18,214,819 (GRCm39) |
|
probably benign |
Het |
Ash1l |
C |
A |
3: 88,914,624 (GRCm39) |
S1751R |
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,006,370 (GRCm39) |
T1675A |
probably benign |
Het |
Bsn |
C |
A |
9: 107,989,336 (GRCm39) |
G2139C |
probably damaging |
Het |
Ccdc148 |
T |
C |
2: 58,717,629 (GRCm39) |
E530G |
probably benign |
Het |
Cct3 |
A |
G |
3: 88,225,772 (GRCm39) |
D365G |
probably benign |
Het |
Chd2 |
A |
T |
7: 73,134,282 (GRCm39) |
S688R |
probably damaging |
Het |
Crispld1 |
A |
G |
1: 17,823,212 (GRCm39) |
T398A |
possibly damaging |
Het |
Ctbp2 |
A |
C |
7: 132,591,788 (GRCm39) |
V906G |
possibly damaging |
Het |
Cwf19l1 |
A |
T |
19: 44,119,938 (GRCm39) |
Y68N |
probably damaging |
Het |
Dlc1 |
T |
A |
8: 37,404,875 (GRCm39) |
M305L |
probably benign |
Het |
Dnm1l |
C |
A |
16: 16,141,883 (GRCm39) |
G288C |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,611,648 (GRCm39) |
S497P |
probably benign |
Het |
Fignl2 |
A |
T |
15: 100,952,129 (GRCm39) |
I51N |
probably damaging |
Het |
Flnb |
A |
G |
14: 7,915,290 (GRCm38) |
N1474D |
possibly damaging |
Het |
Ghrhr |
C |
T |
6: 55,357,849 (GRCm39) |
|
probably benign |
Het |
Hltf |
G |
A |
3: 20,113,254 (GRCm39) |
R9H |
probably damaging |
Het |
Hps5 |
A |
G |
7: 46,426,466 (GRCm39) |
|
probably benign |
Het |
Itpr3 |
T |
C |
17: 27,323,034 (GRCm39) |
|
probably benign |
Het |
Kansl1l |
A |
G |
1: 66,760,047 (GRCm39) |
V911A |
probably benign |
Het |
Kdm3b |
C |
T |
18: 34,957,827 (GRCm39) |
T1064I |
probably benign |
Het |
Lrriq1 |
T |
A |
10: 102,899,279 (GRCm39) |
Q1654L |
probably benign |
Het |
Ltbp1 |
A |
G |
17: 75,666,404 (GRCm39) |
T1366A |
probably damaging |
Het |
Mroh1 |
A |
G |
15: 76,330,892 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
GT |
GTT |
1: 88,183,888 (GRCm39) |
|
probably null |
Het |
Napb |
G |
A |
2: 148,540,843 (GRCm39) |
|
probably benign |
Het |
Npc1 |
G |
C |
18: 12,341,424 (GRCm39) |
P532A |
probably benign |
Het |
Nrp2 |
G |
T |
1: 62,784,536 (GRCm39) |
K228N |
possibly damaging |
Het |
Or13f5 |
T |
A |
4: 52,825,503 (GRCm39) |
Y35* |
probably null |
Het |
Plekhg1 |
A |
T |
10: 3,890,504 (GRCm39) |
K241* |
probably null |
Het |
Poln |
T |
C |
5: 34,234,432 (GRCm39) |
|
probably benign |
Het |
Ppil1 |
A |
T |
17: 29,471,230 (GRCm39) |
F92I |
probably damaging |
Het |
Ppp1r9b |
T |
G |
11: 94,892,046 (GRCm39) |
F154V |
probably damaging |
Het |
Ptchd3 |
T |
G |
11: 121,733,798 (GRCm39) |
L896R |
probably damaging |
Het |
Rev3l |
A |
G |
10: 39,700,827 (GRCm39) |
N1775D |
possibly damaging |
Het |
Rusc2 |
T |
C |
4: 43,424,100 (GRCm39) |
|
probably benign |
Het |
Selenbp2 |
T |
C |
3: 94,610,816 (GRCm39) |
V294A |
probably benign |
Het |
Slc25a48 |
T |
C |
13: 56,599,024 (GRCm39) |
V118A |
probably damaging |
Het |
Slc38a10 |
T |
C |
11: 120,025,679 (GRCm39) |
D219G |
probably damaging |
Het |
Slc39a12 |
A |
G |
2: 14,440,489 (GRCm39) |
E480G |
probably benign |
Het |
Tab2 |
C |
A |
10: 7,795,441 (GRCm39) |
R347L |
probably damaging |
Het |
Tas2r123 |
T |
C |
6: 132,824,955 (GRCm39) |
I284T |
possibly damaging |
Het |
Tnks1bp1 |
T |
A |
2: 84,892,696 (GRCm39) |
D212E |
probably benign |
Het |
Trim67 |
T |
C |
8: 125,521,307 (GRCm39) |
V223A |
probably damaging |
Het |
Ugcg |
A |
G |
4: 59,217,130 (GRCm39) |
D218G |
probably benign |
Het |
Vmn2r59 |
A |
G |
7: 41,695,725 (GRCm39) |
L229S |
probably damaging |
Het |
Zfp451 |
A |
T |
1: 33,816,706 (GRCm39) |
L198I |
probably damaging |
Het |
|
Other mutations in Slc38a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01116:Slc38a2
|
APN |
15 |
96,591,066 (GRCm39) |
splice site |
probably benign |
|
IGL01522:Slc38a2
|
APN |
15 |
96,590,936 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01679:Slc38a2
|
APN |
15 |
96,595,835 (GRCm39) |
nonsense |
probably null |
|
IGL01720:Slc38a2
|
APN |
15 |
96,589,092 (GRCm39) |
splice site |
probably benign |
|
IGL02198:Slc38a2
|
APN |
15 |
96,590,258 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02685:Slc38a2
|
APN |
15 |
96,589,306 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03211:Slc38a2
|
APN |
15 |
96,596,153 (GRCm39) |
splice site |
probably null |
|
P0014:Slc38a2
|
UTSW |
15 |
96,588,042 (GRCm39) |
missense |
probably damaging |
0.96 |
R0068:Slc38a2
|
UTSW |
15 |
96,589,173 (GRCm39) |
splice site |
probably null |
|
R0684:Slc38a2
|
UTSW |
15 |
96,593,168 (GRCm39) |
nonsense |
probably null |
|
R1537:Slc38a2
|
UTSW |
15 |
96,591,034 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1638:Slc38a2
|
UTSW |
15 |
96,590,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R1922:Slc38a2
|
UTSW |
15 |
96,589,043 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2294:Slc38a2
|
UTSW |
15 |
96,589,643 (GRCm39) |
missense |
probably benign |
|
R4672:Slc38a2
|
UTSW |
15 |
96,596,518 (GRCm39) |
missense |
probably benign |
0.00 |
R5799:Slc38a2
|
UTSW |
15 |
96,592,970 (GRCm39) |
missense |
probably benign |
0.29 |
R5878:Slc38a2
|
UTSW |
15 |
96,590,465 (GRCm39) |
missense |
probably damaging |
0.96 |
R6188:Slc38a2
|
UTSW |
15 |
96,590,397 (GRCm39) |
critical splice donor site |
probably null |
|
R7097:Slc38a2
|
UTSW |
15 |
96,591,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R7122:Slc38a2
|
UTSW |
15 |
96,591,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R7130:Slc38a2
|
UTSW |
15 |
96,589,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R7224:Slc38a2
|
UTSW |
15 |
96,589,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R7776:Slc38a2
|
UTSW |
15 |
96,588,033 (GRCm39) |
missense |
probably benign |
0.04 |
R7896:Slc38a2
|
UTSW |
15 |
96,591,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R7964:Slc38a2
|
UTSW |
15 |
96,590,453 (GRCm39) |
missense |
probably benign |
0.29 |
R8427:Slc38a2
|
UTSW |
15 |
96,590,294 (GRCm39) |
missense |
probably damaging |
0.98 |
R8487:Slc38a2
|
UTSW |
15 |
96,593,172 (GRCm39) |
nonsense |
probably null |
|
R8845:Slc38a2
|
UTSW |
15 |
96,592,900 (GRCm39) |
missense |
probably benign |
0.00 |
R9400:Slc38a2
|
UTSW |
15 |
96,591,053 (GRCm39) |
missense |
probably benign |
0.14 |
R9606:Slc38a2
|
UTSW |
15 |
96,591,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|