Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
T |
C |
1: 179,581,078 (GRCm39) |
N1708S |
probably benign |
Het |
Ahnak2 |
C |
T |
12: 112,748,991 (GRCm39) |
M285I |
probably benign |
Het |
Angptl1 |
A |
T |
1: 156,684,806 (GRCm39) |
D325V |
probably damaging |
Het |
Anln |
A |
T |
9: 22,262,298 (GRCm39) |
V931E |
probably damaging |
Het |
Ascc3 |
C |
T |
10: 50,526,021 (GRCm39) |
R578* |
probably null |
Het |
B3galnt2 |
C |
T |
13: 14,150,161 (GRCm39) |
A168V |
probably benign |
Het |
Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
Cd22 |
T |
C |
7: 30,577,182 (GRCm39) |
I42V |
probably benign |
Het |
Cyp2b19 |
C |
T |
7: 26,466,280 (GRCm39) |
T361I |
probably benign |
Het |
D930048N14Rik |
C |
A |
11: 51,544,576 (GRCm39) |
|
probably benign |
Het |
Ehf |
T |
C |
2: 103,113,928 (GRCm39) |
N23S |
probably damaging |
Het |
Eif2ak3 |
T |
A |
6: 70,860,699 (GRCm39) |
I425N |
probably damaging |
Het |
Fbxo4 |
C |
T |
15: 4,005,305 (GRCm39) |
V192M |
probably damaging |
Het |
Gm21190 |
T |
C |
5: 15,730,849 (GRCm39) |
Q169R |
possibly damaging |
Het |
Gngt1 |
A |
G |
6: 3,994,246 (GRCm39) |
D8G |
possibly damaging |
Het |
Ift140 |
T |
C |
17: 25,251,147 (GRCm39) |
L31P |
probably damaging |
Het |
Keg1 |
C |
T |
19: 12,686,994 (GRCm39) |
Q8* |
probably null |
Het |
Lama3 |
T |
A |
18: 12,682,283 (GRCm39) |
M1083K |
possibly damaging |
Het |
Lrp1b |
A |
T |
2: 40,527,876 (GRCm39) |
Y68* |
probably null |
Het |
Lyz3 |
A |
G |
10: 117,071,534 (GRCm39) |
V115A |
probably benign |
Het |
Mctp1 |
A |
T |
13: 77,178,055 (GRCm39) |
K947N |
probably damaging |
Het |
Muc5ac |
A |
G |
7: 141,357,065 (GRCm39) |
Y1113C |
probably damaging |
Het |
Myb |
C |
T |
10: 21,028,844 (GRCm39) |
V85M |
probably damaging |
Het |
Npas2 |
T |
G |
1: 39,401,029 (GRCm39) |
S798A |
unknown |
Het |
Or13a21 |
G |
T |
7: 139,999,517 (GRCm39) |
H56Q |
probably damaging |
Het |
Orc2 |
A |
G |
1: 58,532,818 (GRCm39) |
|
probably null |
Het |
Parpbp |
T |
C |
10: 87,946,175 (GRCm39) |
T415A |
probably benign |
Het |
Pcdha3 |
T |
C |
18: 37,080,875 (GRCm39) |
V539A |
probably benign |
Het |
Piwil4 |
T |
C |
9: 14,621,230 (GRCm39) |
E601G |
probably damaging |
Het |
Pramel51 |
A |
T |
12: 88,142,763 (GRCm39) |
L285Q |
possibly damaging |
Het |
Ptpn3 |
T |
A |
4: 57,205,905 (GRCm39) |
I696F |
probably damaging |
Het |
Sec63 |
C |
T |
10: 42,692,379 (GRCm39) |
Q617* |
probably null |
Het |
Sgip1 |
C |
A |
4: 102,762,765 (GRCm39) |
|
probably benign |
Het |
Tktl2 |
T |
C |
8: 66,965,381 (GRCm39) |
V313A |
probably benign |
Het |
Tmem63b |
C |
A |
17: 45,978,634 (GRCm39) |
R325L |
probably benign |
Het |
Ttn |
C |
T |
2: 76,539,700 (GRCm39) |
G34429R |
probably damaging |
Het |
|
Other mutations in Sirpd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Sirpd
|
APN |
3 |
15,397,205 (GRCm39) |
splice site |
probably null |
|
IGL03104:Sirpd
|
APN |
3 |
15,397,283 (GRCm39) |
utr 5 prime |
probably benign |
|
R0239:Sirpd
|
UTSW |
3 |
15,361,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Sirpd
|
UTSW |
3 |
15,361,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R0771:Sirpd
|
UTSW |
3 |
15,385,506 (GRCm39) |
missense |
probably benign |
0.33 |
R1452:Sirpd
|
UTSW |
3 |
15,397,212 (GRCm39) |
missense |
unknown |
|
R1541:Sirpd
|
UTSW |
3 |
15,385,744 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5124:Sirpd
|
UTSW |
3 |
15,385,639 (GRCm39) |
nonsense |
probably null |
|
R5328:Sirpd
|
UTSW |
3 |
15,397,234 (GRCm39) |
missense |
unknown |
|
R5991:Sirpd
|
UTSW |
3 |
15,385,818 (GRCm39) |
missense |
probably benign |
0.00 |
R6333:Sirpd
|
UTSW |
3 |
15,385,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R7270:Sirpd
|
UTSW |
3 |
15,385,704 (GRCm39) |
missense |
probably benign |
0.18 |
R7615:Sirpd
|
UTSW |
3 |
15,385,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R7799:Sirpd
|
UTSW |
3 |
15,361,723 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8536:Sirpd
|
UTSW |
3 |
15,361,614 (GRCm39) |
makesense |
probably null |
|
R9777:Sirpd
|
UTSW |
3 |
15,385,813 (GRCm39) |
nonsense |
probably null |
|
|