Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
T |
C |
15: 81,949,036 (GRCm39) |
S978P |
possibly damaging |
Het |
Ago3 |
G |
A |
4: 126,262,315 (GRCm39) |
R412C |
probably damaging |
Het |
Ampd3 |
C |
T |
7: 110,399,917 (GRCm39) |
T344M |
probably damaging |
Het |
Arl10 |
G |
T |
13: 54,722,962 (GRCm39) |
V19L |
probably benign |
Het |
Aspm |
C |
T |
1: 139,407,086 (GRCm39) |
A1991V |
probably damaging |
Het |
Axdnd1 |
A |
T |
1: 156,193,221 (GRCm39) |
D655E |
probably benign |
Het |
Bdp1 |
T |
C |
13: 100,196,878 (GRCm39) |
H1169R |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,023,586 (GRCm39) |
F942L |
probably damaging |
Het |
Camk2g |
A |
G |
14: 20,789,455 (GRCm39) |
I205T |
probably damaging |
Het |
Cdh5 |
C |
A |
8: 104,852,304 (GRCm39) |
H140N |
possibly damaging |
Het |
Cog8 |
C |
A |
8: 107,782,993 (GRCm39) |
G99W |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 16,240,101 (GRCm39) |
C1104R |
probably damaging |
Het |
Dhrs7c |
G |
A |
11: 67,706,690 (GRCm39) |
V283M |
probably benign |
Het |
Emilin2 |
T |
A |
17: 71,617,219 (GRCm39) |
Q64L |
probably benign |
Het |
Fam169a |
T |
A |
13: 97,255,043 (GRCm39) |
|
probably benign |
Het |
Gvin-ps3 |
T |
C |
7: 105,681,374 (GRCm39) |
E627G |
possibly damaging |
Het |
Hmcn1 |
T |
A |
1: 150,441,135 (GRCm39) |
M5374L |
probably benign |
Het |
Hsd17b1 |
A |
T |
11: 100,969,289 (GRCm39) |
I8F |
probably damaging |
Het |
Itgae |
A |
G |
11: 73,036,395 (GRCm39) |
E1111G |
probably benign |
Het |
Kcmf1 |
A |
G |
6: 72,835,755 (GRCm39) |
|
probably null |
Het |
Kdm1b |
T |
A |
13: 47,227,231 (GRCm39) |
F574L |
probably damaging |
Het |
Lgr4 |
T |
C |
2: 109,842,738 (GRCm39) |
Y908H |
probably damaging |
Het |
Lig1 |
T |
C |
7: 13,037,722 (GRCm39) |
|
probably benign |
Het |
Ltbp3 |
C |
A |
19: 5,801,551 (GRCm39) |
C698* |
probably null |
Het |
Ncor2 |
A |
G |
5: 125,113,144 (GRCm39) |
V1216A |
possibly damaging |
Het |
Or52e3 |
A |
T |
7: 102,869,815 (GRCm39) |
T297S |
possibly damaging |
Het |
Or5b109 |
T |
C |
19: 13,212,085 (GRCm39) |
V157A |
probably benign |
Het |
Or5l13 |
T |
C |
2: 87,779,741 (GRCm39) |
T279A |
probably damaging |
Het |
Pmepa1 |
G |
A |
2: 173,069,926 (GRCm39) |
R210W |
probably damaging |
Het |
Ppp5c |
A |
G |
7: 16,740,040 (GRCm39) |
Y434H |
probably damaging |
Het |
Pwwp2b |
A |
G |
7: 138,835,366 (GRCm39) |
E269G |
probably damaging |
Het |
Rgs3 |
A |
T |
4: 62,544,124 (GRCm39) |
T299S |
probably benign |
Het |
Skint5 |
G |
A |
4: 113,403,733 (GRCm39) |
T1163I |
unknown |
Het |
Slc35f4 |
A |
G |
14: 49,543,660 (GRCm39) |
|
probably null |
Het |
Smr2l |
T |
G |
5: 88,430,413 (GRCm39) |
M103R |
probably benign |
Het |
Trmt5 |
A |
G |
12: 73,331,888 (GRCm39) |
I4T |
probably benign |
Het |
Ttc7b |
A |
G |
12: 100,321,260 (GRCm39) |
|
probably null |
Het |
Utp6 |
A |
G |
11: 79,826,831 (GRCm39) |
S582P |
possibly damaging |
Het |
Zbtb41 |
T |
C |
1: 139,351,552 (GRCm39) |
S222P |
probably damaging |
Het |
Zfp988 |
A |
C |
4: 147,417,242 (GRCm39) |
K559Q |
probably benign |
Het |
|
Other mutations in Enpp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Enpp3
|
APN |
10 |
24,663,670 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00778:Enpp3
|
APN |
10 |
24,674,160 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01147:Enpp3
|
APN |
10 |
24,650,805 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01343:Enpp3
|
APN |
10 |
24,681,820 (GRCm39) |
nonsense |
probably null |
|
IGL01642:Enpp3
|
APN |
10 |
24,674,167 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01814:Enpp3
|
APN |
10 |
24,667,923 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02083:Enpp3
|
APN |
10 |
24,652,692 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02152:Enpp3
|
APN |
10 |
24,649,900 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02186:Enpp3
|
APN |
10 |
24,667,881 (GRCm39) |
splice site |
probably benign |
|
IGL02517:Enpp3
|
APN |
10 |
24,685,746 (GRCm39) |
splice site |
probably benign |
|
IGL02956:Enpp3
|
APN |
10 |
24,650,841 (GRCm39) |
splice site |
probably benign |
|
R0017:Enpp3
|
UTSW |
10 |
24,675,051 (GRCm39) |
splice site |
probably null |
|
R0042:Enpp3
|
UTSW |
10 |
24,650,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Enpp3
|
UTSW |
10 |
24,652,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0218:Enpp3
|
UTSW |
10 |
24,652,767 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0403:Enpp3
|
UTSW |
10 |
24,680,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Enpp3
|
UTSW |
10 |
24,696,495 (GRCm39) |
missense |
probably benign |
0.00 |
R0450:Enpp3
|
UTSW |
10 |
24,652,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0510:Enpp3
|
UTSW |
10 |
24,652,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0826:Enpp3
|
UTSW |
10 |
24,671,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R1245:Enpp3
|
UTSW |
10 |
24,660,851 (GRCm39) |
splice site |
probably benign |
|
R1261:Enpp3
|
UTSW |
10 |
24,650,832 (GRCm39) |
missense |
probably damaging |
0.97 |
R1633:Enpp3
|
UTSW |
10 |
24,671,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Enpp3
|
UTSW |
10 |
24,654,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1913:Enpp3
|
UTSW |
10 |
24,652,669 (GRCm39) |
nonsense |
probably null |
|
R1966:Enpp3
|
UTSW |
10 |
24,683,389 (GRCm39) |
missense |
probably damaging |
0.99 |
R2157:Enpp3
|
UTSW |
10 |
24,652,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R2179:Enpp3
|
UTSW |
10 |
24,681,793 (GRCm39) |
missense |
probably benign |
0.00 |
R2410:Enpp3
|
UTSW |
10 |
24,650,716 (GRCm39) |
missense |
probably benign |
0.00 |
R3794:Enpp3
|
UTSW |
10 |
24,707,630 (GRCm39) |
splice site |
probably null |
|
R3896:Enpp3
|
UTSW |
10 |
24,653,847 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4334:Enpp3
|
UTSW |
10 |
24,669,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R4569:Enpp3
|
UTSW |
10 |
24,652,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Enpp3
|
UTSW |
10 |
24,649,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R4951:Enpp3
|
UTSW |
10 |
24,674,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4998:Enpp3
|
UTSW |
10 |
24,683,436 (GRCm39) |
missense |
probably benign |
0.01 |
R5045:Enpp3
|
UTSW |
10 |
24,652,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R5276:Enpp3
|
UTSW |
10 |
24,685,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R5331:Enpp3
|
UTSW |
10 |
24,684,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R5569:Enpp3
|
UTSW |
10 |
24,654,719 (GRCm39) |
missense |
probably damaging |
0.98 |
R5975:Enpp3
|
UTSW |
10 |
24,650,740 (GRCm39) |
missense |
probably benign |
0.37 |
R6117:Enpp3
|
UTSW |
10 |
24,663,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R6419:Enpp3
|
UTSW |
10 |
24,684,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R6677:Enpp3
|
UTSW |
10 |
24,653,855 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6735:Enpp3
|
UTSW |
10 |
24,683,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R6833:Enpp3
|
UTSW |
10 |
24,685,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R6999:Enpp3
|
UTSW |
10 |
24,684,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Enpp3
|
UTSW |
10 |
24,702,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R7173:Enpp3
|
UTSW |
10 |
24,649,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R7224:Enpp3
|
UTSW |
10 |
24,652,782 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7227:Enpp3
|
UTSW |
10 |
24,693,742 (GRCm39) |
missense |
unknown |
|
R7487:Enpp3
|
UTSW |
10 |
24,681,821 (GRCm39) |
missense |
probably benign |
0.02 |
R7529:Enpp3
|
UTSW |
10 |
24,674,072 (GRCm39) |
missense |
probably damaging |
0.97 |
R7583:Enpp3
|
UTSW |
10 |
24,711,990 (GRCm39) |
start codon destroyed |
probably null |
0.83 |
R7692:Enpp3
|
UTSW |
10 |
24,660,739 (GRCm39) |
nonsense |
probably null |
|
R7962:Enpp3
|
UTSW |
10 |
24,660,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Enpp3
|
UTSW |
10 |
24,654,717 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8153:Enpp3
|
UTSW |
10 |
24,685,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R8262:Enpp3
|
UTSW |
10 |
24,653,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R8305:Enpp3
|
UTSW |
10 |
24,700,827 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8393:Enpp3
|
UTSW |
10 |
24,702,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R8776:Enpp3
|
UTSW |
10 |
24,650,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R8776-TAIL:Enpp3
|
UTSW |
10 |
24,650,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Enpp3
|
UTSW |
10 |
24,696,513 (GRCm39) |
missense |
probably benign |
0.12 |
R9047:Enpp3
|
UTSW |
10 |
24,674,172 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9093:Enpp3
|
UTSW |
10 |
24,671,702 (GRCm39) |
missense |
probably benign |
0.00 |
R9117:Enpp3
|
UTSW |
10 |
24,702,078 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9194:Enpp3
|
UTSW |
10 |
24,675,092 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9224:Enpp3
|
UTSW |
10 |
24,650,716 (GRCm39) |
missense |
probably benign |
0.00 |
R9244:Enpp3
|
UTSW |
10 |
24,654,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R9387:Enpp3
|
UTSW |
10 |
24,711,990 (GRCm39) |
start codon destroyed |
probably null |
0.83 |
R9644:Enpp3
|
UTSW |
10 |
24,685,801 (GRCm39) |
missense |
probably damaging |
0.98 |
R9658:Enpp3
|
UTSW |
10 |
24,649,802 (GRCm39) |
makesense |
probably null |
|
X0026:Enpp3
|
UTSW |
10 |
24,702,140 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Enpp3
|
UTSW |
10 |
24,663,691 (GRCm39) |
missense |
probably benign |
|
|