Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503E14Rik |
G |
A |
14: 44,401,391 (GRCm39) |
H152Y |
probably benign |
Het |
Abca1 |
T |
C |
4: 53,086,132 (GRCm39) |
D457G |
probably benign |
Het |
Atp8a1 |
T |
G |
5: 67,817,246 (GRCm39) |
K913N |
possibly damaging |
Het |
Cd180 |
G |
A |
13: 102,841,917 (GRCm39) |
S321N |
probably benign |
Het |
Cdc14b |
T |
C |
13: 64,363,470 (GRCm39) |
N264D |
probably damaging |
Het |
Cenpf |
A |
T |
1: 189,387,109 (GRCm39) |
C1724S |
probably benign |
Het |
Chil4 |
A |
G |
3: 106,109,113 (GRCm39) |
S397P |
probably benign |
Het |
Clpb |
C |
T |
7: 101,427,815 (GRCm39) |
R387* |
probably null |
Het |
Csgalnact2 |
A |
T |
6: 118,103,233 (GRCm39) |
M1K |
probably null |
Het |
Gtf3c1 |
G |
A |
7: 125,266,546 (GRCm39) |
R967W |
probably damaging |
Het |
Hnrnpr |
T |
A |
4: 136,066,856 (GRCm39) |
D472E |
unknown |
Het |
Klhl28 |
A |
T |
12: 64,996,840 (GRCm39) |
D500E |
probably damaging |
Het |
Lmo7 |
C |
T |
14: 102,148,321 (GRCm39) |
|
probably benign |
Het |
Mphosph8 |
A |
G |
14: 56,911,900 (GRCm39) |
I308V |
probably benign |
Het |
Myo6 |
T |
A |
9: 80,190,868 (GRCm39) |
|
probably null |
Het |
Nsmaf |
C |
T |
4: 6,435,056 (GRCm39) |
|
probably null |
Het |
Padi6 |
T |
A |
4: 140,454,934 (GRCm39) |
I668L |
possibly damaging |
Het |
Pigw |
A |
G |
11: 84,768,150 (GRCm39) |
I393T |
possibly damaging |
Het |
Prg3 |
G |
A |
2: 84,824,076 (GRCm39) |
C212Y |
probably damaging |
Het |
Pwp1 |
T |
C |
10: 85,715,752 (GRCm39) |
V267A |
probably benign |
Het |
Raver2 |
C |
A |
4: 100,953,468 (GRCm39) |
Q79K |
probably benign |
Het |
Sdr9c7 |
T |
C |
10: 127,745,697 (GRCm39) |
S270P |
probably damaging |
Het |
Sfmbt2 |
A |
G |
2: 10,406,818 (GRCm39) |
E39G |
probably damaging |
Het |
Strada |
A |
G |
11: 106,061,976 (GRCm39) |
|
probably benign |
Het |
Xrn1 |
T |
C |
9: 95,855,500 (GRCm39) |
|
probably benign |
Het |
Zic3 |
A |
G |
X: 57,079,779 (GRCm39) |
Y424C |
probably damaging |
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 |
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 |
R2380:Enpp3
|
UTSW |
10 |
24,652,770 (GRCm39) |
missense |
probably benign |
|
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 |
|
|