Incidental Mutation 'IGL02286:Nt5dc3'
ID |
289993 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Nt5dc3
|
Ensembl Gene |
ENSMUSG00000054027 |
Gene Name |
5'-nucleotidase domain containing 3 |
Synonyms |
Gnn, C630002B14Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL02286
|
Quality Score |
|
Status
|
|
Chromosome |
10 |
Chromosomal Location |
86614869-86674253 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
G to A
at 86656644 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099396]
|
AlphaFold |
Q3UHB1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000099396
|
SMART Domains |
Protein: ENSMUSP00000096994 Gene: ENSMUSG00000054027
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
25 |
N/A |
INTRINSIC |
Pfam:5_nucleotid
|
83 |
526 |
1.8e-159 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000218792
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000218802
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 15 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Dab1 |
A |
G |
4: 104,537,267 (GRCm39) |
T187A |
probably damaging |
Het |
Eno2 |
C |
T |
6: 124,743,543 (GRCm39) |
R132H |
probably damaging |
Het |
Fgb |
T |
G |
3: 82,950,633 (GRCm39) |
M374L |
probably benign |
Het |
Fgf21 |
T |
C |
7: 45,264,561 (GRCm39) |
D57G |
possibly damaging |
Het |
Gcgr |
A |
G |
11: 120,428,757 (GRCm39) |
T354A |
probably damaging |
Het |
Gm12790 |
T |
C |
4: 101,824,918 (GRCm39) |
T117A |
probably benign |
Het |
Myo18a |
C |
T |
11: 77,668,811 (GRCm39) |
Q224* |
probably null |
Het |
N4bp2 |
A |
G |
5: 65,960,895 (GRCm39) |
Y522C |
probably damaging |
Het |
Or12e13 |
G |
A |
2: 87,663,592 (GRCm39) |
A70T |
probably damaging |
Het |
Ppp1r3b |
C |
T |
8: 35,851,515 (GRCm39) |
A118V |
probably benign |
Het |
Slc37a2 |
C |
T |
9: 37,146,455 (GRCm39) |
A351T |
probably damaging |
Het |
Tlr11 |
T |
C |
14: 50,598,328 (GRCm39) |
F105L |
possibly damaging |
Het |
Vwa8 |
G |
A |
14: 79,184,713 (GRCm39) |
|
probably null |
Het |
Xrra1 |
A |
T |
7: 99,563,434 (GRCm39) |
I474F |
possibly damaging |
Het |
Zfp790 |
A |
G |
7: 29,529,160 (GRCm39) |
K615R |
possibly damaging |
Het |
|
Other mutations in Nt5dc3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Nt5dc3
|
APN |
10 |
86,669,838 (GRCm39) |
splice site |
probably null |
|
IGL00767:Nt5dc3
|
APN |
10 |
86,656,137 (GRCm39) |
splice site |
probably benign |
|
IGL01318:Nt5dc3
|
APN |
10 |
86,661,089 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01369:Nt5dc3
|
APN |
10 |
86,656,139 (GRCm39) |
splice site |
probably benign |
|
IGL01376:Nt5dc3
|
APN |
10 |
86,670,028 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01568:Nt5dc3
|
APN |
10 |
86,669,802 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02692:Nt5dc3
|
APN |
10 |
86,640,642 (GRCm39) |
splice site |
probably null |
|
R0372:Nt5dc3
|
UTSW |
10 |
86,661,155 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0714:Nt5dc3
|
UTSW |
10 |
86,648,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R1755:Nt5dc3
|
UTSW |
10 |
86,660,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Nt5dc3
|
UTSW |
10 |
86,669,926 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1888:Nt5dc3
|
UTSW |
10 |
86,669,926 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3973:Nt5dc3
|
UTSW |
10 |
86,660,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R4097:Nt5dc3
|
UTSW |
10 |
86,669,820 (GRCm39) |
missense |
probably benign |
0.01 |
R4871:Nt5dc3
|
UTSW |
10 |
86,652,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5286:Nt5dc3
|
UTSW |
10 |
86,640,656 (GRCm39) |
missense |
probably benign |
0.08 |
R5482:Nt5dc3
|
UTSW |
10 |
86,647,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R5530:Nt5dc3
|
UTSW |
10 |
86,656,857 (GRCm39) |
missense |
probably damaging |
0.99 |
R5861:Nt5dc3
|
UTSW |
10 |
86,651,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Nt5dc3
|
UTSW |
10 |
86,647,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R8251:Nt5dc3
|
UTSW |
10 |
86,656,091 (GRCm39) |
missense |
probably damaging |
0.98 |
R8734:Nt5dc3
|
UTSW |
10 |
86,669,863 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
Posted On |
2015-04-16 |