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) question?
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

DomainStartEndE-ValueType
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
GeneRefVarChr/LocMutationPredicted EffectZygosity
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
AlleleSourceChrCoordTypePredicted EffectPPH 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