Incidental Mutation 'IGL01554:Nudt7'
ID 90687
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Nudt7
Ensembl Gene ENSMUSG00000031767
Gene Name nudix hydrolase 7
Synonyms 1300007B24Rik, 2210404C19Rik, nudix (nucleoside diphosphate linked moiety X)-type motif 7
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # IGL01554
Quality Score
Status
Chromosome 8
Chromosomal Location 114860314-114881471 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 114874625 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000114598 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000066514] [ENSMUST00000073521] [ENSMUST00000109109] [ENSMUST00000134593] [ENSMUST00000147605]
AlphaFold Q99P30
Predicted Effect probably benign
Transcript: ENSMUST00000066514
SMART Domains Protein: ENSMUSP00000065791
Gene: ENSMUSG00000031767

DomainStartEndE-ValueType
Pfam:NUDIX 15 140 4.1e-15 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000073521
SMART Domains Protein: ENSMUSP00000073213
Gene: ENSMUSG00000031767

DomainStartEndE-ValueType
Pfam:NUDIX 38 168 4.4e-17 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000109109
SMART Domains Protein: ENSMUSP00000104737
Gene: ENSMUSG00000031767

DomainStartEndE-ValueType
Pfam:NUDIX 62 193 3.2e-18 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000134593
SMART Domains Protein: ENSMUSP00000116868
Gene: ENSMUSG00000031767

DomainStartEndE-ValueType
Pfam:NUDIX 38 146 4.2e-12 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000147605
SMART Domains Protein: ENSMUSP00000114598
Gene: ENSMUSG00000031767

DomainStartEndE-ValueType
Pfam:NUDIX 38 107 1.2e-8 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the Nudix hydrolase family. Nudix hydrolases eliminate potentially toxic nucleotide metabolites from the cell and regulate the concentrations and availability of many different nucleotide substrates, cofactors, and signaling molecules. Alternatively spliced transcript variants encoding multiple isoforms have been found for this gene. [provided by RefSeq, Aug 2011]
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8a T C 11: 109,932,992 (GRCm39) I1211V probably benign Het
Adgre4 A G 17: 56,124,090 (GRCm39) S497G probably damaging Het
Ankrd55 T C 13: 112,459,601 (GRCm39) M65T possibly damaging Het
Entrep3 A G 3: 89,092,888 (GRCm39) T257A probably damaging Het
Ermard A G 17: 15,271,855 (GRCm39) D338G possibly damaging Het
Espl1 T C 15: 102,221,660 (GRCm39) L983P probably damaging Het
Ext2 A C 2: 93,642,294 (GRCm39) L192V probably damaging Het
Fam83b T A 9: 76,409,403 (GRCm39) Y241F probably benign Het
Fbxl12 G A 9: 20,550,215 (GRCm39) P170S possibly damaging Het
Fsip2 C A 2: 82,807,622 (GRCm39) P1314T possibly damaging Het
Greb1l A G 18: 10,522,144 (GRCm39) R747G probably benign Het
Hspa1a G T 17: 35,189,500 (GRCm39) P468T probably damaging Het
Lamb1 T C 12: 31,356,976 (GRCm39) C1028R probably damaging Het
Lcn8 C T 2: 25,544,198 (GRCm39) A40V possibly damaging Het
Lmbrd2 A G 15: 9,165,906 (GRCm39) Y260C possibly damaging Het
Mex3d G T 10: 80,217,869 (GRCm39) N449K possibly damaging Het
Mgat4f A G 1: 134,317,696 (GRCm39) N156S probably damaging Het
Ncam2 A G 16: 81,309,823 (GRCm39) K438E possibly damaging Het
Nup214 C A 2: 31,941,084 (GRCm39) S39* probably null Het
Opn5 A G 17: 42,918,089 (GRCm39) S58P probably damaging Het
Or6c74 T C 10: 129,870,052 (GRCm39) S186P probably damaging Het
Or7e173 T C 9: 19,938,704 (GRCm39) I177V possibly damaging Het
Pcsk1 T A 13: 75,280,426 (GRCm39) N750K probably benign Het
Pdzrn3 T C 6: 101,127,502 (GRCm39) N1055D probably damaging Het
Phf2 T A 13: 48,959,355 (GRCm39) K884* probably null Het
Prkdc A G 16: 15,470,166 (GRCm39) N191S probably benign Het
Prpf8 A T 11: 75,386,472 (GRCm39) Q987L probably damaging Het
Prrc2c G A 1: 162,538,355 (GRCm39) P425L probably damaging Het
Rab36 T C 10: 74,886,520 (GRCm39) I166T possibly damaging Het
Rab3gap1 G T 1: 127,855,745 (GRCm39) L461F possibly damaging Het
Rnls A T 19: 33,368,499 (GRCm39) Y27N possibly damaging Het
Sncaip A T 18: 53,002,006 (GRCm39) I176F possibly damaging Het
Tagap G A 17: 8,151,780 (GRCm39) G322S probably benign Het
Tas2r130 C T 6: 131,607,046 (GRCm39) A250T probably benign Het
Tgs1 A G 4: 3,593,632 (GRCm39) S507G probably null Het
Ttn T C 2: 76,706,056 (GRCm39) probably benign Het
Zp2 T C 7: 119,737,548 (GRCm39) K246E possibly damaging Het
Other mutations in Nudt7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02549:Nudt7 APN 8 114,878,688 (GRCm39) missense probably damaging 1.00
R0525:Nudt7 UTSW 8 114,878,392 (GRCm39) critical splice acceptor site probably null
R0781:Nudt7 UTSW 8 114,862,111 (GRCm39) intron probably benign
R5167:Nudt7 UTSW 8 114,878,567 (GRCm39) nonsense probably null
R5198:Nudt7 UTSW 8 114,862,185 (GRCm39) splice site probably null
R5562:Nudt7 UTSW 8 114,874,723 (GRCm39) missense probably damaging 1.00
R5597:Nudt7 UTSW 8 114,878,506 (GRCm39) missense probably benign 0.12
R6957:Nudt7 UTSW 8 114,860,385 (GRCm39) missense probably benign 0.03
R7410:Nudt7 UTSW 8 114,860,559 (GRCm39) intron probably benign
R8245:Nudt7 UTSW 8 114,863,080 (GRCm39) missense probably damaging 0.99
R8248:Nudt7 UTSW 8 114,878,737 (GRCm39) missense probably benign 0.08
R9602:Nudt7 UTSW 8 114,878,499 (GRCm39) missense probably damaging 1.00
Posted On 2013-12-09