Incidental Mutation 'IGL01697:9430015G10Rik'
ID 104319
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 9430015G10Rik
Ensembl Gene ENSMUSG00000059939
Gene Name RIKEN cDNA 9430015G10 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.066) question?
Stock # IGL01697
Quality Score
Status
Chromosome 4
Chromosomal Location 156194455-156211720 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 156203613 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000131817 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072554] [ENSMUST00000105576] [ENSMUST00000169550]
AlphaFold A2ASP7
Predicted Effect probably benign
Transcript: ENSMUST00000072554
SMART Domains Protein: ENSMUSP00000072366
Gene: ENSMUSG00000059939

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:DUF4501 23 199 1.5e-94 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000105576
SMART Domains Protein: ENSMUSP00000101201
Gene: ENSMUSG00000059939

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:DUF4501 20 51 4e-12 PFAM
Pfam:DUF4501 49 167 7.7e-69 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125786
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127332
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141802
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141882
Predicted Effect noncoding transcript
Transcript: ENSMUST00000154944
Predicted Effect probably benign
Transcript: ENSMUST00000169550
SMART Domains Protein: ENSMUSP00000131817
Gene: ENSMUSG00000059939

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:DUF4501 20 199 1e-109 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous mutant null mice show a decreased mean percentage of CD4 cells and an increased mean percentage of B cells in peripheral blood. Female mutant mice also exhibit abnormal thermal nociception, showing decreased sensitivity to acute pain during hot plate testing. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arid2 A C 15: 96,259,453 (GRCm39) probably null Het
Cadm1 C A 9: 47,761,622 (GRCm39) D435E probably damaging Het
Dagla A G 19: 10,248,562 (GRCm39) F33L probably benign Het
Edrf1 A G 7: 133,245,459 (GRCm39) H199R probably benign Het
F5 T A 1: 164,021,621 (GRCm39) N1365K probably benign Het
Gipc2 T G 3: 151,843,245 (GRCm39) I131L probably benign Het
Gpc1 C T 1: 92,786,132 (GRCm39) S507F possibly damaging Het
Grid1 A G 14: 35,031,214 (GRCm39) D269G probably benign Het
Ighv12-3 A T 12: 114,330,573 (GRCm39) M1K probably null Het
Kif5b T C 18: 6,226,871 (GRCm39) H129R possibly damaging Het
Lipo3 A T 19: 33,536,965 (GRCm39) C252S probably damaging Het
Mast4 A C 13: 102,904,401 (GRCm39) N645K probably damaging Het
Megf9 T A 4: 70,351,709 (GRCm39) T471S possibly damaging Het
Mmrn1 A G 6: 60,953,477 (GRCm39) D586G possibly damaging Het
Ninl A T 2: 150,781,867 (GRCm39) L1206Q probably damaging Het
Oog2 T A 4: 143,921,754 (GRCm39) N221K possibly damaging Het
Or13a17 T C 7: 140,271,565 (GRCm39) V249A possibly damaging Het
Or5b96 T A 19: 12,867,831 (GRCm39) T37S probably benign Het
Or6c8b C A 10: 128,882,371 (GRCm39) C187F probably damaging Het
Pik3ap1 G A 19: 41,313,018 (GRCm39) A365V probably damaging Het
Ppwd1 T C 13: 104,356,972 (GRCm39) E181G probably benign Het
Scaf11 A C 15: 96,321,504 (GRCm39) probably benign Het
Skic3 C T 13: 76,276,852 (GRCm39) L479F probably benign Het
Skint7 T A 4: 111,837,654 (GRCm39) probably benign Het
Sox14 T C 9: 99,757,716 (GRCm39) I8V probably benign Het
Spata31f3 T A 4: 42,874,163 (GRCm39) M2L probably benign Het
Stim1 A T 7: 102,075,176 (GRCm39) probably benign Het
Ttll3 T C 6: 113,376,690 (GRCm39) S357P probably benign Het
Vmn1r178 T A 7: 23,593,114 (GRCm39) I54N probably damaging Het
Zdhhc2 T C 8: 40,920,460 (GRCm39) probably benign Het
Other mutations in 9430015G10Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1162:9430015G10Rik UTSW 4 156,206,875 (GRCm39) critical splice donor site probably null
R3824:9430015G10Rik UTSW 4 156,203,607 (GRCm39) splice site probably null
R5664:9430015G10Rik UTSW 4 156,208,016 (GRCm39) missense probably damaging 1.00
R7711:9430015G10Rik UTSW 4 156,203,649 (GRCm39) missense probably damaging 0.96
R8388:9430015G10Rik UTSW 4 156,209,888 (GRCm39) missense probably damaging 1.00
Z1176:9430015G10Rik UTSW 4 156,206,468 (GRCm39) missense probably benign 0.09
Z1177:9430015G10Rik UTSW 4 156,206,834 (GRCm39) missense probably benign 0.38
Posted On 2014-01-21