Incidental Mutation 'IGL00741:1810009J06Rik'
ID 8430
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1810009J06Rik
Ensembl Gene ENSMUSG00000094808
Gene Name RIKEN cDNA 1810009J06 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.162) question?
Stock # IGL00741
Quality Score
Status
Chromosome 6
Chromosomal Location 40941706-40945361 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 40941768 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000075935 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076638]
AlphaFold Q9CPN7
Predicted Effect probably benign
Transcript: ENSMUST00000076638
SMART Domains Protein: ENSMUSP00000075935
Gene: ENSMUSG00000094808

DomainStartEndE-ValueType
Tryp_SPc 23 240 4.94e-97 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 12 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc9 A C 6: 142,632,956 (GRCm39) V262G probably benign Het
Adamtsl1 T C 4: 86,195,185 (GRCm39) V534A probably damaging Het
Arhgap31 A G 16: 38,423,363 (GRCm39) V901A probably damaging Het
C3 A G 17: 57,527,206 (GRCm39) probably benign Het
Chd7 T C 4: 8,839,454 (GRCm39) V1330A probably damaging Het
Dop1a A G 9: 86,404,859 (GRCm39) T255A possibly damaging Het
Eef1a2 T C 2: 180,794,803 (GRCm39) Q132R possibly damaging Het
Pamr1 A C 2: 102,416,966 (GRCm39) S93R possibly damaging Het
Tacc3 A G 5: 33,826,984 (GRCm39) Y531C probably damaging Het
Tcerg1 A G 18: 42,701,518 (GRCm39) E860G possibly damaging Het
Tmco4 T A 4: 138,723,885 (GRCm39) probably null Het
Zfyve16 A G 13: 92,660,761 (GRCm39) L16P probably damaging Het
Other mutations in 1810009J06Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00952:1810009J06Rik APN 6 40,941,733 (GRCm39) missense probably benign 0.00
IGL01146:1810009J06Rik APN 6 40,943,217 (GRCm39) missense probably damaging 1.00
IGL02815:1810009J06Rik APN 6 40,941,729 (GRCm39) missense probably benign
R1543:1810009J06Rik UTSW 6 40,945,138 (GRCm39) missense probably damaging 1.00
R1708:1810009J06Rik UTSW 6 40,941,732 (GRCm39) missense probably benign
R1964:1810009J06Rik UTSW 6 40,945,141 (GRCm39) missense probably damaging 1.00
R5786:1810009J06Rik UTSW 6 40,945,122 (GRCm39) missense probably damaging 1.00
R6611:1810009J06Rik UTSW 6 40,943,713 (GRCm39) missense probably benign 0.09
R7057:1810009J06Rik UTSW 6 40,945,181 (GRCm39) missense probably benign 0.00
R9371:1810009J06Rik UTSW 6 40,943,663 (GRCm39) missense probably damaging 1.00
Posted On 2012-12-06