Incidental Mutation 'P0017:C030017K20Rik'
ID 7776
Institutional Source Beutler Lab
Gene Symbol C030017K20Rik
Ensembl Gene
Gene Name RIKEN cDNA C030017K20 gene
Synonyms LOC381581
MMRRC Submission 038270-MU
Accession Numbers
Essential gene? Not available question?
Stock # P0017 (G1)
Quality Score
Status Validated
Chromosome 4
Chromosomal Location 155536022-155550862 bp(+) (GRCm39)
Type of Mutation splice site (5 bp from exon)
DNA Base Change (assembly) G to T at 155547574 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000123626 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105619] [ENSMUST00000105619] [ENSMUST00000151083] [ENSMUST00000151083]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000105619
Predicted Effect probably null
Transcript: ENSMUST00000105619
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135407
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144157
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144625
Predicted Effect probably null
Transcript: ENSMUST00000151083
SMART Domains Protein: ENSMUSP00000123626
Gene: ENSMUSG00000078490

DomainStartEndE-ValueType
low complexity region 44 59 N/A INTRINSIC
coiled coil region 134 162 N/A INTRINSIC
coiled coil region 333 378 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000151083
SMART Domains Protein: ENSMUSP00000123626
Gene: ENSMUSG00000078490

DomainStartEndE-ValueType
low complexity region 44 59 N/A INTRINSIC
coiled coil region 134 162 N/A INTRINSIC
coiled coil region 333 378 N/A INTRINSIC
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 82.5%
  • 3x: 74.9%
  • 10x: 52.3%
  • 20x: 31.8%
Validation Efficiency 59% (51/87)
Allele List at MGI

All alleles(2) : Targeted(2)

Other mutations in this stock
Total: 6 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ano4 A T 10: 88,817,052 (GRCm39) L591* probably null Het
Arhgap30 C T 1: 171,236,272 (GRCm39) P882L probably benign Het
Crb1 T C 1: 139,176,678 (GRCm39) E435G possibly damaging Het
Fam193a G T 5: 34,597,807 (GRCm39) D535Y probably damaging Het
Hmcn1 T A 1: 150,596,440 (GRCm39) T1799S possibly damaging Het
Il20ra A G 10: 19,635,154 (GRCm39) E465G probably damaging Het
Posted On 2012-10-29