Incidental Mutation 'IGL02168:2010007H06Rik'
ID 282782
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2010007H06Rik
Ensembl Gene ENSMUSG00000044694
Gene Name RIKEN cDNA 2010007H06 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02168
Quality Score
Status
Chromosome 9
Chromosomal Location 51189813-51195510 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 51191801 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150539 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000114427] [ENSMUST00000215038]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000050829
Predicted Effect probably benign
Transcript: ENSMUST00000114427
SMART Domains Protein: ENSMUSP00000110070
Gene: ENSMUSG00000079559

DomainStartEndE-ValueType
low complexity region 114 135 N/A INTRINSIC
low complexity region 148 161 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186025
Predicted Effect probably benign
Transcript: ENSMUST00000215038
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6030468B19Rik T A 11: 117,689,244 (GRCm39) probably benign Het
Ankra2 G A 13: 98,409,882 (GRCm39) probably benign Het
Astn1 C A 1: 158,436,911 (GRCm39) A823E possibly damaging Het
Cfap43 T C 19: 47,740,362 (GRCm39) probably benign Het
Clec4b2 T A 6: 123,181,156 (GRCm39) N180K probably damaging Het
Col7a1 A G 9: 108,813,143 (GRCm39) probably benign Het
Dhrs7c T C 11: 67,706,693 (GRCm39) F284L probably benign Het
Dock1 T C 7: 134,678,860 (GRCm39) probably benign Het
Entpd5 A T 12: 84,433,752 (GRCm39) probably null Het
Heatr5b A T 17: 79,139,020 (GRCm39) probably benign Het
Kdm3a A G 6: 71,577,101 (GRCm39) V738A probably damaging Het
Klf10 A T 15: 38,297,085 (GRCm39) F318L probably damaging Het
Mcc A C 18: 44,582,366 (GRCm39) I770S probably damaging Het
Muc19 C T 15: 91,778,292 (GRCm39) noncoding transcript Het
Or9a4 A T 6: 40,548,317 (GRCm39) probably benign Het
Pcdh17 A G 14: 84,770,635 (GRCm39) T1038A probably benign Het
Pole2 A G 12: 69,248,660 (GRCm39) probably benign Het
Polr2c A G 8: 95,584,394 (GRCm39) R36G probably damaging Het
Ptgs2 A G 1: 149,979,430 (GRCm39) probably null Het
Scart1 A T 7: 139,803,399 (GRCm39) H321L probably benign Het
Taf5 A G 19: 47,070,917 (GRCm39) D747G probably damaging Het
Tll1 T G 8: 64,507,001 (GRCm39) K580T possibly damaging Het
Tmc3 A T 7: 83,269,203 (GRCm39) N768I possibly damaging Het
Top1 G T 2: 160,546,893 (GRCm39) probably null Het
Ubtf T C 11: 102,204,994 (GRCm39) K97E probably damaging Het
Vcl T C 14: 21,057,355 (GRCm39) V509A probably benign Het
Vmn2r110 A T 17: 20,804,062 (GRCm39) probably benign Het
Zfp106 A G 2: 120,364,712 (GRCm39) V565A possibly damaging Het
Zfp458 A T 13: 67,406,098 (GRCm39) C111S probably damaging Het
Posted On 2015-04-16