Incidental Mutation 'IGL02667:6530409C15Rik'
ID302781
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 6530409C15Rik
Ensembl Gene ENSMUSG00000043340
Gene NameRIKEN cDNA 6530409C15 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02667
Quality Score
Status
Chromosome6
Chromosomal Location28215555-28260862 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 28217671 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143099
SMART Domains Protein: ENSMUSP00000133161
Gene: ENSMUSG00000043340

DomainStartEndE-ValueType
low complexity region 34 48 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143551
SMART Domains Protein: ENSMUSP00000132432
Gene: ENSMUSG00000043340

DomainStartEndE-ValueType
low complexity region 34 48 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000201159
Predicted Effect noncoding transcript
Transcript: ENSMUST00000202392
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1e1 G A 13: 4,595,667 P174L possibly damaging Het
Arf5 C A 6: 28,425,199 N95K probably damaging Het
Atl3 T C 19: 7,509,416 F39L possibly damaging Het
Atp2a3 C A 11: 72,975,339 H262N probably benign Het
Cyp2a12 T C 7: 27,031,158 S183P probably damaging Het
Dicer1 T A 12: 104,714,906 R449S probably damaging Het
Dlec1 T C 9: 119,127,466 I736T probably benign Het
Eny2 T A 15: 44,429,588 M12K possibly damaging Het
Fbxl21 C T 13: 56,537,129 R349C probably benign Het
Gstm2 A G 3: 107,986,108 L13P probably damaging Het
Gucy2g G A 19: 55,206,177 T936M possibly damaging Het
Mbp G T 18: 82,554,615 K12N probably damaging Het
Mon1b G T 8: 113,638,823 R261L possibly damaging Het
Myo18a A G 11: 77,857,852 probably benign Het
Nr2f2 T C 7: 70,357,985 S117G probably damaging Het
Pi4k2b T C 5: 52,750,605 probably benign Het
Pi4ka A G 16: 17,295,461 F1504L possibly damaging Het
Ppm1d T C 11: 85,332,285 W239R probably damaging Het
Setd1b T A 5: 123,157,497 S1043T unknown Het
Tgfbrap1 T C 1: 43,067,620 I298V probably benign Het
Tmem190 T A 7: 4,783,158 D20E probably benign Het
Tph2 A T 10: 115,080,045 C408S probably benign Het
Trmt44 A C 5: 35,571,052 Y295D probably damaging Het
Trpm2 C T 10: 77,935,942 R621H probably damaging Het
Ubn1 A G 16: 5,062,599 E134G probably damaging Het
Zcchc11 T C 4: 108,558,708 probably benign Het
Posted On2015-04-16