Incidental Mutation 'IGL00436:A530083I20Rik'
ID 28105
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol A530083I20Rik
Ensembl Gene ENSMUSG00000097322
Gene Name RIKEN cDNA A530083I20 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL00436
Quality Score
Status
Chromosome 9
Chromosomal Location 122714145-122732596 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 122725197 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150648 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063980] [ENSMUST00000215872]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000063980
SMART Domains Protein: ENSMUSP00000071695
Gene: ENSMUSG00000063488

DomainStartEndE-ValueType
SCAN 45 156 1.18e-65 SMART
ZnF_C2H2 350 372 5.59e-4 SMART
ZnF_C2H2 378 400 3.69e-4 SMART
ZnF_C2H2 434 456 8.4e1 SMART
ZnF_C2H2 487 509 4.24e-4 SMART
ZnF_C2H2 515 537 8.34e-3 SMART
ZnF_C2H2 543 565 7.37e-4 SMART
ZnF_C2H2 571 593 1.92e-2 SMART
ZnF_C2H2 599 621 1.13e-4 SMART
ZnF_C2H2 627 649 2.24e-3 SMART
ZnF_C2H2 655 677 4.17e-3 SMART
ZnF_C2H2 683 705 1.04e-3 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180486
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180877
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214426
Predicted Effect probably benign
Transcript: ENSMUST00000215872
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216429
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216924
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 11 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bop1 T C 15: 76,338,728 (GRCm39) T436A probably benign Het
Dnah11 G T 12: 118,000,194 (GRCm39) T2277K possibly damaging Het
F13b A T 1: 139,438,325 (GRCm39) E313D probably benign Het
Fsd1 T C 17: 56,300,943 (GRCm39) probably null Het
Gm14326 T C 2: 177,587,491 (GRCm39) K502E probably damaging Het
Kmt2c T C 5: 25,486,259 (GRCm39) N1385D probably damaging Het
Pdc T C 1: 150,209,006 (GRCm39) V163A probably damaging Het
Rapgef6 T C 11: 54,570,091 (GRCm39) S873P probably benign Het
Spsb4 T A 9: 96,826,646 (GRCm39) Y269F probably benign Het
Sult6b2 T G 6: 142,743,563 (GRCm39) probably benign Het
Tfpi2 A G 6: 3,965,407 (GRCm39) V17A probably benign Het
Posted On 2013-04-17