Incidental Mutation 'IGL01930:4930433N12Rik'
ID 180422
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930433N12Rik
Ensembl Gene ENSMUSG00000042360
Gene Name RIKEN cDNA 4930433N12 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.088) question?
Stock # IGL01930
Quality Score
Status
Chromosome 9
Chromosomal Location 3190269-3199813 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to T at 3134875 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000048921
SMART Domains Protein: ENSMUSP00000044865
Gene: ENSMUSG00000042360

DomainStartEndE-ValueType
low complexity region 4 16 N/A INTRINSIC
low complexity region 43 54 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212713
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsf3 A G 8: 123,507,085 (GRCm39) Y126C probably benign Het
Akr1c20 T A 13: 4,557,647 (GRCm39) probably benign Het
Cdan1 T C 2: 120,557,063 (GRCm39) probably benign Het
Cdc42bpg C T 19: 6,361,398 (GRCm39) A308V probably damaging Het
Dek T C 13: 47,241,611 (GRCm39) I318V probably benign Het
Dvl1 A G 4: 155,940,645 (GRCm39) M422V possibly damaging Het
Dync2i1 A G 12: 116,189,583 (GRCm39) probably null Het
Erbin G A 13: 103,977,680 (GRCm39) L626F probably damaging Het
Fa2h A T 8: 112,075,936 (GRCm39) V229E possibly damaging Het
Gfpt1 T A 6: 87,036,397 (GRCm39) H193Q possibly damaging Het
Gm10717 C T 9: 3,025,616 (GRCm39) S67L probably benign Het
Gpr162 A G 6: 124,838,575 (GRCm39) L25P possibly damaging Het
Hsd3b5 T C 3: 98,529,475 (GRCm39) T52A probably benign Het
Megf8 T A 7: 25,034,286 (GRCm39) V668D probably damaging Het
Or10j2 T C 1: 173,098,177 (GRCm39) V145A probably benign Het
Prkdc A G 16: 15,516,751 (GRCm39) T1042A probably damaging Het
Rasgrf2 A G 13: 92,130,857 (GRCm39) S735P probably damaging Het
Serpina3n T A 12: 104,375,231 (GRCm39) L101H probably damaging Het
Sipa1l2 T C 8: 126,145,978 (GRCm39) D1674G probably damaging Het
Sval3 A G 6: 41,949,455 (GRCm39) N98D probably benign Het
Tbc1d16 G A 11: 119,046,901 (GRCm39) R449C possibly damaging Het
Tm7sf3 A C 6: 146,512,431 (GRCm39) I321S possibly damaging Het
Tmem273 G A 14: 32,538,814 (GRCm39) E92K probably benign Het
Trappc13 A G 13: 104,284,586 (GRCm39) probably benign Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Wdr76 A G 2: 121,341,303 (GRCm39) D116G possibly damaging Het
Zscan18 T C 7: 12,509,275 (GRCm39) probably benign Het
Other mutations in 4930433N12Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01458:4930433N12Rik APN 9 3,134,008 (GRCm39) unclassified noncoding transcript
R4393:4930433N12Rik UTSW 9 3,134,944 (GRCm39) unclassified noncoding transcript
Posted On 2014-05-07