Incidental Mutation 'IGL02528:C920021L13Rik'
ID 297179
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol C920021L13Rik
Ensembl Gene ENSMUSG00000080727
Gene Name RIKEN cDNA C920021L13 gene
Synonyms 100042889
Accession Numbers
Essential gene? Not available question?
Stock # IGL02528
Quality Score
Status
Chromosome 3
Chromosomal Location 95778834-95796405 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to G at 95794628 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000127666 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036360] [ENSMUST00000090476] [ENSMUST00000171519]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000036360
SMART Domains Protein: ENSMUSP00000046810
Gene: ENSMUSG00000038543

DomainStartEndE-ValueType
Pfam:DUF4634 1 145 3.6e-64 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000090476
SMART Domains Protein: ENSMUSP00000102749
Gene: ENSMUSG00000038543

DomainStartEndE-ValueType
Pfam:DUF4634 1 146 1.8e-65 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000120398
Predicted Effect noncoding transcript
Transcript: ENSMUST00000133611
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142433
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145949
Predicted Effect probably benign
Transcript: ENSMUST00000171519
SMART Domains Protein: ENSMUSP00000127666
Gene: ENSMUSG00000038543

DomainStartEndE-ValueType
Pfam:DUF4634 1 146 1.5e-65 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930544G11Rik T A 6: 65,930,357 (GRCm39) probably benign Het
4933416I08Rik T A X: 52,580,792 (GRCm39) N54I probably damaging Het
Abcc2 A G 19: 43,786,943 (GRCm39) D188G probably benign Het
Akap11 T C 14: 78,748,307 (GRCm39) Y1360C probably damaging Het
Bltp2 T C 11: 78,162,802 (GRCm39) V888A possibly damaging Het
Ccdc89 A T 7: 90,076,819 (GRCm39) Q343L probably damaging Het
Cep350 A T 1: 155,770,361 (GRCm39) M1843K probably damaging Het
Ces2b T C 8: 105,561,601 (GRCm39) S232P probably damaging Het
Eprs1 G T 1: 185,145,686 (GRCm39) R1165L probably damaging Het
Ercc5 A G 1: 44,206,962 (GRCm39) E625G probably benign Het
Evi5l T C 8: 4,243,172 (GRCm39) V352A probably benign Het
Ggt5 T C 10: 75,446,254 (GRCm39) probably benign Het
Gm11564 T A 11: 99,706,293 (GRCm39) R46* probably null Het
Herc2 A G 7: 55,758,641 (GRCm39) probably benign Het
Kash5 T C 7: 44,833,170 (GRCm39) probably benign Het
Kcnh8 A G 17: 53,110,556 (GRCm39) S256G probably damaging Het
Man2a2 G A 7: 80,009,388 (GRCm39) A822V probably damaging Het
Mast4 T C 13: 102,990,331 (GRCm39) *255W probably null Het
Muc5b A G 7: 141,417,754 (GRCm39) M3567V probably benign Het
Noxa1 A G 2: 24,980,645 (GRCm39) probably benign Het
Nsd2 T C 5: 34,036,395 (GRCm39) probably benign Het
Pcna-ps2 A T 19: 9,261,331 (GRCm39) I197L probably benign Het
Pde8a A G 7: 80,942,937 (GRCm39) probably benign Het
Polr1a C A 6: 71,941,701 (GRCm39) Q1070K probably benign Het
Pum2 G T 12: 8,778,696 (GRCm39) G449* probably null Het
Rab29 T C 1: 131,797,749 (GRCm39) probably benign Het
Rpap1 T A 2: 119,605,431 (GRCm39) probably null Het
Scn7a A G 2: 66,530,519 (GRCm39) Y609H probably damaging Het
Slit3 T C 11: 35,469,801 (GRCm39) S268P probably benign Het
Stat2 C T 10: 128,126,534 (GRCm39) T753I probably benign Het
Susd6 T C 12: 80,916,945 (GRCm39) V160A probably damaging Het
Tex52 A G 6: 128,356,460 (GRCm39) E51G possibly damaging Het
Tmem102 T A 11: 69,694,532 (GRCm39) probably null Het
Ttn A G 2: 76,720,582 (GRCm39) probably benign Het
Ubtd2 T A 11: 32,449,249 (GRCm39) L32* probably null Het
Usp38 T C 8: 81,719,864 (GRCm39) Y455C probably damaging Het
Wwp2 T C 8: 108,281,099 (GRCm39) F671L probably benign Het
Xlr3a T C X: 72,138,573 (GRCm39) N29D possibly damaging Het
Zan T C 5: 137,463,403 (GRCm39) E592G possibly damaging Het
Zmat4 T A 8: 24,505,212 (GRCm39) S151T probably damaging Het
Znfx1 T C 2: 166,892,324 (GRCm39) T631A probably benign Het
Other mutations in C920021L13Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00478:C920021L13Rik APN 3 95,794,797 (GRCm39) intron probably benign
Posted On 2015-04-16