Incidental Mutation 'R0080:4732465J04Rik'
ID 65757
Institutional Source Beutler Lab
Gene Symbol 4732465J04Rik
Ensembl Gene ENSMUSG00000101517
Gene Name RIKEN cDNA 4732465J04 gene
Synonyms
MMRRC Submission 038367-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.404) question?
Stock # R0080 (G1)
Quality Score 133
Status Validated
Chromosome 10
Chromosomal Location 95608995-95630846 bp(+) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) GATCTATCTATCTATCTATCTATCTATCTATCTATCTATC to GATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATC at 95630440 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000084674
SMART Domains Protein: ENSMUSP00000081726
Gene: ENSMUSG00000071107

DomainStartEndE-ValueType
transmembrane domain 24 43 N/A INTRINSIC
transmembrane domain 50 72 N/A INTRINSIC
transmembrane domain 82 104 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185499
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187483
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 97.6%
  • 10x: 93.1%
  • 20x: 79.7%
Validation Efficiency 88% (175/200)
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam17 A C 12: 21,379,049 (GRCm39) probably benign Het
Adcy1 T C 11: 7,099,497 (GRCm39) probably benign Het
Adgb T C 10: 10,253,583 (GRCm39) probably benign Het
Antkmt T C 17: 26,010,548 (GRCm39) I89V probably benign Het
Ccdc180 A G 4: 45,896,205 (GRCm39) D118G probably null Het
Coro7 A T 16: 4,448,328 (GRCm39) L714Q probably damaging Het
D2hgdh A G 1: 93,754,177 (GRCm39) Y50C probably damaging Het
Dsg1b T G 18: 20,530,424 (GRCm39) S360A probably damaging Het
Ednra T C 8: 78,401,688 (GRCm39) I201V probably benign Het
Ggt6 A G 11: 72,328,021 (GRCm39) T136A possibly damaging Het
Gnb5 A T 9: 75,221,636 (GRCm39) E28V possibly damaging Het
Golgb1 T C 16: 36,718,973 (GRCm39) L293P probably damaging Het
Gpr179 A G 11: 97,242,295 (GRCm39) V183A probably benign Het
Grk6 T C 13: 55,606,723 (GRCm39) S474P probably benign Het
Hectd4 A G 5: 121,487,435 (GRCm39) S3477G probably benign Het
Hoatz T C 9: 51,013,102 (GRCm39) T57A probably benign Het
Irx3 T C 8: 92,526,954 (GRCm39) D250G possibly damaging Het
Jsrp1 T G 10: 80,646,349 (GRCm39) M70L probably benign Het
Kcmf1 G T 6: 72,827,470 (GRCm39) probably null Het
Med23 T C 10: 24,788,715 (GRCm39) V1368A probably benign Het
Myl3 A C 9: 110,596,997 (GRCm39) D119A probably damaging Het
Ncoa6 TGC TGCGC 2: 155,250,211 (GRCm39) probably null Het
Nos1 G T 5: 118,031,943 (GRCm39) C297F probably damaging Het
Oas1d G A 5: 121,054,955 (GRCm39) A176T possibly damaging Het
Odf2l A T 3: 144,830,084 (GRCm39) I19F possibly damaging Het
Or6c1b T C 10: 129,273,140 (GRCm39) I153T possibly damaging Het
Or6c209 G A 10: 129,483,522 (GRCm39) C175Y probably benign Het
Pfkfb2 A T 1: 130,642,279 (GRCm39) S5R probably benign Het
Pign G T 1: 105,480,130 (GRCm39) A848E probably damaging Het
Pomgnt2 A T 9: 121,811,326 (GRCm39) V485E probably damaging Het
Ryr2 T A 13: 11,583,361 (GRCm39) K4764N probably damaging Het
Scgb1b19 A G 7: 32,987,067 (GRCm39) T73A probably damaging Het
Slc35d3 T C 10: 19,724,944 (GRCm39) E304G probably damaging Het
Snta1 A G 2: 154,225,757 (GRCm39) V209A probably benign Het
Spdye4b A T 5: 143,181,430 (GRCm39) D95V probably damaging Het
Srek1 T C 13: 103,880,194 (GRCm39) T455A unknown Het
Tie1 T A 4: 118,341,550 (GRCm39) E254V probably damaging Het
Tigd4 A G 3: 84,501,452 (GRCm39) H123R probably benign Het
Tmem144 G A 3: 79,746,580 (GRCm39) probably benign Het
Trim60 C T 8: 65,453,251 (GRCm39) A333T probably damaging Het
Vmn2r82 A T 10: 79,232,339 (GRCm39) R779S probably benign Het
Wdr91 T C 6: 34,883,620 (GRCm39) R132G possibly damaging Het
Zfp445 A G 9: 122,681,421 (GRCm39) V840A probably damaging Het
Other mutations in 4732465J04Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01958:4732465J04Rik APN 10 95,629,659 (GRCm39) missense probably damaging 0.99
R0164:4732465J04Rik UTSW 10 95,630,440 (GRCm39) frame shift probably null
R1717:4732465J04Rik UTSW 10 95,629,641 (GRCm39) critical splice donor site probably null
Predicted Primers
Posted On 2013-08-19