Incidental Mutation 'R0946:9230112D13Rik'
ID 82125
Institutional Source Beutler Lab
Gene Symbol 9230112D13Rik
Ensembl Gene ENSMUSG00000021797
Gene Name RIKEN cDNA 9230112D13 gene
Synonyms
MMRRC Submission 039085-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.186) question?
Stock # R0946 (G1)
Quality Score 225
Status Not validated
Chromosome 14
Chromosomal Location 34233578-34244758 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 34234099 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Threonine at position 64 (M64T)
Ref Sequence ENSEMBL: ENSMUSP00000022325 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022325]
AlphaFold Q9D260
Predicted Effect unknown
Transcript: ENSMUST00000022325
AA Change: M64T
Predicted Effect noncoding transcript
Transcript: ENSMUST00000227512
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.9%
  • 10x: 97.5%
  • 20x: 95.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts15 C T 9: 30,813,493 (GRCm39) G891R probably damaging Het
Adck5 G A 15: 76,477,486 (GRCm39) V107I possibly damaging Het
Aoc3 G A 11: 101,223,131 (GRCm39) V456M possibly damaging Het
Apbb1 A T 7: 105,223,062 (GRCm39) L183Q probably benign Het
Camsap3 A G 8: 3,654,442 (GRCm39) H693R probably benign Het
Ccdc88a A G 11: 29,406,509 (GRCm39) T414A probably benign Het
Cdh17 T C 4: 11,795,581 (GRCm39) V387A probably benign Het
Coasy G T 11: 100,976,696 (GRCm39) V489F probably damaging Het
Ercc6 A T 14: 32,274,578 (GRCm39) M574L probably benign Het
Esrrb T C 12: 86,552,598 (GRCm39) L180P probably damaging Het
Fam83b A T 9: 76,398,679 (GRCm39) V808D probably damaging Het
Fat3 C T 9: 15,909,100 (GRCm39) V2301I possibly damaging Het
Ftdc1 C A 16: 58,435,075 (GRCm39) R83S probably damaging Het
Hyal4 T A 6: 24,755,912 (GRCm39) Y43* probably null Het
Hydin C A 8: 111,257,685 (GRCm39) L2372M probably benign Het
Lrrc4c T C 2: 97,459,809 (GRCm39) V145A probably benign Het
Lypd10 A G 7: 24,413,167 (GRCm39) K162R probably benign Het
Muc21 A C 17: 35,929,105 (GRCm39) S1581A probably benign Het
Myh4 A G 11: 67,142,577 (GRCm39) I913V possibly damaging Het
Nat10 C T 2: 103,561,719 (GRCm39) G654D probably damaging Het
Nbn A T 4: 15,970,719 (GRCm39) probably null Het
Nup50l A T 6: 96,142,677 (GRCm39) N122K possibly damaging Het
Oas3 T C 5: 120,907,128 (GRCm39) Y503C unknown Het
Or11g7 C A 14: 50,691,130 (GRCm39) T207K probably benign Het
Pappa G T 4: 65,233,029 (GRCm39) probably null Het
Pfas A G 11: 68,884,121 (GRCm39) probably null Het
Pfas G T 11: 68,881,573 (GRCm39) probably null Het
Pign A T 1: 105,519,422 (GRCm39) M500K probably benign Het
Pkhd1 T C 1: 20,269,605 (GRCm39) K3313R probably benign Het
Ptk2b A G 14: 66,396,047 (GRCm39) V807A probably benign Het
Ptpdc1 C T 13: 48,740,286 (GRCm39) E382K probably damaging Het
Rfpl4b A T 10: 38,696,833 (GRCm39) I256N probably benign Het
Skap1 C G 11: 96,432,295 (GRCm39) S88* probably null Het
Slc4a2 T C 5: 24,640,884 (GRCm39) S742P probably damaging Het
Supv3l1 T C 10: 62,265,599 (GRCm39) D647G probably damaging Het
Tmem184c A C 8: 78,331,386 (GRCm39) V121G probably damaging Het
Tonsl T C 15: 76,507,421 (GRCm39) I118V probably benign Het
Top1 T A 2: 160,554,588 (GRCm39) Y446* probably null Het
Trim37 A G 11: 87,037,781 (GRCm39) R172G probably damaging Het
Vgll4 C A 6: 114,867,768 (GRCm39) probably null Het
Vgll4 T A 6: 114,867,769 (GRCm39) probably null Het
Vmn1r5 T G 6: 56,963,150 (GRCm39) I275S possibly damaging Het
Vwde A T 6: 13,187,874 (GRCm39) H584Q probably damaging Het
Zbtb14 C A 17: 69,695,497 (GRCm39) F398L probably damaging Het
Zfp282 T A 6: 47,856,943 (GRCm39) W59R probably damaging Het
Zfp329 T A 7: 12,545,395 (GRCm39) N43I probably benign Het
Zswim2 T A 2: 83,754,103 (GRCm39) T186S probably benign Het
Other mutations in 9230112D13Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0532:9230112D13Rik UTSW 14 34,234,054 (GRCm39) missense unknown
R1475:9230112D13Rik UTSW 14 34,234,012 (GRCm39) missense unknown
R2369:9230112D13Rik UTSW 14 34,233,913 (GRCm39) missense unknown
R2903:9230112D13Rik UTSW 14 34,233,898 (GRCm39) missense unknown
R7627:9230112D13Rik UTSW 14 34,234,055 (GRCm39) missense unknown
R8971:9230112D13Rik UTSW 14 34,236,383 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- AAGCTGAATTTTGGACATTAACGCGG -3'
(R):5'- GCCTTCTGACATCCTAGCAATTAGCC -3'

Sequencing Primer
(F):5'- AATTTTGGACATTAACGCGGTTTTG -3'
(R):5'- ATCTCCAGAGAGGTGCCAC -3'
Posted On 2013-11-08