Incidental Mutation 'R0021:2310016G11Rik'
ID 64763
Institutional Source Beutler Lab
Gene Symbol 2310016G11Rik
Ensembl Gene ENSMUSG00000070574
Gene Name RIKEN cDNA 2310016G11 gene
Synonyms
MMRRC Submission 038316-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.098) question?
Stock # R0021 (G1)
Quality Score 176
Status Validated
Chromosome 7
Chromosomal Location 44317657-44327659 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to G at 44326620 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: ENSMUST00000094460
SMART Domains Protein: ENSMUSP00000092031
Gene: ENSMUSG00000070574

DomainStartEndE-ValueType
Blast:HOX 14 79 8e-10 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209111
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 95.8%
Validation Efficiency 97% (60/62)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc5 T A 16: 20,197,411 (GRCm39) K647* probably null Het
Aplp1 A G 7: 30,135,241 (GRCm39) probably benign Het
Arhgef25 A G 10: 127,025,423 (GRCm39) I43T probably benign Het
Brinp3 T G 1: 146,777,189 (GRCm39) S545R probably benign Het
Btnl1 A G 17: 34,598,468 (GRCm39) E28G probably benign Het
C5ar2 A G 7: 15,971,601 (GRCm39) F109L probably benign Het
D630045J12Rik G A 6: 38,160,902 (GRCm39) Q1081* probably null Het
Dhx36 T C 3: 62,385,016 (GRCm39) I699V possibly damaging Het
Dnah9 A G 11: 65,860,805 (GRCm39) I2855T probably benign Het
Dock8 T C 19: 25,140,411 (GRCm39) I1317T probably benign Het
Galnt11 A T 5: 25,453,855 (GRCm39) D27V probably damaging Het
Gm5134 T A 10: 75,829,718 (GRCm39) C335S probably damaging Het
Hdhd2 A T 18: 77,058,311 (GRCm39) K227N probably damaging Het
Impg1 A T 9: 80,317,479 (GRCm39) L36Q probably damaging Het
Krtcap3 A G 5: 31,410,303 (GRCm39) H227R probably benign Het
Lrrc7 A G 3: 157,866,298 (GRCm39) Y1148H probably damaging Het
Map2k4 A G 11: 65,603,110 (GRCm39) I174T probably damaging Het
Mef2c C A 13: 83,804,359 (GRCm39) L282M probably damaging Het
Nkapd1 A C 9: 50,521,725 (GRCm39) D65E probably damaging Het
Nqo2 T C 13: 34,165,490 (GRCm39) I129T probably benign Het
Pdgfrb T A 18: 61,197,998 (GRCm39) probably benign Het
Phf7 C T 14: 30,960,443 (GRCm39) probably benign Het
Plac8 T A 5: 100,704,434 (GRCm39) T88S probably benign Het
Pou2f1 G A 1: 165,703,587 (GRCm39) T654M probably damaging Het
Ptprk T A 10: 28,468,891 (GRCm39) V1425E probably damaging Het
Saal1 A T 7: 46,342,316 (GRCm39) S376T probably damaging Het
Scart2 G A 7: 139,876,310 (GRCm39) R594H probably benign Het
Serpini1 T C 3: 75,526,620 (GRCm39) Y291H probably damaging Het
Siah2 T C 3: 58,583,713 (GRCm39) H191R probably benign Het
Spaca6 T A 17: 18,058,498 (GRCm39) Y39* probably null Het
Tbc1d10a T C 11: 4,163,680 (GRCm39) C277R probably damaging Het
Trim45 A T 3: 100,832,736 (GRCm39) D323V probably damaging Het
Trim55 A C 3: 19,698,866 (GRCm39) M32L probably benign Het
Unc5b T C 10: 60,614,698 (GRCm39) T200A probably benign Het
Uqcc4 A G 17: 25,403,957 (GRCm39) E99G possibly damaging Het
V1rd19 A T 7: 23,703,029 (GRCm39) D165V probably damaging Het
Other mutations in 2310016G11Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0021:2310016G11Rik UTSW 7 44,326,620 (GRCm39) intron noncoding transcript
R0863:2310016G11Rik UTSW 7 44,327,232 (GRCm39) exon noncoding transcript
R4380:2310016G11Rik UTSW 7 44,326,580 (GRCm39) intron noncoding transcript
R5110:2310016G11Rik UTSW 7 44,327,286 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- TCCACGGATAGTAACTCTGCACCC -3'
(R):5'- CAGAAATCCTGTGACATGCCATCCC -3'

Sequencing Primer
(F):5'- CACCCTTGAGCAGTTCCTGG -3'
(R):5'- ACTGCTTTGTAGAACCCGATG -3'
Posted On 2013-08-06