Incidental Mutation 'R4130:1700021A07Rik'
ID 315511
Institutional Source Beutler Lab
Gene Symbol 1700021A07Rik
Ensembl Gene ENSMUSG00000037535
Gene Name RIKEN cDNA 1700021A07 gene
Synonyms
MMRRC Submission 041636-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.086) question?
Stock # R4130 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 21295257-21302464 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 21301441 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: ENSMUST00000042671
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187763
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188024
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.7%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency 100% (29/29)
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A4gnt A G 9: 99,502,671 (GRCm39) D277G possibly damaging Het
Adam12 C T 7: 133,514,653 (GRCm39) V345I probably damaging Het
Ankrd29 G A 18: 12,387,757 (GRCm39) A275V possibly damaging Het
Arpp21 T A 9: 111,984,376 (GRCm39) probably benign Het
Bbx T C 16: 50,045,221 (GRCm39) K447E probably damaging Het
Bcar1 A G 8: 112,440,797 (GRCm39) L399P possibly damaging Het
Cytl1 T C 5: 37,892,985 (GRCm39) S32P probably damaging Het
Eif4e1b C T 13: 54,935,130 (GRCm39) T219M probably benign Het
F10 A G 8: 13,105,584 (GRCm39) D383G possibly damaging Het
Gm37267 T G 1: 180,336,643 (GRCm39) noncoding transcript Het
Golga2 G A 2: 32,178,178 (GRCm39) R29H probably benign Het
Gpd1 A T 15: 99,617,158 (GRCm39) probably null Het
Lrrk2 G A 15: 91,639,997 (GRCm39) R1514Q probably benign Het
Map1b T C 13: 99,568,188 (GRCm39) E1511G unknown Het
Nup35 G A 2: 80,486,443 (GRCm39) probably benign Het
Or13n4 C T 7: 106,422,792 (GRCm39) G314S probably benign Het
Pdzd9 A T 7: 120,262,092 (GRCm39) D123E possibly damaging Het
Pramel29 T A 4: 143,935,379 (GRCm39) I121F probably damaging Het
Rab3gap2 A G 1: 184,936,494 (GRCm39) D19G possibly damaging Het
Rnf213 T C 11: 119,373,832 (GRCm39) S4972P probably damaging Het
Skap1 A G 11: 96,416,871 (GRCm39) Y52C probably damaging Het
Sphkap T C 1: 83,255,619 (GRCm39) N710S probably damaging Het
Tedc1 T A 12: 113,126,828 (GRCm39) D363E probably benign Het
Vmn2r44 T A 7: 8,370,918 (GRCm39) Q709H probably damaging Het
Wdr5 G T 2: 27,410,441 (GRCm39) probably benign Het
Other mutations in 1700021A07Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5095:1700021A07Rik UTSW 10 21,301,492 (GRCm39) intron noncoding transcript
Predicted Primers PCR Primer
(F):5'- CAGGATGGATGCTAGCATGG -3'
(R):5'- GAGAATTCAGTTTCCCTGCTGC -3'

Sequencing Primer
(F):5'- ACTCCAAGGAGCCTCTCTC -3'
(R):5'- CCCTGCTGCTTGTATTTACTGG -3'
Posted On 2015-05-14