Incidental Mutation 'R3438:1700017G19Rik'
ID 267272
Institutional Source Beutler Lab
Gene Symbol 1700017G19Rik
Ensembl Gene ENSMUSG00000037884
Gene Name RIKEN cDNA 1700017G19 gene
Synonyms
MMRRC Submission 040656-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R3438 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 40559016-40577061 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 40575673 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: ENSMUST00000035860
SMART Domains Protein: ENSMUSP00000143577
Gene: ENSMUSG00000037884

DomainStartEndE-ValueType
low complexity region 42 55 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000175150
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.4%
Validation Efficiency 97% (37/38)
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 C T 6: 128,557,349 (GRCm39) A115T probably benign Het
Ampd3 T C 7: 110,402,433 (GRCm39) I479T probably damaging Het
Aoah G A 13: 21,101,242 (GRCm39) R254K probably benign Het
Appbp2 T C 11: 85,088,966 (GRCm39) E358G probably damaging Het
Col6a5 A G 9: 105,752,991 (GRCm39) S2294P possibly damaging Het
Cux1 T C 5: 136,340,414 (GRCm39) E632G probably damaging Het
Cyp7a1 T C 4: 6,272,769 (GRCm39) N148S probably damaging Het
Dgkz A T 2: 91,764,395 (GRCm39) probably benign Het
Dlgap1 A T 17: 70,823,356 (GRCm39) S114C probably damaging Het
Dmtn T A 14: 70,850,156 (GRCm39) I263F probably damaging Het
Gigyf2 C A 1: 87,368,302 (GRCm39) H1029N probably damaging Het
Gm10770 T A 2: 150,021,469 (GRCm39) probably null Het
Gnb1l A G 16: 18,371,117 (GRCm39) T203A probably benign Het
Kng2 T C 16: 22,830,821 (GRCm39) I163V probably benign Het
Lamc1 T C 1: 153,102,161 (GRCm39) D1479G probably benign Het
Larp7-ps A C 4: 92,079,919 (GRCm39) V23G possibly damaging Het
Lhx4 T A 1: 155,578,230 (GRCm39) D304V probably benign Het
Mybl1 G T 1: 9,757,870 (GRCm39) T143K probably damaging Het
Notch3 C T 17: 32,372,564 (GRCm39) C630Y probably damaging Het
Oas1e T C 5: 120,933,475 (GRCm39) E30G probably damaging Het
Or4c114 T C 2: 88,904,707 (GRCm39) I243V probably benign Het
Or8b55 T G 9: 38,727,512 (GRCm39) F238V probably damaging Het
Or9e1 G T 11: 58,732,698 (GRCm39) G253* probably null Het
Otoa A G 7: 120,759,566 (GRCm39) E1056G possibly damaging Het
Plin4 A G 17: 56,414,193 (GRCm39) V144A probably benign Het
Sec16b T C 1: 157,384,328 (GRCm39) probably benign Het
Stk31 A G 6: 49,414,455 (GRCm39) S485G probably benign Het
Tanc2 C T 11: 105,748,401 (GRCm39) P511L probably damaging Het
Utrn T C 10: 12,357,062 (GRCm39) D309G probably damaging Het
Vpreb3 C T 10: 75,779,056 (GRCm39) probably benign Het
Vsx2 A T 12: 84,616,985 (GRCm39) Q90L probably damaging Het
Other mutations in 1700017G19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4558:1700017G19Rik UTSW 3 40,567,240 (GRCm39) unclassified noncoding transcript
R4559:1700017G19Rik UTSW 3 40,567,240 (GRCm39) unclassified noncoding transcript
R4812:1700017G19Rik UTSW 3 40,575,633 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- TGTGTGCCTACAAAGAGCTTC -3'
(R):5'- GAGTGACAATCTGAGACGCTC -3'

Sequencing Primer
(F):5'- TAATGGCCCTTCTGGAGAAAG -3'
(R):5'- CCAAGCTTCGTATTCCTG -3'
Posted On 2015-02-18