Incidental Mutation 'R4558:1700017G19Rik'
ID 342937
Institutional Source Beutler Lab
Gene Symbol 1700017G19Rik
Ensembl Gene ENSMUSG00000037884
Gene Name RIKEN cDNA 1700017G19 gene
Synonyms
MMRRC Submission 042005-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # R4558 (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 40567240 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: ENSMUST00000202778
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.1%
Validation Efficiency 100% (36/36)
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A830018L16Rik C A 1: 12,042,300 (GRCm39) S440* probably null Het
Acot11 T C 4: 106,605,563 (GRCm39) N583S probably damaging Het
Alox12 T G 11: 70,143,889 (GRCm39) M164L probably benign Het
Atad2b A G 12: 4,993,223 (GRCm39) I247M probably benign Het
Bmpr2 T A 1: 59,884,851 (GRCm39) M279K probably damaging Het
Cacna2d3 T C 14: 28,825,670 (GRCm39) T502A possibly damaging Het
Casp12 A T 9: 5,352,742 (GRCm39) Y188F probably damaging Het
Catsperb A G 12: 101,557,799 (GRCm39) Y790C possibly damaging Het
Cnbd1 G T 4: 19,055,095 (GRCm39) N110K possibly damaging Het
Entrep1 G A 19: 24,007,913 (GRCm39) S130L probably damaging Het
Fam227b C T 2: 125,968,963 (GRCm39) S37N probably benign Het
Fsip2 T C 2: 82,815,297 (GRCm39) S3677P possibly damaging Het
Gm10764 A G 10: 87,126,682 (GRCm39) noncoding transcript Het
H2-Q6 T C 17: 35,647,291 (GRCm39) V312A probably benign Het
Hecw1 T A 13: 14,422,190 (GRCm39) D972V probably damaging Het
Kalrn G A 16: 33,807,578 (GRCm39) T2597I possibly damaging Het
Kng1 C A 16: 22,896,168 (GRCm39) probably null Het
Med13 T C 11: 86,189,880 (GRCm39) T1010A probably damaging Het
Nbeal1 C T 1: 60,320,469 (GRCm39) R2021* probably null Het
Ncapg A T 5: 45,833,986 (GRCm39) T341S probably benign Het
Obscn T C 11: 59,022,472 (GRCm39) R758G possibly damaging Het
Pabir2 G A X: 52,349,554 (GRCm39) probably benign Het
Pcdhb4 A G 18: 37,443,017 (GRCm39) I776V probably benign Het
Ppp4r4 T C 12: 103,573,192 (GRCm39) V697A probably benign Het
Pramel13 T C 4: 144,122,542 (GRCm39) M1V probably null Het
Psd4 G A 2: 24,294,806 (GRCm39) V789M probably damaging Het
Rasa3 T C 8: 13,648,259 (GRCm39) E135G probably damaging Het
Serpinb9c T A 13: 33,338,482 (GRCm39) E139V probably benign Het
Sgsm1 G A 5: 113,405,977 (GRCm39) probably benign Het
Tmem161b A G 13: 84,399,363 (GRCm39) I6M possibly damaging Het
Upf2 A G 2: 5,978,404 (GRCm39) M423V unknown Het
Vmn1r207 A G 13: 22,910,581 (GRCm39) noncoding transcript Het
Other mutations in 1700017G19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3438:1700017G19Rik UTSW 3 40,575,673 (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'- CTACTGAGCAGGGTTCATGAG -3'
(R):5'- CCCAGCTTTCTGTAGAGCTG -3'

Sequencing Primer
(F):5'- CAGGGTTCATGAGGCACAG -3'
(R):5'- CTTTCTGTAGAGCTGCTAGCCAAAG -3'
Posted On 2015-09-24