Incidental Mutation 'R0574:2700099C18Rik'
ID 46592
Institutional Source Beutler Lab
Gene Symbol 2700099C18Rik
Ensembl Gene ENSMUSG00000098090
Gene Name RIKEN cDNA 2700099C18 gene
Synonyms
MMRRC Submission 038764-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.288) question?
Stock # R0574 (G1)
Quality Score 225
Status Validated
Chromosome 17
Chromosomal Location 95059923-95082454 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 95068919 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: ENSMUST00000084298
SMART Domains Protein: ENSMUSP00000081321
Gene: ENSMUSG00000066057

DomainStartEndE-ValueType
low complexity region 25 48 N/A INTRINSIC
transmembrane domain 90 112 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000157966
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182313
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182402
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182475
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182639
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182794
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183133
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.2%
  • 20x: 92.4%
Validation Efficiency 100% (34/34)
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca14 A G 7: 119,823,720 (GRCm39) I416V probably damaging Het
Actrt3 T C 3: 30,653,829 (GRCm39) E57G probably benign Het
Adamts5 A G 16: 85,696,372 (GRCm39) S262P probably damaging Het
Aldh1a2 T C 9: 71,188,990 (GRCm39) probably null Het
Arhgap29 A G 3: 121,801,274 (GRCm39) I670V probably benign Het
Bptf T C 11: 106,967,353 (GRCm39) D1009G probably damaging Het
Ddr2 G T 1: 169,809,532 (GRCm39) probably benign Het
Ift140 T A 17: 25,270,734 (GRCm39) probably null Het
Itga1 A C 13: 115,103,097 (GRCm39) S1111R probably damaging Het
Klk1b27 T A 7: 43,705,525 (GRCm39) L199Q probably damaging Het
Lhx3 T C 2: 26,091,323 (GRCm39) S329G probably benign Het
Man2b1 T G 8: 85,823,405 (GRCm39) M913R probably benign Het
Mmp15 G A 8: 96,092,029 (GRCm39) A80T possibly damaging Het
Mpo A T 11: 87,686,902 (GRCm39) Y177F probably damaging Het
Mynn T C 3: 30,670,888 (GRCm39) S587P probably benign Het
Nfkbib C T 7: 28,461,213 (GRCm39) V145I probably benign Het
Or1o3 G T 17: 37,573,772 (GRCm39) S261Y probably damaging Het
Or4k15 A T 14: 50,364,139 (GRCm39) Y35F probably damaging Het
Or6k8-ps1 T C 1: 173,979,132 (GRCm39) F17L probably benign Het
Pole2 G A 12: 69,258,231 (GRCm39) probably benign Het
Ppargc1b C T 18: 61,435,810 (GRCm39) G906D probably benign Het
Prl8a2 T A 13: 27,532,883 (GRCm39) C32S probably damaging Het
Rhno1 A T 6: 128,335,113 (GRCm39) probably null Het
Rprd2 T C 3: 95,681,669 (GRCm39) E408G possibly damaging Het
Ryr2 T A 13: 11,746,555 (GRCm39) H1999L probably benign Het
Shprh T C 10: 11,038,821 (GRCm39) probably benign Het
Snx3 T A 10: 42,378,383 (GRCm39) N19K probably benign Het
Stx8 C T 11: 67,864,078 (GRCm39) T46M probably damaging Het
Tbc1d17 A G 7: 44,492,547 (GRCm39) probably benign Het
Ush1c A G 7: 45,846,228 (GRCm39) S855P possibly damaging Het
Usp54 A G 14: 20,606,322 (GRCm39) V1338A probably benign Het
Vmn1r214 A G 13: 23,218,663 (GRCm39) I52M probably benign Het
Predicted Primers PCR Primer
(F):5'- AGAAAACCTTGGCCTCGGGAAC -3'
(R):5'- ACGAGCCTAAAGAGCTGTCCAGTG -3'

Sequencing Primer
(F):5'- GGCCTCGGGAACTCATATTC -3'
(R):5'- GAGCTGTCCAGTGATTTCAGAAAC -3'
Posted On 2013-06-11