Incidental Mutation 'R2400:7530416G11Rik'
ID 248666
Institutional Source Beutler Lab
Gene Symbol 7530416G11Rik
Ensembl Gene ENSMUSG00000096607
Gene Name RIKEN cDNA 7530416G11 gene
Synonyms
MMRRC Submission 040366-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # R2400 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 85376937-85387428 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 85377566 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 133 (T133A)
Ref Sequence ENSEMBL: ENSMUSP00000136090 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000178942]
AlphaFold J3QJX6
Predicted Effect unknown
Transcript: ENSMUST00000178942
AA Change: T133A
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 24 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl2 G T 3: 148,557,570 (GRCm39) S519R probably damaging Het
AU041133 A T 10: 81,986,742 (GRCm39) K132* probably null Het
Bhlhe22 A G 3: 18,109,615 (GRCm39) N222D probably damaging Het
Cep72 C A 13: 74,197,096 (GRCm39) A69S probably damaging Het
Csn1s2a T A 5: 87,928,014 (GRCm39) probably null Het
Dapk1 T A 13: 60,900,030 (GRCm39) F872I probably benign Het
Dhx57 T C 17: 80,567,845 (GRCm39) D746G probably damaging Het
Dnah17 T A 11: 118,017,210 (GRCm39) probably null Het
Fgg A G 3: 82,915,494 (GRCm39) D37G possibly damaging Het
Fnip2 G T 3: 79,386,941 (GRCm39) S958R probably benign Het
Gfpt1 A G 6: 87,064,330 (GRCm39) D640G probably damaging Het
Golgb1 C A 16: 36,738,828 (GRCm39) T2389K possibly damaging Het
Hmgcl C A 4: 135,679,679 (GRCm39) probably null Het
Mmp11 T A 10: 75,761,344 (GRCm39) T419S probably benign Het
Myg1 G C 15: 102,246,171 (GRCm39) G349R probably damaging Het
Nkiras1 T A 14: 18,280,011 (GRCm38) V108E possibly damaging Het
Pcsk1 T C 13: 75,238,245 (GRCm39) L22P probably benign Het
Rnf213 T C 11: 119,334,021 (GRCm39) Y3077H probably damaging Het
Sec62 A G 3: 30,864,681 (GRCm39) N182D unknown Het
Serpinb5 A G 1: 106,809,682 (GRCm39) T363A probably damaging Het
Usf3 T A 16: 44,036,110 (GRCm39) S197T probably benign Het
Vmn2r11 T A 5: 109,199,928 (GRCm39) E508D probably benign Het
Wdr81 A G 11: 75,339,861 (GRCm39) F1376L probably benign Het
Zfp260 T C 7: 29,804,126 (GRCm39) S9P possibly damaging Het
Other mutations in 7530416G11Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
FR4340:7530416G11Rik UTSW 15 85,378,508 (GRCm39) missense unknown
FR4342:7530416G11Rik UTSW 15 85,378,508 (GRCm39) missense unknown
FR4589:7530416G11Rik UTSW 15 85,378,508 (GRCm39) missense unknown
R3889:7530416G11Rik UTSW 15 85,378,292 (GRCm39) missense unknown
R4609:7530416G11Rik UTSW 15 85,378,370 (GRCm39) missense unknown
R6005:7530416G11Rik UTSW 15 85,378,310 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- CTGCATACCAGGTGGGAAAG -3'
(R):5'- ACTCCACTTTGGTGAAGAGAACC -3'

Sequencing Primer
(F):5'- AAAGTGTAGTGTCCGTCTTTCC -3'
(R):5'- CTATTTCCAATAGGCAAGCTGTGG -3'
Posted On 2014-11-11