Incidental Mutation 'IGL00852:Cypt15-ps'
ID 278019
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cypt15-ps
Ensembl Gene ENSMUSG00000079619
Gene Name cysteine-rich perinuclear theca 15
Synonyms 1700085A12Rik, Cypt15
Accession Numbers
Essential gene? Not available question?
Stock # IGL00852
Quality Score
Status
Chromosome X
Chromosomal Location 38435144-38435840 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 38435507 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 56 (R56*)
Ref Sequence ENSEMBL: ENSMUSP00000110767 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115114]
AlphaFold B1AXS0
Predicted Effect probably null
Transcript: ENSMUST00000115114
AA Change: R56*
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cfap157 T A 2: 32,669,827 (GRCm39) Q252L possibly damaging Het
Chd9 C A 8: 91,699,835 (GRCm39) Q622K probably benign Het
Crygd C T 1: 65,101,250 (GRCm39) R115Q probably benign Het
Dbt G A 3: 116,339,763 (GRCm39) G384S probably benign Het
Dmxl2 A T 9: 54,330,597 (GRCm39) L721* probably null Het
Dsc2 C T 18: 20,167,740 (GRCm39) V718I probably benign Het
Eef1b2 G A 1: 63,217,665 (GRCm39) G91R probably damaging Het
Epb41l1 C T 2: 156,345,638 (GRCm39) L214F probably damaging Het
Ibtk A C 9: 85,595,654 (GRCm39) Y971D probably benign Het
Lancl1 G A 1: 67,043,996 (GRCm39) L335F probably damaging Het
Pcm1 T C 8: 41,740,858 (GRCm39) W1035R probably damaging Het
Pkn2 T A 3: 142,515,577 (GRCm39) probably benign Het
Ranbp2 G A 10: 58,313,723 (GRCm39) R1481Q probably benign Het
Scn5a T C 9: 119,366,748 (GRCm39) N313S probably benign Het
Septin10 A G 10: 59,028,642 (GRCm39) probably benign Het
Serpinb6c A T 13: 34,081,321 (GRCm39) probably null Het
Slc22a19 C T 19: 7,660,323 (GRCm39) M362I probably benign Het
Spmip4 T A 6: 50,566,164 (GRCm39) probably null Het
Tnni3k T A 3: 154,760,206 (GRCm39) Q43L probably benign Het
Trpm3 T A 19: 22,964,435 (GRCm39) V1310D possibly damaging Het
Zdhhc13 T A 7: 48,455,349 (GRCm39) S260R probably benign Het
Other mutations in Cypt15-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
Z1176:Cypt15-ps UTSW X 38,435,261 (GRCm39) missense possibly damaging 0.82
Z1177:Cypt15-ps UTSW X 38,435,207 (GRCm39) missense probably damaging 0.96
Posted On 2015-04-16