Incidental Mutation 'IGL01966:1500002C15Rik'
ID 181539
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1500002C15Rik
Ensembl Gene ENSMUSG00000096221
Gene Name RIKEN cDNA 1500002C15 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01966
Quality Score
Status
Chromosome 4
Chromosomal Location 155818180-155818927 bp(-) (GRCm39)
Type of Mutation splice site (1880 bp from exon)
DNA Base Change (assembly) A to G at 155818526 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000101220 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030905] [ENSMUST00000105595] [ENSMUST00000127188] [ENSMUST00000147721]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000030905
SMART Domains Protein: ENSMUSP00000030905
Gene: ENSMUSG00000029038

DomainStartEndE-ValueType
Pfam:Ssu72 6 194 1.3e-96 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000105595
SMART Domains Protein: ENSMUSP00000101220
Gene: ENSMUSG00000029038

DomainStartEndE-ValueType
Pfam:Ssu72 4 176 2.8e-81 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000127188
SMART Domains Protein: ENSMUSP00000127341
Gene: ENSMUSG00000084845

DomainStartEndE-ValueType
Pfam:TMEM240 1 173 3.8e-108 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000147721
SMART Domains Protein: ENSMUSP00000130974
Gene: ENSMUSG00000084845

DomainStartEndE-ValueType
Pfam:TMEM240 1 173 1.5e-100 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000176526
Predicted Effect noncoding transcript
Transcript: ENSMUST00000178987
SMART Domains Protein: ENSMUSP00000136958
Gene: ENSMUSG00000096221

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 41 52 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000197451
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acer2 T A 4: 86,835,815 (GRCm39) *230R probably null Het
Adamts12 A G 15: 11,258,269 (GRCm39) K527E probably damaging Het
Anks1b C A 10: 90,730,994 (GRCm39) R937S probably damaging Het
C2cd5 G T 6: 142,957,767 (GRCm39) C989* probably null Het
Calhm5 T C 10: 33,972,129 (GRCm39) H102R probably benign Het
Col14a1 A G 15: 55,312,121 (GRCm39) probably benign Het
Cramp1 T A 17: 25,201,917 (GRCm39) T522S probably benign Het
Cyp2c70 A T 19: 40,142,016 (GRCm39) probably benign Het
Elmod1 T A 9: 53,828,611 (GRCm39) I224F probably benign Het
Emx2 T A 19: 59,448,021 (GRCm39) I24N possibly damaging Het
Fga A T 3: 82,936,461 (GRCm39) I86F probably damaging Het
Fig4 C A 10: 41,108,098 (GRCm39) probably null Het
Gm10234 T C 6: 95,299,118 (GRCm39) probably null Het
Gm12588 A T 11: 121,797,561 (GRCm39) I96N probably benign Het
Grm3 A G 5: 9,561,486 (GRCm39) I788T probably damaging Het
Homer3 A G 8: 70,742,807 (GRCm39) K173E probably damaging Het
Kansl1l A G 1: 66,777,227 (GRCm39) V635A probably damaging Het
Kctd3 C T 1: 188,724,859 (GRCm39) G241R probably damaging Het
Krt8 G T 15: 101,906,105 (GRCm39) S423R probably benign Het
Lrrc24 C A 15: 76,602,511 (GRCm39) A125S probably benign Het
Muc4 T C 16: 32,570,244 (GRCm39) S435P possibly damaging Het
Nfkb2 G A 19: 46,298,129 (GRCm39) G502D probably benign Het
Nlrp6 G A 7: 140,505,103 (GRCm39) C750Y probably damaging Het
Or8b1b A T 9: 38,376,225 (GRCm39) D296V possibly damaging Het
Oxsm T C 14: 16,242,520 (GRCm38) N83S probably benign Het
Paqr3 A G 5: 97,247,502 (GRCm39) L202P probably benign Het
Pcdh10 T A 3: 45,334,733 (GRCm39) L349Q probably benign Het
Ptdss2 A G 7: 140,715,304 (GRCm39) T29A possibly damaging Het
Rbbp8nl G A 2: 179,922,782 (GRCm39) probably benign Het
Rc3h2 A G 2: 37,272,789 (GRCm39) probably benign Het
Ric1 A T 19: 29,572,963 (GRCm39) Y801F probably benign Het
Sgcz A T 8: 38,107,169 (GRCm39) S114R probably damaging Het
Tenm4 A G 7: 96,202,757 (GRCm39) D124G probably damaging Het
Zscan22 T G 7: 12,640,398 (GRCm39) M214R probably benign Het
Other mutations in 1500002C15Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01526:1500002C15Rik APN 4 155,818,628 (GRCm39) unclassified probably benign
IGL03268:1500002C15Rik APN 4 155,818,648 (GRCm39) unclassified probably benign
Posted On 2014-05-07