Incidental Mutation 'IGL02581:1700034H15Rik'
ID 299357
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700034H15Rik
Ensembl Gene ENSMUSG00000055833
Gene Name RIKEN cDNA 1700034H15 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02581
Quality Score
Status
Chromosome 1
Chromosomal Location 191626184-191639639 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 191635652 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000124176 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000044954] [ENSMUST00000161756]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000044954
SMART Domains Protein: ENSMUSP00000042410
Gene: ENSMUSG00000037434

DomainStartEndE-ValueType
Pfam:Cation_efflux 11 278 7.3e-43 PFAM
transmembrane domain 306 328 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000069573
SMART Domains Protein: ENSMUSP00000063209
Gene: ENSMUSG00000055833

DomainStartEndE-ValueType
low complexity region 106 117 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139827
SMART Domains Protein: ENSMUSP00000136990
Gene: ENSMUSG00000055833

DomainStartEndE-ValueType
low complexity region 106 117 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000140401
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145050
Predicted Effect noncoding transcript
Transcript: ENSMUST00000154116
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190327
Predicted Effect probably benign
Transcript: ENSMUST00000161756
SMART Domains Protein: ENSMUSP00000124176
Gene: ENSMUSG00000037434

DomainStartEndE-ValueType
Pfam:Cation_efflux 1 119 1.5e-17 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 C T 11: 9,349,132 (GRCm39) probably benign Het
Aga T C 8: 53,974,079 (GRCm39) probably benign Het
Atp2a3 C A 11: 72,866,165 (GRCm39) H262N probably benign Het
C1rl T C 6: 124,470,113 (GRCm39) S2P possibly damaging Het
Cstdc5 T C 16: 36,179,860 (GRCm39) T86A probably damaging Het
Dgkd T C 1: 87,845,724 (GRCm39) probably benign Het
Dnajb11 A G 16: 22,689,768 (GRCm39) N311D probably benign Het
Flg2 A C 3: 93,127,199 (GRCm39) Q2037P unknown Het
Glyctk T C 9: 106,034,980 (GRCm39) T29A probably benign Het
Gtf3c1 C A 7: 125,245,687 (GRCm39) R1672L possibly damaging Het
Hps3 A T 3: 20,057,385 (GRCm39) probably benign Het
Kcnh3 G T 15: 99,136,052 (GRCm39) C683F possibly damaging Het
Lmtk2 T G 5: 144,085,166 (GRCm39) F213V probably damaging Het
Malrd1 C A 2: 16,147,123 (GRCm39) C1988* probably null Het
Map3k11 T A 19: 5,750,834 (GRCm39) M684K probably benign Het
Oga T A 19: 45,740,630 (GRCm39) M902L possibly damaging Het
Pip5k1c C A 10: 81,153,155 (GRCm39) probably null Het
Plekhh1 T C 12: 79,125,882 (GRCm39) probably null Het
Rev3l C A 10: 39,697,277 (GRCm39) N591K probably benign Het
Rrp9 T A 9: 106,360,827 (GRCm39) N269K probably damaging Het
Sec14l4 T C 11: 3,989,941 (GRCm39) I80T possibly damaging Het
Srpra G A 9: 35,126,328 (GRCm39) probably null Het
Tmc8 G A 11: 117,674,714 (GRCm39) R143H probably benign Het
Trank1 T C 9: 111,212,193 (GRCm39) I1777T probably benign Het
Trim17 C A 11: 58,861,902 (GRCm39) Y311* probably null Het
Vps13a C T 19: 16,632,686 (GRCm39) A2557T probably benign Het
Vps53 T G 11: 75,992,883 (GRCm39) N106T probably damaging Het
Other mutations in 1700034H15Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01634:1700034H15Rik APN 1 191,633,016 (GRCm39) unclassified noncoding transcript
Posted On 2015-04-16