Incidental Mutation 'IGL02310:Gm44805'
ID287779
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm44805
Ensembl Gene ENSMUSG00000109350
Gene Namepredicted gene 44805
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02310
Quality Score
Status
Chromosome7
Chromosomal Location19671584-19681423 bp(-) (GRCm38)
Type of Mutationmakesense
DNA Base Change (assembly) A to G at 19671763 bp
ZygosityHeterozygous
Amino Acid Change Stop codon to Glutamine at position 98 (*98Q)
Ref Sequence ENSEMBL: ENSMUSP00000114512 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000003074] [ENSMUST00000127648] [ENSMUST00000134116] [ENSMUST00000142352] [ENSMUST00000150569]
Predicted Effect probably null
Transcript: ENSMUST00000003074
AA Change: *98Q
SMART Domains Protein: ENSMUSP00000003074
Gene: ENSMUSG00000002992
AA Change: *98Q

DomainStartEndE-ValueType
Pfam:Apo-CII 20 97 4.4e-46 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000127648
AA Change: *98Q
SMART Domains Protein: ENSMUSP00000118305
Gene: ENSMUSG00000109350
AA Change: *98Q

DomainStartEndE-ValueType
Pfam:Apo-CII 20 68 2.7e-24 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000134116
AA Change: *98Q
SMART Domains Protein: ENSMUSP00000118291
Gene: ENSMUSG00000002992
AA Change: *98Q

DomainStartEndE-ValueType
Pfam:Apo-CII 20 97 4.4e-46 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000142352
AA Change: *98Q
SMART Domains Protein: ENSMUSP00000115173
Gene: ENSMUSG00000002992
AA Change: *98Q

DomainStartEndE-ValueType
Pfam:Apo-CII 21 97 1.8e-42 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000150569
AA Change: *98Q
SMART Domains Protein: ENSMUSP00000114512
Gene: ENSMUSG00000109350
AA Change: *98Q

DomainStartEndE-ValueType
Pfam:Apo-CII 20 97 4.4e-46 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: This locus represents naturally occurring read-through transcription between the neighboring apolipoprotein C-IV (Apoc4) and apolipoprotein C-II (Apoc2) genes on chromosome 7. The readthrough transcript encodes a protein that shares sequence identity with the downstream gene (Apoc2). [provided by RefSeq, Jun 2015]
Allele List at MGI
Other mutations in this stock
Total: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9530077C05Rik A G 9: 22,424,428 Y114C probably benign Het
Ano4 T A 10: 89,023,878 K382* probably null Het
Bcl9l A G 9: 44,509,305 Y1299C probably damaging Het
Best1 T A 19: 9,989,152 H357L probably benign Het
Cdc26 T C 4: 62,395,029 probably benign Het
Esyt2 C T 12: 116,365,921 L700F probably benign Het
Fkbp15 T C 4: 62,340,316 Y138C probably damaging Het
Gbp6 T C 5: 105,290,975 N16D probably benign Het
Hecw2 T C 1: 53,923,916 D812G probably null Het
Hic2 G A 16: 17,257,757 R150Q probably damaging Het
Kif21b T A 1: 136,159,757 L937Q probably damaging Het
Klhl36 T A 8: 119,869,617 probably null Het
Mug2 C T 6: 122,059,123 probably benign Het
Olfr1410 T C 1: 92,608,065 V76A possibly damaging Het
Pdcl2 A T 5: 76,317,881 I116N probably damaging Het
Pkn2 A G 3: 142,811,580 I482T probably damaging Het
Prss53 T G 7: 127,886,614 D518A probably benign Het
Psme4 A G 11: 30,837,484 D1093G probably benign Het
Tmcc2 A T 1: 132,358,907 I602N probably damaging Het
Tmem55b T C 14: 50,929,210 T187A possibly damaging Het
Ttn C T 2: 76,788,691 V16115I possibly damaging Het
Zbtb21 G T 16: 97,951,790 T459K possibly damaging Het
Posted On2015-04-16