Incidental Mutation 'IGL03348:Or4ac1-ps1'
ID 419560
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or4ac1-ps1
Ensembl Gene ENSMUSG00000068810
Gene Name olfactory receptor family 4 subfamily AC member 1, pseudogene 1
Synonyms Olfr1187-ps1, GA_x6K02T2Q125-50027818-50027495
Accession Numbers
Essential gene? Probably non essential (E-score: 0.243) question?
Stock # IGL03348
Quality Score
Status
Chromosome 2
Chromosomal Location 88370468-88370791 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 88370485 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect
SMART Domains Protein: ENSMUSP00000088203
Gene: ENSMUSG00000068810
AA Change: T95A

DomainStartEndE-ValueType
SCOP:d1l9ha_ 19 99 9e-3 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000177576
SMART Domains Protein: ENSMUSP00000137535
Gene: ENSMUSG00000068810

DomainStartEndE-ValueType
transmembrane domain 19 41 N/A INTRINSIC
transmembrane domain 51 73 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A330008L17Rik A C 8: 100,148,324 (GRCm39) noncoding transcript Het
Actmap T G 7: 26,896,545 (GRCm39) probably null Het
Adgrv1 T C 13: 81,647,177 (GRCm39) N3121S possibly damaging Het
Aldh16a1 C T 7: 44,791,399 (GRCm39) R102Q possibly damaging Het
Atp9b A T 18: 80,879,637 (GRCm39) I346K possibly damaging Het
Baiap2l1 T C 5: 144,215,341 (GRCm39) K388R probably benign Het
Cfap65 A C 1: 74,966,778 (GRCm39) I303S probably damaging Het
Chd5 C T 4: 152,461,142 (GRCm39) P1244L probably damaging Het
Col12a1 A G 9: 79,600,712 (GRCm39) S791P possibly damaging Het
Ctsz T A 2: 174,270,490 (GRCm39) I231F probably damaging Het
Dnah8 A G 17: 30,965,960 (GRCm39) T2431A probably damaging Het
Eif4b T C 15: 102,001,466 (GRCm39) probably benign Het
Epha4 T C 1: 77,483,809 (GRCm39) I67V possibly damaging Het
Exoc1 T A 5: 76,683,440 (GRCm39) V55D probably damaging Het
Exosc8 A T 3: 54,640,143 (GRCm39) D72E possibly damaging Het
F5 C T 1: 164,021,721 (GRCm39) P1399S possibly damaging Het
Fmo1 T A 1: 162,677,720 (GRCm39) N132I possibly damaging Het
Fndc1 T A 17: 7,991,479 (GRCm39) H739L unknown Het
Glb1l2 T C 9: 26,676,976 (GRCm39) D415G probably benign Het
Gphn T A 12: 78,673,893 (GRCm39) H498Q probably damaging Het
Lrrc56 A G 7: 140,787,153 (GRCm39) N342S probably benign Het
Mbnl3 G A X: 50,253,425 (GRCm39) T16I probably damaging Het
Mrps5 T G 2: 127,443,305 (GRCm39) H294Q probably damaging Het
Neu4 A G 1: 93,952,696 (GRCm39) Y355C possibly damaging Het
Obscn A T 11: 58,941,188 (GRCm39) D5105E probably damaging Het
Or4f56 C A 2: 111,703,493 (GRCm39) A236S probably damaging Het
Or4k15b A G 14: 50,272,212 (GRCm39) I216T probably benign Het
Or5p73 A G 7: 108,064,615 (GRCm39) D28G probably benign Het
Parp1 T A 1: 180,405,272 (GRCm39) probably benign Het
Plac1 A T X: 52,159,517 (GRCm39) N64K probably damaging Het
Plcd1 C A 9: 118,901,558 (GRCm39) K655N possibly damaging Het
Psme4 T C 11: 30,826,796 (GRCm39) S1772P probably damaging Het
Shcbp1 C T 8: 4,815,089 (GRCm39) V130I probably benign Het
Slc25a11 T C 11: 70,536,170 (GRCm39) probably benign Het
Svep1 C T 4: 58,113,635 (GRCm39) G1004E probably damaging Het
Tars2 T C 3: 95,647,580 (GRCm39) probably null Het
Tbc1d12 C T 19: 38,905,064 (GRCm39) T593I probably damaging Het
Tcerg1l T A 7: 137,815,100 (GRCm39) E526D probably damaging Het
Tmcc3 G A 10: 94,414,942 (GRCm39) V215M possibly damaging Het
Trappc8 T C 18: 20,985,838 (GRCm39) D601G probably damaging Het
Trp53bp2 T A 1: 182,281,313 (GRCm39) N971K probably damaging Het
Ube2g2 A T 10: 77,466,711 (GRCm39) E36D probably benign Het
Uggt2 T A 14: 119,308,300 (GRCm39) R360S probably benign Het
Utp20 A G 10: 88,594,179 (GRCm39) V2182A probably benign Het
Other mutations in Or4ac1-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02974:Or4ac1-ps1 APN 2 88,370,579 (GRCm39) synonymous silent
R0784:Or4ac1-ps1 UTSW 2 88,370,511 (GRCm39) exon noncoding transcript
R3724:Or4ac1-ps1 UTSW 2 88,370,630 (GRCm39) exon noncoding transcript
R3805:Or4ac1-ps1 UTSW 2 88,370,700 (GRCm39) exon noncoding transcript
R3806:Or4ac1-ps1 UTSW 2 88,370,700 (GRCm39) exon noncoding transcript
R5235:Or4ac1-ps1 UTSW 2 88,370,769 (GRCm39) exon noncoding transcript
R5464:Or4ac1-ps1 UTSW 2 88,370,599 (GRCm39) splice site probably null
R5888:Or4ac1-ps1 UTSW 2 88,370,588 (GRCm39) exon noncoding transcript
Posted On 2016-08-02