Incidental Mutation 'IGL03373:Mup1'
ID 420397
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mup1
Ensembl Gene ENSMUSG00000078683
Gene Name major urinary protein 1
Synonyms Mup-a, Mup-1, Ltn-1, Lvtn-1, Up-1
Accession Numbers
Essential gene? Not available question?
Stock # IGL03373
Quality Score
Status
Chromosome 4
Chromosomal Location 60454011-60457959 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to G at 60457849 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000118299 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084548] [ENSMUST00000103012] [ENSMUST00000107499] [ENSMUST00000135953]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000084548
SMART Domains Protein: ENSMUSP00000081596
Gene: ENSMUSG00000078683

DomainStartEndE-ValueType
low complexity region 4 16 N/A INTRINSIC
Pfam:Lipocalin 34 173 1.6e-33 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000103012
SMART Domains Protein: ENSMUSP00000100077
Gene: ENSMUSG00000078683

DomainStartEndE-ValueType
low complexity region 4 16 N/A INTRINSIC
Pfam:Lipocalin 34 173 5.7e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000107499
SMART Domains Protein: ENSMUSP00000103123
Gene: ENSMUSG00000078683

DomainStartEndE-ValueType
low complexity region 4 16 N/A INTRINSIC
Pfam:Lipocalin 34 173 5.7e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000135953
Predicted Effect noncoding transcript
Transcript: ENSMUST00000156693
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Three haplotypes for the Mup1 complex are known: the a haplotype in BALB/c, DBA/2 and C57BR/cd; b haplotype in C57BL/6, C57L and C58; and c (null) haplotype in BALB/cJPt. Female electrophoretic pattern differs from male in some strains, but converts to the male pattern with androgen treatment. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam6a A T 12: 113,509,172 (GRCm39) Y515F possibly damaging Het
Adgrv1 A G 13: 81,711,751 (GRCm39) V1075A probably damaging Het
Alox8 T C 11: 69,077,443 (GRCm39) T436A probably benign Het
Cdc7 T A 5: 107,120,785 (GRCm39) probably benign Het
Cdhr1 T A 14: 36,818,257 (GRCm39) D65V possibly damaging Het
Dnase1 A G 16: 3,857,707 (GRCm39) E278G probably damaging Het
Eif3g A T 9: 20,805,722 (GRCm39) probably benign Het
Flnb G A 14: 7,890,867 (GRCm38) probably null Het
Hars2 G T 18: 36,918,998 (GRCm39) R86L probably damaging Het
Lmod1 C T 1: 135,292,264 (GRCm39) A373V possibly damaging Het
Mdga2 A G 12: 66,763,496 (GRCm39) I200T probably damaging Het
Nat8f5 A C 6: 85,794,529 (GRCm39) S144A probably benign Het
Ndnf A C 6: 65,681,272 (GRCm39) Y517S possibly damaging Het
Nedd4l G A 18: 65,314,391 (GRCm39) probably benign Het
Nlrp4g A T 9: 124,349,853 (GRCm38) noncoding transcript Het
Nob1 C T 8: 108,144,678 (GRCm39) probably benign Het
Nploc4 G A 11: 120,300,455 (GRCm39) R326* probably null Het
Obox3 A T 7: 15,359,715 (GRCm39) V318D probably benign Het
Or10a3m G A 7: 108,313,339 (GRCm39) V248I probably damaging Het
Or10ag57 T C 2: 87,218,577 (GRCm39) F176S probably damaging Het
Pgm1 T C 4: 99,818,741 (GRCm39) I130T probably damaging Het
Ptprk A T 10: 28,442,533 (GRCm39) D845V probably damaging Het
Ptx4 T A 17: 25,339,873 (GRCm39) S17T probably benign Het
Rasgrf1 T C 9: 89,899,084 (GRCm39) probably benign Het
Rfx6 A G 10: 51,596,096 (GRCm39) T426A probably damaging Het
Sfpq C A 4: 126,920,578 (GRCm39) R564S possibly damaging Het
Spint2 A G 7: 28,957,634 (GRCm39) probably benign Het
Vmn1r27 A G 6: 58,192,689 (GRCm39) I105T probably damaging Het
Vmn1r78 T C 7: 11,887,270 (GRCm39) S294P possibly damaging Het
Vmn2r40 T C 7: 8,923,092 (GRCm39) D423G probably benign Het
Other mutations in Mup1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6420:Mup1 UTSW 4 60,457,758 (GRCm39) missense possibly damaging 0.67
R9500:Mup1 UTSW 4 60,456,488 (GRCm39) missense possibly damaging 0.95
Posted On 2016-08-02