Incidental Mutation 'IGL01392:Prb1b'
ID 79239
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prb1b
Ensembl Gene ENSMUSG00000107874
Gene Name proline-rich protein BstNI subfamily 1B
Synonyms MP5, Prpmp5
Accession Numbers
Essential gene? Probably non essential (E-score: 0.127) question?
Stock # IGL01392
Quality Score
Status
Chromosome 6
Chromosomal Location 132288553-132291706 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 132289383 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 147 (N147S)
Ref Sequence ENSEMBL: ENSMUSP00000047347 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000048686]
AlphaFold E9PXN1
Predicted Effect unknown
Transcript: ENSMUST00000048686
AA Change: N147S
SMART Domains Protein: ENSMUSP00000047347
Gene: ENSMUSG00000107874
AA Change: N147S

DomainStartEndE-ValueType
Pfam:Pro-rich 1 136 2.2e-36 PFAM
Pfam:Pro-rich 84 169 6.1e-17 PFAM
Pfam:Pro-rich 131 182 2.5e-10 PFAM
Pfam:Pro-rich 171 228 4.7e-10 PFAM
Pfam:Pro-rich 222 290 1.1e-11 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acvr1 A G 2: 58,390,558 (GRCm39) V2A probably benign Het
Adgrf5 A T 17: 43,760,903 (GRCm39) Q866L probably benign Het
Ankrd13a A G 5: 114,935,914 (GRCm39) E295G probably benign Het
Arid1a T C 4: 133,408,348 (GRCm39) D2053G unknown Het
Calr4 A G 4: 109,111,071 (GRCm39) E272G probably benign Het
Cmya5 T C 13: 93,225,714 (GRCm39) S3125G probably damaging Het
Dnah7b T C 1: 46,165,948 (GRCm39) Y538H probably damaging Het
Eri3 T C 4: 117,446,356 (GRCm39) probably null Het
Fmo6 T A 1: 162,757,580 (GRCm39) R63* probably null Het
Gm7168 G A 17: 14,169,169 (GRCm39) D179N probably benign Het
Got1l1 T C 8: 27,688,019 (GRCm39) T337A probably damaging Het
Gvin-ps3 T C 7: 105,682,962 (GRCm39) I98V probably benign Het
Igf2r A G 17: 12,923,236 (GRCm39) M1191T probably benign Het
Ighv1-54 A G 12: 115,157,557 (GRCm39) L30P probably damaging Het
Igkv8-30 A G 6: 70,094,331 (GRCm39) S27P probably benign Het
Kcnab2 A T 4: 152,478,254 (GRCm39) V335E possibly damaging Het
Klf12 A T 14: 100,387,193 (GRCm39) I3N probably damaging Het
Megf8 T C 7: 25,063,174 (GRCm39) V2510A probably benign Het
Mme A G 3: 63,269,467 (GRCm39) D592G probably damaging Het
Myh1 A G 11: 67,112,127 (GRCm39) N1727S probably benign Het
Ncor1 A G 11: 62,231,420 (GRCm39) S796P probably damaging Het
Nlrp14 A G 7: 106,797,120 (GRCm39) probably benign Het
Or51f23 T A 7: 102,453,061 (GRCm39) Y125* probably null Het
Or5b95 T A 19: 12,658,167 (GRCm39) Y232N probably benign Het
Or5p80 C T 7: 108,229,885 (GRCm39) R229C probably benign Het
Plekhm2 A G 4: 141,369,737 (GRCm39) V86A probably damaging Het
Popdc2 G T 16: 38,194,493 (GRCm39) V305L probably benign Het
Rttn C T 18: 89,013,737 (GRCm39) H469Y probably benign Het
Slc2a12 T C 10: 22,540,583 (GRCm39) V146A probably damaging Het
Sptlc3 A G 2: 139,388,341 (GRCm39) E111G possibly damaging Het
Zfp108 T C 7: 23,957,872 (GRCm39) probably benign Het
Zfp719 T A 7: 43,240,554 (GRCm39) F714Y probably damaging Het
Other mutations in Prb1b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02259:Prb1b APN 6 132,289,637 (GRCm39) missense unknown
IGL02434:Prb1b APN 6 132,289,339 (GRCm39) missense unknown
IGL03238:Prb1b APN 6 132,289,308 (GRCm39) missense unknown
R0971:Prb1b UTSW 6 132,290,618 (GRCm39) missense unknown
R1900:Prb1b UTSW 6 132,291,661 (GRCm39) missense unknown
R3800:Prb1b UTSW 6 132,289,657 (GRCm39) missense unknown
R3951:Prb1b UTSW 6 132,289,657 (GRCm39) missense unknown
R3952:Prb1b UTSW 6 132,289,657 (GRCm39) missense unknown
R3981:Prb1b UTSW 6 132,289,657 (GRCm39) missense unknown
R4083:Prb1b UTSW 6 132,289,657 (GRCm39) missense unknown
R4348:Prb1b UTSW 6 132,290,624 (GRCm39) missense unknown
R4351:Prb1b UTSW 6 132,290,624 (GRCm39) missense unknown
R4352:Prb1b UTSW 6 132,290,624 (GRCm39) missense unknown
R4353:Prb1b UTSW 6 132,290,624 (GRCm39) missense unknown
R6190:Prb1b UTSW 6 132,289,692 (GRCm39) missense unknown
R7001:Prb1b UTSW 6 132,289,527 (GRCm39) missense unknown
R9023:Prb1b UTSW 6 132,289,174 (GRCm39) frame shift probably null
R9028:Prb1b UTSW 6 132,289,618 (GRCm39) missense unknown
R9193:Prb1b UTSW 6 132,288,996 (GRCm39) missense unknown
R9256:Prb1b UTSW 6 132,288,972 (GRCm39) missense unknown
R9388:Prb1b UTSW 6 132,289,437 (GRCm39) missense unknown
R9644:Prb1b UTSW 6 132,289,218 (GRCm39) missense unknown
Posted On 2013-11-05