Incidental Mutation 'IGL01604:Mpi'
ID92680
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mpi
Ensembl Gene ENSMUSG00000032306
Gene Namemannose phosphate isomerase
Synonyms1110002E17Rik, Mpi-1, Mpi1
Accession Numbers

Genbank: NM_025837; MGI: 97075

Is this an essential gene? Essential (E-score: 1.000) question?
Stock #IGL01604
Quality Score
Status
Chromosome9
Chromosomal Location57544256-57552763 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 57550742 bp
ZygosityHeterozygous
Amino Acid Change Alanine to Valine at position 59 (A59V)
Ref Sequence ENSEMBL: ENSMUSP00000034856 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034856]
Predicted Effect possibly damaging
Transcript: ENSMUST00000034856
AA Change: A59V

PolyPhen 2 Score 0.846 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000034856
Gene: ENSMUSG00000032306
AA Change: A59V

DomainStartEndE-ValueType
Pfam:PMI_typeI 6 384 4.3e-145 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000124593
Predicted Effect noncoding transcript
Transcript: ENSMUST00000140671
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145543
Predicted Effect unknown
Transcript: ENSMUST00000156428
AA Change: A55V
SMART Domains Protein: ENSMUSP00000119342
Gene: ENSMUSG00000032306
AA Change: A55V

DomainStartEndE-ValueType
Pfam:PMI_typeI 3 119 3.1e-45 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Phosphomannose isomerase catalyzes the interconversion of fructose-6-phosphate and mannose-6-phosphate and plays a critical role in maintaining the supply of D-mannose derivatives, which are required for most glycosylation reactions. Mutations in the MPI gene were found in patients with carbohydrate-deficient glycoprotein syndrome, type Ib. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
PHENOTYPE: Homozygous null mice display embryonic lethality during organogenesis, variable abnormalities of the yolk sac and embryonic vasculature, and partial penetrance of abnormal chorioallantoic fusion, placental defects, impaired emrbyo turning, increased apoptosis, and posterior axial truncations. [provided by MGI curators]
Allele List at MGI

All alleles(6) : Targeted, other(2) Gene trapped(4)

Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9530053A07Rik A G 7: 28,155,324 N1792D probably benign Het
Abca5 T A 11: 110,277,636 I1416L possibly damaging Het
Abcc4 A T 14: 118,527,994 M992K possibly damaging Het
Adnp A G 2: 168,184,338 S346P probably damaging Het
Atad2b A T 12: 4,965,837 probably benign Het
Ccl12 A G 11: 82,103,233 *105W probably null Het
Chd1 A G 17: 15,770,097 D1637G possibly damaging Het
Cpeb2 T C 5: 43,278,695 probably null Het
Cul4a T C 8: 13,133,843 probably null Het
Dlg1 T A 16: 31,856,438 probably benign Het
Fam171b A G 2: 83,879,600 T539A possibly damaging Het
Gif A G 19: 11,757,762 T249A probably benign Het
Gm9696 A C 3: 59,972,302 noncoding transcript Het
Jmjd1c T C 10: 67,249,762 F2444L probably damaging Het
Knl1 T A 2: 119,070,001 F728I probably damaging Het
Megf9 C A 4: 70,448,791 C318F probably null Het
Mrps28 A G 3: 8,900,070 I103T probably damaging Het
Msantd2 G A 9: 37,522,848 R329H probably benign Het
Myh7b C T 2: 155,632,407 L1681F probably damaging Het
Nf1 C T 11: 79,441,709 probably benign Het
Olfr1302 A G 2: 111,780,590 K90R possibly damaging Het
Olfr1475 G A 19: 13,479,248 probably benign Het
Rapgef6 G A 11: 54,694,563 E1596K probably damaging Het
Serpinb3b T C 1: 107,154,724 E270G probably benign Het
Skor2 C A 18: 76,859,951 A456E possibly damaging Het
Slc13a2 A G 11: 78,403,395 I220T possibly damaging Het
Slc6a1 T A 6: 114,314,401 M361K probably damaging Het
Tars2 G A 3: 95,740,278 R608C probably damaging Het
Tctn3 T C 19: 40,605,302 probably null Het
Tex14 A G 11: 87,509,698 I439V possibly damaging Het
Thbs2 T A 17: 14,678,769 I690F probably benign Het
Vwa8 A G 14: 79,180,804 I1684V possibly damaging Het
Xdh T C 17: 73,909,337 I705V probably benign Het
Other mutations in Mpi
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00921:Mpi APN 9 57552266 missense probably damaging 1.00
IGL01071:Mpi APN 9 57550592 missense probably damaging 1.00
IGL02090:Mpi APN 9 57550653 missense probably benign 0.00
benadryl UTSW 9 57550757 missense probably damaging 1.00
sleepies UTSW 9 57545189 unclassified probably benign
Zyrtec UTSW 9 57545217 missense probably damaging 1.00
F6893:Mpi UTSW 9 57546549 missense probably benign 0.12
R0751:Mpi UTSW 9 57550614 missense probably damaging 1.00
R1146:Mpi UTSW 9 57545189 unclassified probably benign
R3727:Mpi UTSW 9 57544849 missense possibly damaging 0.69
R3944:Mpi UTSW 9 57545253 missense probably damaging 1.00
R4645:Mpi UTSW 9 57550757 missense probably damaging 1.00
R4772:Mpi UTSW 9 57544898 missense probably damaging 1.00
R4856:Mpi UTSW 9 57545307 missense probably damaging 1.00
R5088:Mpi UTSW 9 57550604 missense probably damaging 0.97
R5504:Mpi UTSW 9 57545217 missense probably damaging 1.00
R5886:Mpi UTSW 9 57548462 unclassified probably benign
R7038:Mpi UTSW 9 57545217 missense probably damaging 1.00
R8043:Mpi UTSW 9 57550598 missense probably damaging 1.00
RF013:Mpi UTSW 9 57548641 missense probably benign 0.31
Posted On2013-12-09