Incidental Mutation 'IGL03068:G6pc'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol G6pc
Ensembl Gene ENSMUSG00000078650
Gene Nameglucose-6-phosphatase, catalytic
SynonymsGlc-6-Pase, G6Pase, G6pt, Glc-6-Pase-alpha
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock #IGL03068
Quality Score
Chromosomal Location101367561-101377903 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 101370750 bp
Amino Acid Change Aspartic acid to Glycine at position 92 (D92G)
Ref Sequence ENSEMBL: ENSMUSP00000019469 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000019469]
Predicted Effect probably benign
Transcript: ENSMUST00000019469
AA Change: D92G

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000019469
Gene: ENSMUSG00000078650
AA Change: D92G

acidPPc 56 196 2.28e-40 SMART
transmembrane domain 214 236 N/A INTRINSIC
transmembrane domain 256 278 N/A INTRINSIC
transmembrane domain 291 308 N/A INTRINSIC
transmembrane domain 323 345 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: The enzyme encoded by this gene is a multisubunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for glucose-6-phosphate, inorganic phosphate, and glucose. This gene is one of three glucose-6-phosphatase catalytic-subunit-encoding genes in mouse. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). [provided by RefSeq, Sep 2015]
PHENOTYPE: Mice homozygous for disruptions in this gene tend to die within a couple of weeks of weaning. Blood chemistry and glucose metabolism are abnormal as is glycogen storage. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ago3 A G 4: 126,417,378 L14P probably damaging Het
Ak2 G T 4: 129,008,026 probably benign Het
Appbp2 T C 11: 85,201,420 Y311C probably damaging Het
Arl9 C A 5: 77,007,378 L119I possibly damaging Het
Atp1a1 T C 3: 101,583,859 H620R probably benign Het
Cfap52 T C 11: 67,935,856 D381G probably benign Het
Cngb3 T C 4: 19,375,246 F292S possibly damaging Het
Comtd1 G A 14: 21,847,643 R203C probably damaging Het
Crmp1 G T 5: 37,265,289 A147S possibly damaging Het
Csmd3 T A 15: 47,847,121 H1586L possibly damaging Het
Ctnna1 G A 18: 35,249,732 E644K possibly damaging Het
Dock3 T C 9: 106,964,759 D957G possibly damaging Het
Ear1 G T 14: 43,819,045 S122* probably null Het
Eefsec G T 6: 88,258,227 Q576K probably benign Het
Efcab5 T A 11: 77,104,101 I1215L probably benign Het
Etfa A T 9: 55,487,482 D160E probably benign Het
Exoc7 G A 11: 116,301,134 R197C possibly damaging Het
Gm3182 T A 14: 4,483,921 probably null Het
Gm4952 A G 19: 12,623,704 N96S probably damaging Het
Gpr156 G A 16: 37,992,129 V276M probably damaging Het
Irs2 A G 8: 11,004,974 S1153P probably damaging Het
Kif21b T C 1: 136,158,355 probably benign Het
Lmo7 A T 14: 101,875,492 probably benign Het
Mapk4 G T 18: 73,970,344 N31K probably damaging Het
Mccc2 T C 13: 99,963,811 T357A probably damaging Het
Mpeg1 A G 19: 12,462,206 T343A probably benign Het
Myo3b G T 2: 70,426,816 probably benign Het
Pald1 T C 10: 61,321,184 E829G possibly damaging Het
Pde11a A G 2: 76,017,864 I873T probably damaging Het
Samd9l T A 6: 3,375,348 K638* probably null Het
Sema4d A G 13: 51,708,886 S479P probably damaging Het
Slc12a2 T C 18: 57,904,335 probably benign Het
Slc47a2 T C 11: 61,303,943 N470S probably damaging Het
Spag17 C T 3: 100,080,205 P1604S probably benign Het
Taf8 C A 17: 47,501,365 V39L probably damaging Het
Tlr11 A G 14: 50,361,484 E309G probably benign Het
Tmem260 A G 14: 48,486,914 probably benign Het
Tsc1 A T 2: 28,681,258 K816M probably damaging Het
Ttc29 A G 8: 78,325,551 I354V probably benign Het
Ttll3 A T 6: 113,409,197 N665Y probably damaging Het
Ubr4 A G 4: 139,409,730 T971A probably benign Het
Vmn2r96 T A 17: 18,582,875 I349N probably benign Het
Vwa5a A G 9: 38,734,847 T504A probably benign Het
Ythdf3 T A 3: 16,204,718 V354E possibly damaging Het
Zan C A 5: 137,476,415 G13V probably damaging Het
Other mutations in G6pc
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00863:G6pc APN 11 101370723 missense probably damaging 1.00
R1988:G6pc UTSW 11 101367942 missense probably damaging 0.97
R3936:G6pc UTSW 11 101374603 missense probably benign
R4601:G6pc UTSW 11 101372741 missense probably damaging 1.00
R4677:G6pc UTSW 11 101376613 missense probably benign
R6073:G6pc UTSW 11 101367976 missense probably benign
R6304:G6pc UTSW 11 101367909 missense probably damaging 1.00
R7103:G6pc UTSW 11 101374587 splice site probably null
R7143:G6pc UTSW 11 101370723 missense probably damaging 1.00
R7438:G6pc UTSW 11 101376677 missense probably benign 0.17
R7499:G6pc UTSW 11 101376694 nonsense probably null
R7960:G6pc UTSW 11 101376533 missense probably damaging 1.00
R8339:G6pc UTSW 11 101376488 missense possibly damaging 0.87
Posted On2016-08-02