Version: 8.1.0
Date: Fri Apr 18 2025
80 results for GPI2

GPI2

(Saccharomyces cerevisiae)
Gene
Name: GlycosylPhosphatidylInositol anchor biosynthesis
Synonyms: YPL076W, GCR4
Source: SGD:S000005997
Biotype: protein coding gene
Symbol: GPI2 (Sce)
Symbol: GPI2
Alleles: gpi2-5A (Sce)...gpi2-774 (Sce)...gpi2-1-7b (Sce)...gpi2-7 (Sce)...gpi2-Δ (Sce)

gpi2-1-7b

(Saccharomyces cerevisiae)
Allele/Variant
Source: SGD:S000277753
Genes: GPI2 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: gpi2-1-7b (Sce)
Genes: GPI2 (Sce)
Symbol: gpi2-1-7b

gpi2-774

(Saccharomyces cerevisiae)
Allele/Variant
Source: SGD:S000277507
Genes: GPI2 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: gpi2-774 (Sce)
Genes: GPI2 (Sce)
Symbol: gpi2-774

gpi2-Δ

(Saccharomyces cerevisiae)
Allele/Variant
Source: SGD:S000308571
Genes: GPI2 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: gpi2-Δ (Sce)
Genes: GPI2 (Sce)
Symbol: gpi2-Δ

gpi2-7

(Saccharomyces cerevisiae)
Allele/Variant
Source: SGD:S000284377
Genes: GPI2 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: gpi2-7 (Sce)
Genes: GPI2 (Sce)
Symbol: gpi2-7

gpi2-5A

(Saccharomyces cerevisiae)
Allele/Variant
Source: SGD:S000284779
Genes: GPI2 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: gpi2-5A (Sce)
Genes: GPI2 (Sce)
Symbol: gpi2-5A

gpi2-(gcr4-2)

(Saccharomyces cerevisiae)
Allele/Variant
Source: SGD:S000284893
Genes: GPI2 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: gpi2-(gcr4-2) (Sce)
Genes: GPI2 (Sce)
Symbol: gpi2-(gcr4-2)

PIGC

(Homo sapiens)
Gene
Name: phosphatidylinositol glycan anchor biosynthesis class C
Synonyms: GPI2, phosphatidylinositol N-acetylglucosaminyltransferase subunit C, MGC2049, phosphatidylinositol-glycan biosynthesis, class C protein, phosphatidylinositol glycan anchor biosynthesis, class C, GPIBD16, MRT62, PIG-C, phosphatidylinositol-glycan biosynthesis class C protein
Source: HGNC:8960
Biotype: protein coding gene
Synonyms: GPI2...GPI2...GPI2
Strict Orthology Symbols: GPI2

Pigc

(Mus musculus)
Gene
Name: phosphatidylinositol glycan anchor biosynthesis, class C
Synonyms: 3110030E07Rik, RIKEN cDNA 3110030E07 gene, AW212108, expressed sequence AW212108
Source: MGI:1914542
Biotype: protein coding gene
Strict Orthology Symbols: GPI2

pigc

(Danio rerio)
Gene
Name: phosphatidylinositol glycan anchor biosynthesis, class C
Synonyms: zgc:85894, wu:fc16d03
Source: ZFIN:ZDB-GENE-030131-2714
Biotype: protein coding gene
Strict Orthology Symbols: GPI2

PIG-C

(Drosophila melanogaster)
Gene
Name: Phosphatidylinositol glycan anchor biosynthesis class C
Synonyms: PIGC, CG12077, Phosphatidylinositol glycan anchor biosynthesis, class C ortholog, Phosphatidylinositol glycan anchor biosynthesis, class C
Source: FB:FBgn0035435
Biotype: protein coding gene
Strict Orthology Symbols: GPI2

pigc-1

(Caenorhabditis elegans)
Gene
Name: PhosphatidylInositol Glycan anchor biosynthesis class C 1
Synonyms: CELE_T20D3.8, T20D3.8
Source: WB:WBGene00011860
Biotype: protein coding gene
Strict Orthology Symbols: GPI2

Pigc

(Rattus norvegicus)
Gene
Name: phosphatidylinositol glycan anchor biosynthesis, class C
Synonyms: phosphatidylinositol N-acetylglucosaminyltransferase subunit C, LOC364032, PIG-C, phosphatidylinositol-glycan biosynthesis class C protein, phosphatidylinositol glycan, class C
Source: RGD:1311337
Biotype: protein coding gene
Strict Orthology Symbols: GPI2

glycosylphosphatidylinositol biosynthesis defect 16

Disease
Source: DOID:0081223
Definition: An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PIGC gene on chromosome 1q23.
Genes: GPI2 (Sce)

pigc

(Xenopus tropicalis)
Gene
Name: phosphatidylinositol glycan anchor biosynthesis class C
Synonyms: pigc, phosphatidylinositol glycan anchor biosynthesis class C
Source: Xenbase:XB-GENE-951705
Biotype: gene
Strict Orthology Symbols: GPI2

phosphatidylinositol N-acetylglucosaminyltransferase activity

Gene Ontology
Source: GO:0017176
Synonyms:
  • UDP-N-acetyl-D-glucosamine:1-phosphatidyl-1D-myo-inositol 6-(N-acetyl-alpha-D-glucosaminyl)transferase activity
  • UDP-N-acetyl-D-glucosamine:phosphatidylinositol N-acetyl-D-glucosaminyltransferase activity
Branch: molecular function
Genes: GPI2 (Sce)

glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex

Gene Ontology
Source: GO:0000506
Synonyms:
  • GPI-GlcNAc transferase complex
  • GPI-GnT complex
Branch: cellular component
Genes: GPI2 (Sce)

GPI anchor biosynthetic process

Gene Ontology
Source: GO:0006506
Synonyms:
  • GPI anchor anabolism
  • GPI anchor biosynthesis
Branch: biological process
Genes: GPI2 (Sce)

glycosyltransferase activity

Gene Ontology
Source: GO:0016757
Synonyms:
  • transferase activity, transferring glycosyl groups
  • transferase activity, transferring other glycosyl groups
Branch: molecular function
Genes: GPI2 (Sce)

(GRCh38)1:172441758T>G

(Homo sapiens)
Allele/Variant
Source: rs777363797
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441758T>G
Gene Synonyms: GPI2

(GRCh38)1:172442092T>C

(Homo sapiens)
Allele/Variant
Source: rs756094179
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442092T>C
Gene Synonyms: GPI2

(GRCh38)1:172442293C>A

(Homo sapiens)
Allele/Variant
Source: rs151276937
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442293C>A
Gene Synonyms: GPI2

(GRCh38)1:172441762T>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.172441762T>C
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441762T>C
Gene Synonyms: GPI2

(GRCh38)1:172442337C>T

(Homo sapiens)
Allele/Variant
Source: rs781352019
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442337C>T
Gene Synonyms: GPI2

(GRCh38)1:172442497A>G

(Homo sapiens)
Allele/Variant
Source: rs149404118
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442497A>G
Gene Synonyms: GPI2

(GRCh38)1:172442485G>T

(Homo sapiens)
Allele/Variant
Source: rs375570541
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442485G>T
Gene Synonyms: GPI2

(GRCh38)1:172442607C>T

(Homo sapiens)
Allele/Variant
Source: rs1416846556
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442607C>T
Gene Synonyms: GPI2

(GRCh38)1:172441988A>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.172441988A>C
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441988A>C
Gene Synonyms: GPI2

(GRCh38)1:172441979A>G

(Homo sapiens)
Allele/Variant
Source: rs1278813615
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441979A>G
Gene Synonyms: GPI2

(GRCh38)1:172441988A>G

(Homo sapiens)
Allele/Variant
Source: rs1553259602
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441988A>G
Gene Synonyms: GPI2

(GRCh38)1:172442510C>T

(Homo sapiens)
Allele/Variant
Source: rs201429163
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442510C>T
Gene Synonyms: GPI2

(GRCh38)1:172442504T>C

(Homo sapiens)
Allele/Variant
Source: rs779814454
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442504T>C
Gene Synonyms: GPI2

(GRCh38)1:172442529G>T

(Homo sapiens)
Allele/Variant
Source: rs762595686
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442529G>T
Gene Synonyms: GPI2

(GRCh38)1:172442315A>G

(Homo sapiens)
Allele/Variant
Source: rs61747503
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442315A>G
Gene Synonyms: GPI2

(GRCh38)1:172442356A>G

(Homo sapiens)
Allele/Variant
Source: rs2230471
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442356A>G
Gene Synonyms: GPI2

(GRCh38)1:172442367A>T

(Homo sapiens)
Allele/Variant
Source: rs2149169681
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442367A>T
Gene Synonyms: GPI2

(GRCh38)1:172441827G>A

(Homo sapiens)
Allele/Variant
Source: rs1063412
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441827G>A
Gene Synonyms: GPI2

(GRCh38)1:172441884T>C

(Homo sapiens)
Allele/Variant
Source: rs751068367
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441884T>C
Gene Synonyms: GPI2

(GRCh38)1:172442090G>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.172442090G>A
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442090G>A
Gene Synonyms: GPI2

(GRCh38)1:172442540T>C

(Homo sapiens)
Allele/Variant
Source: rs750452407
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442540T>C
Gene Synonyms: GPI2

(GRCh38)1:172442376G>A

(Homo sapiens)
Allele/Variant
Source: rs139238043
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442376G>A
Gene Synonyms: GPI2

(GRCh38)1:172442400T>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.172442400T>C
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442400T>C
Gene Synonyms: GPI2

(GRCh38)1:172442587G>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.172442587G>C
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442587G>C
Gene Synonyms: GPI2

(GRCh38)1:172441947G>A

(Homo sapiens)
Allele/Variant
Source: rs34001453
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441947G>A
Gene Synonyms: GPI2

(GRCh38)1:172442049G>A

(Homo sapiens)
Allele/Variant
Source: rs768479943
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442049G>A
Gene Synonyms: GPI2

(GRCh38)1:172441773C>T

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.172441773C>T
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441773C>T
Gene Synonyms: GPI2

(GRCh38)1:172441964A>G

(Homo sapiens)
Allele/Variant
Source: rs786205667
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172441964A>G
Gene Synonyms: GPI2

(GRCh38)1:172442057A>C

(Homo sapiens)
Allele/Variant
Source: rs1553259614
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442057A>C
Gene Synonyms: GPI2

(GRCh38)1:172442066G>C

(Homo sapiens)
Allele/Variant
Source: rs140958278
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442066G>C
Gene Synonyms: GPI2

(GRCh38)1:172442125A>G

(Homo sapiens)
Allele/Variant
Source: rs138512059
Genes: C1orf105 (Hsa), PIGC (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:172442125A>G
Gene Synonyms: GPI2