Version: 8.0.0
Date: Tue Jan 28 2025
2,794 results for armc8

armc8

(Danio rerio)
Gene
Name: armadillo repeat containing 8
Synonyms: zgc:153683, im:6908171
Source: ZFIN:ZDB-GENE-061027-88
Biotype: protein coding gene
Symbol: armc8 (Dre)
Symbol: armc8
Automated Gene Synopsis: Orthologous to human ARMC8 (armadillo repeat containing 8).
Strict Orthology Symbols: armc8

ARMC8

(Homo sapiens)
Gene
Name: armadillo repeat containing 8
Synonyms: GID5, GID complex subunit 5, VID28 homolog, MGC4880, S863-2, MGC10058, VID28, HSPC056, armadillo repeat-containing protein 8
Source: HGNC:24999
Biotype: protein coding gene
Symbol: ARMC8 (Hsa)
Symbol: ARMC8
Strict Orthology Symbols: armc8

Armc8

(Mus musculus)
Gene
Name: armadillo repeat containing 8
Synonyms: 1200015K23Rik, RIKEN cDNA 1200015K23 gene, Gid5, RGD1310477, HSPC056
Source: MGI:1921375
Biotype: protein coding gene
Symbol: Armc8 (Mmu)
Symbol: Armc8
Automated Gene Synopsis: Orthologous to human ARMC8 (armadillo repeat containing 8).
Strict Orthology Symbols: armc8
Alleles: Armc8 (Mmu)...Armc8 (Mmu)...Armc8 (Mmu)

Armc8

(Rattus norvegicus)
Gene
Name: armadillo repeat containing 8
Synonyms: LOC315949, RGD1310477, similar to RIKEN cDNA 1200015K23, armadillo repeat-containing protein 8
Source: RGD:1310477
Biotype: protein coding gene
Symbol: Armc8 (Rno)
Symbol: Armc8
Gene Synopsis: Orthologous to human ARMC8 (armadillo repeat containing 8); INTERACTS WITH 2,4-dinitrotoluene; 2,6-dinitrotoluene
Automated Gene Synopsis: Orthologous to human ARMC8 (armadillo repeat containing 8).
Strict Orthology Symbols: armc8

armc8

(Xenopus tropicalis)
Gene
Name: armadillo repeat containing 8
Synonyms: armadillo repeat containing 8, armc8
Source: Xenbase:XB-GENE-493289
Biotype: gene
Symbol: armc8
Symbol: armc8 (Xtr)
Automated Gene Synopsis: Orthologous to human ARMC8 (armadillo repeat containing 8).
Synonyms: armc8...armc8...armc8
Strict Orthology Symbols: armc8

armc8.L

(Xenopus laevis)
Gene
Name: armadillo repeat containing 8
Synonyms: armadillo repeat containing 8, armc8.L
Source: Xenbase:XB-GENE-866242
Biotype: gene
Symbol: armc8.L (Xla)
Automated Gene Synopsis: Orthologous to human ARMC8 (armadillo repeat containing 8).
Strict Orthology Symbols: armc8
Symbol: armc8.L

armc8.S

(Xenopus laevis)
Gene
Name: armadillo repeat containing 8
Synonyms: armc8.S, armadillo repeat containing 8
Source: Xenbase:XB-GENE-17330911
Biotype: gene
Symbol: armc8.S (Xla)
Automated Gene Synopsis: Orthologous to human ARMC8 (armadillo repeat containing 8).
Strict Orthology Symbols: armc8
Symbol: armc8.S

Armc8tm1.1Geno

(Mus musculus)
Allele/Variant
Source: MGI:5439655
Genes: Armc8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Armc8 (Mmu)
Genes: Armc8 (Mmu)
Symbol: Armc8tm1.1Geno

Armc8em1(IMPC)Ccpcz

(Mus musculus)
Allele/Variant
Source: MGI:7425523
Genes: Armc8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Armc8 (Mmu)
Genes: Armc8 (Mmu)
Symbol: Armc8em1(IMPC)Ccpcz

Armc8em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7295484
Genes: Armc8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Armc8 (Mmu)
Genes: Armc8 (Mmu)
Symbol: Armc8em1Gpt

ARMC8P1

(Homo sapiens)
Gene
Name: armadillo repeat containing 8 pseudogene 1
Synonyms: Not Available
Source: HGNC:49918
Biotype: pseudogene
Symbol: ARMC8P1 (Hsa)
Symbol: ARMC8P1

VID28

(Saccharomyces cerevisiae)
Gene
Name: Vacuolar Import and Degradation
Synonyms: GID5, YIL017C, YIL017W
Source: SGD:S000001279
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human ARMC8 (armadillo repeat containing 8).
Strict Orthology Symbols: armc8

GID complex

Gene Ontology
Source: GO:0034657
Synonyms:
  • C-terminal to LisH complex
  • CTLH complex
Branch: cellular component
Genes: Armc8 (Mmu)...ARMC8 (Hsa)...armc8 (Dre)...Armc8 (Rno)

sa31717

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-1202
Genes: armc8 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: armc8 (Dre)

tertiary granule lumen

Gene Ontology
Source: GO:1904724
Synonyms:
  • gelatinase granule membrane-enclosed lumen
  • membrane-enclosed lumen of gelatinase granule
Branch: cellular component
Genes: ARMC8 (Hsa)

specific granule lumen

Gene Ontology
Source: GO:0035580
Synonyms:
  • secondary granule lumen
Branch: cellular component
Genes: ARMC8 (Hsa)

ubiquitin ligase complex

Gene Ontology
Source: GO:0000151
Synonyms: Not Available
Branch: cellular component
Genes: ARMC8 (Hsa)...Armc8 (Rno)...Armc8 (Mmu)...armc8 (Dre)

animal organ development

Gene Ontology
Source: GO:0048513
Synonyms:
  • development of an organ
  • organogenesis
Branch: biological process
Genes: armc8 (Dre)

proteasome-mediated ubiquitin-dependent protein catabolic process

Gene Ontology
Source: GO:0043161
Synonyms:
  • proteasomal pathway
  • proteasomal processing
Branch: biological process
Genes: Armc8 (Rno)...Armc8 (Mmu)...armc8 (Dre)...ARMC8 (Hsa)

intracellular membrane-bounded organelle

Gene Ontology
Source: GO:0043231
Synonyms:
  • intracellular membrane-enclosed organelle
Branch: cellular component
Genes: Armc8 (Rno)...ARMC8 (Hsa)...Armc8 (Mmu)

sa41433

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-7432
Genes: armc8 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: armc8 (Dre)

sa21497

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-15948
Genes: armc8 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: armc8 (Dre)

sa21498

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-15949
Genes: armc8 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: armc8 (Dre)

sa9128

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-19806
Genes: armc8 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: armc8 (Dre)

nucleoplasm

Gene Ontology
Source: GO:0005654
Synonyms: Not Available
Branch: cellular component
Genes: ARMC8 (Hsa)...Armc8 (Mmu)...Armc8 (Rno)

cytosol

Gene Ontology
Source: GO:0005829
Synonyms: Not Available
Branch: cellular component
Genes: Armc8 (Mmu)...Armc8 (Rno)...ARMC8 (Hsa)

extracellular region

Gene Ontology
Source: GO:0005576
Synonyms:
  • extracellular
Branch: cellular component
Genes: ARMC8 (Hsa)

nucleus

Gene Ontology
Source: GO:0005634
Synonyms:
  • cell nucleus
  • horsetail nucleus
Branch: cellular component
Genes: Armc8 (Mmu)...ARMC8 (Hsa)...armc8 (Dre)...Armc8 (Rno)

cytoplasm

Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: Armc8 (Mmu)...ARMC8 (Hsa)...armc8 (Dre)...Armc8 (Rno)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: Armc8 (Mmu)

protein binding

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: ARMC8 (Hsa)

(GRCh38)3:138223524A>C

(Homo sapiens)
Allele/Variant
Source: rs759475910
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138223524A>C

(GRCh38)3:138223661T>A

(Homo sapiens)
Allele/Variant
Source: NC_000003.12:g.138223661T>A
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138223661T>A

(GRCh38)3:138245175C>T

(Homo sapiens)
Allele/Variant
Source: rs1450402393
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138245175C>T

(GRCh38)3:138223468A>G

(Homo sapiens)
Allele/Variant
Source: rs148160525
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138223468A>G

(GRCh38)3:138239502A>G

(Homo sapiens)
Allele/Variant
Source: rs1175834278
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138239502A>G

(GRCh38)3:138223693T>C

(Homo sapiens)
Allele/Variant
Source: rs1357762909
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138223693T>C

(GRCh38)3:138241862A>G

(Homo sapiens)
Allele/Variant
Source: rs764449578
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138241862A>G

(GRCh38)3:138239500G>A

(Homo sapiens)
Allele/Variant
Source: rs200770718
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138239500G>A

(GRCh38)3:138223516C>G

(Homo sapiens)
Allele/Variant
Source: rs141108325
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138223516C>G

(GRCh38)3:138223654T>C

(Homo sapiens)
Allele/Variant
Source: rs1299410710
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_lost, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138223654T>C

(GRCh38)3:138237358C>T

(Homo sapiens)
Allele/Variant
Source: rs757421910
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138237358C>T

(GRCh38)3:138241874C>G

(Homo sapiens)
Allele/Variant
Source: rs377149557
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138241874C>G

(GRCh38)3:138241831G>C

(Homo sapiens)
Allele/Variant
Source: rs143059438
Genes: ARMC8 (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)3:138241831G>C

(GRCh38)3:138239499C>T

(Homo sapiens)
Allele/Variant
Source: rs1426021184
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138239499C>T

(GRCh38)3:138228964G>A

(Homo sapiens)
Allele/Variant
Source: rs200413853
Genes: ARMC8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:138228964G>A

(GRCh38)3:138241822T>G

(Homo sapiens)
Allele/Variant
Source: rs2046640666
Genes: ARMC8 (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)3:138241822T>G

(GRCh38)3:138295866A>G

(Homo sapiens)
Allele/Variant
Source: NC_000003.12:g.138295866A>G
Genes: NME9 (Hsa), ARMC8 (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)3:138295866A>G

(GRCh38)3:138273015A>G

(Homo sapiens)
Allele/Variant
Source: rs750096434
Genes: NME9 (Hsa), ARMC8 (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)3:138273015A>G

(GRCh38)3:138274467A>G

(Homo sapiens)
Allele/Variant
Source: rs771125727
Genes: NME9 (Hsa), ARMC8 (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)3:138274467A>G