Version: 8.0.0
Date: Tue Jan 28 2025
2,652 results for ap4s1

Ap4s1

(Rattus norvegicus)
Gene
Name: adaptor related protein complex 4 subunit sigma 1
Synonyms: adaptor-related protein complex 4, sigma 1 subunit, LOC366618, adaptor-related protein complex AP-4, sigma 1, AP-4 complex subunit sigma-1, MGC187750
Source: RGD:1311990
Biotype: protein coding gene
Symbol: Ap4s1 (Rno)
Symbol: Ap4s1
Gene Synopsis: Orthologous to human AP4S1 (adaptor related protein complex 4 subunit sigma 1); INTERACTS WITH 2,3,7,8
Automated Gene Synopsis: Orthologous to human AP4S1 (adaptor related protein complex 4 subunit sigma 1).
Strict Orthology Symbols: ap4s1

ap4s1

(Danio rerio)
Gene
Name: adaptor related protein complex 4 subunit sigma 1
Synonyms: si:dz115o7.1, si:dz234g15.5, zgc:136677
Source: ZFIN:ZDB-GENE-030616-404
Biotype: protein coding gene
Symbol: ap4s1 (Dre)
Symbol: ap4s1
Automated Gene Synopsis: Orthologous to human AP4S1 (adaptor related protein complex 4 subunit sigma 1).
Strict Orthology Symbols: ap4s1

AP4S1

(Homo sapiens)
Gene
Name: adaptor related protein complex 4 subunit sigma 1
Synonyms: CLA20, FLJ32366, FLJ41011, AP47B, AP-4 adaptor complex subunit sigma-1, clathrin-associated/assembly/adaptor protein, sigma 4, adapter-related protein complex 4 subunit sigma-1, SPG52, adaptor-related protein complex 4, sigma 1 subunit, sigma-1 subunit of AP-4, adaptor related protein complex 4 sigma 1 subunit, adaptor related protein complex 4, sigma 1 subunit, AP-4 adapter complex subunit sigma-1, AP-4 complex subunit sigma-1, sigma-4-adaptin, CLAPS4, adaptor-related protein complex 4 subunit sigma-1, sigma4-adaptin, CPSQ6
Source: HGNC:575
Biotype: protein coding gene
Symbol: AP4S1 (Hsa)
Symbol: AP4S1
Strict Orthology Symbols: ap4s1

Ap4s1

(Mus musculus)
Gene
Name: adaptor-related protein complex AP-4, sigma 1
Synonyms: AI314282, expressed sequence AI314282
Source: MGI:1337065
Biotype: protein coding gene
Symbol: Ap4s1 (Mmu)
Symbol: Ap4s1
Automated Gene Synopsis: Orthologous to human AP4S1 (adaptor related protein complex 4 subunit sigma 1).
Strict Orthology Symbols: ap4s1
Alleles: Ap4s1 (Mmu)...Ap4s1 (Mmu)

ap4s1

(Xenopus tropicalis)
Gene
Name: adaptor related protein complex 4, sigma 1 subunit
Synonyms: adaptor related protein complex 4, sigma 1 subunit, ap4s1
Source: Xenbase:XB-GENE-941798
Biotype: gene
Symbol: ap4s1
Symbol: ap4s1 (Xtr)
Automated Gene Synopsis: Orthologous to human AP4S1 (adaptor related protein complex 4 subunit sigma 1).
Synonyms: ap4s1...ap4s1...ap4s1
Strict Orthology Symbols: ap4s1

ap4s1.L

(Xenopus laevis)
Gene
Name: adaptor related protein complex 4, sigma 1 subunit
Synonyms: adaptor related protein complex 4, sigma 1 subunit, ap4s1.L
Source: Xenbase:XB-GENE-941803
Biotype: gene
Symbol: ap4s1.L (Xla)
Automated Gene Synopsis: Orthologous to human AP4S1 (adaptor related protein complex 4 subunit sigma 1).
Strict Orthology Symbols: ap4s1
Symbol: ap4s1.L

Ap4s1em1(IMPC)Bay

(Mus musculus)
Allele/Variant
Source: MGI:7425516
Genes: Ap4s1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ap4s1 (Mmu)
Genes: Ap4s1 (Mmu)
Symbol: Ap4s1em1(IMPC)Bay

Ap4s1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7309918
Genes: Ap4s1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ap4s1 (Mmu)
Genes: Ap4s1 (Mmu)
Symbol: Ap4s1em1Gpt

Ap4s1-ps1

(Rattus norvegicus)
Gene
Name: adaptor related protein complex 4 subunit sigma 1, pseudogene 1
Synonyms: LOC100360746, adaptor-related protein complex AP-4, sigma 1
Source: RGD:2321512
Biotype: pseudogene
Symbol: Ap4s1-ps1 (Rno)
Symbol: Ap4s1-ps1

ap4s1zf3882/+ (AB)

(Danio rerio)
Model
Id: ZFIN:ZDB-FISH-240816-6
Synonyms: Not Available
Symbol: ap4s1 (AB) (Dre)
Genes: ap4s1 (Dre)
Name: ap4s1 (AB)

ap4s1zf3882/zf3882 (AB)

(Danio rerio)
Model
Id: ZFIN:ZDB-FISH-240816-5
Synonyms: Not Available
Symbol: ap4s1 (AB) (Dre)
Genes: ap4s1 (Dre)
Name: ap4s1 (AB)

hereditary spastic paraplegia 52

Disease
Source: DOID:0110804
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4S1 gene on chromosome 14q12.
Genes: AP4S1 (Hsa)...ap4s1.L (Xla)...Ap4s1 (Rno)...ap4s1 (Dre)...Ap4s1 (Mmu)

AP-4 adaptor complex

Gene Ontology
Source: GO:0030124
Synonyms: Not Available
Branch: cellular component
Genes: Ap4s1 (Rno)...AP4S1 (Hsa)...Ap4s1 (Mmu)

zf3882

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-240815-3
Genes: ap4s1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: hereditary spastic paraplegia 52
Variant Name: Not Available
Genes: ap4s1 (Dre)

zf3881

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-240815-2
Genes: ap4s1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: ap4s1 (Dre)

icm05Tg + MO2-ap4s1

(Danio rerio)
Model
Id: ZFIN:ZDB-FISH-210129-13
Synonyms: Not Available
Genes: ap4s1 (Dre)
Name: icm05Tg + MO2-ap4s1

AB + MO2-ap4s1

(Danio rerio)
Model
Id: ZFIN:ZDB-FISH-210128-27
Synonyms: Not Available
Genes: ap4s1 (Dre)
Name: AB + MO2-ap4s1

central nervous system neuron axonogenesis

Gene Ontology
Source: GO:0021955
Synonyms: Not Available
Branch: biological process
Genes: ap4s1 (Dre)

endosome lumen

Gene Ontology
Source: GO:0031904
Synonyms: Not Available
Branch: cellular component
Genes: AP4S1 (Hsa)

regulation of axonogenesis

Gene Ontology
Source: GO:0050770
Synonyms: Not Available
Branch: biological process
Genes: ap4s1 (Dre)

protein targeting

Gene Ontology
Source: GO:0006605
Synonyms:
  • nascent polypeptide association
  • protein sorting along secretory pathway
Branch: biological process
Genes: AP4S1 (Hsa)

trans-Golgi network membrane

Gene Ontology
Source: GO:0032588
Synonyms:
  • Golgi trans face membrane
  • trans Golgi network membrane
Branch: cellular component
Genes: AP4S1 (Hsa)

intracellular protein transport

Gene Ontology
Source: GO:0006886
Synonyms:
  • copper-induced intracellular protein transport
Branch: biological process
Genes: Ap4s1 (Rno)...AP4S1 (Hsa)...Ap4s1 (Mmu)...ap4s1 (Dre)

vesicle-mediated transport

Gene Ontology
Source: GO:0016192
Synonyms:
  • nonselective vesicle transport
  • protein sorting along secretory pathway
Branch: biological process
Genes: Ap4s1 (Rno)...AP4S1 (Hsa)...Ap4s1 (Mmu)...ap4s1 (Dre)

trans-Golgi network

Gene Ontology
Source: GO:0005802
Synonyms:
  • Golgi trans face
  • Golgi trans-face
Branch: cellular component
Genes: AP4S1 (Hsa)...Ap4s1 (Mmu)

neurogenesis

Gene Ontology
Source: GO:0022008
Synonyms:
  • nervous system cell generation
  • neural cell differentiation
Branch: biological process
Genes: ap4s1 (Dre)

endomembrane system

Gene Ontology
Source: GO:0012505
Synonyms: Not Available
Branch: cellular component
Genes: Ap4s1 (Rno)...AP4S1 (Hsa)...ap4s1 (Dre)

intracellular membrane-bounded organelle

Gene Ontology
Source: GO:0043231
Synonyms:
  • intracellular membrane-enclosed organelle
Branch: cellular component
Genes: AP4S1 (Hsa)...ap4s1 (Dre)...Ap4s1 (Rno)...Ap4s1 (Mmu)

protein localization

Gene Ontology
Source: GO:0008104
Synonyms:
  • asymmetric protein localisation
  • asymmetric protein localization
Branch: biological process
Genes: AP4S1 (Hsa)

Golgi apparatus

Gene Ontology
Source: GO:0005794
Synonyms:
  • Golgi
  • Golgi complex
Branch: cellular component
Genes: AP4S1 (Hsa)

protein transport

Gene Ontology
Source: GO:0015031
Synonyms:
  • enzyme transport
Branch: biological process
Genes: AP4S1 (Hsa)...ap4s1 (Dre)

cytoplasm

Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: AP4S1 (Hsa)

(GRCh38)14:31066278C>T

(Homo sapiens)
Allele/Variant
Source: rs112987601
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31066278C>T

(GRCh38)14:31066320C>A

(Homo sapiens)
Allele/Variant
Source: rs387906970
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31066320C>A

(GRCh38)14:31069778C>G

(Homo sapiens)
Allele/Variant
Source: rs7155228
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31069778C>G

(GRCh38)14:31084514T>G

(Homo sapiens)
Allele/Variant
Source: rs7157080
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31084514T>G

(GRCh38)14:31084835G>C

(Homo sapiens)
Allele/Variant
Source: rs1226099981
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31084835G>C

(GRCh38)14:31084859G>C

(Homo sapiens)
Allele/Variant
Source: rs528491755
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31084859G>C

(GRCh38)14:31084865A>G

(Homo sapiens)
Allele/Variant
Source: rs1228214819
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31084865A>G

(GRCh38)14:31072896T>C

(Homo sapiens)
Allele/Variant
Source: NC_000014.9:g.31072896T>C
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31072896T>C

(GRCh38)14:31072968C>T

(Homo sapiens)
Allele/Variant
Source: rs200440467
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31072968C>T

(GRCh38)14:31073212A>C

(Homo sapiens)
Allele/Variant
Source: rs111925674
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31073212A>C

(GRCh38)14:31066230G>A

(Homo sapiens)
Allele/Variant
Source: rs996367496
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31066230G>A

(GRCh38)14:31066240G>A

(Homo sapiens)
Allele/Variant
Source: rs1594680613
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31066240G>A

(GRCh38)14:31066279G>A

(Homo sapiens)
Allele/Variant
Source: rs201972703
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31066279G>A

(GRCh38)14:31066282C>G

(Homo sapiens)
Allele/Variant
Source: rs557132648
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31066282C>G

(GRCh38)14:31073220A>G

(Homo sapiens)
Allele/Variant
Source: rs73252184
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31073220A>G

(GRCh38)14:31080560T>C

(Homo sapiens)
Allele/Variant
Source: rs369709330
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31080560T>C

(GRCh38)14:31084751T>C

(Homo sapiens)
Allele/Variant
Source: NC_000014.9:g.31084751T>C
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31084751T>C

(GRCh38)14:31084837C>A

(Homo sapiens)
Allele/Variant
Source: rs864309596
Genes: AP4S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:31084837C>A