Version: 8.0.0Date: Tue Jan 28 2025
Category
RNF175
(Homo sapiens)Gene
Name: ring finger protein 175
Synonyms: FLJ34190
Source: HGNC:27735
Biotype: protein coding gene
Symbol: RNF175 (Hsa)
Symbol: RNF175
Strict Orthology Symbols: rnf175
rnf175
(Danio rerio)Gene
Name: ring finger protein 175
Synonyms: zgc:56665
Source: ZFIN:ZDB-GENE-040426-1104
Biotype: protein coding gene
Symbol: rnf175 (Dre)
Symbol: rnf175
Automated Gene Synopsis: Orthologous to human RNF175 (ring finger protein 175).
Strict Orthology Symbols: RNF175
CG15814
(Drosophila melanogaster)Gene
Name: Not Available
Synonyms: Not Available
Source: FB:FBgn0030873
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human RNF121 (ring finger protein 121) and RNF175 (ring finger protein 175).
Strict Orthology Symbols: rnf175
rnf-121
(Caenorhabditis elegans)Gene
Name: RiNg Finger protein 121
Synonyms: CELE_C16C10.5, C16C10.5
Source: WB:WBGene00007626
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human RNF121 (ring finger protein 121) and RNF175 (ring finger protein 175).
Strict Orthology Symbols: rnf175
zko210b
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-171115-166
Genes: rnf175 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: rnf175 (Dre)
la028203Tg
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-130129-2604
Genes: rnf175 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: rnf175 (Dre)
zko210a
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-171115-165
Genes: rnf175 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: rnf175 (Dre)
Gene Ontology
Source: GO:0036503
Synonyms:
- ER-associated degradation pathway
- endoplasmic reticulum-associated degradation
Branch: biological process
Genes: RNF175 (Hsa)...rnf175 (Dre)
Gene Ontology
Source: GO:0061630
Synonyms:
- E3
- ER-associated E3 ligase
Branch: molecular function
Genes: RNF175 (Hsa)...rnf175 (Dre)
Gene Ontology
Source: GO:0000139
Synonyms:
- Golgi apparatus membrane
Branch: cellular component
Genes: RNF175 (Hsa)...rnf175 (Dre)
sa19435
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-10676
Genes: rnf175 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: rnf175 (Dre)
Gene Ontology
Source: GO:0005789
Synonyms:
- ER membrane
Branch: cellular component
Genes: RNF175 (Hsa)...rnf175 (Dre)
Gene Ontology
Source: GO:0046872
Synonyms:
- heavy metal binding
- metal binding
Branch: molecular function
Genes: rnf175 (Dre)...RNF175 (Hsa)
Gene Ontology
Source: GO:0016020
Synonyms:
- integral component of membrane
- integral to membrane
Branch: cellular component
Genes: rnf175 (Dre)...RNF175 (Hsa)
Gene Ontology
Source: GO:0005515
Synonyms:
- glycoprotein binding
- protein amino acid binding
Branch: molecular function
Genes: RNF175 (Hsa)
(GRCh38)4:153728297C>T
(Homo sapiens)Allele/Variant
Source: rs746352762
Genes: RNF175 (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)4:153728297C>T
(GRCh38)4:153728211G>A
(Homo sapiens)Allele/Variant
Source: rs201556317
Genes: RNF175 (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)4:153728211G>A
(GRCh38)4:153748763T>C
(Homo sapiens)Allele/Variant
Source: rs764889075
Genes: RNF175 (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)4:153748763T>C
(GRCh38)4:153712575A>G
(Homo sapiens)Allele/Variant
Source: rs781620641
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153712575A>G
(GRCh38)4:153720219C>T
(Homo sapiens)Allele/Variant
Source: rs201891647
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153720219C>T
(GRCh38)4:153715537A>C
(Homo sapiens)Allele/Variant
Source: rs142224306
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153715537A>C
(GRCh38)4:153723355A>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.153723355A>G
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153723355A>G
(GRCh38)4:153720197G>A
(Homo sapiens)Allele/Variant
Source: rs765834231
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153720197G>A
(GRCh38)4:153728211G>T
(Homo sapiens)Allele/Variant
Source: rs201556317
Genes: RNF175 (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)4:153728211G>T
(GRCh38)4:153748728T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.153748728T>C
Genes: RNF175 (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)4:153748728T>C
(GRCh38)4:153720281T>C
(Homo sapiens)Allele/Variant
Source: rs766883578
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153720281T>C
(GRCh38)4:153723406C>T
(Homo sapiens)Allele/Variant
Source: rs1219355122
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153723406C>T
(GRCh38)4:153728307A>G
(Homo sapiens)Allele/Variant
Source: rs374840860
Genes: RNF175 (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)4:153728307A>G
(GRCh38)4:153720284A>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.153720284A>G
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153720284A>G
(GRCh38)4:153712496A>G
(Homo sapiens)Allele/Variant
Source: rs528121328
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153712496A>G
(GRCh38)4:153712556C>T
(Homo sapiens)Allele/Variant
Source: rs200984268
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153712556C>T
(GRCh38)4:153712533T>C
(Homo sapiens)Allele/Variant
Source: rs774478741
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153712533T>C
(GRCh38)4:153723399C>T
(Homo sapiens)Allele/Variant
Source: rs764124998
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153723399C>T
(GRCh38)4:153728243C>G
(Homo sapiens)Allele/Variant
Source: rs754691648
Genes: RNF175 (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)4:153728243C>G
(GRCh38)4:153748749G>A
(Homo sapiens)Allele/Variant
Source: rs200438202
Genes: RNF175 (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)4:153748749G>A
(GRCh38)4:153751442A>G
(Homo sapiens)Allele/Variant
Source: rs554858143
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153751442A>G
(GRCh38)4:153710412A>G
(Homo sapiens)Allele/Variant
Source: rs1250695710
Genes: TLR2 (Hsa), RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153710412A>G