Version: 8.0.0Date: Tue Jan 28 2025
Category
CLUL1
(Homo sapiens)Gene
Name: clusterin like 1
Synonyms: retinal-specific clusterin-like protein, clusterin-like protein 1, RA337M, clusterin-like 1 (retinal)
Source: HGNC:2096
Biotype: protein coding gene
Symbol: CLUL1 (Hsa)
Symbol: CLUL1
Strict Orthology Symbols: clul1
clul1
(Danio rerio)Gene
Name: clusterin-like 1 (retinal)
Synonyms: wu:fb51b10
Source: ZFIN:ZDB-GENE-031118-57
Biotype: protein coding gene
Symbol: clul1 (Dre)
Symbol: clul1
Automated Gene Synopsis: Orthologous to human CLUL1 (clusterin like 1).
Strict Orthology Symbols: CLUL1...Clul1
Clul1
(Rattus norvegicus)Gene
Name: clusterin like 1
Synonyms: clusterin-like protein 1, LOC367345, clusterin-like 1 (retinal)
Source: RGD:1306852
Biotype: protein coding gene
Symbol: Clul1 (Rno)
Symbol: Clul1
Gene Synopsis: Orthologous to human CLUL1 (clusterin like 1); INTERACTS WITH bisphenol A; copper atom; copper(0).
Automated Gene Synopsis: Orthologous to human CLUL1 (clusterin like 1).
Strict Orthology Symbols: clul1
clul1.L
(Xenopus laevis)Gene
Name: clusterin like 1
Synonyms: ra337m, clusterin like 1, clul1.L
Source: Xenbase:XB-GENE-6488856
Biotype: gene
Symbol: clul1.L (Xla)
Automated Gene Synopsis: Orthologous to human CLUL1 (clusterin like 1).
Strict Orthology Symbols: clul1
Symbol: clul1.L
clul1
(Xenopus tropicalis)Gene
Name: clusterin like 1
Synonyms: ra337m, clul1, clusterin like 1
Source: Xenbase:XB-GENE-984639
Biotype: gene
Symbol: clul1 (Xtr)
Symbol: clul1
Synonyms: clul1...clul1...clul1
Strict Orthology Symbols: clul1.L
Clul1-ps2
(Mus musculus)Gene
Name: clusterin like 1, pseudogene 2
Synonyms: predicted gene 3778, predicted gene, 100042299, Gm3778, 100042299
Source: MGI:3781951
Biotype: pseudogene
Symbol: Clul1-ps2 (Mmu)
Symbol: Clul1-ps2
Clul1-ps
(Mus musculus)Gene
Name: clusterin like 1, pseudogene 1
Synonyms: predicted gene, 41522, Gm41522
Source: MGI:5624407
Biotype: pseudogene
Symbol: Clul1-ps (Mmu)
Symbol: Clul1-ps
Gene Ontology
Source: GO:0051787
Synonyms: Not Available
Branch: molecular function
Genes: Clul1 (Rno)...CLUL1 (Hsa)...clul1 (Dre)
Gene Ontology
Source: GO:0005615
Synonyms:
- intercellular space
Branch: cellular component
Genes: Clul1 (Rno)...clul1 (Dre)...CLUL1 (Hsa)
sa19790
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-131217-14928
Genes: clul1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: clul1 (Dre)
Gene Ontology
Source: GO:0005576
Synonyms:
- extracellular
Branch: cellular component
Genes: Clul1 (Rno)...clul1 (Dre)...CLUL1 (Hsa)
Gene Ontology
Source: GO:0005634
Synonyms:
- cell nucleus
- horsetail nucleus
Branch: cellular component
Genes: clul1 (Dre)...Clul1 (Rno)...CLUL1 (Hsa)
(GRCh38)18:619282T>C
(Homo sapiens)Allele/Variant
Source: NC_000018.10:g.619282T>C
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:619282T>C
(GRCh38)18:627250T>A
(Homo sapiens)Allele/Variant
Source: rs766077524
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:627250T>A
(GRCh38)18:627274G>A
(Homo sapiens)Allele/Variant
Source: rs200242838
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:627274G>A
(GRCh38)18:627251C>G
(Homo sapiens)Allele/Variant
Source: rs753466551
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:627251C>G
(GRCh38)18:624968T>C
(Homo sapiens)Allele/Variant
Source: rs370390666
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:624968T>C
(GRCh38)18:619260G>C
(Homo sapiens)Allele/Variant
Source: NC_000018.10:g.619260G>C
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:619260G>C
(GRCh38)18:624878T>A
(Homo sapiens)Allele/Variant
Source: rs371171982
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:624878T>A
(GRCh38)18:627200A>G
(Homo sapiens)Allele/Variant
Source: NC_000018.10:g.627200A>G
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:627200A>G
(GRCh38)18:624955T>C
(Homo sapiens)Allele/Variant
Source: rs760704789
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:624955T>C
(GRCh38)18:627325A>G
(Homo sapiens)Allele/Variant
Source: rs529629931
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:627325A>G
(GRCh38)18:627328T>C
(Homo sapiens)Allele/Variant
Source: NC_000018.10:g.627328T>C
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:627328T>C
(GRCh38)18:618061G>A
(Homo sapiens)Allele/Variant
Source: rs758691813
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:618061G>A
(GRCh38)18:627313C>G
(Homo sapiens)Allele/Variant
Source: rs550555452
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:627313C>G
(GRCh38)18:618032G>T
(Homo sapiens)Allele/Variant
Source: rs766168896
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:618032G>T
(GRCh38)18:618067A>G
(Homo sapiens)Allele/Variant
Source: rs200703485
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:618067A>G
(GRCh38)18:619313A>T
(Homo sapiens)Allele/Variant
Source: rs895852297
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:619313A>T
(GRCh38)18:625004A>C
(Homo sapiens)Allele/Variant
Source: rs368036645
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:625004A>C
(GRCh38)18:625012T>C
(Homo sapiens)Allele/Variant
Source: rs890279081
Genes: CLUL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:625012T>C
(GRCh38)18:644962T>C
(Homo sapiens)Allele/Variant
Source: rs2074431690
Genes: CLUL1 (Hsa), TYMSOS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:644962T>C
(GRCh38)18:633366G>T
(Homo sapiens)Allele/Variant
Source: NC_000018.10:g.633366G>T
Genes: CLUL1 (Hsa), TYMSOS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:633366G>T
(GRCh38)18:645034C>T
(Homo sapiens)Allele/Variant
Source: rs1188686355
Genes: CLUL1 (Hsa), TYMSOS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:645034C>T
(GRCh38)18:633327A>T
(Homo sapiens)Allele/Variant
Source: NC_000018.10:g.633327A>T
Genes: CLUL1 (Hsa), TYMSOS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:633327A>T
(GRCh38)18:633370A>G
(Homo sapiens)Allele/Variant
Source: rs779281882
Genes: CLUL1 (Hsa), TYMSOS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:633370A>G
(GRCh38)18:633326G>T
(Homo sapiens)Allele/Variant
Source: NC_000018.10:g.633326G>T
Genes: CLUL1 (Hsa), TYMSOS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:633326G>T
(GRCh38)18:641365G>A
(Homo sapiens)Allele/Variant
Source: rs527661052
Genes: CLUL1 (Hsa), TYMSOS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:641365G>A
(GRCh38)18:641536A>G
(Homo sapiens)Allele/Variant
Source: rs761168896
Genes: CLUL1 (Hsa), TYMSOS (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)18:641536A>G
(GRCh38)18:633345A>G
(Homo sapiens)Allele/Variant
Source: rs368695647
Genes: CLUL1 (Hsa), TYMSOS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:633345A>G
(GRCh38)18:641341C>A
(Homo sapiens)Allele/Variant
Source: NC_000018.10:g.641341C>A
Genes: CLUL1 (Hsa), TYMSOS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:641341C>A
(mRatBN7.2)9:113347971T>C
(Rattus norvegicus)Allele/Variant
Source: rs3321728843
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113347971T>C
(mRatBN7.2)9:113348720A>C
(Rattus norvegicus)Allele/Variant
Source: rs106566153
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113348720A>C
(mRatBN7.2)9:113350901G>A
(Rattus norvegicus)Allele/Variant
Source: rs197521069
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113350901G>A
(mRatBN7.2)9:113353131T>C
(Rattus norvegicus)Allele/Variant
Source: rs107269274
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113353131T>C
(mRatBN7.2)9:113356585A>G
(Rattus norvegicus)Allele/Variant
Source: rs106195255
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113356585A>G
(mRatBN7.2)9:113356873T>A
(Rattus norvegicus)Allele/Variant
Source: rs105355477
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113356873T>A
(mRatBN7.2)9:113365213G>T
(Rattus norvegicus)Allele/Variant
Source: rs3321728947
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113365213G>T
(mRatBN7.2)9:113367058A>G
(Rattus norvegicus)Allele/Variant
Source: rs3321765014
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113367058A>G
(mRatBN7.2)9:113369416A>G
(Rattus norvegicus)Allele/Variant
Source: rs105847777
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113369416A>G
(mRatBN7.2)9:113369561C>A
(Rattus norvegicus)Allele/Variant
Source: rs197514928
Genes: Clul1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:113369561C>A