Version: 8.0.0Date: Tue Jan 28 2025
Category
Tcerg1l
(Mus musculus)Gene
Name: transcription elongation regulator 1-like
Synonyms: 5730476P14Rik, RGD1562437, RIKEN cDNA 5730476P14 gene
Source: MGI:1917821
Biotype: protein coding gene
Symbol: Tcerg1l (Mmu)
Symbol: Tcerg1l
Automated Gene Synopsis: Orthologous to human TCERG1L (transcription elongation regulator 1 like).
Strict Orthology Symbols: tcerg1l
Alleles: Tcerg1l
tcerg1l
(Danio rerio)Gene
Name: transcription elongation regulator 1 like
Synonyms: si:ch211-177d9.1
Source: ZFIN:ZDB-GENE-131121-319
Biotype: protein coding gene
Symbol: tcerg1l (Dre)
Symbol: tcerg1l
Automated Gene Synopsis: Orthologous to human TCERG1L (transcription elongation regulator 1 like).
Strict Orthology Symbols: TCERG1L...Tcerg1l
TCERG1L
(Homo sapiens)Gene
Name: transcription elongation regulator 1 like
Synonyms: 5730476P14Rik, MGC126584, transcription elongation regulator 1-like protein
Source: HGNC:23533
Biotype: protein coding gene
Symbol: TCERG1L (Hsa)
Symbol: TCERG1L
Strict Orthology Symbols: tcerg1l
Tcerg1l
(Rattus norvegicus)Gene
Name: transcription elongation regulator 1-like
Synonyms: transcription elongation regulator 1-like protein, similar to transcription elongation regulator 1-like, RGD1562437, LOC361669
Source: RGD:1562437
Biotype: protein coding gene
Symbol: Tcerg1l (Rno)
Symbol: Tcerg1l
Gene Synopsis: Orthologous to human TCERG1L (transcription elongation regulator 1 like); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine
Automated Gene Synopsis: Orthologous to human TCERG1L (transcription elongation regulator 1 like).
Strict Orthology Symbols: tcerg1l
tcerg1l
(Xenopus tropicalis)Gene
Name: transcription elongation regulator 1 like
Synonyms: tcerg1l, LOC108697180, transcription elongation regulator 1 like
Source: Xenbase:XB-GENE-982107
Biotype: gene
Symbol: tcerg1l (Xtr)
Symbol: tcerg1l
Automated Gene Synopsis: Orthologous to human TCERG1L (transcription elongation regulator 1 like).
Synonyms: tcerg1l...tcerg1l...tcerg1l
Strict Orthology Symbols: tcerg1l.L...TCERG1L...Tcerg1l
TCERG1L-AS1
(Homo sapiens)Gene
Name: TCERG1L antisense RNA 1
Synonyms: Not Available
Source: HGNC:49532
Biotype: ncRNA gene
Symbol: TCERG1L-AS1 (Hsa)
Symbol: TCERG1L-AS1
tcerg1l.L
(Xenopus laevis)Gene
Name: transcription elongation regulator 1 like
Synonyms: tcerg1l.L, LOC108697180, transcription elongation regulator 1 like
Source: Xenbase:XB-GENE-17334607
Biotype: gene
Symbol: tcerg1l.L (Xla)
Automated Gene Synopsis: Orthologous to human TCERG1L (transcription elongation regulator 1 like).
Strict Orthology Symbols: tcerg1l
Symbol: tcerg1l.L
Tcerg1ltm1a(KOMP)Wtsi
(Mus musculus)Allele/Variant
Source: MGI:4820071
Genes: Tcerg1l (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tcerg1l
Genes: Tcerg1l (Mmu)
Symbol: Tcerg1ltm1a(KOMP)Wtsi
Tcerg1ltm1.1(cre/ERT2)Zjh
(Mus musculus)Allele/Variant
Source: MGI:6360921
Genes: Tcerg1l (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tcerg1l
Genes: Tcerg1l (Mmu)
Symbol: Tcerg1ltm1.1(cre/ERT2)Zjh
Construct Regulatory Region: Tcerg1l (Mmu)
Constructs: Tcerg1l< construct
Tcerg1ltm1a(KOMP)Wtsi/Tcerg1ltm1a(KOMP)Wtsi [background:] C57BL/6N-Tcerg1ltm1a(KOMP)Wtsi/Wtsi
(Mus musculus)Model
Id: MGI:6263654
Synonyms: Not Available
Symbol: Tcerg1l/Tcerg1l [background:] C57BL/6N-Tcerg1l/Wtsi
Genes: Tcerg1l (Mmu)
Alleles: Tcerg1l
Name: Tcerg1l/Tcerg1l [background:] C57BL/6N-Tcerg1l/Wtsi
CG42724
(Drosophila melanogaster)Gene
Name: Not Available
Synonyms: CG33097, CG15187, CG31367
Source: FB:FBgn0261641
Biotype: protein coding gene
Strict Orthology Symbols: TCERG1L...Tcerg1l
tcer-1
(Caenorhabditis elegans)Gene
Name: TransCription Elongation Regulator homolog 1
Synonyms: gos-1, CELE_ZK1127.9, ZK1127.9
Source: WB:WBGene00022855
Biotype: protein coding gene
Strict Orthology Symbols: TCERG1L...Tcerg1l
Gene Ontology
Source: GO:0070063
Synonyms: Not Available
Branch: molecular function
Genes: TCERG1L (Hsa)...Tcerg1l (Rno)...tcerg1l (Dre)...Tcerg1l (Mmu)
Gene Ontology
Source: GO:0003712
Synonyms:
- RNA polymerase II transcriptional cofactor activity
- nuclear receptor coreceptor activity
Branch: molecular function
Genes: Tcerg1l (Mmu)...tcerg1l (Dre)...TCERG1L (Hsa)...Tcerg1l (Rno)
sa28008
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-20327
Genes: tcerg1l (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: tcerg1l (Dre)
Gene Ontology
Source: GO:0005634
Synonyms:
- cell nucleus
- horsetail nucleus
Branch: cellular component
Genes: Tcerg1l (Rno)...Tcerg1l (Mmu)...TCERG1L (Hsa)...tcerg1l (Dre)
(GRCh38)10:131260340G>A
(Homo sapiens)Allele/Variant
Source: rs372812956
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131260340G>A
(GRCh38)10:131093283C>T
(Homo sapiens)Allele/Variant
Source: rs201034812
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131093283C>T
(GRCh38)10:131116837G>A
(Homo sapiens)Allele/Variant
Source: rs759083298
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131116837G>A
(GRCh38)10:131166826T>G
(Homo sapiens)Allele/Variant
Source: rs565261722
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131166826T>G
(GRCh38)10:131260312T>G
(Homo sapiens)Allele/Variant
Source: rs762386085
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131260312T>G
(GRCh38)10:131104329T>C
(Homo sapiens)Allele/Variant
Source: rs762126091
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131104329T>C
(GRCh38)10:131116863G>A
(Homo sapiens)Allele/Variant
Source: rs199911619
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131116863G>A
(GRCh38)10:131260386G>A
(Homo sapiens)Allele/Variant
Source: rs149055623
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131260386G>A
(GRCh38)10:131260385C>T
(Homo sapiens)Allele/Variant
Source: rs750754103
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131260385C>T
(GRCh38)10:131311413G>A
(Homo sapiens)Allele/Variant
Source: rs1800227124
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131311413G>A
(GRCh38)10:131311313A>G
(Homo sapiens)Allele/Variant
Source: rs1032169405
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131311313A>G
(GRCh38)10:131104343A>T
(Homo sapiens)Allele/Variant
Source: rs1402069579
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131104343A>T
(GRCh38)10:131116838C>G
(Homo sapiens)Allele/Variant
Source: rs894288962
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131116838C>G
(GRCh38)10:131116889C>T
(Homo sapiens)Allele/Variant
Source: rs760903688
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131116889C>T
(GRCh38)10:131146556T>C
(Homo sapiens)Allele/Variant
Source: rs1314319228
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131146556T>C
(GRCh38)10:131146634C>T
(Homo sapiens)Allele/Variant
Source: rs145173247
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131146634C>T
(GRCh38)10:131309194T>C
(Homo sapiens)Allele/Variant
Source: rs576330871
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131309194T>C
(GRCh38)10:131309160T>A
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.131309160T>A
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131309160T>A
(GRCh38)10:131093276C>G
(Homo sapiens)Allele/Variant
Source: rs769421483
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131093276C>G
(GRCh38)10:131309277G>A
(Homo sapiens)Allele/Variant
Source: rs745908436
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131309277G>A
(GRCh38)10:131246239G>A
(Homo sapiens)Allele/Variant
Source: rs207471605
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131246239G>A
(GRCh38)10:131262699C>T
(Homo sapiens)Allele/Variant
Source: rs207471606
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131262699C>T
(GRCh38)10:131308273G>C
(Homo sapiens)Allele/Variant
Source: rs41282900
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131308273G>C
(GRCh38)10:131260265C>T
(Homo sapiens)Allele/Variant
Source: rs367822256
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131260265C>T
(GRCh38)10:131311599G>T
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.131311599G>T
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131311599G>T
(GRCh38)10:131116930C>T
(Homo sapiens)Allele/Variant
Source: rs145788961
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131116930C>T
(GRCh38)10:131134385C>T
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.131134385C>T
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131134385C>T
(GRCh38)10:131260394C>T
(Homo sapiens)Allele/Variant
Source: rs768205119
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131260394C>T
(GRCh38)10:131260349G>A
(Homo sapiens)Allele/Variant
Source: rs768095460
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131260349G>A
(GRCh38)10:131098331G>C
(Homo sapiens)Allele/Variant
Source: rs751858553
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131098331G>C
(GRCh38)10:131116872G>A
(Homo sapiens)Allele/Variant
Source: rs150958404
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131116872G>A
(GRCh38)10:131311389G>C
(Homo sapiens)Allele/Variant
Source: rs540582305
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131311389G>C
(GRCh38)10:131093268C>T
(Homo sapiens)Allele/Variant
Source: rs147204742
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131093268C>T
(GRCh38)10:131260316G>A
(Homo sapiens)Allele/Variant
Source: rs761569207
Genes: TCERG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:131260316G>A