Version: 7.5.0
Date: Fri Dec 13 2024
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Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Category
Allele/Variant
65
Gene
1
Filter
66
results
for
T10B5.2
Page 1 of 2
T10B5.2
(
Caenorhabditis elegans
)
Gene
Name:
Not Available
Synonyms:
CELE_T10B5.2
Source:
WB:WBGene00020388
Biotype:
pseudogene
Symbol:
T10B5.2
(Cel)
Symbol:
T10B5.2
Cross References:
WB:
T10B5.2
...
T10B5.2
...
T10B5.2
Allele/Variant (65)
(WBcel235)V:1851254C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1851254C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1851254C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1848832A>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848832A>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848832A>T
Gene Cross References:
T10B5.2
(WBcel235)V:1849241C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849241C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849241C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1848268G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848268G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848268G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1848337C>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848337C>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848337C>A
Gene Cross References:
T10B5.2
(WBcel235)V:1850999A>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850999A>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850999A>T
Gene Cross References:
T10B5.2
(WBcel235)V:1848507G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848507G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848507G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1850197T>C
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850197T>C
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850197T>C
Gene Cross References:
T10B5.2
(WBcel235)V:1850610G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850610G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850610G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1851426G>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1851426G>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1851426G>T
Gene Cross References:
T10B5.2
(WBcel235)V:1849761C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849761C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849761C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1849660G>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849660G>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849660G>T
Gene Cross References:
T10B5.2
(WBcel235)V:1848562G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848562G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848562G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1851173G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1851173G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1851173G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1848149T>C
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848149T>C
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848149T>C
Gene Cross References:
T10B5.2
(WBcel235)V:1850006A>G
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850006A>G
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850006A>G
Gene Cross References:
T10B5.2
(WBcel235)V:1850873C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850873C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850873C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1849794T>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849794T>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849794T>A
Gene Cross References:
T10B5.2
(WBcel235)V:1848711C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848711C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848711C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1848073C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848073C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848073C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1849721C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849721C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849721C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1849929G>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849929G>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849929G>T
Gene Cross References:
T10B5.2
(WBcel235)V:1851366G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1851366G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1851366G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1850097C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850097C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850097C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1848075C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848075C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848075C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1851081T>G
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1851081T>G
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1851081T>G
Gene Cross References:
T10B5.2
(WBcel235)V:1848463T>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848463T>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848463T>A
Gene Cross References:
T10B5.2
(WBcel235)V:1850565T>C
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850565T>C
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850565T>C
Gene Cross References:
T10B5.2
(WBcel235)V:1848650A>G
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848650A>G
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848650A>G
Gene Cross References:
T10B5.2
(WBcel235)V:1848674T>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848674T>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848674T>A
Gene Cross References:
T10B5.2
(WBcel235)V:1849083G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849083G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849083G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1849161T>G
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849161T>G
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849161T>G
Gene Cross References:
T10B5.2
(WBcel235)V:1848795G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848795G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848795G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1850087C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850087C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850087C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1850491G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850491G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850491G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1849951G>C
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849951G>C
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849951G>C
Gene Cross References:
T10B5.2
(WBcel235)V:1851222G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1851222G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1851222G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1851438T>C
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1851438T>C
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1851438T>C
Gene Cross References:
T10B5.2
(WBcel235)V:1848629A>G
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848629A>G
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848629A>G
Gene Cross References:
T10B5.2
(WBcel235)V:1849490A>G
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849490A>G
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849490A>G
Gene Cross References:
T10B5.2
(WBcel235)V:1848106T>C
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848106T>C
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848106T>C
Gene Cross References:
T10B5.2
(WBcel235)V:1848560G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848560G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848560G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1850598T>C
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850598T>C
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850598T>C
Gene Cross References:
T10B5.2
(WBcel235)V:1850985C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850985C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850985C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1851016C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1851016C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1851016C>T
Gene Cross References:
T10B5.2
(WBcel235)V:1848905A>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1848905A>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1848905A>T
Gene Cross References:
T10B5.2
(WBcel235)V:1849774G>A
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849774G>A
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849774G>A
Gene Cross References:
T10B5.2
(WBcel235)V:1849850A>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1849850A>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_variant, intron_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1849850A>T
Gene Cross References:
T10B5.2
(WBcel235)V:1850821C>T
(
Caenorhabditis elegans
)
Allele/Variant
Source:
NC_003283.11:g.1850821C>T
Genes:
T10B5.2
(Cel)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
non_coding_transcript_exon_variant
Diseases:
Not Available
Variant Name:
(WBcel235)V:1850821C>T
Gene Cross References:
T10B5.2
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