132 results for tns3.2

tns3.2

(Danio rerio)
Gene
Name: tensin 3, tandem duplicate 2
Synonyms: tns3.1, si:ch211-39i19.4, si:ch211-39i19.6
Source: ZFIN:ZDB-GENE-081031-95
Biotype: protein coding gene
Symbol: tns3.2 (Dre)
Symbol: tns3.2

TNS3

(Homo sapiens)
Gene
Name: tensin 3
Synonyms: tensin-like SH2 domain-containing protein 1, H_NH0549I23.2, DKFZp686K12123, FLJ35545, FLJ13732, tensin-like SH2 domain-containing 1, DKFZp686M1045, MGC88434, thyroid specific PTB domain protein, tensin-3, tensin-like SH2 domain containing 1, TENS1, H_NH049I23.2, tumor endothelial marker 6, TEM6
Source: HGNC:21616
Biotype: protein coding gene
Strict Orthology Symbols: tns3.2

Tns3

(Rattus norvegicus)
Gene
Name: tensin 3
Synonyms: LOC360980, TSN3, similar to novel protein similar to Tensin Tns, tensin3, LOC498410, RGD1564174, tensin-3
Source: RGD:1564174
Biotype: protein coding gene
Strict Orthology Symbols: tns3.2

tns-1

(Caenorhabditis elegans)
Gene
Name: TeNSin homolog 1
Synonyms: tag-163, tag-83, M01E11.7, CELE_M01E11.7
Source: WB:WBGene00006508
Biotype: protein coding gene
Strict Orthology Symbols: tns3.2

by

(Drosophila melanogaster)
Gene
Name: blistery
Synonyms: Tensin, BcDNA:RE65113, CT26639, CG9379, 3R-B, tensin
Source: FB:FBgn0000244
Biotype: protein coding gene
Strict Orthology Symbols: tns3.2

Tns3

(Mus musculus)
Gene
Name: tensin 3
Synonyms: F830010I22Rik, TSN3, Tens1, tensin3, tensin-like SH2 domain containing 1, RGD1564174, cDNA sequence BC023928, RIKEN cDNA F830010I22 gene, TEM6, BC023928
Source: MGI:2443012
Biotype: protein coding gene
Strict Orthology Symbols: tns3.2

tns3

(Xenopus tropicalis)
Gene
Name: tensin 3
Synonyms: tensin 3, tns3
Source: Xenbase:XB-GENE-1011198
Biotype: gene
Strict Orthology Symbols: tns3.2

Source: GO:0004721
Synonyms:
  • phosphoprotein phosphohydrolase activity
  • protein phosphatase activity
Branch: molecular function
Genes: tns3.2 (Dre)

Gene Ontology
Source: GO:0005925
Synonyms:
  • HAJ
  • adhesion plaque
Branch: cellular component
Genes: tns3.2 (Dre)

sa17437

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-10281
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_acceptor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: tns3.2 (Dre)

sa7478

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-18998
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
Genes: tns3.2 (Dre)

Gene Ontology
Source: GO:0016787
Synonyms: Not Available
Branch: molecular function
Genes: tns3.2 (Dre)

Allele/Variant
Source: ss5199710925
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6658031G>A

Allele/Variant
Source: ss5199710955
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6658037A>G

Allele/Variant
Source: ss5199711061
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659120T>C

Allele/Variant
Source: ss5199710996
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6655403A>T

Allele/Variant
Source: ss5199710931
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6656306T>A

Allele/Variant
Source: ss5199710912
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6656374A>G

Allele/Variant
Source: ss5199710972
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6656550G>A

Allele/Variant
Source: ss5199711031
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6660871T>C

Allele/Variant
Source: ss5199711044
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6661135C>G

Allele/Variant
Source: ss5199710910
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6657038G>T

Allele/Variant
Source: ss5199711029
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6658987T>G

Allele/Variant
Source: ss5199711019
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659193T>G

Allele/Variant
Source: ss5199710948
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6655887G>T

Allele/Variant
Source: ss5199710970
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6656364A>C

Allele/Variant
Source: ss5199710938
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6657817C>A

Allele/Variant
Source: ss5199710947
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6657852A>G

Allele/Variant
Source: ss5199710946
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6658052A>G

Allele/Variant
Source: ss5199711049
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659032G>A

Allele/Variant
Source: ss5199711080
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659055A>G

Allele/Variant
Source: ss5199711030
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6660149C>G

Allele/Variant
Source: ss5199710990
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6658072G>A

Allele/Variant
Source: ss5199711063
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659101A>G

Allele/Variant
Source: ss5199711027
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659125T>G

Allele/Variant
Source: ss5199711052
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659148T>A

Allele/Variant
Source: ss5199710911
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6657456C>T

Allele/Variant
Source: ss5199710994
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6657876A>G

Allele/Variant
Source: ss5199711036
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659056T>G

Allele/Variant
Source: ss5199711032
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6660134T>C

Allele/Variant
Source: ss5199711001
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659079T>G

Allele/Variant
Source: ss5199711099
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659488T>A

Allele/Variant
Source: ss5199711040
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659565T>C

Allele/Variant
Source: ss5199711012
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659738T>G

Allele/Variant
Source: ss5199711016
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659964T>C

Allele/Variant
Source: ss5199710926
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6656029C>A

Allele/Variant
Source: ss5199710951
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6658669G>T

Allele/Variant
Source: ss5199710949
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6658941T>G

Allele/Variant
Source: ss5199711035
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659042A>G

Allele/Variant
Source: ss5199711085
Genes: tns3.2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)20:6659429T>A