1,863 results for nav2b

nav2b

(Danio rerio)
Gene
Name: neuron navigator 2b
Synonyms: im:7156396, im:7155999, si:ch211-169k21.2
Source: ZFIN:ZDB-GENE-061207-13
Biotype: protein coding gene
Symbol: nav2b (Dre)
Symbol: nav2b

NAV2

(Homo sapiens)
Gene
Name: neuron navigator 2
Synonyms: RAINB1, FLJ77876, STEERIN2, retinoic acid inducible gene in neuroblastoma 1, unc-53 homolog 2, helicase, APC down-regulated 1, UNC53H2, POMFIL2, FLJ10633, pore membrane and/or filament-interacting-like protein 2, helicase APC down-regulated 1, FLJ23707, FLJ11030, HELAD1, pore membrane and/or filament interacting like protein 2, steerin-2, retinoic acid inducible in neuroblastoma 1, KIAA1419
Source: HGNC:15997
Biotype: protein coding gene
Strict Orthology Symbols: nav2b

unc-53

(Caenorhabditis elegans)
Gene
Name: UNCoordinated 53
Synonyms: CELE_F45E10.1, F45E10.1
Source: WB:WBGene00006788
Biotype: protein coding gene
Strict Orthology Symbols: nav2b

Nav2

(Mus musculus)
Gene
Name: neuron navigator 2
Synonyms: Unc53H2, 5330421F07Rik, expressed sequence BQ960892, HELAD1, mKIAA3015, RIKEN cDNA 5330421F07 gene, Rainb1, expressed sequence AU067780, RAINB2, BQ960892, POMFIL2, AU067780
Source: MGI:2183691
Biotype: protein coding gene
Strict Orthology Symbols: nav2b

Nav2

(Rattus norvegicus)
Gene
Name: neuron navigator 2
Synonyms: LOC361581, Rainb1, retinoic acid inducible in neuroblastoma cells 1
Source: RGD:619778
Biotype: protein coding gene
Strict Orthology Symbols: nav2b

Nav

(Drosophila melanogaster)
Gene
Name: Neuron navigator
Synonyms: Dm_2L:104545, CG13958, Sickie, CG13959, CG33316, CG13964, CG42589, sickie, sick, CG43720, CG13960, CG13961, CG10662, CG34343
Source: FB:FBgn0263873
Biotype: protein coding gene
Strict Orthology Symbols: nav2b

la014661Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120806-9970
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: nav2b (Dre)

la023148Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120806-10720
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: nav2b (Dre)

nav2

(Xenopus tropicalis)
Gene
Name: neuron navigator 2
Synonyms: neuron navigator 2, rainb1, pomfil2, steerin2, helad1, nav2
Source: Xenbase:XB-GENE-1008034
Biotype: gene
Strict Orthology Symbols: nav2b

Source: DOID:0070338
Definition: A cerebellar disease that is characterized by a cerebellum that is smaller than usual or not completely developed.
Genes: nav2b (Dre)

Gene Ontology
Source: GO:0022008
Synonyms:
  • nervous system cell generation
  • neural cell differentiation
Branch: biological process
Genes: nav2b (Dre)

Source: GO:0009653
Synonyms:
  • anatomical structure organization
  • embryogenesis and morphogenesis
Branch: biological process
Genes: nav2b (Dre)

sa14752

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-3428
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: nav2b (Dre)

Source: GO:0016887
Synonyms:
  • ATP hydrolase activity
  • ATP monophosphatase activity
Branch: molecular function
Genes: nav2b (Dre)

sa14333

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-12700
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: nav2b (Dre)

Gene Ontology
Source: GO:0005524
Synonyms:
  • Mg-ATP binding
  • MgATP binding
Branch: molecular function
Genes: nav2b (Dre)

Gene Ontology
Source: GO:0005575
Synonyms:
  • cell or subcellular entity
  • cellular component
Branch: cellular component
Genes: nav2b (Dre)

Allele/Variant
Source: ss5200201338
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14534567A>G

Allele/Variant
Source: ss5200201347
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14534708T>A

Allele/Variant
Source: ss5200201440
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14537493T>G

Allele/Variant
Source: ss5200201444
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14538409G>A

Allele/Variant
Source: ss5200201521
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14544371C>G

Allele/Variant
Source: ss5200201517
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14545035T>C

Allele/Variant
Source: ss5200201931
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14567989C>T

Allele/Variant
Source: ss5200202172
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14581493C>T

Allele/Variant
Source: ss5200202115
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14582265G>T

Allele/Variant
Source: ss5200202209
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14591186C>T

Allele/Variant
Source: ss5200202134
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14585842A>G

Allele/Variant
Source: ss5200202205
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14587154A>G

Allele/Variant
Source: ss5200202236
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14592201T>A

Allele/Variant
Source: ss5200202387
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14595414A>C

Allele/Variant
Source: ss5200202367
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14595415A>C

Allele/Variant
Source: ss5200202360
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14595432T>C

Allele/Variant
Source: ss5200202378
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14597852T>A

Allele/Variant
Source: ss5200202644
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14613373G>A

Allele/Variant
Source: ss5200202648
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14613829G>A

Allele/Variant
Source: ss5200202812
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14624739A>T

Allele/Variant
Source: ss5200200976
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14517755A>T

Allele/Variant
Source: ss5200201045
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14520698T>G

Allele/Variant
Source: ss5200201025
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14521124C>G

Allele/Variant
Source: ss5200201027
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14521602G>A

Allele/Variant
Source: ss5200201085
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14521797C>T

Allele/Variant
Source: ss5200201113
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14525353G>C

Allele/Variant
Source: ss5200201206
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14525476C>T

Allele/Variant
Source: ss5200201139
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14525564T>A

Allele/Variant
Source: ss5200201269
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14534399T>A

Allele/Variant
Source: ss5200201197
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14527049T>G

Allele/Variant
Source: ss5200200982
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14514196C>T

Allele/Variant
Source: ss5200200952
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14515021G>A

Allele/Variant
Source: ss5200200983
Genes: nav2b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)25:14515983C>T