Gene: ENSG00000157423 (Homo sapiens)

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Gene Identifier
ENSG00000157423
Transcript Identifier
ENST00000393567
Gene Type
Coding gene
Location
16 : 70807580-71186895 : negative

Family Information

Homologous gene family
HOM03P004095
(23 genes in 12 species)
specific family

Descriptions

gene_descr
HYDIN, axonemal central pair apparatus protein

Identifiers

Type Value
pidENSP00000377197
HGNC19368
UniprotQ4G0P3

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0002064
IEA
Genome Projectepithelial cell development
GO:0003341
IEA
Genome Projectcilium movement
GO:0007275
IEA
Genome Projectmulticellular organismal development
GO:0021591
IEA
Genome Projectventricular system development
GO:0042384
IEA
Genome Projectcilium assembly
GO:0060438
IEA
Genome Projecttrachea development

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005929
IEA
Genome Projectcilium
GO:0042995
IEA
Genome Projectcell projection

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
Show redundant parents:  
 
InterPro Description
IPR008962PapD-like
IPR027417P-loop containing nucleoside triphosphate hydrolase
IPR031549Abnormal spindle-like microcephaly-associated protein, ASH domain

No MapMan annotations defined for this gene.