Homo sapiens Protein: SEMA3A
Summary
InnateDB Protein IDBP-24548.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SEMA3A
Protein Name sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
Synonyms coll-1; COLL1; HH16; Hsema-I; Hsema-III; SEMA1; SEMAD; SEMAIII; SEMAL; SemD;
Species Homo sapiens
Ensembl Protein ENSP00000265362
InnateDB Gene IDBG-24546 (SEMA3A)
Protein Structure
UniProt Annotation
Function Involved in the development of the olfactory system and in neuronal control of puberty. Induces the collapse and paralysis of neuronal growth cones. Could serve as a ligand that guides specific growth cones by a motility-inhibiting mechanism. Binds to the complex neuropilin-1/plexin-1. {ECO:0000269PubMed:22416012}.
Subcellular Localization Secreted {ECO:0000250}.
Disease Associations Hypogonadotropic hypogonadism 16 with or without anosmia (HH16) [MIM:614897]: A disorder characterized by absent or incomplete sexual maturation by the age of 18 years, in conjunction with low levels of circulating gonadotropins and testosterone and no other abnormalities of the hypothalamic- pituitary axis. In some cases, it is associated with non- reproductive phenotypes, such as anosmia, cleft palate, and sensorineural hearing loss. Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts. Hypogonadism is due to deficiency in gonadotropin-releasing hormone and probably results from a failure of embryonic migration of gonadotropin-releasing hormone-synthesizing neurons. In the presence of anosmia, idiopathic hypogonadotropic hypogonadism is referred to as Kallmann syndrome, whereas in the presence of a normal sense of smell, it has been termed normosmic idiopathic hypogonadotropic hypogonadism (nIHH). {ECO:0000269PubMed:22416012, ECO:0000269PubMed:22927827}. Note=The disease may be caused by mutations affecting distinct genetic loci, including the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 3 [view]
Protein-Protein 3 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004872 receptor activity
GO:0005515 protein binding
GO:0030215 semaphorin receptor binding
GO:0038191 neuropilin binding
GO:0045499 chemorepellent activity
Biological Process
GO:0001764 neuron migration
GO:0002027 regulation of heart rate
GO:0006915 apoptotic process
GO:0007275 multicellular organismal development
GO:0007411 axon guidance
GO:0007413 axonal fasciculation
GO:0008045 motor neuron axon guidance
GO:0010633 negative regulation of epithelial cell migration
GO:0021612 facial nerve structural organization
GO:0021637 trigeminal nerve structural organization
GO:0021675 nerve development
GO:0021772 olfactory bulb development
GO:0021785 branchiomotor neuron axon guidance
GO:0021828 gonadotrophin-releasing hormone neuronal migration to the hypothalamus
GO:0030517 negative regulation of axon extension
GO:0045087 innate immune response (InnateDB)
GO:0048485 sympathetic nervous system development
GO:0048813 dendrite morphogenesis
GO:0048841 regulation of axon extension involved in axon guidance
GO:0048843 negative regulation of axon extension involved in axon guidance
GO:0048846 axon extension involved in axon guidance
GO:0048880 sensory system development
GO:0050919 negative chemotaxis
GO:0060385 axonogenesis involved in innervation
GO:0060666 dichotomous subdivision of terminal units involved in salivary gland branching
GO:0061549 sympathetic ganglion development
GO:0071526 semaphorin-plexin signaling pathway
GO:0097490 sympathetic neuron projection extension
GO:0097491 sympathetic neuron projection guidance
GO:1901166 neural crest cell migration involved in autonomic nervous system development
GO:1902285 semaphorin-plexin signaling pathway involved in neuron projection guidance
GO:1902287 semaphorin-plexin signaling pathway involved in axon guidance
GO:1903045 neural crest cell migration involved in sympathetic nervous system development
GO:2000020 positive regulation of male gonad development
GO:2001224 positive regulation of neuron migration
Cellular Component
GO:0005576 extracellular region
GO:0016020 membrane
GO:0030424 axon
GO:0030425 dendrite
Protein Structure and Domains
PDB ID
InterPro IPR001627 Sema domain
IPR003599 Immunoglobulin subtype
IPR007110 Immunoglobulin-like domain
IPR016201 Plexin-like fold
PFAM PF01403
PRINTS
PIRSF
SMART SM00630
SM00409
SM00423
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q14563
PhosphoSite PhosphoSite-Q14563
TrEMBL Q86UJ2
UniProt Splice Variant
Entrez Gene 10371
UniGene Hs.252451
RefSeq NP_006071
HUGO HGNC:10723
OMIM 603961
CCDS CCDS5599
HPRD 04908
IMGT
EMBL AC004028 AC004451 AC004848 AC004907 AC006322 AC073221 L26081
GenPept AAA65938 AAC78622 AAP22350 AAS00353 AAS02028