CDB25:0004267 SEMA3G — PLXNA4

Experimentally validated in Human; Orthology-inferred in Mouse, Rat, Frog, Zebrafish, Macaque, Pig, Dog, Cow, Chimp, Horse, Marmoset, Sheep

Title

Journal:; Year Published:

Abstract

A Novel SEMA3G Mutation in Two Siblings Affected by Syndromic GnRH Deficiency.

Neuroendocrinology, 2021; PubMed, Homo sapiens SEMA3G — Homo sapiens PLXNA4
ABSTRACT: Gonadotropin-releasing hormone (GnRH) deficiency causes hypogonadotropic hypogonadism (HH), a rare genetic disorder that impairs sexual reproduction. HH can be due to defective GnRH-secreting neuron development or function and may be associated with other clinical signs in overlapping genetic syndromes. With most of the cases being idiopathic, genetics underlying HH is still largely unknown.
Basic Information on SEMA3G
Ligand Name: semaphorin 3G
Other Symbols: FLJ00014, sem2
Ligand Location: secreted based on perplexity, uniprot
HGNC Gene Symbol Report: SEMA3G
GeneCards: SEMA3G
Interactions with other Receptors for SEMA3G
Basic Information on PLXNA4
Receptor Name: plexin A4
Other Symbols: PLXNA4A, PLXNA4B, KIAA1550, DKFZp434G0625PRO34003, FAYV2820
Receptor Location: cell membrane based on hpa, perplexity, uniprot
HGNC Gene Symbol Report: PLXNA4
GeneCards: PLXNA4
HGNC Gene Group: IPT domain containing, Plexins