espn gene marker
2021年8月20日 — ESPN (Espin) is a Protein Coding gene. Diseases associated with ESPN include Deafness, Autosomal Recessive 36, With Or Without Vestibular ...
Expression; Interaction; Structure; Family & Domains; Sequences (2+); Similar proteins; Cross-references; Entry information; Miscellaneous.
Molecular function： Actin-binding
HGNCi： HGNC:13281, ESPN
Biological process： Hearing
View mouse Espn Chr4:152204788-152236828 with: phenotypes, sequences, polymorphisms, proteins, references, function, expression.
作者：S Naz3 STR markers. The grey shaded haplotypes represent the ancestral chromosome harbouring the ESPN mutation. ESPN, a gene in the DFNB36 critical interval at 1p36. 2004 被引用次数：143 —
2021年7月4日 — ESPN espin [ Homo sapiens (human) ] · Summary · Genomic context · Genomic regions, transcripts, and products · Expression · Bibliography · Phenotypes.
ID: ZDB-GENE-081105-173; Name: espin; Symbol: espn Nomenclature History; Previous Names. si:dkey-77h17.1 ... Exclude altered gene expression phenotypes.
Espin, also known as autosomal recessive deafness type 36 protein or ectoplasmic specialization protein, is a protein that in humans is encoded by the ESPN gene ...
marker | 必须包含： marker
Gene: Espn (espin) Rattus norvegicus ... 6480464, [Estradiol co-treated with TGFB1 protein] results in decreased expression of ESPN mRNA, CTD, PMID:30165855.
2005年2月14日 — And its researchers must work hard to understand the value of each genetic marker, so coaches don't just cut a player for atypical DNA.
A recessive mutation in the espin gene (Espn) has been detected in the jerker. ... expression in photoreceptors is altered in whirlin-knockout mice (28).