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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
Biological process: Hearing
View mouse Espn Chr4:152204788-152236828 with: phenotypes, sequences, polymorphisms, proteins, references, function, expression.
作者:S Naz2004被引用次数:143 — 3 STR markers. The grey shaded haplotypes represent the ancestral chromosome harbouring the ESPN mutation. ESPN, a gene in the DFNB36 critical interval at 1p36.


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 ...
缺少字词: 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).

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