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Browse our EYA4 (EYA4) ELISA Kits

Full name:
Eyes Absent Homolog 4 (Drosophila) ELISA Kits (EYA4)
On www.antibodies-online.com are 0 Eyes Absent Homolog 4 (Drosophila) (EYA4) ELISA Kits from different suppliers available. Additionally we are shipping EYA4 Antibodies (64) and EYA4 Proteins (4) and many more products for this protein. A total of 71 EYA4 products are currently listed.
Synonyms:
B130023L16Rik, CMD1J, DFNA10
list all ELISA KIts Gene Name GeneID UniProt
Mouse EYA4 EYA4 14051  
Human EYA4 EYA4 2070 O95677
Rat EYA4 EYA4 292172  

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More ELISA Kits for EYA4 Interaction Partners

Mouse (Murine) Eyes Absent Homolog 4 (Drosophila) (EYA4) interaction partners

  1. results implicate Eya4/Six1 (show SIX1 ELISA Kits) regulates normal cardiac function via p27 (show CDKN1B ELISA Kits)/casein kinase-2alpha/histone deacetylase 2 (show HDAC2 ELISA Kits) and indicate that mutations within this transcriptional complex and signaling cascade lead to the development of cardiomyopathy.

  2. constructs of the homologous region ( Eya1HR and Eya4HR) interact with Six1 (show SIX1 ELISA Kits) prey constructs, although no interaction with Dach1 (show DACH1 ELISA Kits) prey was demonstrable

  3. Eya4(-/-) mice developed otitis media with effusion; anatomic studies revealed abnormal middle ear cavity and eustachian tube dysmorphology.

  4. that Eyes absent 4 (EYA4), originally identified as a co-transcription factor, stimulates the expression of IFN-beta (show IFNB1 ELISA Kits) and CXCL10 (show CXCL10 ELISA Kits) in response to the undigested DNA of apoptotic cells

Human Eyes Absent Homolog 4 (Drosophila) (EYA4) interaction partners

  1. Up to now, merely 7 loci have been linked to mid-frequency hearing loss. Only four genetic mid-frequency deafness genes, namely, DFNA10 (EYA4), DFNA8 (show TECTA ELISA Kits)/12 (TECTA (show TECTA ELISA Kits)), DFNA13 (COL11A2 (show COL11A2 ELISA Kits)), DFNA44 (CCDC50 (show CCDC50 ELISA Kits)), have been reported to date. [review]

  2. study identified EYA4 gene as targets for AML1 (show RUNX1 ELISA Kits)-ETO (show RUNX1T1 ELISA Kits) and indicated it as a novel tumor suppressor gene. In addition, we provided evidence that EYA4 gene might be a novel therapeutic target and a potential candidate for treating AML1 (show RUNX1 ELISA Kits)-ETO (show RUNX1T1 ELISA Kits)+ t (8;21) AML (show RUNX1 ELISA Kits).

  3. Loss of EYA4 expression is associated with intrahepatic cholangiocarcinoma.

  4. The identification of a novel EYA4 truncation mutation associated with DFNA10, rather than syndromic hearing loss, supports a previously reported genotype-phenotype correlation in this gene.

  5. results implicate Eya4/Six1 (show SIX1 ELISA Kits) regulates normal cardiac function via p27 (show PAK2 ELISA Kits)/casein kinase-2alpha/histone deacetylase 2 (show HDAC2 ELISA Kits) and indicate that mutations within this transcriptional complex and signaling cascade lead to the development of cardiomyopathy.

  6. In a Dutch family with c.464del EYA4 mutation, hearing impairment begins as a mid-frequency hearing impairment in childhood and develops into a high-frequency, moderate hearing impairment later in life.

  7. Genetic variations in the EYA4, GRHL2 and DFNA5 genes and their interactions with occupational noise exposure may play an important role in the incidence of noise-induced hearing loss (NIHL).

  8. analysis of an EYA4 mutation causing hearing loss in a Chinese DFNA family

  9. A novel missense mutation c.1643C>G (p.T548R) in EYA4 may cause autosomal dominant non-syndromic hearing impairment.

  10. EYA4 mutations are associated with autosomal dominant non-syndromic hearing loss.

EYA4 Antigen Profile

Antigen Summary

This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, and it may be important for eye development, and for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant nonsyndromic sensorineural 10 locus. Defects in this gene are also associated with dilated cardiomyopathy 1J. Three transcript variants encoding distinct isoforms have been identified for this gene.

Alternative names and synonyms associated with EYA4

  • eyes absent 4 homolog (Drosophila) (Eya4) Elisa Kit
  • eyes absent homolog 4 (Drosophila) (EYA4) Elisa Kit
  • eyes absent homolog 4 (Drosophila) (Eya4) Elisa Kit
  • B130023L16Rik Elisa Kit
  • CMD1J Elisa Kit
  • DFNA10 Elisa Kit

Protein level used designations for EYA4

eyes absent homolog 4 , dJ78N10.1 (eyes absent) , eyes absent 4

GENE ID SPECIES
14051 Mus musculus
2070 Homo sapiens
395716 Gallus gallus
483991 Canis lupus familiaris
100157256 Sus scrofa
538786 Bos taurus
292172 Rattus norvegicus
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