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Validated All-in-One™ qPCR Primer for ATOH1(NM_005172.1) Search again
Product ID:
HQP011762
(click here to view gene annotation page)
Species:
Human
Symbol:
Alias:
ATH1, DFNA89, HATH1, MATH-1, bHLHa14
Gene Description:
atonal bHLH transcription factor 1
Target Gene Accession:
NM_005172.1(click here to view gene page)
Estimated Delivery:
Approximately 1-3 weeks, but may vary. Please email sales@genecopoeia.com or call 301-762-0888 to confirm ETA.
Important Note:
By default, qPCR primer pairs are designed to measure the expression level of the splice variant (accession number) you selected for this gene WITHOUT consideration of other possible variants of this gene. If this gene has multiple variants, and you would like to measure the expression levels of one particular variant, multiple variants, or all variants, please contact us for a custom service project at inquiry@genecopoeia.com.
Validated result:
Summary
This protein belongs to the basic helix-loop-helix (BHLH) family of transcription factors. It activates E-box dependent transcription along with E47. [provided by RefSeq].
Gene References into function
- Maps to 10q21-22. Candidate gene for optic nerve aplasia and related syndromes.
- Proneural and proneuroendocrine transcription factor expression in cutaneous mechanoreceptor (Merkel) cells and Merkel cell carcinoma
- Hath1 may regulate the expression of MUC2, a mucin secreted by goblet cells, and Hath1 may also be a novel factor normally repressed as a consequence of activation of the Wnt signaling pathway [review]
- Hath1 is one of the transcriptional regulators for MUC6 and MUC5AC in gastric cancer cells.
- Based on these results, we hypothesize that Cdx2 is involved in activating Math1 expression in intestinal epithelial cells.
- HATH1 is an important factor in the up-regulation of MUC2 expression that occurs in mucinous cancers and signet ring carcinomas.
- GSK3beta-dependent protein degradation was switched between Hath1 and beta-catenin by Wnt signaling, leading to the dramatic alteration of cell status between proliferation and differentiation in colon cancer
- In the chimeric environment, genotypically wild-type cells that possess Math1 have the competence to differentiate into hair cells by providing appropriate environmental interactions.
- Patients with ATOH1-expressing adenocarcinomas might have a worse prognosis.
- ATOH1 activates hairy and enhancer of split 6 transcription through binding to three clustered E boxes of its promoter
- Hath1 protein degradation may be required for maintaining the undifferentiated state of colon cancers, and that GSK3 inhibitors have potential for use in cancer therapy.
