QuickView for Sohlh1 (gene)

Gene Symbol:

SOHLH1 Homo sapiens

Full name:

spermatogenesis and oogenesis specific basic helix-loop-helix 1

Synonyms:

C9orf157, NOHLH, ODG5, SPATA27, TEB2, bA100C15.3, bHLHe80, spermatogenesis- and oogenesis-specific basic helix-loop-helix-containing protein 1, newborn ovary helix loop helix, spermatogenesis associated 27

Genomic Location:

Chr 9: 137725074-137731195

Description:

This gene encodes one of testis-specific transcription factors which are essential for spermatogenesis, oogenesis and folliculogenesis. This gene is located on chromosome 9. Mutations in this gene are associated with nonobstructive azoospermia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

This gene encodes one of testis-specific transcription factors which are essential for spermatogenesis, oogenesis and folliculogenesis. This gene is located on chromosome 9. Mutations in this gene are associated with nonobstructive azoospermia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Pan troglodytes ,  Bos taurus ,  Canis lupus familiaris

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

CAGGGTC_MIR504

miRNA binding sites
(Source: TargetScan):

Predicted Gene Targets for miR-504

Cytogenetic Map:

9q34.3

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