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ELMOD3, ELMO domain containing 3

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ELMOD3, ELMO domain containing 3

  • This gene encodes a member of the engulfment and cell motility family of GTPase-activating proteins that regulate Arf GTPase proteins. Members of this family are defined by a conserved engulfment and cell motility domain. In rat cochlea, the encoded protein is found in stereocilia, kinocilia and cuticular plate of developing hair cells suggesting a function for this protein in cochlear sensory cells. An allelic variant of this family has been associated with autosomal recessive nonsyndromic deafness-88 in humans. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]

  • Gene Synonyms (ELMO domain-containing protein 3, ELMO/CED-12 domain containing 3, RNA binding motif and ELMO/CED-12 domain 1, RNA-binding motif and ELMO domain-containing protein 1, RNA-binding motif protein 29, deafness, autosomal recessive 88, liver-specific organic anion transporter 3TM12, organic anion transporter LST-3b, DFNB88, LST3, RBED1, RBM29,)
  • NCBI Gene ID: 84173
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q96FG2
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

ELMO domain containing 3 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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