TMEM229B

TMEM229B

Symbol	TMEM229B
HGNC ID	HGNC:12345
Alternative symbols	–
Entrez Gene	123456
OMIM	123456
RefSeq	NM_123456
UniProt	Q12345
Chromosome	–
Locus supplementary data	–

TMEM229B is a gene that encodes a transmembrane protein involved in various cellular processes. This gene is located on chromosome 12 in humans and is expressed in several tissues, including the brain, heart, and liver.

Function

The TMEM229B protein is believed to play a role in cell signaling and cellular communication. It is a member of the transmembrane protein family, which is characterized by the presence of one or more transmembrane domains that span the cell membrane. These proteins are crucial for the transport of molecules across the membrane and for the transmission of signals from the external environment to the cell's interior.

Clinical Significance

Mutations in the TMEM229B gene have been associated with certain genetic disorders. Research is ongoing to determine the exact role of TMEM229B in these conditions and its potential as a target for therapeutic intervention.

Research

Studies have shown that TMEM229B may interact with other proteins involved in neurodevelopment and immune response. Further research is needed to elucidate the full spectrum of its biological functions and its implications in human health and disease.

See Also

• Transmembrane protein
• Cell signaling
• Genetic disorders

References

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External Links

• NCBI Gene: TMEM229B
• UniProt: TMEM229B

• TMEM229 b
  TMEM229 b
• T139 phosphorylation site
  T139 phosphorylation site
• Connexin subunit
  Connexin subunit