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SEPT5

SEPT5

Protein-coding gene in the species Homo sapiens

Septin-5 is a protein that in humans is encoded by the SEPT5 gene. This gene is a member of the septin gene family of nucleotide binding proteins, originally

SEPT5

DiGeorge syndrome

Medical condition caused by chromosomal abnormality

These include DGCR8, which is important for biogenesis of brain microRNA, SEPT5, which encodes a protein that interacts with the PARK2 protein, COMT, which

DiGeorge syndrome

DiGeorge_syndrome

Chromosome 22

Human chromosome

component 50 homolog SEPT3: encoding protein neuronal-specific septin-3 SEPT5 SHFM3P1: SOX10 SYNGR1: encoding protein synaptogyrin-1 TBC1D10A: encoding

Chromosome 22

Chromosome_22

Septin

Family of proteins

subfamilies each named after its founding member: (i) SEPT2 (SEPT1, SEPT4, SEPT5), (ii) SEPT3 (SEPT9, SEPT12), (iii) SEPT6 (SEPT8, SEPT10, SEPT11, SEPT14)

Septin

Parkin (protein)

Mammalian protein found in humans

HSPA1A, HSPA8, Multisynthetase complex auxiliary component p38, PDCD2, SEPT5, SNCAIP, STUB1, SYT11, and Ubiquitin C. GRCh38: Ensembl release 89: ENSG00000185345

Parkin (protein)

Parkin_(protein)

SEPT8

Protein-coding gene in the species Homo sapiens

in vesicle trafficking. SEPT8 has been shown to interact with PFTK1 and SEPT5. GRCh38: Ensembl release 89: ENSG00000164402 – Ensembl, May 2017 GRCm38:

SEPT8

SEPT4

Protein-coding gene in the species Homo sapiens

D'Adamio L, Lee JM, Cochran E, Bowser R, Dawson TM, Wolozin B (October 2003). "SEPT5_v2 is a parkin-binding protein". Brain Research. Molecular Brain Research

SEPT4

Tropomyosin receptor kinase C

Protein found in humans

at promoter or exon 1 region of eight genes (including DDIT3, FES, FLT3, SEPT5, SEPT9, SOX1, SOX17, and NTRK3) for prognostic prediction in ESCC (esophageal

Tropomyosin receptor kinase C