SERINC1 - serine incorporator 1 Gene

Also Known as TDE2; TMS2; TDE1L; TMS-2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 57515

About SERINC1

Cytogenetic location: 6q22.31 Genomic coordinates (GRCh38): 6:122,443,351-122,471,807 (from NCBI)

This gene has 1 transcript (splice variant), 219 orthologues and 4 paralogues. Ubiquitous expression in brain (RPKM 241.4), adrenal (RPKM 145.5) and 25 other tissues.

Summary

Predicted to enable protein-macromolecule adaptor activity. Predicted to be involved in several processes, including phosphatidylserine metabolic process; positive regulation of CDP-diacylglycerol-serine O-phosphatidyltransferase activity; and positive regulation of serine C-palmitoyltransferase activity. Predicted to be located in endoplasmic reticulum membrane and plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Apr 2022]

SERINC1 Products (1)

mRNA Protein Name
NM_020755.4 NP_065806.1 serine incorporator 1 precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
20195357 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SERINC1 Protein Structure

Serinc

Serinc: Serine incorporator (Serinc) (16 - 452)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 453 a.a.
Protein Preferred Names Protein Names

serine incorporator 1

  • tumor differentially expressed protein 2

SERINC1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SERINC1 Q9NRX5 GPX8 Homo sapiens Q8TED1 32296183
Intra
SERINC1 Q9NRX5 GPX8 Homo sapiens Q8TED1 32296183
Intra
SERINC1 Q9NRX5 AQP9 Homo sapiens O43315 32296183
Intra
SERINC1 Q9NRX5 AQP9 Homo sapiens O43315 32296183
Intra
SERINC1 Q9NRX5 FFAR3 Homo sapiens O14843 32296183
Intra
SERINC1 Q9NRX5 FFAR3 Homo sapiens O14843 32296183
Intra
SERINC1 Q9NRX5 GPR42 Homo sapiens O15529 32296183
Intra
SERINC1 Q9NRX5 GPR42 Homo sapiens O15529 32296183
Intra
SERINC1 Q9NRX5 PAX8 Homo sapiens Q06710
TAP
20195357
Intra
SERINC1 Q9NRX5 PAX8 Homo sapiens Q06710 20195357
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Spastic Paraplegia 50, Autosomal Recessive
  • Hereditary Spastic Paraplegia 50

  • SPG50

  • Ap-4 Deficiency Syndrome

  • Ap-4-Associated Hereditary Spastic Paraplegia

  • Adaptor Protein Complex 4 Deficiency

  • Cerebral Palsy, Spastic Quadriplegic, 3, Formerly

  • Cpsq3, Formerly

  • Autosomal Recessive Spastic Paraplegia 50

  • Cpsq3

  • Spastic Quadriplegic Cerebral Palsy 3

  • Ap-4 Deficiency

  • Ap-4-Associated Hsp

  • Paraplegia, Spastic, Autosomal Recessive, Type 50

  • Spastic Paraplegia-50, Autosomal Recessive

Duane Retraction Syndrome
  • Stilling-Turk-Duane Syndrome

  • Duane'S Syndrome

  • Duane Syndrome

  • Isolated Duane Retraction Syndrome

  • Co-Contractive Retraction Syndrome

  • Duane Anomaly, Isolated

  • Ocular Retraction Syndrome

  • Drs

  • Durs

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus SERINC1 RGD RGD:727843
Canis familiaris SERINC1 VGNC VGNC:46019
Macaca mulatta SERINC1 VGNC VGNC:77226
Felis catus SERINC1 VGNC VGNC:65017
Mus musculus SERINC1 MGD MGI:1926228
Others SERINC1 NCBI