PTDSS2 - phosphatidylserine synthase 2 Gene

Also Known as PSS2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 81490

About PTDSS2

Cytogenetic location: 11p15.5 Genomic coordinates (GRCh38): 11:448,268-491,399 (from NCBI)

This gene has 13 transcripts (splice variants), 1 gene allele, 198 orthologues and 1 paralogue. Broad expression in testis (RPKM 10.7), kidney (RPKM 4.4) and 25 other tissues.

Summary

The protein encoded by this gene catalyzes the conversion of phosphatidylethanolamine to phosphatidylserine, a structural membrane phospholipid that functions in cell signaling, blood coagulation, and Apoptosis. The encoded enzyme also has a high affinity for docosahexaenoic acid (DHA) and can use it to make DHA-containing phosphatidylserine. [provided by RefSeq, Jul 2016]

PTDSS2 Products (4)

mRNA Protein Name
NM_001329544.2 NP_001316473.1 phosphatidylserine synthase 2 isoform 1
NM_001329545.2 NP_001316474.1 phosphatidylserine synthase 2 isoform 3
NM_001329548.2 NP_001316477.1 phosphatidylserine synthase 2 isoform 4 precursor
NM_030783.3 NP_110410.1 phosphatidylserine synthase 2 isoform 2
Molecular Function GO Annotation Evidence References Source
enables L-serine-phosphatidylethanolamine phosphatidyltransferase activity IDA
IDA: Inferred from direct assay
19014349 GOA
Biological Process GO Annotation Evidence References Source
involved in phosphatidylserine biosynthetic process IDA
IDA: Inferred from direct assay
19014349 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

PTDSS2 Protein Structure

PSS

PSS: Phosphatidyl serine synthase (120 - 400)

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

phosphatidylserine synthase 2

  • PSS-2

PTDSS2 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82025 PSS2 Antibody (YA1770) WB, IP Human
HY-P82025A PSS2 Antibody (YA1770)(PBS only) WB, IP Human
HY-P86281 PSS2 Antibody (YA5973) WB, FC, IP Human

Related Diseases

Diseases Alias
Lenz-Majewski Hyperostotic Dwarfism
  • Lenz-Majewski Syndrome

  • Lenz Majewski Hyperostotic Dwarfism

  • LMHD

  • Hyperostotic Dwarfism Lenz-Majewski Type

  • Lenz-Majewski Hyperostotic Dysplasia

  • Multiple Congenital Anomalies, Intellectual Disability And Progressive Skeletal Sclerosis

  • Lms

Neuronopathy, Distal Hereditary Motor, Type Viia
  • HMN7A

  • Hmn Viia

  • Dhmn7a

  • Neuropathy, Distal Hereditary Motor, Type Viia

  • Dhmnvp

  • Harper-Young Myopathy

  • Distal Hereditary Motor Neuronopathy Type 7a

  • Distal Hereditary Motor Neuropathy Type Viia

  • Neuronopathy, Distal Hereditary Motor, Type 7a

  • Spinal Muscular Atrophy, Distal, With Vocal Cord Paralysis

  • Distal Spinal Muscular Atrophy With Vocal Cord Paralysis Type 7a

  • Harper-Young Myopath

  • Neuronopathy, Distal Hereditary Motor, 7a

  • Distal Hereditary Motor Neuronopathy Type Viia

  • Distal Hereditary Motor Neuropathy With Vocal Cord Paralysis

  • Distal Spinal Muscular Atrophy With Vocal Cord Paralysis

  • Neuropathy, Motor, Distal, Hereditary, Type Viia

Myasthenic Syndrome, Congenital, 20, Presynaptic
  • Congenital Myasthenic Syndrome 20

  • CMS20

  • Congenital Myasthenic Syndrome 20 Presynaptic

  • Myasthenic Syndrome, Congenital, Type 20, Presynaptic

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
Canis familiaris PTDSS2 VGNC VGNC:45137
Bos taurus PTDSS2 VGNC VGNC:106882
Felis catus PTDSS2 VGNC VGNC:64427
Rattus norvegicus PTDSS2 RGD RGD:1307914
Mus musculus PTDSS2 MGD MGI:1351664
Others PTDSS2 NCBI