phosphatidylserine synthase 1

Summary
Gene Symbol
  • PTDSS1
Aliases
  • KIAA0024
  • PSS1
  • PSSA
Organism
Homo sapiens (human)
External Links
NCBI Gene
9791
HGNC
9587
KEGG Gene ID
hsa:9791
PubChem
9791
Alliance of Genome Resources
Annotation
Keyword
  • Acetylation
  • Alternative splicing
  • Disease variant
  • Dwarfism
  • Endoplasmic reticulum
  • Intellectual disability
  • Phospholipid biosynthesis
  • Phosphoprotein
  • Reference proteome
  • Transferase
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
P48651
  • Serine-exchange enzyme I
Gene Ontology (GO)
Displaying 1 entry
GO Term Evidence Code PMID
phosphatidylserine biosynthetic process
GO Hierarchy
KEGG BRITE Database
Orthology
K08729
Name
phosphatidylserine synthase 1 [EC:2.7.8.-]
References
Disease
Disease Ontology
Displaying entries 11 - 20 of 68 in total
DO ID Disease Name Source
DOID:0070133 autosomal recessive cutis laxa type IB
DOID:0070134 autosomal recessive cutis laxa type IIA
DOID:0070135 autosomal recessive cutis laxa type IA
DOID:0070136 autosomal dominant cutis laxa 2
DOID:0070137 autosomal recessive cutis laxa type IIB
DOID:0070138 autosomal recessive cutis laxa type IIIB
DOID:0070140 autosomal recessive cutis laxa type IIC
DOID:0070141 autosomal recessive cutis laxa type II classic type
DOID:0070142 autosomal dominant cutis laxa
DOID:0080334 aortic valve disease 2
The Human Phenotype Ontology
Displaying entries 21 - 30 of 102 in total
HPO ID HPO Term
HP:0000316 Hypertelorism
HP:0000337 Broad forehead
HP:0000347 Micrognathia
HP:0000400 Macrotia
HP:0000407 Sensorineural hearing impairment
HP:0000452 Choanal stenosis
HP:0000453 Choanal atresia
HP:0000614 Abnormal nasolacrimal system morphology
HP:0000682 Abnormal dental enamel morphology
HP:0000885 Broad ribs
Displaying all 2 entries
Disease ID Disease Name
ORPHA:2658
  • Lenz-Majewski hyperostotic dwarfism
OMIM:151050
  • Lenz-Majewski hyperostotic dwarfism
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP002660
Gene Name
phosphatidylserine synthase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024