NIPAL3
NIPA-like protein 3
Also known as: DJ462O23.2, NPAL3, NPAL3_HUMAN, SLC57A5
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6P499
- Gene
- NIPAL3
- Ensembl
- ENSG00000001461
- Chromosome
- 1
- Canonical length
- 406 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable magnesium ion transmembrane transporter activity. Predicted to be involved in magnesium ion transport. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
406 residues, UniProt reviewed canonical sequence.
>Q6P499|NIPAL3
1 MDGSHSAALK LQQLPPTSSS SAVSEASFSY KENLIGALLA IFGHLVVSIA LNLQKYCHIR
61 LAGSKDPRAY FKTKTWWLGL FLMLLGELGV FASYAFAPLS LIVPLSAVSV IASAIIGIIF
121 IKEKWKPKDF LRRYVLSFVG CGLAVVGTYL LVTFAPNSHE KMTGENVTRH LVSWPFLLYM
181 LVEIILFCLL LYFYKEKNAN NIVVILLLVA LLGSMTVVTV KAVAGMLVLS IQGNLQLDYP
241 IFYVMFVCMV ATAVYQAAFL SQASQMYDSS LIASVGYILS TTIAITAGAI FYLDFIGEDV
301 LHICMFALGC LIAFLGVFLI TRNRKKPIPF EPYISMDAMP GMQNMHDKGM TVQPELKASF
361 SYGALENNDN ISEIYAPATL PVMQEEHGSR SASGVPYRVL EHTKKELocalizationUniProt · AlphaFold · HPA
Whether an antibody against NIPAL3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Unknown
- Secreted
- No
- Transmembrane segments
- 9
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 60 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 60 nTPM
- cerebellum: 59 nTPM
- midbrain: 56 nTPM
- prostate: 53 nTPM
- hippocampal formation: 39 nTPM
- cerebral cortex: 38 nTPM
Single-cell type
- prostatic glandular cells: 612 nCPM
- oligodendrocytes: 130 nCPM
- megakaryocytes: 124 nCPM
- lacrimal acinar cells: 121 nCPM
- cone photoreceptor cells: 118 nCPM
- esophageal apical cells: 116 nCPM
Immune cell
- naive CD4 T-cell: 39 nTPM
- T-reg: 32 nTPM
- memory CD4 T-cell: 29 nTPM
- naive CD8 T-cell: 25 nTPM
- memory CD8 T-cell: 23 nTPM
- memory B-cell: 22 nTPM
Brain region
- white matter: 166 nTPM
- cerebellum: 128 nTPM
- basal ganglia: 127 nTPM
- cerebral cortex: 127 nTPM
- pons: 125 nTPM
- thalamus: 125 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.84
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.68
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NIPAL3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads NIPAL3 as an antibody target. Whether an autoantibody or antibody against NIPAL3 could matter depends on whether native NIPAL3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NIPAL3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label NIPAL3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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