TRAM1L1
Translocating chain-associated membrane protein 1-like 1
Also known as: MGC26568, TR1L1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N609
- Gene
- TRAM1L1
- Ensembl
- ENSG00000174599
- Chromosome
- 4
- Canonical length
- 369 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Predicted to be involved in protein insertion into ER membrane. Predicted to be located in endoplasmic reticulum and membrane. Predicted to be active in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
369 residues, UniProt reviewed canonical sequence.
>Q8N609|TRAM1L1
1 MGLRKKSTKN PPVLSQEFIL QNHADIVSCV GMFFLLGLVF EGTAEASIVF LTLQHSVAVP
61 AAEEQATGSK SLYYYGVKDL ATVFFYMLVA IIIHATIQEY VLDKINKRMQ FTKAKQNKFN
121 ESGQFSVFYF FSCIWGTFIL ISENCLSDPT LIWKARPHSM MTFQMKFFYI SQLAYWFHAF
181 PELYFQKTKK QDIPRQLVYI GLHLFHITGA YLLYLNHLGL LLLVLHYFVE LLSHMCGLFY
241 FSDEKYQKGI SLWAIVFILG RLVTLIVSVL TVGFHLAGSQ NRNPDALTGN VNVLAAKIAV
301 LSSSCTIQAY VTWNLITLWL QRWVEDSNIQ ASCMKKKRSR SSKKRTENGV GVETSNRVDC
361 PPKRKEKSSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRAM1L1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 8
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 7.9 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 7.9 nTPM
- spinal cord: 7.4 nTPM
- kidney: 6.4 nTPM
- basal ganglia: 6.3 nTPM
- hippocampal formation: 5.9 nTPM
- epididymis: 5.7 nTPM
Single-cell type
- oligodendrocytes: 15 nCPM
- retinal pigment epithelial cells: 13 nCPM
- oligodendrocyte progenitor cells: 11 nCPM
- epididymal principal cells: 9.1 nCPM
- other brain neurons: 7.6 nCPM
- decidual stromal cells: 7.1 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 9.6 nTPM
- hypothalamus: 9.1 nTPM
- pons: 9 nTPM
- basal ganglia: 8.7 nTPM
- medulla oblongata: 8.2 nTPM
- spinal cord: 8.1 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)
- 1.39
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
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
- protein insertion into ER membrane
- SRP-dependent cotranslational protein targeting to membrane, translocation
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TRAM1L1 as an antibody target. Whether an autoantibody or antibody against TRAM1L1 could matter depends on whether native TRAM1L1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRAM1L1 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 TRAM1L1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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