LMCD1
LIM and cysteine-rich domains protein 1
Also known as: LMCD1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NZU5
- Gene
- LMCD1
- Ensembl
- ENSG00000071282
- Chromosome
- 3
- Canonical length
- 365 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Cell Junctions,Cytosol
OverviewNCBI Gene
This gene encodes a member of the LIM-domain family of zinc finger proteins. The encoded protein contains an N-terminal cysteine-rich domain and two C-terminal LIM domains. The presence of LIM domains suggests involvement in protein-protein interactions. The protein may act as a co-regulator of transcription along with other transcription factors. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]
Canonical amino-acid sequenceUniProt
365 residues, UniProt reviewed canonical sequence.
>Q9NZU5|LMCD1
1 MAKVAKDLNP GVKKMSLGQL QSARGVACLG CKGTCSGFEP HSWRKICKSC KCSQEDHCLT
61 SDLEDDRKIG RLLMDSKYST LTARVKGGDG IRIYKRNRMI MTNPIATGKD PTFDTITYEW
121 APPGVTQKLG LQYMELIPKE KQPVTGTEGA FYRRRQLMHQ LPIYDQDPSR CRGLLENELK
181 LMEEFVKQYK SEALGVGEVA LPGQGGLPKE EGKQQEKPEG AETTAATTNG SLSDPSKEVE
241 YVCELCKGAA PPDSPVVYSD RAGYNKQWHP TCFVCAKCSE PLVDLIYFWK DGAPWCGRHY
301 CESLRPRCSG CDEIIFAEDY QRVEDLAWHR KHFVCEGCEQ LLSGRAYIVT KGQLLCPTCS
361 KSKRSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LMCD1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 537 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 537 nTPM
- blood vessel: 382 nTPM
- tongue: 243 nTPM
- choroid plexus: 135 nTPM
- lung: 128 nTPM
- adipose tissue: 124 nTPM
Single-cell type
- smooth muscle cells: 1,090 nCPM
- thymic myoid cells: 522 nCPM
- myonuclei: 489 nCPM
- decidual stromal cells: 480 nCPM
- hepatic stellate cells: 458 nCPM
- vascular endothelial cells: 279 nCPM
Immune cell
- T-reg: 21 nTPM
- myeloid DC: 3.3 nTPM
- memory CD4 T-cell: 2.9 nTPM
- memory B-cell: 2 nTPM
- plasmacytoid DC: 1 nTPM
- memory CD8 T-cell: 0.6 nTPM
Brain region
- choroid plexus: 72 nTPM
- white matter: 22 nTPM
- medulla oblongata: 21 nTPM
- hippocampal formation: 20 nTPM
- cerebellum: 20 nTPM
- spinal cord: 19 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)
- 0.77
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.66
- DepMap mean gene effect
- 0.12
- 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
- negative regulation of transcription by RNA polymerase II
- positive regulation of calcineurin-NFAT signaling cascade
- regulation of cardiac muscle hypertrophy
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LMCD1 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 LMCD1 as an antibody target. Whether an autoantibody or antibody against LMCD1 could matter depends on whether native LMCD1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LMCD1 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 LMCD1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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