DCAF12L2
DDB1- and CUL4-associated factor 12-like protein 2
Also known as: DC122_HUMAN, WDR40C
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5VW00
- Gene
- DCAF12L2
- Ensembl
- ENSG00000198354
- Chromosome
- X
- Canonical length
- 463 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by Gly-His and Trp-Asp (GH-WD), which may facilitate formation of heterotrimeric or multi-protein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene appears to represent an intronless retrocopy of a related multi-exon gene located on chromosome 9. However, the CDS of this intronless gene remains intact, it is conserved in other mammalian species, it is known to be transcribed, and it is therefore thought to encode a functional protein. [provided by RefSeq, May 2010]
Canonical amino-acid sequenceUniProt
463 residues, UniProt reviewed canonical sequence.
>Q5VW00|DCAF12L2
1 MAQQQTGSRK RKAPAVEAGA GSSSSQGLAA ADGEGPLLPK KQKRPATRRR LVHYLKGREV
61 GARGPAGLQG FEGELRGYAV QRLPELLTER QLDLGTLNKV FASQWLNARQ VVCGTKCNTL
121 FVVDVQSGHI TRIPLMRDKE AGLAQAHQGC GIHAIELNPS KTLLATGGEN PNSLAIYQLP
181 TLDPLCLGDR HGHKDWIFAV AWLSDTVAVS GSRDGTVALW RMDPDMFNGS IAWHSEVGLP
241 VYAHIRPRDV EAIPRASTNP SNRKVRALAF SGKNQELGAV SLDGYFHLWK ARSTLSRLLS
301 IRLPYCRENV CLTYCDELSL YAVGSQSHVS FLDPRQRQQN IRPLCSREGG TGVRSLSFYQ
361 HIITVGTGHG SLLFYDIRAQ KFLEERASSS LDSMPGPAGR KLKLACGRGW LNQDDVWVNY
421 FGGMGEFPNA LYTHCYNWPE MKLFVAGGPL PSGLHGNYAG LWSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DCAF12L2 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
- 0
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 20 nTPM
- testis: 5 nTPM
- hypothalamus: 4 nTPM
- seminal vesicle: 4 nTPM
- parathyroid gland: 2.4 nTPM
- fallopian tube: 2.2 nTPM
Single-cell type
- epididymal principal cells: 53 nCPM
- epididymal efferent duct absorptive cells: 15 nCPM
- sertoli cells: 8.8 nCPM
- oocytes: 4.6 nCPM
- peritubular myoid cells: 4.4 nCPM
- other brain neurons: 4.3 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
- medulla oblongata: 21 nTPM
- cerebral cortex: 13 nTPM
- pons: 10 nTPM
- hypothalamus: 8.5 nTPM
- hippocampal formation: 6.7 nTPM
- basal ganglia: 5.1 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)
- 1.04
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.94
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DCAF12L2 as an antibody target. Whether an autoantibody or antibody against DCAF12L2 could matter depends on whether native DCAF12L2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DCAF12L2 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 DCAF12L2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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