ZC3H12B
Probable ribonuclease ZC3H12B
Also known as: CXorf32, MCPIP2, ZC12B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5HYM0
- Gene
- ZC3H12B
- Ensembl
- ENSG00000102053
- Chromosome
- X
- Canonical length
- 836 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli fibrillar center,Golgi apparatus
OverviewNCBI Gene
The protein encoded by this gene belongs to a family of CCCH-type zinc finger proteins that are involved in the proinflammatory activation of macrophages. The exact function of this family member is unknown, but it is thought to function as a ribonuclease. [provided by RefSeq, May 2010]
Canonical amino-acid sequenceUniProt
836 residues, UniProt reviewed canonical sequence.
>Q5HYM0|ZC3H12B
1 MTATAEVETP KMEKSASKEE KQQPKQDSTE QGNADSEEWM SSESDPEQIS LKSSDNSKSC
61 QPRDGQLKKK EMHSKPHRQL CRSPCLDRPS FSQSSILQDG KLDLEKEYQA KMEFALKLGY
121 AEEQIQSVLN KLGPESLIND VLAELVRLGN KGDSEGQINL SLLVPRGPSS REIASPELSL
181 EDEIDNSDNL RPVVIDGSNV AMSHGNKEEF SCRGIQLAVD WFLDKGHKDI TVFVPAWRKE
241 QSRPDAPITD QDILRKLEKE KILVFTPSRR VQGRRVVCYD DRFIVKLAFD SDGIIVSNDN
301 YRDLQVEKPE WKKFIEERLL MYSFVNDKFM PPDDPLGRHG PSLENFLRKR PIVPEHKKQP
361 CPYGKKCTYG HKCKYYHPER ANQPQRSVAD ELRISAKLST VKTMSEGTLA KCGTGMSSAK
421 GEITSEVKRV APKRQSDPSI RSVAMEPEEW LSIARKPEAS SVPSLVTALS VPTIPPPKSH
481 AVGALNTRSA SSPVPGSSHF PHQKASLEHM ASMQYPPILV TNSHGTPISY AEQYPKFESM
541 GDHGYYSMLG DFSKLNINSM HNREYYMAEV DRGVYARNPN LCSDSRVSHT RNDNYSSYNN
601 VYLAVADTHP EGNLKLHRSA SQNRLQPFPH GYHEALTRVQ SYGPEDSKQG PHKQSVPHLA
661 LHAQHPSTGT RSSCPADYPM PPNIHPGATP QPGRALVMTR MDSISDSRLY ESNPVRQRRP
721 PLCREQHASW DPLPCTTDSY GYHSYPLSNS LMQPCYEPVM VRSVPEKMEQ LWRNPWVGMC
781 NDSREHMIPE HQYQTYKNLC NIFPSNIVLA VMEKNPHTAD AQQLAALIVA KLRAARLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZC3H12B 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)
- 0.58
- Highest tissue expression
- 2.9 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 2.9 nTPM
- basal ganglia: 2.6 nTPM
- cerebellum: 2.3 nTPM
- hippocampal formation: 2.2 nTPM
- pituitary gland: 2.1 nTPM
- retina: 2.1 nTPM
Single-cell type
- somatotrophs: 713 nCPM
- lactotrophs: 660 nCPM
- thyrotrophs: 591 nCPM
- fibro-adipogenic progenitors: 578 nCPM
- corticotrophs: 509 nCPM
- gonadotrophs: 456 nCPM
Immune cell
- naive CD4 T-cell: 0.3 nTPM
- memory B-cell: 0.2 nTPM
- naive B-cell: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
- gdT-cell: 0.1 nTPM
- MAIT T-cell: 0.1 nTPM
Brain region
- basal ganglia: 11 nTPM
- cerebral cortex: 10 nTPM
- white matter: 9.9 nTPM
- hippocampal formation: 9.4 nTPM
- hypothalamus: 8.8 nTPM
- cerebellum: 8.6 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)
- 0.21
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.54
- DepMap mean gene effect
- -0.02
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZC3H12B as an antibody target. Whether an autoantibody or antibody against ZC3H12B could matter depends on whether native ZC3H12B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZC3H12B 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 ZC3H12B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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