ZFAND4
AN1-type zinc finger protein 4
Also known as: ANUBL1, FLJ40185, ZFAN4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86XD8
- Gene
- ZFAND4
- Ensembl
- ENSG00000172671
- Chromosome
- 10
- Canonical length
- 727 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Golgi apparatus
OverviewNCBI Gene
Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
727 residues, UniProt reviewed canonical sequence.
>Q86XD8|ZFAND4
1 MDNRKEPPFF NDDNMGPFYY RLHFCDTMEL FIETLTGTCF ELRVSPFETV ISVKAKIRRL
61 EGIPICRQHL IWNNMELEND YCLNDYNISE GCTLKLVLAM RGGPINTRRV PTDDPLRKMA
121 EYLDSSRVEV WEKTSCSKQV TFLVYQEGDQ LNFFPAVDRG DGTLTPLSDS SKKIDFHLHV
181 LRRKGEHRMS GGSMYNSDTD EDEETEPSSS GQQIIENSIT MNKMKLLKAK MKNMNLSKKP
241 KKAVKIKPHP PVAPRPSSGS TAPSRHRLLR VLPNIGQSCS PAFGNAYPPE ISRNGISSLA
301 TQLSAERYIS SITGEFLKED NSWENNTLSH FSSNVKLPPQ IPHLELGNDQ ELADSVLHLG
361 SSLPRQTKHF LGNLPSSNGN IVLPSEECVT EQSLLPKVGS LASFAEGNAD EQSSGLEGAC
421 KVNLELLLTN ADKGLKAPEQ HLKHVAGVLN GESVETSVLN YRELSPHKNR LLSPLRCSAP
481 MSLHNSLVKP ERQSKCFEFG KLQPSSSQSL DVQNITDSSF SRTTCFQGVK VDSLGKRSDV
541 ISKVEARDIT EMTNKASKEP VGCVNNISFL ASLAGSTSRN RLQSTRGAGR LQNSGTGLST
601 NLQHFQEENF RKSSPQLEHT GVFLSTHGVG MNGNNAAAGK SVGECTTHHL PPVKAPLQTK
661 KKTTNHCFLC GKKTGLASSY ECRCGNNFCA SHRYAETHGC TYDYKSAGRR YLHEANPVVN
721 APKLPKILocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZFAND4 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)
- 0.64
- Highest tissue expression
- 35 nTPM
Expression across tissuesHPA
Tissue
- testis: 35 nTPM
- cerebellum: 5.4 nTPM
- lymph node: 4.6 nTPM
- tonsil: 4.4 nTPM
- spinal cord: 3.4 nTPM
- thyroid gland: 3.1 nTPM
Single-cell type
- late spermatids: 1,225 nCPM
- early spermatids: 540 nCPM
- late primary spermatocytes: 266 nCPM
- cardiomyocytes: 99 nCPM
- adrenal cortex cells: 77 nCPM
- corticotrophs: 58 nCPM
Immune cell
- NK-cell: 0.7 nTPM
- MAIT T-cell: 0.5 nTPM
- gdT-cell: 0.4 nTPM
- memory B-cell: 0.4 nTPM
- naive CD8 T-cell: 0.4 nTPM
- non-classical monocyte: 0.4 nTPM
Brain region
- cerebellum: 7.5 nTPM
- medulla oblongata: 4.5 nTPM
- midbrain: 4.5 nTPM
- hypothalamus: 4.4 nTPM
- pons: 4.3 nTPM
- white matter: 4.3 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)
- 1.06
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.68
- DepMap mean gene effect
- 0.05
- 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
Molecular functions
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, AN1-type
- Ubiquitin-like domain
- Ubiquitin domain
- Ubiquitin-like domain superfamily
- AN1-like Zinc finger
- Ubiquitin family
- AN1-like Zinc finger
- AN1-type zinc finger domain-containing protein
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZFAND4 as an antibody target. Whether an autoantibody or antibody against ZFAND4 could matter depends on whether native ZFAND4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZFAND4 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 ZFAND4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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