Gene Gene information from NCBI Gene database.
Entrez ID 25925
Gene name Zinc finger protein 521
Gene symbol ZNF521
Synonyms (NCBI Gene)
EHZFEvi3
Chromosome 18
Chromosome location 18q11.2
miRNA miRNA information provided by mirtarbase database.
13
miRTarBase ID miRNA Experiments Reference
MIRT031286 hsa-miR-19b-3p Sequencing 20371350
MIRT2696068 hsa-miR-23a CLIP-seq
MIRT2696069 hsa-miR-23b CLIP-seq
MIRT2696070 hsa-miR-23c CLIP-seq
MIRT2696071 hsa-miR-3151 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 32296183, 33961781
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IDA 12393497
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610974 24605 ENSG00000198795
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96K83
Protein name Zinc finger protein 521 (Early hematopoietic zinc finger protein) (LYST-interacting protein 3)
Protein function Transcription factor that can both act as an activator or a repressor depending on the context. Involved in BMP signaling and in the regulation of the immature compartment of the hematopoietic system. Associates with SMADs in response to BMP2 le
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13912 zf-C2H2_6 46 68 Domain
PF00096 zf-C2H2 118 140 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 174 196 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 311 335 Domain
PF13912 zf-C2H2_6 436 463 Domain
PF13912 zf-C2H2_6 633 659 Domain
PF00096 zf-C2H2 664 686 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 693 715 Domain
PF13912 zf-C2H2_6 929 955 Domain
PF13912 zf-C2H2_6 958 984 Domain
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in hematopoietic cells. Present in organs and tissues that contain stem and progenitor cells, myeloid and/or lymphoid: placenta, spleen, lymph nodes, thymus, bone marrow and fetal liver. Within the hematopoietic
Sequence
MSRRKQAKPRSLKDPNCKLEDKTEDGEALDCKKRPEDGEELEDEAVHSCDSCLQVFESLS
DITEHKIN
QCQLTDGVDVEDDPTCSWPASSPSSKDQTSPSHGEGCDFGEEEGGPGLPYPC
QFCDKSFSRLSYLKHHEQSH
SDKLPFKCTYCSRLFKHKRSRDRHIKLHTGDKKYHCSECD
AAFSRSDHLKIHLKTH
TSNKPYKCAICRRGFLSSSSLHGHMQVHERNKDGSQSGSRMEDW
KMKDTQKCSQCEEGFDFPEDLQKHIAECHPECSPNEDRAALQCVYCHELFVEETSLMNHM
EQVHSGEKKNSCSICSESFHTVEELYSHMDSHQQPESCNHSNSPSLVTVGYTSVSSTTPD
SNLSVDSSTMVEAAPPIPKSRGRKRAAQQTPDMTGPSSKQAKVTYSCIYCNKQLFSSLAV
LQIHLKTMHLDKPEQAHICQYCLEVLPSLYNLNEHLKQVHEAQDPGLIVSAMPAIVYQCN
FCSEVVNDLNTLQEHIRCSHGFANPAAKDSNAFFCPHCYMGFLTDSSLEEHIRQVHCDLS
GSRFGSPVLGTPKEPVVEVYSCSYCTNSPIFNSVLKLNKHIKENHKNIPLALNYIHNGKK
SRALSPLSPVAIEQTSLKMMQAVGGAPARPTGEYICNQCGAKYTSLDSFQTHLKTHLDTV
LPKLTCPQCNKEFPNQESLLKHVTIHFMITSTYYICESCDKQFTSVDDLQKHLLDMHTFV
FFRCTLCQEVFDSKVSIQLHLAVKHSNEKKVYRCTSCNWDFRNETDLQLHVKHNHLENQG
KVHKCIFCGESFGTEVELQCHITTHSKKYNCKFCSKAFHAIILLEKHLREKHCVFETKTP
NCGTNGASEQVQKEEVELQTLLTNSQESHNSHDGSEEDVDTSEPMYGCDICGAAYTMETL
LQNHQLRDHNIRPGESAIVKKKAELIKGNYKCNVCSRTFFSENGLREHMQTHLGPVKHYM
CPICGERFPSLLTLTEHKVTHSKS
LDTGNCRICKMPLQSEEEFLEHCQMHPDLRNSLTGF
RCVVCMQTVTSTLELKIHGTFHMQKTGNGSAVQTTGRGQHVQKLYKCASCLKEFRSKQDL
VKLDINGLPYGLCAGCVNLSKSASPGINVPPGTNRPGLGQNENLSAIEGKGKVGGLKTRC
SSCNVKFESESELQNHIQTIHRELVPDSNSTQLKTPQVSPMPRISPSQSDEKKTYQCIKC
QMVFYNEWDIQVHVANHMIDEGLNHECKLCSQTFDSPAKLQCHLIEHSFEGMGGTFKCPV
CFTVFVQANKLQQHIFSAHGQEDKIYDCTQCPQKFFFQTELQNHTMTQHSS
Sequence length 1311
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ANDROGENETIC ALOPECIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 27805002
★☆☆☆☆
Found in Text Mining only
Carcinoma Pancreatic Ductal Associate 35061935
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Associate 27144525, 38268058
★☆☆☆☆
Found in Text Mining only
Cell Transformation Viral Associate 34639154
★☆☆☆☆
Found in Text Mining only
Leukemia Associate 34639154
★☆☆☆☆
Found in Text Mining only
Leukemia Myeloid Acute Associate 34639154
★☆☆☆☆
Found in Text Mining only
Liposarcoma Associate 35313831
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Stimulate 31526099
★☆☆☆☆
Found in Text Mining only
Medulloblastoma Associate 37083768
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 27144525, 31526099, 36191006, 37834202
★☆☆☆☆
Found in Text Mining only