Gene Gene information from NCBI Gene database.
Entrez ID 127665
Gene name Zinc finger protein 648
Gene symbol ZNF648
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1q25.3
miRNA miRNA information provided by mirtarbase database.
35
miRTarBase ID miRNA Experiments Reference
MIRT1533401 hsa-miR-1324 CLIP-seq
MIRT1533402 hsa-miR-135a CLIP-seq
MIRT1533403 hsa-miR-135b CLIP-seq
MIRT1533404 hsa-miR-153 CLIP-seq
MIRT1533405 hsa-miR-298 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 32296183
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
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5T619
Protein name Zinc finger protein 648
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 279 301 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 335 358 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 364 386 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 420 442 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 448 470 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 476 498 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 504 526 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 532 554 Zinc finger, C2H2 type Domain
Sequence
MAQVDSQDRWGEASPLSSLTEEAHDTQMLSMNLESDDEDGGEAEKEGTADPVACPRGSSP
VTHENPDLPWPHPLGKEEEKFSDSSSAGGMGQKPVEMSGKASWSRDVTKINETQGSPGAS
RALGSLPSGLAHKLLGQMQPLGDRLPAGDDGYSGANQDAVLDVPPSFPSNGKYLCAHKSV
DTSAGNSSLLCFPRPGSNWDLPTQETHTPAQASATPASLAAAVLAKARNSRKVQNQAGRR
EGGEAEARPYRCLRGGRAFQKPSKPLSPAETRGGAAKRYACELCGKAYSHRGTLQQHRRL
H
TGERPYQCSFCDKAYTWSSDHRKHIRTHTGEKPYPCPDCGKAFVRSSDLRKHQRNMHSN
NKPFPCSECGLTFNKPLSLLRHQRTHLGAKPFRCPACDREFAVASRMVEHQRVHSGERPF
PCPTCGKCFTKSSNLSEHQTLH
TGQRPFKCADCGVAFAQPSRLVRHQRIHTGERPFPCTQ
CGQAFARSSTLKRHQQIH
SGEKGFLCAECGRAFRIASELAQHIRMHNGERPYQCEDCGQA
FTRSNHLQRHRAKH
GTCKKEPIPSSSDE
Sequence length 568
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
CARDIOVASCULAR DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
IDIOPATHIC OSTEONECROSIS OF THE FEMORAL HEAD GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PERIPHERAL NEUROPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations