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NBPF14 NBPF member 14 [ Homo sapiens (human) ]

Gene ID: 25832, updated on 25-Jul-2021


Official Symbol
NBPF14provided by HGNC
Official Full Name
NBPF member 14provided by HGNC
Primary source
See related
Ensembl:ENSG00000270629 MIM:614003
Gene type
protein coding
RefSeq status
Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NBPF; DJ328E19.C1.1
This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, May 2013]
Ubiquitous expression in skin (RPKM 28.2), ovary (RPKM 24.3) and 25 other tissues See more
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Genomic context

See NBPF14 in Genome Data Viewer
Exon count:
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (148531385..148595717, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (146395342..146467744)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene peptidylprolyl isomerase A like 4G Neighboring gene tRNA-Asn (anticodon GTT) 2-1 Neighboring gene notch 2 N-terminal like B Neighboring gene uncharacterized LOC105371223 Neighboring gene uncharacterized LOC105371222

Genomic regions, transcripts, and products


  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018


Associated conditions

Description Tests
Genome-wide association study implicates PARD3B-based AIDS restriction.
GeneReviews: Not available


Products Interactant Other Gene Complex Source Pubs Description

General gene information


Clone Names

  • FLJ35032, FLJ60520

Gene Ontology Provided by GOA

Component Evidence Code Pubs
located_in cytoplasm IEA
Inferred from Electronic Annotation
more info

General protein information

Preferred Names
neuroblastoma breakpoint family member 14

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001395631.1NP_001382560.1  neuroblastoma breakpoint family member 14 isoform 2

    Status: REVIEWED

    Source sequence(s)
  2. NM_015383.2NP_056198.2  neuroblastoma breakpoint family member 14 isoform 1

    See identical proteins and their annotated locations for NP_056198.2

    Status: REVIEWED

    Source sequence(s)
    ENSP00000482693.1, ENST00000614999.4
    Conserved Domains (1) summary
    DUF1220; Repeat of unknown function (DUF1220)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly


  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    148531385..148595717 complement
    GenBank, FASTA, Sequence Viewer (Graphics)
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