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NBPF12 NBPF member 12 [ Homo sapiens (human) ]

Gene ID: 149013, updated on 25-Jul-2021

Summary

Official Symbol
NBPF12provided by HGNC
Official Full Name
NBPF member 12provided by HGNC
Primary source
HGNC:HGNC:24297
See related
Ensembl:ENSG00000268043 MIM:608607
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
COAS1; KIAA1245
Summary
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]
Expression
Ubiquitous expression in ovary (RPKM 12.2), testis (RPKM 12.2) and 25 other tissues See more
Orthologs
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Genomic context

See NBPF12 in Genome Data Viewer
Location:
1q21.1
Exon count:
37
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (146938324..146996093)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 Unlocalized Scaffold NT_167207.1 (5292..16348, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985591 Neighboring gene HYDIN axonemal central pair apparatus protein 2 (pseudogene) Neighboring gene RNA, 5S ribosomal pseudogene 536 Neighboring gene profilin 1 pseudogene 8 Neighboring gene phosphodiesterase 4D interacting protein pseudogene Neighboring gene insulin like growth factor 2 mRNA binding protein 2 pseudogene

Genomic regions, transcripts, and products

Expression

  • 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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Clone Names

  • DKFZp434O1213

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 12
Names
chomosome one amplified sequence 1 cyclophilin
chromosome 1 amplified sequence 1

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_001278141.3NP_001265070.1  neuroblastoma breakpoint family member 12

    Status: VALIDATED

    Source sequence(s)
    AC244394
    Consensus CDS
    CCDS72881.1
    UniProtKB/TrEMBL
    A0A087WUF1
    Related
    ENSP00000478609.1, ENST00000617931.4
    Conserved Domains (2) summary
    pfam06758
    Location:12721337
    DUF1220; Repeat of unknown function (DUF1220)
    cl26511
    Location:29469
    Neuromodulin_N; Gap junction protein N-terminal region

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

Genomic

  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    146938324..146996093
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_024453443.1XP_024309211.1  neuroblastoma breakpoint family member 12 isoform X1

    Conserved Domains (2) summary
    pfam06758
    Location:757822
    DUF1220; Repeat of unknown function (DUF1220)
    cl26511
    Location:22467
    Neuromodulin_N; Gap junction protein N-terminal region
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