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NBPF12 neuroblastoma breakpoint family, member 12 [ Homo sapiens (human) ]

Gene ID: 440675, discontinued on 22-Nov-2011

Summary

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Official Symbol
NBPF12provided by HGNC
Official Full Name
neuroblastoma breakpoint family, member 12provided by HGNC
Primary source
HGNC:HGNC:31994
Gene type
protein coding
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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Location:
1q21.1
Exon count:
10
Sequence:
Chromosome: 1; NC_000001.9 (144926050..144934268)

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000001.9 chromosome

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

General protein information

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Names
neuroblastoma breakpoint family, member 12

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Build 36.3 (NOTE: not current)

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

Reference assembly

Genomic

  1. NC_000001.9 Reference assembly

    Range
    144926050..144934268
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_001715810.1 → XP_001715862.1  

Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
Q5TAG4.2 GenPept UniProtKB/Swiss-Prot:Q5TAG4

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.