BRINP1 BMP/retinoic acid inducible neural specific 1 [Bos taurus (domestic cattle)] - Gene

Summary

Official Symbol: BRINP1provided by VGNC
Official Full Name: BMP/retinoic acid inducible neural specific 1provided by VGNC
Primary source: VGNC:VGNC:26567
See related: BGD:BT28178; Ensembl:ENSBTAG00000015936
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Bos taurus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Artiodactyla; Ruminantia; Pecora; Bovidae; Bovinae; Bos
Also known as: DBC1
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 8

Exon count:: 8

Annotation release	Status	Assembly	Chr	Location
RS_2023_09	current	ARS-UCD2.0 (GCF_002263795.3)	8	NC_037335.1 (108637081..108834345, complement)

Chromosome 8 - NC_037335.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Go to reference sequence details

Genomic Sequence:: NC_037335.1 Chromosome 8 Reference ARS-UCD2.0 Primary Assembly

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

BZ849893 (e-PCR)
- UniSTS:475693

STS-Z41452 (e-PCR)
- UniSTS:68790

Gene Ontology Provided by RefSeq

Process	Evidence Code	Pubs
involved_in negative regulation of mitotic cell cycle	IEA Inferred from Electronic Annotation more info	PubMed
involved_in positive regulation of neuron differentiation	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: BMP/retinoic acid-inducible neural-specific protein 1

Names: deleted in bladder cancer 1; deleted in bladder cancer protein 1 homolog

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.