CBLN1 cerebellin 1 precursor [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: CBLN1provided by VGNC
Official Full Name: cerebellin 1 precursorprovided by VGNC
Primary source: VGNC:VGNC:70556
See related: Ensembl:ENSMMUG00000022217
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Macaca mulatta
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 20

Exon count:: 3

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	20	NC_041773.1 (36355415..36358147, complement)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	20	NC_027912.1 (33144720..33147382, complement)

Chromosome 20 - NC_041773.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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

NoName (e-PCR)
- UniSTS:483614

Cbln1 (e-PCR), detects polymorphism
- UniSTS:525884

D16S2661 (e-PCR)
- UniSTS:57151

SHGC-60807 (e-PCR)
- UniSTS:76374

G15895 (e-PCR)
- UniSTS:72832

CBLN1_8243 (e-PCR)
- UniSTS:467596

D16S2966 (e-PCR)
- UniSTS:60594

Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables protein binding	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in glutamatergic synapse	IEA Inferred from Electronic Annotation more info	PubMed
located_in synaptic cleft	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: cerebellin-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.