Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: CT47B1 ENSG00000288466

Description

cancer/testis antigen family 47 member B1 [Source:HGNC Symbol;Acc:HGNC:33293]

Gene Synonyms

CT47.13

Location

GRCh38:ML143381.1

View this gene on the primary assembly.

About this gene

This gene has 1 transcript (splice variant) and 1 gene allele.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000672355.1	CT47B1-202	1328	299aa	ENSP00000500741.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		P0C2W7	-	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

Summary