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

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Gene: SHBG ENSBTAG00000004226

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Description

sex hormone binding globulin [Source:VGNC Symbol;Acc:VGNC:34589]

Location

Primary_assembly 19: 27,345,719-27,350,666 forward strand.

ARS-UCD2.0:CM008186.2

About this gene

This gene has 6 transcripts (splice variants), 112 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000005537.8	SHBG-204	1609	425aa	ENSBTAP00000005537.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6PWN7	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, APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,
ENSBTAT00000127571.2	SHBG-205	1606	424aa	ENSBTAP00000089161.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SRZ8	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSBTAT00000125912.2	SHBG-206	1444	370aa	ENSBTAP00000094646.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TD21	-
ENSBTAT00000094296.2	SHBG-201	1266	316aa	ENSBTAP00000082851.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S9U6	-
ENSBTAT00000095127.2	SHBG-203	1248	309aa	ENSBTAP00000087012.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SSP0	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSBTAT00000108186.2	SHBG-202	807	163aa	ENSBTAP00000075794.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RX83	-

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Summary

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