Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Hgs ENSRNOG00000036696

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Description

hepatocyte growth factor-regulated tyrosine kinase substrate [Source:RGD Symbol;Acc:69225]

Gene Synonyms

Hrs

Location

Primary_assembly 10: 106,237,824-106,256,174 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 5 transcripts (splice variants), 198 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000054966.6	Hgs-201	3150	836aa	ENSRNOP00000051849.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A140TAH1	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 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,
ENSRNOT00000135875.1	Hgs-203	3455	708aa	ENSRNOP00000102539.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000110912.2	Hgs-202	2843	786aa	ENSRNOP00000087685.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A993	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,
ENSRNOT00000172328.1	Hgs-205	2813	762aa	ENSRNOP00000108384.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000168248.1	Hgs-204	2783	756aa	ENSRNOP00000103548.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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