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

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Gene: PTHLH ENSBTAG00000006538

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Description

parathyroid hormone like hormone [Source:VGNC Symbol;Acc:VGNC:33517]

Location

Primary_assembly 5: 81,846,683-81,858,759 forward strand.

ARS-UCD2.0:CM008172.2

About this gene

This gene has 3 transcripts (splice variants) and 268 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000008581.7	PTHLH-202	855	182aa	ENSBTAP00000008581.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6YQ87	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,
ENSBTAT00000122595.2	PTHLH-201	1218	175aa	ENSBTAP00000080329.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SA76	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSBTAT00000043154.6	PTHLH-203	1199	177aa	ENSBTAP00000040744.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P58073	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,

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Summary

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