Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: PHLDB1 ENSBTAG00000016197

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Description

pleckstrin homology like domain family B member 1 [Source:VGNC Symbol;Acc:VGNC:32837]

Location

Primary_assembly 15: 29,261,949-29,310,613 forward strand.

ARS-UCD2.0:CM008182.2

About this gene

This gene has 3 transcripts (splice variants), 318 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000064299.4	PHLDB1-201	5617	1412aa	ENSBTAP00000056309.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3N336	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,
ENSBTAT00000079193.3	PHLDB1-203	5777	1381aa	ENSBTAP00000073320.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MN58	-
ENSBTAT00000065315.4	PHLDB1-202	5392	1337aa	ENSBTAP00000054368.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3MXU7	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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