Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: PITPNB ENSBTAG00000017799

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Description

phosphatidylinositol transfer protein beta [Source:VGNC Symbol;Acc:VGNC:32920]

Location

Primary_assembly 17: 67,268,876-67,330,126 reverse strand.

ARS-UCD2.0:CM008184.2

About this gene

This gene has 6 transcripts (splice variants), 214 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000115179.1	PITPNB-202	3065	306aa	ENSBTAP00000098349.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TMY3	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,
ENSBTAT00000051852.4	PITPNB-203	2960	271aa	ENSBTAP00000048516.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A452DJF3 Q9TR36	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,
ENSBTAT00000103556.1	PITPNB-201	2898	273aa	ENSBTAP00000077388.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S151	-
ENSBTAT00000081439.2	PITPNB-204	1888	272aa	ENSBTAP00000061142.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF7A0N3	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,
ENSBTAT00000121666.1	PITPNB-206	1822	250aa	ENSBTAP00000093016.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T2J7	-
ENSBTAT00000081931.2	PITPNB-205	756	251aa	ENSBTAP00000061832.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M1B1	-

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Summary

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