Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
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  - Orthologues
  - Paralogues
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: TBCD ENSSSCG00000017136

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Description

tubulin folding cofactor D [Source:NCBI gene (formerly Entrezgene);Acc:100512127]

Location

Primary_assembly 12: 329,714-449,556 reverse strand.

Sscrofa11.1:CM000823.5

About this gene

This gene has 3 transcripts (splice variants) and 205 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000018654.5	TBCD-201	3760	1193aa	ENSSSCP00000018153.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RZZ1	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,
ENSSSCT00000091144.2	TBCD-202	3715	1177aa	ENSSSCP00000060544.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QAV5	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,
ENSSSCT00000099785.1	TBCD-203	3691	1169aa	ENSSSCP00000076549.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4FB51	-

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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data