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
External references
Supporting evidence
ID History
- Gene history

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Gene: Tcp10b ENSRNOG00000013374

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Description

t-complex protein 10b [Source:RGD Symbol;Acc:1307454]

Gene Synonyms

LOC308169

Location

Primary_assembly 1: 55,485,411-55,508,836 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 153 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000143938.1	Tcp10b-204	2254	513aa	ENSRNOP00000102497.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000109422.2	Tcp10b-203	2158	481aa	ENSRNOP00000087403.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A4A8	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,
ENSRNOT00000077340.3	Tcp10b-202	2098	461aa	ENSRNOP00000070785.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JYT7 A6KK47	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,
ENSRNOT00000018015.9	Tcp10b-201	2015	434aa	ENSRNOP00000018015.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZUW1	-

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Summary

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