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

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Gene: RAD9B ENSSSCG00000009824

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Description

RAD9 checkpoint clamp component B [Source:VGNC Symbol;Acc:VGNC:92063]

Location

Primary_assembly 14: 31,869,684-31,903,823 forward strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 5 transcripts (splice variants), 193 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000094483.1	RAD9B-202	2198	398aa	ENSSSCP00000079116.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4FI43	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,
ENSSSCT00000100502.1	RAD9B-201	2174	390aa	ENSSSCP00000074952.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4F6T4	-
ENSSSCT00000093225.1	RAD9B-203	2171	389aa	ENSSSCP00000075241.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4F7J5	-
ENSSSCT00000096358.1	RAD9B-204	2168	388aa	ENSSSCP00000074975.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4F6Y0	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,
ENSSSCT00000010767.5	RAD9B-205	1905	398aa	ENSSSCP00000010487.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1TZ49 F1RNM9	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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