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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Numa1 ENSRNOG00000000417

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Description

nuclear mitotic apparatus protein 1 [Source:RGD Symbol;Acc:1308777]

Location

Primary_assembly 1: 165,709,905-165,784,848 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 150 orthologues, 3 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000000474.8	Numa1-201	7203	2106aa	ENSRNOP00000000474.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LW91	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 P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,
ENSRNOT00000094333.2	Numa1-203	7793	2092aa	ENSRNOP00000094619.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AMK5	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,
ENSRNOT00000055249.4	Numa1-202	6258	2086aa	ENSRNOP00000052124.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7FF45	-

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Paralogues

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