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

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Tinf2 ENSRNOG00000020189

.

Description

TERF1 interacting nuclear factor 2 [Source:RGD Symbol;Acc:1359192]

Gene Synonyms

MGC94711

Location

Primary_assembly 15: 33,140,714-33,146,930 reverse strand.

GRCr8:CM070405.1

About this gene

This gene has 4 transcripts (splice variants), 311 orthologues and is associated with 18 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000122224.1	Tinf2-203	2470	404aa	ENSRNOP00000109835.1	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,
ENSRNOT00000110822.2	Tinf2-202	2464	402aa	ENSRNOP00000077645.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZKC5	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,
ENSRNOT00000167823.1	Tinf2-204	2404	382aa	ENSRNOP00000099026.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000027362.7	Tinf2-201	1655	397aa	ENSRNOP00000027362.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KH37 F7F4I8	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,

.

Strains

.

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.

.

Personal Data