Transcript: ENST00000379881.8 SOHLH2-202

Description

spermatogenesis and oogenesis specific basic helix-loop-helix 2 [Source:HGNC Symbol;Acc:HGNC:26026]

Gene Synonyms

BHLHE81, FLJ20449, SPATA28, TEB1

Location

Chromosome 13: 36,168,217-36,214,556 reverse strand.

About this transcript

This transcript has 11 exons, is annotated with 8 domains and features, is associated with 18796 variant alleles and maps to 374 oligo probes.

Gene

This transcript is a product of gene ENSG00000120669.16 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000379881.8	SOHLH2-202	2125	425aa	ENSP00000369210.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS9355	Q9NX45-1	NM_017826.3	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENST00000317764.6	SOHLH2-201	1909	225aa	ENSP00000326838.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS61309	Q9NX45-2	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,

Summary

Statistics

Exons: 11, Coding exons: 11, Transcript length: 2,125 bps, Translation length: 425 residues

MANE

This MANE Select transcript contains ENSP00000369210 and matches to NM_017826.3 and NP_060296.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NX45

CCDS

This transcript is a member of the Human CCDS set: CCDS9355

Transcript Support Level (TSL)

TSL:1

Version

ENST00000379881.8

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

Transcript: ENST00000379881.8 SOHLH2-202

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Transcript: ENST00000379881.8 SOHLH2-202

Summary

About Us

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