Transcript: ENST00000366618.8 SLC35F3-202

Description

solute carrier family 35 member F3 [Source:HGNC Symbol;Acc:HGNC:23616]

Gene Synonyms

FLJ37712

Location

Chromosome 1: 233,904,676-234,324,511 forward strand.

About this transcript

This transcript has 8 exons, is annotated with 18 domains and features, is associated with 177104 variant alleles and maps to 362 oligo probes.

Gene

This transcript is a product of gene ENSG00000183780.13 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000366618.8	SLC35F3-202	3143	490aa	ENSP00000355577.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS1600	Q8IY50-2	NM_173508.4	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, TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs 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:2,
ENST00000366617.3	SLC35F3-201	2762	421aa	ENSP00000355576.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS73050	Q8IY50-1	-	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,

Summary

Statistics

Exons: 8, Coding exons: 8, Transcript length: 3,143 bps, Translation length: 490 residues

MANE

This MANE Select transcript contains ENSP00000355577 and matches to NM_173508.4 and NP_775779.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8IY50

CCDS

This transcript is a member of the Human CCDS set: CCDS1600

Transcript Support Level (TSL)

TSL:2

Version

ENST00000366618.8

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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

Transcript: ENST00000366618.8 SLC35F3-202

Summary

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Transcript: ENST00000366618.8 SLC35F3-202

Summary

About Us

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