Gene: FAM66B ENSG00000215374

Description

family with sequence similarity 66 member B [Source:HGNC Symbol;Acc:HGNC:28890]

Location

Chromosome 8: 7,298,744-7,355,359 reverse strand.

GRCh38:CM000670.2

View alleles of this gene on alternative sequences

About this gene

This gene has 9 transcripts (splice variants) and 1 gene allele.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	RefSeq Match	Flags
ENST00000653873.1	FAM66B-203	2209	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-
ENST00000670717.1	FAM66B-209	2188	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-
ENST00000664195.1	FAM66B-207	4238	No protein	-	lncRNA	-	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,
ENST00000663272.1	FAM66B-206	4350	No protein	-	lncRNA	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000665607.1	FAM66B-208	4069	No protein	-	lncRNA	-	-
ENST00000656213.1	FAM66B-204	4029	No protein	-	lncRNA	-	-
ENST00000656567.1	FAM66B-205	3774	No protein	-	lncRNA	-	-
ENST00000606573.1	FAM66B-202	2630	No protein	-	lncRNA	-	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,
ENST00000529456.1	FAM66B-201	1432	No protein	-	lncRNA	-	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,

Gene: FAM66B ENSG00000215374

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Gene: FAM66B ENSG00000215374

Summary

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