Gene: HMX1 ENSG00000215612

Description

H6 family homeobox 1 [Source:HGNC Symbol;Acc:HGNC:5017]

Gene Synonyms

H6, NKX5-3

Location

Chromosome 4: 8,846,076-8,871,839 reverse strand.

GRCh38:CM000666.2

View alleles of this gene on alternative sequences

About this gene

This gene has 2 transcripts (splice variants), 1 gene allele, 186 orthologues, 3 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000400677.5	HMX1-201	1917	348aa	ENSP00000383516.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS47018	Q9NP08	NM_018942.3	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,
ENST00000506970.2	HMX1-202	651	190aa	ENSP00000446997.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS77900	F1T0J4	-	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,

Gene: HMX1 ENSG00000215612

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Gene: HMX1 ENSG00000215612

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