Human (GRCh38.p14)
Description

distal-less homeobox 1 [Source:HGNC Symbol;Acc:HGNC:2914]

About this transcript

This transcript has 3 exons, is annotated with 18 domains and features, is associated with 2213 variant alleles and maps to 386 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000361725.5DLX1-2032356255aaENSP00000354478.4
 
Protein coding
CCDS2247P56177-1 NM_178120.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000341900.6DLX1-2012130129aaENSP00000341786.6
 
Protein coding
CCDS33328P56177-2 -GENCODE basicTSL:1
ENST00000361609.4DLX1-2021022171aaENSP00000354865.4
 
Protein coding
J3KP55 -TSL:5CDS 3' incomplete
ENST00000469444.6DLX1-205762187aaENSP00000448827.1
 
Protein coding
F8VXJ2 -TSL:3CDS 3' incomplete
ENST00000550686.1DLX1-207573No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000475989.2DLX1-2061897No protein-
 
Retained intron
--TSL:2
ENST00000409492.1DLX1-204919No protein-
 
Retained intron
--TSL:1
Statistics

Exons: 3, Coding exons: 3, Transcript length: 2,356 bps, Translation length: 255 residues

MANE

This MANE Select transcript contains ENSP00000354478 and matches to NM_178120.5 and NP_835221.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P56177

CCDS

This transcript is a member of the Human CCDS set: CCDS2247

Transcript Support Level (TSL)

TSL:1

Version

ENST00000361725.5

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.

Annotation Attributes

retained intron first [Definitions]

GENCODE basic gene

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