Human (GRCh37.p13)
Description

Sp1 transcription factor [Source:HGNC Symbol;Acc:11205]

Gene Synonyms

TSFP1

Location

Chromosome 12: 53,773,960-53,810,230 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 4 transcripts (splice variants) and 25 paralogues.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000327443.4SP1-0012846785aa
 
Protein coding
CCDS8857C4PGM0 G5E9M8 H3BVI2
P08047 Q9NR52
NM_138473.2Ensembl CanonicalGENCODE Basic
ENST00000426431.2SP1-0027603778aa
 
Protein coding
CCDS44898C4PGM0 G5E9M8 H3BVI2
NM_003109.1GENCODE Basic
ENST00000548560.1SP1-0041061230aa
 
Protein coding
H3BVI2 -CDS 3' incomplete
ENST00000551969.1SP1-003602162aa
 
Protein coding
H3BUU5 -CDS 3' incomplete
Name

SP1 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: P08047

CCDS

This gene is a member of the Human CCDS set: CCDS44898.1, CCDS8857.1

Ensembl version

ENSG00000185591.5

Other assemblies

This gene maps to 53,380,176-53,416,446 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000170047 (version 3)

Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Contigs

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