Human (GRCh37.p13)
Description

SPANX family, member B2 [Source:HGNC Symbol;Acc:14330]

Gene Synonyms

B1, CT11.2, SPANX, SPANX-B, SPANXB

Location

Chromosome X: 140,084,756-140,085,871 forward strand.

GRCh37:CM000685.1

About this gene

This gene has 1 transcript (splice variant) and 5 paralogues.

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  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000449283.1SPANXB2-001469103aa
 
Protein coding
CCDS48177Q9NS25 NM_145664.1Ensembl CanonicalGENCODE Basic
Name

SPANXB2 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q9NS25

CCDS

This gene is a member of the Human CCDS set: CCDS48177.1

Ensembl version

ENSG00000227234.1

Other assemblies

There is no ungapped mapping of this gene onto the GRCh38 assembly.

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:
OTTHUMG00000022554 (version 1)

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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