Human (GRCh37.p13)
Description

cat eye syndrome chromosome region, candidate 5 [Source:HGNC Symbol;Acc:1843]

Location

Chromosome 22: 17,618,401-17,646,177 reverse strand.

GRCh37:CM000684.1

About this gene

This gene has 7 transcripts (splice variants).

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000336737.4CECR5-0021799423aa
 
Protein coding
CCDS33595Q9BXW7 NM_033070.2Ensembl CanonicalGENCODE Basic
ENST00000155674.5CECR5-0011735393aa
 
Protein coding
CCDS13741Q9BXW7 NM_017829.5GENCODE Basic
ENST00000399852.3CECR5-0031118223aa
 
Protein coding
A8MYZ9 -GENCODE Basic
ENST00000480451.1CECR5-0061028No protein
 
Processed transcript
---
ENST00000463033.1CECR5-007643No protein
 
Processed transcript
---
ENST00000477157.1CECR5-0043614No protein
 
Retained intron
---
ENST00000486462.1CECR5-0051591No protein
 
Retained intron
---
Name

CECR5 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q9BXW7

CCDS

This gene is a member of the Human CCDS set: CCDS13741.1, CCDS33595.1

Ensembl version

ENSG00000069998.8

Other assemblies

This gene maps to 17,137,511-17,165,287 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:
OTTHUMG00000150071 (version 2)

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