Human (GRCh37.p13)
Description

cat eye syndrome chromosome region, candidate 1 [Source:HGNC Symbol;Acc:1839]

Gene Synonyms

ADA2, ADGF, IDGFL

Location
About this transcript

This transcript has 7 exons, is annotated with 6 domains and features, is associated with 9901 variant alleles and maps to 343 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000399839.1CECR1-0023986511aaENSP00000382733.1
 
Protein coding
CCDS13742B4DHM2 B4E3Q4 C9IZA8
F5H7J3 Q9NZK5
NM_001282228.1GENCODE basic
ENST00000262607.3CECR1-0033925511aaENSP00000262607.2
 
Protein coding
CCDS13742B4DHM2 B4E3Q4 C9IZA8
F5H7J3 Q9NZK5
NM_017424.2GENCODE basic
ENST00000330232.4CECR1-0043195270aaENSP00000332871.4
 
Protein coding
CCDS13743Q9NZK5 NM_177405.1GENCODE basic
ENST00000449907.2CECR1-2022072469aaENSP00000406443.2
 
Protein coding
CCDS63395B4DHM2 B4E3Q4 NM_001282227.1GENCODE basic
ENST00000399837.2CECR1-2011603511aaENSP00000382731.2
 
Protein coding
CCDS13742B4DHM2 B4E3Q4 C9IZA8
F5H7J3 Q9NZK5
-GENCODE basic
ENST00000441548.1CECR1-005581135aaENSP00000392078.1
 
Protein coding
C9IZA8 -CDS 3' incomplete
ENST00000543038.1CECR1-001549152aaENSP00000442482.1
 
Protein coding
C9IZA8 F5H7J3 -CDS 3' incomplete
ENST00000480276.1CECR1-006570No protein-
 
Processed transcript
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ENST00000469063.1CECR1-007510No protein-
 
Processed transcript
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Statistics

Exons: 7, Coding exons: 7, Transcript length: 3,195 bps, Translation length: 270 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NZK5

CCDS

This transcript is a member of the Human CCDS set: CCDS13743

Version

ENST00000330232.4

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.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000316081 (version 1)
GENCODE basic gene

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