Human (GRCh37.p13)
Description

SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 [Source:HGNC Symbol;Acc:11107]

Gene Synonyms

BAF60B, CRACD2, PRO2451, Rsc6p

Location

Chromosome 17: 61,909,444-61,920,425 reverse strand.

GRCh37:CM000679.1

About this gene

This gene has 11 transcripts (splice variants), 2 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000448276.2SMARCD2-0012716531aaENSP00000392617.2
 
Protein coding
CCDS45756J3KMX2 J3KT18 Q92925
NM_001098426.1GENCODE basic
ENST00000323347.10SMARCD2-0031935483aaENSP00000318451.10
 
Protein coding
J3KMX2 Q92925 -GENCODE basic
ENST00000225742.9SMARCD2-0021800456aaENSP00000225742.9
 
Protein coding
J3KMX2 -GENCODE basic
ENST00000450364.3SMARCD2-012993231aaENSP00000398946.3
 
Protein coding
--CDS 5' incomplete
ENST00000577990.1SMARCD2-00544969aaENSP00000462761.1
 
Protein coding
J3KT18 -CDS 3' incomplete
ENST00000584400.1SMARCD2-006101780aaENSP00000464503.1
 
Nonsense mediated decay
J3KT18 J3QS33 --
ENST00000580054.1SMARCD2-007477109aaENSP00000463793.1
 
Nonsense mediated decay
J3QQL7 -CDS 5' incomplete
ENST00000584483.1SMARCD2-010821No protein-
 
Retained intron
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ENST00000578234.1SMARCD2-009595No protein-
 
Retained intron
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ENST00000581832.1SMARCD2-011562No protein-
 
Retained intron
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ENST00000577686.1SMARCD2-008394No protein-
 
Retained intron
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