SMARCAD1

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SMARCAD1
Identifiers
Aliases SMARCAD1, ADERM, ETL1, HEL1, SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
External IDs MGI: 95453 HomoloGene: 5301 GeneCards: SMARCAD1
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001128429
NM_001128430
NM_001254949
NM_020159

NM_001253392
NM_007958

RefSeq (protein)

NP_001121901
NP_001121902
NP_001241878
NP_064544

NP_001240321.1
NP_031984.1
NP_001240321
NP_031984

Location (UCSC) Chr 4: 94.21 – 94.29 Mb Chr 6: 65.04 – 65.12 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 is a protein that in humans is encoded by the SMARCAD1 gene.[3][4]

Proper expression of SMARCAD1 may be important to fingerprint development,[5] and the disruption of its expression is believed to cause adermatoglyphia, the absence of fingerprints.

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ Adra CN, Donato JL, Badovinac R, Syed F, Kheraj R, Cai H, Moran C, Kolker MT, Turner H, Weremowicz S, Shirakawa T, Morton CC, Schnipper LE, Drews R (Jan 2001). "SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases". Genomics. 69 (2): 162–73. doi:10.1006/geno.2000.6281. PMID 11031099. 
  4. ^ "Entrez Gene: SMARCAD1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1". 
  5. ^ "The Mystery of the Missing Fingerprints". 

Further reading[edit]