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.[5][6]
Proper expression of SMARCAD1 may be important to fingerprint development,[7] and the disruption of its expression is believed to cause adermatoglyphia, the absence of fingerprints.
^ abcGRCh38: Ensembl release 89: ENSG00000163104 – Ensembl, May 2017
^ abcGRCm38: Ensembl release 89: ENSMUSG00000029920 – Ensembl, May 2017
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^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.
^"Entrez Gene: SMARCAD1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1".
box 1 is a protein that in humans is encoded by the SMARCAD1 gene. Proper expression of SMARCAD1 may be important to fingerprint development, and the...
mapped to chromosome 4q22. In the splice-site of a 3' exon of the gene for SMARCAD1-helicase, a point mutation was detected. It results in a shortened form...
that adermatoglyphia is caused by the improper expression of the protein SMARCAD1. The condition has been called immigration delay disease by the researchers...
captured by the Nebulin-family actin filament anchoring protein Cyk3 and the SMARCAD1 family ATP-dependent DNA helicase Fft3. Bbc1 competes with WIP homolog...