Details for: DEAF1
Associated with
Other Information
Genular Protein ID: 955192056
Symbol: DEAF1_HUMAN
Name: Deformed epidermal autoregulatory factor 1 homolog
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9773984
Title: Characterization of a nuclear deformed epidermal autoregulatory factor-1 (DEAF-1)-related (NUDR) transcriptional regulator protein.
PubMed ID: 9773984
PubMed ID: 11705868
Title: Altered subcellular localization of suppressin, a novel inhibitor of cell-cycle entry, is an independent prognostic factor in colorectal adenocarcinomas.
PubMed ID: 11705868
PubMed ID: 19668219
Title: Deaf1 isoforms control the expression of genes encoding peripheral tissue antigens in the pancreatic lymph nodes during type 1 diabetes.
PubMed ID: 19668219
DOI: 10.1038/ni.1773
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 10521432
Title: Nuclear DEAF-1-related (NUDR) protein contains a novel DNA binding domain and represses transcription of the heterogeneous nuclear ribonucleoprotein A2/B1 promoter.
PubMed ID: 10521432
PubMed ID: 11427895
Title: The SAND domain structure defines a novel DNA-binding fold in transcriptional regulation.
PubMed ID: 11427895
DOI: 10.1038/89675
PubMed ID: 18826651
Title: Deaf-1 regulates epithelial cell proliferation and side-branching in the mammary gland.
PubMed ID: 18826651
PubMed ID: 19413330
Title: Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.
PubMed ID: 19413330
DOI: 10.1021/ac9004309
PubMed ID: 22442688
Title: Deformed epidermal autoregulatory factor-1 (DEAF1) interacts with the Ku70 subunit of the DNA-dependent protein kinase complex.
PubMed ID: 22442688
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 24726472
Title: Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems.
PubMed ID: 24726472
PubMed ID: 16527309
Title: Structure and functional analysis of the MYND domain.
PubMed ID: 16527309
PubMed ID: 18286714
Title: Retraction notice to 'Structure and functional analysis of the MYND domain' [J. Mol. Biol. (2006) 358, 498-508].
PubMed ID: 18286714
PubMed ID: 23372760
Title: Structural and functional analysis of the DEAF-1 and BS69 MYND domains.
PubMed ID: 23372760
PubMed ID: 21076407
PubMed ID: 26048982
Title: Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsy.
PubMed ID: 26048982
PubMed ID: 24668509
Title: Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly.
PubMed ID: 24668509
DOI: 10.1002/ajmg.a.36482
Sequence Information:
- Length: 565
- Mass: 59327
- Checksum: 3BDFEDBF6AD4BDDE
- Sequence:
MEDSDSAAKQ LGLAEAAAVA AAAAVAAAAA AAAGGEAEEP VLSRDEDSEE DADSEAERET PRVTAVAVMA AEPGHMDMGA EALPGPDEAA AAAAFAEVTT VTVANVGAAA DNVFTTSVAN AASISGHVLS GRTALQIGDS LNTEKATLIV VHTDGSIVET TGLKGPAAPL TPGPQSPPTP LAPGQEKGGT KYNWDPSVYD SELPVRCRNI SGTLYKNRLG SGGRGRCIKQ GENWYSPTEF EAMAGRASSK DWKRSIRYAG RPLQCLIQDG ILNPHAASCT CAACCDDMTL SGPVRLFVPY KRRKKENELP TTPVKKDSPK NITLLPATAA TTFTVTPSGQ ITTSGALTFD RASTVEATAV ISESPAQGDV FAGATVQEAS VQPPCRASHP EPHYPGYQDS CQIAPFPEAA LPTSHPKIVL TSLPALAVPP PTPTKAAPPA LVNGLELSEP RSWLYLEEMV NSLLNTAQQL KTLFEQAKHA STYREAATNQ AKIHADAERK EQSCVNCGRE AMSECTGCHK VNYCSTFCQR KDWKDHQHIC GQSAAVTVQA DEVHVAESVM EKVTV
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.