Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
112869
Gene name Gene Name - the full gene name approved by the HGNC.
SAGA complex associated factor 29
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SGF29
Synonyms (NCBI Gene) Gene synonyms aliases
CCDC101, STAF36, TDRD29
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16p11.2
Summary Summary of gene provided in NCBI Entrez Gene.
CCDC101 is a subunit of 2 histone acetyltransferase complexes: the ADA2A (TADA2A; MIM 602276)-containing (ATAC) complex and the SPT3 (SUPT3H; MIM 602947)-TAF9 (MIM 600822)-GCN5 (KAT2A; MIM 602301)/PCAF (KAT2B; MIM 602303) acetylase (STAGA) complex. Both o
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000124 Component SAGA complex IBA 21873635
GO:0005515 Function Protein binding IPI 16189514, 21685874, 24981860, 25416956, 25609649, 26496610, 28514442, 31515488, 32296183
GO:0005671 Component Ada2/Gcn5/Ada3 transcription activator complex IBA 21873635
GO:0005671 Component Ada2/Gcn5/Ada3 transcription activator complex IDA 18838386
GO:0016573 Process Histone acetylation IDA 23894581
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
613374 25156 ENSG00000176476
Protein
UniProt ID Q96ES7
Protein name SAGA-associated factor 29 (Coiled-coil domain-containing protein 101) (SAGA complex-associated factor 29)
Protein function Chromatin reader component of some histone acetyltransferase (HAT) SAGA-type complexes like the TFTC-HAT, ATAC or STAGA complexes (PubMed:19103755, PubMed:20850016, PubMed:21685874, PubMed:26421618, PubMed:26578293). SGF29 specifically recognize
PDB 3LX7 , 3ME9 , 3MEA , 3MET , 3MEU , 3MEV , 3MEW , 5C0M
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07039 DUF1325 158 288 SGF29 tudor-like domain Domain
Sequence
MALVSADSRIAELLTELHQLIKQTQEERSRSEHNLVNIQKTHERMQTENKISPYYRTKLR
GLYTTAKADAEAECNILRKALDKIAEIKSLLEERRIAAKIAGLYNDSEPPRKTMRRGVLM
TLLQQSAMTLPLWIGKPGDKPPPLCGAIPASGDYVARPGDKVAARVKAVDGDEQWILAEV
VSYSHATNKYEVDDIDEEGKERHTLSRRRVIPLPQWKANPETDPEALFQKEQLVLALYPQ
TTCFYRALIHAPPQRPQDDYSVLFEDTSYADGYSPPLNVAQRYVVACK
EPKKK
Sequence length 293
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Diabetes mellitus Diabetes Mellitus, Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
21980299
Esophagus neoplasm Esophageal Neoplasms rs28934578, rs121918714, rs1567556006, rs1575166666 22960999
Unknown
Disease term Disease name Evidence References Source
Chronic obstructive pulmonary disease Chronic Obstructive Airway Disease 28166215 ClinVar
Eczema Eczema GWAS
Associations from Text Mining
Disease Name Relationship Type References
Congenital central hypoventilation syndrome Associate 38048593
Dyserythropoiesis Congenital with Internuclear Chromatin Bridges and Ultrastructurally Normal Erythroblast Heterochromatin Associate 38048593
Leukemia Myeloid Acute Associate 38048593
Polycystic Ovary Syndrome Associate 39585802