Hs03981464_cn

• Gene Symbol: BAHCC1
• Assay Reference Genome Location: Chr.17:81451156 on build GRCh38
• Cytoband: 17q25.3

Target Gene Details

• Entrez Gene ID: 57597
• Gene Name: BAH domain and coiled-coil containing 1
• Gene Aliases: BAHD2
• Location: Chr.17:81395431-81466332 on Build GRCh38
• Assay Gene Location: Within Intron 12

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
BAHCC1	NM_001291324.1			NP_001278253.1
	XM_011525063.2			XP_011523365.1
	XM_017024898.1			XP_016880387.1
	XM_017024899.1			XP_016880388.1
	AB040880.1			BAA95971.1

Target Gene Details

• Entrez Gene ID: 100422944
• Gene Name: microRNA 3186
• Gene Aliases: mir-3186
• Location: Chr.17:81451104-81451188 on Build GRCh38
• Assay Gene Location: Overlaps - Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MIR3186	NR_036152.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv26223	Chr.17:80659041 - 81736487 on Build GRCh38	Gain+Loss	BAHCC1 BAIAP2 MIR3186 MIR1250 LOC100129503 CHMP6 AATK TEPSIN MIR4740 RPTOR PDE6G BAIAP2-AS1 ARL16 LINC00482 SLC38A10 TSPAN10 MRPL12 C17orf89 HGS LOC105371925 LOC107985022 CCDC137 SLC25A10 MIR657 LOC400627 LOC105371921 LOC101928855 OXLD1 TMEM105 MIR6786 FSCN2 NPLOC4 LOC107985021 MIR3065 LOC100130370 CEP131 FAAP100 AATK-AS1 MIR338 ACTG1
nsv576177	Chr.17:81450374 - 81483574 on Build GRCh38	Gain	BAHCC1 MIR3186
nsv428351	Chr.17:81152631 - 83064073 on Build GRCh38	Gain	BAHCC1 FASN UTS2R MIR3186 LOC101929552 NOTUM AATK TEPSIN MYADML2 PDE6G SLC16A3 ARHGDIA CD7 ARL16 SNORD134 OGFOD3 CSNK1D PPP1R27 HGS RAC3 TEX19 CCDC137 FOXK2 P4HB B3GNTL1 SECTM1 MIR6786 MAFG LOC100130370 FN3K CEP131 FAAP100 LOC105376791 FN3KRP PCYT2 GCGR ACTG1 NARF WDR45B PYCR1 MIR6787 LRRC45 CCDC57 MIR4740 MCRIP1 HEXDC ALYREF ASPSCR1 DCXR GPS1 SIRT7 LINC00482 TBCD SLC38A10 TSPAN10 LOC101929511 MRPL12 LOC105371944 C17orf89 NPB ANAPC11 LOC105371925 STRA13 DUS1L RFNG SLC25A10 MIR4525 MAFG-AS1 C17orf62 OXLD1 TMEM105 ZNF750 FSCN2 LOC105376790 NPLOC4 RAB40B AATK-AS1
nsv576175	Chr.17:81349843 - 81509075 on Build GRCh38	Loss	BAHCC1 MIR4740 MIR3186 LOC100130370
nsv457973	Chr.17:81406747 - 81526679 on Build GRCh38	Loss	BAHCC1 MIR3186 FSCN2 ACTG1
dgv3294n100	Chr.17:81415451 - 81473664 on Build GRCh38	Loss	BAHCC1 MIR3186
nsv1057744	Chr.17:81402199 - 81462332 on Build GRCh38	Gain	BAHCC1 MIR3186
nsv952389	Chr.17:81137501 - 81593774 on Build GRCh38	Deletion	BAHCC1 LOC105371925 MIR3186 AATK TEPSIN TMEM105 FSCN2 MIR4740 NPLOC4 LOC100130370 CEP131 FAAP100 LINC00482 SLC38A10 AATK-AS1 C17orf89 ACTG1
nsv1056174	Chr.17:81416245 - 81457288 on Build GRCh38	Gain	BAHCC1 MIR3186

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

DNA-binding transcription factor

Gene Ontology Categories:

Process(es)

chromatin silencing
heterochromatin assembly

Function(s)

transcription regulatory region sequence-specific DNA binding
chromatin binding