Hs05455769_cn

• Gene Symbol: ANKRD11
• Assay Reference Genome Location: Chr.16:89276377 on build GRCh38
• Cytoband: 16q24.3

Target Gene Details

• Entrez Gene ID: 29123
• Gene Name: ankyrin repeat domain 11
• Gene Aliases: ANCO-1, ANCO1, LZ16, T13
• Location: Chr.16:89267619-89490561 on Build GRCh38
• Assay Gene Location: Within Intron 16

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ANKRD11	NM_001256182.1			NP_001243111.1
	NM_001256183.1			NP_001243112.1
	NM_013275.5			NP_037407.4
	XM_006721181.1			XP_006721244.1
	XM_006721184.2			XP_006721247.1
	XM_011523051.2			XP_011521353.1
	XM_011523053.2			XP_011521355.1
	XM_011523054.2			XP_011521356.1
	XM_011523055.2			XP_011521357.1
	XM_011523056.2			XP_011521358.1
	XM_011523057.2			XP_011521359.1
	XM_017023182.1			XP_016878671.1
	XM_017023183.1			XP_016878672.1
	XM_017023184.1			XP_016878673.1
	XM_017023185.1			XP_016878674.1
	XM_017023186.1			XP_016878675.1
	XM_017023187.1			XP_016878676.1
	AY373756.1			AAR25661.1
	AY533563.1			AAS45544.1
	KJ534770.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv509638	Chr.16:89152681 - 89296203 on Build GRCh38	Insertion	LOC105371414 LOC400558 ZNF778 LINC00304 ACSF3 CDH15 ANKRD11 SLC22A31
nsv428331	Chr.16:89216635 - 90185980 on Build GRCh38	Gain+Loss	MC1R DPEP1 VPS9D1 SPIRE2 TUBB8P7 URAHP GAS8 SPATA33 LOC101927817 ZNF276 FANCA LOC100287036 RPL13 CDK10 TUBB3 ANKRD11 DBNDD1 TCF25 AFG3L1P CPNE7 PRDM7 CENPBD1 DEF8 VPS9D1-AS1 FAM157C LOC107984817 LOC105371419 LOC105371414 ZNF778 SPG7 GAS8-AS1 SPATA2L CHMP1A SNORD68
nsv469681	Chr.16:89206785 - 89364930 on Build GRCh38	Loss	LOC100287036 LOC105371414 ZNF778 ANKRD11
nsv573674	Chr.16:88738775 - 89325907 on Build GRCh38	Gain	LOC107987238 LOC101927793 LOC105371409 APRT TRAPPC2L LOC100129697 LOC339059 LOC100287036 PABPN1L LOC105371414 CDT1 LOC400558 CBFA2T3 ZNF778 LINC00304 ACSF3 CDH15 ANKRD11 PIEZO1 LOC100289580 SLC22A31 GALNS
nsv827843	Chr.16:89216602 - 89298922 on Build GRCh38	Gain	LOC105371414 ZNF778 ANKRD11
nsv457622	Chr.16:89207475 - 89319153 on Build GRCh38	Loss	LOC105371414 ZNF778 ANKRD11
dgv3066n100	Chr.16:89067685 - 89301626 on Build GRCh38	Gain	LOC105371414 LOC400558 ZNF778 LINC00304 ACSF3 CDH15 ANKRD11 SLC22A31
nsv482951	Chr.16:88633593 - 90228345 on Build GRCh38	Loss	VPS9D1 SPIRE2 LOC105371409 TUBB8P7 URAHP GAS8 SPATA33 LOC101927817 CYBA FANCA CBFA2T3 RNF166 MVD PIEZO1 SLC22A31 GALNS DBNDD1 LOC101927793 CPNE7 PRDM7 DEF8 FAM157C TRAPPC2L LOC107984817 SNAI3 SNAI3-AS1 LOC400558 ZNF778 SPATA2L CHMP1A CTU2 LOC100289580 LOC107987238 MC1R DPEP1 ZNF276 MIR4722 LOC100129697 LOC339059 LOC100287036 PABPN1L RPL13 CDK10 TUBB3 CDH15 ANKRD11 TCF25 AFG3L1P CENPBD1 IL17C VPS9D1-AS1 APRT LOC105371419 LOC105371414 CDT1 LINC00304 ACSF3 SPG7 GAS8-AS1 SNORD68
esv2763149	Chr.16:89179547 - 89368114 on Build GRCh38	Gain	LOC100287036 LOC105371414 ZNF778 CDH15 ANKRD11 SLC22A31
nsv952073	Chr.16:89247293 - 89304992 on Build GRCh38	Deletion	LOC105371414 ANKRD11

More Information

Additional Information:

For this assay, SNP(s) [rs144774327] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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

Gene Ontology Categories:

Process(es)

in utero embryonic development
tissue homeostasis
multicellular organism growth
odontogenesis of dentin-containing tooth
skeletal system morphogenesis
face morphogenesis
bone development