Hs02488212_cn

• Gene Symbol: ANKRD11
• Assay Reference Genome Location: Chr.16:89283811 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 Exon 16

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ANKRD11	NM_001256182.1	10	3263	NP_001243111.1
	NM_001256183.1	9	3189	NP_001243112.1
	NM_013275.5	9	3192	NP_037407.4
	XM_006721181.1	9	2969	XP_006721244.1
	XM_006721184.2	8	3007	XP_006721247.1
	XM_011523051.2	10	3252	XP_011521353.1
	XM_011523053.2	10	3358	XP_011521355.1
	XM_011523054.2	10	3272	XP_011521356.1
	XM_011523055.2	11	3557	XP_011521357.1
	XM_011523056.2	10	3294	XP_011521358.1
	XM_011523057.2	9	3175	XP_011521359.1
	XM_017023182.1	9	3625	XP_016878671.1
	XM_017023183.1	10	3361	XP_016878672.1
	XM_017023184.1	10	3358	XP_016878673.1
	XM_017023185.1	8	2999	XP_016878674.1
	XM_017023186.1	12	3735	XP_016878675.1
	XM_017023187.1	8	3087	XP_016878676.1
	AK057803.1	1	235
	AK290994.1	8	2871
	AY131227.1	1	1588	AAN07913.1
	AY373756.1	9	3195	AAR25661.1
	AY533563.1	10	3020	AAS45544.1
	BC041585.1	1	531
	DA172996.1	1	300
	KJ534770.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv508n67	Chr.16:89283130 - 89285501 on Build GRCh38	Gain	ANKRD11
nsv509638	Chr.16:89152681 - 89296203 on Build GRCh38	Insertion	ANKRD11 CDH15 LOC105371414 LINC00304 LOC400558 ACSF3 ZNF778 SLC22A31
nsv428331	Chr.16:89216635 - 90185980 on Build GRCh38	Gain+Loss	LOC100287036 ANKRD11 SPG7 GAS8-AS1 SNORD68 TUBB8P7 LOC105371414 PRDM7 VPS9D1 ZNF778 MC1R DBNDD1 SPATA2L FAM157C CHMP1A DEF8 TUBB3 AFG3L1P URAHP CDK10 LOC105371419 VPS9D1-AS1 SPATA33 FANCA LOC101927817 GAS8 DPEP1 TCF25 RPL13 CPNE7 ZNF276 SPIRE2 CENPBD1 LOC107984817
nsv469681	Chr.16:89206785 - 89364930 on Build GRCh38	Loss	LOC100287036 ANKRD11 LOC105371414 ZNF778
nsv827843	Chr.16:89216602 - 89298922 on Build GRCh38	Gain	ANKRD11 LOC105371414 ZNF778
nsv573674	Chr.16:88738775 - 89325907 on Build GRCh38	Gain	LOC105371409 LOC100287036 ANKRD11 CBFA2T3 LOC100129697 PABPN1L CDH15 LOC105371414 LINC00304 LOC400558 PIEZO1 ACSF3 ZNF778 SLC22A31 LOC339059 GALNS TRAPPC2L LOC100289580 CDT1 LOC101927793 LOC107987238 APRT
nsv457622	Chr.16:89207475 - 89319153 on Build GRCh38	Loss	ANKRD11 LOC105371414 ZNF778
dgv3066n100	Chr.16:89067685 - 89301626 on Build GRCh38	Gain	ANKRD11 CDH15 LOC105371414 LINC00304 LOC400558 ACSF3 ZNF778 SLC22A31
nsv482951	Chr.16:88633593 - 90228345 on Build GRCh38	Loss	LOC100287036 ANKRD11 SPG7 CBFA2T3 CDH15 GAS8-AS1 TUBB8P7 SNAI3-AS1 PRDM7 PIEZO1 VPS9D1 ZNF778 SLC22A31 DBNDD1 LOC339059 AFG3L1P LOC105371419 VPS9D1-AS1 FANCA CTU2 LOC101927817 SNAI3 ACSF3 GAS8 DPEP1 TCF25 RPL13 CPNE7 MIR4722 CDT1 SPIRE2 CENPBD1 LOC107984817 APRT LOC105371409 LOC100129697 SNORD68 LOC105371414 LINC00304 LOC400558 IL17C MC1R CYBA SPATA2L FAM157C CHMP1A LOC101927793 DEF8 TUBB3 LOC107987238 URAHP CDK10 PABPN1L MVD SPATA33 RNF166 GALNS TRAPPC2L ZNF276 LOC100289580
esv2763149	Chr.16:89179547 - 89368114 on Build GRCh38	Gain	LOC100287036 ANKRD11 CDH15 LOC105371414 ZNF778 SLC22A31
nsv952073	Chr.16:89247293 - 89304992 on Build GRCh38	Deletion	ANKRD11 LOC105371414

More Information

• Set Membership: Intragenic, 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