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Gene: ZDHHC1 (zinc finger DHHC-type containing 1) Homo sapiens

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Symbol:

ZDHHC1

Name:

zinc finger DHHC-type containing 1

RGD ID:

1348828

HGNC Page

HGNC:17916

Description:

Enables protein-cysteine S-palmitoyltransferase activity. Involved in antiviral innate immune response; protein palmitoylation; and regulation of defense response. Located in Golgi apparatus and endoplasmic reticulum membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C16orf1; DHHC domain-containing cysteine-rich protein 1; DHHC-1; DHHC-domain-containing cysteine-rich protein; HSU90653; palmitoyltransferase ZDHHC1; probable palmitoyltransferase ZDHHC1; zinc finger DHHC domain-containing protein 1; zinc finger protein 377; zinc finger, DHHC domain containing 1; zinc finger, DHHC-type containing 1; ZNF377

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Zdhhc1 (zinc finger, DHHC domain containing 1)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Zdhhc1 (zinc finger, DHHC-type containing 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Zdhhc1 (zDHHC palmitoyltransferase 1)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	ZDHHC1 (zDHHC palmitoyltransferase 1)	NCBI	Ortholog
Canis lupus familiaris (dog):	ZDHHC1 (zinc finger DHHC-type containing 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Zdhhc1 (zDHHC palmitoyltransferase 1)	NCBI	Ortholog
Sus scrofa (pig):	ZDHHC1 (zinc finger DHHC-type containing 1)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	ZDHHC1 (zDHHC palmitoyltransferase 1)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Zdhhc1 (zDHHC palmitoyltransferase 1)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Fam221a (family with sequence similarity 221, member A)	HGNC	OMA
Alliance orthologs ³
Mus musculus (house mouse):	Zdhhc1 (zinc finger, DHHC domain containing 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Zdhhc1 (zinc finger, DHHC-type containing 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	zdhhc1 (zinc finger, DHHC-type containing 1)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Drosophila melanogaster (fruit fly):	CG17075	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|OrthoInspector\|PhylomeDB\|SonicParanoid)
Caenorhabditis elegans (roundworm):	dhhc-11	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoInspector\|PANTHER\|SonicParanoid)
Xenopus laevis (African clawed frog):	zdhhc1.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	zdhhc1	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|OrthoInspector\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	zdhhc1.L	Alliance	DIOPT (Xenbase)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	67,394,152 - 67,416,477 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	67,394,152 - 67,416,833 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	67,428,055 - 67,450,380 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	65,985,829 - 66,007,878 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	16	65,985,828 - 66,007,878	NCBI
Celera	16	51,936,522 - 51,958,539 (-)	NCBI		Celera
Cytogenetic Map	16	q22.1	NCBI
HuRef	16	53,301,558 - 53,323,519 (-)	NCBI		HuRef
CHM1_1	16	68,835,705 - 68,857,722 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	73,188,923 - 73,211,253 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZDHHC1	Human	autosomal dominant dyskeratosis congenita 6		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Dyskeratosis congenita and autosomal dominant 6	ClinVar	PMID:28492532
ZDHHC1	Human	Chromosome 16q12 Duplication Syndrome		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Chromosome 16q12 duplication syndrome	ClinVar	PMID:25741868

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZDHHC1	Human	17beta-estradiol	decreases expression	EXP		6480464	Estradiol results in decreased expression of ZDHHC1 mRNA	CTD	PMID:31614463
ZDHHC1	Human	2,3,7,8-tetrachlorodibenzodioxine	affects expression	ISO	Zdhhc1 (Mus musculus)	6480464	Tetrachlorodibenzodioxin affects the expression of ZDHHC1 mRNA	CTD	PMID:21570461
ZDHHC1	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in increased expression of ZDHHC1 mRNA	CTD	PMID:33387578
ZDHHC1	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in decreased expression of ZDHHC1 mRNA	CTD	PMID:22808131 and PMID:34747641
ZDHHC1	Human	3-isobutyl-1-methyl-7H-xanthine	multiple interactions	EXP		6480464	[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol S] results in increased expression of ZDHHC1 mRNA	CTD	PMID:28628672
ZDHHC1	Human	4,4'-diaminodiphenylmethane	increases expression	ISO	Zdhhc1 (Mus musculus)	6480464	4 and 4'-diaminodiphenylmethane results in increased expression of ZDHHC1 mRNA	CTD	PMID:18648102
ZDHHC1	Human	4,4'-sulfonyldiphenol	multiple interactions	EXP		6480464	[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol S] results in increased expression of ZDHHC1 mRNA	CTD	PMID:28628672
ZDHHC1	Human	6-propyl-2-thiouracil	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Propylthiouracil results in decreased expression of ZDHHC1 mRNA	CTD	PMID:30047161
ZDHHC1	Human	amitrole	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Amitrole results in decreased expression of ZDHHC1 mRNA	CTD	PMID:30047161
ZDHHC1	Human	amphetamine	increases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Amphetamine results in increased expression of ZDHHC1 mRNA	CTD	PMID:30779732
ZDHHC1	Human	aristolochic acid A	increases expression	EXP		6480464	aristolochic acid I results in increased expression of ZDHHC1 mRNA	CTD	PMID:33212167
ZDHHC1	Human	benzo[a]pyrene	decreases methylation	EXP		6480464	Benzo(a)pyrene results in decreased methylation of ZDHHC1 5' UTR	CTD	PMID:27901495
ZDHHC1	Human	benzo[a]pyrene	increases methylation	EXP		6480464	Benzo(a)pyrene results in increased methylation of ZDHHC1 promoter	CTD	PMID:27901495
ZDHHC1	Human	beta-lapachone	decreases expression	EXP		6480464	beta-lapachone results in decreased expression of ZDHHC1 mRNA	CTD	PMID:38218311
ZDHHC1	Human	bisphenol A	increases expression	ISO	Zdhhc1 (Mus musculus)	6480464	bisphenol A results in increased expression of ZDHHC1 mRNA	CTD	PMID:26063408
ZDHHC1	Human	bisphenol A	decreases methylation	EXP		6480464	bisphenol A results in decreased methylation of ZDHHC1 gene	CTD	PMID:31601247
ZDHHC1	Human	bisphenol A	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in decreased methylation of ZDHHC1 gene	CTD	PMID:31601247
ZDHHC1	Human	bisphenol A	increases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	bisphenol A results in increased expression of ZDHHC1 mRNA	CTD	PMID:25181051 and PMID:34947998
ZDHHC1	Human	bisphenol F	decreases expression	ISO	Zdhhc1 (Mus musculus)	6480464	bisphenol F results in decreased expression of ZDHHC1 mRNA	CTD	PMID:38685157
ZDHHC1	Human	cadmium dichloride	decreases expression	EXP		6480464	Cadmium Chloride results in decreased expression of ZDHHC1 mRNA	CTD	PMID:38568856
ZDHHC1	Human	carbon nanotube	decreases expression	ISO	Zdhhc1 (Mus musculus)	6480464	Nanotubes more ...	CTD	PMID:25554681
ZDHHC1	Human	cisplatin	decreases expression	EXP		6480464	Cisplatin results in decreased expression of ZDHHC1 mRNA	CTD	PMID:27392435
ZDHHC1	Human	crocidolite asbestos	decreases expression	ISO	Zdhhc1 (Mus musculus)	6480464	Asbestos and Crocidolite results in decreased expression of ZDHHC1 mRNA	CTD	PMID:29279043
ZDHHC1	Human	Cuprizon	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Cuprizone results in decreased expression of ZDHHC1 mRNA	CTD	PMID:27523638
ZDHHC1	Human	cyclophosphamide	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Cyclophosphamide results in decreased expression of ZDHHC1 mRNA	CTD	PMID:27281708
ZDHHC1	Human	dexamethasone	multiple interactions	EXP		6480464	[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol S] results in increased expression of ZDHHC1 mRNA	CTD	PMID:28628672
ZDHHC1	Human	endosulfan	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Endosulfan results in decreased expression of ZDHHC1 mRNA	CTD	PMID:29391264
ZDHHC1	Human	formaldehyde	increases expression	EXP		6480464	Formaldehyde results in increased expression of ZDHHC1 mRNA	CTD	PMID:27664576
ZDHHC1	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in decreased methylation of ZDHHC1 gene	CTD	PMID:31601247
ZDHHC1	Human	indometacin	multiple interactions	EXP		6480464	[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol S] results in increased expression of ZDHHC1 mRNA	CTD	PMID:28628672
ZDHHC1	Human	methimazole	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Methimazole results in decreased expression of ZDHHC1 mRNA	CTD	PMID:30047161
ZDHHC1	Human	paracetamol	increases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Acetaminophen results in increased expression of ZDHHC1 mRNA	CTD	PMID:33387578
ZDHHC1	Human	pregnenolone 16alpha-carbonitrile	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Pregnenolone Carbonitrile results in decreased expression of ZDHHC1 mRNA	CTD	PMID:30047161
ZDHHC1	Human	sulfadimethoxine	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Sulfadimethoxine results in decreased expression of ZDHHC1 mRNA	CTD	PMID:30047161
ZDHHC1	Human	sunitinib	increases expression	EXP		6480464	Sunitinib results in increased expression of ZDHHC1 mRNA	CTD	PMID:31533062
ZDHHC1	Human	temozolomide	decreases expression	EXP		6480464	Temozolomide results in decreased expression of ZDHHC1 mRNA	CTD	PMID:31758290
ZDHHC1	Human	thioacetamide	decreases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Thioacetamide results in decreased expression of ZDHHC1 mRNA	CTD	PMID:34492290
ZDHHC1	Human	trichloroethene	increases expression	ISO	Zdhhc1 (Rattus norvegicus)	6480464	Trichloroethylene results in increased expression of ZDHHC1 mRNA	CTD	PMID:33387578
ZDHHC1	Human	trimellitic anhydride	decreases expression	ISO	Zdhhc1 (Mus musculus)	6480464	trimellitic anhydride results in decreased expression of ZDHHC1 mRNA	CTD	PMID:19042947
ZDHHC1	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of ZDHHC1 mRNA	CTD	PMID:37042841
ZDHHC1	Human	triptonide	increases expression	ISO	Zdhhc1 (Mus musculus)	6480464	triptonide results in increased expression of ZDHHC1 mRNA	CTD	PMID:33045310

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZDHHC1	Human	antiviral innate immune response	involved_in	IMP		150520179	PMID:25299331	UniProt	PMID:25299331
ZDHHC1	Human	antiviral innate immune response	involved_in	IBA	MGI:1918046 more ...	150520179		GO_Central	GO_REF:0000033
ZDHHC1	Human	antiviral innate immune response	involved_in	IEA	UniProtKB:Q8R0N9 and ensembl:ENSMUSP00000148381	150520179		Ensembl	GO_REF:0000107
ZDHHC1	Human	peptidyl-L-cysteine S-palmitoylation	involved_in	ISO	Zdhhc1 (Mus musculus)	9068941	PMID:23687301	UniProt	PMID:23687301
ZDHHC1	Human	positive regulation of defense response to virus by host	involved_in	IMP		150520179	PMID:25299331	UniProt	PMID:25299331
ZDHHC1	Human	positive regulation of defense response to virus by host	involved_in	IEA	UniProtKB:Q8R0N9 and ensembl:ENSMUSP00000148381	150520179		Ensembl	GO_REF:0000107
ZDHHC1	Human	positive regulation of NLRP3 inflammasome complex assembly	involved_in	IDA		150520179	PMID:39173637	UniProt	PMID:39173637
ZDHHC1	Human	positive regulation of NLRP3 inflammasome complex assembly	involved_in	IEA	UniProtKB:Q8R0N9 and ensembl:ENSMUSP00000148381	150520179		Ensembl	GO_REF:0000107
ZDHHC1	Human	positive regulation of protein localization to endosome	involved_in	IEA	UniProtKB:Q8R0N9 and ensembl:ENSMUSP00000148381	150520179		Ensembl	GO_REF:0000107
ZDHHC1	Human	positive regulation of protein oligomerization	involved_in	IEA	UniProtKB:Q8R0N9 and ensembl:ENSMUSP00000148381	150520179		Ensembl	GO_REF:0000107
ZDHHC1	Human	protein palmitoylation	involved_in	IDA		150520179	PMID:23034182	UniProt	PMID:23034182
ZDHHC1	Human	protein palmitoylation	acts_upstream_of_or_within	ISO	Zdhhc1 (Mus musculus)	9068941	PMID:15603741	MGI	PMID:15603741
ZDHHC1	Human	protein targeting to membrane	involved_in	IBA	PANTHER:PTN000525256 more ...	150520179		GO_Central	GO_REF:0000033

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZDHHC1	Human	endoplasmic reticulum	is_active_in	IBA	FB:FBgn0027453 more ...	150520179		GO_Central	GO_REF:0000033
ZDHHC1	Human	endoplasmic reticulum	located_in	IEA	UniProtKB-KW:KW-0256	150520179		UniProt	GO_REF:0000043
ZDHHC1	Human	endoplasmic reticulum	located_in	IDA		150520179	PMID:16647879	UniProt	PMID:16647879
ZDHHC1	Human	endoplasmic reticulum membrane	located_in	IDA		150520179	PMID:25299331	UniProt	PMID:25299331
ZDHHC1	Human	endoplasmic reticulum membrane	located_in	IEA	UniProtKB-SubCell:SL-0097	150520179		UniProt	GO_REF:0000044
ZDHHC1	Human	endosome	located_in	IEA	UniProtKB-KW:KW-0967	150520179		UniProt	GO_REF:0000043
ZDHHC1	Human	endosome membrane	located_in	IEA	UniProtKB:Q8R0N9 and ensembl:ENSMUSP00000148381	150520179		Ensembl	GO_REF:0000107
ZDHHC1	Human	endosome membrane	located_in	IEA	UniProtKB-SubCell:SL-0100	150520179		UniProt	GO_REF:0000044
ZDHHC1	Human	extracellular exosome	located_in	HDA		150520179	PMID:19056867	UniProt	PMID:19056867
ZDHHC1	Human	Golgi apparatus	located_in	IEA	UniProtKB-SubCell:SL-0132	150520179		UniProt	GO_REF:0000044
ZDHHC1	Human	Golgi apparatus	is_active_in	IBA	FB:FBgn0031495 more ...	150520179		GO_Central	GO_REF:0000033
ZDHHC1	Human	Golgi apparatus	located_in	IEA	UniProtKB-KW:KW-0333	150520179		UniProt	GO_REF:0000043
ZDHHC1	Human	Golgi apparatus	located_in	IDA		150520179	PMID:25299331	UniProt	PMID:25299331
ZDHHC1	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043
ZDHHC1	Human	membrane	located_in	IEA	UniProtKB-SubCell:SL-0162	150520179		UniProt	GO_REF:0000044

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZDHHC1	Human	acyltransferase activity	enables	IEA	UniProtKB-KW:KW-0012	150520179		UniProt	GO_REF:0000043
ZDHHC1	Human	acyltransferase activity	enables	IEA	UniRule:UR000079119	150520179		UniProt	GO_REF:0000104
ZDHHC1	Human	DNA binding	enables	NAS		150520179	PMID:10395086	UniProt	PMID:10395086
ZDHHC1	Human	palmitoyltransferase activity	enables	IEA	InterPro:IPR001594 and InterPro:IPR039859	150520179		InterPro	GO_REF:0000002
ZDHHC1	Human	palmitoyltransferase activity	enables	IDA		150520179	PMID:23034182	UniProt	PMID:23034182
ZDHHC1	Human	palmitoyltransferase activity	enables	IEA	UniProtKB:Q8R0N9 and ensembl:ENSMUSP00000148381	150520179		Ensembl	GO_REF:0000107
ZDHHC1	Human	protein binding	enables	IPI	UniProtKB:Q86WV6	150520179	PMID:25299331	UniProt	PMID:25299331
ZDHHC1	Human	protein binding	enables	IPI	UniProtKB:A8MQ03 more ...	150520179	PMID:32296183	IntAct	PMID:32296183
ZDHHC1	Human	protein-cysteine S-palmitoyltransferase activity	enables	IEA	RHEA:36683	150520179		RHEA	GO_REF:0000116
ZDHHC1	Human	protein-cysteine S-palmitoyltransferase activity	enables	IBA	MGI:1913470 more ...	150520179		GO_Central	GO_REF:0000033
ZDHHC1	Human	protein-cysteine S-palmitoyltransferase activity	enables	IEA	EC:2.3.1.225	150520179		UniProt	GO_REF:0000003
ZDHHC1	Human	protein-cysteine S-palmitoyltransferase activity	enables	IEA	UniProtKB:Q8R0N9 and ensembl:ENSMUSP00000148381	150520179		Ensembl	GO_REF:0000107
ZDHHC1	Human	protein-cysteine S-palmitoyltransferase activity	enables	IDA		150520179	PMID:39173637	UniProt	PMID:39173637
ZDHHC1	Human	transferase activity	enables	IEA	UniProtKB-KW:KW-0808	150520179		UniProt	GO_REF:0000043

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZDHHC1	Human	Immunodeficiency		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Immunodeficiency	ClinVar

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:8889548	PMID:10395086	PMID:12477932	PMID:15489334	PMID:16647879	PMID:19056867	PMID:20549515	PMID:21873635	PMID:23034182	PMID:23687301	PMID:25299331	PMID:28514442
PMID:32296183	PMID:32863941	PMID:33961781	PMID:34282274	PMID:36949045	PMID:39069526	PMID:39173637

ZDHHC1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	67,394,152 - 67,416,477 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	67,394,152 - 67,416,833 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	67,428,055 - 67,450,380 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	65,985,829 - 66,007,878 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	16	65,985,828 - 66,007,878	NCBI
Celera	16	51,936,522 - 51,958,539 (-)	NCBI		Celera
Cytogenetic Map	16	q22.1	NCBI
HuRef	16	53,301,558 - 53,323,519 (-)	NCBI		HuRef
CHM1_1	16	68,835,705 - 68,857,722 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	73,188,923 - 73,211,253 (-)	NCBI		T2T-CHM13v2.0

Zdhhc1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	8	106,199,055 - 106,223,694 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	8	106,199,055 - 106,223,534 (-)	Ensembl		GRCm39 Ensembl
GRCm38	8	105,472,419 - 105,497,062 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	8	105,472,423 - 105,496,902 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	8	107,996,325 - 108,020,770 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	8	108,361,554 - 108,385,999 (-)	NCBI		MGSCv36	mm8
Celera	8	109,695,617 - 109,720,060 (-)	NCBI		Celera
Cytogenetic Map	8	D3	NCBI
cM Map	8	53.04	NCBI

Zdhhc1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	19	50,260,445 - 50,285,634 (-)	NCBI		GRCr8
mRatBN7.2	19	33,350,533 - 33,375,717 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	19	33,350,533 - 33,375,616 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	19	40,166,123 - 40,191,049 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	19	40,819,451 - 40,844,381 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	19	43,110,095 - 43,142,033 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	19	37,428,959 - 37,454,150 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	19	37,428,959 - 37,454,040 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	19	48,294,576 - 48,319,729 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	19	35,288,675 - 35,314,178 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	19	32,778,838 - 32,803,771 (-)	NCBI		Celera
Cytogenetic Map	19	q12	NCBI

Zdhhc1
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955484	9,234,319 - 9,245,894 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955484	9,224,559 - 9,245,894 (+)	NCBI	ChiLan1.0	ChiLan1.0

ZDHHC1
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	18	76,924,075 - 76,946,138 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	16	82,836,755 - 82,858,767 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	16	47,739,857 - 47,761,887 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	16	67,129,090 - 67,150,646 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	16	67,129,091 - 67,142,001 (-)	Ensembl	panpan1.1		panPan2

ZDHHC1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	5	81,985,974 - 82,006,877 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	5	81,985,998 - 82,006,885 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	5	81,975,651 - 81,996,458 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	5	82,421,311 - 82,442,105 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	5	82,421,230 - 82,442,095 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	5	82,247,436 - 82,268,237 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	5	81,928,559 - 81,949,345 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	5	82,571,977 - 82,592,795 (+)	NCBI		UU_Cfam_GSD_1.0

Zdhhc1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024409349	41,719,938 - 41,739,343 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936475	17,849,802 - 17,861,465 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936475	17,849,772 - 17,869,140 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZDHHC1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	6	28,049,949 - 28,071,540 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	6	28,046,099 - 28,071,535 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	6	25,317,029 - 25,338,632 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZDHHC1
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	5	60,040,264 - 60,062,531 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	5	60,040,266 - 60,062,548 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666047	22,789,567 - 22,811,886 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Zdhhc1
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624746	18,901,589 - 18,922,066 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624746	18,901,622 - 18,921,798 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in ZDHHC1
51 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 16q13-22.2(chr16:56883592-71279975)x3	copy number gain	See cases [RCV000052405]	Chr16:56883592..71279975 [GRCh38] Chr16:56917504..71313878 [GRCh37] Chr16:55475005..69871379 [NCBI36] Chr16:16q13-22.2	pathogenic
GRCh38/hg38 16q21-23.1(chr16:58456122-74708723)x3	copy number gain	See cases [RCV000052408]	Chr16:58456122..74708723 [GRCh38] Chr16:58490026..74742621 [GRCh37] Chr16:57047527..73300122 [NCBI36] Chr16:16q21-23.1	pathogenic
GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3	copy number gain	See cases [RCV000052421]	Chr16:65313395..90081985 [GRCh38] Chr16:65347298..90148393 [GRCh37] Chr16:63904799..88675894 [NCBI36] Chr16:16q21-24.3	pathogenic
GRCh38/hg38 16q21-22.1(chr16:62179331-67770414)x1	copy number loss	See cases [RCV000053333]	Chr16:62179331..67770414 [GRCh38] Chr16:62213235..67804317 [GRCh37] Chr16:60770736..66361818 [NCBI36] Chr16:16q21-22.1	pathogenic
GRCh38/hg38 16q21-22.1(chr16:63318997-70555249)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]\|See cases [RCV000053334]	Chr16:63318997..70555249 [GRCh38] Chr16:63352901..70589152 [GRCh37] Chr16:61910402..69146653 [NCBI36] Chr16:16q21-22.1	pathogenic
GRCh38/hg38 16q21-22.1(chr16:64311275-68062011)x1	copy number loss	See cases [RCV000053335]	Chr16:64311275..68062011 [GRCh38] Chr16:64345179..68095914 [GRCh37] Chr16:62902680..66653415 [NCBI36] Chr16:16q21-22.1	pathogenic
GRCh38/hg38 16q22.1(chr16:66694180-67865445)x1	copy number loss	See cases [RCV000053336]	Chr16:66694180..67865445 [GRCh38] Chr16:66728083..67899348 [GRCh37] Chr16:65285584..66456849 [NCBI36] Chr16:16q22.1	pathogenic
GRCh38/hg38 16q21-24.1(chr16:62925929-84585795)x3	copy number gain	See cases [RCV000135863]	Chr16:62925929..84585795 [GRCh38] Chr16:62959833..84619401 [GRCh37] Chr16:61517334..83176902 [NCBI36] Chr16:16q21-24.1	pathogenic
NM_015964.3(TPPP3):c.312A>G (p.Ala104=)	single nucleotide variant	Malignant melanoma [RCV000071182]	Chr16:67390509 [GRCh38] Chr16:67424412 [GRCh37] Chr16:65981913 [NCBI36] Chr16:16q22.1	not provided
GRCh38/hg38 16q21-22.1(chr16:66245888-67473023)x1	copy number loss	See cases [RCV000134709]	Chr16:66245888..67473023 [GRCh38] Chr16:66279791..67506926 [GRCh37] Chr16:64837292..66064427 [NCBI36] Chr16:16q21-22.1	pathogenic
GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3	copy number gain	See cases [RCV000139426]	Chr16:65511483..90096995 [GRCh38] Chr16:65545386..90163403 [GRCh37] Chr16:64102887..88690904 [NCBI36] Chr16:16q21-24.3	pathogenic
GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3	copy number gain	See cases [RCV000142578]	Chr16:64389378..90081985 [GRCh38] Chr16:64423281..90148393 [GRCh37] Chr16:62980782..88675894 [NCBI36] Chr16:16q21-24.3	pathogenic\|likely pathogenic
GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3	copy number gain	See cases [RCV000143425]	Chr16:52899183..90088654 [GRCh38] Chr16:52933095..90155062 [GRCh37] Chr16:51490596..88682563 [NCBI36] Chr16:16q12.2-24.3	pathogenic
GRCh38/hg38 16q12.1-22.1(chr16:49685521-68401712)x3	copy number gain	See cases [RCV000143752]	Chr16:49685521..68401712 [GRCh38] Chr16:49719432..68435615 [GRCh37] Chr16:48276933..66993116 [NCBI36] Chr16:16q12.1-22.1	pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46615804-90142285)x1	copy number loss	Breast ductal adenocarcinoma [RCV000207138]	Chr16:46615804..90142285 [GRCh37] Chr16:16q11.2-24.3	uncertain significance
GRCh37/hg19 16q12.2-22.2(chr16:55359026-70884455)x1	copy number loss	Breast ductal adenocarcinoma [RCV000207067]	Chr16:55359026..70884455 [GRCh37] Chr16:16q12.2-22.2	likely pathogenic\|uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46464488-90155062)x3	copy number gain	See cases [RCV000446110]	Chr16:46464488..90155062 [GRCh37] Chr16:16q11.2-24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	copy number gain	See cases [RCV000446684]	Chr16:69193..90274381 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3	copy number gain	See cases [RCV000511622]	Chr16:9273328..89548493 [GRCh37] Chr16:16p13.2-q24.3	uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46497599-90354753)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626429]	Chr16:46497599..90354753 [GRCh37] Chr16:16q11.2-24.3	drug response
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	copy number gain	See cases [RCV000511296]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16q22.1(chr16:67132790-68166320)	copy number loss	not provided [RCV000767617]	Chr16:67132790..68166320 [GRCh37] Chr16:16q22.1	pathogenic
NM_001323627.2(ZDHHC1):c.1169C>G (p.Pro390Arg)	single nucleotide variant	not specified [RCV004325729]	Chr16:67394890 [GRCh38] Chr16:67428793 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46455960-90354753)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626435]	Chr16:46455960..90354753 [GRCh37] Chr16:16q11.2-24.3	drug response
NM_001323627.2(ZDHHC1):c.70C>T (p.Pro24Ser)	single nucleotide variant	not specified [RCV004291907]	Chr16:67406382 [GRCh38] Chr16:67440285 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q13-24.3(chr16:57051473-89797669)x3	copy number gain	See cases [RCV000512511]	Chr16:57051473..89797669 [GRCh37] Chr16:16q13-24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	copy number gain	See cases [RCV000512138]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16q12.2-22.2(chr16:54416050-72453266)x3	copy number gain	not provided [RCV000683820]	Chr16:54416050..72453266 [GRCh37] Chr16:16q12.2-22.2	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3	copy number gain	not provided [RCV000738917]	Chr16:88165..90163275 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3	copy number gain	not provided [RCV000738918]	Chr16:88165..90274695 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3	copy number gain	not provided [RCV000738915]	Chr16:61451..90294632 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16q21-22.1(chr16:65669673-70180183)x1	copy number loss	not provided [RCV001006797]	Chr16:65669673..70180183 [GRCh37] Chr16:16q21-22.1	pathogenic
GRCh37/hg19 16q21-24.3(chr16:61524229-90155062)x3	copy number gain	not provided [RCV001249359]	Chr16:61524229..90155062 [GRCh37] Chr16:16q21-24.3	not provided
NM_001323627.2(ZDHHC1):c.355C>A (p.Leu119Met)	single nucleotide variant	not specified [RCV004686231]	Chr16:67401030 [GRCh38] Chr16:67434933 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.151C>A (p.Leu51Ile)	single nucleotide variant	not specified [RCV004686235]	Chr16:67406301 [GRCh38] Chr16:67440204 [GRCh37] Chr16:16q22.1	uncertain significance
NC_000016.9:g.(?_66545871)_(72146396_?)dup	duplication	Dyskeratosis congenita, autosomal dominant 6 [RCV001900384]\|Immunodeficiency [RCV001900385]\|not provided [RCV001900386]	Chr16:66545871..72146396 [GRCh37] Chr16:16q21-22.2	uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46503968-90155062)x3	copy number gain	not provided [RCV002221458]	Chr16:46503968..90155062 [GRCh37] Chr16:16q11.2-24.3	pathogenic
NM_001323627.2(ZDHHC1):c.1346G>A (p.Arg449Gln)	single nucleotide variant	not specified [RCV004295048]	Chr16:67394713 [GRCh38] Chr16:67428616 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1166G>A (p.Gly389Glu)	single nucleotide variant	not specified [RCV004149323]	Chr16:67394893 [GRCh38] Chr16:67428796 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.313C>G (p.Pro105Ala)	single nucleotide variant	not specified [RCV004110507]	Chr16:67401072 [GRCh38] Chr16:67434975 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1196C>T (p.Ser399Leu)	single nucleotide variant	not specified [RCV004081259]	Chr16:67394863 [GRCh38] Chr16:67428766 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1355C>T (p.Thr452Met)	single nucleotide variant	not specified [RCV004217867]	Chr16:67394704 [GRCh38] Chr16:67428607 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1104+33G>A	single nucleotide variant	not specified [RCV004242873]	Chr16:67395154 [GRCh38] Chr16:67429057 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.700G>A (p.Ala234Thr)	single nucleotide variant	not specified [RCV004140290]	Chr16:67398687 [GRCh38] Chr16:67432590 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.328G>A (p.Val110Met)	single nucleotide variant	not specified [RCV004160169]	Chr16:67401057 [GRCh38] Chr16:67434960 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.71C>T (p.Pro24Leu)	single nucleotide variant	not specified [RCV004245457]	Chr16:67406381 [GRCh38] Chr16:67440284 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.310G>A (p.Asp104Asn)	single nucleotide variant	not specified [RCV004227752]	Chr16:67401075 [GRCh38] Chr16:67434978 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1105-49T>C	single nucleotide variant	not specified [RCV004224830]	Chr16:67395111 [GRCh38] Chr16:67429014 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1148C>T (p.Thr383Ile)	single nucleotide variant	not specified [RCV004146548]	Chr16:67395019 [GRCh38] Chr16:67428922 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.743C>T (p.Ala248Val)	single nucleotide variant	not specified [RCV004100535]	Chr16:67398644 [GRCh38] Chr16:67432547 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.589G>C (p.Ala197Pro)	single nucleotide variant	not specified [RCV004125695]	Chr16:67398886 [GRCh38] Chr16:67432789 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.56G>A (p.Ser19Asn)	single nucleotide variant	not specified [RCV004157266]	Chr16:67406396 [GRCh38] Chr16:67440299 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.368A>T (p.Asn123Ile)	single nucleotide variant	not specified [RCV004223323]	Chr16:67401017 [GRCh38] Chr16:67434920 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1104+52A>C	single nucleotide variant	not specified [RCV004277190]	Chr16:67395135 [GRCh38] Chr16:67429038 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1347A>T (p.Arg449=)	single nucleotide variant	not specified [RCV004361117]	Chr16:67394712 [GRCh38] Chr16:67428615 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.775G>A (p.Ala259Thr)	single nucleotide variant	not specified [RCV004362218]	Chr16:67398612 [GRCh38] Chr16:67432515 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1104+3A>T	single nucleotide variant	not specified [RCV004483546]	Chr16:67395184 [GRCh38] Chr16:67429087 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1149C>T (p.Thr383=)	single nucleotide variant	not specified [RCV004483547]	Chr16:67395018 [GRCh38] Chr16:67428921 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1157C>T (p.Pro386Leu)	single nucleotide variant	not specified [RCV004483548]	Chr16:67395010 [GRCh38] Chr16:67428913 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1326C>T (p.Ala442=)	single nucleotide variant	not specified [RCV004483549]	Chr16:67394733 [GRCh38] Chr16:67428636 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1337G>C (p.Gly446Ala)	single nucleotide variant	not specified [RCV004483550]	Chr16:67394722 [GRCh38] Chr16:67428625 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.248A>G (p.Tyr83Cys)	single nucleotide variant	not specified [RCV004483551]	Chr16:67406204 [GRCh38] Chr16:67440107 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.603C>T (p.Phe201=)	single nucleotide variant	not specified [RCV004483553]	Chr16:67398872 [GRCh38] Chr16:67432775 [GRCh37] Chr16:16q22.1	likely benign
NM_001323627.2(ZDHHC1):c.641A>G (p.Asn214Ser)	single nucleotide variant	not specified [RCV004483554]	Chr16:67398834 [GRCh38] Chr16:67432737 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.706G>A (p.Val236Met)	single nucleotide variant	not specified [RCV004483555]	Chr16:67398681 [GRCh38] Chr16:67432584 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.71C>A (p.Pro24Gln)	single nucleotide variant	not specified [RCV004483556]	Chr16:67406381 [GRCh38] Chr16:67440284 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.870G>T (p.Glu290Asp)	single nucleotide variant	not specified [RCV004483557]	Chr16:67398269 [GRCh38] Chr16:67432172 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.875A>C (p.Lys292Thr)	single nucleotide variant	not specified [RCV004686233]	Chr16:67398264 [GRCh38] Chr16:67432167 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.988G>C (p.Gly330Arg)	single nucleotide variant	not specified [RCV004686236]	Chr16:67395506 [GRCh38] Chr16:67429409 [GRCh37] Chr16:16q22.1	likely benign
NM_001323627.2(ZDHHC1):c.1259C>T (p.Ser420Leu)	single nucleotide variant	not specified [RCV004888172]	Chr16:67394800 [GRCh38] Chr16:67428703 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q21-24.1(chr16:62746020-84485022)x3	copy number gain	not provided [RCV004819314]	Chr16:62746020..84485022 [GRCh37] Chr16:16q21-24.1	pathogenic
NM_001323627.2(ZDHHC1):c.515G>A (p.Gly172Asp)	single nucleotide variant	not specified [RCV004877239]	Chr16:67399370 [GRCh38] Chr16:67433273 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh38/hg38 16q21-23.3(chr16:65957829-83611443)x3	copy number gain	See cases [RCV000143742]	Chr16:65957829..83611443 [GRCh38] Chr16:65991732..83645048 [GRCh37] Chr16:64549233..82202549 [NCBI36] Chr16:16q21-23.3	pathogenic
Single allele	complex	Breast ductal adenocarcinoma [RCV000207314]	Chr16:56368689..90141355 [GRCh37] Chr16:16q12.2-24.3	uncertain significance
NM_001323627.2(ZDHHC1):c.150G>A (p.Pro50=)	single nucleotide variant	not provided [RCV000973542]	Chr16:67406302 [GRCh38] Chr16:67440205 [GRCh37] Chr16:16q22.1	benign
NM_001323627.2(ZDHHC1):c.625A>T (p.Met209Leu)	single nucleotide variant	not specified [RCV004328362]	Chr16:67398850 [GRCh38] Chr16:67432753 [GRCh37] Chr16:16q22.1	uncertain significance
NC_000016.9:g.(?_65821800)_(72146396_?)del	deletion	Dyskeratosis congenita, autosomal dominant 6 [RCV003122496]	Chr16:65821800..72146396 [GRCh37] Chr16:16q21-22.2	uncertain significance
NM_001323627.2(ZDHHC1):c.863C>A (p.Pro288Gln)	single nucleotide variant	not specified [RCV004308727]	Chr16:67398276 [GRCh38] Chr16:67432179 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.857G>A (p.Arg286His)	single nucleotide variant	not specified [RCV004298792]	Chr16:67398282 [GRCh38] Chr16:67432185 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1105-13C>T	single nucleotide variant	not specified [RCV004104282]	Chr16:67395075 [GRCh38] Chr16:67428978 [GRCh37] Chr16:16q22.1	likely benign
NM_001323627.2(ZDHHC1):c.635G>A (p.Arg212His)	single nucleotide variant	not specified [RCV004084509]	Chr16:67398840 [GRCh38] Chr16:67432743 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.917G>A (p.Arg306Gln)	single nucleotide variant	not specified [RCV004262223]	Chr16:67398222 [GRCh38] Chr16:67432125 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1007C>T (p.Ala336Val)	single nucleotide variant	not specified [RCV004483545]	Chr16:67395487 [GRCh38] Chr16:67429390 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.298G>A (p.Ala100Thr)	single nucleotide variant	not specified [RCV004483552]	Chr16:67401087 [GRCh38] Chr16:67434990 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001323627.2(ZDHHC1):c.1364G>T (p.Arg455Leu)	single nucleotide variant	not specified [RCV004686230]	Chr16:67394695 [GRCh38] Chr16:67428598 [GRCh37] Chr16:16q22.1	likely benign
NM_001323627.2(ZDHHC1):c.89C>T (p.Pro30Leu)	single nucleotide variant	not specified [RCV004686232]	Chr16:67406363 [GRCh38] Chr16:67440266 [GRCh37] Chr16:16q22.1	uncertain significance
NC_000016.9:g.(?_48799549)_(70756330_?)dup	duplication	Chromosome 16q12 duplication syndrome [RCV004595820]	Chr16:48799549..70756330 [GRCh37] Chr16:16q12.1-22.1	likely pathogenic
NM_001323627.2(ZDHHC1):c.551C>T (p.Ala184Val)	single nucleotide variant	not specified [RCV004877240]	Chr16:67398924 [GRCh38] Chr16:67432827 [GRCh37] Chr16:16q22.1	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	1955
Count of miRNA genes:	787
Interacting mature miRNAs:	936
Transcripts:	ENST00000348579, ENST00000562122, ENST00000565726, ENST00000566075, ENST00000567311, ENST00000568650
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597098162	GWAS1194236_H	comparative body size at age 10, self-reported QTL GWAS1194236 (human)		3e-16	comparative body size at age 10, self-reported		16	67415736	67415737	Human
597042899	GWAS1138973_H	volumetric bone mineral density QTL GWAS1138973 (human)		0.0000009	volumetric bone mineral density	volumetric bone mineral density (CMO:0001553)	16	67406386	67406387	Human
597346097	GWAS1442171_H	body mass index QTL GWAS1442171 (human)		3e-11	body mass index	body mass index (BMI) (CMO:0000105)	16	67415736	67415737	Human

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2436	2788	2243	4972	1722	2347	6	624	1852	465	2269	7216	6383	52	3733	1	852	1744	1613	174	1


RefSeq Transcripts	NM_001323627	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_013304	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006721185	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011523060	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450245	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450246	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450247	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450248	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054380184	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054380185	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054380186	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054380187	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054380188	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC009061	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK307155	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC021908	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC045169	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM724650	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX111231	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CA432496	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471092	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY054038	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U90653	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000348579 ⟹ ENSP00000340299

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,394,419 - 67,416,474 (-)	Ensembl

Ensembl Acc Id:

ENST00000562122

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,395,505 - 67,404,553 (-)	Ensembl

Ensembl Acc Id:

ENST00000565726 ⟹ ENSP00000459264

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,394,152 - 67,416,477 (-)	Ensembl

Ensembl Acc Id:

ENST00000566075

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,394,425 - 67,396,257 (-)	Ensembl

Ensembl Acc Id:

ENST00000567311

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,395,566 - 67,396,287 (-)	Ensembl

Ensembl Acc Id:

ENST00000568650

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	67,404,158 - 67,416,833 (-)	Ensembl

RefSeq Acc Id:

NM_001323627 ⟹ NP_001310556

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,394,152 - 67,416,477 (-)	NCBI
CHM1_1	16	68,835,705 - 68,857,780 (-)	NCBI
T2T-CHM13v2.0	16	73,188,923 - 73,211,253 (-)	NCBI

Sequence:

show sequence

AGCGCCGGACGAGGCCCAGCCAGTCTGGGTCTGGCCTGGCCGCCCCTCCAGCCTGCTGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCAGAGCCAGAGCTCGAGGACTCACCGGCCC
AGTCTCCGTCCGGGATGGGGCCCCGCTCCCGGGCGCGTTGCCGCCCAGTCCCGGGGACCGTCCCTACCGCGAGGGTCTGAGGCGCGGCTGCCCCGGGGAGGGTGGAAGGCCAGGCGTGGGGCCCGAAC
CTCTGGCTGACTTTGGCAGGGCCCATCTGGCACGGCCTCCGCGGCGCGCAGCTGTTTTCAAGTCAGCAAACATTTACTGAGGATCTACTATGTACAAGATGAACATCTGCAACAAGCCCTCCAACAAG
ACGGCCCCTGAGAAGAGTGTGTGGACGGCACCGGCACAGCCCAGCGGACCCTCCCCTGAGCTGCAGGGCCAGCGATCCCGCCGGAATGGGTGGAGCTGGCCCCCTCACCCGCTCCAGATTGTGGCCTG
GCTGCTGTACCTCTTCTTTGCTGTGATCGGCTTTGGGATCCTTGTTCCCCTCCTGCCTCACCACTGGGTGCCCGCTGGCTACGCTTGCATGGGCGCCATCTTTGCTGGCCACCTTGTGGTGCACCTGA
CCGCCGTCTCCATCGATCCAGCAGATGCCAACGTGCGGGACAAGAGCTATGCGGGGCCCCTGCCCATCTTCAACCGAAGCCAGCACGCACATGTCATTGAAGACCTGCACTGCAACTTGTGCAACGTG
GATGTGAGCGCTCGCTCCAAGCACTGCAGCGCCTGCAACAAGTGCGTGTGCGGTTTCGACCACCACTGCAAGTGGCTCAACAACTGTGTGGGCGAGCGGAACTACCGGCTCTTTCTACACAGTGTTGC
ATCCGCTTTACTGGGCGTCCTGCTCCTGGTGCTGGTGGCCACATATGTCTTCGTGGAGTTCTTTGTCAACCCCATGCGTCTGCGCACCAACCGACACTTTGAAGTCCTGAAGAATCACACGGATGTGT
GGTTCGTGTTCCTGCCTGCCGCCCCCGTGGAGACCCAGGCCCCTGCCATCCTGGCCCTGGCCGCCCTGCTCATCCTTCTGGGCCTCCTGTCCACAGCCCTCCTGGGGCACCTGCTCTGCTTCCACATT
TATCTCATGTGGCACAAGCTCACCACCTATGAGTACATCGTGCAGCACCGCCCACCACAGGAGGCCAAGGGGGTTCACAGGGAGCTCGAGTCATGTCCTCCCAAGATGCGGCCCATTCAGGAGATGGA
GTTCTACATGCGGACCTTCAGACATATGCGCCCAGAGCCCCCTGGCCAGGCCGGGCCAGCAGCAGTGAATGCCAATCCCTCCCAGTTTCTTGCCACCCGTGGCCAAGCGGAACCTCCACCACCCTCTT
CCCCAGACACTCTCGCCCTGCCTCCCCGGATCCGACCCCAGAAAAAGAGGAAGAGGCGCGTGTATAAAGTGCGAACGTCTGAGACCTCGGATCCGGCGTCGGGGCCTAGGGCCCCCAGCCGCCGCTCC
AGCTCGTCGACGGATTCCGCGGACGCCAGCCCTGTGCACGCCGCTGGCCCTGCCGGCGCCTACCACTCGGCGTCGGCAGAGTCCGTGGACGAGATTCCAGTGGCGCAGACGCGCCTGGGCAGCGCCGC
TCTGGCCGCCCCGCGGGGCCGGGGCCGACAGCCCACGCTGGCGCGGCAGGCGCGTGCGCCCGCCGTTTTCGTGAGCCCGAGCAGCGGCGAGCCCAGGGCGCCGGGCGGCCGGGAGGCTGGTCTGGCTT
AGCTGGGCCGAGAGGCCGGAGGGCCGAGTTAGAGCGGCCGGCCTGACTCTCTATGCAACACCCCATCCTTGCCGCACCGAGTGCACTTTAGGGGCCCCTACGGCCGGCGGGATCGGCCTCCCTCCCCC
ACGACTCAGCAATACCCGCCCCACCGGCTGTGATGCTCCAATAAACTTTTTTATGCTTTTGCGGACGTCGCGCTTACTTTCTTAATGGCAGGGGCCACGGGCCATCCAGAAGCCCGACCCTGGCCAGT
GGACCGGGGGCGGGGAGGAGGTCCCTGTATAGTAGGTAGCCACCCAGGCTGCCCTGTGGAGGTGCTCACGTGCGGCTCGTGGTTAGGAAAGGCCTTAGAAGGCGGCCTGGAGGAGGTTATTTTTCTTA
AAGATGGGCTTTGCACTGGGAGGCCGAGAGAAAGCAGGCTTTGGGCTCCGAAAGCAGCAGTGGGCGCTGAGGCTGC

hide sequence

RefSeq Acc Id:

NM_013304 ⟹ NP_037436

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,394,152 - 67,416,477 (-)	NCBI
GRCh37	16	67,428,322 - 67,450,339 (-)	RGD
Build 36	16	65,985,829 - 66,007,878 (-)	NCBI Archive
Celera	16	51,936,522 - 51,958,539 (-)	RGD
HuRef	16	53,301,558 - 53,323,519 (-)	RGD
CHM1_1	16	68,835,705 - 68,857,722 (-)	NCBI
T2T-CHM13v2.0	16	73,188,923 - 73,211,253 (-)	NCBI

Sequence:

show sequence

AGCGCCGGACGAGGCCCAGCCAGTCTGGGTCTGGCCTGGCCGCCCCTCCAGCCTGCTGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCAGAGCCAGAGCTCGAGGACTCACCGGCCC
AGTCTCCGTCCGGGATGGGGCCCCGCTCCCGGGCGCGTTGCCGCCCAGTCCCGGGGACCGTCCCTACCGCGAGGGTCTGAGGCGCGGCTGCCCCGGGGAGGGTGGAAGGCCAGGCGTGGGGCCCGAAC
CTCTGGCTGACTTTGGCAGGGCCCATCTGGCACGGCCTCCGCGGCGCGCAGCTGTTTTCAAGTCAGCAAACATTTACTGAGGATCTACTATGTACAAGATGAACATCTGCAACAAGCCCTCCAACAAG
ACGGCCCCTGAGAAGAGTGTGTGGACGGCACCGGCACAGCCCAGCGGACCCTCCCCTGAGCTGCAGGGCCAGCGATCCCGCCGGAATGGGTGGAGCTGGCCCCCTCACCCGCTCCAGATTGTGGCCTG
GCTGCTGTACCTCTTCTTTGCTGTGATCGGCTTTGGGATCCTTGTTCCCCTCCTGCCTCACCACTGGGTGCCCGCTGGCTACGCTTGCATGGGCGCCATCTTTGCTGGCCACCTTGTGGTGCACCTGA
CCGCCGTCTCCATCGATCCAGCAGATGCCAACGTGCGGGACAAGAGCTATGCGGGGCCCCTGCCCATCTTCAACCGAAGCCAGCACGCACATGTCATTGAAGACCTGCACTGCAACTTGTGCAACGTG
GATGTGAGCGCTCGCTCCAAGCACTGCAGCGCCTGCAACAAGTGCGTGTGCGGTTTCGACCACCACTGCAAGTGGCTCAACAACTGTGTGGGCGAGCGGAACTACCGGCTCTTTCTACACAGTGTTGC
ATCCGCTTTACTGGGCGTCCTGCTCCTGGTGCTGGTGGCCACATATGTCTTCGTGGAGTTCTTTGTCAACCCCATGCGTCTGCGCACCAACCGACACTTTGAAGTCCTGAAGAATCACACGGATGTGT
GGTTCGTGTTCCTGCCTGCCGCCCCCGTGGAGACCCAGGCCCCTGCCATCCTGGCCCTGGCCGCCCTGCTCATCCTTCTGGGCCTCCTGTCCACAGCCCTCCTGGGGCACCTGCTCTGCTTCCACATT
TATCTCATGTGGCACAAGCTCACCACCTATGAGTACATCGTGCAGCACCGCCCACCACAGGAGGCCAAGGGGGTTCACAGGGAGCTCGAGTCATGTCCTCCCAAGATGCGGCCCATTCAGGAGATGGA
GTTCTACATGCGGACCTTCAGACATATGCGCCCAGAGCCCCCTGGCCAGGCCGGGCCAGCAGCAGTGAATGCCAAACACTCTCGCCCTGCCTCCCCGGATCCGACCCCAGGTAGGAGGGACTGTGCTG
GGCCTCCGGTCCAGGTGGAGTGGGATAGAAAGAAGCCTCTACCCTGGCGCTCGCCTCTGCTTCTTTTGGCGATGTGGGGCCCTCAGGCTCCCCCGTGTCTCTGCAGAAAAAGAGGAAGAGGCGCGTGT
ATAAAGTGCGAACGTCTGAGACCTCGGATCCGGCGTCGGGGCCTAGGGCCCCCAGCCGCCGCTCCAGCTCGTCGACGGATTCCGCGGACGCCAGCCCTGTGCACGCCGCTGGCCCTGCCGGCGCCTAC
CACTCGGCGTCGGCAGAGTCCGTGGACGAGATTCCAGTGGCGCAGACGCGCCTGGGCAGCGCCGCTCTGGCCGCCCCGCGGGGCCGGGGCCGACAGCCCACGCTGGCGCGGCAGGCGCGTGCGCCCGC
CGTTTTCGTGAGCCCGAGCAGCGGCGAGCCCAGGGCGCCGGGCGGCCGGGAGGCTGGTCTGGCTTAGCTGGGCCGAGAGGCCGGAGGGCCGAGTTAGAGCGGCCGGCCTGACTCTCTATGCAACACCC
CATCCTTGCCGCACCGAGTGCACTTTAGGGGCCCCTACGGCCGGCGGGATCGGCCTCCCTCCCCCACGACTCAGCAATACCCGCCCCACCGGCTGTGATGCTCCAATAAACTTTTTTATGCTTTTGCG
GACGTCGCGCTTACTTTCTTAATGGCAGGGGCCACGGGCCATCCAGAAGCCCGACCCTGGCCAGTGGACCGGGGGCGGGGAGGAGGTCCCTGTATAGTAGGTAGCCACCCAGGCTGCCCTGTGGAGGT
GCTCACGTGCGGCTCGTGGTTAGGAAAGGCCTTAGAAGGCGGCCTGGAGGAGGTTATTTTTCTTAAAGATGGGCTTTGCACTGGGAGGCCGAGAGAAAGCAGGCTTTGGGCTCCGAAAGCAGCAGTGG
GCGCTGAGGCTGC

hide sequence

RefSeq Acc Id:

XM_006721185 ⟹ XP_006721248

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,394,152 - 67,416,477 (-)	NCBI

Sequence:

show sequence

GTCAGGGGAACGGGCCCAGCGCCGGACGAGGCCCAGCCAGTCTGGGTCTGGCCTGGCCGCCCCT
CCAGCCTGCTGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCAGAGCCAGAGCTCGAGGACTCACCGGCCCAGTCTCCGTCCGGGATGGGGCCCCGCTCCCGGGCGCGTTGCCGCCCA
GTCCCGGGGACCGTCCCTACCGCGAGGGTCTGAGGCGCGGCTGCCCCGGGGAGGGTGGAAGGCCAGGCGTGGGGCCCGAACCTCTGGCTGACTTTGGCAGGGCCCATCTGGCACGGCCTCCGCGGCGC
GCAGCTGTTTTCAAGTCAGCAAACATTTACTGAGGATCTACTATGTACAAGATGAACATCTGCAACAAGCCCTCCAACAAGACGGCCCCTGAGAAGAGTGTGTGGACGGCACCGGCACAGCCCAGCGG
ACCCTCCCCTGAGCTGCAGGGCCAGCGATCCCGCCGGAATGGGTGGAGCTGGCCCCCTCACCCGCTCCAGATTGTGGCCTGGCTGCTGTACCTCTTCTTTGCTGTGATCGGCTTTGGGATCCTTGTTC
CCCTCCTGCCTCACCACTGGGTGCCCGCTGGCTACGCTTGCATGGGCGCCATCTTTGCTGGCCACCTTGTGGTGCACCTGACCGCCGTCTCCATCGATCCAGCAGATGCCAACGTGCGGGACAAGAGC
TATGCGGGGCCCCTGCCCATCTTCAACCGAAGCCAGCACGCACATGTCATTGAAGACCTGCACTGCAACTTGTGCAACGTGGATGTGAGCGCTCGCTCCAAGCACTGCAGCGCCTGCAACAAGTGCGT
GTGCGGTTTCGACCACCACTGCAAGTGGCTCAACAACTGTGTGGGCGAGCGGAACTACCGGCTCTTTCTACACAGTGTTGCATCCGCTTTACTGGGCGTCCTGCTCCTGGTGCTGGTGGCCACATATG
TCTTCGTGGAGTTCTTTGTCAACCCCATGCGTCTGCGCACCAACCGACACTTTGAAGTCCTGAAGAATCACACGGATGTGTGGTTCGTGTTCCTGCCTGCCGCCCCCGTGGAGACCCAGGCCCCTGCC
ATCCTGGCCCTGGCCGCCCTGCTCATCCTTCTGGGCCTCCTGTCCACAGCCCTCCTGGGGCACCTGCTCTGCTTCCACATTTATCTCATGTGGCACAAGCTCACCACCTATGAGTACATCGTGCAGCA
CCGCCCACCACAGGAGGCCAAGGGGGTTCACAGGGAGCTCGAGTCATGTCCTCCCAAGATGCGGCCCATTCAGGAGATGGAGTTCTACATGCGGACCTTCAGACATATGCGCCCAGAGCCCCCTGGCC
AGGCCGGGCCAGCAGCAGTGAATGCCAATCCCTCCCAGTTTCTTGCCACCCGTGGCCAAGCGGAACCTCCACCACCCTCTTCCCCAGACACTCTCGCCCTGCCTCCCCGGATCCGACCCCAGGCTCCC
CCGTGTCTCTGCAGAAAAAGAGGAAGAGGCGCGTGTATAAAGTGCGAACGTCTGAGACCTCGGATCCGGCGTCGGGGCCTAGGGCCCCCAGCCGCCGCTCCAGCTCGTCGACGGATTCCGCGGACGCC
AGCCCTGTGCACGCCGCTGGCCCTGCCGGCGCCTACCACTCGGCGTCGGCAGAGTCCGTGGACGAGATTCCAGTGGCGCAGACGCGCCTGGGCAGCGCCGCTCTGGCCGCCCCGCGGGGCCGGGGCCG
ACAGCCCACGCTGGCGCGGCAGGCGCGTGCGCCCGCCGTTTTCGTGAGCCCGAGCAGCGGCGAGCCCAGGGCGCCGGGCGGCCGGGAGGCTGGTCTGGCTTAGCTGGGCCGAGAGGCCGGAGGGCCGA
GTTAGAGCGGCCGGCCTGACTCTCTATGCAACACCCCATCCTTGCCGCACCGAGTGCACTTTAGGGGCCCCTACGGCCGGCGGGATCGGCCTCCCTCCCCCACGACTCAGCAATACCCGCCCCACCGG
CTGTGATGCTCCAATAAACTTTTTTATGCTTTTGCGGA

hide sequence

RefSeq Acc Id:

XM_011523060 ⟹ XP_011521362

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,394,152 - 67,406,367 (-)	NCBI

Sequence:

show sequence

GCTGCTGTACCTCTTCTTTGCTGTGATCGGCTTTGGGATCCTTGTTCCCCTCCTGCCTCACCAC
TGGGTGCCCGCTGGCTACGCTCCAGTGCATGGGCGCCATCTTTGCTGGCCACCTTGTGGTGCACCTGACCGCCGTCTCCATCGATCCAGCAGATGCCAACGTGCGGGACAAGAGCTATGCGGGGCCCC
TGCCCATCTTCAACCGAAGCCAGCACGCACATGTCATTGAAGACCTGCACTGCAACTTGTGCAACGTGGATGTGAGCGCTCGCTCCAAGCACTGCAGCGCCTGCAACAAGTGCGTGTGCGGTTTCGAC
CACCACTGCAAGTGGCTCAACAACTGTGTGGGCGAGCGGAACTACCGGCTCTTTCTACACAGTGTTGCATCCGCTTTACTGGGCGTCCTGCTCCTGGTGCTGGTGGCCACATATGTCTTCGTGGAGTT
CTTTGTCAACCCCATGCGTCTGCGCACCAACCGACACTTTGAAGTCCTGAAGAATCACACGGATGTGTGGTTCGTGTTCCTGCCTGCCGCCCCCGTGGAGACCCAGGCCCCTGCCATCCTGGCCCTGG
CCGCCCTGCTCATCCTTCTGGGCCTCCTGTCCACAGCCCTCCTGGGGCACCTGCTCTGCTTCCACATTTATCTCATGTGGCACAAGCTCACCACCTATGAGTACATCGTGCAGCACCGCCCACCACAG
GAGGCCAAGGGGGTTCACAGGGAGCTCGAGTCATGTCCTCCCAAGATGCGGCCCATTCAGGAGATGGAGTTCTACATGCGGACCTTCAGACATATGCGCCCAGAGCCCCCTGGCCAGGCCGGGCCAGC
AGCAGTGAATGCCAAACACTCTCGCCCTGCCTCCCCGGATCCGACCCCAGGTAGGAGGGACTGTGCTGGGCCTCCGGTCCAGGTGGAGTGGGATAGAAAGAAGCCTCTACCCTGGCGCTCGCCTCTGC
TTCTTTTGGCGATGTGGGGCCCTCAGGCTCCCCCGTGTCTCTGCAGAAAAAGAGGAAGAGGCGCGTGTATAAAGTGCGAACGTCTGAGACCTCGGATCCGGCGTCGGGGCCTAGGGCCCCCAGCCGCC
GCTCCAGCTCGTCGACGGATTCCGCGGACGCCAGCCCTGTGCACGCCGCTGGCCCTGCCGGCGCCTACCACTCGGCGTCGGCAGAGTCCGTGGACGAGATTCCAGTGGCGCAGACGCGCCTGGGCAGC
GCCGCTCTGGCCGCCCCGCGGGGCCGGGGCCGACAGCCCACGCTGGCGCGGCAGGCGCGTGCGCCCGCCGTTTTCGTGAGCCCGAGCAGCGGCGAGCCCAGGGCGCCGGGCGGCCGGGAGGCTGGTCT
GGCTTAGCTGGGCCGAGAGGCCGGAGGGCCGAGTTAGAGCGGCCGGCCTGACTCTCTATGCAACACCCCATCCTTGCCGCACCGAGTGCACTTTAGGGGCCCCTACGGCCGGCGGGATCGGCCTCCCT
CCCCCACGACTCAGCAATACCCGCCCCACCGGCTGTGATGCTCCAATAAACTTTTTTATGCTTTTGCGGA

hide sequence

RefSeq Acc Id:

XM_024450245 ⟹ XP_024306013

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,394,152 - 67,416,477 (-)	NCBI

Sequence:

show sequence

GTGATGGTGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGATCCTGTCTCAGAAGAAAAAAAAAAACCCTAAACCCAAAACCCAAATACCACCAGTTGAATCCCTGGGGGAAAACTAAGTCCTCCAT
TTAGCTTTGAGATGGGACAACTCAGAGGTCACTTCAAATAATGCTTGGCTTGGCCTGCAGGAGGCTCTGAGCCTCAGGTGGGCTGAAGGGCAGGGTGGCTAGGAGTGAGTGTCTGGCAGTCAGGGTGG
TAGCCAGCCGGCAGAGGGAGATGGGCTGCGGGAGGCATGGGTTCACGACCCTGCAGAAAGAGGGCAGGGCTGGATGGATGGAAGGCAGGAGAAAGCAGGCCAGATGGCTTAGGGTGGACCAGGATTCC
ACACCATTTACTGTGCCCACGTTTCCTTTTATTTCAGCTGTTTTCAAGTCAGCAAACATTTACTGAGGATCTACTATGTACAAGATGAACATCTGCAACAAGCCCTCCAACAAGACGGCCCCTGAGAA
GAGTGTGTGGACGGCACCGGCACAGCCCAGCGGACCCTCCCCTGAGCTGCAGGGCCAGCGATCCCGCCGGAATGGGTGGAGCTGGCCCCCTCACCCGCTCCAGATTGTGGCCTGGCTGCTGTACCTCT
TCTTTGCTGTGATCGGCTTTGGGATCCTTGTTCCCCTCCTGCCTCACCACTGGGTGCCCGCTGGCTACGCTTGCATGGGCGCCATCTTTGCTGGCCACCTTGTGGTGCACCTGACCGCCGTCTCCATC
GATCCAGCAGATGCCAACGTGCGGGACAAGAGCTATGCGGGGCCCCTGCCCATCTTCAACCGAAGCCAGCACGCACATGTCATTGAAGACCTGCACTGCAACTTGTGCAACGTGGATGTGAGCGCTCG
CTCCAAGCACTGCAGCGCCTGCAACAAGTGCGTGTGCGGTTTCGACCACCACTGCAAGTGGCTCAACAACTGTGTGGGCGAGCGGAACTACCGGCTCTTTCTACACAGTGTTGCATCCGCTTTACTGG
GCGTCCTGCTCCTGGTGCTGGTGGCCACATATGTCTTCGTGGAGTTCTTTGTCAACCCCATGCGTCTGCGCACCAACCGACACTTTGAAGTCCTGAAGAATCACACGGATGTGTGGTTCGTGTTCCTG
CCTGCCGCCCCCGTGGAGACCCAGGCCCCTGCCATCCTGGCCCTGGCCGCCCTGCTCATCCTTCTGGGCCTCCTGTCCACAGCCCTCCTGGGGCACCTGCTCTGCTTCCACATTTATCTCATGTGGCA
CAAGCTCACCACCTATGAGTACATCGTGCAGCACCGCCCACCACAGGAGGCCAAGGGGGTTCACAGGGAGCTCGAGTCATGTCCTCCCAAGATGCGGCCCATTCAGGAGATGGAGTTCTACATGCGGA
CCTTCAGACATATGCGCCCAGAGCCCCCTGGCCAGGCCGGGCCAGCAGCAGTGAATGCCAAACACTCTCGCCCTGCCTCCCCGGATCCGACCCCAGGTAGGAGGGACTGTGCTGGGCCTCCGGTCCAG
GTGGAGTGGGATAGAAAGAAGCCTCTACCCTGGCGCTCGCCTCTGCTTCTTTTGGCGATGTGGGGCCCTCAGGCTCCCCCGTGTCTCTGCAGAAAAAGAGGAAGAGGCGCGTGTATAAAGTGCGAACG
TCTGAGACCTCGGATCCGGCGTCGGGGCCTAGGGCCCCCAGCCGCCGCTCCAGCTCGTCGACGGATTCCGCGGACGCCAGCCCTGTGCACGCCGCTGGCCCTGCCGGCGCCTACCACTCGGCGTCGGC
AGAGTCCGTGGACGAGATTCCAGTGGCGCAGACGCGCCTGGGCAGCGCCGCTCTGGCCGCCCCGCGGGGCCGGGGCCGACAGCCCACGCTGGCGCGGCAGGCGCGTGCGCCCGCCGTTTTCGTGAGCC
CGAGCAGCGGCGAGCCCAGGGCGCCGGGCGGCCGGGAGGCTGGTCTGGCTTAGCTGGGCCGAGAGGCCGGAGGGCCGAGTTAGAGCGGCCGGCCTGACTCTCTATGCAACACCCCATCCTTGCCGCAC
CGAGTGCACTTTAGGGGCCCCTACGGCCGGCGGGATCGGCCTCCCTCCCCCACGACTCAGCAATACCCGCCCCACCGGCTGTGATGCTCCAATAAACTTTTTTATGCTTTTGCGGA

hide sequence

RefSeq Acc Id:

XM_024450246 ⟹ XP_024306014

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,394,152 - 67,416,477 (-)	NCBI

Sequence:

show sequence

GTCAGGGGAACGGGCCCAGCGCCGGACGAGGCCCAGCCAGTCTGGGTCTGGCCTGGCCGCCCCTCCAGCCTGCTGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCAGAGCCAGAGCT
CGAGGACTCACCGGCCCAGTCTCCGTCCGGGATGGGGCCCCGCTCCCGGGCGCGTTGCCGCCCAGTCCCGGGGACCGTCCCTACCGCGAGGGTCTGAGGCGCGGCTGCCCCGGGGAGGGTGGAAGGCC
AGGCGTGGGGCCCGAACCTCTGGCTGACTTTGGCAGGGCCCATCTGGCACGGCCTCCGCGGCGCGCAGCTGTTTTCAAGTCAGCAAACATTTACTGAGGATCTACTATGTACAAGATGAACATCTGCA
ACAAGCCCTCCAACAAGACGGCCCCTGAGAAGAGTGTGTGGACGGCACCGGCACAGCCCAGCGGACCCTCCCCTGAGCTGCAGGGCCAGCGATCCCGCCGGAATGGGTGGAGCTGGCCCCCTCACCCG
CTCCAGATTGTGGCCTGGCTGCTGTACCTCTTCTTTGCTGTGATCGGCTTTGGGATCCTTGTTCCCCTCCTGCCTCACCACTGGGTGCCCGCTGGCTACGCTTGCATGGGCGCCATCTTTGCTGGCCA
CCTTGTGGTGCACCTGACCGCCGTCTCCATCGATCCAGCAGATGCCAACGTGCGGGACAAGAGCTATGCGGGGCCCCTGCCCATCTTCAACCGAAGCCAGCACGCACATGTCATTGAAGACCTGCACT
GCAACTTGTGCAACGTGGATGTGAGCGCTCGCTCCAAGCACTGCAGCGCCTGCAACAAGTGCGTGTGCGGTTTCGACCACCACTGCAAGTGGCTCAACAACTGTGTGGGCGAGCGGAACTACCGGCTC
TTTCTACACAGTGTTGCATCCGCTTTACTGGGCGTCCTGCTCCTGGTGCTGGTGGCCACATATGTCTTCGTGGAGTTCTTTGTCAACCCCATGCGTCTGCGCACCAACCGACACTTTGAAGTCCTGAA
GAATCACACGGATGTGTGGTTCGTGTTCCTGCCTGCCGCCCCCGTGGAGACCCAGGCCCCTGCCATCCTGGCCCTGGCCGCCCTGCTCATCCTTCTGGGCCTCCTGTCCACAGCCCTCCTGGGGCACC
TGCTCTGCTTCCACATTTATCTCATGTGGCACAAGCTCACCACCTATGAGTACATCGTGCAGCACCGCCCACCACAGGAGGCCAAGGGGGTTCACAGGGAGCTCGAGTCATGTCCTCCCAAGATGCGG
CCCATTCAGGAGATGGAGTTCTACATGCGGACCTTCAGACATATGCGCCCAGAGCCCCCTGGCCAGGCCGGGCCAGCAGCAGTGAATGCCAAACACTCTCGCCCTGCCTCCCCGGATCCGACCCCAGG
CTCCCCCGTGTCTCTGCAGAAAAAGAGGAAGAGGCGCGTGTATAAAGTGCGAACGTCTGAGACCTCGGATCCGGCGTCGGGGCCTAGGGCCCCCAGCCGCCGCTCCAGCTCGTCGACGGATTCCGCGG
ACGCCAGCCCTGTGCACGCCGCTGGCCCTGCCGGCGCCTACCACTCGGCGTCGGCAGAGTCCGTGGACGAGATTCCAGTGGCGCAGACGCGCCTGGGCAGCGCCGCTCTGGCCGCCCCGCGGGGCCGG
GGCCGACAGCCCACGCTGGCGCGGCAGGCGCGTGCGCCCGCCGTTTTCGTGAGCCCGAGCAGCGGCGAGCCCAGGGCGCCGGGCGGCCGGGAGGCTGGTCTGGCTTAGCTGGGCCGAGAGGCCGGAGG
GCCGAGTTAGAGCGGCCGGCCTGACTCTCTATGCAACACCCCATCCTTGCCGCACCGAGTGCACTTTAGGGGCCCCTACGGCCGGCGGGATCGGCCTCCCTCCCCCACGACTCAGCAATACCCGCCCC
ACCGGCTGTGATGCTCCAATAAACTTTTTTATGCTTTTGCGGA

hide sequence

RefSeq Acc Id:

XM_024450247 ⟹ XP_024306015

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,394,152 - 67,416,477 (-)	NCBI

Sequence:

show sequence

GTCAGGGGAACGGGCCCAGCGCCGGACGAGGCCCAGCCAGTCTGGGTCTGGCCTGGCCGCCCCT
CCAGCCTGCTGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCGGAGCCAGAGCCAGAGCTCGAGGACTCACCGGCCCAGTCTCCGTCCGGGATGGGGCCCCGCTCCCGGGCGCGTTGCCGCCCA
GTCCCGGGGACCGTCCCTACCGCGAGGGTCTGAGGCGCGGCTGCCCCGGGGAGGGTGGAAGGCCAGGCGTGGGGCCCGAACCTCTGGCTGACTTTGGCAGGGCCCATCTGGCACGGCCTCCGCGGCGC
GCAGCTGTTTTCAAGTCAGCAAACATTTACTGAGGATCTACTATGTACAAGATGAACATCTGCAACAAGCCCTCCAACAAGACGGCCCCTGAGAAGAGTGTGTGGACGGCACCGGCACAGCCCAGCGG
ACCCTCCCCTGAGCTGCAGGGCCAGCGATCCCGCCGGAATGGGTGGAGCTGGCCCCCTCACCCGCTCCAGATTGTGGCCTGGCTGCTGTACCTCTTCTTTGCTGTGATCGGCTTTGGGATCCTTGTTC
CCCTCCTGCCTCACCACTGGGTGCCCGCTGGCTACGCTTGCATGGGCGCCATCTTTGCTGGCCACCTTGTGGTGCACCTGACCGCCGTCTCCATCGATCCAGCAGATGCCAACGTGCGGGACAAGAGC
TATGCGGGGCCCCTGCCCATCTTCAACCGAAGCCAGCACGCACATGTCATTGAAGACCTGCACTGCAACTTGTGCAACGTGGATGTGAGCGCTCGCTCCAAGCACTGCAGCGCCTGCAACAAGTGCGT
GTGCGGTTTCGACCACCACTGCAAGTGGCTCAACAACTGTGTGGGCGAGCGGAACTACCGGCTCTTTCTACACAGTGTTGCATCCGCTTTACTGGGCGTCCTGCTCCTGGTGCTGGTGGCCACATATG
TCTTCGTGGAGTTCTTTGTCAACCCCATGCGTCTGCGCACCAACCGACACTTTGAAGTCCTGAAGAATCACACGGATGTGTGGTTCGTGTTCCTGCCTGCCGCCCCCGTGGAGACCCAGGCCCCTGCC
ATCCTGGCCCTGGCCGCCCTGCTCATCCTTCTGGGCCTCCTGTCCACAGCCCTCCTGGGGCACCTGCTCTGCTTCCACATTTATCTCATGTGGCACAAGCTCACCACCTATGAGTACATCGTGCAGCA
CCGCCCACCACAGGAGGCCAAGGGGGTTCACAGGGAGCTCGAGTCATGTCCTCCCAAGATGCGGCCCATTCAGGAGATGGAGTTCTACATGCGGACCTTCAGACATATGCGCCCAGAGCCCCCTGGCC
AGGCCGGGCCAGCAGCAGTGAATGCCAAAAAAAGAGGAAGAGGCGCGTGTATAAAGTGCGAACGTCTGAGACCTCGGATCCGGCGTCGGGGCCTAGGGCCCCCAGCCGCCGCTCCAGCTCGTCGACGG
ATTCCGCGGACGCCAGCCCTGTGCACGCCGCTGGCCCTGCCGGCGCCTACCACTCGGCGTCGGCAGAGTCCGTGGACGAGATTCCAGTGGCGCAGACGCGCCTGGGCAGCGCCGCTCTGGCCGCCCCG
CGGGGCCGGGGCCGACAGCCCACGCTGGCGCGGCAGGCGCGTGCGCCCGCCGTTTTCGTGAGCCCGAGCAGCGGCGAGCCCAGGGCGCCGGGCGGCCGGGAGGCTGGTCTGGCTTAGCTGGGCCGAGA
GGCCGGAGGGCCGAGTTAGAGCGGCCGGCCTGACTCTCTATGCAACACCCCATCCTTGCCGCACCGAGTGCACTTTAGGGGCCCCTACGGCCGGCGGGATCGGCCTCCCTCCCCCACGACTCAGCAAT
ACCCGCCCCACCGGCTGTGATGCTCCAATAAACTTTTTTATGCTTTTGCGGA

hide sequence

RefSeq Acc Id:

XM_054380184 ⟹ XP_054236159

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,188,923 - 73,211,253 (-)	NCBI

RefSeq Acc Id:

XM_054380185 ⟹ XP_054236160

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,188,923 - 73,211,253 (-)	NCBI

RefSeq Acc Id:

XM_054380186 ⟹ XP_054236161

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,188,923 - 73,211,253 (-)	NCBI

RefSeq Acc Id:

XM_054380187 ⟹ XP_054236162

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,188,923 - 73,211,253 (-)	NCBI

RefSeq Acc Id:

XM_054380188 ⟹ XP_054236163

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	73,188,923 - 73,201,055 (-)	NCBI


Protein RefSeqs	NP_001310556	(Get FASTA)	NCBI Sequence Viewer
	NP_037436	(Get FASTA)	NCBI Sequence Viewer
	XP_006721248	(Get FASTA)	NCBI Sequence Viewer
	XP_011521362	(Get FASTA)	NCBI Sequence Viewer
	XP_024306013	(Get FASTA)	NCBI Sequence Viewer
	XP_024306014	(Get FASTA)	NCBI Sequence Viewer
	XP_024306015	(Get FASTA)	NCBI Sequence Viewer
	XP_054236159	(Get FASTA)	NCBI Sequence Viewer
	XP_054236160	(Get FASTA)	NCBI Sequence Viewer
	XP_054236161	(Get FASTA)	NCBI Sequence Viewer
	XP_054236162	(Get FASTA)	NCBI Sequence Viewer
	XP_054236163	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAB86591	(Get FASTA)	NCBI Sequence Viewer
	AAH21908	(Get FASTA)	NCBI Sequence Viewer
	EAW83132	(Get FASTA)	NCBI Sequence Viewer
	EAW83133	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000340299
	ENSP00000340299.2
	ENSP00000459264
GenBank Protein	Q8WTX9	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_037436 ⟸ NM_013304
- Peptide Label:	isoform 1
- UniProtKB:	O15461 (UniProtKB/Swiss-Prot), Q8WTX9 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MYKMNICNKPSNKTAPEKSVWTAPAQPSGPSPELQGQRSRRNGWSWPPHPLQIVAWLLYLFFAVIGFGILVPLLPHHWVPAGYACMGAIFAGHLVVHLTAVSIDPADANVRDKSYAGPLPIFNRSQHA HVIEDLHCNLCNVDVSARSKHCSACNKCVCGFDHHCKWLNNCVGERNYRLFLHSVASALLGVLLLVLVATYVFVEFFVNPMRLRTNRHFEVLKNHTDVWFVFLPAAPVETQAPAILALAALLILLGLL STALLGHLLCFHIYLMWHKLTTYEYIVQHRPPQEAKGVHRELESCPPKMRPIQEMEFYMRTFRHMRPEPPGQAGPAAVNAKHSRPASPDPTPGRRDCAGPPVQVEWDRKKPLPWRSPLLLLAMWGPQA PPCLCRKRGRGACIKCERLRPRIRRRGLGPPAAAPARRRIPRTPALCTPLALPAPTTRRRQSPWTRFQWRRRAWAAPLWPPRGAGADSPRWRGRRVRPPFS hide sequence

RefSeq Acc Id:

XP_006721248 ⟸ XM_006721185

- Peptide Label:

isoform X2

- Sequence:

show sequence

MYKMNICNKPSNKTAPEKSVWTAPAQPSGPSPELQGQRSRRNGWSWPPHPLQIVAWLLYLFFAVIGFGILVPLLPHHWVPAGYACMGAIFAGHLVVHLTAVSIDPADANVRDKSYAGPLPIFNRSQHA
HVIEDLHCNLCNVDVSARSKHCSACNKCVCGFDHHCKWLNNCVGERNYRLFLHSVASALLGVLLLVLVATYVFVEFFVNPMRLRTNRHFEVLKNHTDVWFVFLPAAPVETQAPAILALAALLILLGLL
STALLGHLLCFHIYLMWHKLTTYEYIVQHRPPQEAKGVHRELESCPPKMRPIQEMEFYMRTFRHMRPEPPGQAGPAAVNANPSQFLATRGQAEPPPPSSPDTLALPPRIRPQAPPCLCRKRGRGACIK
CERLRPRIRRRGLGPPAAAPARRRIPRTPALCTPLALPAPTTRRRQSPWTRFQWRRRAWAAPLWPPRGAGADSPRWRGRRVRPPFS

hide sequence

RefSeq Acc Id:

XP_011521362 ⟸ XM_011523060

- Peptide Label:

isoform X5

- Sequence:

show sequence

MGAIFAGHLVVHLTAVSIDPADANVRDKSYAGPLPIFNRSQHAHVIEDLHCNLCNVDVSARSKHCSACNKCVCGFDHHCKWLNNCVGERNYRLFLHSVASALLGVLLLVLVATYVFVEFFVNPMRLRT
NRHFEVLKNHTDVWFVFLPAAPVETQAPAILALAALLILLGLLSTALLGHLLCFHIYLMWHKLTTYEYIVQHRPPQEAKGVHRELESCPPKMRPIQEMEFYMRTFRHMRPEPPGQAGPAAVNAKHSRP
ASPDPTPGRRDCAGPPVQVEWDRKKPLPWRSPLLLLAMWGPQAPPCLCRKRGRGACIKCERLRPRIRRRGLGPPAAAPARRRIPRTPALCTPLALPAPTTRRRQSPWTRFQWRRRAWAAPLWPPRGAG
ADSPRWRGRRVRPPFS

hide sequence

RefSeq Acc Id:	NP_001310556 ⟸ NM_001323627
- Peptide Label:	isoform 2
- UniProtKB:	I3L202 (UniProtKB/TrEMBL)
- Sequence:	show sequence MYKMNICNKPSNKTAPEKSVWTAPAQPSGPSPELQGQRSRRNGWSWPPHPLQIVAWLLYLFFAV IGFGILVPLLPHHWVPAGYACMGAIFAGHLVVHLTAVSIDPADANVRDKSYAGPLPIFNRSQHAHVIEDLHCNLCNVDVSARSKHCSACNKCVCGFDHHCKWLNNCVGERNYRLFLHSVASALLGVLL LVLVATYVFVEFFVNPMRLRTNRHFEVLKNHTDVWFVFLPAAPVETQAPAILALAALLILLGLLSTALLGHLLCFHIYLMWHKLTTYEYIVQHRPPQEAKGVHRELESCPPKMRPIQEMEFYMRTFRH MRPEPPGQAGPAAVNANPSQFLATRGQAEPPPPSSPDTLALPPRIRPQKKRKRRVYKVRTSETSDPASGPRAPSRRSSSSTDSADASPVHAAGPAGAYHSASAESVDEIPVAQTRLGSAALAAPRGRG RQPTLARQARAPAVFVSPSSGEPRAPGGREAGLA hide sequence

RefSeq Acc Id:

XP_024306015 ⟸ XM_024450247

- Peptide Label:

isoform X4

- Sequence:

show sequence

MYKMNICNKPSNKTAPEKSVWTAPAQPSGPSPELQGQRSRRNGWSWPPHPLQIVAWLLYLFFAV
IGFGILVPLLPHHWVPAGYACMGAIFAGHLVVHLTAVSIDPADANVRDKSYAGPLPIFNRSQHAHVIEDLHCNLCNVDVSARSKHCSACNKCVCGFDHHCKWLNNCVGERNYRLFLHSVASALLGVLL
LVLVATYVFVEFFVNPMRLRTNRHFEVLKNHTDVWFVFLPAAPVETQAPAILALAALLILLGLLSTALLGHLLCFHIYLMWHKLTTYEYIVQHRPPQEAKGVHRELESCPPKMRPIQEMEFYMRTFRH
MRPEPPGQAGPAAVNAKKRGRGACIKCERLRPRIRRRGLGPPAAAPARRRIPRTPALCTPLALPAPTTRRRQSPWTRFQWRRRAWAAPLWPPRGAGADSPRWRGRRVRPPFS

hide sequence

Protein Domains

DHHC Palmitoyltransferase DHHC

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8WTX9-F1-model_v2	AlphaFold	Q8WTX9	1-485	view protein structure

RGD ID:

6793617

Promoter ID:

HG_KWN:24035

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, Lymphoblastoid

Transcripts:

OTTHUMT00000268845, UC002ETC.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	66,007,536 - 66,008,036 (-)	MPROMDB

RGD ID:

7232545

Promoter ID:

EPDNEW_H22018

Type:

initiation region

Name:

ZDHHC1_1

Description:

zinc finger DHHC-type containing 1

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	67,416,477 - 67,416,537	EPDNEW

Database	Acc Id	Source(s)
COSMIC	ZDHHC1	COSMIC
Ensembl Genes	ENSG00000159714	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000348579	ENTREZGENE
	ENST00000348579.6	UniProtKB/Swiss-Prot
	ENST00000565726	ENTREZGENE
GTEx	ENSG00000159714	GTEx
HGNC ID	HGNC:17916	ENTREZGENE
Human Proteome Map	ZDHHC1	Human Proteome Map
InterPro	Palmitoyltrfase_DHHC	UniProtKB/Swiss-Prot
	PFA4/ZDH16/20/ERF2-like	UniProtKB/Swiss-Prot
KEGG Report	hsa:29800	UniProtKB/Swiss-Prot
NCBI Gene	29800	ENTREZGENE
PANTHER	PALMITOYLTRANSFERASE ZDHHC1	UniProtKB/Swiss-Prot
	ZINC FINGER DHHC DOMAIN CONTAINING PROTEIN	UniProtKB/Swiss-Prot
Pfam	DHHC	UniProtKB/Swiss-Prot
PharmGKB	PA38261	PharmGKB
PROSITE	DHHC	UniProtKB/Swiss-Prot
UniProt	I3L202	ENTREZGENE, UniProtKB/TrEMBL
	O15461	ENTREZGENE
	Q8WTX9	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	O15461	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-02-16	ZDHHC1	zinc finger DHHC-type containing 1		zinc finger, DHHC-type containing 1	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailable


InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailable


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar