ZDHHC23 (zinc finger DHHC-type palmitoyltransferase 23) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: ZDHHC23 (zinc finger DHHC-type palmitoyltransferase 23) Homo sapiens
Analyze
Symbol: ZDHHC23
Name: zinc finger DHHC-type palmitoyltransferase 23
RGD ID: 1345232
HGNC Page HGNC:28654
Description: Predicted to enable protein-cysteine S-palmitoyltransferase activity. Involved in protein localization to plasma membrane. Predicted to be located in Golgi membrane. Predicted to be active in Golgi apparatus and endoplasmic reticulum.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DHHC-23; MGC42530; NIDD; palmitoyltransferase ZDHHC23; probable palmitoyltransferase ZDHHC23; zinc finger DHHC domain-containing protein 23; zinc finger DHHC-type containing 23; zinc finger, DHHC domain containing 23; zinc finger, DHHC-type containing 23
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh383113,947,901 - 113,979,508 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl3113,947,901 - 113,965,401 (+)EnsemblGRCh38hg38GRCh38
GRCh373113,666,748 - 113,682,220 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 363115,149,438 - 115,164,519 (+)NCBINCBI36Build 36hg18NCBI36
Build 343115,149,437 - 115,164,515NCBI
Celera3112,075,199 - 112,090,278 (+)NCBICelera
Cytogenetic Map3q13.31NCBI
HuRef3111,040,938 - 111,055,875 (+)NCBIHuRef
CHM1_13113,630,124 - 113,645,199 (+)NCBICHM1_1
T2T-CHM13v2.03116,669,165 - 116,719,588 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:8619474   PMID:9110174   PMID:12107410   PMID:14702039   PMID:15105416   PMID:15489334   PMID:21832049   PMID:21873635   PMID:22399288   PMID:22482804   PMID:28514442   PMID:30658672  
PMID:32296183   PMID:33961781  


Genomics

Comparative Map Data
ZDHHC23
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh383113,947,901 - 113,979,508 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl3113,947,901 - 113,965,401 (+)EnsemblGRCh38hg38GRCh38
GRCh373113,666,748 - 113,682,220 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 363115,149,438 - 115,164,519 (+)NCBINCBI36Build 36hg18NCBI36
Build 343115,149,437 - 115,164,515NCBI
Celera3112,075,199 - 112,090,278 (+)NCBICelera
Cytogenetic Map3q13.31NCBI
HuRef3111,040,938 - 111,055,875 (+)NCBIHuRef
CHM1_13113,630,124 - 113,645,199 (+)NCBICHM1_1
T2T-CHM13v2.03116,669,165 - 116,719,588 (+)NCBIT2T-CHM13v2.0
Zdhhc23
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391643,785,396 - 43,800,295 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1643,785,396 - 43,800,154 (-)EnsemblGRCm39 Ensembl
GRCm381643,965,033 - 43,979,820 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1643,965,033 - 43,979,791 (-)EnsemblGRCm38mm10GRCm38
MGSCv371643,969,259 - 43,979,163 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361643,888,478 - 43,898,382 (-)NCBIMGSCv36mm8
Celera1644,324,294 - 44,334,213 (-)NCBICelera
Cytogenetic Map16B4NCBI
cM Map1628.44NCBI
Zdhhc23
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81170,224,581 - 70,240,971 (+)NCBIGRCr8
mRatBN7.21156,718,702 - 56,735,063 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1156,718,826 - 56,734,194 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1165,532,953 - 65,543,533 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01158,195,202 - 58,205,782 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01157,243,748 - 57,254,331 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01161,661,119 - 61,677,547 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1161,661,310 - 61,676,684 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01160,791,638 - 60,807,948 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41158,286,189 - 58,296,769 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11158,342,817 - 58,358,183 (+)NCBI
Celera1156,272,859 - 56,283,439 (+)NCBICelera
Cytogenetic Map11q21NCBI
Zdhhc23
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542714,045,657 - 14,057,202 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495542714,045,659 - 14,057,226 (+)NCBIChiLan1.0ChiLan1.0
ZDHHC23
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22111,940,243 - 111,955,562 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan13111,945,021 - 111,960,340 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v03111,086,166 - 111,101,631 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.13118,007,264 - 118,022,595 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl3118,007,270 - 118,022,204 (+)Ensemblpanpan1.1panPan2
ZDHHC23
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13318,215,822 - 18,227,626 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3318,215,678 - 18,223,268 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3318,323,605 - 18,335,904 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03318,461,154 - 18,473,451 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3318,461,254 - 18,469,090 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13318,264,528 - 18,276,815 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03318,316,321 - 18,328,618 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03318,861,187 - 18,873,505 (+)NCBIUU_Cfam_GSD_1.0
Zdhhc23
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405602136,071,082 - 136,086,926 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365361,434,748 - 1,450,854 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365361,434,774 - 1,450,872 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZDHHC23
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl13145,970,851 - 145,997,044 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.113145,981,955 - 145,997,599 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.213155,569,093 - 155,584,573 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ZDHHC23
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12266,905,388 - 66,917,104 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2266,901,395 - 66,915,702 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604199,551,890 - 99,567,107 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Zdhhc23
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473134,544,250 - 34,560,790 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473134,544,476 - 34,561,284 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZDHHC23
26 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 3q13.2-13.31(chr3:112168829-117393356)x1 copy number loss See cases [RCV000050766] Chr3:112168829..117393356 [GRCh38]
Chr3:111887676..117112203 [GRCh37]
Chr3:113370366..118594893 [NCBI36]
Chr3:3q13.2-13.31		 pathogenic
GRCh38/hg38 3q11.1-21.1(chr3:93886671-123216683)x1 copy number loss See cases [RCV000051543] Chr3:93886671..123216683 [GRCh38]
Chr3:93605515..122935530 [GRCh37]
Chr3:95088205..124418220 [NCBI36]
Chr3:3q11.1-21.1		 pathogenic
GRCh38/hg38 3q13.13-13.31(chr3:108242572-116169331)x1 copy number loss See cases [RCV000051544] Chr3:108242572..116169331 [GRCh38]
Chr3:107961419..115888178 [GRCh37]
Chr3:109444109..117370868 [NCBI36]
Chr3:3q13.13-13.31		 pathogenic
GRCh38/hg38 3q13.2-13.31(chr3:112479482-115774102)x1 copy number loss See cases [RCV000051545] Chr3:112479482..115774102 [GRCh38]
Chr3:112198329..115492949 [GRCh37]
Chr3:113681019..116975639 [NCBI36]
Chr3:3q13.2-13.31		 pathogenic
GRCh38/hg38 3q13.11-13.31(chr3:104621220-116093884)x3 copy number gain See cases [RCV000051722] Chr3:104621220..116093884 [GRCh38]
Chr3:104340064..115812731 [GRCh37]
Chr3:105822754..117295421 [NCBI36]
Chr3:3q13.11-13.31		 pathogenic
GRCh38/hg38 3q11.1-13.31(chr3:93819623-116887056)x1 copy number loss See cases [RCV000135320] Chr3:93819623..116887056 [GRCh38]
Chr3:93538467..116605903 [GRCh37]
Chr3:95021157..118088593 [NCBI36]
Chr3:3q11.1-13.31		 pathogenic
GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3 copy number gain See cases [RCV000134948] Chr3:103426882..198110178 [GRCh38]
Chr3:103145726..197837049 [GRCh37]
Chr3:104628416..199321446 [NCBI36]
Chr3:3q13.11-29		 pathogenic
GRCh38/hg38 3q13.2-13.31(chr3:112465096-115774102)x1 copy number loss See cases [RCV000135592] Chr3:112465096..115774102 [GRCh38]
Chr3:112183943..115492949 [GRCh37]
Chr3:113666633..116975639 [NCBI36]
Chr3:3q13.2-13.31		 likely pathogenic
GRCh38/hg38 3q11.2-13.31(chr3:97795369-115663349)x1 copy number loss See cases [RCV000138186] Chr3:97795369..115663349 [GRCh38]
Chr3:97514213..115382196 [GRCh37]
Chr3:98996903..116864886 [NCBI36]
Chr3:3q11.2-13.31		 pathogenic|uncertain significance
GRCh38/hg38 3q13.2-13.31(chr3:112465094-115774111)x1 copy number loss See cases [RCV000138434] Chr3:112465094..115774111 [GRCh38]
Chr3:112183941..115492958 [GRCh37]
Chr3:113666631..116975648 [NCBI36]
Chr3:3q13.2-13.31		 pathogenic
GRCh38/hg38 3q13.2-21.3(chr3:112620977-128734134)x1 copy number loss See cases [RCV000139033] Chr3:112620977..128734134 [GRCh38]
Chr3:112339824..128452977 [GRCh37]
Chr3:113822514..129935667 [NCBI36]
Chr3:3q13.2-21.3		 pathogenic
GRCh38/hg38 3q11.1-24(chr3:93800620-145695381)x3 copy number gain See cases [RCV000142340] Chr3:93800620..145695381 [GRCh38]
Chr3:93519464..145413168 [GRCh37]
Chr3:95002154..146895858 [NCBI36]
Chr3:3q11.1-24		 pathogenic
GRCh38/hg38 3q13.2-13.31(chr3:112425234-115795585)x1 copy number loss See cases [RCV000142219] Chr3:112425234..115795585 [GRCh38]
Chr3:112144081..115514432 [GRCh37]
Chr3:113626771..116997122 [NCBI36]
Chr3:3q13.2-13.31		 pathogenic
GRCh38/hg38 3q13.2-13.33(chr3:112520553-120031022)x1 copy number loss See cases [RCV000142725] Chr3:112520553..120031022 [GRCh38]
Chr3:112239400..119749869 [GRCh37]
Chr3:113722090..121232559 [NCBI36]
Chr3:3q13.2-13.33		 pathogenic
GRCh37/hg19 3q13.12-13.31(chr3:106598767-115704696) copy number loss Chromosome 3q13.31 deletion syndrome [RCV002280741] Chr3:106598767..115704696 [GRCh37]
Chr3:3q13.12-13.31		 pathogenic
GRCh37/hg19 3q13.2-13.31(chr3:112144081-115514432)x1 copy number loss See cases [RCV000446223] Chr3:112144081..115514432 [GRCh37]
Chr3:3q13.2-13.31		 pathogenic
GRCh37/hg19 3q13.11-13.32(chr3:105094834-117441953)x1 copy number loss See cases [RCV000448410] Chr3:105094834..117441953 [GRCh37]
Chr3:3q13.11-13.32		 pathogenic
GRCh37/hg19 3q13.2-13.31(chr3:112590339-116461450)x1 copy number loss See cases [RCV000511086] Chr3:112590339..116461450 [GRCh37]
Chr3:3q13.2-13.31		 pathogenic
NM_001320466.2(ZDHHC23):c.826C>T (p.Arg276Trp) single nucleotide variant Inborn genetic diseases [RCV003299116] Chr3:113954364 [GRCh38]
Chr3:113673211 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.620G>A (p.Ser207Asn) single nucleotide variant Inborn genetic diseases [RCV003280299] Chr3:113954158 [GRCh38]
Chr3:113673005 [GRCh37]
Chr3:3q13.31		 uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3 copy number gain See cases [RCV000511055] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986) copy number gain See cases [RCV000512358] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
NM_001320466.2(ZDHHC23):c.468C>A (p.Phe156Leu) single nucleotide variant Inborn genetic diseases [RCV003300458] Chr3:113954006 [GRCh38]
Chr3:113672853 [GRCh37]
Chr3:3q13.31		 uncertain significance
GRCh37/hg19 3q13.13-13.31(chr3:110645295-115103586)x1 copy number loss not provided [RCV000682294] Chr3:110645295..115103586 [GRCh37]
Chr3:3q13.13-13.31		 pathogenic
GRCh37/hg19 3q13.2-13.31(chr3:111894832-116930109)x1 copy number loss not provided [RCV000682296] Chr3:111894832..116930109 [GRCh37]
Chr3:3q13.2-13.31		 pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3 copy number gain not provided [RCV000742138] Chr3:61495..197838262 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3 copy number gain not provided [RCV000742133] Chr3:60174..197948027 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
GRCh37/hg19 3q13.31(chr3:113666402-113667160)x1 copy number loss not provided [RCV000742697] Chr3:113666402..113667160 [GRCh37]
Chr3:3q13.31		 benign
GRCh37/hg19 3q13.31(chr3:113666511-113667160)x1 copy number loss not provided [RCV000742698] Chr3:113666511..113667160 [GRCh37]
Chr3:3q13.31		 benign
GRCh37/hg19 3q13.31(chr3:113666511-113673125)x1 copy number loss not provided [RCV000742699] Chr3:113666511..113673125 [GRCh37]
Chr3:3q13.31		 benign
GRCh37/hg19 3q13.2-13.31(chr3:112183943-115492949)x1 copy number loss not provided [RCV000856645] Chr3:112183943..115492949 [GRCh37]
Chr3:3q13.2-13.31		 pathogenic
GRCh37/hg19 3q13.31(chr3:113594376-114060961)x3 copy number gain not provided [RCV000848094] Chr3:113594376..114060961 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.452A>G (p.Tyr151Cys) single nucleotide variant Inborn genetic diseases [RCV003271376] Chr3:113953990 [GRCh38]
Chr3:113672837 [GRCh37]
Chr3:3q13.31		 uncertain significance
NC_000003.11:g.(?_113503051)_(114070745_?)dup duplication not provided [RCV003105597] Chr3:113503051..114070745 [GRCh37]
Chr3:3q13.31		 uncertain significance
NC_000003.11:g.(?_113010404)_(114099634_?)del deletion not provided [RCV003105596] Chr3:113010404..114099634 [GRCh37]
Chr3:3q13.2-13.31		 uncertain significance
GRCh37/hg19 3q13.2-13.32(chr3:113233952-118525556)x1 copy number loss See cases [RCV001194596] Chr3:113233952..118525556 [GRCh37]
Chr3:3q13.2-13.32		 pathogenic
GRCh37/hg19 3q13.2-13.31(chr3:112135341-115509260)x3 copy number gain not provided [RCV001259226] Chr3:112135341..115509260 [GRCh37]
Chr3:3q13.2-13.31		 pathogenic
GRCh37/hg19 3q13.31(chr3:113623035-114368128)x1 copy number loss Chromosome 3q13.31 deletion syndrome [RCV001391300] Chr3:113623035..114368128 [GRCh37]
Chr3:3q13.31		 pathogenic
GRCh37/hg19 3q13.2-13.31(chr3:112144081-115514432) copy number loss not specified [RCV002053367] Chr3:112144081..115514432 [GRCh37]
Chr3:3q13.2-13.31		 pathogenic
NM_001320466.2(ZDHHC23):c.829A>G (p.Ile277Val) single nucleotide variant Inborn genetic diseases [RCV003282602] Chr3:113954367 [GRCh38]
Chr3:113673214 [GRCh37]
Chr3:3q13.31		 uncertain significance
GRCh37/hg19 3q13.12-13.31(chr3:107059705-115005256)x1 copy number loss not provided [RCV002472579] Chr3:107059705..115005256 [GRCh37]
Chr3:3q13.12-13.31		 pathogenic
NM_001320466.2(ZDHHC23):c.352A>T (p.Thr118Ser) single nucleotide variant Inborn genetic diseases [RCV002689862] Chr3:113953890 [GRCh38]
Chr3:113672737 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_020817.2(CCDC191):c.2369G>A (p.Arg790His) single nucleotide variant Inborn genetic diseases [RCV002783882] Chr3:113978949 [GRCh38]
Chr3:113697796 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_020817.2(CCDC191):c.2399C>T (p.Ala800Val) single nucleotide variant Inborn genetic diseases [RCV002925274] Chr3:113978919 [GRCh38]
Chr3:113697766 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_020817.2(CCDC191):c.2515A>C (p.Lys839Gln) single nucleotide variant Inborn genetic diseases [RCV002704705] Chr3:113978277 [GRCh38]
Chr3:113697124 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.997T>G (p.Phe333Val) single nucleotide variant Inborn genetic diseases [RCV002956457] Chr3:113956463 [GRCh38]
Chr3:113675310 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_020817.2(CCDC191):c.2416T>G (p.Tyr806Asp) single nucleotide variant Inborn genetic diseases [RCV002983566] Chr3:113978902 [GRCh38]
Chr3:113697749 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_020817.2(CCDC191):c.2429T>C (p.Leu810Pro) single nucleotide variant Inborn genetic diseases [RCV002703218] Chr3:113978889 [GRCh38]
Chr3:113697736 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.*2099G>A single nucleotide variant Inborn genetic diseases [RCV002747747] Chr3:113960729 [GRCh38]
Chr3:113679576 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_020817.2(CCDC191):c.2752G>A (p.Glu918Lys) single nucleotide variant Inborn genetic diseases [RCV002680429] Chr3:113965214 [GRCh38]
Chr3:113684061 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.524C>G (p.Thr175Ser) single nucleotide variant Inborn genetic diseases [RCV003175633] Chr3:113954062 [GRCh38]
Chr3:113672909 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_020817.2(CCDC191):c.2687G>A (p.Arg896Gln) single nucleotide variant Inborn genetic diseases [RCV003172855] Chr3:113965279 [GRCh38]
Chr3:113684126 [GRCh37]
Chr3:3q13.31		 uncertain significance
GRCh37/hg19 3q13.13-13.31(chr3:110966195-115843176)x1 copy number loss Chromosome 3q13.31 deletion syndrome [RCV003222552] Chr3:110966195..115843176 [GRCh37]
Chr3:3q13.13-13.31		 pathogenic
NM_020817.2(CCDC191):c.2734G>A (p.Val912Ile) single nucleotide variant Inborn genetic diseases [RCV003218721] Chr3:113965232 [GRCh38]
Chr3:113684079 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.403A>C (p.Lys135Gln) single nucleotide variant Inborn genetic diseases [RCV003195467] Chr3:113953941 [GRCh38]
Chr3:113672788 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.758C>T (p.Pro253Leu) single nucleotide variant Inborn genetic diseases [RCV003185519] Chr3:113954296 [GRCh38]
Chr3:113673143 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.1043C>T (p.Ser348Leu) single nucleotide variant Inborn genetic diseases [RCV003191064] Chr3:113958365 [GRCh38]
Chr3:113677212 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.831A>G (p.Ile277Met) single nucleotide variant Inborn genetic diseases [RCV003197392] Chr3:113954369 [GRCh38]
Chr3:113673216 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.869T>A (p.Val290Asp) single nucleotide variant Inborn genetic diseases [RCV003309061] Chr3:113954407 [GRCh38]
Chr3:113673254 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_001320466.2(ZDHHC23):c.7C>G (p.Gln3Glu) single nucleotide variant Inborn genetic diseases [RCV003266115] Chr3:113948809 [GRCh38]
Chr3:113667656 [GRCh37]
Chr3:3q13.31		 uncertain significance
GRCh38/hg38 3q11.1-21.2(chr3:93979547-124774010)x1 copy number loss Chromosome 3q13.31 deletion syndrome [RCV003327614] Chr3:93979547..124774010 [GRCh38]
Chr3:3q11.1-21.2		 pathogenic
NM_020817.2(CCDC191):c.2350A>C (p.Met784Leu) single nucleotide variant Inborn genetic diseases [RCV003360192] Chr3:113978968 [GRCh38]
Chr3:113697815 [GRCh37]
Chr3:3q13.31		 likely benign
NM_020817.2(CCDC191):c.2363T>C (p.Phe788Ser) single nucleotide variant Inborn genetic diseases [RCV003346843] Chr3:113978955 [GRCh38]
Chr3:113697802 [GRCh37]
Chr3:3q13.31		 uncertain significance
NM_020817.2(CCDC191):c.2722C>T (p.Pro908Ser) single nucleotide variant Inborn genetic diseases [RCV003376067] Chr3:113965244 [GRCh38]
Chr3:113684091 [GRCh37]
Chr3:3q13.31		 uncertain significance
GRCh37/hg19 3q13.13-13.31(chr3:110398276-113879363)x1 copy number loss not provided [RCV003485398] Chr3:110398276..113879363 [GRCh37]
Chr3:3q13.13-13.31		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2318
Count of miRNA genes:869
Interacting mature miRNAs:1042
Transcripts:ENST00000330212, ENST00000478793, ENST00000488129, ENST00000491556, ENST00000496083, ENST00000498275
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.

Markers in Region
D3S3585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373113,674,140 - 113,674,408UniSTSGRCh37
Build 363115,156,830 - 115,157,098RGDNCBI36
Celera3112,082,592 - 112,082,858RGD
Cytogenetic Map3q13.31UniSTS
HuRef3111,048,189 - 111,048,455UniSTS
Marshfield Genetic Map3129.73UniSTS
Marshfield Genetic Map3129.73RGD
Genethon Genetic Map3132.1UniSTS
Whitehead-YAC Contig Map3 UniSTS
GeneMap99-G3 RH Map35530.0UniSTS
RH12338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373113,680,473 - 113,680,629UniSTSGRCh37
Build 363115,163,163 - 115,163,319RGDNCBI36
Celera3112,088,922 - 112,089,078RGD
Cytogenetic Map3q13.31UniSTS
HuRef3111,054,519 - 111,054,675UniSTS
GeneMap99-GB4 RH Map3411.59UniSTS
RH93691  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373113,665,590 - 113,665,713UniSTSGRCh37
Build 363115,148,280 - 115,148,403RGDNCBI36
Celera3112,074,041 - 112,074,164RGD
Cytogenetic Map3q13.31UniSTS
HuRef3111,039,589 - 111,039,712UniSTS
GeneMap99-GB4 RH Map3393.8UniSTS
D3S2836E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373113,681,696 - 113,681,795UniSTSGRCh37
Build 363115,164,386 - 115,164,485RGDNCBI36
Celera3112,090,145 - 112,090,244RGD
Cytogenetic Map3q13.31UniSTS
HuRef3111,055,742 - 111,055,841UniSTS
D3S3313  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373113,681,602 - 113,681,801UniSTSGRCh37
Build 363115,164,292 - 115,164,491RGDNCBI36
Celera3112,090,051 - 112,090,250RGD
Cytogenetic Map3q13.31UniSTS
HuRef3111,055,648 - 111,055,847UniSTS
GeneMap99-GB4 RH Map3411.49UniSTS
Whitehead-RH Map3512.8UniSTS
Whitehead-YAC Contig Map3 UniSTS
NCBI RH Map3919.7UniSTS
G20226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373113,681,595 - 113,681,710UniSTSGRCh37
Build 363115,164,285 - 115,164,400RGDNCBI36
Celera3112,090,044 - 112,090,159RGD
Cytogenetic Map3q13.31UniSTS
HuRef3111,055,641 - 111,055,756UniSTS
A005A39  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373113,681,595 - 113,681,710UniSTSGRCh37
Build 363115,164,285 - 115,164,400RGDNCBI36
Celera3112,090,044 - 112,090,159RGD
Cytogenetic Map3q13.31UniSTS
HuRef3111,055,641 - 111,055,756UniSTS
GeneMap99-GB4 RH Map3412.11UniSTS
NCBI RH Map3928.3UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 344 1 638 34 224 32 86 12 288 75 500 683 8 3
Low 2073 2221 1057 584 1125 427 4012 1790 3206 340 948 921 164 1198 2547 4 1
Below cutoff 17 759 28 5 592 6 257 390 224 4 4 4 6 238

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001320466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001320467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001320468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363952 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_173570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005247269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005247270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006713562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011512618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011512619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017006084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017006086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017006087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447891 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447893 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447894 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345989 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345991 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345993 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345994 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345996 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345997 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345998 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345999 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054346000 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054346001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054346002 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054346003 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054346004 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054346005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001740079 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001740080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001740081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007095654 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007095655 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007095656 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007095657 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007095658 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486683 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486685 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486687 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486691 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486692 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_924118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_924119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC128687 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF131818 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK022842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK127025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK127260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK127996 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC035230 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA389626 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000330212   ⟹   ENSP00000330485
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl3113,947,901 - 113,962,982 (+)Ensembl
RefSeq Acc Id: ENST00000478793   ⟹   ENSP00000420251
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl3113,948,065 - 113,962,978 (+)Ensembl
RefSeq Acc Id: ENST00000488129
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl3113,957,574 - 113,963,364 (+)Ensembl
RefSeq Acc Id: ENST00000491556   ⟹   ENSP00000420292
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl3113,948,507 - 113,953,982 (+)Ensembl
RefSeq Acc Id: ENST00000496083   ⟹   ENSP00000417579
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl3113,958,454 - 113,965,401 (+)Ensembl
RefSeq Acc Id: ENST00000498275   ⟹   ENSP00000417840
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl3113,947,975 - 113,961,314 (+)Ensembl
RefSeq Acc Id: ENST00000638807   ⟹   ENSP00000492287
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl3113,948,013 - 113,963,373 (+)Ensembl
RefSeq Acc Id: NM_001320466   ⟹   NP_001307395
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,948,013 - 113,963,373 (+)NCBI
CHM1_13113,630,124 - 113,645,590 (+)NCBI
T2T-CHM13v2.03116,669,277 - 116,684,637 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001320467   ⟹   NP_001307396
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,948,013 - 113,963,373 (+)NCBI
CHM1_13113,630,124 - 113,645,590 (+)NCBI
T2T-CHM13v2.03116,669,277 - 116,684,637 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001320468   ⟹   NP_001307397
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,948,013 - 113,963,373 (+)NCBI
CHM1_13113,630,124 - 113,645,590 (+)NCBI
T2T-CHM13v2.03116,669,277 - 116,684,637 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363952   ⟹   NP_001350881
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
Sequence:
RefSeq Acc Id: NM_173570   ⟹   NP_775841
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,948,013 - 113,963,373 (+)NCBI
GRCh373113,666,748 - 113,705,706 (+)NCBI
Build 363115,149,438 - 115,164,519 (+)NCBI Archive
Celera3112,075,199 - 112,090,278 (+)RGD
HuRef3111,040,938 - 111,055,875 (+)ENTREZGENE
CHM1_13113,630,124 - 113,645,590 (+)NCBI
T2T-CHM13v2.03116,669,277 - 116,684,637 (+)NCBI
Sequence:
RefSeq Acc Id: NR_135271
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,948,013 - 113,963,373 (+)NCBI
CHM1_13113,630,124 - 113,645,590 (+)NCBI
T2T-CHM13v2.03116,669,277 - 116,684,637 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005247269   ⟹   XP_005247326
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
GRCh373113,666,748 - 113,705,706 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005247270   ⟹   XP_005247327
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
GRCh373113,666,748 - 113,705,706 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006713562   ⟹   XP_006713625
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,979,508 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011512618   ⟹   XP_011510920
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011512619   ⟹   XP_011510921
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017006084   ⟹   XP_016861573
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017006086   ⟹   XP_016861575
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017006087   ⟹   XP_016861576
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047447882   ⟹   XP_047303838
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_047447883   ⟹   XP_047303839
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_047447885   ⟹   XP_047303841
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,979,508 (+)NCBI
RefSeq Acc Id: XM_047447886   ⟹   XP_047303842
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,978,427 (+)NCBI
RefSeq Acc Id: XM_047447887   ⟹   XP_047303843
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_047447888   ⟹   XP_047303844
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_047447890   ⟹   XP_047303846
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_047447891   ⟹   XP_047303847
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_047447892   ⟹   XP_047303848
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_047447893   ⟹   XP_047303849
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_047447894   ⟹   XP_047303850
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,948,580 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_047447895   ⟹   XP_047303851
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XM_054345987   ⟹   XP_054201962
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345988   ⟹   XP_054201963
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345989   ⟹   XP_054201964
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345990   ⟹   XP_054201965
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345991   ⟹   XP_054201966
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,699,974 (+)NCBI
RefSeq Acc Id: XM_054345992   ⟹   XP_054201967
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,699,974 (+)NCBI
RefSeq Acc Id: XM_054345993   ⟹   XP_054201968
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345994   ⟹   XP_054201969
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345995   ⟹   XP_054201970
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345996   ⟹   XP_054201971
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345997   ⟹   XP_054201972
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345998   ⟹   XP_054201973
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054345999   ⟹   XP_054201974
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054346000   ⟹   XP_054201975
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054346001   ⟹   XP_054201976
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054346002   ⟹   XP_054201977
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054346003   ⟹   XP_054201978
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054346004   ⟹   XP_054201979
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,756 - 116,684,637 (+)NCBI
RefSeq Acc Id: XM_054346005   ⟹   XP_054201980
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XR_001740081
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,978,427 (+)NCBI
Sequence:
RefSeq Acc Id: XR_007095654
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XR_007095655
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XR_007095656
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XR_007095657
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XR_007095658
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
RefSeq Acc Id: XR_008486683
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XR_008486684
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XR_008486685
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,708,864 (+)NCBI
RefSeq Acc Id: XR_008486686
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,713,494 (+)NCBI
RefSeq Acc Id: XR_008486687
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,719,588 (+)NCBI
RefSeq Acc Id: XR_008486688
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,713,497 (+)NCBI
RefSeq Acc Id: XR_008486689
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XR_008486690
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,699,645 (+)NCBI
RefSeq Acc Id: XR_008486691
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XR_008486692
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XR_008486693
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.03116,669,165 - 116,684,637 (+)NCBI
RefSeq Acc Id: XR_924119
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,901 - 113,963,373 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001307395 (Get FASTA)   NCBI Sequence Viewer  
  NP_001307396 (Get FASTA)   NCBI Sequence Viewer  
  NP_001307397 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350881 (Get FASTA)   NCBI Sequence Viewer  
  NP_775841 (Get FASTA)   NCBI Sequence Viewer  
  XP_005247326 (Get FASTA)   NCBI Sequence Viewer  
  XP_005247327 (Get FASTA)   NCBI Sequence Viewer  
  XP_006713625 (Get FASTA)   NCBI Sequence Viewer  
  XP_011510920 (Get FASTA)   NCBI Sequence Viewer  
  XP_011510921 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861573 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861575 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861576 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303838 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303839 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303841 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303842 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303843 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303844 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303846 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303847 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303848 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303849 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303850 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303851 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201962 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201963 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201964 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201965 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201966 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201967 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201968 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201969 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201970 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201971 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201972 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201973 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201974 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201975 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201976 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201977 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201978 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201979 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201980 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH35230 (Get FASTA)   NCBI Sequence Viewer  
  BAG54425 (Get FASTA)   NCBI Sequence Viewer  
  BAG54615 (Get FASTA)   NCBI Sequence Viewer  
  EAW79616 (Get FASTA)   NCBI Sequence Viewer  
  EAW79617 (Get FASTA)   NCBI Sequence Viewer  
  EAW79618 (Get FASTA)   NCBI Sequence Viewer  
  EAW79619 (Get FASTA)   NCBI Sequence Viewer  
  EAW79620 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000330485
  ENSP00000330485.3
  ENSP00000417579.1
  ENSP00000417840
  ENSP00000417840.1
  ENSP00000420251
  ENSP00000420251.1
  ENSP00000420292.1
  ENSP00000492287
  ENSP00000492287.2
GenBank Protein Q8IYP9 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_775841   ⟸   NM_173570
- Peptide Label: isoform c
- UniProtKB: D3DN76 (UniProtKB/Swiss-Prot),   Q8IYP9 (UniProtKB/Swiss-Prot),   B3KXV3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005247326   ⟸   XM_005247269
- Peptide Label: isoform X6
- UniProtKB: D3DN76 (UniProtKB/Swiss-Prot),   Q8IYP9 (UniProtKB/Swiss-Prot),   B3KXV3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005247327   ⟸   XM_005247270
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_006713625   ⟸   XM_006713562
- Peptide Label: isoform X3
- UniProtKB: B3KXB3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011510920   ⟸   XM_011512618
- Peptide Label: isoform X1
- UniProtKB: A0A1W2PRJ8 (UniProtKB/TrEMBL),   B3KXB3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011510921   ⟸   XM_011512619
- Peptide Label: isoform X4
- UniProtKB: E9PAP7 (UniProtKB/TrEMBL),   B3KXB3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001307395   ⟸   NM_001320466
- Peptide Label: isoform a
- UniProtKB: A0A1W2PRJ8 (UniProtKB/TrEMBL),   B3KXB3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001307397   ⟸   NM_001320468
- Peptide Label: isoform b
- UniProtKB: B3KXB3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001307396   ⟸   NM_001320467
- Peptide Label: isoform a
- UniProtKB: A0A1W2PRJ8 (UniProtKB/TrEMBL),   B3KXB3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016861576   ⟸   XM_017006087
- Peptide Label: isoform X5
- UniProtKB: B3KXB3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016861573   ⟸   XM_017006084
- Peptide Label: isoform X2
- UniProtKB: B3KXB3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016861575   ⟸   XM_017006086
- Peptide Label: isoform X7
- UniProtKB: B3KXV3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001350881   ⟸   NM_001363952
- Peptide Label: isoform d
- UniProtKB: E9PAP7 (UniProtKB/TrEMBL),   B3KXB3 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000420251   ⟸   ENST00000478793
RefSeq Acc Id: ENSP00000420292   ⟸   ENST00000491556
RefSeq Acc Id: ENSP00000492287   ⟸   ENST00000638807
RefSeq Acc Id: ENSP00000417579   ⟸   ENST00000496083
RefSeq Acc Id: ENSP00000417840   ⟸   ENST00000498275
RefSeq Acc Id: ENSP00000330485   ⟸   ENST00000330212
RefSeq Acc Id: XP_047303841   ⟸   XM_047447885
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047303842   ⟸   XM_047447886
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047303843   ⟸   XM_047447887
- Peptide Label: isoform X4
- UniProtKB: E9PAP7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047303839   ⟸   XM_047447883
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047303846   ⟸   XM_047447890
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047303851   ⟸   XM_047447895
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047303838   ⟸   XM_047447882
- Peptide Label: isoform X1
- UniProtKB: A0A1W2PRJ8 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047303847   ⟸   XM_047447891
- Peptide Label: isoform X6
- UniProtKB: Q8IYP9 (UniProtKB/Swiss-Prot),   D3DN76 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047303849   ⟸   XM_047447893
- Peptide Label: isoform X8
RefSeq Acc Id: XP_047303844   ⟸   XM_047447888
- Peptide Label: isoform X4
- UniProtKB: E9PAP7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047303848   ⟸   XM_047447892
- Peptide Label: isoform X6
- UniProtKB: Q8IYP9 (UniProtKB/Swiss-Prot),   D3DN76 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047303850   ⟸   XM_047447894
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054201967   ⟸   XM_054345992
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054201966   ⟸   XM_054345991
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054201971   ⟸   XM_054345996
- Peptide Label: isoform X4
- UniProtKB: E9PAP7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054201964   ⟸   XM_054345989
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054201974   ⟸   XM_054345999
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054201980   ⟸   XM_054346005
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054201963   ⟸   XM_054345988
- Peptide Label: isoform X1
- UniProtKB: A0A1W2PRJ8 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054201975   ⟸   XM_054346000
- Peptide Label: isoform X6
- UniProtKB: Q8IYP9 (UniProtKB/Swiss-Prot),   D3DN76 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054201977   ⟸   XM_054346002
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054201968   ⟸   XM_054345993
- Peptide Label: isoform X4
- UniProtKB: E9PAP7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054201970   ⟸   XM_054345995
- Peptide Label: isoform X6
- UniProtKB: Q8IYP9 (UniProtKB/Swiss-Prot),   D3DN76 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054201969   ⟸   XM_054345994
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054201973   ⟸   XM_054345998
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054201962   ⟸   XM_054345987
- Peptide Label: isoform X1
- UniProtKB: A0A1W2PRJ8 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054201972   ⟸   XM_054345997
- Peptide Label: isoform X4
- UniProtKB: E9PAP7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054201976   ⟸   XM_054346001
- Peptide Label: isoform X6
- UniProtKB: Q8IYP9 (UniProtKB/Swiss-Prot),   D3DN76 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054201965   ⟸   XM_054345990
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054201978   ⟸   XM_054346003
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054201979   ⟸   XM_054346004
- Peptide Label: isoform X9
Protein Domains
DHHC   Palmitoyltransferase DHHC

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8IYP9-F1-model_v2 AlphaFold Q8IYP9 1-409 view protein structure

Promoters
RGD ID:6865290
Promoter ID:EPDNEW_H5810
Type:initiation region
Name:ZDHHC23_1
Description:zinc finger DHHC-type containing 23
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh383113,947,906 - 113,947,966EPDNEW
RGD ID:6801969
Promoter ID:HG_KWN:45873
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Lymphoblastoid,   NB4
Transcripts:ENST00000393809,   NM_173570,   UC003EAV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 363115,149,031 - 115,149,627 (+)MPROMDB
RGD ID:6814717
Promoter ID:HG_XEF:5567
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour
Transcripts:NM_001003757,   NM_001007460,   NM_213627
Position:
Human AssemblyChrPosition (strand)Source
Build 363115,149,756 - 115,150,256 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:28654 AgrOrtholog
COSMIC ZDHHC23 COSMIC
Ensembl Genes ENSG00000184307 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000330212 ENTREZGENE
  ENST00000330212.7 UniProtKB/Swiss-Prot
  ENST00000478793 ENTREZGENE
  ENST00000478793.1 UniProtKB/TrEMBL
  ENST00000491556.1 UniProtKB/TrEMBL
  ENST00000496083.1 UniProtKB/TrEMBL
  ENST00000498275 ENTREZGENE
  ENST00000498275.5 UniProtKB/TrEMBL
  ENST00000638807 ENTREZGENE
  ENST00000638807.2 UniProtKB/TrEMBL
GTEx ENSG00000184307 GTEx
HGNC ID HGNC:28654 ENTREZGENE
Human Proteome Map ZDHHC23 Human Proteome Map
InterPro Palmitoyltrfase_DHHC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:254887 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 254887 ENTREZGENE
OMIM 617334 OMIM
PANTHER PALMITOYLTRANSFERASE ZDHHC23 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC FINGER DHHC DOMAIN CONTAINING PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DHHC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134960347 PharmGKB
PROSITE DHHC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A1W2PRJ8 ENTREZGENE, UniProtKB/TrEMBL
  B3KXB3 ENTREZGENE, UniProtKB/TrEMBL
  B3KXV3 ENTREZGENE, UniProtKB/TrEMBL
  C9JPJ8_HUMAN UniProtKB/TrEMBL
  D3DN76 ENTREZGENE
  E9PAP7 ENTREZGENE, UniProtKB/TrEMBL
  H7C4L2_HUMAN UniProtKB/TrEMBL
  Q8IYP9 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary D3DN76 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-10-22 ZDHHC23  zinc finger DHHC-type palmitoyltransferase 23  ZDHHC23  zinc finger DHHC-type containing 23  Symbol and/or name change 5135510 APPROVED
2016-02-18 ZDHHC23  zinc finger DHHC-type containing 23    zinc finger, DHHC-type containing 23  Symbol and/or name change 5135510 APPROVED