ZNF346 (zinc finger protein 346) - Rat Genome Database

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Gene: ZNF346 (zinc finger protein 346) Homo sapiens
Analyze
Symbol: ZNF346
Name: zinc finger protein 346
RGD ID: 1317625
HGNC Page HGNC:16403
Description: Enables double-stranded RNA binding activity; enzyme binding activity; and miRNA binding activity. Predicted to act upstream of or within positive regulation of apoptotic process. Located in nucleolus and nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DKFZp547M223; double-stranded RNA-binding zinc finger protein JAZ; JAZ; just another zinc finger protein; Zfp346
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385177,022,696 - 177,081,189 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5177,022,696 - 177,081,189 (+)EnsemblGRCh38hg38GRCh38
GRCh375176,449,697 - 176,508,190 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365176,382,303 - 176,426,364 (+)NCBINCBI36Build 36hg18NCBI36
Build 345176,382,302 - 176,426,349NCBI
Celera5172,007,563 - 172,051,635 (-)NCBICelera
Cytogenetic Map5q35.2NCBI
HuRef5171,371,845 - 171,415,482 (+)NCBIHuRef
CHM1_15175,882,099 - 175,926,642 (+)NCBICHM1_1
T2T-CHM13v2.05177,565,869 - 177,624,397 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
ZNF346HumanChromosome 5, Trisomy 5q  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: 5q35 microduplication syndromeClinVarPMID:31690835
ZNF346HumanEhlers-Danlos syndrome dermatosparaxis type  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Ehlers-Danlos syndrome and dermatosparaxis typeClinVarPMID:16770806 more ...
ZNF346HumanEhlers-Danlos syndrome spondylodysplastic type 2  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Ehlers-Danlos syndrome progeroid typeClinVarPMID:28492532
ZNF346HumanMarfanoid Mental Retardation Syndrome, Autosomal  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Marfanoid habitus and intellectual disabilityClinVarPMID:25741868
ZNF346HumanSilver-Russell syndrome  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Russell-Silver syndromeClinVarPMID:27172843
ZNF346HumanSotos syndrome  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Sotos syndromeClinVarPMID:12464997 more ...
ZNF346HumanSotos syndrome  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Sotos syndromeClinVarPMID:16770806 more ...

1 to 20 of 59 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
ZNF346Human(-)-alpha-phellandrene decreases expressionEXP 6480464alpha phellandrene results in decreased expression of ZFP346 mRNACTDPMID:25075043
ZNF346Human17beta-estradiol decreases expressionISOZfp346 (Rattus norvegicus)6480464Estradiol results in decreased expression of ZFP346 mRNACTDPMID:32145629
ZNF346Human2,3,7,8-tetrachlorodibenzodioxine affects expressionISOZfp346 (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of ZFP346 mRNACTDPMID:21570461
ZNF346Human2,3,7,8-tetrachlorodibenzodioxine increases expressionISOZfp346 (Rattus norvegicus)6480464Tetrachlorodibenzodioxin results in increased expression of ZFP346 mRNACTDPMID:33387578
ZNF346Human3,3',5,5'-tetrabromobisphenol A increases expressionISOZfp346 (Rattus norvegicus)6480464tetrabromobisphenol A results in increased expression of ZNF346 mRNACTDPMID:27914987
ZNF346Human3,4-methylenedioxymethamphetamine decreases expressionISOZfp346 (Mus musculus)6480464N-Methyl-3 and 4-methylenedioxyamphetamine results in decreased expression of ZFP346 mRNACTDPMID:26251327
ZNF346Humanaflatoxin B1 increases expressionISOZfp346 (Mus musculus)6480464Aflatoxin B1 results in increased expression of ZFP346 mRNACTDPMID:19770486
ZNF346Humanalpha-phellandrene decreases expressionEXP 6480464alpha phellandrene results in decreased expression of ZFP346 mRNACTDPMID:25075043
ZNF346Humanantirheumatic drug increases expressionEXP 6480464Antirheumatic Agents results in increased expression of ZNF346 mRNACTDPMID:24449571
ZNF346Humanaristolochic acid A increases expressionEXP 6480464aristolochic acid I results in increased expression of ZNF346 mRNACTDPMID:33212167
ZNF346Humanarsane affects methylationEXP 6480464Arsenic affects the methylation of ZNF346 geneCTDPMID:25304211
ZNF346Humanarsenic atom affects methylationEXP 6480464Arsenic affects the methylation of ZNF346 geneCTDPMID:25304211
ZNF346Humanatrazine decreases expressionEXP 6480464Atrazine results in decreased expression of ZNF346 mRNACTDPMID:22378314
ZNF346Humanbenzo[a]pyrene increases expressionISOZfp346 (Mus musculus)6480464Benzo(a)pyrene results in increased expression of ZFP346 mRNACTDPMID:22228805
ZNF346Humanbenzo[a]pyrene multiple interactionsISOZfp346 (Mus musculus)6480464[Benzo(a)pyrene co-treated with benz(a)anthracene co-treated with benzo(b)fluoranthene co-treated with chrysene] results in increased expression of ZFP346 mRNACTDPMID:27858113
ZNF346Humanbenzo[b]fluoranthene multiple interactionsISOZfp346 (Mus musculus)6480464[Benzo(a)pyrene co-treated with benz(a)anthracene co-treated with benzo(b)fluoranthene co-treated with chrysene] results in increased expression of ZFP346 mRNACTDPMID:27858113
ZNF346Humanbisphenol A affects expressionISOZfp346 (Rattus norvegicus)6480464bisphenol A affects the expression of ZNF346 mRNACTDPMID:25181051
ZNF346Humanbisphenol A multiple interactionsEXP 6480464[bisphenol A co-treated with Fulvestrant] results in increased methylation of ZNF346 geneCTDPMID:31601247
ZNF346Humanbisphenol A increases expressionISOZfp346 (Rattus norvegicus)6480464bisphenol A results in increased expression of ZFP346 mRNACTDPMID:34947998
ZNF346Humanbisphenol A decreases expressionEXP 6480464bisphenol A results in decreased expression of ZNF346 mRNACTDPMID:29275510

1 to 20 of 59 rows

Biological Process

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
ZNF346Humanpositive regulation of apoptotic process acts_upstream_of_or_withinISOZfp346 (Mus musculus)9068941 PMID:10488071MGIPMID:10488071

Cellular Component

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
ZNF346Humancytoplasm located_inIEAUniProtKB-KW:KW-0963150520179 UniProtGO_REF:0000043
ZNF346Humancytoplasm located_inIEAUniProtKB-SubCell:SL-0086150520179 UniProtGO_REF:0000044
ZNF346Humannucleolus located_inIEAUniProtKB-SubCell:SL-0188150520179 UniProtGO_REF:0000044
ZNF346Humannucleolus located_inIDA 150520179 PMID:10488071UniProtGO_REF:0000054 and PMID:10488071
ZNF346Humannucleoplasm located_inIDA 150520179 HPAGO_REF:0000052
ZNF346Humannucleus located_inIEAUniProtKB-SubCell:SL-0191150520179 UniProtGO_REF:0000044
ZNF346Humannucleus located_inIDA 150520179 PMID:10488071UniProtPMID:10488071
ZNF346Humannucleus located_inIEAUniProtKB-KW:KW-0539150520179 UniProtGO_REF:0000043

Molecular Function
1 to 15 of 15 rows

  
1 to 15 of 15 rows


#
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
PMID:10488071   PMID:11076863   PMID:11230166   PMID:11256614   PMID:12477932   PMID:14702039   PMID:15254228   PMID:15489334   PMID:15489336   PMID:16344560   PMID:16381901   PMID:18029348  
PMID:19828471   PMID:20020773   PMID:21145461   PMID:21715977   PMID:21873635   PMID:21903422   PMID:21913182   PMID:21988832   PMID:22681889   PMID:23382074   PMID:24457600   PMID:24521053  
PMID:24778252   PMID:25331946   PMID:25416956   PMID:25544563   PMID:25875936   PMID:26186194   PMID:26496610   PMID:28208259   PMID:28431233   PMID:28514442   PMID:28524877   PMID:28712289  
PMID:29229926   PMID:29395067   PMID:29845934   PMID:30196744   PMID:31091453   PMID:31527615   PMID:32203420   PMID:32296183   PMID:32433965   PMID:32707033   PMID:32814053   PMID:33060197  
PMID:33301849   PMID:33658012   PMID:33961781   PMID:34079125   PMID:34578187   PMID:34650049   PMID:35013218   PMID:35271311   PMID:35915203   PMID:35944360   PMID:36232890   PMID:36273042  
PMID:36373674   PMID:36537216   PMID:36834567   PMID:36949045   PMID:37314180   PMID:37314216   PMID:37723588  



ZNF346
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385177,022,696 - 177,081,189 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5177,022,696 - 177,081,189 (+)EnsemblGRCh38hg38GRCh38
GRCh375176,449,697 - 176,508,190 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365176,382,303 - 176,426,364 (+)NCBINCBI36Build 36hg18NCBI36
Build 345176,382,302 - 176,426,349NCBI
Celera5172,007,563 - 172,051,635 (-)NCBICelera
Cytogenetic Map5q35.2NCBI
HuRef5171,371,845 - 171,415,482 (+)NCBIHuRef
CHM1_15175,882,099 - 175,926,642 (+)NCBICHM1_1
T2T-CHM13v2.05177,565,869 - 177,624,397 (+)NCBIT2T-CHM13v2.0
Zfp346
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391355,253,079 - 55,282,884 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1355,253,124 - 55,282,638 (+)EnsemblGRCm39 Ensembl
GRCm381355,105,271 - 55,135,071 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1355,105,311 - 55,134,825 (+)EnsemblGRCm38mm10GRCm38
MGSCv371355,206,670 - 55,236,432 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361355,114,933 - 55,144,438 (+)NCBIMGSCv36mm8
Celera1356,166,301 - 56,196,016 (+)NCBICelera
Cytogenetic Map13B1NCBI
cM Map1329.8NCBI
Zfp346
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8179,498,933 - 9,528,824 (-)NCBIGRCr8
mRatBN7.2179,493,787 - 9,523,681 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl179,493,803 - 9,523,635 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx179,510,640 - 9,541,007 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01711,039,927 - 11,069,987 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0179,507,045 - 9,537,410 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01710,021,596 - 10,061,803 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1710,021,420 - 10,061,772 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01712,130,909 - 12,168,917 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41715,544,785 - 15,575,512 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11715,547,045 - 15,575,515 (-)NCBI
Celera179,571,731 - 9,601,487 (-)NCBICelera
Cytogenetic Map17p14NCBI
Znf346
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540829,312,274 - 29,349,316 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540829,312,273 - 29,346,983 (+)NCBIChiLan1.0ChiLan1.0
ZNF346
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v24172,104,227 - 172,165,684 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan15170,243,769 - 170,307,038 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v05172,321,875 - 172,386,462 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.15179,390,239 - 179,449,071 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl5179,390,239 - 179,449,071 (+)Ensemblpanpan1.1panPan2
ZNF346
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1436,269,126 - 36,303,647 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl436,271,853 - 36,303,594 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha436,235,147 - 36,269,673 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0436,633,379 - 36,667,914 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl436,633,413 - 36,667,875 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1436,460,298 - 36,494,813 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0436,647,499 - 36,682,090 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0437,155,749 - 37,190,501 (-)NCBIUU_Cfam_GSD_1.0
Znf346
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213122,286,077 - 122,338,890 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365971,310,999 - 1,366,227 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365971,311,007 - 1,363,731 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZNF346
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl280,871,595 - 80,895,585 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1280,871,576 - 80,895,592 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2282,445,038 - 82,469,063 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ZNF346
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12379,010,203 - 79,072,063 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2379,027,548 - 79,070,705 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607510,173,143 - 10,236,987 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Znf346
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473312,995,358 - 13,068,150 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473312,997,728 - 13,057,640 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in ZNF346
31 total Variants

1 to 10 of 97 rows
Name
Type
Condition(s)
Position(s)
Clinical significance
GRCh38/hg38 5q35.2-35.3(chr5:176132340-177586960)x1 copy number loss See cases [RCV000050645] Chr5:176132340..177586960 [GRCh38]
Chr5:175559343..177013961 [GRCh37]
Chr5:175491949..176946567 [NCBI36]
Chr5:5q35.2-35.3
pathogenic
GRCh38/hg38 5q32-35.3(chr5:149714592-181272151)x3 copy number gain See cases [RCV000051863] Chr5:149714592..181272151 [GRCh38]
Chr5:149094155..180699152 [GRCh37]
Chr5:149074348..180631758 [NCBI36]
Chr5:5q32-35.3
pathogenic
GRCh38/hg38 5q33.3-35.3(chr5:160029980-181269805)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051865]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051865]|See cases [RCV000051865] Chr5:160029980..181269805 [GRCh38]
Chr5:159456987..180696806 [GRCh37]
Chr5:159389565..180629412 [NCBI36]
Chr5:5q33.3-35.3
pathogenic
GRCh38/hg38 5q34-35.3(chr5:168689326-181269946)x3 copy number gain See cases [RCV000051866] Chr5:168689326..181269946 [GRCh38]
Chr5:168116331..180696947 [GRCh37]
Chr5:168048909..180629553 [NCBI36]
Chr5:5q34-35.3
pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:175851047-178365049)x3 copy number gain See cases [RCV000051867] Chr5:175851047..178365049 [GRCh38]
Chr5:175278050..177792050 [GRCh37]
Chr5:175210656..177724656 [NCBI36]
Chr5:5q35.2-35.3
pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:175889986-180793986)x3 copy number gain See cases [RCV000051868] Chr5:175889986..180793986 [GRCh38]
Chr5:175316989..180220986 [GRCh37]
Chr5:175249595..180153592 [NCBI36]
Chr5:5q35.2-35.3
pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:175007241-179089812)x1 copy number loss See cases [RCV000052151] Chr5:175007241..179089812 [GRCh38]
Chr5:174434244..178516813 [GRCh37]
Chr5:174366850..178449419 [NCBI36]
Chr5:5q35.2-35.3
pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176043476-177995759)x1 copy number loss See cases [RCV000053127] Chr5:176043476..177995759 [GRCh38]
Chr5:175470479..177422760 [GRCh37]
Chr5:175403085..177355366 [NCBI36]
Chr5:5q35.2-35.3
pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176115257-177646633)x1 copy number loss See cases [RCV000053128] Chr5:176115257..177646633 [GRCh38]
Chr5:175542260..177073634 [GRCh37]
Chr5:175474866..177006240 [NCBI36]
Chr5:5q35.2-35.3
pathogenic
GRCh38/hg38 5q35.2-35.3(chr5:176152073-177986213)x1 copy number loss See cases [RCV000053129] Chr5:176152073..177986213 [GRCh38]
Chr5:175579076..177413214 [GRCh37]
Chr5:175511682..177345820 [NCBI36]
Chr5:5q35.2-35.3
pathogenic
1 to 10 of 97 rows

Predicted Target Of
Summary Value
Count of predictions:6716
Count of miRNA genes:1058
Interacting mature miRNAs:1294
Transcripts:ENST00000261948, ENST00000358149, ENST00000503039, ENST00000503425, ENST00000504600, ENST00000506693, ENST00000508155, ENST00000510933, ENST00000511834, ENST00000512315, ENST00000513587
Prediction methods:Microtar, Miranda, Rnahybrid
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.


1 to 10 of 22 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
2289409BW320_HBody weight QTL 320 (human)3.50.0002Body weightlean mass5160925164181538259Human
406998406GWAS647382_HBMI-adjusted waist circumference QTL GWAS647382 (human)9e-10body size trait (VT:0100005)5177024077177024078Human
597067411GWAS1163485_Hage at menopause QTL GWAS1163485 (human)9e-14age at menopause5177038269177038270Human
597166397GWAS1262471_Huterine fibroid QTL GWAS1262471 (human)1e-09uterine fibroid5177038269177038270Human
597156785GWAS1252859_Hestradiol measurement QTL GWAS1252859 (human)6e-15estradiol measurementblood estradiol level (CMO:0000513)5177039010177039011Human
597264031GWAS1360105_Heducational attainment QTL GWAS1360105 (human)4e-17educational attainment5177065556177065557Human
597102672GWAS1198746_Hword reading QTL GWAS1198746 (human)0.000003word reading5177051625177051626Human
407115340GWAS764316_Huterine fibroid, Menorrhagia QTL GWAS764316 (human)4e-10uterine fibroid, Menorrhagia5177023836177023837Human
597276209GWAS1372283_HUterine leiomyoma QTL GWAS1372283 (human)2e-09Uterine leiomyoma5177023836177023837Human
597278481GWAS1374555_Hinsomnia QTL GWAS1374555 (human)6e-09insomnia5177036550177036551Human

1 to 10 of 22 rows
D5S2196E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375176,486,351 - 176,486,462UniSTSGRCh37
Build 365176,418,957 - 176,419,068RGDNCBI36
Celera5172,014,865 - 172,014,976RGD
Cytogenetic Map5q35.2UniSTS
HuRef5171,408,072 - 171,408,183UniSTS
D5S2703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375176,488,890 - 176,489,109UniSTSGRCh37
Build 365176,421,496 - 176,421,715RGDNCBI36
Celera5172,012,212 - 172,012,431RGD
Cytogenetic Map5q35.2UniSTS
HuRef5171,410,614 - 171,410,833UniSTS
RH47837  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375176,507,938 - 176,508,126UniSTSGRCh37
Build 365176,440,544 - 176,440,732RGDNCBI36
Celera5171,993,195 - 171,993,383RGD
Cytogenetic Map5q35.2UniSTS
HuRef5171,429,662 - 171,429,850UniSTS
GeneMap99-GB4 RH Map5636.91UniSTS
NCBI RH Map5973.0UniSTS
D5S2863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375176,492,824 - 176,492,981UniSTSGRCh37
Build 365176,425,430 - 176,425,587RGDNCBI36
Celera5172,008,340 - 172,008,498RGD
Cytogenetic Map5q35.2UniSTS
HuRef5171,414,548 - 171,414,705UniSTS
ZNF346__4826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375176,493,067 - 176,493,743UniSTSGRCh37
Build 365176,425,673 - 176,426,349RGDNCBI36
Celera5172,007,578 - 172,008,254RGD
HuRef5171,414,791 - 171,415,467UniSTS
SGC32143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375176,492,807 - 176,492,954UniSTSGRCh37
Build 365176,425,413 - 176,425,560RGDNCBI36
Celera5172,008,367 - 172,008,515RGD
Cytogenetic Map5q35.2UniSTS
HuRef5171,414,531 - 171,414,678UniSTS
GeneMap99-GB4 RH Map5636.91UniSTS
Whitehead-RH Map5540.8UniSTS
NCBI RH Map5973.0UniSTS




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 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 174 1


1 to 30 of 78 rows
RefSeq Transcripts NM_001308213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001308214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001308215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001308216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001308218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001308219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001308221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001308223 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363713 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_012279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_131773 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_131774 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005265860 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005265864 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534493 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534494 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534497 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 30 of 78 rows

Ensembl Acc Id: ENST00000358149   ⟹   ENSP00000350869
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,022,696 - 177,067,985 (+)Ensembl
Ensembl Acc Id: ENST00000503039   ⟹   ENSP00000424495
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,022,735 - 177,081,189 (+)Ensembl
Ensembl Acc Id: ENST00000503425   ⟹   ENSP00000421212
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,022,704 - 177,064,966 (+)Ensembl
Ensembl Acc Id: ENST00000504600
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,044,327 - 177,050,892 (+)Ensembl
Ensembl Acc Id: ENST00000506693   ⟹   ENSP00000423515
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,022,696 - 177,065,241 (+)Ensembl
Ensembl Acc Id: ENST00000508155   ⟹   ENSP00000421388
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,022,716 - 177,065,458 (+)Ensembl
Ensembl Acc Id: ENST00000510933
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,022,904 - 177,042,249 (+)Ensembl
Ensembl Acc Id: ENST00000511834   ⟹   ENSP00000425725
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,022,732 - 177,065,965 (+)Ensembl
Ensembl Acc Id: ENST00000512315   ⟹   ENSP00000421089
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,022,696 - 177,080,554 (+)Ensembl
Ensembl Acc Id: ENST00000513587   ⟹   ENSP00000423690
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5177,022,735 - 177,065,018 (+)Ensembl
RefSeq Acc Id: NM_001308213   ⟹   NP_001295142
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,081,189 (+)NCBI
CHM1_15175,882,083 - 175,941,073 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,624,397 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001308214   ⟹   NP_001295143
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
CHM1_15175,882,083 - 175,927,867 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001308215   ⟹   NP_001295144
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
CHM1_15175,882,083 - 175,927,867 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001308216   ⟹   NP_001295145
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
CHM1_15175,882,083 - 175,927,867 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001308218   ⟹   NP_001295147
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
CHM1_15175,882,083 - 175,927,867 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001308219   ⟹   NP_001295148
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,081,189 (+)NCBI
CHM1_15175,882,083 - 175,941,073 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,624,397 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001308221   ⟹   NP_001295150
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
CHM1_15175,882,083 - 175,927,867 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001308223   ⟹   NP_001295152
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,081,189 (+)NCBI
CHM1_15175,882,083 - 175,941,073 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,624,397 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363713   ⟹   NP_001350642
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,081,189 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,624,397 (+)NCBI
Sequence:
RefSeq Acc Id: NM_012279   ⟹   NP_036411
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
GRCh375176,449,681 - 176,508,189 (+)NCBI
Build 365176,382,303 - 176,426,364 (+)NCBI Archive
Celera5172,007,563 - 172,051,635 (-)RGD
HuRef5171,371,845 - 171,415,482 (+)ENTREZGENE
CHM1_15175,882,083 - 175,927,867 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
Sequence:
RefSeq Acc Id: NR_131773
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
CHM1_15175,882,083 - 175,927,867 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
Sequence:
RefSeq Acc Id: NR_131774
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
CHM1_15175,882,083 - 175,927,867 (+)NCBI
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005265864   ⟹   XP_005265921
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
GRCh375176,449,681 - 176,508,189 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011534494   ⟹   XP_011532796
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,081,189 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011534495   ⟹   XP_011532797
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,065,983 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011534496   ⟹   XP_011532798
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009297   ⟹   XP_016864786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009298   ⟹   XP_016864787
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,060,242 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009299   ⟹   XP_016864788
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009303   ⟹   XP_016864792
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,043,727 - 177,067,985 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047417051   ⟹   XP_047273007
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
RefSeq Acc Id: XM_047417052   ⟹   XP_047273008
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
RefSeq Acc Id: XM_047417053   ⟹   XP_047273009
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,065,983 (+)NCBI
RefSeq Acc Id: XM_047417054   ⟹   XP_047273010
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
RefSeq Acc Id: XM_047417055   ⟹   XP_047273011
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
RefSeq Acc Id: XM_047417056   ⟹   XP_047273012
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,060,242 (+)NCBI
RefSeq Acc Id: XM_047417057   ⟹   XP_047273013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385177,022,696 - 177,067,985 (+)NCBI
RefSeq Acc Id: XM_054352256   ⟹   XP_054208231
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
RefSeq Acc Id: XM_054352257   ⟹   XP_054208232
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,624,397 (+)NCBI
RefSeq Acc Id: XM_054352258   ⟹   XP_054208233
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,609,186 (+)NCBI
RefSeq Acc Id: XM_054352259   ⟹   XP_054208234
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
RefSeq Acc Id: XM_054352260   ⟹   XP_054208235
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
RefSeq Acc Id: XM_054352261   ⟹   XP_054208236
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
RefSeq Acc Id: XM_054352262   ⟹   XP_054208237
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,603,448 (+)NCBI
RefSeq Acc Id: XM_054352263   ⟹   XP_054208238
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
RefSeq Acc Id: XM_054352264   ⟹   XP_054208239
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,609,186 (+)NCBI
RefSeq Acc Id: XM_054352265   ⟹   XP_054208240
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
RefSeq Acc Id: XM_054352266   ⟹   XP_054208241
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
RefSeq Acc Id: XM_054352267   ⟹   XP_054208242
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
RefSeq Acc Id: XM_054352268   ⟹   XP_054208243
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,603,448 (+)NCBI
RefSeq Acc Id: XM_054352269   ⟹   XP_054208244
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,565,869 - 177,611,193 (+)NCBI
RefSeq Acc Id: XM_054352270   ⟹   XP_054208245
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05177,586,922 - 177,611,193 (+)NCBI
1 to 30 of 62 rows
Protein RefSeqs NP_001295142 (Get FASTA)   NCBI Sequence Viewer  
  NP_001295143 (Get FASTA)   NCBI Sequence Viewer  
  NP_001295144 (Get FASTA)   NCBI Sequence Viewer  
  NP_001295145 (Get FASTA)   NCBI Sequence Viewer  
  NP_001295147 (Get FASTA)   NCBI Sequence Viewer  
  NP_001295148 (Get FASTA)   NCBI Sequence Viewer  
  NP_001295150 (Get FASTA)   NCBI Sequence Viewer  
  NP_001295152 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350642 (Get FASTA)   NCBI Sequence Viewer  
  NP_036411 (Get FASTA)   NCBI Sequence Viewer  
  XP_005265921 (Get FASTA)   NCBI Sequence Viewer  
  XP_011532796 (Get FASTA)   NCBI Sequence Viewer  
  XP_011532797 (Get FASTA)   NCBI Sequence Viewer  
  XP_011532798 (Get FASTA)   NCBI Sequence Viewer  
  XP_016864786 (Get FASTA)   NCBI Sequence Viewer  
  XP_016864787 (Get FASTA)   NCBI Sequence Viewer  
  XP_016864788 (Get FASTA)   NCBI Sequence Viewer  
  XP_016864792 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273007 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273008 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273009 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273010 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273011 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273012 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273013 (Get FASTA)   NCBI Sequence Viewer  
  XP_054208231 (Get FASTA)   NCBI Sequence Viewer  
  XP_054208232 (Get FASTA)   NCBI Sequence Viewer  
  XP_054208233 (Get FASTA)   NCBI Sequence Viewer  
  XP_054208234 (Get FASTA)   NCBI Sequence Viewer  
  XP_054208235 (Get FASTA)   NCBI Sequence Viewer  
1 to 30 of 62 rows
1 to 5 of 48 rows
1 to 5 of 48 rows
RefSeq Acc Id: NP_036411   ⟸   NM_012279
- Peptide Label: isoform a
- UniProtKB: Q68CV9 (UniProtKB/Swiss-Prot),   B7Z367 (UniProtKB/Swiss-Prot),   Q6ZMW1 (UniProtKB/Swiss-Prot),   Q9UL40 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005265921   ⟸   XM_005265864
- Peptide Label: isoform X11
- Sequence:
RefSeq Acc Id: XP_011532796   ⟸   XM_011534494
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011532797   ⟸   XM_011534495
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011532798   ⟸   XM_011534496
- Peptide Label: isoform X5
- Sequence:
C2H2-type   U1-type

Name Modeler Protein Id AA Range Protein Structure
AF-Q9UL40-F1-model_v2 AlphaFold Q9UL40 1-294 view protein structure

RGD ID:6803719
Promoter ID:HG_KWN:51890
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000261948,   NM_012279,   UC003MFJ.1,   UC003MFK.1
Position:
Human AssemblyChrPosition (strand)Source
Build 365176,381,676 - 176,382,392 (+)MPROMDB
RGD ID:6871660
Promoter ID:EPDNEW_H8994
Type:initiation region
Name:ZNF346_1
Description:zinc finger protein 346
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
GRCh385177,022,696 - 177,022,756EPDNEW


1 to 40 of 41 rows
Database
Acc Id
Source(s)
COSMIC ZNF346 COSMIC
Ensembl Genes ENSG00000113761 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000358149 ENTREZGENE
  ENST00000358149.8 UniProtKB/Swiss-Prot
  ENST00000503039 ENTREZGENE
  ENST00000503039.1 UniProtKB/Swiss-Prot
  ENST00000503425 ENTREZGENE
  ENST00000503425.5 UniProtKB/Swiss-Prot
  ENST00000506693 ENTREZGENE
  ENST00000511834 ENTREZGENE
  ENST00000512315 ENTREZGENE
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot
GTEx ENSG00000113761 GTEx
HGNC ID HGNC:16403 ENTREZGENE
Human Proteome Map ZNF346 Human Proteome Map
InterPro Matrin/U1-like-C_Znf_C2H2 UniProtKB/Swiss-Prot
  ZN346_ZMAT4 UniProtKB/Swiss-Prot
  Znf_C2H2_sf UniProtKB/Swiss-Prot
  Znf_C2H2_type UniProtKB/Swiss-Prot
KEGG Report hsa:23567 UniProtKB/Swiss-Prot
NCBI Gene 23567 ENTREZGENE
OMIM 605308 OMIM
PANTHER ZINC FINGER PROTEIN 346 UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN 385B-LIKE UniProtKB/Swiss-Prot
Pfam zf-met UniProtKB/Swiss-Prot
PharmGKB PA134898181 PharmGKB
SMART ZnF_C2H2 UniProtKB/Swiss-Prot
  ZnF_U1 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF57667 UniProtKB/Swiss-Prot
UniProt B7Z367 ENTREZGENE
  B7Z4J8 ENTREZGENE, UniProtKB/TrEMBL
  B7Z4N4 ENTREZGENE, UniProtKB/TrEMBL
  B7Z6B6_HUMAN UniProtKB/TrEMBL
  B7Z6Q2_HUMAN UniProtKB/TrEMBL
  D6RJ07 ENTREZGENE, UniProtKB/TrEMBL
  Q68CV9 ENTREZGENE
  Q6ZMW1 ENTREZGENE
  Q9UL40 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B7Z367 UniProtKB/Swiss-Prot
  Q68CV9 UniProtKB/Swiss-Prot
1 to 40 of 41 rows