PDCL3 (phosducin like 3) - Rat Genome Database

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Gene: PDCL3 (phosducin like 3) Homo sapiens
Analyze
Symbol: PDCL3
Name: phosducin like 3
RGD ID: 1320124
HGNC Page HGNC:28860
Description: Enables protein folding chaperone. Involved in several processes, including chaperone-mediated protein folding; negative regulation of chaperone-mediated protein folding; and protein stabilization. Acts upstream of or within positive regulation of angiogenesis; positive regulation of endothelial cell proliferation; and regulation of protein metabolic process. Located in cytosol; endoplasmic reticulum; and nuclear lumen.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: HTPHLP; IAP-associated factor VIAF1; MGC3062; PHLP2A; PHLP3; phosducin-like 3; phosducin-like protein 3; phPL3; VIAF; VIAF-1; VIAF1; viral IAP-associated factor 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: PDCL3P1   PDCL3P2   PDCL3P3   PDCL3P4   PDCL3P5   PDCL3P6  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382100,562,993 - 100,576,739 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl2100,562,993 - 100,576,739 (+)EnsemblGRCh38hg38GRCh38
GRCh372101,179,455 - 101,193,201 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362100,545,859 - 100,559,633 (+)NCBINCBI36Build 36hg18NCBI36
Build 342100,637,944 - 100,651,719NCBI
Celera295,384,039 - 95,397,821 (+)NCBICelera
Cytogenetic Map2q11.2NCBI
HuRef294,943,898 - 94,957,677 (+)NCBIHuRef
CHM1_12101,183,727 - 101,197,486 (+)NCBICHM1_1
T2T-CHM13v2.02101,021,740 - 101,035,465 (+)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

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
Additional References at PubMed
PMID:12477932   PMID:15371430   PMID:15489334   PMID:17207965   PMID:17429077   PMID:18029348   PMID:19012568   PMID:19322201   PMID:20360068   PMID:21873635   PMID:22658674   PMID:23792958  
PMID:25515538   PMID:26059764   PMID:26167880   PMID:26186194   PMID:26344197   PMID:26496610   PMID:26638075   PMID:26830138   PMID:26912792   PMID:27496612   PMID:28514442   PMID:28718761  
PMID:29128334   PMID:29507755   PMID:29568061   PMID:30572598   PMID:30890647   PMID:31586073   PMID:31617661   PMID:31932471   PMID:31980649   PMID:32621347   PMID:32877691   PMID:33961781  
PMID:34079125   PMID:35271311   PMID:35384245   PMID:35831314  


Genomics

Comparative Map Data
PDCL3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382100,562,993 - 100,576,739 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl2100,562,993 - 100,576,739 (+)EnsemblGRCh38hg38GRCh38
GRCh372101,179,455 - 101,193,201 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362100,545,859 - 100,559,633 (+)NCBINCBI36Build 36hg18NCBI36
Build 342100,637,944 - 100,651,719NCBI
Celera295,384,039 - 95,397,821 (+)NCBICelera
Cytogenetic Map2q11.2NCBI
HuRef294,943,898 - 94,957,677 (+)NCBIHuRef
CHM1_12101,183,727 - 101,197,486 (+)NCBICHM1_1
T2T-CHM13v2.02101,021,740 - 101,035,465 (+)NCBIT2T-CHM13v2.0
Pdcl3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39139,026,895 - 39,036,317 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl139,024,689 - 39,036,319 (+)EnsemblGRCm39 Ensembl
GRCm38138,987,814 - 38,997,236 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl138,985,608 - 38,997,238 (+)EnsemblGRCm38mm10GRCm38
MGSCv37139,044,659 - 39,054,081 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36138,932,360 - 38,941,782 (+)NCBIMGSCv36mm8
Celera138,777,037 - 38,786,281 (+)NCBICelera
Cytogenetic Map1BNCBI
Pdcl3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2941,234,322 - 41,243,769 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl941,234,234 - 41,243,735 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx949,728,486 - 49,736,952 (+)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.0954,851,230 - 54,859,696 (+)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.0953,135,081 - 53,143,552 (+)NCBIRnor_WKY
Rnor_6.0945,672,257 - 45,680,728 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl945,672,157 - 45,680,799 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0945,362,541 - 45,371,012 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4938,004,222 - 38,012,693 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1938,005,635 - 38,014,107 (+)NCBI
Celera938,984,793 - 38,993,264 (+)NCBICelera
Cytogenetic Map9q22NCBI
Pdcl3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049554706,553,450 - 6,563,814 (+)NCBIChiLan1.0ChiLan1.0
PDCL3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.12A101,538,872 - 101,551,669 (+)NCBIpanpan1.1PanPan1.1panPan2
PDCL3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11042,214,127 - 42,223,986 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1042,215,120 - 42,223,906 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1042,137,411 - 42,147,413 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01043,080,268 - 43,090,236 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1043,079,573 - 43,090,129 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11042,791,342 - 42,801,288 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01043,075,653 - 43,085,591 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01043,266,979 - 43,276,929 (-)NCBIUU_Cfam_GSD_1.0
Pdcl3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440629286,141,438 - 86,150,373 (+)NCBIHiC_Itri_2
SpeTri2.0NW_004936661419,113 - 428,032 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PDCL3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl353,674,509 - 53,692,928 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1353,681,798 - 53,693,034 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2356,244,971 - 56,256,183 (+)NCBISscrofa10.2Sscrofa10.2susScr3
PDCL3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1144,275,182 - 4,289,041 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666041171,892,827 - 171,907,083 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Pdcl3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247495,410,476 - 5,422,533 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247495,410,501 - 5,419,625 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2q11.2-12.3(chr2:100378510-108472871)x3 copy number gain See cases [RCV000050836] Chr2:100378510..108472871 [GRCh38]
Chr2:100994972..109089327 [GRCh37]
Chr2:100361404..108455759 [NCBI36]
Chr2:2q11.2-12.3		 pathogenic
GRCh38/hg38 2q11.1-12.1(chr2:94817406-103252396)x3 copy number gain See cases [RCV000052946] Chr2:94817406..103252396 [GRCh38]
Chr2:95618109..103868854 [GRCh37]
Chr2:94846878..103235286 [NCBI36]
Chr2:2q11.1-12.1		 pathogenic
GRCh38/hg38 2q11.2-13(chr2:97672522-110211318)x3 copy number gain See cases [RCV000052947] Chr2:97672522..110211318 [GRCh38]
Chr2:98288985..110968895 [GRCh37]
Chr2:97655417..110326184 [NCBI36]
Chr2:2q11.2-13		 pathogenic
GRCh38/hg38 2p11.2-q11.2(chr2:91443218-102334856)x3 copy number gain See cases [RCV000052945] Chr2:91443218..102334856 [GRCh38]
Chr2:91617683..102951316 [GRCh37]
Chr2:90981410..102317748 [NCBI36]
Chr2:2p11.2-q11.2		 pathogenic
GRCh38/hg38 2q11.2(chr2:98787057-100785053)x1 copy number loss See cases [RCV000054057] Chr2:98787057..100785053 [GRCh38]
Chr2:99403520..101401515 [GRCh37]
Chr2:98769952..100767947 [NCBI36]
Chr2:2q11.2		 pathogenic
GRCh38/hg38 2q11.2(chr2:99253497-101559639)x3 copy number gain See cases [RCV000136916] Chr2:99253497..101559639 [GRCh38]
Chr2:99869960..102176101 [GRCh37]
Chr2:99236392..101542533 [NCBI36]
Chr2:2q11.2		 uncertain significance
GRCh38/hg38 2q11.2(chr2:100404604-100908738)x3 copy number gain See cases [RCV000139353] Chr2:100404604..100908738 [GRCh38]
Chr2:101021066..101525200 [GRCh37]
Chr2:100387498..100891632 [NCBI36]
Chr2:2q11.2		 likely benign
GRCh38/hg38 2q11.2(chr2:98411773-101636907)x1 copy number loss See cases [RCV000139206] Chr2:98411773..101636907 [GRCh38]
Chr2:99028236..102253369 [GRCh37]
Chr2:98394668..101619801 [NCBI36]
Chr2:2q11.2		 likely pathogenic
GRCh38/hg38 2q11.1-13(chr2:94678532-110602409)x3 copy number gain See cases [RCV000141075] Chr2:94678532..110602409 [GRCh38]
Chr2:95344257..111359986 [GRCh37]
Chr2:94707984..111076455 [NCBI36]
Chr2:2q11.1-13		 pathogenic
GRCh38/hg38 2q11.2-12.2(chr2:100478285-106498909)x3 copy number gain See cases [RCV000141445] Chr2:100478285..106498909 [GRCh38]
Chr2:101094747..107115365 [GRCh37]
Chr2:100461179..106481797 [NCBI36]
Chr2:2q11.2-12.2		 uncertain significance
GRCh38/hg38 2q11.2(chr2:100406992-100919730)x3 copy number gain See cases [RCV000143677] Chr2:100406992..100919730 [GRCh38]
Chr2:101023454..101536192 [GRCh37]
Chr2:100389886..100902624 [NCBI36]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q11.1-12.3(chr2:95529039-108518266) copy number gain See cases [RCV000449270] Chr2:95529039..108518266 [GRCh37]
Chr2:2q11.1-12.3		 pathogenic
GRCh37/hg19 2q11.1-13(chr2:95327499-111370025)x4 copy number gain See cases [RCV000446842] Chr2:95327499..111370025 [GRCh37]
Chr2:2q11.1-13		 pathogenic
GRCh37/hg19 2q11.2(chr2:100890121-101188008)x3 copy number gain See cases [RCV000445655] Chr2:100890121..101188008 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q11.1-12.2(chr2:95518497-107186127) copy number gain See cases [RCV000511158] Chr2:95518497..107186127 [GRCh37]
Chr2:2q11.1-12.2		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q11.2(chr2:101022472-101536192)x3 copy number gain not provided [RCV000682080] Chr2:101022472..101536192 [GRCh37]
Chr2:2q11.2		 likely benign|uncertain significance
Single allele deletion not provided [RCV000714264] Chr2:40608411..146900718 [GRCh37]
Chr2:2p22.1-q22.3		 likely pathogenic
GRCh37/hg19 2q11.1-13(chr2:96353030-114045463)x3 copy number gain not provided [RCV000682168] Chr2:96353030..114045463 [GRCh37]
Chr2:2q11.1-13		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1 copy number loss See cases [RCV002287563] Chr2:11504318..111365996 [GRCh37]
Chr2:2p25.1-q13		 pathogenic
NM_024065.5(PDCL3):c.403A>C (p.Ser135Arg) single nucleotide variant Inborn genetic diseases [RCV002858958] Chr2:100571624 [GRCh38]
Chr2:101188086 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_024065.5(PDCL3):c.470A>G (p.Asn157Ser) single nucleotide variant Inborn genetic diseases [RCV002704258] Chr2:100571691 [GRCh38]
Chr2:101188153 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_024065.5(PDCL3):c.20A>G (p.Asp7Gly) single nucleotide variant Inborn genetic diseases [RCV002743014] Chr2:100566516 [GRCh38]
Chr2:101182978 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_024065.5(PDCL3):c.673C>T (p.Arg225Trp) single nucleotide variant Inborn genetic diseases [RCV002699566] Chr2:100576449 [GRCh38]
Chr2:101192911 [GRCh37]
Chr2:2q11.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:279
Count of miRNA genes:261
Interacting mature miRNAs:268
Transcripts:ENST00000264254, ENST00000416255, ENST00000450127
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.

Markers in Region
SHGC-146357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372101,191,912 - 101,192,113UniSTSGRCh37
Build 362100,558,344 - 100,558,545RGDNCBI36
Celera295,396,533 - 95,396,734RGD
Cytogenetic Map2q11.2UniSTS
HuRef294,956,389 - 94,956,590UniSTS
TNG Radiation Hybrid Map259085.0UniSTS
SHGC-57056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376151,149,285 - 151,149,522UniSTSGRCh37
Build 366151,190,978 - 151,191,215RGDNCBI36
Celera6151,883,144 - 151,883,381RGD
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map2q11.2UniSTS
HuRef6148,712,854 - 148,713,091UniSTS


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 visual system adipose tissue appendage entire extraembryonic component
High
Medium 2183 1925 1257 264 1198 160 4305 1930 2327 360 1412 1496 117 1135 2755 3
Low 252 1063 469 358 751 304 50 262 1399 59 44 116 57 69 33 1
Below cutoff 1 2 1 1 3 5 3 1 1 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000264254   ⟹   ENSP00000264254
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2100,562,993 - 100,576,739 (+)Ensembl
RefSeq Acc Id: ENST00000416255   ⟹   ENSP00000413936
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2100,563,258 - 100,571,632 (+)Ensembl
RefSeq Acc Id: ENST00000450127   ⟹   ENSP00000390585
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2100,568,955 - 100,572,040 (+)Ensembl
RefSeq Acc Id: NM_024065   ⟹   NP_076970
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382100,562,993 - 100,576,739 (+)NCBI
GRCh372101,179,418 - 101,193,201 (+)RGD
Build 362100,545,859 - 100,559,633 (+)NCBI Archive
Celera295,384,039 - 95,397,821 (+)RGD
HuRef294,943,898 - 94,957,677 (+)ENTREZGENE
CHM1_12101,183,727 - 101,197,486 (+)NCBI
T2T-CHM13v2.02101,021,740 - 101,035,465 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017004890   ⟹   XP_016860379
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382100,563,305 - 100,576,739 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_076970   ⟸   NM_024065
- UniProtKB: Q53S68 (UniProtKB/Swiss-Prot),   Q9H2J4 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016860379   ⟸   XM_017004890
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000390585   ⟸   ENST00000450127
RefSeq Acc Id: ENSP00000413936   ⟸   ENST00000416255
RefSeq Acc Id: ENSP00000264254   ⟸   ENST00000264254
Protein Domains
Phosducin thioredoxin-like

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9H2J4-F1-model_v2 AlphaFold Q9H2J4 1-239 view protein structure

Promoters
RGD ID:6797925
Promoter ID:HG_KWN:34129
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:OTTHUMT00000329734,   OTTHUMT00000329736
Position:
Human AssemblyChrPosition (strand)Source
Build 362100,544,931 - 100,546,162 (+)MPROMDB
RGD ID:6861168
Promoter ID:EPDNEW_H3749
Type:initiation region
Name:PDCL3_1
Description:phosducin like 3
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
GRCh382100,562,993 - 100,563,053EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:28860 AgrOrtholog
COSMIC PDCL3 COSMIC
Ensembl Genes ENSG00000115539 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000264254 ENTREZGENE
  ENSP00000264254.6 UniProtKB/Swiss-Prot
  ENSP00000390585.1 UniProtKB/TrEMBL
  ENSP00000413936.1 UniProtKB/TrEMBL
Ensembl Transcript ENST00000264254 ENTREZGENE
  ENST00000264254.11 UniProtKB/Swiss-Prot
  ENST00000416255.5 UniProtKB/TrEMBL
  ENST00000450127.1 UniProtKB/TrEMBL
Gene3D-CATH Glutaredoxin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000115539 GTEx
HGNC ID HGNC:28860 ENTREZGENE
Human Proteome Map PDCL3 Human Proteome Map
InterPro Phosducin_thioredoxin-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Thioredoxin-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:79031 UniProtKB/Swiss-Prot
NCBI Gene 79031 ENTREZGENE
OMIM 611678 OMIM
PANTHER PHOSDUCIN-LIKE PROTEIN 3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VIRAL IAP-ASSOCIATED FACTOR HOMOLOG UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Phosducin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134979849 PharmGKB
Superfamily-SCOP SSF52833 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
TIGRFAMs phd_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt C9JST4_HUMAN UniProtKB/TrEMBL
  H7BZP2_HUMAN UniProtKB/TrEMBL
  PDCL3_HUMAN UniProtKB/Swiss-Prot
  Q53S68 ENTREZGENE
  Q9H2J4 ENTREZGENE
UniProt Secondary B2RA00 UniProtKB/Swiss-Prot
  Q53S68 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-17 PDCL3  phosducin like 3  PDCL3  phosducin-like 3  Symbol and/or name change 5135510 APPROVED