WASH5P (WASP family homolog 5, pseudogene) - Rat Genome Database

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Gene: WASH5P (WASP family homolog 5, pseudogene) Homo sapiens
Analyze
Symbol: WASH5P
Name: WASP family homolog 5, pseudogene
RGD ID: 2302258
HGNC Page HGNC:33884
Description: INTERACTS WITH 2-hydroxypropanoic acid; 3-isobutyl-1-methyl-7H-xanthine; 4,4'-sulfonyldiphenol
Type: pseudo (Ensembl: transcribed_processed_pseudogene)
RefSeq Status: VALIDATED
Previously known as: FAM39F; family with sequence similarity 39, member F; FLJ35264; FLJ50976; FLJ51139; FLJ98676; FLJ99967; WAS protein family homolog 5 pseudogene; WAS protein family homolog 5, pseudogene
Related Functional Gene: WASHC1  
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381960,951 - 70,966 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1966,320 - 66,492 (-)EnsemblGRCh38hg38GRCh38
GRCh38.p14 Ensembl1960,951 - 72,334 (-)EnsemblGRCh38hg38GRCh38
GRCh371960,951 - 70,966 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3694,517 - 7,479 (-)NCBINCBI36Build 36hg18NCBI36
CeleraX155,394,459 - 155,407,034 (+)NCBICelera
Cytogenetic Map19p13.3NCBI
HuRefX143,732,815 - 143,733,266 (+)NCBIHuRef
CHM1_115102,352,063 - 102,362,078 (+)NCBICHM1_1
T2T-CHM13v2.01911,934 - 21,953 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
References
Additional References at PubMed
PMID:14702039  


Genomics

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3059
Count of miRNA genes:884
Interacting mature miRNAs:1064
Transcripts:ENST00000391654, ENST00000606546, ENST00000606554, ENST00000606592, ENST00000606728, ENST00000606872, ENST00000607444, ENST00000607556, ENST00000607633, ENST00000607872
Prediction methods: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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1298499UAE1_HUrinary albumin excretion QTL 1 (human)2.730.0009Urinary albumin excretionurine albumin:creatinine ratio (ACR)19116075902Human
1643451SLIPL6_HSerum lipid level QTL 6 (human)2.190.0008Lipid level19116075902Human
1581534BP76_HBlood pressure QTL 76 (human)20.001Blood pressurepulse pressure19116075902Human
1581535BP65_HBlood pressure QTL 65 (human)3.10.001Blood pressurepulse pressure19116075902Human
2314591INSUL4_HInsulin level QTL 4 (human)3.80.000038Insulin levelfasting19116075902Human
1298476BP3_HBlood pressure QTL 3 (human)2.4Blood pressuresystolic19116075902Human

Markers in Region
REN94418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371673,597 - 73,849UniSTSGRCh37
Build 361613,597 - 13,849RGDNCBI36
CeleraX155,402,216 - 155,402,468RGD
Cytogenetic MapYq12UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic MapXq28UniSTS
HuRefX143,728,486 - 143,728,738UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
sensory system
1201 2214 2782 2204 4509 1436 1719 404 1369 242 1963 6007 5793 3567 528 1426 1232 162

Sequence


Ensembl Acc Id: ENST00000631796
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,820 - 70,971 (-)Ensembl
Ensembl Acc Id: ENST00000631994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1966,378 - 71,566 (-)Ensembl
Ensembl Acc Id: ENST00000632089
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,792 - 71,003 (-)Ensembl
Ensembl Acc Id: ENST00000632292
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1970,652 - 71,626 (-)Ensembl
Ensembl Acc Id: ENST00000632496
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,820 - 70,990 (-)Ensembl
Ensembl Acc Id: ENST00000632506
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1960,951 - 70,976 (-)Ensembl
Ensembl Acc Id: ENST00000633703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1963,821 - 70,951 (-)Ensembl
Ensembl Acc Id: ENST00000633719
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1962,113 - 66,524 (-)Ensembl
Ensembl Acc Id: ENST00000633742
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1966,320 - 66,492 (-)Ensembl
Ensembl Acc Id: ENST00000634023
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1964,779 - 72,315 (-)Ensembl
Ensembl Acc Id: ENST00000816397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,820 - 72,334 (-)Ensembl
Ensembl Acc Id: ENST00000816398
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1964,775 - 70,973 (-)Ensembl
Ensembl Acc Id: ENST00000816399
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1964,775 - 70,968 (-)Ensembl
Ensembl Acc Id: ENST00000816400
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,820 - 70,974 (-)Ensembl
Ensembl Acc Id: ENST00000816401
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,820 - 70,966 (-)Ensembl
Ensembl Acc Id: ENST00000816402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,820 - 70,965 (-)Ensembl
Ensembl Acc Id: ENST00000816403
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,824 - 70,963 (-)Ensembl
Ensembl Acc Id: ENST00000816404
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,822 - 70,961 (-)Ensembl
Ensembl Acc Id: ENST00000816405
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1965,824 - 70,957 (-)Ensembl
Ensembl Acc Id: ENST00000816406
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1968,160 - 70,954 (-)Ensembl
RefSeq Acc Id: NR_033266
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381960,951 - 70,966 (-)NCBI
GRCh371960,951 - 70,966 (-)RGD
Celera19155,394,459 - 155,407,034 (+)RGD
HuRef19143,732,815 - 143,733,266 (+)RGD
CHM1_115102,352,063 - 102,362,078 (+)NCBI
T2T-CHM13v2.01911,934 - 21,953 (-)NCBI
Sequence:

Additional Information

Database Acc Id Source(s)
COSMIC WASH5P COSMIC
Ensembl Genes ENSG00000282458 Ensembl
  ENSG00000292982 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000632506 ENTREZGENE
GTEx ENSG00000282458 GTEx
  ENSG00000292982 GTEx
HGNC ID HGNC:33884 ENTREZGENE
Human Proteome Map WASH5P Human Proteome Map
NCBI Gene WASH5P ENTREZGENE


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-02-19 WASH5P  WASP family homolog 5, pseudogene    WAS protein family homolog 5, pseudogene  Symbol and/or name change 5135510 APPROVED
2018-06-12 WASH5P  WAS protein family homolog 5, pseudogene    WAS protein family homolog 5 pseudogene  Symbol and/or name change 5135510 APPROVED