PARVB (parvin beta) - Rat Genome Database

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Gene: PARVB (parvin beta) Homo sapiens
Analyze
Symbol: PARVB
Name: parvin beta
RGD ID: 1322969
HGNC Page HGNC
Description: Predicted to enable actin binding activity. Involved in actin cytoskeleton reorganization; establishment or maintenance of cell polarity regulating cell shape; and lamellipodium assembly. Located in focal adhesion and lamellipodium.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: affixin; beta-parvin; CGI-56; FLJ17029; parvin, beta
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
GRCh38.p13 Ensembl2243,999,211 - 44,172,939 (+)EnsemblGRCh38hg38GRCh38
GRCh382243,999,164 - 44,172,939 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372244,395,091 - 44,568,819 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362242,726,506 - 42,896,439 (+)NCBINCBI36hg18NCBI36
Build 342242,745,068 - 42,890,002NCBI
Celera2228,306,774 - 28,479,077 (+)NCBI
Cytogenetic Map22q13.31NCBI
HuRef2227,348,952 - 27,516,946 (+)NCBIHuRef
CHM1_12244,353,851 - 44,522,290 (+)NCBICHM1_1
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
actin cytoskeleton  (IBA)
cytoplasm  (IBA,IEA)
cytoskeleton  (IEA)
cytosol  (TAS)
focal adhesion  (IBA,IDA)
lamellipodium  (IBA,IDA)
plasma membrane  (IEA)
Z disc  (IEA)

Molecular Function
actin binding  (IBA,IEA)
protein binding  (IPI)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:10591208   PMID:10810093   PMID:11171322   PMID:11402068   PMID:11722847   PMID:12372433   PMID:12477932   PMID:12499396   PMID:12529303   PMID:15005707   PMID:15159419   PMID:15284246  
PMID:15342556   PMID:15467740   PMID:15489334   PMID:15835269   PMID:16314921   PMID:17353931   PMID:17998334   PMID:18325335   PMID:18976975   PMID:19885839   PMID:19924298   PMID:20139978  
PMID:20164304   PMID:20345489   PMID:20379614   PMID:20467437   PMID:20736946   PMID:21295579   PMID:21483694   PMID:21625516   PMID:21873635   PMID:22719876   PMID:22869380   PMID:22939629  
PMID:23099104   PMID:23382691   PMID:23455922   PMID:23535033   PMID:23535911   PMID:23950981   PMID:24621583   PMID:25117820   PMID:25422907   PMID:25776890   PMID:26115385   PMID:26186194  
PMID:26343796   PMID:26344197   PMID:26496610   PMID:26549231   PMID:28514442   PMID:28611215   PMID:30021884   PMID:30463901   PMID:31586073   PMID:33961781  


Genomics

Comparative Map Data
PARVB
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2243,999,211 - 44,172,939 (+)EnsemblGRCh38hg38GRCh38
GRCh382243,999,164 - 44,172,939 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372244,395,091 - 44,568,819 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362242,726,506 - 42,896,439 (+)NCBINCBI36hg18NCBI36
Build 342242,745,068 - 42,890,002NCBI
Celera2228,306,774 - 28,479,077 (+)NCBI
Cytogenetic Map22q13.31NCBI
HuRef2227,348,952 - 27,516,946 (+)NCBIHuRef
CHM1_12244,353,851 - 44,522,290 (+)NCBICHM1_1
Parvb
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391584,116,244 - 84,199,890 (+)NCBIGRCm39mm39
GRCm39 Ensembl1584,116,244 - 84,199,889 (+)Ensembl
GRCm381584,232,043 - 84,315,689 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1584,232,043 - 84,315,688 (+)EnsemblGRCm38mm10GRCm38
MGSCv371584,062,473 - 84,146,039 (+)NCBIGRCm37mm9NCBIm37
MGSCv361584,059,809 - 84,143,375 (+)NCBImm8
MGSCv361585,033,050 - 85,115,036 (+)NCBImm8
Celera1586,363,102 - 86,447,450 (+)NCBICelera
Cytogenetic Map15E2NCBI
Parvb
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.27115,360,254 - 115,445,767 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl7115,360,261 - 115,445,766 (+)Ensembl
Rnor_6.07125,189,827 - 125,275,977 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl7125,189,827 - 125,277,689 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0763,181,011 - 63,268,380 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47122,223,325 - 122,310,356 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.17122,235,509 - 122,344,586 (+)NCBI
Celera7111,665,408 - 111,748,729 (+)NCBICelera
Cytogenetic Map7q34NCBI
Parvb
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541328,961,804 - 29,020,430 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495541328,962,614 - 29,020,430 (+)NCBIChiLan1.0ChiLan1.0
PARVB
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.12243,107,009 - 43,245,932 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2243,079,786 - 43,245,932 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v02224,913,710 - 25,061,603 (+)NCBIMhudiblu_PPA_v0panPan3
PARVB
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11021,549,654 - 21,629,771 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1021,551,998 - 21,640,781 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1021,492,217 - 21,589,726 (-)NCBI
ROS_Cfam_1.01022,300,594 - 22,397,773 (-)NCBI
UMICH_Zoey_3.11022,019,817 - 22,117,314 (-)NCBI
UNSW_CanFamBas_1.01022,340,152 - 22,437,648 (-)NCBI
UU_Cfam_GSD_1.01022,513,879 - 22,611,416 (-)NCBI
LOC101965678
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049455,222,742 - 5,258,715 (-)NCBI
SpeTri2.0NW_0049367181,721,452 - 1,757,423 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PARVB
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl54,906,684 - 5,015,441 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.154,906,667 - 5,015,494 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.252,124,672 - 2,160,970 (+)NCBISscrofa10.2Sscrofa10.2susScr3
PARVB
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11926,536,346 - 26,672,740 (+)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl1926,606,974 - 26,672,190 (+)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604598,764,422 - 98,868,527 (-)NCBIVero_WHO_p1.0
Parvb
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247525,039,180 - 5,121,056 (-)NCBIHetGla_female_1.0hetGla2

Position Markers
D22S1171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,417,584 - 44,417,739UniSTSGRCh37
Build 362242,748,917 - 42,749,072RGDNCBI36
Celera2228,329,186 - 28,329,341RGD
Cytogenetic Map22q13.2-q13.33UniSTS
Marshfield Genetic Map2248.19UniSTS
Marshfield Genetic Map2248.19RGD
Genethon Genetic Map2242.2UniSTS
deCODE Assembly Map2253.45UniSTS
Stanford-G3 RH Map221464.0UniSTS
GeneMap99-GB4 RH Map22144.18UniSTS
Whitehead-RH Map22170.9UniSTS
NCBI RH Map22212.8UniSTS
GeneMap99-G3 RH Map221464.0UniSTS
RH75363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,400,403 - 44,400,602UniSTSGRCh37
Build 362242,731,736 - 42,731,935RGDNCBI36
Celera2228,312,004 - 28,312,203RGD
Cytogenetic Map22q13.2-q13.33UniSTS
HuRef2227,354,264 - 27,354,463UniSTS
G65730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,475,055 - 44,475,422UniSTSGRCh37
Build 362242,806,388 - 42,806,755RGDNCBI36
Celera2228,386,624 - 28,386,991RGD
Cytogenetic Map22q13.2-q13.33UniSTS
HuRef2227,428,911 - 27,429,278UniSTS
G65736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,465,127 - 44,465,394UniSTSGRCh37
Build 362242,796,460 - 42,796,727RGDNCBI36
Celera2228,376,696 - 28,376,963RGD
Cytogenetic Map22q13.2-q13.33UniSTS
HuRef2227,418,983 - 27,419,250UniSTS
SHGC-132012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,564,717 - 44,564,994UniSTSGRCh37
Build 362242,896,050 - 42,896,327RGDNCBI36
Celera2228,478,688 - 28,478,965RGD
Cytogenetic Map22q13.2-q13.33UniSTS
HuRef2227,516,550 - 27,516,827UniSTS
TNG Radiation Hybrid Map2210947.0UniSTS
stbK70A10TV  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,409,074 - 44,409,205UniSTSGRCh37
Build 362242,740,407 - 42,740,538RGDNCBI36
Celera2228,320,675 - 28,320,806RGD
Cytogenetic Map22q13.2-q13.33UniSTS
HuRef2227,362,935 - 27,363,066UniSTS
SHGC-132330  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,417,518 - 44,417,808UniSTSGRCh37
Build 362242,748,851 - 42,749,141RGDNCBI36
Celera2228,329,120 - 28,329,410RGD
Cytogenetic Map22q13.2-q13.33UniSTS
TNG Radiation Hybrid Map2211002.0UniSTS
G65608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,398,528 - 44,398,855UniSTSGRCh37
Build 362242,729,861 - 42,730,188RGDNCBI36
Celera2228,310,129 - 28,310,456RGD
Cytogenetic Map22q13.2-q13.33UniSTS
HuRef2227,352,389 - 27,352,716UniSTS
D22S1241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372244,564,748 - 44,564,855UniSTSGRCh37
Build 362242,896,081 - 42,896,188RGDNCBI36
Celera2228,478,719 - 28,478,826RGD
Cytogenetic Map22q13.2-q13.33UniSTS
HuRef2227,516,581 - 27,516,688UniSTS
GeneMap99-G3 RH Map221486.0UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3552
Count of miRNA genes:1149
Interacting mature miRNAs:1451
Transcripts:ENST00000338758, ENST00000402876, ENST00000404989, ENST00000406477, ENST00000444029, ENST00000477438, ENST00000477795, ENST00000484345, ENST00000495824
Prediction methods: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.


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 1357 851 478 68 921 60 1878 1914 979 191 667 820 16 1178 1048 1
Low 1046 2131 1237 546 992 395 2477 272 2717 220 771 781 155 1 26 1740 1
Below cutoff 29 3 8 8 36 10 9 18 7 14 9 3 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001003828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001243385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001243386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_013327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005261596 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB048276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF151814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF237769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF303887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313957 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL031595 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL033543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL035398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL159142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC017461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC039811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC046103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG743702 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP339885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA308417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB044150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF457476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF457484 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z82174 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z82178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000338758   ⟹   ENSP00000342492
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2244,024,302 - 44,172,939 (+)Ensembl
RefSeq Acc Id: ENST00000402876
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2244,024,302 - 44,119,934 (+)Ensembl
RefSeq Acc Id: ENST00000404989   ⟹   ENSP00000384353
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2244,069,061 - 44,169,184 (+)Ensembl
RefSeq Acc Id: ENST00000406477   ⟹   ENSP00000384515
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2243,999,211 - 44,168,923 (+)Ensembl
RefSeq Acc Id: ENST00000444029   ⟹   ENSP00000393758
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2244,031,365 - 44,132,965 (+)Ensembl
RefSeq Acc Id: ENST00000477438
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2244,168,179 - 44,168,927 (+)Ensembl
RefSeq Acc Id: ENST00000477795
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2244,086,684 - 44,100,089 (+)Ensembl
RefSeq Acc Id: ENST00000484345
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2244,162,734 - 44,168,243 (+)Ensembl
RefSeq Acc Id: ENST00000495824
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2244,136,464 - 44,139,124 (+)Ensembl
RefSeq Acc Id: ENST00000619710   ⟹   ENSP00000482511
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2244,026,304 - 44,169,221 (+)Ensembl
RefSeq Acc Id: NM_001003828   ⟹   NP_001003828
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382243,999,211 - 44,172,939 (+)NCBI
GRCh372244,395,091 - 44,565,113 (+)NCBI
Build 362242,726,506 - 42,896,439 (+)NCBI Archive
HuRef2227,348,952 - 27,516,946 (+)NCBI
CHM1_12244,353,851 - 44,522,290 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001243385   ⟹   NP_001230314
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,069,106 - 44,172,939 (+)NCBI
GRCh372244,395,091 - 44,565,113 (+)NCBI
HuRef2227,348,952 - 27,516,946 (+)NCBI
CHM1_12244,423,734 - 44,522,290 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001243386   ⟹   NP_001230315
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,026,304 - 44,172,939 (+)NCBI
GRCh372244,395,091 - 44,565,113 (+)NCBI
HuRef2227,348,952 - 27,516,946 (+)NCBI
CHM1_12244,380,943 - 44,522,290 (+)NCBI
Sequence:
RefSeq Acc Id: NM_013327   ⟹   NP_037459
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,024,302 - 44,172,939 (+)NCBI
GRCh372244,395,091 - 44,565,113 (+)NCBI
Build 362242,751,501 - 42,896,439 (+)NCBI Archive
HuRef2227,348,952 - 27,516,946 (+)NCBI
CHM1_12244,378,922 - 44,522,290 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005261596   ⟹   XP_005261653
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,026,304 - 44,169,226 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028792   ⟹   XP_016884281
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,024,302 - 44,169,227 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024452235   ⟹   XP_024308003
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,081,408 - 44,169,226 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024452236   ⟹   XP_024308004
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382243,999,164 - 44,169,227 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024452237   ⟹   XP_024308005
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,086,666 - 44,169,226 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001003828   ⟸   NM_001003828
- Peptide Label: isoform a
- UniProtKB: Q9HBI1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_037459   ⟸   NM_013327
- Peptide Label: isoform b
- UniProtKB: Q9HBI1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001230315   ⟸   NM_001243386
- Peptide Label: isoform d
- UniProtKB: Q9HBI1 (UniProtKB/Swiss-Prot),   A0A087WZB5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001230314   ⟸   NM_001243385
- Peptide Label: isoform c
- UniProtKB: Q9HBI1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005261653   ⟸   XM_005261596
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_016884281   ⟸   XM_017028792
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_024308004   ⟸   XM_024452236
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_024308003   ⟸   XM_024452235
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024308005   ⟸   XM_024452237
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: ENSP00000342492   ⟸   ENST00000338758
RefSeq Acc Id: ENSP00000384353   ⟸   ENST00000404989
RefSeq Acc Id: ENSP00000393758   ⟸   ENST00000444029
RefSeq Acc Id: ENSP00000384515   ⟸   ENST00000406477
RefSeq Acc Id: ENSP00000482511   ⟸   ENST00000619710
Protein Domains
Calponin-homology (CH)

Promoters
RGD ID:6800193
Promoter ID:HG_KWN:43147
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000355618,   ENST00000402876,   OTTHUMT00000319518
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,751,261 - 42,751,977 (+)MPROMDB
RGD ID:6800197
Promoter ID:HG_KWN:43148
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid,   NB4
Transcripts:UC010GZN.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,752,891 - 42,753,842 (+)MPROMDB
RGD ID:6800196
Promoter ID:HG_KWN:43150
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:UC003BEO.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,795,831 - 42,796,331 (+)MPROMDB
RGD ID:6800192
Promoter ID:HG_KWN:43151
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000319521
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,812,946 - 42,813,446 (+)MPROMDB
RGD ID:6800194
Promoter ID:HG_KWN:43154
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000319524
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,888,861 - 42,889,361 (+)MPROMDB
RGD ID:6800195
Promoter ID:HG_KWN:43155
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000319525
Position:
Human AssemblyChrPosition (strand)Source
Build 362242,894,161 - 42,894,661 (+)MPROMDB
RGD ID:13604364
Promoter ID:EPDNEW_H28366
Type:initiation region
Name:PARVB_1
Description:parvin beta
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28367  EPDNEW_H28368  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,024,302 - 44,024,362EPDNEW
RGD ID:13604366
Promoter ID:EPDNEW_H28367
Type:initiation region
Name:PARVB_3
Description:parvin beta
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28366  EPDNEW_H28368  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,026,311 - 44,026,371EPDNEW
RGD ID:13604368
Promoter ID:EPDNEW_H28368
Type:initiation region
Name:PARVB_2
Description:parvin beta
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28366  EPDNEW_H28367  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382244,069,106 - 44,069,166EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001003828.2(PARVB):c.1044+90C>T single nucleotide variant Lung cancer [RCV000102080] Chr22:44158173 [GRCh38]
Chr22:44554053 [GRCh37]
Chr22:22q13.31
uncertain significance
GRCh38/hg38 22q13.2-13.33(chr22:42138114-50739836)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051370]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051370]|See cases [RCV000051370] Chr22:42138114..50739836 [GRCh38]
Chr22:42513525..51178264 [GRCh37]
Chr22:40843471..49525130 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42433752-50738932)x1 copy number loss See cases [RCV000051371] Chr22:42433752..50738932 [GRCh38]
Chr22:42829758..51177360 [GRCh37]
Chr22:41159702..49524226 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42826246-50739836)x1 copy number loss See cases [RCV000051407] Chr22:42826246..50739836 [GRCh38]
Chr22:43222252..51178264 [GRCh37]
Chr22:41552196..49525130 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.31-13.33(chr22:43807366-50739836)x1 copy number loss See cases [RCV000051408] Chr22:43807366..50739836 [GRCh38]
Chr22:44203246..51178264 [GRCh37]
Chr22:42534579..49525130 [NCBI36]
Chr22:22q13.31-13.33
pathogenic
GRCh38/hg38 22q13.31-13.33(chr22:43993654-50739977)x1 copy number loss See cases [RCV000051409] Chr22:43993654..50739977 [GRCh38]
Chr22:44389534..51178405 [GRCh37]
Chr22:42720867..49525271 [NCBI36]
Chr22:22q13.31-13.33
pathogenic
GRCh38/hg38 22q12.3-13.33(chr22:37061769-50738932)x3 copy number gain See cases [RCV000051684] Chr22:37061769..50738932 [GRCh38]
Chr22:37457809..51177360 [GRCh37]
Chr22:35787755..49524226 [NCBI36]
Chr22:22q12.3-13.33
pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42599757-50725241)x3 copy number gain See cases [RCV000051686] Chr22:42599757..50725241 [GRCh38]
Chr22:42995763..51163669 [GRCh37]
Chr22:41325707..49510535 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42653747-50739836)x3 copy number gain See cases [RCV000051687] Chr22:42653747..50739836 [GRCh38]
Chr22:43049753..51178264 [GRCh37]
Chr22:41379697..49525130 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q12.3-13.33(chr22:33768441-50739977)x3 copy number gain See cases [RCV000051682] Chr22:33768441..50739977 [GRCh38]
Chr22:34164428..51178405 [GRCh37]
Chr22:32494428..49525271 [NCBI36]
Chr22:22q12.3-13.33
pathogenic
GRCh38/hg38 22q13.31(chr22:43841416-44192863)x3 copy number gain See cases [RCV000052857] Chr22:43841416..44192863 [GRCh38]
Chr22:44237296..44588743 [GRCh37]
Chr22:42568629..42920076 [NCBI36]
Chr22:22q13.31
uncertain significance
NM_001003828.2(PARVB):c.7C>T (p.His3Tyr) single nucleotide variant Malignant melanoma [RCV000072989] Chr22:43999347 [GRCh38]
Chr22:44395227 [GRCh37]
Chr22:42726560 [NCBI36]
Chr22:22q13.31
not provided
NM_001003828.2(PARVB):c.1142C>T (p.Ser381Phe) single nucleotide variant Malignant melanoma [RCV000072990] Chr22:44168626 [GRCh38]
Chr22:44564506 [GRCh37]
Chr22:42895839 [NCBI36]
Chr22:22q13.31
not provided
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3 copy number gain See cases [RCV000133646] Chr22:16916608..50739836 [GRCh38]
Chr22:17397498..51178264 [GRCh37]
Chr22:15777498..49525130 [NCBI36]
Chr22:22q11.1-13.33
pathogenic
Single allele deletion Intellectual disability [RCV001293376] Chr22:42333802..51195728 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3 copy number gain See cases [RCV000134730] Chr22:16916743..50739785 [GRCh38]
Chr22:17397633..51178213 [GRCh37]
Chr22:15777633..49525079 [NCBI36]
Chr22:22q11.1-13.33
pathogenic
GRCh38/hg38 22q13.1-13.33(chr22:40202014-50735806)x3 copy number gain See cases [RCV000134513] Chr22:40202014..50735806 [GRCh38]
Chr22:40598018..51174234 [GRCh37]
Chr22:38927964..49521100 [NCBI36]
Chr22:22q13.1-13.33
pathogenic
GRCh38/hg38 22q13.31-13.33(chr22:43902561-50739836)x1 copy number loss See cases [RCV000135444] Chr22:43902561..50739836 [GRCh38]
Chr22:44298441..51178264 [GRCh37]
Chr22:42629774..49525130 [NCBI36]
Chr22:22q13.31-13.33
pathogenic
GRCh38/hg38 22q13.2-13.31(chr22:42197923-47305564)x4 copy number gain See cases [RCV000135528] Chr22:42197923..47305564 [GRCh38]
Chr22:42593929..47701314 [GRCh37]
Chr22:40923873..46079978 [NCBI36]
Chr22:22q13.2-13.31
pathogenic
GRCh38/hg38 22q13.31-13.33(chr22:43992879-50683114)x3 copy number gain See cases [RCV000136124] Chr22:43992879..50683114 [GRCh38]
Chr22:44388759..51121542 [GRCh37]
Chr22:42720092..49468408 [NCBI36]
Chr22:22q13.31-13.33
benign
GRCh38/hg38 22q13.2-13.33(chr22:41871143-50739836)x1 copy number loss See cases [RCV000136921] Chr22:41871143..50739836 [GRCh38]
Chr22:42267147..51178264 [GRCh37]
Chr22:40597093..49525130 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42710276-50739836)x3 copy number gain See cases [RCV000137136] Chr22:42710276..50739836 [GRCh38]
Chr22:43106282..51178264 [GRCh37]
Chr22:41436226..49525130 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42493445-50268479)x1 copy number loss See cases [RCV000136786] Chr22:42493445..50268479 [GRCh38]
Chr22:42889451..50706908 [GRCh37]
Chr22:41219395..49049035 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42837094-50735806)x1 copy number loss See cases [RCV000141415] Chr22:42837094..50735806 [GRCh38]
Chr22:43233100..51174234 [GRCh37]
Chr22:41563044..49521100 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:43187980-50745444)x1 copy number loss See cases [RCV000140901] Chr22:43187980..50745444 [GRCh38]
Chr22:43583986..51183872 [GRCh37]
Chr22:41913930..49530738 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.31(chr22:44031975-44060578)x3 copy number gain See cases [RCV000140781] Chr22:44031975..44060578 [GRCh38]
Chr22:44427855..44456458 [GRCh37]
Chr22:42759188..42787791 [NCBI36]
Chr22:22q13.31
likely benign
GRCh38/hg38 22q13.2-13.33(chr22:42380961-50759410)x3 copy number gain See cases [RCV000141659] Chr22:42380961..50759410 [GRCh38]
Chr22:42776967..51197838 [GRCh37]
Chr22:41106911..49544704 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42080077-50739836)x3 copy number gain See cases [RCV000142755] Chr22:42080077..50739836 [GRCh38]
Chr22:42476081..51178264 [GRCh37]
Chr22:40806027..49525130 [NCBI36]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42416026-51181759) copy number loss 22q13.3 deletion syndrome [RCV000767745] Chr22:42416026..51181759 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3 copy number gain See cases [RCV000240091] Chr22:16054691..51237518 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q12.3-13.33(chr22:35728929-51220961)x3 copy number gain See cases [RCV000240469] Chr22:35728929..51220961 [GRCh37]
Chr22:22q12.3-13.33
pathogenic
GRCh37/hg19 22q13.1-13.33(chr22:40425714-51220961)x3 copy number gain See cases [RCV000240459] Chr22:40425714..51220961 [GRCh37]
Chr22:22q13.1-13.33
pathogenic
GRCh37/hg19 22q13.31(chr22:44367095-44538688)x1 copy number loss See cases [RCV000449150] Chr22:44367095..44538688 [GRCh37]
Chr22:22q13.31
uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3 copy number gain See cases [RCV000446956] Chr22:16054691..51220902 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3 copy number gain See cases [RCV000448847] Chr22:16054691..51237463 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43381459-51197838)x1 copy number loss See cases [RCV000512121] Chr22:43381459..51197838 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q13.31(chr22:44382852-45007914)x1 copy number loss See cases [RCV000511840] Chr22:44382852..45007914 [GRCh37]
Chr22:22q13.31
uncertain significance
GRCh37/hg19 22q13.2-13.33(chr22:43875989-51197838)x1 copy number loss See cases [RCV000511015] Chr22:43875989..51197838 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43050743-51197838)x1 copy number loss See cases [RCV000511256] Chr22:43050743..51197838 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42441918-51197838)x1 copy number loss See cases [RCV000510765] Chr22:42441918..51197838 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838) copy number gain See cases [RCV000510873] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3 copy number gain See cases [RCV000512333] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43320284-51183840)x1 copy number loss not provided [RCV000684527] Chr22:43320284..51183840 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:43111156-51183840)x1 copy number loss not provided [RCV000684528] Chr22:43111156..51183840 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42955616-51183840)x1 copy number loss not provided [RCV000684529] Chr22:42955616..51183840 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q13.31(chr22:44465713-44541738)x1 copy number loss not provided [RCV000684450] Chr22:44465713..44541738 [GRCh37]
Chr22:22q13.31
uncertain significance
GRCh37/hg19 22q13.2-13.31(chr22:44023172-44744568)x3 copy number gain not provided [RCV000684483] Chr22:44023172..44744568 [GRCh37]
Chr22:22q13.2-13.31
uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16054667-51243435)x3 copy number gain not provided [RCV000741689] Chr22:16054667..51243435 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q13.2-13.33(chr22:42151555-51195728)x1 copy number loss not provided [RCV000741989] Chr22:42151555..51195728 [GRCh37]
Chr22:22q13.2-13.33
pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51195728)x3 copy number gain not provided [RCV000741691] Chr22:16114244..51195728 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q13.31(chr22:44349925-44494419)x3 copy number gain not provided [RCV000742021] Chr22:44349925..44494419 [GRCh37]
Chr22:22q13.31
benign
GRCh37/hg19 22q13.31(chr22:44564297-44567854)x1 copy number loss not provided [RCV000742022] Chr22:44564297..44567854 [GRCh37]
Chr22:22q13.31
benign
GRCh37/hg19 22q13.31(chr22:44564407-44565393)x0 copy number loss not provided [RCV000742023] Chr22:44564407..44565393 [GRCh37]
Chr22:22q13.31
benign
GRCh37/hg19 22q13.31(chr22:44564975-44565393)x0 copy number loss not provided [RCV000742024] Chr22:44564975..44565393 [GRCh37]
Chr22:22q13.31
benign
GRCh37/hg19 22q13.31(chr22:44564975-44569346)x1 copy number loss not provided [RCV000742025] Chr22:44564975..44569346 [GRCh37]
Chr22:22q13.31
benign
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51211392)x3 copy number gain not provided [RCV000741692] Chr22:16114244..51211392 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3 copy number gain not provided [RCV001007181] Chr22:30654764..51197838 [GRCh37]
Chr22:22q12.2-13.33
pathogenic
NM_001003828.2(PARVB):c.837C>T (p.Phe279=) single nucleotide variant not provided [RCV000882974] Chr22:44147886 [GRCh38]
Chr22:44543766 [GRCh37]
Chr22:22q13.31
benign
GRCh37/hg19 22q13.1-13.33(chr22:40502364-51197838)x3 copy number gain not provided [RCV001007502] Chr22:40502364..51197838 [GRCh37]
Chr22:22q13.1-13.33
pathogenic
NM_001003828.2(PARVB):c.943-10_943-9insG insertion not provided [RCV000965506] Chr22:44157972..44157973 [GRCh38]
Chr22:44553852..44553853 [GRCh37]
Chr22:22q13.31
benign
NM_001003828.2(PARVB):c.1185C>T (p.Asn395=) single nucleotide variant not provided [RCV000891687] Chr22:44168669 [GRCh38]
Chr22:44564549 [GRCh37]
Chr22:22q13.31
benign
GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3 copy number gain not provided [RCV000846344] Chr22:16888899..51197838 [GRCh37]
Chr22:22q11.1-13.33
pathogenic
NM_013327.5(PARVB):c.155C>G (p.Pro52Arg) single nucleotide variant not provided [RCV000958249] Chr22:44093970 [GRCh38]
Chr22:44489850 [GRCh37]
Chr22:22q13.31
benign
NM_013327.5(PARVB):c.1044C>T (p.Ser348=) single nucleotide variant not provided [RCV000958250] Chr22:44168627 [GRCh38]
Chr22:44564507 [GRCh37]
Chr22:22q13.31
benign
Single allele deletion 22q13.3 deletion syndrome [RCV001254356] Chr22:43032129..50739836 [GRCh38]
Chr22:22q13.2-13.33
pathogenic
Single allele deletion 22q13.3 deletion syndrome [RCV001254364] Chr22:43802117..50806121 [GRCh38]
Chr22:22q13.31-13.33
pathogenic
GRCh37/hg19 22q13.31(chr22:44541184-44783321)x3 copy number gain not provided [RCV001258786] Chr22:44541184..44783321 [GRCh37]
Chr22:22q13.31
uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3 copy number gain See cases [RCV001263056] Chr22:16197005..51224252 [GRCh37]
Chr22:22q11.1-13.33
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14653 AgrOrtholog
COSMIC PARVB COSMIC
Ensembl Genes ENSG00000188677 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000342492 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000384353 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000384515 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000393758 UniProtKB/TrEMBL
  ENSP00000482511 ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENST00000338758 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000404989 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000406477 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000444029 UniProtKB/TrEMBL
  ENST00000619710 ENTREZGENE, UniProtKB/TrEMBL
Gene3D-CATH 1.10.418.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000188677 GTEx
HGNC ID HGNC:14653 ENTREZGENE
Human Proteome Map PARVB Human Proteome Map
InterPro CH-domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CH_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Parvin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:29780 UniProtKB/Swiss-Prot
NCBI Gene 29780 ENTREZGENE
OMIM 608121 OMIM
PANTHER PTHR12114 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam PF00307 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32951 PharmGKB
PIRSF Parvin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE PS50021 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SM00033 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF47576 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WZB5 ENTREZGENE, UniProtKB/TrEMBL
  B0QYP8_HUMAN UniProtKB/TrEMBL
  PARVB_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary B0QYM8 UniProtKB/Swiss-Prot
  B0QYN1 UniProtKB/Swiss-Prot
  B2R9X6 UniProtKB/Swiss-Prot
  Q5TGJ5 UniProtKB/Swiss-Prot
  Q86X93 UniProtKB/Swiss-Prot
  Q96PN1 UniProtKB/Swiss-Prot
  Q9NSP7 UniProtKB/Swiss-Prot
  Q9UGT3 UniProtKB/Swiss-Prot
  Q9Y368 UniProtKB/Swiss-Prot
  Q9Y3L6 UniProtKB/Swiss-Prot
  Q9Y3L7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 PARVB  parvin beta  PARVB  parvin, beta  Symbol and/or name change 5135510 APPROVED