ACTR3B (actin related protein 3B) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: ACTR3B (actin related protein 3B) Homo sapiens
Analyze
Symbol: ACTR3B
Name: actin related protein 3B
RGD ID: 1603621
HGNC Page HGNC:17256
Description: Predicted to enable ATP binding activity and actin binding activity. Predicted to contribute to actin filament binding activity. Predicted to be involved in Arp2/3 complex-mediated actin nucleation. Located in extracellular exosome.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: actin-like protein 3B; actin-related protein 3-beta; actin-related protein 3B; actin-related protein Arp11; actin-related protein ARP4; ARP11; ARP3 actin related protein 3 homolog B; ARP3 actin-related protein 3 homolog B; ARP3 actin-related protein 3 homolog B (yeast); ARP3-beta; ARP3BETA; DKFZp686O24114
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: ACTR3BP1   ACTR3BP2   ACTR3BP3   ACTR3BP4   ACTR3BP5   ACTR3BP6   ACTR3BP7  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387152,759,752 - 152,855,378 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7152,759,749 - 152,855,378 (+)EnsemblGRCh38hg38GRCh38
GRCh377152,456,837 - 152,552,463 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367152,087,784 - 152,183,396 (+)NCBINCBI36Build 36hg18NCBI36
Celera7148,258,695 - 148,259,790 (+)NCBICelera
Cytogenetic Map7q36.1-q36.2NCBI
HuRef7146,267,013 - 146,310,451 (+)NCBIHuRef
HuRef7146,326,572 - 146,359,033 (+)NCBIHuRef
CHM1_17152,465,204 - 152,560,884 (+)NCBICHM1_1
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27151,783,914 - 151,879,544 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Autism  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10047519   PMID:10806390   PMID:11162478   PMID:12477932   PMID:12853948   PMID:12857853   PMID:14651955   PMID:14702039   PMID:15176487   PMID:16169070   PMID:17353931   PMID:20379614  
PMID:21873635   PMID:21988832   PMID:23251661   PMID:23398456   PMID:23533145   PMID:24981860   PMID:25082827   PMID:25963833   PMID:26186194   PMID:26344197   PMID:26618866   PMID:26673895  
PMID:28514442   PMID:29229926   PMID:29568061   PMID:32780723   PMID:33961781   PMID:35271311   PMID:35914814  


Genomics

Comparative Map Data
ACTR3B
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387152,759,752 - 152,855,378 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7152,759,749 - 152,855,378 (+)EnsemblGRCh38hg38GRCh38
GRCh377152,456,837 - 152,552,463 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367152,087,784 - 152,183,396 (+)NCBINCBI36Build 36hg18NCBI36
Celera7148,258,695 - 148,259,790 (+)NCBICelera
Cytogenetic Map7q36.1-q36.2NCBI
HuRef7146,267,013 - 146,310,451 (+)NCBIHuRef
HuRef7146,326,572 - 146,359,033 (+)NCBIHuRef
CHM1_17152,465,204 - 152,560,884 (+)NCBICHM1_1
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27151,783,914 - 151,879,544 (+)NCBI
Actr3b
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39525,964,960 - 26,055,686 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl525,964,995 - 26,055,686 (+)EnsemblGRCm39 Ensembl
GRCm38525,759,941 - 25,850,691 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl525,759,997 - 25,850,688 (+)EnsemblGRCm38mm10GRCm38
MGSCv37525,265,844 - 25,356,160 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36525,270,091 - 25,360,407 (+)NCBIMGSCv36mm8
Celera522,699,772 - 22,788,698 (+)NCBICelera
Cytogenetic Map5B1NCBI
cM Map512.35NCBI
Actr3b
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr849,995,553 - 10,089,422 (-)NCBIGRCr8
mRatBN7.249,261,631 - 9,355,496 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl49,262,233 - 9,355,441 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx414,258,894 - 14,353,572 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0410,073,170 - 10,167,844 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.048,429,951 - 8,518,857 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.045,644,287 - 5,672,708 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl45,644,260 - 5,672,708 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl45,721,261 - 5,773,301 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.045,668,162 - 5,696,597 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.444,654,603 - 4,747,545 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera4963,948 - 1,056,011 (+)NCBICelera
Cytogenetic Map4q11NCBI
Actr3b
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554916,686,420 - 6,742,099 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554916,690,246 - 6,741,900 (+)NCBIChiLan1.0ChiLan1.0
ACTR3B
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26189,175,351 - 190,156,098 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1741,185,617 - 41,281,574 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v07144,340,531 - 144,436,456 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
ACTR3B
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11616,470,965 - 16,555,777 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1616,470,853 - 16,555,259 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1617,087,180 - 17,171,836 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01618,202,406 - 18,287,120 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1618,202,376 - 18,287,112 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11616,575,306 - 16,660,017 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01617,156,385 - 17,241,264 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01617,207,225 - 17,292,092 (+)NCBIUU_Cfam_GSD_1.0
Actr3b
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244051184,972,871 - 5,029,644 (-)NCBIHiC_Itri_2
SpeTri2.0NW_0049365277,873,874 - 7,930,341 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ACTR3B
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1184,637,408 - 4,748,233 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2184,955,097 - 4,999,916 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ACTR3B
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.121120,901,960 - 120,997,307 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl21120,902,030 - 120,998,759 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607216,941,124 - 17,036,500 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Actr3b
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248004,256,748 - 4,322,758 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248004,257,418 - 4,373,677 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ACTR3B
6 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3 copy number gain See cases [RCV000050876] Chr7:129310166..159282390 [GRCh38]
Chr7:128950007..159075079 [GRCh37]
Chr7:128737243..158767840 [NCBI36]
Chr7:7q32.1-36.3		 pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132850196-159325876)x3 copy number gain See cases [RCV000051101] Chr7:132850196..159325876 [GRCh38]
Chr7:132534956..159118566 [GRCh37]
Chr7:132185496..158811327 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:147250465-159325876)x1 copy number loss See cases [RCV000051108] Chr7:147250465..159325876 [GRCh38]
Chr7:146947557..159118566 [GRCh37]
Chr7:146578490..158811327 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q36.1-36.2(chr7:152674212-153187462)x3 copy number gain See cases [RCV000053551] Chr7:152674212..153187462 [GRCh38]
Chr7:152371297..152884547 [GRCh37]
Chr7:152002230..152515480 [NCBI36]
Chr7:7q36.1-36.2		 uncertain significance
GRCh38/hg38 7q36.2(chr7:152807005-153753205)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053552]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053552]|See cases [RCV000053552] Chr7:152807005..153753205 [GRCh38]
Chr7:152504090..153450290 [GRCh37]
Chr7:152135023..153081223 [NCBI36]
Chr7:7q36.2		 uncertain significance
GRCh38/hg38 7q33-36.3(chr7:136309982-159307523)x3 copy number gain See cases [RCV000053576] Chr7:136309982..159307523 [GRCh38]
Chr7:135994730..159100212 [GRCh37]
Chr7:135645270..158792973 [NCBI36]
Chr7:7q33-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:142021716-159325876)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|See cases [RCV000053577] Chr7:142021716..159325876 [GRCh38]
Chr7:142528609..159118566 [GRCh37]
Chr7:141367985..158811327 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:143884559-159282390)x1 copy number loss See cases [RCV000054178] Chr7:143884559..159282390 [GRCh38]
Chr7:143581652..159075079 [GRCh37]
Chr7:143212585..158767840 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:145699944-159296617)x1 copy number loss See cases [RCV000054188] Chr7:145699944..159296617 [GRCh38]
Chr7:145397037..159089306 [GRCh37]
Chr7:145027970..158782067 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.3(chr7:152332476-159296617)x1 copy number loss See cases [RCV000054190] Chr7:152332476..159296617 [GRCh38]
Chr7:152029561..159089306 [GRCh37]
Chr7:151660494..158782067 [NCBI36]
Chr7:7q36.1-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:139365967-159282531)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|See cases [RCV000054175] Chr7:139365967..159282531 [GRCh38]
Chr7:139050713..159075220 [GRCh37]
Chr7:138701253..158767981 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:140754198-159307523)x1 copy number loss See cases [RCV000054176] Chr7:140754198..159307523 [GRCh38]
Chr7:140453998..159100212 [GRCh37]
Chr7:140100467..158792973 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:142358524-159282531)x1 copy number loss See cases [RCV000054177] Chr7:142358524..159282531 [GRCh38]
Chr7:142528609..159075220 [GRCh37]
Chr7:141726947..158767981 [NCBI36]
Chr7:7q34-36.3		 pathogenic
NM_001040135.2(ACTR3B):c.45-2039C>A single nucleotide variant Lung cancer [RCV000105831] Chr7:152781148 [GRCh38]
Chr7:152478233 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001040135.2(ACTR3B):c.*1316A>T single nucleotide variant Lung cancer [RCV000105832] Chr7:152855869 [GRCh38]
Chr7:152552954 [GRCh37]
Chr7:7q36.2		 uncertain significance
GRCh38/hg38 7q36.2(chr7:152860576-154126004)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053553]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053553]|See cases [RCV000053553] Chr7:152860576..154126004 [GRCh38]
Chr7:152557661..153823089 [GRCh37]
Chr7:152188594..153454022 [NCBI36]
Chr7:7q36.2		 uncertain significance
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q36.1-36.2(chr7:151214163-153187462)x1 copy number loss See cases [RCV000134853] Chr7:151214163..153187462 [GRCh38]
Chr7:150911249..152884547 [GRCh37]
Chr7:150542182..152515480 [NCBI36]
Chr7:7q36.1-36.2		 pathogenic
GRCh38/hg38 7q35-36.2(chr7:147345844-153833351)x3 copy number gain See cases [RCV000135825] Chr7:147345844..153833351 [GRCh38]
Chr7:147042936..153530436 [GRCh37]
Chr7:146673869..153161369 [NCBI36]
Chr7:7q35-36.2		 pathogenic
GRCh38/hg38 7q36.1-36.3(chr7:151378879-158923762)x1 copy number loss See cases [RCV000136125] Chr7:151378879..158923762 [GRCh38]
Chr7:151075965..158716453 [GRCh37]
Chr7:150706898..158409214 [NCBI36]
Chr7:7q36.1-36.3		 pathogenic|benign
GRCh38/hg38 7q33-36.2(chr7:137751200-154815582)x3 copy number gain See cases [RCV000136592] Chr7:137751200..154815582 [GRCh38]
Chr7:137435946..154607292 [GRCh37]
Chr7:137086486..154238225 [NCBI36]
Chr7:7q33-36.2		 pathogenic
GRCh38/hg38 7q36.1-36.3(chr7:150486071-159335865)x1 copy number loss See cases [RCV000136089] Chr7:150486071..159335865 [GRCh38]
Chr7:150183159..159128555 [GRCh37]
Chr7:149814092..158821316 [NCBI36]
Chr7:7q36.1-36.3		 pathogenic
GRCh38/hg38 7q36.2-36.3(chr7:152807205-159325876)x1 copy number loss See cases [RCV000136940] Chr7:152807205..159325876 [GRCh38]
Chr7:152504290..159118566 [GRCh37]
Chr7:152135223..158811327 [NCBI36]
Chr7:7q36.2-36.3		 pathogenic
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.3(chr7:151104277-159325876)x3 copy number gain See cases [RCV000136683] Chr7:151104277..159325876 [GRCh38]
Chr7:150801364..159118566 [GRCh37]
Chr7:150432297..158811327 [NCBI36]
Chr7:7q36.1-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.2(chr7:152674212-153203028)x3 copy number gain See cases [RCV000137699] Chr7:152674212..153203028 [GRCh38]
Chr7:152371297..152900113 [GRCh37]
Chr7:152002230..152531046 [NCBI36]
Chr7:7q36.1-36.2		 uncertain significance
GRCh38/hg38 7q36.1-36.3(chr7:150802801-159335866)x1 copy number loss See cases [RCV000137465] Chr7:150802801..159335866 [GRCh38]
Chr7:150499889..159128556 [GRCh37]
Chr7:150130822..158821317 [NCBI36]
Chr7:7q36.1-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:141960861-159335866)x1 copy number loss See cases [RCV000137256] Chr7:141960861..159335866 [GRCh38]
Chr7:142528609..159128556 [GRCh37]
Chr7:141307130..158821317 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:145436544-159331441)x1 copy number loss See cases [RCV000137338] Chr7:145436544..159331441 [GRCh38]
Chr7:145133637..159124131 [GRCh37]
Chr7:144764570..158816892 [NCBI36]
Chr7:7q35-36.3		 pathogenic|likely pathogenic
GRCh38/hg38 7q35-36.3(chr7:145250254-159335866)x1 copy number loss See cases [RCV000138005] Chr7:145250254..159335866 [GRCh38]
Chr7:144947347..159128556 [GRCh37]
Chr7:144578280..158821317 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1 copy number loss See cases [RCV000138120] Chr7:134666829..158591882 [GRCh38]
Chr7:134351581..158384574 [GRCh37]
Chr7:134002121..158077335 [NCBI36]
Chr7:7q33-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:146047157-157522158)x1 copy number loss See cases [RCV000137781] Chr7:146047157..157522158 [GRCh38]
Chr7:145744250..157314852 [GRCh37]
Chr7:145375183..157007613 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 copy number gain See cases [RCV000138847] Chr7:121863759..159335865 [GRCh38]
Chr7:121503813..159128555 [GRCh37]
Chr7:121291049..158821316 [NCBI36]
Chr7:7q31.32-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.2(chr7:150113232-154162779)x3 copy number gain See cases [RCV000138566] Chr7:150113232..154162779 [GRCh38]
Chr7:149810321..153859864 [GRCh37]
Chr7:149441254..153490797 [NCBI36]
Chr7:7q36.1-36.2		 likely pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132444095-159335866)x3 copy number gain See cases [RCV000139654] Chr7:132444095..159335866 [GRCh38]
Chr7:132128854..159128556 [GRCh37]
Chr7:131779394..158821317 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.2(chr7:150275734-153342804)x3 copy number gain See cases [RCV000139660] Chr7:150275734..153342804 [GRCh38]
Chr7:149972823..153039889 [GRCh37]
Chr7:149603756..152670822 [NCBI36]
Chr7:7q36.1-36.2		 uncertain significance
GRCh38/hg38 7q36.1-36.3(chr7:152428852-159335865)x3 copy number gain See cases [RCV000139725] Chr7:152428852..159335865 [GRCh38]
Chr7:152125937..159128555 [GRCh37]
Chr7:151756870..158821316 [NCBI36]
Chr7:7q36.1-36.3		 pathogenic
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 copy number gain See cases [RCV000141413] Chr7:115459015..159325817 [GRCh38]
Chr7:115099069..159118507 [GRCh37]
Chr7:114886305..158811268 [NCBI36]
Chr7:7q31.2-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.2(chr7:151424353-153358923)x1 copy number loss See cases [RCV000142444] Chr7:151424353..153358923 [GRCh38]
Chr7:151121439..153056008 [GRCh37]
Chr7:150752372..152686941 [NCBI36]
Chr7:7q36.1-36.2		 uncertain significance
GRCh38/hg38 7q36.1-36.2(chr7:152438976-152964146)x3 copy number gain See cases [RCV000142238] Chr7:152438976..152964146 [GRCh38]
Chr7:152136061..152661231 [GRCh37]
Chr7:151766994..152292164 [NCBI36]
Chr7:7q36.1-36.2		 uncertain significance
GRCh38/hg38 7q32.3-36.3(chr7:131228764-159335866)x3 copy number gain See cases [RCV000142802] Chr7:131228764..159335866 [GRCh38]
Chr7:130913523..159128556 [GRCh37]
Chr7:130564063..158821317 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.3(chr7:150260297-159325876)x1 copy number loss See cases [RCV000142592] Chr7:150260297..159325876 [GRCh38]
Chr7:149957386..159118566 [GRCh37]
Chr7:149588319..158811327 [NCBI36]
Chr7:7q36.1-36.3		 pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:131171478-159327017)x3 copy number gain See cases [RCV000143754] Chr7:131171478..159327017 [GRCh38]
Chr7:130856237..159119707 [GRCh37]
Chr7:130506777..158812468 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132438072-159327017)x3 copy number gain See cases [RCV000143707] Chr7:132438072..159327017 [GRCh38]
Chr7:132122831..159119707 [GRCh37]
Chr7:131773371..158812468 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:147144002-159327017)x1 copy number loss See cases [RCV000143503] Chr7:147144002..159327017 [GRCh38]
Chr7:146841094..159119707 [GRCh37]
Chr7:146472027..158812468 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:137589621-159119707)x3 copy number gain See cases [RCV000449264] Chr7:137589621..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
GRCh37/hg19 7q35-36.3(chr7:143839360-159138663) copy number loss Abnormal esophagus morphology [RCV000416719] Chr7:143839360..159138663 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:133799185-159119707)x1 copy number loss See cases [RCV000448836] Chr7:133799185..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:152094127-152522083)x3 copy number gain See cases [RCV000448843] Chr7:152094127..152522083 [GRCh37]
Chr7:7q36.1		 likely benign
GRCh37/hg19 7q36.1-36.3(chr7:149261179-159075020)x3 copy number gain See cases [RCV000447776] Chr7:149261179..159075020 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7q32.1-36.3(chr7:128276078-159119707)x3 copy number gain See cases [RCV000447956] Chr7:128276078..159119707 [GRCh37]
Chr7:7q32.1-36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:151167135-159119707)x1 copy number loss See cases [RCV000512112] Chr7:151167135..159119707 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:140636858-159119707)x1 copy number loss See cases [RCV000510250] Chr7:140636858..159119707 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:136758593-159119707)x3 copy number gain See cases [RCV000510490] Chr7:136758593..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:151665824-152589802)x3 copy number gain See cases [RCV000510426] Chr7:151665824..152589802 [GRCh37]
Chr7:7q36.1		 likely benign
GRCh37/hg19 7q33-36.3(chr7:137917376-159119707)x1 copy number loss See cases [RCV000511889] Chr7:137917376..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:151566053-159119707)x3 copy number gain See cases [RCV000511775] Chr7:151566053..159119707 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:151681403-152594326)x3 copy number gain See cases [RCV000511239] Chr7:151681403..152594326 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q36.1-36.3(chr7:150553743-159119707)x3 copy number gain See cases [RCV000510762] Chr7:150553743..159119707 [GRCh37]
Chr7:7q36.1-36.3		 likely pathogenic
GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220) copy number gain not provided [RCV000767558] Chr7:128312450..159119220 [GRCh37]
Chr7:7q32.1-36.3		 pathogenic
GRCh37/hg19 7q36.1-36.2(chr7:151387196-154070094)x1 copy number loss See cases [RCV000512509] Chr7:151387196..154070094 [GRCh37]
Chr7:7q36.1-36.2		 likely pathogenic
GRCh37/hg19 7q36.1(chr7:151858920-152501978)x3 copy number gain not provided [RCV000682860] Chr7:151858920..152501978 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q36.1(chr7:151852539-152560660)x3 copy number gain not provided [RCV000682864] Chr7:151852539..152560660 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q34-36.3(chr7:140133025-158982771)x1 copy number loss not provided [RCV000682910] Chr7:140133025..158982771 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
NC_000007.14:g.(?_152454659)_(158705768_?)del deletion Autism [RCV000754327] Chr7:152454659..158705768 [GRCh38]
Chr7:7q36.1-36.3		 likely pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:139623170-158329903)x3 copy number gain not provided [RCV000747070] Chr7:139623170..158329903 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:141938235-159126310)x1 copy number loss not provided [RCV000747083] Chr7:141938235..159126310 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q35-36.1(chr7:143711059-152573935)x3 copy number gain not provided [RCV000747094] Chr7:143711059..152573935 [GRCh37]
Chr7:7q35-36.1		 benign
GRCh37/hg19 7q36.1-36.3(chr7:148238976-159126310)x1 copy number loss not provided [RCV000747115] Chr7:148238976..159126310 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:149968222-152539376)x3 copy number gain not provided [RCV000847582] Chr7:149968222..152539376 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q32.3-36.3(chr7:131414604-159126310)x1 copy number loss See cases [RCV001007432] Chr7:131414604..159126310 [GRCh37]
Chr7:7q32.3-36.3		 pathogenic
GRCh37/hg19 7q36.1-36.2(chr7:151699080-152779856)x3 copy number gain not provided [RCV000847674] Chr7:151699080..152779856 [GRCh37]
Chr7:7q36.1-36.2		 uncertain significance
GRCh37/hg19 7q36.1-36.2(chr7:152539403-152905013)x4 copy number gain not provided [RCV000847583] Chr7:152539403..152905013 [GRCh37]
Chr7:7q36.1-36.2		 uncertain significance
GRCh37/hg19 7q35-36.3(chr7:143107740-156886246)x3 copy number gain not provided [RCV001249383] Chr7:143107740..156886246 [GRCh37]
Chr7:7q35-36.3		 not provided
GRCh37/hg19 7q36.1-36.2(chr7:152502421-153499951)x3 copy number gain not provided [RCV001006028] Chr7:152502421..153499951 [GRCh37]
Chr7:7q36.1-36.2		 likely benign
GRCh37/hg19 7q32.3-36.3(chr7:130592554-159119707)x3 copy number gain not provided [RCV000849569] Chr7:130592554..159119707 [GRCh37]
Chr7:7q32.3-36.3		 pathogenic
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3 copy number gain not provided [RCV001005994] Chr7:109251060..159119707 [GRCh37]
Chr7:7q31.1-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:138620939-159233475)x3 copy number gain Neurodevelopmental disorder [RCV003327610] Chr7:138620939..159233475 [GRCh38]
Chr7:7q34-36.3		 likely pathogenic
GRCh37/hg19 7q35-36.3(chr7:145962558-159119707)x1 copy number loss not provided [RCV001006022] Chr7:145962558..159119707 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:152093605-152539495)x3 copy number gain not provided [RCV001258984] Chr7:152093605..152539495 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q36.1-36.2(chr7:151550461-153195115)x4 copy number gain not provided [RCV001795854] Chr7:151550461..153195115 [GRCh37]
Chr7:7q36.1-36.2		 uncertain significance
GRCh37/hg19 7q33-36.3(chr7:133851002-159119707)x3 copy number gain not provided [RCV001834520] Chr7:133851002..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:148695373-159119707)x1 copy number loss not provided [RCV001832910] Chr7:148695373..159119707 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:148153261-157543640)x3 copy number gain not provided [RCV001827941] Chr7:148153261..157543640 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
NC_000007.13:g.(?_150307047)_(152613597_?)del deletion not provided [RCV003113787] Chr7:150307047..152613597 [GRCh37]
Chr7:7q36.1-36.2		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:149062717-159124131)x1 copy number loss not provided [RCV002279756] Chr7:149062717..159124131 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7q35-36.3(chr7:146927174-159128556)x3 copy number gain not provided [RCV002279740] Chr7:146927174..159128556 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3		 uncertain significance
GRCh37/hg19 7q36.1-36.2(chr7:151581341-153599029)x1 copy number loss not provided [RCV002473720] Chr7:151581341..153599029 [GRCh37]
Chr7:7q36.1-36.2		 pathogenic
GRCh37/hg19 7q36.1-36.2(chr7:152000451-152830642)x3 copy number gain not provided [RCV002474683] Chr7:152000451..152830642 [GRCh37]
Chr7:7q36.1-36.2		 uncertain significance
GRCh37/hg19 7q36.1(chr7:152126966-152539376)x3 copy number gain not provided [RCV002474994] Chr7:152126966..152539376 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q36.1-36.2(chr7:151265288-152929871)x3 copy number gain not provided [RCV002472437] Chr7:151265288..152929871 [GRCh37]
Chr7:7q36.1-36.2		 uncertain significance
NM_020445.6(ACTR3B):c.782C>T (p.Ala261Val) single nucleotide variant Inborn genetic diseases [RCV002844067] Chr7:152823439 [GRCh38]
Chr7:152520524 [GRCh37]
Chr7:7q36.2		 uncertain significance
NM_020445.6(ACTR3B):c.896T>C (p.Val299Ala) single nucleotide variant Inborn genetic diseases [RCV002799058] Chr7:152825067 [GRCh38]
Chr7:152522152 [GRCh37]
Chr7:7q36.2		 uncertain significance
NM_020445.6(ACTR3B):c.770C>T (p.Thr257Met) single nucleotide variant Inborn genetic diseases [RCV002961698] Chr7:152823427 [GRCh38]
Chr7:152520512 [GRCh37]
Chr7:7q36.2		 uncertain significance
NM_020445.6(ACTR3B):c.485C>T (p.Thr162Met) single nucleotide variant Inborn genetic diseases [RCV003212343] Chr7:152816533 [GRCh38]
Chr7:152513618 [GRCh37]
Chr7:7q36.2		 uncertain significance
GRCh38/hg38 7q33-36.3(chr7:137463392-159345973)x3 copy number gain Neurodevelopmental disorder [RCV003327609] Chr7:137463392..159345973 [GRCh38]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q34-36.1(chr7:140154317-152551638)x1 copy number loss not provided [RCV003334300] Chr7:140154317..152551638 [GRCh37]
Chr7:7q34-36.1		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:135639005-159119707)x1 copy number loss not provided [RCV003482988] Chr7:135639005..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:142099013-159119707)x1 copy number loss not provided [RCV003482989] Chr7:142099013..159119707 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q35-36.3(chr7:144940098-159119707)x1 copy number loss not provided [RCV003482991] Chr7:144940098..159119707 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:137456457-159119707)x3 copy number gain not specified [RCV003986713] Chr7:137456457..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1255
Count of miRNA genes:470
Interacting mature miRNAs:509
Transcripts:ENST00000256001, ENST00000377776, ENST00000397282, ENST00000479402, ENST00000488782, ENST00000537264
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-147571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377149,978,428 - 149,978,726UniSTSGRCh37
GRCh377152,525,323 - 152,525,621UniSTSGRCh37
Build 367149,609,361 - 149,609,659RGDNCBI36
Cytogenetic Map7q36.1UniSTS
HuRef7143,794,399 - 143,794,697UniSTS
CRA_TCAGchr7v27151,852,403 - 151,852,701UniSTS
CRA_TCAGchr7v27149,316,295 - 149,316,593UniSTS
TNG Radiation Hybrid Map768950.0UniSTS
GDB:1318002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,531,003 - 152,531,144UniSTSGRCh37
GRCh377149,972,902 - 149,973,043UniSTSGRCh37
Build 367149,603,835 - 149,603,976RGDNCBI36
Cytogenetic Map7q36.1UniSTS
HuRef7143,788,937 - 143,789,078UniSTS
HuRef7146,337,461 - 146,337,602UniSTS
CRA_TCAGchr7v27149,310,769 - 149,310,910UniSTS
CRA_TCAGchr7v27151,858,083 - 151,858,224UniSTS
RH78488  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,551,908 - 152,552,028UniSTSGRCh37
Build 367152,182,841 - 152,182,961RGDNCBI36
Celera7147,098,405 - 147,098,525RGD
Cytogenetic Map7q36.1UniSTS
HuRef7146,358,477 - 146,358,597UniSTS
CRA_TCAGchr7v27151,878,988 - 151,879,108UniSTS
GeneMap99-GB4 RH Map7675.32UniSTS
WI-14223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,552,339 - 152,552,441UniSTSGRCh37
Build 367152,183,272 - 152,183,374RGDNCBI36
Celera7147,098,836 - 147,098,938RGD
Cytogenetic Map7q36.1UniSTS
HuRef7146,358,908 - 146,359,010UniSTS
CRA_TCAGchr7v27151,879,419 - 151,879,521UniSTS
GeneMap99-GB4 RH Map7675.22UniSTS
Whitehead-RH Map7648.4UniSTS
D7S1390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,467,126 - 152,467,261UniSTSGRCh37
GRCh377149,619,772 - 149,619,907UniSTSGRCh37
Build 367149,250,705 - 149,250,840RGDNCBI36
Cytogenetic Map7q36.1UniSTS
HuRef7146,277,298 - 146,277,433UniSTS
CRA_TCAGchr7v27148,957,639 - 148,957,774UniSTS
CRA_TCAGchr7v27151,794,206 - 151,794,341UniSTS
GDB:1318182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,524,232 - 152,524,351UniSTSGRCh37
GRCh377149,979,698 - 149,979,817UniSTSGRCh37
Build 367149,610,631 - 149,610,750RGDNCBI36
Cytogenetic Map7q36.1UniSTS
HuRef7143,795,669 - 143,795,788UniSTS
CRA_TCAGchr7v27149,317,565 - 149,317,684UniSTS
CRA_TCAGchr7v27151,851,312 - 151,851,431UniSTS
SHGC-30943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377149,616,919 - 149,617,060UniSTSGRCh37
GRCh377152,469,963 - 152,470,104UniSTSGRCh37
Build 367149,247,852 - 149,247,993RGDNCBI36
Cytogenetic Map7q36.1UniSTS
HuRef7146,280,135 - 146,280,277UniSTS
CRA_TCAGchr7v27151,797,043 - 151,797,184UniSTS
CRA_TCAGchr7v27148,954,786 - 148,954,927UniSTS
TNG Radiation Hybrid Map768873.0UniSTS
GeneMap99-G3 RH Map78365.0UniSTS
STS-W68401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,551,803 - 152,551,993UniSTSGRCh37
Build 367152,182,736 - 152,182,926RGDNCBI36
Celera7147,098,300 - 147,098,490RGD
Celera7148,259,579 - 148,259,769UniSTS
Cytogenetic Map7q36.1UniSTS
HuRef7146,358,372 - 146,358,562UniSTS
CRA_TCAGchr7v27151,878,883 - 151,879,073UniSTS
GeneMap99-GB4 RH Map7675.32UniSTS
D7S3198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,503,164 - 152,503,345UniSTSGRCh37
GRCh377150,000,738 - 150,000,919UniSTSGRCh37
Build 367149,631,671 - 149,631,852RGDNCBI36
Celera7144,557,827 - 144,558,008RGD
Cytogenetic Map7q36.1UniSTS
HuRef7146,315,547 - 146,315,728UniSTS
HuRef7143,816,682 - 143,816,863UniSTS
CRA_TCAGchr7v27149,338,590 - 149,338,771UniSTS
CRA_TCAGchr7v27151,830,244 - 151,830,425UniSTS
D7S3199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,552,015 - 152,552,230UniSTSGRCh37
Build 367152,182,948 - 152,183,163RGDNCBI36
Celera7147,098,512 - 147,098,727RGD
Cytogenetic Map7q36.1UniSTS
HuRef7146,358,584 - 146,358,799UniSTS
CRA_TCAGchr7v27151,879,095 - 151,879,310UniSTS
D13S1639  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q22.1UniSTS
D3S1673  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic MapXp22.2UniSTS
D1S1423  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p22.3-p21.32UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map9q12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map10p14-p13UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map11q23-q24UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map22cen-q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map4q28UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map1q41-q42UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map11q24.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3q13UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map9p21.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq27.2UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map20q11.21-q11.23UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map15q26UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p15.1-p14UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map7q32.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21-q24UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map8q24.12UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map6q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map20pter-p12UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map14q22.2UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p22-p21UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map10q22.3-q23.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map3p12.3UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map3q11.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6p24.2UniSTS
Cytogenetic Map20q13.33UniSTS


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 pharyngeal arch
High
Medium 91 184 452 112 41 8 1717 160 3102 19 754 278 107 1 141 1223 1
Low 2348 2767 1273 511 1877 456 2640 2029 632 400 705 1335 67 1063 1565 5 2
Below cutoff 40 1 1 33 1 8 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001040135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350942 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350943 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350944 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350945 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350946 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_020445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146946 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146949 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA559050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB209174 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC072057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC073249 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092180 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF023453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF086920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF104455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC008682 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB570472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DN601600 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000256001   ⟹   ENSP00000256001
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7152,759,752 - 152,855,378 (+)Ensembl
RefSeq Acc Id: ENST00000377776   ⟹   ENSP00000367007
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7152,759,749 - 152,854,938 (+)Ensembl
RefSeq Acc Id: ENST00000397282   ⟹   ENSP00000380452
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7152,759,788 - 152,854,949 (+)Ensembl
RefSeq Acc Id: ENST00000479402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7152,810,742 - 152,855,371 (+)Ensembl
RefSeq Acc Id: ENST00000488782
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7152,800,623 - 152,816,522 (+)Ensembl
RefSeq Acc Id: NM_001040135   ⟹   NP_001035225
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
GRCh377152,456,834 - 152,552,464 (+)NCBI
Build 367152,087,784 - 152,183,396 (+)NCBI Archive
Celera7148,258,695 - 148,259,790 (+)RGD
HuRef7146,267,013 - 146,310,451 (+)NCBI
HuRef7146,326,572 - 146,359,033 (+)NCBI
CHM1_17152,465,204 - 152,560,884 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
CRA_TCAGchr7v27151,783,914 - 151,879,544 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001350940   ⟹   NP_001337869
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001350941   ⟹   NP_001337870
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001350942   ⟹   NP_001337871
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001350943   ⟹   NP_001337872
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001350944   ⟹   NP_001337873
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001350945   ⟹   NP_001337874
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001350946   ⟹   NP_001337875
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NM_020445   ⟹   NP_065178
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
GRCh377152,456,834 - 152,552,464 (+)NCBI
Build 367152,087,784 - 152,183,396 (+)NCBI Archive
Celera7148,258,695 - 148,259,790 (+)RGD
HuRef7146,267,013 - 146,310,451 (+)NCBI
HuRef7146,326,572 - 146,359,033 (+)NCBI
CHM1_17152,465,204 - 152,560,884 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
CRA_TCAGchr7v27151,783,914 - 151,879,544 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146946
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146947
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146948
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146949
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146950
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
RefSeq Acc Id: NR_146951
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387152,759,752 - 152,855,378 (+)NCBI
T2T-CHM13v2.07153,933,015 - 154,028,620 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_001035225   ⟸   NM_001040135
- Peptide Label: isoform 2
- UniProtKB: Q59FV6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_065178   ⟸   NM_020445
- Peptide Label: isoform 1
- UniProtKB: Q7Z526 (UniProtKB/Swiss-Prot),   B4DFW4 (UniProtKB/Swiss-Prot),   A8MTG1 (UniProtKB/Swiss-Prot),   Q96BT2 (UniProtKB/Swiss-Prot),   Q9P1U1 (UniProtKB/Swiss-Prot),   Q59FV6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001337871   ⟸   NM_001350942
- Peptide Label: isoform 3
- UniProtKB: B7Z9W3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001337873   ⟸   NM_001350944
- Peptide Label: isoform 4
- UniProtKB: B4DT29 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001337870   ⟸   NM_001350941
- Peptide Label: isoform 3
- UniProtKB: B7Z9W3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001337874   ⟸   NM_001350945
- Peptide Label: isoform 5
- UniProtKB: Q59GD5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001337869   ⟸   NM_001350940
- Peptide Label: isoform 3
- UniProtKB: B7Z9W3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001337875   ⟸   NM_001350946
- Peptide Label: isoform 6
- Sequence:
RefSeq Acc Id: NP_001337872   ⟸   NM_001350943
- Peptide Label: isoform 3
- UniProtKB: B7Z9W3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000256001   ⟸   ENST00000256001
RefSeq Acc Id: ENSP00000367007   ⟸   ENST00000377776
RefSeq Acc Id: ENSP00000380452   ⟸   ENST00000397282

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9P1U1-F1-model_v2 AlphaFold Q9P1U1 1-418 view protein structure

Promoters
RGD ID:6805221
Promoter ID:HG_KWN:60358
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:OTTHUMT00000322803,   OTTHUMT00000322804,   UC003WLG.1
Position:
Human AssemblyChrPosition (strand)Source
Build 367152,087,536 - 152,088,036 (+)MPROMDB
RGD ID:7212409
Promoter ID:EPDNEW_H11951
Type:initiation region
Name:ACTR3B_1
Description:ARP3 actin related protein 3 homolog B
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
GRCh387152,759,752 - 152,759,812EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17256 AgrOrtholog
COSMIC ACTR3B COSMIC
Ensembl Genes ENSG00000133627 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000256001 ENTREZGENE
  ENST00000256001.13 UniProtKB/Swiss-Prot
  ENST00000377776 ENTREZGENE
  ENST00000377776.7 UniProtKB/Swiss-Prot
  ENST00000397282 ENTREZGENE
  ENST00000397282.2 UniProtKB/Swiss-Prot
Gene3D-CATH 3.30.420.40 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000133627 GTEx
HGNC ID HGNC:17256 ENTREZGENE
Human Proteome Map ACTR3B Human Proteome Map
InterPro Actin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Actin/actin-like_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_NBD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:57180 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 57180 ENTREZGENE
PANTHER ACTIN-RELATED PROTEIN 3 UniProtKB/TrEMBL
  ACTIN-RELATED PROTEIN 3B-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR11937 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Actin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142672645 PharmGKB
PRINTS ACTIN UniProtKB/TrEMBL
PROSITE ACTINS_ACT_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ACTIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF53067 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8MTG1 ENTREZGENE
  ARP3B_HUMAN UniProtKB/Swiss-Prot
  B4DFW4 ENTREZGENE
  B4DT29 ENTREZGENE, UniProtKB/TrEMBL
  B7Z9W3 ENTREZGENE, UniProtKB/TrEMBL
  Q59FV6 ENTREZGENE, UniProtKB/TrEMBL
  Q59GD5 ENTREZGENE, UniProtKB/TrEMBL
  Q7Z526 ENTREZGENE
  Q96BT2 ENTREZGENE
  Q9P1U1 ENTREZGENE
UniProt Secondary A8MTG1 UniProtKB/Swiss-Prot
  B4DFW4 UniProtKB/Swiss-Prot
  Q7Z526 UniProtKB/Swiss-Prot
  Q96BT2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-01-15 ACTR3B  actin related protein 3B    ARP3 actin related protein 3 homolog B  Symbol and/or name change 5135510 APPROVED
2016-07-19 ACTR3B  ARP3 actin related protein 3 homolog B    ARP3 actin-related protein 3 homolog B (yeast)  Symbol and/or name change 5135510 APPROVED
2012-07-05 ACTR3B  ARP3 actin-related protein 3 homolog B (yeast)  ACTR3B  ARP3 actin-related protein 3 homolog B (yeast)  Symbol and/or name change 5135510 APPROVED