RFPL2 (ret finger protein like 2) - Rat Genome Database

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Gene: RFPL2 (ret finger protein like 2) Homo sapiens
Analyze
Symbol: RFPL2
Name: ret finger protein like 2
RGD ID: 1342537
HGNC Page HGNC:9979
Description: Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Predicted to be involved in several processes, including positive regulation of autophagy; positive regulation of canonical NF-kappaB signal transduction; and regulation of viral entry into host cell. Predicted to be active in cytosol and nucleoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: ret finger protein-like 2; RING finger protein 79; RNF79
RGD Orthologs
Bonobo
Alliance Orthologs
More Info more info ...
Related Pseudogenes: LOC390358  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382232,190,438 - 32,205,073 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2232,190,435 - 32,205,073 (-)EnsemblGRCh38hg38GRCh38
GRCh372232,586,425 - 32,601,060 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362230,916,425 - 30,919,466 (-)NCBINCBI36Build 36hg18NCBI36
Build 342230,910,979 - 30,914,020NCBI
Celera2216,388,684 - 16,402,982 (-)NCBICelera
Cytogenetic Map22q12.3NCBI
HuRef2215,544,043 - 15,558,342 (-)NCBIHuRef
CHM1_12232,545,769 - 32,560,065 (-)NCBICHM1_1
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IBA,IEA)
cytosol  (IBA)
nucleoplasm  (IBA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10508838   PMID:10591208   PMID:12477932   PMID:14702039   PMID:15461802   PMID:15489334   PMID:18656177   PMID:21873635   PMID:26186194   PMID:27803151   PMID:28514442   PMID:33961781  


Genomics

Comparative Map Data
RFPL2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382232,190,438 - 32,205,073 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2232,190,435 - 32,205,073 (-)EnsemblGRCh38hg38GRCh38
GRCh372232,586,425 - 32,601,060 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362230,916,425 - 30,919,466 (-)NCBINCBI36Build 36hg18NCBI36
Build 342230,910,979 - 30,914,020NCBI
Celera2216,388,684 - 16,402,982 (-)NCBICelera
Cytogenetic Map22q12.3NCBI
HuRef2215,544,043 - 15,558,342 (-)NCBIHuRef
CHM1_12232,545,769 - 32,560,065 (-)NCBICHM1_1
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBIT2T-CHM13v2.0
RFPL2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22342,137,362 - 42,144,939 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12244,838,189 - 44,845,770 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02213,207,617 - 13,216,472 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12231,062,225 - 31,066,651 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2231,062,558 - 31,068,437 (-)Ensemblpanpan1.1panPan2

Variants

.
Variants in RFPL2
19 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 22q12.1-12.3(chr22:26979579-33992220)x3 copy number gain See cases [RCV000050553] Chr22:26979579..33992220 [GRCh38]
Chr22:27375542..34388209 [GRCh37]
Chr22:25705542..32718209 [NCBI36]
Chr22:22q12.1-12.3		 pathogenic
NM_001098527.2(RFPL2):c.618G>A (p.Arg206=) single nucleotide variant Malignant melanoma [RCV000063895] Chr22:32191291 [GRCh38]
Chr22:32587278 [GRCh37]
Chr22:30917278 [NCBI36]
Chr22:22q12.3		 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
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 22q11.23-12.3(chr22:23279231-36247369)x3 copy number gain See cases [RCV000138172] Chr22:23279231..36247369 [GRCh38]
Chr22:23621418..36643415 [GRCh37]
Chr22:21951418..34973361 [NCBI36]
Chr22:22q11.23-12.3		 pathogenic
GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3 copy number gain See cases [RCV000137926] Chr22:20907226..37187347 [GRCh38]
Chr22:21261514..37583387 [GRCh37]
Chr22:19591514..35913333 [NCBI36]
Chr22:22q11.21-12.3		 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
NM_001394555.1(RFPL2):c.263G>A (p.Arg88Lys) single nucleotide variant not specified [RCV004298234] Chr22:32194347 [GRCh38]
Chr22:32590334 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.11:g.(?_32200123)_(32200234_?)del deletion Epilepsy, familial focal, with variable foci 1 [RCV000585830] Chr22:32200123..32200234 [GRCh38]
Chr22:22q12.3		 likely pathogenic
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 22q12.1-12.3(chr22:28349854-33013062)x3 copy number gain See cases [RCV000510523] Chr22:28349854..33013062 [GRCh37]
Chr22:22q12.1-12.3		 likely pathogenic
GRCh37/hg19 22q11.23-12.3(chr22:23637907-36614412)x3 copy number gain See cases [RCV000511098] Chr22:23637907..36614412 [GRCh37]
Chr22:22q11.23-12.3		 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
NM_001394555.1(RFPL2):c.742G>A (p.Gly248Arg) single nucleotide variant not specified [RCV004286707] Chr22:32191167 [GRCh38]
Chr22:32587154 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.895G>C (p.Val299Leu) single nucleotide variant not specified [RCV004308276] Chr22:32191014 [GRCh38]
Chr22:32587001 [GRCh37]
Chr22:22q12.3		 uncertain significance
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 22q11.22-12.3(chr22:22460754-35198232)x3 copy number gain not provided [RCV000684530] Chr22:22460754..35198232 [GRCh37]
Chr22:22q11.22-12.3		 pathogenic
GRCh37/hg19 22q12.2-12.3(chr22:31748161-32659394)x3 copy number gain not provided [RCV000846837] Chr22:31748161..32659394 [GRCh37]
Chr22:22q12.2-12.3		 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 22q12.3(chr22:32518130-32778254)x3 copy number gain not provided [RCV000741911] Chr22:32518130..32778254 [GRCh37]
Chr22:22q12.3		 benign
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 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
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
GRCh37/hg19 22q12.3(chr22:32468505-32780333)x3 copy number gain not provided [RCV000847184] Chr22:32468505..32780333 [GRCh37]
Chr22:22q12.3		 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
NC_000022.10:g.(?_32232938)_(34157463_?)dup duplication Muscular dystrophy-dystroglycanopathy type B6 [RCV001920547] Chr22:32232938..34157463 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.10:g.(?_29083885)_(34046674_?)dup duplication not provided [RCV001979643] Chr22:29083885..34046674 [GRCh37]
Chr22:22q12.1-12.3		 uncertain significance
NC_000022.10:g.(?_32500753)_(32894517_?)dup duplication Congenital glucose-galactose malabsorption [RCV003111075] Chr22:32500753..32894517 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.626G>A (p.Arg209Gln) single nucleotide variant not specified [RCV004088758] Chr22:32191283 [GRCh38]
Chr22:32587270 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.878C>T (p.Pro293Leu) single nucleotide variant not specified [RCV004106699] Chr22:32191031 [GRCh38]
Chr22:32587018 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.358G>A (p.Val120Ile) single nucleotide variant not specified [RCV004083174] Chr22:32193100 [GRCh38]
Chr22:32589087 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.1064G>T (p.Gly355Val) single nucleotide variant not specified [RCV004099768] Chr22:32190845 [GRCh38]
Chr22:32586832 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.307G>A (p.Val103Ile) single nucleotide variant not specified [RCV004073960] Chr22:32193151 [GRCh38]
Chr22:32589138 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.218G>A (p.Ser73Asn) single nucleotide variant not specified [RCV004124990] Chr22:32194392 [GRCh38]
Chr22:32590379 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.494A>G (p.Lys165Arg) single nucleotide variant not specified [RCV004126180] Chr22:32192964 [GRCh38]
Chr22:32588951 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.888C>A (p.Phe296Leu) single nucleotide variant not specified [RCV004103872] Chr22:32191021 [GRCh38]
Chr22:32587008 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.1117C>T (p.Arg373Cys) single nucleotide variant not specified [RCV004245448] Chr22:32190792 [GRCh38]
Chr22:32586779 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.784G>C (p.Val262Leu) single nucleotide variant not specified [RCV004092796] Chr22:32191125 [GRCh38]
Chr22:32587112 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.4G>C (p.Glu2Gln) single nucleotide variant not specified [RCV004118491] Chr22:32202448 [GRCh38]
Chr22:32598435 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.781T>A (p.Ser261Thr) single nucleotide variant not specified [RCV004089667] Chr22:32191128 [GRCh38]
Chr22:32587115 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.458G>A (p.Arg153His) single nucleotide variant not specified [RCV004249013] Chr22:32193000 [GRCh38]
Chr22:32588987 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.128G>A (p.Arg43Lys) single nucleotide variant not specified [RCV004361198] Chr22:32194482 [GRCh38]
Chr22:32590469 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.458G>T (p.Arg153Leu) single nucleotide variant not specified [RCV004350019] Chr22:32193000 [GRCh38]
Chr22:32588987 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.1048C>T (p.Pro350Ser) single nucleotide variant not specified [RCV004446303] Chr22:32190861 [GRCh38]
Chr22:32586848 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.13G>A (p.Glu5Lys) single nucleotide variant not specified [RCV004446306] Chr22:32202439 [GRCh38]
Chr22:32598426 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.931G>T (p.Asp311Tyr) single nucleotide variant not specified [RCV004446311] Chr22:32190978 [GRCh38]
Chr22:32586965 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.1067T>C (p.Val356Ala) single nucleotide variant not specified [RCV004446304] Chr22:32190842 [GRCh38]
Chr22:32586829 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.139G>A (p.Val47Met) single nucleotide variant not specified [RCV004446305] Chr22:32194471 [GRCh38]
Chr22:32590458 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.331C>A (p.Pro111Thr) single nucleotide variant not specified [RCV004446307] Chr22:32193127 [GRCh38]
Chr22:32589114 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_001394555.1(RFPL2):c.425C>G (p.Ser142Cys) single nucleotide variant not specified [RCV004446308] Chr22:32193033 [GRCh38]
Chr22:32589020 [GRCh37]
Chr22:22q12.3		 likely benign
NM_001394555.1(RFPL2):c.791G>A (p.Arg264His) single nucleotide variant not specified [RCV004446310] Chr22:32191118 [GRCh38]
Chr22:32587105 [GRCh37]
Chr22:22q12.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:436
Count of miRNA genes:111
Interacting mature miRNAs:111
Transcripts:ENST00000248980, ENST00000248983, ENST00000400236, ENST00000400237, ENST00000489846
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
ECD05199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,595,443 - 32,596,185UniSTSGRCh37
Build 362230,925,443 - 30,926,185RGDNCBI36
Celera2216,397,705 - 16,398,448RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,553,064 - 15,553,807UniSTS
ECD05345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,593,874 - 32,594,612UniSTSGRCh37
Build 362230,923,874 - 30,924,612RGDNCBI36
Celera2216,396,136 - 16,396,874RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,551,495 - 15,552,233UniSTS
ECD05454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,594,645 - 32,595,380UniSTSGRCh37
Build 362230,924,645 - 30,925,380RGDNCBI36
Celera2216,396,907 - 16,397,642RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,552,266 - 15,553,001UniSTS
ECD05560  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,596,256 - 32,596,988UniSTSGRCh37
Build 362230,926,256 - 30,926,988RGDNCBI36
Celera2216,398,519 - 16,399,251RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,553,878 - 15,554,610UniSTS
ECD06761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,587,142 - 32,587,842UniSTSGRCh37
Build 362230,917,142 - 30,917,842RGDNCBI36
Celera2216,389,404 - 16,390,104RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,544,763 - 15,545,463UniSTS
ECD09581  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,586,510 - 32,587,135UniSTSGRCh37
Build 362230,916,510 - 30,917,135RGDNCBI36
Celera2216,388,772 - 16,389,397RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,544,131 - 15,544,756UniSTS
ECD11094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372229,835,740 - 29,836,298UniSTSGRCh37
GRCh372232,588,008 - 32,588,590UniSTSGRCh37
Build 362228,165,740 - 28,166,298RGDNCBI36
Celera2213,635,589 - 13,636,147RGD
Celera2216,390,271 - 16,390,853UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map22q12.3UniSTS
HuRef2215,545,630 - 15,546,212UniSTS
ECD11272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372229,833,336 - 29,833,913UniSTSGRCh37
GRCh372232,590,138 - 32,590,715UniSTSGRCh37
Build 362228,163,336 - 28,163,913RGDNCBI36
Celera2213,633,184 - 13,633,761RGD
Celera2216,392,400 - 16,392,977UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map22q12.3UniSTS
HuRef2215,547,759 - 15,548,336UniSTS
ECD11371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,592,205 - 32,592,779UniSTSGRCh37
Build 362230,922,205 - 30,922,779RGDNCBI36
Celera2216,394,467 - 16,395,041RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,549,826 - 15,550,400UniSTS
ECD11708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372229,830,688 - 29,831,248UniSTSGRCh37
GRCh372232,592,802 - 32,593,366UniSTSGRCh37
Build 362228,160,688 - 28,161,248RGDNCBI36
Celera2216,395,064 - 16,395,628UniSTS
Celera2213,630,536 - 13,631,096RGD
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map22q12.3UniSTS
HuRef2215,550,423 - 15,550,987UniSTS
ECD13489  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,597,352 - 32,597,868UniSTSGRCh37
Build 362230,927,352 - 30,927,868RGDNCBI36
Celera2216,399,616 - 16,400,132RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,554,975 - 15,555,491UniSTS
ECD14142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,598,562 - 32,599,062UniSTSGRCh37
Build 362230,928,562 - 30,929,062RGDNCBI36
Celera2216,400,826 - 16,401,326RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,556,185 - 15,556,685UniSTS
ECD14678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,590,797 - 32,591,285UniSTSGRCh37
Build 362230,920,797 - 30,921,285RGDNCBI36
Celera2216,393,059 - 16,393,547RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,548,418 - 15,548,906UniSTS
ECD20144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,751,341 - 32,751,636UniSTSGRCh37
GRCh372232,597,428 - 32,597,733UniSTSGRCh37
Build 362230,927,428 - 30,927,733RGDNCBI36
Celera2216,553,513 - 16,553,808UniSTS
Celera2216,399,692 - 16,399,997RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,555,051 - 15,555,356UniSTS
HuRef2215,708,673 - 15,708,968UniSTS
REN76899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,586,046 - 32,586,293UniSTSGRCh37
Build 362230,916,046 - 30,916,293RGDNCBI36
Celera2216,388,308 - 16,388,555RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,543,667 - 15,543,914UniSTS
REN76900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,586,266 - 32,586,528UniSTSGRCh37
Build 362230,916,266 - 30,916,528RGDNCBI36
Celera2216,388,528 - 16,388,790RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,543,887 - 15,544,149UniSTS
REN76901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,586,505 - 32,586,766UniSTSGRCh37
Build 362230,916,505 - 30,916,766RGDNCBI36
Celera2216,388,767 - 16,389,028RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,544,126 - 15,544,387UniSTS
REN76902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,586,655 - 32,586,913UniSTSGRCh37
Build 362230,916,655 - 30,916,913RGDNCBI36
Celera2216,388,917 - 16,389,175RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,544,276 - 15,544,534UniSTS
REN76903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,756,481 - 32,756,730UniSTSGRCh37
GRCh372232,586,848 - 32,587,097UniSTSGRCh37
Build 362230,916,848 - 30,917,097RGDNCBI36
Celera2216,558,653 - 16,558,902UniSTS
Celera2216,389,110 - 16,389,359RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,544,469 - 15,544,718UniSTS
HuRef2215,713,813 - 15,714,062UniSTS
REN76904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,587,043 - 32,587,269UniSTSGRCh37
Build 362230,917,043 - 30,917,269RGDNCBI36
Celera2216,389,305 - 16,389,531RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,544,664 - 15,544,890UniSTS
REN76905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,587,239 - 32,587,486UniSTSGRCh37
Build 362230,917,239 - 30,917,486RGDNCBI36
Celera2216,389,501 - 16,389,748RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,544,860 - 15,545,107UniSTS
REN76906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,587,474 - 32,587,699UniSTSGRCh37
Build 362230,917,474 - 30,917,699RGDNCBI36
Celera2216,389,736 - 16,389,961RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,545,095 - 15,545,320UniSTS
REN76907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,587,645 - 32,587,885UniSTSGRCh37
Build 362230,917,645 - 30,917,885RGDNCBI36
Celera2216,389,907 - 16,390,147RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,545,266 - 15,545,506UniSTS
REN76908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,755,196 - 32,755,463UniSTSGRCh37
GRCh372232,587,861 - 32,588,123UniSTSGRCh37
Build 362230,917,861 - 30,918,123RGDNCBI36
Celera2216,557,368 - 16,557,635UniSTS
Celera2216,390,123 - 16,390,386RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,545,482 - 15,545,745UniSTS
HuRef2215,712,528 - 15,712,795UniSTS
REN76909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,588,103 - 32,588,364UniSTSGRCh37
Build 362230,918,103 - 30,918,364RGDNCBI36
Celera2216,390,366 - 16,390,627RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,545,725 - 15,545,986UniSTS
REN76910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,588,341 - 32,588,600UniSTSGRCh37
Build 362230,918,341 - 30,918,600RGDNCBI36
Celera2216,390,604 - 16,390,863RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,545,963 - 15,546,222UniSTS
REN76911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,754,333 - 32,754,570UniSTSGRCh37
GRCh372232,588,750 - 32,588,987UniSTSGRCh37
Build 362230,918,750 - 30,918,987RGDNCBI36
Celera2216,556,505 - 16,556,742UniSTS
Celera2216,391,013 - 16,391,250RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,546,372 - 15,546,609UniSTS
HuRef2215,711,665 - 15,711,902UniSTS
REN76912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,754,231 - 32,754,455UniSTSGRCh37
GRCh372232,588,865 - 32,589,089UniSTSGRCh37
Build 362230,918,865 - 30,919,089RGDNCBI36
Celera2216,556,403 - 16,556,627UniSTS
Celera2216,391,128 - 16,391,352RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,546,487 - 15,546,711UniSTS
HuRef2215,711,563 - 15,711,787UniSTS
REN76913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,589,064 - 32,589,312UniSTSGRCh37
Build 362230,919,064 - 30,919,312RGDNCBI36
Celera2216,391,327 - 16,391,575RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,546,686 - 15,546,934UniSTS
REN76915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372229,833,810 - 29,834,032UniSTSGRCh37
GRCh372232,590,009 - 32,590,241UniSTSGRCh37
Build 362228,163,810 - 28,164,032RGDNCBI36
Celera2213,633,658 - 13,633,881RGD
Celera2216,392,270 - 16,392,503UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map22q12.3UniSTS
HuRef2215,547,629 - 15,547,862UniSTS
REN76916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372229,833,577 - 29,833,837UniSTSGRCh37
GRCh372232,590,214 - 32,590,474UniSTSGRCh37
Build 362228,163,577 - 28,163,837RGDNCBI36
Celera2213,633,425 - 13,633,685RGD
Celera2216,392,476 - 16,392,736UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map22q12.3UniSTS
HuRef2215,547,835 - 15,548,095UniSTS
REN76917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,590,534 - 32,590,758UniSTSGRCh37
Build 362230,920,534 - 30,920,758RGDNCBI36
Celera2216,392,796 - 16,393,020RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,548,155 - 15,548,379UniSTS
REN76918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,590,707 - 32,590,964UniSTSGRCh37
Build 362230,920,707 - 30,920,964RGDNCBI36
Celera2216,392,969 - 16,393,226RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,548,328 - 15,548,585UniSTS
REN76919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,590,940 - 32,591,196UniSTSGRCh37
Build 362230,920,940 - 30,921,196RGDNCBI36
Celera2216,393,202 - 16,393,458RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,548,561 - 15,548,817UniSTS
REN76920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372229,832,600 - 29,832,872UniSTSGRCh37
GRCh372232,591,177 - 32,591,444UniSTSGRCh37
Build 362228,162,600 - 28,162,872RGDNCBI36
Celera2213,632,448 - 13,632,720RGD
Celera2216,393,439 - 16,393,706UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map22q12.3UniSTS
HuRef2215,548,798 - 15,549,065UniSTS
REN76921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,591,875 - 32,592,125UniSTSGRCh37
Build 362230,921,875 - 30,922,125RGDNCBI36
Celera2216,394,137 - 16,394,387RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,549,496 - 15,549,746UniSTS
REN76922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,592,095 - 32,592,319UniSTSGRCh37
Build 362230,922,095 - 30,922,319RGDNCBI36
Celera2216,394,357 - 16,394,581RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,549,716 - 15,549,940UniSTS
REN76923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,592,293 - 32,592,547UniSTSGRCh37
Build 362230,922,293 - 30,922,547RGDNCBI36
Celera2216,394,555 - 16,394,809RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,549,914 - 15,550,168UniSTS
REN76924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372229,831,318 - 29,831,561UniSTSGRCh37
GRCh372232,592,489 - 32,592,732UniSTSGRCh37
Build 362228,161,318 - 28,161,561RGDNCBI36
Celera2216,394,751 - 16,394,994UniSTS
Celera2213,631,166 - 13,631,409RGD
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map22q12.3UniSTS
HuRef2215,550,110 - 15,550,353UniSTS
REN76925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372229,831,107 - 29,831,341UniSTSGRCh37
GRCh372232,592,709 - 32,592,943UniSTSGRCh37
Build 362228,161,107 - 28,161,341RGDNCBI36
Celera2216,394,971 - 16,395,205UniSTS
Celera2213,630,955 - 13,631,189RGD
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map22q12.3UniSTS
HuRef2215,550,330 - 15,550,564UniSTS
REN76926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,592,920 - 32,593,162UniSTSGRCh37
Build 362230,922,920 - 30,923,162RGDNCBI36
Celera2216,395,182 - 16,395,424RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,550,541 - 15,550,783UniSTS
REN76927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,593,129 - 32,593,379UniSTSGRCh37
Build 362230,923,129 - 30,923,379RGDNCBI36
Celera2216,395,391 - 16,395,641RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,550,750 - 15,551,000UniSTS
REN76928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,593,254 - 32,593,490UniSTSGRCh37
Build 362230,923,254 - 30,923,490RGDNCBI36
Celera2216,395,516 - 16,395,752RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,550,875 - 15,551,111UniSTS
REN76929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,593,463 - 32,593,687UniSTSGRCh37
Build 362230,923,463 - 30,923,687RGDNCBI36
Celera2216,395,725 - 16,395,949RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,551,084 - 15,551,308UniSTS
REN76930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,593,649 - 32,593,900UniSTSGRCh37
Build 362230,923,649 - 30,923,900RGDNCBI36
Celera2216,395,911 - 16,396,162RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,551,270 - 15,551,521UniSTS
REN76931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,593,877 - 32,594,123UniSTSGRCh37
Build 362230,923,877 - 30,924,123RGDNCBI36
Celera2216,396,139 - 16,396,385RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,551,498 - 15,551,744UniSTS
REN76932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,594,103 - 32,594,342UniSTSGRCh37
Build 362230,924,103 - 30,924,342RGDNCBI36
Celera2216,396,365 - 16,396,604RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,551,724 - 15,551,963UniSTS
REN76933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,594,320 - 32,594,583UniSTSGRCh37
Build 362230,924,320 - 30,924,583RGDNCBI36
Celera2216,396,582 - 16,396,845RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,551,941 - 15,552,204UniSTS
REN76934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,594,562 - 32,594,824UniSTSGRCh37
Build 362230,924,562 - 30,924,824RGDNCBI36
Celera2216,396,824 - 16,397,086RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,552,183 - 15,552,445UniSTS
REN76935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,594,808 - 32,595,060UniSTSGRCh37
Build 362230,924,808 - 30,925,060RGDNCBI36
Celera2216,397,070 - 16,397,322RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,552,429 - 15,552,681UniSTS
REN76936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,595,036 - 32,595,276UniSTSGRCh37
Build 362230,925,036 - 30,925,276RGDNCBI36
Celera2216,397,298 - 16,397,538RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,552,657 - 15,552,897UniSTS
REN76937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,595,255 - 32,595,490UniSTSGRCh37
Build 362230,925,255 - 30,925,490RGDNCBI36
Celera2216,397,517 - 16,397,752RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,552,876 - 15,553,111UniSTS
REN76938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,595,447 - 32,595,696UniSTSGRCh37
Build 362230,925,447 - 30,925,696RGDNCBI36
Celera2216,397,709 - 16,397,958RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,553,068 - 15,553,317UniSTS
REN76939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,595,670 - 32,595,916UniSTSGRCh37
Build 362230,925,670 - 30,925,916RGDNCBI36
Celera2216,397,932 - 16,398,178RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,553,291 - 15,553,537UniSTS
REN76940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,595,898 - 32,596,141UniSTSGRCh37
Build 362230,925,898 - 30,926,141RGDNCBI36
Celera2216,398,161 - 16,398,404RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,553,520 - 15,553,763UniSTS
REN76941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,752,519 - 32,752,786UniSTSGRCh37
GRCh372232,596,094 - 32,596,363UniSTSGRCh37
Build 362230,926,094 - 30,926,363RGDNCBI36
Celera2216,554,691 - 16,554,958UniSTS
Celera2216,398,357 - 16,398,626RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,553,716 - 15,553,985UniSTS
HuRef2215,709,851 - 15,710,118UniSTS
REN76942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,596,316 - 32,596,565UniSTSGRCh37
Build 362230,926,316 - 30,926,565RGDNCBI36
Celera2216,398,579 - 16,398,828RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,553,938 - 15,554,187UniSTS
REN76943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,596,495 - 32,596,731UniSTSGRCh37
Build 362230,926,495 - 30,926,731RGDNCBI36
Celera2216,398,758 - 16,398,994RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,554,117 - 15,554,353UniSTS
REN76944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,596,712 - 32,596,970UniSTSGRCh37
Build 362230,926,712 - 30,926,970RGDNCBI36
Celera2216,398,975 - 16,399,233RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,554,334 - 15,554,592UniSTS
REN76945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,596,862 - 32,597,125UniSTSGRCh37
Build 362230,926,862 - 30,927,125RGDNCBI36
Celera2216,399,125 - 16,399,389RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,554,484 - 15,554,748UniSTS
REN76946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,597,103 - 32,597,368UniSTSGRCh37
Build 362230,927,103 - 30,927,368RGDNCBI36
Celera2216,399,367 - 16,399,632RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,554,726 - 15,554,991UniSTS
REN76947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,597,361 - 32,597,602UniSTSGRCh37
Build 362230,927,361 - 30,927,602RGDNCBI36
Celera2216,399,625 - 16,399,866RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,554,984 - 15,555,225UniSTS
REN76948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,597,575 - 32,597,828UniSTSGRCh37
Build 362230,927,575 - 30,927,828RGDNCBI36
Celera2216,399,839 - 16,400,092RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,555,198 - 15,555,451UniSTS
REN76949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,597,803 - 32,598,062UniSTSGRCh37
Build 362230,927,803 - 30,928,062RGDNCBI36
Celera2216,400,067 - 16,400,326RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,555,426 - 15,555,685UniSTS
REN76950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,598,047 - 32,598,293UniSTSGRCh37
Build 362230,928,047 - 30,928,293RGDNCBI36
Celera2216,400,311 - 16,400,557RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,555,670 - 15,555,916UniSTS
REN76951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,598,269 - 32,598,507UniSTSGRCh37
Build 362230,928,269 - 30,928,507RGDNCBI36
Celera2216,400,533 - 16,400,771RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,555,892 - 15,556,130UniSTS
REN76952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,598,480 - 32,598,707UniSTSGRCh37
Build 362230,928,480 - 30,928,707RGDNCBI36
Celera2216,400,744 - 16,400,971RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,556,103 - 15,556,330UniSTS
REN76953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,598,693 - 32,598,938UniSTSGRCh37
Build 362230,928,693 - 30,928,938RGDNCBI36
Celera2216,400,957 - 16,401,202RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,556,316 - 15,556,561UniSTS
REN76954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,598,923 - 32,599,154UniSTSGRCh37
Build 362230,928,923 - 30,929,154RGDNCBI36
Celera2216,401,187 - 16,401,418RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,556,546 - 15,556,777UniSTS
REN76955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,599,133 - 32,599,392UniSTSGRCh37
Build 362230,929,133 - 30,929,392RGDNCBI36
Celera2216,401,397 - 16,401,656RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,556,756 - 15,557,015UniSTS
REN76956  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,599,372 - 32,599,620UniSTSGRCh37
Build 362230,929,372 - 30,929,620RGDNCBI36
Celera2216,401,636 - 16,401,884RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,556,995 - 15,557,243UniSTS
REN76957  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,599,607 - 32,599,855UniSTSGRCh37
Build 362230,929,607 - 30,929,855RGDNCBI36
Celera2216,401,871 - 16,402,119RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,557,230 - 15,557,479UniSTS
REN76958  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,599,823 - 32,600,061UniSTSGRCh37
Build 362230,929,823 - 30,930,061RGDNCBI36
Celera2216,402,087 - 16,402,325RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,557,447 - 15,557,685UniSTS
REN76959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,600,044 - 32,600,276UniSTSGRCh37
Build 362230,930,044 - 30,930,276RGDNCBI36
Celera2216,402,308 - 16,402,540RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,557,668 - 15,557,900UniSTS
REN76960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,600,254 - 32,600,518UniSTSGRCh37
Build 362230,930,254 - 30,930,518RGDNCBI36
Celera2216,402,518 - 16,402,782RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,557,878 - 15,558,142UniSTS
REN76961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,600,498 - 32,600,748UniSTSGRCh37
Build 362230,930,498 - 30,930,748RGDNCBI36
Celera2216,402,762 - 16,403,012RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,558,122 - 15,558,372UniSTS
REN76962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,600,719 - 32,600,965UniSTSGRCh37
Build 362230,930,719 - 30,930,965RGDNCBI36
Celera2216,402,983 - 16,403,229RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,558,343 - 15,558,589UniSTS
REN76963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,600,957 - 32,601,213UniSTSGRCh37
Build 362230,930,957 - 30,931,213RGDNCBI36
Celera2216,403,221 - 16,403,477RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,558,581 - 15,558,837UniSTS
REN76964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,601,192 - 32,601,417UniSTSGRCh37
Build 362230,931,192 - 30,931,417RGDNCBI36
Celera2216,403,456 - 16,403,681RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,558,816 - 15,559,041UniSTS
REN76965  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,601,395 - 32,601,637UniSTSGRCh37
Build 362230,931,395 - 30,931,637RGDNCBI36
Celera2216,403,659 - 16,403,901RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,559,019 - 15,559,261UniSTS
REN76966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,601,615 - 32,601,874UniSTSGRCh37
Build 362230,931,615 - 30,931,874RGDNCBI36
Celera2216,403,879 - 16,404,138RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,559,239 - 15,559,498UniSTS
REN76967  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,601,873 - 32,602,130UniSTSGRCh37
Build 362230,931,873 - 30,932,130RGDNCBI36
Celera2216,404,137 - 16,404,394RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,559,497 - 15,559,754UniSTS
REN76968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,602,107 - 32,602,347UniSTSGRCh37
Build 362230,932,107 - 30,932,347RGDNCBI36
Celera2216,404,371 - 16,404,611RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,559,731 - 15,559,971UniSTS
REN76969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,602,245 - 32,602,510UniSTSGRCh37
Build 362230,932,245 - 30,932,510RGDNCBI36
Celera2216,404,509 - 16,404,774RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,559,869 - 15,560,134UniSTS
REN77564  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,749,892 - 32,750,118UniSTSGRCh37
GRCh372232,601,984 - 32,602,258UniSTSGRCh37
Build 362230,931,984 - 30,932,258RGDNCBI36
Celera2216,552,064 - 16,552,290UniSTS
Celera2216,404,248 - 16,404,522RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,559,608 - 15,559,882UniSTS
HuRef2215,707,224 - 15,707,450UniSTS
REN77572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,751,611 - 32,751,837UniSTSGRCh37
GRCh372232,597,369 - 32,597,453UniSTSGRCh37
Build 362230,927,369 - 30,927,453RGDNCBI36
Celera2216,553,783 - 16,554,009UniSTS
Celera2216,399,633 - 16,399,717RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,554,992 - 15,555,076UniSTS
HuRef2215,708,943 - 15,709,169UniSTS
REN77576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,752,457 - 32,752,710UniSTSGRCh37
GRCh372232,596,171 - 32,596,425UniSTSGRCh37
Build 362230,926,171 - 30,926,425RGDNCBI36
Celera2216,554,629 - 16,554,882UniSTS
Celera2216,398,434 - 16,398,688RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,553,793 - 15,554,047UniSTS
HuRef2215,709,789 - 15,710,042UniSTS
REN77578  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,752,935 - 32,753,161UniSTSGRCh37
GRCh372232,595,719 - 32,595,945UniSTSGRCh37
Build 362230,925,719 - 30,925,945RGDNCBI36
Celera2216,555,107 - 16,555,333UniSTS
Celera2216,397,981 - 16,398,208RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,553,340 - 15,553,567UniSTS
HuRef2215,710,267 - 15,710,493UniSTS
REN77591  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,756,214 - 32,756,472UniSTSGRCh37
GRCh372232,587,106 - 32,587,364UniSTSGRCh37
Build 362230,917,106 - 30,917,364RGDNCBI36
Celera2216,558,386 - 16,558,644UniSTS
Celera2216,389,368 - 16,389,626RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,544,727 - 15,544,985UniSTS
HuRef2215,713,546 - 15,713,804UniSTS
stSG602596  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,586,783 - 32,588,184UniSTSGRCh37
GRCh372232,755,135 - 32,756,795UniSTSGRCh37
Build 362230,916,783 - 30,918,184RGDNCBI36
Celera2216,557,307 - 16,558,967UniSTS
Celera2216,389,045 - 16,390,447RGD
HuRef2215,544,404 - 15,545,806UniSTS
HuRef2215,712,467 - 15,714,127UniSTS
stSG602597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,753,985 - 32,755,150UniSTSGRCh37
GRCh372232,588,169 - 32,589,335UniSTSGRCh37
Build 362230,918,169 - 30,919,335RGDNCBI36
Celera2216,556,157 - 16,557,322UniSTS
Celera2216,390,432 - 16,391,598RGD
HuRef2215,711,317 - 15,712,482UniSTS
HuRef2215,545,791 - 15,546,957UniSTS
stSG602599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,590,291 - 32,591,309UniSTSGRCh37
GRCh372229,832,740 - 29,833,760UniSTSGRCh37
Build 362228,162,740 - 28,163,760RGDNCBI36
Celera2216,392,553 - 16,393,571UniSTS
Celera2213,632,588 - 13,633,608RGD
HuRef2215,547,912 - 15,548,930UniSTS
stSG602606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,598,775 - 32,599,062UniSTSGRCh37
GRCh372232,516,208 - 32,516,520UniSTSGRCh37
Build 362230,846,208 - 30,846,520RGDNCBI36
Celera2216,401,039 - 16,401,326UniSTS
Celera2216,316,666 - 16,316,978RGD
Cytogenetic Map22q12.3UniSTS
HuRef2215,471,947 - 15,472,259UniSTS
HuRef2215,556,398 - 15,556,685UniSTS
RFPL1__5486  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,586,422 - 32,587,071UniSTSGRCh37
GRCh372229,837,799 - 29,838,447UniSTSGRCh37
Build 362228,167,799 - 28,168,447RGDNCBI36
Celera2216,388,684 - 16,389,333UniSTS
Celera2213,637,648 - 13,638,296RGD
HuRef2215,544,043 - 15,544,692UniSTS
REN76914  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map22q12UniSTS


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 adipose tissue appendage entire extraembryonic component
High
Medium 134 97 1
Low 38 61 194 52 135 52 91 11 2317 28 274 144 9 4
Below cutoff 1587 1778 1271 440 1175 337 2428 994 920 247 816 1216 111 870 1301 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001098527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001159545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001159546 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001364982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001364983 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001364984 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001364985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001364986 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394554 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394555 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529832 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054324985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AJ010231 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055999 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL008723 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR456563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB549304 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000248983   ⟹   ENSP00000248983
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,190,435 - 32,202,451 (-)Ensembl
RefSeq Acc Id: ENST00000400237   ⟹   ENSP00000383096
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,190,438 - 32,203,477 (-)Ensembl
RefSeq Acc Id: ENST00000489846
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,190,704 - 32,193,401 (-)Ensembl
RefSeq Acc Id: ENST00000626996   ⟹   ENSP00000486618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,190,438 - 32,202,571 (-)Ensembl
RefSeq Acc Id: ENST00000628378   ⟹   ENSP00000487290
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,190,706 - 32,202,511 (-)Ensembl
RefSeq Acc Id: ENST00000652607   ⟹   ENSP00000498332
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,190,438 - 32,205,073 (-)Ensembl
RefSeq Acc Id: NM_001098527   ⟹   NP_001091997
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,203,477 (-)NCBI
GRCh372232,586,422 - 32,603,223 (-)NCBI
Build 362230,916,425 - 30,919,179 (-)NCBI Archive
Celera2216,388,684 - 16,402,982 (-)RGD
HuRef2215,544,043 - 15,558,342 (-)RGD
CHM1_12232,545,769 - 32,558,811 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,667,560 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001159545   ⟹   NP_001153017
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
GRCh372232,586,422 - 32,603,223 (-)NCBI
Celera2216,388,684 - 16,402,982 (-)RGD
HuRef2215,544,043 - 15,558,342 (-)RGD
CHM1_12232,545,769 - 32,560,065 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001159546   ⟹   NP_001153018
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
GRCh372232,586,422 - 32,603,223 (-)NCBI
Celera2216,388,684 - 16,402,982 (-)RGD
HuRef2215,544,043 - 15,558,342 (-)RGD
CHM1_12232,545,769 - 32,557,884 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001364982   ⟹   NP_001351911
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001364983   ⟹   NP_001351912
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001364984   ⟹   NP_001351913
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001364985   ⟹   NP_001351914
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001364986   ⟹   NP_001351915
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001394554   ⟹   NP_001381483
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001394555   ⟹   NP_001381484
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001394556   ⟹   NP_001381485
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001394557   ⟹   NP_001381486
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001394558   ⟹   NP_001381487
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,205,073 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,669,156 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001394559   ⟹   NP_001381488
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,203,477 (-)NCBI
T2T-CHM13v2.02232,654,520 - 32,667,560 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011529828   ⟹   XP_011528130
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,190,438 - 32,203,477 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054324985   ⟹   XP_054180960
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02232,654,520 - 32,667,560 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001091997 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153017 (Get FASTA)   NCBI Sequence Viewer  
  NP_001153018 (Get FASTA)   NCBI Sequence Viewer  
  NP_001351911 (Get FASTA)   NCBI Sequence Viewer  
  NP_001351912 (Get FASTA)   NCBI Sequence Viewer  
  NP_001351913 (Get FASTA)   NCBI Sequence Viewer  
  NP_001351914 (Get FASTA)   NCBI Sequence Viewer  
  NP_001351915 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381483 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381484 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381485 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381486 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381487 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381488 (Get FASTA)   NCBI Sequence Viewer  
  XP_011528130 (Get FASTA)   NCBI Sequence Viewer  
  XP_054180960 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH51910 (Get FASTA)   NCBI Sequence Viewer  
  AAH69737 (Get FASTA)   NCBI Sequence Viewer  
  AAH69827 (Get FASTA)   NCBI Sequence Viewer  
  CAA09045 (Get FASTA)   NCBI Sequence Viewer  
  CAG30449 (Get FASTA)   NCBI Sequence Viewer  
  EAW60009 (Get FASTA)   NCBI Sequence Viewer  
  EAW60010 (Get FASTA)   NCBI Sequence Viewer  
  EAW60011 (Get FASTA)   NCBI Sequence Viewer  
  EAW60012 (Get FASTA)   NCBI Sequence Viewer  
  EAW60013 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000248983.5
  ENSP00000383096
  ENSP00000383096.1
  ENSP00000486618.1
  ENSP00000487290.1
  ENSP00000498332
  ENSP00000498332.1
GenBank Protein O75678 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001091997   ⟸   NM_001098527
- Peptide Label: isoform 2
- UniProtKB: O75678 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001153017   ⟸   NM_001159545
- Peptide Label: isoform 3
- UniProtKB: Q6NSX6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001153018   ⟸   NM_001159546
- Peptide Label: isoform 3
- UniProtKB: Q6NSX6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011528130   ⟸   XM_011529828
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: NP_001351911   ⟸   NM_001364982
- Peptide Label: isoform 4
- UniProtKB: Q6NSX6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001351913   ⟸   NM_001364984
- Peptide Label: isoform 3
- UniProtKB: Q6NSX6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001351912   ⟸   NM_001364983
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001351914   ⟸   NM_001364985
- Peptide Label: isoform 3
- UniProtKB: Q6NSX6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001351915   ⟸   NM_001364986
- Peptide Label: isoform 5
RefSeq Acc Id: ENSP00000383096   ⟸   ENST00000400237
RefSeq Acc Id: ENSP00000486618   ⟸   ENST00000626996
RefSeq Acc Id: ENSP00000498332   ⟸   ENST00000652607
RefSeq Acc Id: ENSP00000487290   ⟸   ENST00000628378
RefSeq Acc Id: ENSP00000248983   ⟸   ENST00000248983
RefSeq Acc Id: NP_001381484   ⟸   NM_001394555
- Peptide Label: isoform 2
- UniProtKB: O75678 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001381483   ⟸   NM_001394554
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001381486   ⟸   NM_001394557
- Peptide Label: isoform 3
- UniProtKB: Q6NSX6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001381485   ⟸   NM_001394556
- Peptide Label: isoform 6
- UniProtKB: Q6NSX6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001381487   ⟸   NM_001394558
- Peptide Label: isoform 3
- UniProtKB: Q6NSX6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001381488   ⟸   NM_001394559
- Peptide Label: isoform 3
- UniProtKB: Q6NSX6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054180960   ⟸   XM_054324985
- Peptide Label: isoform X1
Protein Domains
B30.2/SPRY

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O75678-F1-model_v2 AlphaFold O75678 1-378 view protein structure

Promoters
RGD ID:13603818
Promoter ID:EPDNEW_H28093
Type:initiation region
Name:RFPL2_2
Description:ret finger protein like 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28094  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,202,520 - 32,202,580EPDNEW
RGD ID:13603820
Promoter ID:EPDNEW_H28094
Type:initiation region
Name:RFPL2_1
Description:ret finger protein like 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28093  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,204,743 - 32,204,803EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9979 AgrOrtholog
COSMIC RFPL2 COSMIC
Ensembl Genes ENSG00000128253 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000248983.8 UniProtKB/Swiss-Prot
  ENST00000400237 ENTREZGENE
  ENST00000400237.2 UniProtKB/Swiss-Prot
  ENST00000626996.2 UniProtKB/Swiss-Prot
  ENST00000628378.1 UniProtKB/TrEMBL
  ENST00000652607 ENTREZGENE
  ENST00000652607.2 UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.120.920 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000128253 GTEx
HGNC ID HGNC:9979 ENTREZGENE
Human Proteome Map RFPL2 Human Proteome Map
InterPro B30.2/SPRY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  B30.2/SPRY_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Butyrophylin_SPRY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ConA-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PRY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RDM_domain_RFPL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SPRY/PRY_RFPL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SPRY_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_RING/FYVE/PHD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:10739 UniProtKB/Swiss-Prot
NCBI Gene 10739 ENTREZGENE
OMIM 605969 OMIM
PANTHER B30.2_SPRY DOMAIN-CONTAINING PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  E3 UBIQUITIN-PROTEIN LIGASE TRIM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam PRY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RDM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SPRY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C3HC4_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34348 PharmGKB
PRINTS BUTYPHLNCDUF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE B302_SPRY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART PRY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SPRY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP RING/U-box UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF49899 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0D9SGA4_HUMAN UniProtKB/TrEMBL
  O75678 ENTREZGENE
  Q6NSX6 ENTREZGENE, UniProtKB/TrEMBL
  RFPL2_HUMAN UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-14 RFPL2  ret finger protein like 2    ret finger protein-like 2  Symbol and/or name change 5135510 APPROVED