MIER3 (MIER family member 3) - Rat Genome Database

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Gene: MIER3 (MIER family member 3) Homo sapiens
Analyze
Symbol: MIER3
Name: MIER family member 3
RGD ID: 1605562
HGNC Page HGNC:26678
Description: Predicted to enable histone deacetylase binding activity and transcription corepressor activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Located in nucleoplasm. Part of protein-containing complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DKFZp686L09111; DKFZp781G1119; DKFZp781I1119; FLJ35954; mesoderm induction early response 1, family member 3; mesoderm induction early response protein 3; mi-er3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38556,919,603 - 56,952,209 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl556,919,602 - 56,971,675 (-)EnsemblGRCh38hg38GRCh38
GRCh37556,215,430 - 56,247,950 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36556,251,186 - 56,283,711 (-)NCBINCBI36Build 36hg18NCBI36
Celera553,169,638 - 53,202,174 (-)NCBICelera
Cytogenetic Map5q11.2NCBI
HuRef553,187,350 - 53,219,884 (-)NCBIHuRef
CHM1_1556,218,436 - 56,250,963 (-)NCBICHM1_1
T2T-CHM13v2.0557,747,855 - 57,780,385 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:11076863   PMID:11230166   PMID:12477932   PMID:14702039   PMID:15489336   PMID:16344560   PMID:16381901   PMID:19274049   PMID:21258344   PMID:21873635   PMID:22993404   PMID:23752268  
PMID:26186194   PMID:26496610   PMID:28046085   PMID:28242625   PMID:28514442   PMID:28887525   PMID:29507755   PMID:32296183   PMID:33961781   PMID:34242623   PMID:35271311  


Genomics

Comparative Map Data
MIER3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38556,919,603 - 56,952,209 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl556,919,602 - 56,971,675 (-)EnsemblGRCh38hg38GRCh38
GRCh37556,215,430 - 56,247,950 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36556,251,186 - 56,283,711 (-)NCBINCBI36Build 36hg18NCBI36
Celera553,169,638 - 53,202,174 (-)NCBICelera
Cytogenetic Map5q11.2NCBI
HuRef553,187,350 - 53,219,884 (-)NCBIHuRef
CHM1_1556,218,436 - 56,250,963 (-)NCBICHM1_1
T2T-CHM13v2.0557,747,855 - 57,780,385 (-)NCBIT2T-CHM13v2.0
Mier3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3913111,822,607 - 111,855,130 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl13111,817,513 - 111,855,130 (+)EnsemblGRCm39 Ensembl
GRCm3813111,686,073 - 111,718,596 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl13111,680,979 - 111,718,596 (+)EnsemblGRCm38mm10GRCm38
MGSCv3713112,476,386 - 112,508,802 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3613112,807,229 - 112,838,514 (+)NCBIMGSCv36mm8
Celera13116,010,054 - 116,024,988 (+)NCBICelera
Cytogenetic Map13D2.2NCBI
cM Map1363.36NCBI
Mier3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8245,021,167 - 45,049,745 (+)NCBIGRCr8
mRatBN7.2243,287,546 - 43,316,422 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl243,287,916 - 43,316,136 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx250,408,447 - 50,432,200 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0248,466,902 - 48,490,655 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0243,318,416 - 43,342,169 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0243,266,301 - 43,295,175 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl243,266,739 - 43,294,889 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0262,313,119 - 62,341,562 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4243,003,828 - 43,027,625 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1242,924,292 - 42,953,309 (+)NCBI
Celera239,077,974 - 39,101,738 (+)NCBICelera
Cytogenetic Map2q14NCBI
Mier3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495544610,961,436 - 10,992,971 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495544610,962,336 - 10,992,645 (+)NCBIChiLan1.0ChiLan1.0
MIER3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2456,971,837 - 57,004,495 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1555,125,468 - 55,158,126 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0557,060,314 - 57,092,948 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1558,690,719 - 58,722,146 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl558,689,857 - 58,722,146 (+)Ensemblpanpan1.1panPan2
MIER3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1244,057,161 - 44,135,210 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl244,060,500 - 44,108,034 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha241,118,466 - 41,196,496 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0244,539,169 - 44,617,541 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl244,539,170 - 44,590,675 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1241,615,980 - 41,694,009 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0242,419,426 - 42,497,469 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0243,239,394 - 43,317,194 (-)NCBIUU_Cfam_GSD_1.0
Mier3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213202,065,171 - 202,095,395 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648011,002,583 - 11,032,329 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648011,001,964 - 11,031,891 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MIER3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1635,990,469 - 36,025,436 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11635,990,468 - 36,025,424 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21638,256,410 - 38,291,399 (-)NCBISscrofa10.2Sscrofa10.2susScr3
MIER3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1453,144,256 - 53,177,429 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl453,147,773 - 53,172,089 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660492,036,468 - 2,069,711 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Mier3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247592,162,981 - 2,324,008 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247592,060,688 - 2,325,104 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MIER3
12 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q11.1-12.1(chr5:50288355-63149770)x1 copy number loss See cases [RCV000050797] Chr5:50288355..63149770 [GRCh38]
Chr5:49584189..62445597 [GRCh37]
Chr5:49619946..62481353 [NCBI36]
Chr5:5q11.1-12.1		 pathogenic
GRCh38/hg38 5q11.2(chr5:53332485-57152396)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053283]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053283]|See cases [RCV000053283] Chr5:53332485..57152396 [GRCh38]
Chr5:52628315..56448223 [GRCh37]
Chr5:52664072..56483980 [NCBI36]
Chr5:5q11.2		 uncertain significance
GRCh38/hg38 5q11.2-12.1(chr5:56947850-61725401)x3 copy number gain See cases [RCV000134066] Chr5:56947850..61725401 [GRCh38]
Chr5:56243677..61021228 [GRCh37]
Chr5:56279434..61056985 [NCBI36]
Chr5:5q11.2-12.1		 pathogenic
GRCh38/hg38 5q11.2(chr5:56717311-57029532)x1 copy number loss See cases [RCV000136937] Chr5:56717311..57029532 [GRCh38]
Chr5:56013138..56325359 [GRCh37]
Chr5:56048895..56361116 [NCBI36]
Chr5:5q11.2		 uncertain significance
GRCh38/hg38 5p13.2-q12.1(chr5:35201559-61903141)x3 copy number gain See cases [RCV000137302] Chr5:35201559..61903141 [GRCh38]
Chr5:35201661..61198968 [GRCh37]
Chr5:35237418..61234725 [NCBI36]
Chr5:5p13.2-q12.1		 pathogenic
GRCh38/hg38 5p15.33-q13.3(chr5:22149-74412725)x3 copy number gain See cases [RCV000138780] Chr5:22149..74412725 [GRCh38]
Chr5:22149..73708550 [GRCh37]
Chr5:75149..73744306 [NCBI36]
Chr5:5p15.33-q13.3		 pathogenic
GRCh37/hg19 5q11.2(chr5:56107595-56694985)x1 copy number loss See cases [RCV000449017] Chr5:56107595..56694985 [GRCh37]
Chr5:5q11.2		 uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
NM_001297599.2(MIER3):c.1058A>G (p.Tyr353Cys) single nucleotide variant Inborn genetic diseases [RCV003277933] Chr5:56923828 [GRCh38]
Chr5:56219655 [GRCh37]
Chr5:5q11.2		 uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5q11.2(chr5:56241959-56248026)x0 copy number loss not provided [RCV000744721] Chr5:56241959..56248026 [GRCh37]
Chr5:5q11.2		 benign
GRCh37/hg19 5q11.2(chr5:56246610-56248186)x1 copy number loss not provided [RCV000744722] Chr5:56246610..56248186 [GRCh37]
Chr5:5q11.2		 benign
GRCh37/hg19 5q11.2(chr5:56247119-56248026)x1 copy number loss not provided [RCV000744723] Chr5:56247119..56248026 [GRCh37]
Chr5:5q11.2		 benign
GRCh37/hg19 5q11.2(chr5:56247119-56248186)x3 copy number gain not provided [RCV000744724] Chr5:56247119..56248186 [GRCh37]
Chr5:5q11.2		 benign
GRCh37/hg19 5q11.2(chr5:56247272-56248026)x1 copy number loss not provided [RCV000744725] Chr5:56247272..56248026 [GRCh37]
Chr5:5q11.2		 benign
GRCh37/hg19 5q11.2(chr5:56247323-56248026)x1 copy number loss not provided [RCV000744726] Chr5:56247323..56248026 [GRCh37]
Chr5:5q11.2		 benign
GRCh37/hg19 5q11.2(chr5:56247344-56248026)x1 copy number loss not provided [RCV000744727] Chr5:56247344..56248026 [GRCh37]
Chr5:5q11.2		 benign
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32		 uncertain significance
NM_001297599.2(MIER3):c.511G>A (p.Asp171Asn) single nucleotide variant Inborn genetic diseases [RCV003291983] Chr5:56935677 [GRCh38]
Chr5:56231504 [GRCh37]
Chr5:5q11.2		 uncertain significance
GRCh37/hg19 5q11.2(chr5:55867380-56217595)x3 copy number gain not provided [RCV001258852] Chr5:55867380..56217595 [GRCh37]
Chr5:5q11.2		 uncertain significance
NM_001297599.2(MIER3):c.1353T>G (p.Asp451Glu) single nucleotide variant Inborn genetic diseases [RCV003308781] Chr5:56923428 [GRCh38]
Chr5:56219255 [GRCh37]
Chr5:5q11.2		 uncertain significance
NM_001297599.2(MIER3):c.1400C>G (p.Pro467Arg) single nucleotide variant Inborn genetic diseases [RCV002868663] Chr5:56923381 [GRCh38]
Chr5:56219208 [GRCh37]
Chr5:5q11.2		 uncertain significance
NM_001297599.2(MIER3):c.1231A>T (p.Thr411Ser) single nucleotide variant Inborn genetic diseases [RCV002916153] Chr5:56923550 [GRCh38]
Chr5:56219377 [GRCh37]
Chr5:5q11.2		 uncertain significance
NM_001297599.2(MIER3):c.1410G>A (p.Met470Ile) single nucleotide variant Inborn genetic diseases [RCV002965738] Chr5:56923371 [GRCh38]
Chr5:56219198 [GRCh37]
Chr5:5q11.2		 uncertain significance
NM_001297599.2(MIER3):c.458A>G (p.Asp153Gly) single nucleotide variant Inborn genetic diseases [RCV002896932] Chr5:56935730 [GRCh38]
Chr5:56231557 [GRCh37]
Chr5:5q11.2		 uncertain significance
NM_001297599.2(MIER3):c.32C>T (p.Pro11Leu) single nucleotide variant Inborn genetic diseases [RCV002989507] Chr5:56950630 [GRCh38]
Chr5:56246457 [GRCh37]
Chr5:5q11.2		 uncertain significance
NM_001297599.2(MIER3):c.602A>G (p.Glu201Gly) single nucleotide variant Inborn genetic diseases [RCV003200024] Chr5:56933392 [GRCh38]
Chr5:56229219 [GRCh37]
Chr5:5q11.2		 uncertain significance
NM_001297599.2(MIER3):c.1616A>G (p.His539Arg) single nucleotide variant Inborn genetic diseases [RCV003364990] Chr5:56923165 [GRCh38]
Chr5:56218992 [GRCh37]
Chr5:5q11.2		 uncertain significance
NM_001297599.2(MIER3):c.1225G>A (p.Asp409Asn) single nucleotide variant Inborn genetic diseases [RCV003342897] Chr5:56923556 [GRCh38]
Chr5:56219383 [GRCh37]
Chr5:5q11.2		 likely benign
GRCh37/hg19 5q11.1-11.2(chr5:49430268-57925870)x1 copy number loss not specified [RCV003986571] Chr5:49430268..57925870 [GRCh37]
Chr5:5q11.1-11.2		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5852
Count of miRNA genes:987
Interacting mature miRNAs:1189
Transcripts:ENST00000336942, ENST00000381199, ENST00000381213, ENST00000381226, ENST00000409421, ENST00000440000, ENST00000451637, ENST00000452157, ENST00000480115, ENST00000497185, ENST00000546593
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
ECD00767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,229,946 - 56,230,836UniSTSGRCh37
Build 36556,265,703 - 56,266,593RGDNCBI36
Celera553,184,163 - 53,185,053RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,201,876 - 53,202,766UniSTS
ECD01199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,218,058 - 56,218,931UniSTSGRCh37
Build 36556,253,815 - 56,254,688RGDNCBI36
Celera553,172,267 - 53,173,140RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,189,979 - 53,190,852UniSTS
ECD01342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,218,991 - 56,219,859UniSTSGRCh37
Build 36556,254,748 - 56,255,616RGDNCBI36
Celera553,173,200 - 53,174,068RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,190,912 - 53,191,780UniSTS
ECD01363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,216,209 - 56,217,076UniSTSGRCh37
Build 36556,251,966 - 56,252,833RGDNCBI36
Celera553,170,418 - 53,171,285RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,188,130 - 53,188,997UniSTS
ECD01856  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,217,134 - 56,217,984UniSTSGRCh37
Build 36556,252,891 - 56,253,741RGDNCBI36
Celera553,171,343 - 53,172,193RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,189,055 - 53,189,905UniSTS
ECD02045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,230,870 - 56,231,713UniSTSGRCh37
Build 36556,266,627 - 56,267,470RGDNCBI36
Celera553,185,087 - 53,185,930RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,202,800 - 53,203,643UniSTS
ECD02583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,229,073 - 56,229,897UniSTSGRCh37
Build 36556,264,830 - 56,265,654RGDNCBI36
Celera553,183,292 - 53,184,114RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,201,005 - 53,201,827UniSTS
ECD02716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,225,468 - 56,226,287UniSTSGRCh37
Build 36556,261,225 - 56,262,044RGDNCBI36
Celera553,179,688 - 53,180,507RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,197,401 - 53,198,220UniSTS
ECD03457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,248,783 - 56,249,577UniSTSGRCh37
Build 36556,284,540 - 56,285,334RGDNCBI36
Celera553,203,003 - 53,203,797RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,220,766 - 53,221,560UniSTS
ECD05325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,219,948 - 56,220,686UniSTSGRCh37
Build 36556,255,705 - 56,256,443RGDNCBI36
Celera553,174,157 - 53,174,895RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,191,869 - 53,192,607UniSTS
ECD05589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,228,118 - 56,228,849UniSTSGRCh37
Build 36556,263,875 - 56,264,606RGDNCBI36
Celera553,182,337 - 53,183,068RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,200,050 - 53,200,781UniSTS
ECD06319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,242,621 - 56,243,332UniSTSGRCh37
Build 36556,278,378 - 56,279,089RGDNCBI36
Celera553,196,838 - 53,197,549RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,214,551 - 53,215,262UniSTS
ECD06667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,226,361 - 56,227,063UniSTSGRCh37
Build 36556,262,118 - 56,262,820RGDNCBI36
Celera553,180,581 - 53,181,282RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,198,294 - 53,198,995UniSTS
ECD08666  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,243,420 - 56,244,068UniSTSGRCh37
Build 36556,279,177 - 56,279,825RGDNCBI36
Celera553,197,637 - 53,198,285RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,215,350 - 53,215,998UniSTS
ECD09476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,215,449 - 56,216,076UniSTSGRCh37
Build 36556,251,206 - 56,251,833RGDNCBI36
Celera553,169,658 - 53,170,285RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,187,370 - 53,187,997UniSTS
ECD09718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,234,058 - 56,234,679UniSTSGRCh37
Build 36556,269,815 - 56,270,436RGDNCBI36
Celera553,188,275 - 53,188,896RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,205,988 - 53,206,609UniSTS
ECD09768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,246,376 - 56,246,996UniSTSGRCh37
Build 36556,282,133 - 56,282,753RGDNCBI36
Celera553,200,596 - 53,201,216RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,218,306 - 53,218,926UniSTS
ECD10148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,245,643 - 56,246,252UniSTSGRCh37
Build 36556,281,400 - 56,282,009RGDNCBI36
Celera553,199,860 - 53,200,469RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,217,573 - 53,218,182UniSTS
ECD10705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,236,691 - 56,237,284UniSTSGRCh37
Build 36556,272,448 - 56,273,041RGDNCBI36
Celera553,190,908 - 53,191,501RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,208,621 - 53,209,214UniSTS
ECD12028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,241,327 - 56,241,881UniSTSGRCh37
Build 36556,277,084 - 56,277,638RGDNCBI36
Celera553,195,544 - 53,196,098RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,213,257 - 53,213,811UniSTS
ECD12821  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,234,753 - 56,235,286UniSTSGRCh37
Build 36556,270,510 - 56,271,043RGDNCBI36
Celera553,188,970 - 53,189,503RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,206,683 - 53,207,216UniSTS
ECD12951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,241,933 - 56,242,463UniSTSGRCh37
Build 36556,277,690 - 56,278,220RGDNCBI36
Celera553,196,150 - 53,196,680RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,213,863 - 53,214,393UniSTS
ECD13041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,248,184 - 56,248,711UniSTSGRCh37
Build 36556,283,941 - 56,284,468RGDNCBI36
Celera553,202,404 - 53,202,931RGD
Cytogenetic Map5q11.2UniSTS
ECD14046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,239,501 - 56,240,003UniSTSGRCh37
Build 36556,275,258 - 56,275,760RGDNCBI36
Celera553,193,718 - 53,194,220RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,211,431 - 53,211,933UniSTS
ECD15039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,238,986 - 56,239,465UniSTSGRCh37
Build 36556,274,743 - 56,275,222RGDNCBI36
Celera553,193,203 - 53,193,682RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,210,916 - 53,211,395UniSTS
ECD16295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,224,231 - 56,224,677UniSTSGRCh37
Build 36556,259,988 - 56,260,434RGDNCBI36
Celera553,178,440 - 53,178,889RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,196,152 - 53,196,602UniSTS
ECD17112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,236,207 - 56,236,619UniSTSGRCh37
Build 36556,271,964 - 56,272,376RGDNCBI36
Celera553,190,424 - 53,190,836RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,208,137 - 53,208,549UniSTS
ECD17438  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,233,236 - 56,233,634UniSTSGRCh37
Build 36556,268,993 - 56,269,391RGDNCBI36
Celera553,187,453 - 53,187,851RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,205,166 - 53,205,564UniSTS
ECD18212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,245,210 - 56,245,578UniSTSGRCh37
Build 36556,280,967 - 56,281,335RGDNCBI36
Celera553,199,427 - 53,199,795RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,217,140 - 53,217,508UniSTS
ECD18213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,247,053 - 56,247,421UniSTSGRCh37
Build 36556,282,810 - 56,283,178RGDNCBI36
Celera553,201,273 - 53,201,641RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,218,983 - 53,219,351UniSTS
ECD18496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,238,326 - 56,238,683UniSTSGRCh37
Build 36556,274,083 - 56,274,440RGDNCBI36
Celera553,192,543 - 53,192,900RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,210,256 - 53,210,613UniSTS
ECD21650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,232,620 - 56,232,863UniSTSGRCh37
Build 36556,268,377 - 56,268,620RGDNCBI36
Celera553,186,837 - 53,187,080RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,204,550 - 53,204,793UniSTS
ECD22476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,235,456 - 56,235,673UniSTSGRCh37
Build 36556,271,213 - 56,271,430RGDNCBI36
Celera553,189,673 - 53,189,890RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,207,386 - 53,207,603UniSTS
ECD22985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,233,753 - 56,233,954UniSTSGRCh37
Build 36556,269,510 - 56,269,711RGDNCBI36
Celera553,187,970 - 53,188,171RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,205,683 - 53,205,884UniSTS
ECD23736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,244,542 - 56,244,720UniSTSGRCh37
Build 36556,280,299 - 56,280,477RGDNCBI36
Celera553,198,759 - 53,198,937RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,216,472 - 53,216,650UniSTS
ECD24053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,240,328 - 56,240,490UniSTSGRCh37
Build 36556,276,085 - 56,276,247RGDNCBI36
Celera553,194,545 - 53,194,707RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,212,258 - 53,212,420UniSTS
ECD24302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,232,099 - 56,232,243UniSTSGRCh37
Build 36556,267,856 - 56,268,000RGDNCBI36
Celera553,186,316 - 53,186,460RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,204,029 - 53,204,173UniSTS
ECD24416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,227,633 - 56,227,763UniSTSGRCh37
Build 36556,263,390 - 56,263,520RGDNCBI36
Celera553,181,852 - 53,181,982RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,199,565 - 53,199,695UniSTS
REN28463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,215,105 - 56,215,343UniSTSGRCh37
Build 36556,250,862 - 56,251,100RGDNCBI36
Celera553,169,314 - 53,169,552RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,187,026 - 53,187,264UniSTS
REN28464  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,215,313 - 56,215,558UniSTSGRCh37
Build 36556,251,070 - 56,251,315RGDNCBI36
Celera553,169,522 - 53,169,767RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,187,234 - 53,187,479UniSTS
REN28465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,215,545 - 56,215,803UniSTSGRCh37
Build 36556,251,302 - 56,251,560RGDNCBI36
Celera553,169,754 - 53,170,012RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,187,466 - 53,187,724UniSTS
REN28466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,215,775 - 56,216,001UniSTSGRCh37
Build 36556,251,532 - 56,251,758RGDNCBI36
Celera553,169,984 - 53,170,210RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,187,696 - 53,187,922UniSTS
REN28467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,215,970 - 56,216,198UniSTSGRCh37
Build 36556,251,727 - 56,251,955RGDNCBI36
Celera553,170,179 - 53,170,407RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,187,891 - 53,188,119UniSTS
REN28468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,216,163 - 56,216,409UniSTSGRCh37
Build 36556,251,920 - 56,252,166RGDNCBI36
Celera553,170,372 - 53,170,618RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,188,084 - 53,188,330UniSTS
REN28469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,216,382 - 56,216,610UniSTSGRCh37
Build 36556,252,139 - 56,252,367RGDNCBI36
Celera553,170,591 - 53,170,819RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,188,303 - 53,188,531UniSTS
REN28470  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,216,544 - 56,216,807UniSTSGRCh37
Build 36556,252,301 - 56,252,564RGDNCBI36
Celera553,170,753 - 53,171,016RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,188,465 - 53,188,728UniSTS
REN28471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,216,780 - 56,217,034UniSTSGRCh37
Build 36556,252,537 - 56,252,791RGDNCBI36
Celera553,170,989 - 53,171,243RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,188,701 - 53,188,955UniSTS
REN28472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,217,020 - 56,217,252UniSTSGRCh37
Build 36556,252,777 - 56,253,009RGDNCBI36
Celera553,171,229 - 53,171,461RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,188,941 - 53,189,173UniSTS
REN28473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,217,223 - 56,217,468UniSTSGRCh37
Build 36556,252,980 - 56,253,225RGDNCBI36
Celera553,171,432 - 53,171,677RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,189,144 - 53,189,389UniSTS
REN28474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,217,441 - 56,217,665UniSTSGRCh37
Build 36556,253,198 - 56,253,422RGDNCBI36
Celera553,171,650 - 53,171,874RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,189,362 - 53,189,586UniSTS
REN28475  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,217,635 - 56,217,891UniSTSGRCh37
Build 36556,253,392 - 56,253,648RGDNCBI36
Celera553,171,844 - 53,172,100RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,189,556 - 53,189,812UniSTS
REN28476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,217,854 - 56,218,087UniSTSGRCh37
Build 36556,253,611 - 56,253,844RGDNCBI36
Celera553,172,063 - 53,172,296RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,189,775 - 53,190,008UniSTS
REN28477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,218,059 - 56,218,307UniSTSGRCh37
Build 36556,253,816 - 56,254,064RGDNCBI36
Celera553,172,268 - 53,172,516RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,189,980 - 53,190,228UniSTS
REN28478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,218,304 - 56,218,548UniSTSGRCh37
Build 36556,254,061 - 56,254,305RGDNCBI36
Celera553,172,513 - 53,172,757RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,190,225 - 53,190,469UniSTS
REN28479  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,218,525 - 56,218,777UniSTSGRCh37
Build 36556,254,282 - 56,254,534RGDNCBI36
Celera553,172,734 - 53,172,986RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,190,446 - 53,190,698UniSTS
REN28480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,218,754 - 56,219,016UniSTSGRCh37
Build 36556,254,511 - 56,254,773RGDNCBI36
Celera553,172,963 - 53,173,225RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,190,675 - 53,190,937UniSTS
REN28481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,218,986 - 56,219,226UniSTSGRCh37
Build 36556,254,743 - 56,254,983RGDNCBI36
Celera553,173,195 - 53,173,435RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,190,907 - 53,191,147UniSTS
REN28482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,219,217 - 56,219,479UniSTSGRCh37
Build 36556,254,974 - 56,255,236RGDNCBI36
Celera553,173,426 - 53,173,688RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,191,138 - 53,191,400UniSTS
REN28483  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,219,463 - 56,219,730UniSTSGRCh37
Build 36556,255,220 - 56,255,487RGDNCBI36
Celera553,173,672 - 53,173,939RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,191,384 - 53,191,651UniSTS
REN28484  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,219,718 - 56,219,946UniSTSGRCh37
Build 36556,255,475 - 56,255,703RGDNCBI36
Celera553,173,927 - 53,174,155RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,191,639 - 53,191,867UniSTS
REN28485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,219,921 - 56,220,176UniSTSGRCh37
Build 36556,255,678 - 56,255,933RGDNCBI36
Celera553,174,130 - 53,174,385RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,191,842 - 53,192,097UniSTS
REN28486  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,220,149 - 56,220,391UniSTSGRCh37
Build 36556,255,906 - 56,256,148RGDNCBI36
Celera553,174,358 - 53,174,600RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,192,070 - 53,192,312UniSTS
REN28487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,220,342 - 56,220,574UniSTSGRCh37
Build 36556,256,099 - 56,256,331RGDNCBI36
Celera553,174,551 - 53,174,783RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,192,263 - 53,192,495UniSTS
REN28488  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,220,545 - 56,220,796UniSTSGRCh37
Build 36556,256,302 - 56,256,553RGDNCBI36
Celera553,174,754 - 53,175,005RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,192,466 - 53,192,717UniSTS
REN28489  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,220,772 - 56,221,022UniSTSGRCh37
Build 36556,256,529 - 56,256,779RGDNCBI36
Celera553,174,981 - 53,175,231RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,192,693 - 53,192,943UniSTS
REN28490  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,220,998 - 56,221,246UniSTSGRCh37
Build 36556,256,755 - 56,257,003RGDNCBI36
Celera553,175,207 - 53,175,455RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,192,919 - 53,193,167UniSTS
REN28491  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,221,231 - 56,221,505UniSTSGRCh37
Build 36556,256,988 - 56,257,262RGDNCBI36
Celera553,175,440 - 53,175,714RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,193,152 - 53,193,426UniSTS
REN28492  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,221,455 - 56,221,679UniSTSGRCh37
Build 36556,257,212 - 56,257,436RGDNCBI36
Celera553,175,664 - 53,175,888RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,193,376 - 53,193,600UniSTS
REN28493  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,221,639 - 56,221,866UniSTSGRCh37
Build 36556,257,396 - 56,257,623RGDNCBI36
Celera553,175,848 - 53,176,075RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,193,560 - 53,193,787UniSTS
REN28494  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,221,847 - 56,222,115UniSTSGRCh37
Build 36556,257,604 - 56,257,872RGDNCBI36
Celera553,176,056 - 53,176,324RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,193,768 - 53,194,036UniSTS
REN28495  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,222,090 - 56,222,330UniSTSGRCh37
Build 36556,257,847 - 56,258,087RGDNCBI36
Celera553,176,299 - 53,176,539RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,194,011 - 53,194,251UniSTS
REN28496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,222,310 - 56,222,562UniSTSGRCh37
Build 36556,258,067 - 56,258,319RGDNCBI36
Celera553,176,519 - 53,176,771RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,194,231 - 53,194,483UniSTS
REN28497  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,222,533 - 56,222,784UniSTSGRCh37
Build 36556,258,290 - 56,258,541RGDNCBI36
Celera553,176,742 - 53,176,993RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,194,454 - 53,194,705UniSTS
REN28498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,222,761 - 56,222,996UniSTSGRCh37
Build 36556,258,518 - 56,258,753RGDNCBI36
Celera553,176,970 - 53,177,205RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,194,682 - 53,194,917UniSTS
REN28499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,222,956 - 56,223,225UniSTSGRCh37
Build 36556,258,713 - 56,258,982RGDNCBI36
Celera553,177,165 - 53,177,434RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,194,877 - 53,195,146UniSTS
REN28500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,223,202 - 56,223,450UniSTSGRCh37
Build 36556,258,959 - 56,259,207RGDNCBI36
Celera553,177,411 - 53,177,659RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,195,123 - 53,195,371UniSTS
REN28501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,223,426 - 56,223,679UniSTSGRCh37
Build 36556,259,183 - 56,259,436RGDNCBI36
Celera553,177,635 - 53,177,888RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,195,347 - 53,195,600UniSTS
REN28502  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,223,645 - 56,223,881UniSTSGRCh37
Build 36556,259,402 - 56,259,638RGDNCBI36
Celera553,177,854 - 53,178,090RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,195,566 - 53,195,802UniSTS
REN28503  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,223,841 - 56,224,065UniSTSGRCh37
Build 36556,259,598 - 56,259,822RGDNCBI36
Celera553,178,050 - 53,178,274RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,195,762 - 53,195,986UniSTS
REN28504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,224,011 - 56,224,260UniSTSGRCh37
Build 36556,259,768 - 56,260,017RGDNCBI36
Celera553,178,220 - 53,178,469RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,195,932 - 53,196,181UniSTS
REN28505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,224,243 - 56,224,492UniSTSGRCh37
Build 36556,260,000 - 56,260,249RGDNCBI36
Cytogenetic Map5q11.2UniSTS
REN28506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,224,434 - 56,224,695UniSTSGRCh37
Build 36556,260,191 - 56,260,452RGDNCBI36
Celera553,178,643 - 53,178,907RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,196,355 - 53,196,620UniSTS
REN28507  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,224,659 - 56,224,906UniSTSGRCh37
Build 36556,260,416 - 56,260,663RGDNCBI36
Celera553,178,871 - 53,179,126RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,196,584 - 53,196,839UniSTS
REN28508  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,224,876 - 56,225,118UniSTSGRCh37
Build 36556,260,633 - 56,260,875RGDNCBI36
Celera553,179,096 - 53,179,338RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,196,809 - 53,197,051UniSTS
REN28509  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,225,098 - 56,225,355UniSTSGRCh37
Build 36556,260,855 - 56,261,112RGDNCBI36
Celera553,179,318 - 53,179,575RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,197,031 - 53,197,288UniSTS
REN28510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,225,313 - 56,225,561UniSTSGRCh37
Build 36556,261,070 - 56,261,318RGDNCBI36
Celera553,179,533 - 53,179,781RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,197,246 - 53,197,494UniSTS
REN28511  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,225,547 - 56,225,788UniSTSGRCh37
Build 36556,261,304 - 56,261,545RGDNCBI36
Celera553,179,767 - 53,180,008RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,197,480 - 53,197,721UniSTS
REN28512  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,225,743 - 56,225,967UniSTSGRCh37
Build 36556,261,500 - 56,261,724RGDNCBI36
Celera553,179,963 - 53,180,187RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,197,676 - 53,197,900UniSTS
REN28513  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,225,935 - 56,226,160UniSTSGRCh37
Build 36556,261,692 - 56,261,917RGDNCBI36
Celera553,180,155 - 53,180,380RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,197,868 - 53,198,093UniSTS
REN28514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,226,131 - 56,226,380UniSTSGRCh37
Build 36556,261,888 - 56,262,137RGDNCBI36
Celera553,180,351 - 53,180,600RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,198,064 - 53,198,313UniSTS
REN28515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,226,366 - 56,226,591UniSTSGRCh37
Build 36556,262,123 - 56,262,348RGDNCBI36
Celera553,180,586 - 53,180,811RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,198,299 - 53,198,524UniSTS
REN28516  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,226,571 - 56,226,818UniSTSGRCh37
Build 36556,262,328 - 56,262,575RGDNCBI36
Celera553,180,791 - 53,181,038RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,198,504 - 53,198,751UniSTS
REN28517  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,226,802 - 56,227,064UniSTSGRCh37
Build 36556,262,559 - 56,262,821RGDNCBI36
Celera553,181,022 - 53,181,283RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,198,735 - 53,198,996UniSTS
REN28518  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,227,027 - 56,227,276UniSTSGRCh37
Build 36556,262,784 - 56,263,033RGDNCBI36
Celera553,181,246 - 53,181,495RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,198,959 - 53,199,208UniSTS
REN28519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,227,084 - 56,227,315UniSTSGRCh37
Build 36556,262,841 - 56,263,072RGDNCBI36
Celera553,181,303 - 53,181,534RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,199,016 - 53,199,247UniSTS
REN28520  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,227,290 - 56,227,526UniSTSGRCh37
Build 36556,263,047 - 56,263,283RGDNCBI36
Celera553,181,509 - 53,181,745RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,199,222 - 53,199,458UniSTS
REN28521  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,227,524 - 56,227,753UniSTSGRCh37
Build 36556,263,281 - 56,263,510RGDNCBI36
Celera553,181,743 - 53,181,972RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,199,456 - 53,199,685UniSTS
REN28522  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,227,730 - 56,227,976UniSTSGRCh37
Build 36556,263,487 - 56,263,733RGDNCBI36
Celera553,181,949 - 53,182,195RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,199,662 - 53,199,908UniSTS
REN28523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,227,887 - 56,228,140UniSTSGRCh37
Build 36556,263,644 - 56,263,897RGDNCBI36
Celera553,182,106 - 53,182,359RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,199,819 - 53,200,072UniSTS
REN28524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,228,117 - 56,228,359UniSTSGRCh37
Build 36556,263,874 - 56,264,116RGDNCBI36
Celera553,182,336 - 53,182,578RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,200,049 - 53,200,291UniSTS
REN28525  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,228,331 - 56,228,557UniSTSGRCh37
Build 36556,264,088 - 56,264,314RGDNCBI36
Celera553,182,550 - 53,182,776RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,200,263 - 53,200,489UniSTS
REN28526  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,228,532 - 56,228,802UniSTSGRCh37
Build 36556,264,289 - 56,264,559RGDNCBI36
Celera553,182,751 - 53,183,021RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,200,464 - 53,200,734UniSTS
REN28527  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,228,786 - 56,229,045UniSTSGRCh37
Build 36556,264,543 - 56,264,802RGDNCBI36
Celera553,183,005 - 53,183,264RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,200,718 - 53,200,977UniSTS
REN28528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,229,033 - 56,229,280UniSTSGRCh37
Build 36556,264,790 - 56,265,037RGDNCBI36
Celera553,183,252 - 53,183,499RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,200,965 - 53,201,212UniSTS
REN28529  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,229,256 - 56,229,498UniSTSGRCh37
Build 36556,265,013 - 56,265,255RGDNCBI36
Celera553,183,475 - 53,183,717RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,201,188 - 53,201,430UniSTS
REN28530  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,229,475 - 56,229,728UniSTSGRCh37
Build 36556,265,232 - 56,265,485RGDNCBI36
Celera553,183,694 - 53,183,947RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,201,407 - 53,201,660UniSTS
REN28531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,229,707 - 56,229,951UniSTSGRCh37
Build 36556,265,464 - 56,265,708RGDNCBI36
Celera553,183,926 - 53,184,168RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,201,639 - 53,201,881UniSTS
REN28532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,229,933 - 56,230,157UniSTSGRCh37
Build 36556,265,690 - 56,265,914RGDNCBI36
Celera553,184,150 - 53,184,374RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,201,863 - 53,202,087UniSTS
REN28533  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,230,132 - 56,230,404UniSTSGRCh37
Build 36556,265,889 - 56,266,161RGDNCBI36
Celera553,184,349 - 53,184,621RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,202,062 - 53,202,334UniSTS
REN28534  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,230,392 - 56,230,642UniSTSGRCh37
Build 36556,266,149 - 56,266,399RGDNCBI36
Celera553,184,609 - 53,184,859RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,202,322 - 53,202,572UniSTS
REN28535  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,230,622 - 56,230,891UniSTSGRCh37
Build 36556,266,379 - 56,266,648RGDNCBI36
Celera553,184,839 - 53,185,108RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,202,552 - 53,202,821UniSTS
REN28536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,230,871 - 56,231,145UniSTSGRCh37
Build 36556,266,628 - 56,266,902RGDNCBI36
Celera553,185,088 - 53,185,362RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,202,801 - 53,203,075UniSTS
REN28537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,231,065 - 56,231,290UniSTSGRCh37
Build 36556,266,822 - 56,267,047RGDNCBI36
Celera553,185,282 - 53,185,507RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,202,995 - 53,203,220UniSTS
REN28538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,231,288 - 56,231,541UniSTSGRCh37
Build 36556,267,045 - 56,267,298RGDNCBI36
Celera553,185,505 - 53,185,758RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,203,218 - 53,203,471UniSTS
REN28539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,231,530 - 56,231,778UniSTSGRCh37
Build 36556,267,287 - 56,267,535RGDNCBI36
Celera553,185,747 - 53,185,995RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,203,460 - 53,203,708UniSTS
REN28540  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,231,760 - 56,231,998UniSTSGRCh37
Build 36556,267,517 - 56,267,755RGDNCBI36
Celera553,185,977 - 53,186,215RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,203,690 - 53,203,928UniSTS
REN28541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,231,861 - 56,232,117UniSTSGRCh37
Build 36556,267,618 - 56,267,874RGDNCBI36
Celera553,186,078 - 53,186,334RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,203,791 - 53,204,047UniSTS
REN28542  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,232,094 - 56,232,325UniSTSGRCh37
Build 36556,267,851 - 56,268,082RGDNCBI36
Celera553,186,311 - 53,186,542RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,204,024 - 53,204,255UniSTS
REN28543  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,232,307 - 56,232,567UniSTSGRCh37
Build 36556,268,064 - 56,268,324RGDNCBI36
Celera553,186,524 - 53,186,784RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,204,237 - 53,204,497UniSTS
REN28544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,232,558 - 56,232,782UniSTSGRCh37
Build 36556,268,315 - 56,268,539RGDNCBI36
Celera553,186,775 - 53,186,999RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,204,488 - 53,204,712UniSTS
REN28545  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,232,749 - 56,232,979UniSTSGRCh37
Build 36556,268,506 - 56,268,736RGDNCBI36
Celera553,186,966 - 53,187,196RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,204,679 - 53,204,909UniSTS
REN28546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,233,078 - 56,233,345UniSTSGRCh37
Build 36556,268,835 - 56,269,102RGDNCBI36
Celera553,187,295 - 53,187,562RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,205,008 - 53,205,275UniSTS
REN28547  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,233,312 - 56,233,549UniSTSGRCh37
Build 36556,269,069 - 56,269,306RGDNCBI36
Celera553,187,529 - 53,187,766RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,205,242 - 53,205,479UniSTS
REN28548  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,233,538 - 56,233,785UniSTSGRCh37
Build 36556,269,295 - 56,269,542RGDNCBI36
Celera553,187,755 - 53,188,002RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,205,468 - 53,205,715UniSTS
REN28549  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,233,762 - 56,234,020UniSTSGRCh37
Build 36556,269,519 - 56,269,777RGDNCBI36
Celera553,187,979 - 53,188,237RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,205,692 - 53,205,950UniSTS
REN28550  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,234,014 - 56,234,273UniSTSGRCh37
Build 36556,269,771 - 56,270,030RGDNCBI36
Celera553,188,231 - 53,188,490RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,205,944 - 53,206,203UniSTS
REN28551  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,234,257 - 56,234,513UniSTSGRCh37
Build 36556,270,014 - 56,270,270RGDNCBI36
Celera553,188,474 - 53,188,730RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,206,187 - 53,206,443UniSTS
REN28552  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,234,505 - 56,234,754UniSTSGRCh37
Build 36556,270,262 - 56,270,511RGDNCBI36
Celera553,188,722 - 53,188,971RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,206,435 - 53,206,684UniSTS
REN28553  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,234,742 - 56,234,973UniSTSGRCh37
Build 36556,270,499 - 56,270,730RGDNCBI36
Celera553,188,959 - 53,189,190RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,206,672 - 53,206,903UniSTS
REN28554  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,234,948 - 56,235,174UniSTSGRCh37
Build 36556,270,705 - 56,270,931RGDNCBI36
Celera553,189,165 - 53,189,391RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,206,878 - 53,207,104UniSTS
REN28555  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,235,160 - 56,235,408UniSTSGRCh37
Build 36556,270,917 - 56,271,165RGDNCBI36
Celera553,189,377 - 53,189,625RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,207,090 - 53,207,338UniSTS
REN28556  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,235,388 - 56,235,635UniSTSGRCh37
Build 36556,271,145 - 56,271,392RGDNCBI36
Celera553,189,605 - 53,189,852RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,207,318 - 53,207,565UniSTS
REN28557  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,235,614 - 56,235,883UniSTSGRCh37
Build 36556,271,371 - 56,271,640RGDNCBI36
Celera553,189,831 - 53,190,100RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,207,544 - 53,207,813UniSTS
REN28558  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,235,860 - 56,236,112UniSTSGRCh37
Build 36556,271,617 - 56,271,869RGDNCBI36
Celera553,190,077 - 53,190,329RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,207,790 - 53,208,042UniSTS
REN28559  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,236,085 - 56,236,333UniSTSGRCh37
Build 36556,271,842 - 56,272,090RGDNCBI36
Celera553,190,302 - 53,190,550RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,208,015 - 53,208,263UniSTS
REN28560  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,236,310 - 56,236,542UniSTSGRCh37
Build 36556,272,067 - 56,272,299RGDNCBI36
Celera553,190,527 - 53,190,759RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,208,240 - 53,208,472UniSTS
REN28561  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,236,537 - 56,236,784UniSTSGRCh37
Build 36556,272,294 - 56,272,541RGDNCBI36
Celera553,190,754 - 53,191,001RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,208,467 - 53,208,714UniSTS
REN28562  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,236,782 - 56,237,023UniSTSGRCh37
Build 36556,272,539 - 56,272,780RGDNCBI36
Celera553,190,999 - 53,191,240RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,208,712 - 53,208,953UniSTS
REN28563  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,237,000 - 56,237,248UniSTSGRCh37
Build 36556,272,757 - 56,273,005RGDNCBI36
Celera553,191,217 - 53,191,465RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,208,930 - 53,209,178UniSTS
REN28564  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,237,204 - 56,237,445UniSTSGRCh37
Build 36556,272,961 - 56,273,202RGDNCBI36
Celera553,191,421 - 53,191,662RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,209,134 - 53,209,375UniSTS
REN28565  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,237,436 - 56,237,679UniSTSGRCh37
Build 36556,273,193 - 56,273,436RGDNCBI36
Celera553,191,653 - 53,191,896RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,209,366 - 53,209,609UniSTS
REN28566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,237,646 - 56,237,885UniSTSGRCh37
Build 36556,273,403 - 56,273,642RGDNCBI36
Celera553,191,863 - 53,192,102RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,209,576 - 53,209,815UniSTS
REN28567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,237,861 - 56,238,123UniSTSGRCh37
Build 36556,273,618 - 56,273,880RGDNCBI36
Celera553,192,078 - 53,192,340RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,209,791 - 53,210,053UniSTS
REN28568  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,238,101 - 56,238,348UniSTSGRCh37
Build 36556,273,858 - 56,274,105RGDNCBI36
Celera553,192,318 - 53,192,565RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,210,031 - 53,210,278UniSTS
REN28569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,238,304 - 56,238,550UniSTSGRCh37
Build 36556,274,061 - 56,274,307RGDNCBI36
Celera553,192,521 - 53,192,767RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,210,234 - 53,210,480UniSTS
REN28570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,238,514 - 56,238,758UniSTSGRCh37
Build 36556,274,271 - 56,274,515RGDNCBI36
Celera553,192,731 - 53,192,975RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,210,444 - 53,210,688UniSTS
REN28571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,238,733 - 56,239,003UniSTSGRCh37
Build 36556,274,490 - 56,274,760RGDNCBI36
Celera553,192,950 - 53,193,220RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,210,663 - 53,210,933UniSTS
REN28572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,238,980 - 56,239,235UniSTSGRCh37
Build 36556,274,737 - 56,274,992RGDNCBI36
Celera553,193,197 - 53,193,452RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,210,910 - 53,211,165UniSTS
REN28573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,239,232 - 56,239,470UniSTSGRCh37
Build 36556,274,989 - 56,275,227RGDNCBI36
Celera553,193,449 - 53,193,687RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,211,162 - 53,211,400UniSTS
REN28574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,239,440 - 56,239,675UniSTSGRCh37
Build 36556,275,197 - 56,275,432RGDNCBI36
Celera553,193,657 - 53,193,892RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,211,370 - 53,211,605UniSTS
REN28575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,239,630 - 56,239,874UniSTSGRCh37
Build 36556,275,387 - 56,275,631RGDNCBI36
Celera553,193,847 - 53,194,091RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,211,560 - 53,211,804UniSTS
REN28576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,239,792 - 56,240,024UniSTSGRCh37
Build 36556,275,549 - 56,275,781RGDNCBI36
Celera553,194,009 - 53,194,241RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,211,722 - 53,211,954UniSTS
REN28577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,240,338 - 56,240,585UniSTSGRCh37
Build 36556,276,095 - 56,276,342RGDNCBI36
Celera553,194,555 - 53,194,802RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,212,268 - 53,212,515UniSTS
REN28578  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,240,423 - 56,240,681UniSTSGRCh37
Build 36556,276,180 - 56,276,438RGDNCBI36
Celera553,194,640 - 53,194,898RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,212,353 - 53,212,611UniSTS
REN28579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,240,673 - 56,240,922UniSTSGRCh37
Build 36556,276,430 - 56,276,679RGDNCBI36
Celera553,194,890 - 53,195,139RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,212,603 - 53,212,852UniSTS
REN28580  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,240,792 - 56,241,019UniSTSGRCh37
Build 36556,276,549 - 56,276,776RGDNCBI36
Celera553,195,009 - 53,195,236RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,212,722 - 53,212,949UniSTS
REN28581  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,241,270 - 56,241,494UniSTSGRCh37
Build 36556,277,027 - 56,277,251RGDNCBI36
Celera553,195,487 - 53,195,711RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,213,200 - 53,213,424UniSTS
REN28582  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,241,435 - 56,241,659UniSTSGRCh37
Build 36556,277,192 - 56,277,416RGDNCBI36
Celera553,195,652 - 53,195,876RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,213,365 - 53,213,589UniSTS
REN28583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,241,625 - 56,241,875UniSTSGRCh37
Build 36556,277,382 - 56,277,632RGDNCBI36
Celera553,195,842 - 53,196,092RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,213,555 - 53,213,805UniSTS
REN28584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,241,873 - 56,242,130UniSTSGRCh37
Build 36556,277,630 - 56,277,887RGDNCBI36
Celera553,196,090 - 53,196,347RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,213,803 - 53,214,060UniSTS
REN28585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,242,105 - 56,242,375UniSTSGRCh37
Build 36556,277,862 - 56,278,132RGDNCBI36
Celera553,196,322 - 53,196,592RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,214,035 - 53,214,305UniSTS
REN28586  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,242,339 - 56,242,563UniSTSGRCh37
Build 36556,278,096 - 56,278,320RGDNCBI36
Celera553,196,556 - 53,196,780RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,214,269 - 53,214,493UniSTS
REN28587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,242,522 - 56,242,780UniSTSGRCh37
Build 36556,278,279 - 56,278,537RGDNCBI36
Celera553,196,739 - 53,196,997RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,214,452 - 53,214,710UniSTS
REN28588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,242,752 - 56,243,004UniSTSGRCh37
Build 36556,278,509 - 56,278,761RGDNCBI36
Celera553,196,969 - 53,197,221RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,214,682 - 53,214,934UniSTS
REN28589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,242,982 - 56,243,238UniSTSGRCh37
Build 36556,278,739 - 56,278,995RGDNCBI36
Celera553,197,199 - 53,197,455RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,214,912 - 53,215,168UniSTS
REN28590  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,243,226 - 56,243,450UniSTSGRCh37
Build 36556,278,983 - 56,279,207RGDNCBI36
Celera553,197,443 - 53,197,667RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,215,156 - 53,215,380UniSTS
REN28591  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,243,421 - 56,243,652UniSTSGRCh37
Build 36556,279,178 - 56,279,409RGDNCBI36
Celera553,197,638 - 53,197,869RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,215,351 - 53,215,582UniSTS
REN28592  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,243,621 - 56,243,895UniSTSGRCh37
Build 36556,279,378 - 56,279,652RGDNCBI36
Celera553,197,838 - 53,198,112RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,215,551 - 53,215,825UniSTS
REN28593  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,243,878 - 56,244,136UniSTSGRCh37
Build 36556,279,635 - 56,279,893RGDNCBI36
Celera553,198,095 - 53,198,353RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,215,808 - 53,216,066UniSTS
REN28594  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,243,960 - 56,244,219UniSTSGRCh37
Build 36556,279,717 - 56,279,976RGDNCBI36
Celera553,198,177 - 53,198,436RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,215,890 - 53,216,149UniSTS
REN28595  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,244,168 - 56,244,393UniSTSGRCh37
Build 36556,279,925 - 56,280,150RGDNCBI36
Celera553,198,385 - 53,198,610RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,216,098 - 53,216,323UniSTS
REN28596  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,244,363 - 56,244,612UniSTSGRCh37
Build 36556,280,120 - 56,280,369RGDNCBI36
Celera553,198,580 - 53,198,829RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,216,293 - 53,216,542UniSTS
REN28597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,244,604 - 56,244,853UniSTSGRCh37
Build 36556,280,361 - 56,280,610RGDNCBI36
Celera553,198,821 - 53,199,070RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,216,534 - 53,216,783UniSTS
REN28598  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,244,835 - 56,245,077UniSTSGRCh37
Build 36556,280,592 - 56,280,834RGDNCBI36
Celera553,199,052 - 53,199,294RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,216,765 - 53,217,007UniSTS
REN28599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,245,056 - 56,245,307UniSTSGRCh37
Build 36556,280,813 - 56,281,064RGDNCBI36
Celera553,199,273 - 53,199,524RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,216,986 - 53,217,237UniSTS
REN28600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,245,295 - 56,245,564UniSTSGRCh37
Build 36556,281,052 - 56,281,321RGDNCBI36
Celera553,199,512 - 53,199,781RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,217,225 - 53,217,494UniSTS
REN28601  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,245,562 - 56,245,786UniSTSGRCh37
Build 36556,281,319 - 56,281,543RGDNCBI36
Celera553,199,779 - 53,200,003RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,217,492 - 53,217,716UniSTS
REN28602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,245,746 - 56,246,003UniSTSGRCh37
Build 36556,281,503 - 56,281,760RGDNCBI36
Celera553,199,963 - 53,200,220RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,217,676 - 53,217,933UniSTS
REN28603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,245,982 - 56,246,247UniSTSGRCh37
Build 36556,281,739 - 56,282,004RGDNCBI36
Celera553,200,199 - 53,200,464RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,217,912 - 53,218,177UniSTS
REN28604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,246,224 - 56,246,483UniSTSGRCh37
Build 36556,281,981 - 56,282,240RGDNCBI36
Celera553,200,441 - 53,200,703RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,218,154 - 53,218,413UniSTS
REN28605  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,246,468 - 56,246,696UniSTSGRCh37
Build 36556,282,225 - 56,282,453RGDNCBI36
Celera553,200,688 - 53,200,916RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,218,398 - 53,218,626UniSTS
REN28606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,246,667 - 56,246,897UniSTSGRCh37
Build 36556,282,424 - 56,282,654RGDNCBI36
Celera553,200,887 - 53,201,117RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,218,597 - 53,218,827UniSTS
REN28607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,246,862 - 56,247,100UniSTSGRCh37
Build 36556,282,619 - 56,282,857RGDNCBI36
Celera553,201,082 - 53,201,320RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,218,792 - 53,219,030UniSTS
REN28608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,247,088 - 56,247,315UniSTSGRCh37
Build 36556,282,845 - 56,283,072RGDNCBI36
Celera553,201,308 - 53,201,535RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,219,018 - 53,219,245UniSTS
REN28609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,247,708 - 56,247,942UniSTSGRCh37
Build 36556,283,465 - 56,283,699RGDNCBI36
Celera553,201,928 - 53,202,162RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,219,638 - 53,219,872UniSTS
REN28610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,247,933 - 56,248,205UniSTSGRCh37
Build 36556,283,690 - 56,283,962RGDNCBI36
Celera553,202,153 - 53,202,425RGD
Cytogenetic Map5q11.2UniSTS
REN28611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,248,198 - 56,248,453UniSTSGRCh37
Build 36556,283,955 - 56,284,210RGDNCBI36
Celera553,202,418 - 53,202,673RGD
Cytogenetic Map5q11.2UniSTS
REN28612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,248,432 - 56,248,672UniSTSGRCh37
Build 36556,284,189 - 56,284,429RGDNCBI36
Celera553,202,652 - 53,202,892RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,220,415 - 53,220,655UniSTS
REN28613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,248,660 - 56,248,906UniSTSGRCh37
Build 36556,284,417 - 56,284,663RGDNCBI36
Celera553,202,880 - 53,203,126RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,220,643 - 53,220,889UniSTS
REN28614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,248,884 - 56,249,136UniSTSGRCh37
Build 36556,284,641 - 56,284,893RGDNCBI36
Celera553,203,104 - 53,203,356RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,220,867 - 53,221,119UniSTS
REN28615  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,249,115 - 56,249,339UniSTSGRCh37
Build 36556,284,872 - 56,285,096RGDNCBI36
Celera553,203,335 - 53,203,559RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,221,098 - 53,221,322UniSTS
REN28616  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,249,317 - 56,249,569UniSTSGRCh37
Build 36556,285,074 - 56,285,326RGDNCBI36
Celera553,203,537 - 53,203,789RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,221,300 - 53,221,552UniSTS
REN28617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,249,564 - 56,249,791UniSTSGRCh37
Build 36556,285,321 - 56,285,548RGDNCBI36
Celera553,203,784 - 53,204,011RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,221,547 - 53,221,774UniSTS
stSG625181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,215,632 - 56,217,036UniSTSGRCh37
Build 36556,251,389 - 56,252,793RGDNCBI36
Celera553,169,841 - 53,171,245RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,187,553 - 53,188,957UniSTS
stSG625182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,217,017 - 56,218,143UniSTSGRCh37
Build 36556,252,774 - 56,253,900RGDNCBI36
Celera553,171,226 - 53,172,352RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,188,938 - 53,190,064UniSTS
stSG625183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,218,124 - 56,219,272UniSTSGRCh37
Build 36556,253,881 - 56,255,029RGDNCBI36
Celera553,172,333 - 53,173,481RGD
Cytogenetic Map5q11.2UniSTS
HuRef553,190,045 - 53,191,193UniSTS
stSG625184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,219,254 - 56,220,408UniSTSGRCh37
Build 36556,255,011 - 56,256,165RGDNCBI36
Celera553,173,463 - 53,174,617RGD
HuRef553,191,175 - 53,192,329UniSTS
stSG625185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,220,391 - 56,220,651UniSTSGRCh37
Build 36556,256,148 - 56,256,408RGDNCBI36
Celera553,174,600 - 53,174,860RGD
HuRef553,192,312 - 53,192,572UniSTS
stSG625186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,223,271 - 56,224,301UniSTSGRCh37
Build 36556,259,028 - 56,260,058RGDNCBI36
Celera553,177,480 - 53,178,510RGD
HuRef553,195,192 - 53,196,222UniSTS
stSG625187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,224,285 - 56,225,603UniSTSGRCh37
Build 36556,260,042 - 56,261,360RGDNCBI36
Celera553,178,494 - 53,179,823RGD
HuRef553,196,206 - 53,197,536UniSTS
stSG625188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,225,584 - 56,226,998UniSTSGRCh37
Build 36556,261,341 - 56,262,755RGDNCBI36
Celera553,179,804 - 53,181,217RGD
HuRef553,197,517 - 53,198,930UniSTS
stSG625189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,226,983 - 56,228,437UniSTSGRCh37
Build 36556,262,740 - 56,264,194RGDNCBI36
Celera553,181,202 - 53,182,656RGD
HuRef553,198,915 - 53,200,369UniSTS
stSG625190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,228,430 - 56,229,486UniSTSGRCh37
Build 36556,264,187 - 56,265,243RGDNCBI36
Celera553,182,649 - 53,183,705RGD
HuRef553,200,362 - 53,201,418UniSTS
stSG625191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,229,473 - 56,230,521UniSTSGRCh37
Build 36556,265,230 - 56,266,278RGDNCBI36
Celera553,183,692 - 53,184,738RGD
HuRef553,201,405 - 53,202,451UniSTS
stSG625192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,230,502 - 56,231,645UniSTSGRCh37
Build 36556,266,259 - 56,267,402RGDNCBI36
Celera553,184,719 - 53,185,862RGD
HuRef553,202,432 - 53,203,575UniSTS
stSG625193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,231,627 - 56,232,762UniSTSGRCh37
Build 36556,267,384 - 56,268,519RGDNCBI36
Celera553,185,844 - 53,186,979RGD
HuRef553,203,557 - 53,204,692UniSTS
stSG625194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,232,743 - 56,234,187UniSTSGRCh37
Build 36556,268,500 - 56,269,944RGDNCBI36
Celera553,186,960 - 53,188,404RGD
HuRef553,204,673 - 53,206,117UniSTS
stSG625195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,234,167 - 56,234,359UniSTSGRCh37
Build 36556,269,924 - 56,270,116RGDNCBI36
Celera553,188,384 - 53,188,576RGD
HuRef553,206,097 - 53,206,289UniSTS
stSG625196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,234,362 - 56,235,585UniSTSGRCh37
Build 36556,270,119 - 56,271,342RGDNCBI36
Celera553,188,579 - 53,189,802RGD
HuRef553,206,292 - 53,207,515UniSTS
stSG625197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,235,566 - 56,236,789UniSTSGRCh37
Build 36556,271,323 - 56,272,546RGDNCBI36
Celera553,189,783 - 53,191,006RGD
HuRef553,207,496 - 53,208,719UniSTS
stSG625198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,236,770 - 56,238,203UniSTSGRCh37
Build 36556,272,527 - 56,273,960RGDNCBI36
Celera553,190,987 - 53,192,420RGD
HuRef553,208,700 - 53,210,133UniSTS
stSG625199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,238,184 - 56,239,421UniSTSGRCh37
Build 36556,273,941 - 56,275,178RGDNCBI36
Celera553,192,401 - 53,193,638RGD
HuRef553,210,114 - 53,211,351UniSTS
stSG625200  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,239,402 - 56,240,431UniSTSGRCh37
Build 36556,275,159 - 56,276,188RGDNCBI36
Celera553,193,619 - 53,194,648RGD
HuRef553,211,332 - 53,212,361UniSTS
stSG625201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,240,416 - 56,241,527UniSTSGRCh37
Build 36556,276,173 - 56,277,284RGDNCBI36
Celera553,194,633 - 53,195,744RGD
HuRef553,212,346 - 53,213,457UniSTS
stSG625202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,241,509 - 56,242,871UniSTSGRCh37
Build 36556,277,266 - 56,278,628RGDNCBI36
Celera553,195,726 - 53,197,088RGD
HuRef553,213,439 - 53,214,801UniSTS
stSG625203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,242,852 - 56,243,999UniSTSGRCh37
Build 36556,278,609 - 56,279,756RGDNCBI36
Celera553,197,069 - 53,198,216RGD
HuRef553,214,782 - 53,215,929UniSTS
stSG625204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,243,987 - 56,245,477UniSTSGRCh37
Build 36556,279,744 - 56,281,234RGDNCBI36
Celera553,198,204 - 53,199,694RGD
HuRef553,215,917 - 53,217,407UniSTS
stSG625205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,245,458 - 56,246,776UniSTSGRCh37
Build 36556,281,215 - 56,282,533RGDNCBI36
Celera553,199,675 - 53,200,996RGD
HuRef553,217,388 - 53,218,706UniSTS
stSG625207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,248,382 - 56,249,495UniSTSGRCh37
Build 36556,284,139 - 56,285,252RGDNCBI36
Celera553,202,602 - 53,203,715RGD
HuRef553,220,365 - 53,221,478UniSTS
MIER3  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37556,219,343 - 56,219,595UniSTSGRCh37
Celera553,173,552 - 53,173,804UniSTS
HuRef553,191,264 - 53,191,516UniSTS


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 1280 875 796 138 824 103 1759 405 1261 189 1181 1046 48 378 1164 4
Low 1159 1880 930 486 896 362 2597 1787 2471 230 279 567 127 1 826 1624 2 2
Below cutoff 236 231 5 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001297598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001297599 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_152622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011543216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011543217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047416839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047416840 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054351877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054351878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC008937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC016644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI470450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK002183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC041348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX640907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647359 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471123 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB136129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000336942   ⟹   ENSP00000337027
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,935,671 - 56,952,203 (-)Ensembl
RefSeq Acc Id: ENST00000381199   ⟹   ENSP00000370596
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,919,603 - 56,952,123 (-)Ensembl
RefSeq Acc Id: ENST00000381213   ⟹   ENSP00000370611
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,919,603 - 56,952,125 (-)Ensembl
RefSeq Acc Id: ENST00000381226   ⟹   ENSP00000370624
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,919,602 - 56,952,118 (-)Ensembl
RefSeq Acc Id: ENST00000409421   ⟹   ENSP00000386584
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,922,584 - 56,941,133 (-)Ensembl
RefSeq Acc Id: ENST00000440000   ⟹   ENSP00000407169
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,947,031 - 56,971,675 (-)Ensembl
RefSeq Acc Id: ENST00000451637   ⟹   ENSP00000400693
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,935,744 - 56,938,971 (-)Ensembl
RefSeq Acc Id: ENST00000452157   ⟹   ENSP00000408076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,919,604 - 56,952,122 (-)Ensembl
RefSeq Acc Id: ENST00000480115
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,938,814 - 56,952,112 (-)Ensembl
RefSeq Acc Id: ENST00000497185
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,947,032 - 56,971,675 (-)Ensembl
RefSeq Acc Id: ENST00000546593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl556,947,031 - 56,971,675 (-)Ensembl
RefSeq Acc Id: NM_001297598   ⟹   NP_001284527
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38556,919,603 - 56,952,123 (-)NCBI
CHM1_1556,218,436 - 56,250,966 (-)NCBI
T2T-CHM13v2.0557,747,855 - 57,780,385 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001297599   ⟹   NP_001284528
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38556,919,603 - 56,952,123 (-)NCBI
CHM1_1556,218,436 - 56,250,966 (-)NCBI
T2T-CHM13v2.0557,747,855 - 57,780,385 (-)NCBI
Sequence:
RefSeq Acc Id: NM_152622   ⟹   NP_689835
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38556,919,603 - 56,952,123 (-)NCBI
GRCh37556,215,429 - 56,247,957 (-)NCBI
Build 36556,251,186 - 56,283,711 (-)NCBI Archive
Celera553,169,638 - 53,202,174 (-)RGD
HuRef553,187,350 - 53,219,884 (-)RGD
CHM1_1556,218,436 - 56,250,966 (-)NCBI
T2T-CHM13v2.0557,747,855 - 57,780,385 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011543216   ⟹   XP_011541518
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38556,919,603 - 56,951,571 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011543217   ⟹   XP_011541519
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38556,919,603 - 56,951,571 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047416839   ⟹   XP_047272795
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38556,919,603 - 56,951,424 (-)NCBI
RefSeq Acc Id: XM_047416840   ⟹   XP_047272796
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38556,919,603 - 56,952,209 (-)NCBI
RefSeq Acc Id: XM_054351877   ⟹   XP_054207852
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0557,747,855 - 57,779,833 (-)NCBI
RefSeq Acc Id: XM_054351878   ⟹   XP_054207853
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0557,747,855 - 57,779,833 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_689835   ⟸   NM_152622
- Peptide Label: isoform 3
- UniProtKB: Q7Z3K6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001284528   ⟸   NM_001297599
- Peptide Label: isoform 2
- UniProtKB: Q86YG8 (UniProtKB/Swiss-Prot),   Q6MZS7 (UniProtKB/Swiss-Prot),   Q68CS3 (UniProtKB/Swiss-Prot),   Q5CZI0 (UniProtKB/Swiss-Prot),   B8ZZQ0 (UniProtKB/Swiss-Prot),   B4DRI9 (UniProtKB/Swiss-Prot),   Q8NA13 (UniProtKB/Swiss-Prot),   Q7Z3K6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001284527   ⟸   NM_001297598
- Peptide Label: isoform 1
- UniProtKB: Q7Z3K6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011541519   ⟸   XM_011543217
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011541518   ⟸   XM_011543216
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000400693   ⟸   ENST00000451637
RefSeq Acc Id: ENSP00000408076   ⟸   ENST00000452157
RefSeq Acc Id: ENSP00000337027   ⟸   ENST00000336942
RefSeq Acc Id: ENSP00000407169   ⟸   ENST00000440000
RefSeq Acc Id: ENSP00000386584   ⟸   ENST00000409421
RefSeq Acc Id: ENSP00000370596   ⟸   ENST00000381199
RefSeq Acc Id: ENSP00000370611   ⟸   ENST00000381213
RefSeq Acc Id: ENSP00000370624   ⟸   ENST00000381226
RefSeq Acc Id: XP_047272796   ⟸   XM_047416840
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047272795   ⟸   XM_047416839
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054207853   ⟸   XM_054351878
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054207852   ⟸   XM_054351877
- Peptide Label: isoform X1
Protein Domains
ELM2   SANT

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q7Z3K6-F1-model_v2 AlphaFold Q7Z3K6 1-550 view protein structure

Promoters
RGD ID:6814753
Promoter ID:HG_XEF:6331
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_2Hour,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001030149,   NM_001168932
Position:
Human AssemblyChrPosition (strand)Source
Build 36556,282,441 - 56,283,157 (-)MPROMDB
RGD ID:6803078
Promoter ID:HG_KWN:50165
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000336942,   NM_152622,   OTTHUMT00000132525,   UC003JRB.1,   UC003JRC.1,   UC003JRD.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36556,283,494 - 56,283,994 (-)MPROMDB
RGD ID:6869648
Promoter ID:EPDNEW_H7989
Type:initiation region
Name:MIER3_1
Description:MIER family member 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38556,952,123 - 56,952,183EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26678 AgrOrtholog
COSMIC MIER3 COSMIC
Ensembl Genes ENSG00000155545 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000336942.9 UniProtKB/TrEMBL
  ENST00000381199 ENTREZGENE
  ENST00000381199.8 UniProtKB/Swiss-Prot
  ENST00000381213 ENTREZGENE
  ENST00000381213.7 UniProtKB/Swiss-Prot
  ENST00000381226 ENTREZGENE
  ENST00000381226.7 UniProtKB/Swiss-Prot
  ENST00000409421 ENTREZGENE
  ENST00000409421.5 UniProtKB/Swiss-Prot
  ENST00000440000.5 UniProtKB/TrEMBL
  ENST00000451637.1 UniProtKB/TrEMBL
  ENST00000452157.5 UniProtKB/Swiss-Prot
Gene3D-CATH 4.10.1240.50 UniProtKB/Swiss-Prot
  Homeodomain-like UniProtKB/Swiss-Prot
GTEx ENSG00000155545 GTEx
HGNC ID HGNC:26678 ENTREZGENE
Human Proteome Map MIER3 Human Proteome Map
InterPro ELM2_dom UniProtKB/Swiss-Prot
  Homeobox-like_sf UniProtKB/Swiss-Prot
  MIER/MTA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIER1/3_C UniProtKB/Swiss-Prot
  SANT/Myb UniProtKB/Swiss-Prot
  SANT_dom UniProtKB/Swiss-Prot
KEGG Report hsa:166968 UniProtKB/Swiss-Prot
NCBI Gene 166968 ENTREZGENE
OMIM 620100 OMIM
PANTHER MESODERM INDUCTION EARLY RESPONSE PROTEIN 3 UniProtKB/TrEMBL
  METASTASIS-ASSOCIATED PROTEIN AND MESODERM INDUCTION EARLY RESPONSE PROTEIN UniProtKB/TrEMBL, UniProtKB/Swiss-Prot
  PTHR10865:SF22 UniProtKB/Swiss-Prot
Pfam ELM2 UniProtKB/Swiss-Prot
  MIER1_beta_C UniProtKB/Swiss-Prot
  Myb_DNA-binding UniProtKB/Swiss-Prot
PharmGKB PA145008088 PharmGKB
PROSITE ELM2 UniProtKB/Swiss-Prot
  SANT UniProtKB/Swiss-Prot
SMART ELM2 UniProtKB/Swiss-Prot
  SANT UniProtKB/Swiss-Prot
Superfamily-SCOP SSF46689 UniProtKB/Swiss-Prot
UniProt A8MQD4_HUMAN UniProtKB/TrEMBL
  B4DRI9 ENTREZGENE
  B8ZZQ0 ENTREZGENE
  C9JXP7_HUMAN UniProtKB/TrEMBL
  H7C1J9_HUMAN UniProtKB/TrEMBL
  MIER3_HUMAN UniProtKB/Swiss-Prot
  Q5CZI0 ENTREZGENE
  Q68CS3 ENTREZGENE
  Q6MZS7 ENTREZGENE
  Q7Z3K6 ENTREZGENE
  Q86YG8 ENTREZGENE
  Q8NA13 ENTREZGENE
UniProt Secondary B4DRI9 UniProtKB/Swiss-Prot
  B8ZZQ0 UniProtKB/Swiss-Prot
  Q5CZI0 UniProtKB/Swiss-Prot
  Q68CS3 UniProtKB/Swiss-Prot
  Q6MZS7 UniProtKB/Swiss-Prot
  Q86YG8 UniProtKB/Swiss-Prot
  Q8NA13 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-02 MIER3  MIER family member 3    mesoderm induction early response 1, family member 3  Symbol and/or name change 5135510 APPROVED