FRMD5 (FERM domain containing 5) - Rat Genome Database

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Gene: FRMD5 (FERM domain containing 5) Homo sapiens
Analyze
Symbol: FRMD5
Name: FERM domain containing 5
RGD ID: 1605911
HGNC Page HGNC:28214
Description: Enables integrin binding activity and protein kinase binding activity. Involved in negative regulation of cell motility; positive regulation of cell adhesion; and regulation of cell migration. Located in adherens junction. Implicated in neurodevelopmental disorder with eye movement abnormalities and ataxia.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FERM domain-containing protein 5; FLJ41022; MGC14161; NEDEMA
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
GRCh381543,870,764 - 44,199,473 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1543,870,761 - 44,195,271 (-)EnsemblGRCh38hg38GRCh38
GRCh371544,162,962 - 44,487,469 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361541,953,022 - 42,274,721 (-)NCBINCBI36Build 36hg18NCBI36
Celera1521,055,188 - 21,376,921 (-)NCBICelera
Cytogenetic Map15q15.3NCBI
HuRef1520,988,457 - 21,310,775 (-)NCBIHuRef
CHM1_11544,283,981 - 44,605,691 (-)NCBICHM1_1
T2T-CHM13v2.01541,678,124 - 42,006,910 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:14702039   PMID:15489334   PMID:16169070   PMID:16344560   PMID:18029348   PMID:20686565   PMID:21873635   PMID:22846708   PMID:23022100   PMID:24097068   PMID:24366813  
PMID:25448675   PMID:26186194   PMID:26760575   PMID:28117551   PMID:28332615   PMID:28514442   PMID:30583072   PMID:33961781   PMID:34201607   PMID:35696571   PMID:36206744   PMID:36215168  


Genomics

Comparative Map Data
FRMD5
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381543,870,764 - 44,199,473 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1543,870,761 - 44,195,271 (-)EnsemblGRCh38hg38GRCh38
GRCh371544,162,962 - 44,487,469 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361541,953,022 - 42,274,721 (-)NCBINCBI36Build 36hg18NCBI36
Celera1521,055,188 - 21,376,921 (-)NCBICelera
Cytogenetic Map15q15.3NCBI
HuRef1520,988,457 - 21,310,775 (-)NCBIHuRef
CHM1_11544,283,981 - 44,605,691 (-)NCBICHM1_1
T2T-CHM13v2.01541,678,124 - 42,006,910 (-)NCBIT2T-CHM13v2.0
Frmd5
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392121,376,010 - 121,637,580 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2121,376,010 - 121,637,568 (-)EnsemblGRCm39 Ensembl
GRCm382121,545,529 - 121,807,087 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2121,545,529 - 121,807,087 (-)EnsemblGRCm38mm10GRCm38
MGSCv372121,371,265 - 121,632,793 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362121,236,970 - 121,498,455 (-)NCBIMGSCv36mm8
Celera2122,692,965 - 122,957,219 (-)NCBICelera
Cytogenetic Map2E5NCBI
cM Map260.42NCBI
Frmd5
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83128,945,812 - 129,217,134 (-)NCBIGRCr8
mRatBN7.23108,492,099 - 108,763,715 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3108,474,562 - 108,763,498 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.03113,480,780 - 113,755,286 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3113,483,269 - 113,525,864 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03120,021,152 - 120,295,167 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43108,323,041 - 108,591,163 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera3107,393,126 - 107,664,345 (-)NCBICelera
Cytogenetic Map3q35NCBI
Frmd5
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541610,338,061 - 10,682,810 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541610,338,061 - 10,683,069 (-)NCBIChiLan1.0ChiLan1.0
FRMD5
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21633,122,498 - 33,539,936 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11537,284,225 - 37,614,938 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01522,830,850 - 23,161,693 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11540,920,868 - 41,251,759 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1540,919,053 - 41,250,981 (-)Ensemblpanpan1.1panPan2
FRMD5
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13010,611,986 - 10,923,444 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3010,614,406 - 10,923,261 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3010,670,228 - 10,980,961 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03010,748,561 - 11,060,094 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3010,748,564 - 11,060,055 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13010,657,550 - 10,967,594 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03010,779,973 - 11,091,358 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03010,899,408 - 11,210,322 (-)NCBIUU_Cfam_GSD_1.0
Frmd5
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864089,077,981 - 89,385,165 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364716,928,398 - 7,232,765 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364716,926,044 - 7,233,006 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FRMD5
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1127,317,701 - 127,650,665 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11127,317,660 - 127,653,112 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21142,444,648 - 142,478,602 (+)NCBISscrofa10.2Sscrofa10.2susScr3
FRMD5
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12638,847,310 - 39,179,487 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2639,119,525 - 39,170,954 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666048101,819,536 - 102,191,869 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Frmd5
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462480410,906,958 - 11,239,995 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462480410,906,085 - 11,240,249 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in FRMD5
41 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001286490.1(FRMD5):c.-238+10530A>C single nucleotide variant Lung cancer [RCV000099494] Chr15:44183697 [GRCh38]
Chr15:44475895 [GRCh37]
Chr15:15q15.3		 uncertain significance
GRCh38/hg38 15q15.3-21.1(chr15:43696563-44541320)x1 copy number loss See cases [RCV000143109] Chr15:43696563..44541320 [GRCh38]
Chr15:43988761..44833518 [GRCh37]
Chr15:41776053..42620810 [NCBI36]
Chr15:15q15.3-21.1		 uncertain significance
GRCh37/hg19 15q15.3-21.1(chr15:44484701-47475522)x1 copy number loss See cases [RCV000240380] Chr15:44484701..47475522 [GRCh37]
Chr15:15q15.3-21.1		 uncertain significance
NM_032892.5(FRMD5):c.1073G>A (p.Gly358Asp) single nucleotide variant Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV003314406] Chr15:43883765 [GRCh38]
Chr15:44175963 [GRCh37]
Chr15:15q15.3		 uncertain significance
GRCh37/hg19 15q15.1-26.3(chr15:41745084-102354798)x4 copy number gain See cases [RCV000447123] Chr15:41745084..102354798 [GRCh37]
Chr15:15q15.1-26.3		 pathogenic
GRCh37/hg19 15q15.2-21.2(chr15:42850434-49592633)x1 copy number loss See cases [RCV000447035] Chr15:42850434..49592633 [GRCh37]
Chr15:15q15.2-21.2		 pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4 copy number gain See cases [RCV000447765] Chr15:20733395..102511616 [GRCh37]
Chr15:15q11.2-26.3		 pathogenic
GRCh37/hg19 15q15.1-21.2(chr15:41689327-52446981)x1 copy number loss See cases [RCV000448968] Chr15:41689327..52446981 [GRCh37]
Chr15:15q15.1-21.2		 pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3 copy number gain See cases [RCV000510717] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3		 pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112) copy number gain See cases [RCV000512019] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3		 pathogenic
NM_032892.5(FRMD5):c.483C>G (p.Phe161Leu) single nucleotide variant Inborn genetic diseases [RCV003253407] Chr15:43905896 [GRCh38]
Chr15:44198094 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.584T>G (p.Phe195Cys) single nucleotide variant Inborn genetic diseases [RCV003242949] Chr15:43902230 [GRCh38]
Chr15:44194428 [GRCh37]
Chr15:15q15.3		 uncertain significance
Single allele duplication not provided [RCV000677926] Chr15:31115047..102354857 [GRCh37]
Chr15:15q13.2-26.3		 pathogenic
GRCh37/hg19 15q15.3-21.3(chr15:43759773-53252240)x1 copy number loss not provided [RCV000683686] Chr15:43759773..53252240 [GRCh37]
Chr15:15q15.3-21.3		 pathogenic
GRCh37/hg19 15q15.3-21.1(chr15:44038893-44838835)x1 copy number loss not provided [RCV000751289] Chr15:44038893..44838835 [GRCh37]
Chr15:15q15.3-21.1		 uncertain significance
GRCh37/hg19 15q15.3(chr15:44391572-44673140)x3 copy number gain not provided [RCV000751295] Chr15:44391572..44673140 [GRCh37]
Chr15:15q15.3		 benign
GRCh37/hg19 15q11.1-26.3(chr15:20016811-102493540)x3 copy number gain not provided [RCV000751155] Chr15:20016811..102493540 [GRCh37]
Chr15:15q11.1-26.3		 pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20071673-102461162)x3 copy number gain not provided [RCV000751156] Chr15:20071673..102461162 [GRCh37]
Chr15:15q11.1-26.3		 pathogenic
NM_032892.5(FRMD5):c.701G>A (p.Gly234Glu) single nucleotide variant Inborn genetic diseases [RCV003244608] Chr15:43892008 [GRCh38]
Chr15:44184206 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.542C>T (p.Thr181Met) single nucleotide variant not provided [RCV000905778] Chr15:43905837 [GRCh38]
Chr15:44198035 [GRCh37]
Chr15:15q15.3		 benign
GRCh37/hg19 15q15.2-15.3(chr15:43420601-44198616)x3 copy number gain not provided [RCV001006684] Chr15:43420601..44198616 [GRCh37]
Chr15:15q15.2-15.3		 uncertain significance
NM_032892.5(FRMD5):c.285G>C (p.Lys95Asn) single nucleotide variant Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV003128078] Chr15:43919503 [GRCh38]
Chr15:44211701 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1304T>C (p.Val435Ala) single nucleotide variant Inborn genetic diseases [RCV003275726] Chr15:43874294 [GRCh38]
Chr15:44166492 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.615T>C (p.Tyr205=) single nucleotide variant not provided [RCV000885285] Chr15:43902199 [GRCh38]
Chr15:44194397 [GRCh37]
Chr15:15q15.3		 benign
NM_032892.5(FRMD5):c.1278T>C (p.Pro426=) single nucleotide variant not provided [RCV000886999] Chr15:43874320 [GRCh38]
Chr15:44166518 [GRCh37]
Chr15:15q15.3		 benign
NC_000015.9:g.(?_32964879)_(91358519_?)dup duplication Bloom syndrome [RCV001343104]|Familial colorectal cancer [RCV001325176] Chr15:32964879..91358519 [GRCh37]
Chr15:15q13.3-26.1		 uncertain significance
GRCh37/hg19 15q15.2-21.2(chr15:42850434-49592633) copy number loss not specified [RCV002052466] Chr15:42850434..49592633 [GRCh37]
Chr15:15q15.2-21.2		 pathogenic
GRCh37/hg19 15q15.3-21.1(chr15:44346958-44853978) copy number gain not specified [RCV002052468] Chr15:44346958..44853978 [GRCh37]
Chr15:15q15.3-21.1		 uncertain significance
GRCh37/hg19 15q15.2-15.3(chr15:43215243-44632384)x1 copy number loss not provided [RCV001829144] Chr15:43215243..44632384 [GRCh37]
Chr15:15q15.2-15.3		 uncertain significance
NM_032892.5(FRMD5):c.1054T>C (p.Cys352Arg) single nucleotide variant Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV002294528]|See cases [RCV002279917] Chr15:43883784 [GRCh38]
Chr15:44175982 [GRCh37]
Chr15:15q15.3		 pathogenic|uncertain significance
NM_032892.5(FRMD5):c.1045A>C (p.Ser349Arg) single nucleotide variant Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV002468661]|See cases [RCV002279918] Chr15:43883793 [GRCh38]
Chr15:44175991 [GRCh37]
Chr15:15q15.3		 likely pathogenic|uncertain significance
NM_032892.5(FRMD5):c.1637A>G (p.Tyr546Cys) single nucleotide variant Neurodevelopmental delay [RCV002279919]|Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV002294529] Chr15:43873961 [GRCh38]
Chr15:44166159 [GRCh37]
Chr15:15q15.3		 pathogenic|uncertain significance
NM_032892.5(FRMD5):c.1053C>G (p.Ser351Arg) single nucleotide variant Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV002294527]|See cases [RCV002279916] Chr15:43883785 [GRCh38]
Chr15:44175983 [GRCh37]
Chr15:15q15.3		 pathogenic|uncertain significance
NM_032892.5(FRMD5):c.178A>G (p.Ile60Val) single nucleotide variant not specified [RCV003230830] Chr15:43924234 [GRCh38]
Chr15:44216432 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1051A>G (p.Ser351Gly) single nucleotide variant Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV002294748] Chr15:43883787 [GRCh38]
Chr15:44175985 [GRCh37]
Chr15:15q15.3		 pathogenic
NM_032892.5(FRMD5):c.1060T>C (p.Ser354Pro) single nucleotide variant Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV002294749] Chr15:43883778 [GRCh38]
Chr15:44175976 [GRCh37]
Chr15:15q15.3		 pathogenic
NM_032892.5(FRMD5):c.1288G>A (p.Val430Met) single nucleotide variant Inborn genetic diseases [RCV002968215] Chr15:43874310 [GRCh38]
Chr15:44166508 [GRCh37]
Chr15:15q15.3		 uncertain significance
NC_000015.10:g.(?_43890333)_(43940887_?)del deletion Autosomal recessive nonsyndromic hearing loss 16 [RCV002461604] Chr15:43890333..43940887 [GRCh38]
Chr15:15q15.3		 pathogenic
GRCh37/hg19 15q15.3(chr15:44178691-44301065)x1 copy number loss not provided [RCV002472454] Chr15:44178691..44301065 [GRCh37]
Chr15:15q15.3		 uncertain significance
NC_000015.10:g.(?_43890333)_(43893072_?)del deletion Autosomal recessive nonsyndromic hearing loss 16 [RCV002444390] Chr15:43890333..43893072 [GRCh38]
Chr15:15q15.3		 pathogenic
NC_000015.10:g.(?_43890333)_(43897714_?)del deletion Autosomal recessive nonsyndromic hearing loss 16 [RCV002444389] Chr15:43890333..43897714 [GRCh38]
Chr15:15q15.3		 pathogenic
NM_032892.5(FRMD5):c.1613C>A (p.Thr538Asn) single nucleotide variant Inborn genetic diseases [RCV002818826] Chr15:43873985 [GRCh38]
Chr15:44166183 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1391C>T (p.Ala464Val) single nucleotide variant Inborn genetic diseases [RCV002749498] Chr15:43874207 [GRCh38]
Chr15:44166405 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.505G>A (p.Glu169Lys) single nucleotide variant Inborn genetic diseases [RCV002888285] Chr15:43905874 [GRCh38]
Chr15:44198072 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1080G>C (p.Arg360Ser) single nucleotide variant Inborn genetic diseases [RCV002699031] Chr15:43883758 [GRCh38]
Chr15:44175956 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1294C>T (p.Pro432Ser) single nucleotide variant Inborn genetic diseases [RCV002762988] Chr15:43874304 [GRCh38]
Chr15:44166502 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1166C>T (p.Ser389Phe) single nucleotide variant Inborn genetic diseases [RCV002709406] Chr15:43874432 [GRCh38]
Chr15:44166630 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1379A>T (p.Lys460Met) single nucleotide variant Inborn genetic diseases [RCV002809739] Chr15:43874219 [GRCh38]
Chr15:44166417 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1090G>A (p.Val364Ile) single nucleotide variant Inborn genetic diseases [RCV002746953] Chr15:43883748 [GRCh38]
Chr15:44175946 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1661G>A (p.Arg554Gln) single nucleotide variant Inborn genetic diseases [RCV002964343] Chr15:43873937 [GRCh38]
Chr15:44166135 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1052G>A (p.Ser351Asn) single nucleotide variant Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV003227553] Chr15:43883786 [GRCh38]
Chr15:44175984 [GRCh37]
Chr15:15q15.3		 likely pathogenic
NM_032892.5(FRMD5):c.1687G>C (p.Val563Leu) single nucleotide variant Inborn genetic diseases [RCV003196020] Chr15:43873911 [GRCh38]
Chr15:44166109 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.86A>G (p.Tyr29Cys) single nucleotide variant Inborn genetic diseases [RCV003210481] Chr15:44194969 [GRCh38]
Chr15:44487167 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1141G>C (p.Glu381Gln) single nucleotide variant Inborn genetic diseases [RCV003181382] Chr15:43874457 [GRCh38]
Chr15:44166655 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.1508G>A (p.Arg503His) single nucleotide variant Inborn genetic diseases [RCV003366277] Chr15:43874090 [GRCh38]
Chr15:44166288 [GRCh37]
Chr15:15q15.3		 uncertain significance
Single allele deletion not provided [RCV003448697] Chr15:41321409..51718601 [GRCh37]
Chr15:15q15.1-21.2		 pathogenic
NM_032892.5(FRMD5):c.793-18_793-9del deletion not specified [RCV003490878] Chr15:43888275..43888284 [GRCh38]
Chr15:44180473..44180482 [GRCh37]
Chr15:15q15.3		 likely benign
NM_032892.5(FRMD5):c.510_516del (p.Leu171fs) deletion not provided [RCV003542503] Chr15:43905863..43905869 [GRCh38]
Chr15:44198061..44198067 [GRCh37]
Chr15:15q15.3		 uncertain significance
GRCh37/hg19 15q11.2-21.2(chr15:22770421-50347130)x3 copy number gain not specified [RCV003987108] Chr15:22770421..50347130 [GRCh37]
Chr15:15q11.2-21.2		 pathogenic
GRCh37/hg19 15q15.3(chr15:43988438-44216507)x3 copy number gain not provided [RCV003885469] Chr15:43988438..44216507 [GRCh37]
Chr15:15q15.3		 uncertain significance
NM_032892.5(FRMD5):c.694C>G (p.Leu232Val) single nucleotide variant Neurodevelopmental disorder with eye movement abnormalities and ataxia [RCV003885423] Chr15:43892015 [GRCh38]
Chr15:44184213 [GRCh37]
Chr15:15q15.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:7385
Count of miRNA genes:1295
Interacting mature miRNAs:1658
Transcripts:ENST00000402883, ENST00000417257, ENST00000421674, ENST00000449926, ENST00000451277, ENST00000458630, ENST00000473965, ENST00000479319, ENST00000484674, ENST00000558108
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
D15S1307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,351,482 - 44,351,607UniSTSGRCh37
Build 361542,138,774 - 42,138,899RGDNCBI36
Celera1521,240,979 - 21,241,104RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,174,818 - 21,174,943UniSTS
TNG Radiation Hybrid Map1512688.0UniSTS
D15S783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,244,063 - 44,244,261UniSTSGRCh37
Build 361542,031,355 - 42,031,553RGDNCBI36
Celera1521,133,544 - 21,133,740RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,066,780 - 21,066,976UniSTS
SHGC-111270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,245,667 - 44,245,938UniSTSGRCh37
Build 361542,032,959 - 42,033,230RGDNCBI36
Celera1521,135,146 - 21,135,417RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,068,382 - 21,068,653UniSTS
TNG Radiation Hybrid Map1512649.0UniSTS
SHGC-141950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,211,553 - 44,211,824UniSTSGRCh37
Build 361541,998,845 - 41,999,116RGDNCBI36
Celera1521,101,034 - 21,101,305RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,034,270 - 21,034,541UniSTS
TNG Radiation Hybrid Map1512629.0UniSTS
SHGC-144561  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,193,563 - 44,193,888UniSTSGRCh37
Build 361541,980,855 - 41,981,180RGDNCBI36
Celera1521,083,021 - 21,083,346RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,016,290 - 21,016,615UniSTS
TNG Radiation Hybrid Map1512603.0UniSTS
ECD00002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,179,421 - 44,180,407UniSTSGRCh37
Build 361541,966,713 - 41,967,699RGDNCBI36
Celera1521,068,879 - 21,069,865RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,002,147 - 21,003,133UniSTS
ECD00013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,182,412 - 44,183,377UniSTSGRCh37
Build 361541,969,704 - 41,970,669RGDNCBI36
Celera1521,071,870 - 21,072,835RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,005,138 - 21,006,103UniSTS
ECD00067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,178,435 - 44,179,378UniSTSGRCh37
Build 361541,965,727 - 41,966,670RGDNCBI36
Celera1521,067,893 - 21,068,836RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,001,161 - 21,002,104UniSTS
ECD00337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,181,403 - 44,182,315UniSTSGRCh37
Build 361541,968,695 - 41,969,607RGDNCBI36
Celera1521,070,861 - 21,071,773RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,004,129 - 21,005,041UniSTS
ECD00354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,180,409 - 44,181,320UniSTSGRCh37
Build 361541,967,701 - 41,968,612RGDNCBI36
Celera1521,069,867 - 21,070,778RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,003,135 - 21,004,046UniSTS
ECD00631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,183,457 - 44,184,353UniSTSGRCh37
Build 361541,970,749 - 41,971,645RGDNCBI36
Celera1521,072,915 - 21,073,811RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,006,183 - 21,007,079UniSTS
ECD01454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,190,737 - 44,191,601UniSTSGRCh37
Build 361541,978,029 - 41,978,893RGDNCBI36
Celera1521,080,195 - 21,081,059RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,013,464 - 21,014,328UniSTS
ECD02610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,176,495 - 44,177,318UniSTSGRCh37
Build 361541,963,787 - 41,964,610RGDNCBI36
Celera1521,065,953 - 21,066,776RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,999,221 - 21,000,044UniSTS
ECD03001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,175,617 - 44,176,426UniSTSGRCh37
Build 361541,962,909 - 41,963,718RGDNCBI36
Celera1521,065,075 - 21,065,884RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,998,343 - 20,999,152UniSTS
ECD04065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,226,565 - 44,227,340UniSTSGRCh37
Build 361542,013,857 - 42,014,632RGDNCBI36
Celera1521,116,046 - 21,116,821RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,049,282 - 21,050,057UniSTS
ECD04356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,195,732 - 44,196,498UniSTSGRCh37
Build 361541,983,024 - 41,983,790RGDNCBI36
Celera1521,085,191 - 21,085,957RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,018,460 - 21,019,226UniSTS
ECD04630  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,219,502 - 44,220,260UniSTSGRCh37
Build 361542,006,794 - 42,007,552RGDNCBI36
Celera1521,108,983 - 21,109,741RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,042,219 - 21,042,977UniSTS
ECD04670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,220,365 - 44,221,122UniSTSGRCh37
Build 361542,007,657 - 42,008,414RGDNCBI36
Celera1521,109,846 - 21,110,603RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,043,082 - 21,043,839UniSTS
ECD05443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,228,740 - 44,229,475UniSTSGRCh37
Build 361542,016,032 - 42,016,767RGDNCBI36
Celera1521,118,221 - 21,118,956RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,051,457 - 21,052,192UniSTS
ECD05546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,211,400 - 44,212,132UniSTSGRCh37
Build 361541,998,692 - 41,999,424RGDNCBI36
Celera1521,100,881 - 21,101,613RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,034,117 - 21,034,849UniSTS
ECD05751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,225,715 - 44,226,442UniSTSGRCh37
Build 361542,013,007 - 42,013,734RGDNCBI36
Celera1521,115,196 - 21,115,923RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,048,432 - 21,049,159UniSTS
ECD05954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,221,206 - 44,221,927UniSTSGRCh37
Build 361542,008,498 - 42,009,219RGDNCBI36
Celera1521,110,687 - 21,111,408RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,043,923 - 21,044,644UniSTS
ECD06553  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,200,552 - 44,201,257UniSTSGRCh37
Build 361541,987,844 - 41,988,549RGDNCBI36
Celera1521,090,009 - 21,090,714RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,023,279 - 21,023,984UniSTS
ECD06586  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,222,050 - 44,222,754UniSTSGRCh37
Build 361542,009,342 - 42,010,046RGDNCBI36
Celera1521,111,531 - 21,112,235RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,044,767 - 21,045,471UniSTS
ECD06636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,222,819 - 44,223,522UniSTSGRCh37
Build 361542,010,111 - 42,010,814RGDNCBI36
Celera1521,112,300 - 21,113,003RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,045,536 - 21,046,239UniSTS
ECD07248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,212,202 - 44,212,888UniSTSGRCh37
Build 361541,999,494 - 42,000,180RGDNCBI36
Celera1521,101,683 - 21,102,369RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,034,919 - 21,035,605UniSTS
ECD07431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,210,678 - 44,211,359UniSTSGRCh37
Build 361541,997,970 - 41,998,651RGDNCBI36
Celera1521,100,159 - 21,100,840RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,033,395 - 21,034,076UniSTS
ECD07735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,201,993 - 44,202,666UniSTSGRCh37
Build 361541,989,285 - 41,989,958RGDNCBI36
Celera1521,091,450 - 21,092,123RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,024,710 - 21,025,383UniSTS
ECD08036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,185,387 - 44,186,052UniSTSGRCh37
Build 361541,972,679 - 41,973,344RGDNCBI36
Celera1521,074,845 - 21,075,510RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,008,113 - 21,008,778UniSTS
ECD08252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,172,965 - 44,173,624UniSTSGRCh37
Build 361541,960,257 - 41,960,916RGDNCBI36
Celera1521,062,423 - 21,063,082RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,995,691 - 20,996,350UniSTS
ECD08290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,172,266 - 44,172,924UniSTSGRCh37
Build 361541,959,558 - 41,960,216RGDNCBI36
Celera1521,061,724 - 21,062,382RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,994,992 - 20,995,650UniSTS
ECD08436  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,186,181 - 44,186,835UniSTSGRCh37
Build 361541,973,473 - 41,974,127RGDNCBI36
Celera1521,075,639 - 21,076,293RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,008,907 - 21,009,561UniSTS
ECD08552  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,171,523 - 44,172,174UniSTSGRCh37
Build 361541,958,815 - 41,959,466RGDNCBI36
Celera1521,060,981 - 21,061,632RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,994,249 - 20,994,900UniSTS
ECD09299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,205,276 - 44,205,908UniSTSGRCh37
Build 361541,992,568 - 41,993,200RGDNCBI36
Celera1521,094,733 - 21,095,365RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,027,993 - 21,028,625UniSTS
ECD09481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,213,691 - 44,214,318UniSTSGRCh37
Build 361542,000,983 - 42,001,610RGDNCBI36
Celera1521,103,172 - 21,103,799RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,036,408 - 21,037,035UniSTS
ECD09482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,227,707 - 44,228,334UniSTSGRCh37
Build 361542,014,999 - 42,015,626RGDNCBI36
Celera1521,117,188 - 21,117,815RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,050,424 - 21,051,051UniSTS
ECD09527  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,212,990 - 44,213,616UniSTSGRCh37
Build 361542,000,282 - 42,000,908RGDNCBI36
Celera1521,102,471 - 21,103,097RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,035,707 - 21,036,333UniSTS
ECD10584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,168,739 - 44,169,336UniSTSGRCh37
Build 361541,956,031 - 41,956,628RGDNCBI36
Celera1521,058,197 - 21,058,794RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,991,465 - 20,992,062UniSTS
ECD11085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,194,150 - 44,194,732UniSTSGRCh37
Build 361541,981,442 - 41,982,024RGDNCBI36
Celera1521,083,608 - 21,084,190RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,016,877 - 21,017,459UniSTS
ECD11158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,224,959 - 44,225,539UniSTSGRCh37
Build 361542,012,251 - 42,012,831RGDNCBI36
Celera1521,114,440 - 21,115,020RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,047,676 - 21,048,256UniSTS
ECD11725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,224,337 - 44,224,900UniSTSGRCh37
Build 361542,011,629 - 42,012,192RGDNCBI36
Celera1521,113,818 - 21,114,381RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,047,054 - 21,047,617UniSTS
ECD11764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,187,306 - 44,187,868UniSTSGRCh37
Build 361541,974,598 - 41,975,160RGDNCBI36
Celera1521,076,764 - 21,077,326RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,010,032 - 21,010,594UniSTS
ECD11795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,193,562 - 44,194,123UniSTSGRCh37
Build 361541,980,854 - 41,981,415RGDNCBI36
Celera1521,083,020 - 21,083,581RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,016,289 - 21,016,850UniSTS
ECD11796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,208,184 - 44,208,745UniSTSGRCh37
Build 361541,995,476 - 41,996,037RGDNCBI36
Celera1521,097,665 - 21,098,226RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,030,901 - 21,031,462UniSTS
ECD12293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,207,574 - 44,208,121UniSTSGRCh37
Build 361541,994,866 - 41,995,413RGDNCBI36
Celera1521,097,055 - 21,097,602RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,030,291 - 21,030,838UniSTS
ECD12363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,173,959 - 44,174,504UniSTSGRCh37
Build 361541,961,251 - 41,961,796RGDNCBI36
Celera1521,063,417 - 21,063,962RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,996,685 - 20,997,230UniSTS
ECD12468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,187,923 - 44,188,465UniSTSGRCh37
Build 361541,975,215 - 41,975,757RGDNCBI36
Celera1521,077,381 - 21,077,923RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,010,649 - 21,011,191UniSTS
ECD12469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,188,629 - 44,189,171UniSTSGRCh37
Build 361541,975,921 - 41,976,463RGDNCBI36
Celera1521,078,087 - 21,078,629RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,011,355 - 21,011,897UniSTS
ECD12594  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,177,702 - 44,178,241UniSTSGRCh37
Build 361541,964,994 - 41,965,533RGDNCBI36
Celera1521,067,160 - 21,067,699RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,000,428 - 21,000,967UniSTS
ECD12826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,204,391 - 44,204,924UniSTSGRCh37
Build 361541,991,683 - 41,992,216RGDNCBI36
Celera1521,093,848 - 21,094,381RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,027,108 - 21,027,641UniSTS
ECD13207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,216,297 - 44,216,820UniSTSGRCh37
Build 361542,003,589 - 42,004,112RGDNCBI36
Celera1521,105,778 - 21,106,301RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,039,014 - 21,039,537UniSTS
ECD13400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,170,573 - 44,171,091UniSTSGRCh37
Build 361541,957,865 - 41,958,383RGDNCBI36
Celera1521,060,031 - 21,060,549RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,993,299 - 20,993,817UniSTS
ECD13719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,168,087 - 44,168,597UniSTSGRCh37
Build 361541,955,379 - 41,955,889RGDNCBI36
Celera1521,057,545 - 21,058,055RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,990,813 - 20,991,323UniSTS
ECD13764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,169,357 - 44,169,866UniSTSGRCh37
Build 361541,956,649 - 41,957,158RGDNCBI36
Celera1521,058,815 - 21,059,324RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,992,083 - 20,992,592UniSTS
ECD13962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,195,077 - 44,195,581UniSTSGRCh37
Build 361541,982,369 - 41,982,873RGDNCBI36
Celera1521,084,536 - 21,085,040RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,017,805 - 21,018,309UniSTS
ECD14620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,191,814 - 44,192,303UniSTSGRCh37
Build 361541,979,106 - 41,979,595RGDNCBI36
Celera1521,081,272 - 21,081,761RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,014,541 - 21,015,030UniSTS
ECD15043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,166,304 - 44,166,783UniSTSGRCh37
Build 361541,953,596 - 41,954,075RGDNCBI36
Celera1521,055,762 - 21,056,241RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,989,031 - 20,989,510UniSTS
ECD15135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,198,163 - 44,198,640UniSTSGRCh37
Build 361541,985,455 - 41,985,932RGDNCBI36
Celera1521,087,622 - 21,088,099RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,020,891 - 21,021,368UniSTS
ECD15173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,197,676 - 44,198,152UniSTSGRCh37
Build 361541,984,968 - 41,985,444RGDNCBI36
Celera1521,087,135 - 21,087,611RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,020,404 - 21,020,880UniSTS
ECD15217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,223,629 - 44,224,104UniSTSGRCh37
Build 361542,010,921 - 42,011,396RGDNCBI36
Celera1521,113,110 - 21,113,585RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,046,346 - 21,046,821UniSTS
ECD15268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,206,044 - 44,206,518UniSTSGRCh37
Build 361541,993,336 - 41,993,810RGDNCBI36
Celera1521,095,501 - 21,095,975RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,028,761 - 21,029,235UniSTS
ECD15884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,192,322 - 44,192,781UniSTSGRCh37
Build 361541,979,614 - 41,980,073RGDNCBI36
Celera1521,081,780 - 21,082,239RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,015,049 - 21,015,508UniSTS
ECD16266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,165,836 - 44,166,283UniSTSGRCh37
Build 361541,953,128 - 41,953,575RGDNCBI36
Celera1521,055,294 - 21,055,741RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,988,563 - 20,989,010UniSTS
ECD16544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,199,130 - 44,199,565UniSTSGRCh37
Build 361541,986,422 - 41,986,857RGDNCBI36
Celera1521,088,589 - 21,089,024RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,021,858 - 21,022,293UniSTS
ECD16994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,209,900 - 44,210,316UniSTSGRCh37
Build 361541,997,192 - 41,997,608RGDNCBI36
Celera1521,099,381 - 21,099,797RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,032,617 - 21,033,033UniSTS
ECD17168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,196,922 - 44,197,332UniSTSGRCh37
Build 361541,984,214 - 41,984,624RGDNCBI36
Celera1521,086,381 - 21,086,791RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,019,650 - 21,020,060UniSTS
ECD17924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,230,681 - 44,231,060UniSTSGRCh37
Build 361542,017,973 - 42,018,352RGDNCBI36
Celera1521,120,162 - 21,120,541RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,053,398 - 21,053,777UniSTS
ECD19442  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,203,872 - 44,204,193UniSTSGRCh37
Build 361541,991,164 - 41,991,485RGDNCBI36
Celera1521,093,329 - 21,093,650RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,026,589 - 21,026,910UniSTS
ECD19802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,231,430 - 44,231,738UniSTSGRCh37
Build 361542,018,722 - 42,019,030RGDNCBI36
Celera1521,120,911 - 21,121,219RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,054,147 - 21,054,455UniSTS
ECD20742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,209,296 - 44,209,569UniSTSGRCh37
Build 361541,996,588 - 41,996,861RGDNCBI36
Celera1521,098,777 - 21,099,050RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,032,013 - 21,032,286UniSTS
ECD20998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,218,629 - 44,218,893UniSTSGRCh37
Build 361542,005,921 - 42,006,185RGDNCBI36
Celera1521,108,110 - 21,108,374RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,041,346 - 21,041,610UniSTS
ECD21151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,214,606 - 44,214,865UniSTSGRCh37
Build 361542,001,898 - 42,002,157RGDNCBI36
Celera1521,104,087 - 21,104,346RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,037,323 - 21,037,582UniSTS
ECD21612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,215,872 - 44,216,116UniSTSGRCh37
Build 361542,003,164 - 42,003,408RGDNCBI36
Celera1521,105,353 - 21,105,597RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,038,589 - 21,038,833UniSTS
ECD23058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,189,714 - 44,189,913UniSTSGRCh37
Build 361541,977,006 - 41,977,205RGDNCBI36
Celera1521,079,172 - 21,079,371RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,012,441 - 21,012,640UniSTS
ECD23273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,218,343 - 44,218,536UniSTSGRCh37
Build 361542,005,635 - 42,005,828RGDNCBI36
Celera1521,107,824 - 21,108,017RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,041,060 - 21,041,253UniSTS
ECD23491  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,203,168 - 44,203,355UniSTSGRCh37
Build 361541,990,460 - 41,990,647RGDNCBI36
Celera1521,092,625 - 21,092,812RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,025,885 - 21,026,072UniSTS
ECD23544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,189,218 - 44,189,403UniSTSGRCh37
Build 361541,976,510 - 41,976,695RGDNCBI36
Celera1521,078,676 - 21,078,861RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,011,944 - 21,012,129UniSTS
ECD23631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,215,195 - 44,215,377UniSTSGRCh37
Build 361542,002,487 - 42,002,669RGDNCBI36
Celera1521,104,676 - 21,104,858RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,037,912 - 21,038,094UniSTS
REN37997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,165,466 - 44,165,714UniSTSGRCh37
Build 361541,952,758 - 41,953,006RGDNCBI36
Celera1521,054,924 - 21,055,172RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,988,193 - 20,988,441UniSTS
REN37998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,165,686 - 44,165,931UniSTSGRCh37
Build 361541,952,978 - 41,953,223RGDNCBI36
Celera1521,055,144 - 21,055,389RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,988,413 - 20,988,658UniSTS
REN37999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,165,906 - 44,166,163UniSTSGRCh37
Build 361541,953,198 - 41,953,455RGDNCBI36
Celera1521,055,364 - 21,055,621RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,988,633 - 20,988,890UniSTS
REN38000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,166,155 - 44,166,403UniSTSGRCh37
Build 361541,953,447 - 41,953,695RGDNCBI36
Celera1521,055,613 - 21,055,861RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,988,882 - 20,989,130UniSTS
REN38001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,166,402 - 44,166,628UniSTSGRCh37
Build 361541,953,694 - 41,953,920RGDNCBI36
Celera1521,055,860 - 21,056,086RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,989,129 - 20,989,355UniSTS
REN38002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,166,609 - 44,166,856UniSTSGRCh37
Build 361541,953,901 - 41,954,148RGDNCBI36
Celera1521,056,067 - 21,056,314RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,989,336 - 20,989,583UniSTS
REN38003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,166,823 - 44,167,076UniSTSGRCh37
Build 361541,954,115 - 41,954,368RGDNCBI36
Celera1521,056,281 - 21,056,534RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,989,550 - 20,989,803UniSTS
REN38004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,167,401 - 44,167,626UniSTSGRCh37
Build 361541,954,693 - 41,954,918RGDNCBI36
Celera1521,056,859 - 21,057,084RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,990,128 - 20,990,353UniSTS
REN38005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,167,430 - 44,167,693UniSTSGRCh37
Build 361541,954,722 - 41,954,985RGDNCBI36
Celera1521,056,888 - 21,057,151RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,990,157 - 20,990,420UniSTS
REN38006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,167,770 - 44,167,995UniSTSGRCh37
Build 361541,955,062 - 41,955,287RGDNCBI36
Celera1521,057,228 - 21,057,453RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,990,497 - 20,990,722UniSTS
REN38007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,167,974 - 44,168,246UniSTSGRCh37
Build 361541,955,266 - 41,955,538RGDNCBI36
Celera1521,057,432 - 21,057,704RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,990,701 - 20,990,972UniSTS
REN38008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,168,237 - 44,168,469UniSTSGRCh37
Build 361541,955,529 - 41,955,761RGDNCBI36
Celera1521,057,695 - 21,057,927RGD
Cytogenetic MapXq13UniSTS
Cytogenetic Map15q15.3UniSTS
HuRef1520,990,963 - 20,991,195UniSTS
REN38009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,168,442 - 44,168,688UniSTSGRCh37
Build 361541,955,734 - 41,955,980RGDNCBI36
Celera1521,057,900 - 21,058,146RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,991,168 - 20,991,414UniSTS
REN38010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,168,685 - 44,168,943UniSTSGRCh37
Build 361541,955,977 - 41,956,235RGDNCBI36
Celera1521,058,143 - 21,058,401RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,991,411 - 20,991,669UniSTS
REN38011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,168,911 - 44,169,175UniSTSGRCh37
Build 361541,956,203 - 41,956,467RGDNCBI36
Celera1521,058,369 - 21,058,633RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,991,637 - 20,991,901UniSTS
REN38012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,169,142 - 44,169,400UniSTSGRCh37
Build 361541,956,434 - 41,956,692RGDNCBI36
Celera1521,058,600 - 21,058,858RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,991,868 - 20,992,126UniSTS
REN38013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,169,360 - 44,169,619UniSTSGRCh37
Build 361541,956,652 - 41,956,911RGDNCBI36
Celera1521,058,818 - 21,059,077RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,992,086 - 20,992,345UniSTS
REN38014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,169,608 - 44,169,863UniSTSGRCh37
Build 361541,956,900 - 41,957,155RGDNCBI36
Celera1521,059,066 - 21,059,321RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,992,334 - 20,992,589UniSTS
REN38015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,169,854 - 44,170,086UniSTSGRCh37
Build 361541,957,146 - 41,957,378RGDNCBI36
Celera1521,059,312 - 21,059,544RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,992,580 - 20,992,812UniSTS
REN38016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,170,000 - 44,170,251UniSTSGRCh37
Build 361541,957,292 - 41,957,543RGDNCBI36
Celera1521,059,458 - 21,059,709RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,992,726 - 20,992,977UniSTS
REN38017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,170,220 - 44,170,462UniSTSGRCh37
Build 361541,957,512 - 41,957,754RGDNCBI36
Celera1521,059,678 - 21,059,920RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,992,946 - 20,993,188UniSTS
REN38018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,170,488 - 44,170,718UniSTSGRCh37
Build 361541,957,780 - 41,958,010RGDNCBI36
Celera1521,059,946 - 21,060,176RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,993,214 - 20,993,444UniSTS
REN38019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,170,695 - 44,170,945UniSTSGRCh37
Build 361541,957,987 - 41,958,237RGDNCBI36
Celera1521,060,153 - 21,060,403RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,993,421 - 20,993,671UniSTS
REN38020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,170,918 - 44,171,176UniSTSGRCh37
Build 361541,958,210 - 41,958,468RGDNCBI36
Celera1521,060,376 - 21,060,634RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,993,644 - 20,993,902UniSTS
REN38021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,170,959 - 44,171,183UniSTSGRCh37
Build 361541,958,251 - 41,958,475RGDNCBI36
Celera1521,060,417 - 21,060,641RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,993,685 - 20,993,909UniSTS
REN38022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,171,414 - 44,171,639UniSTSGRCh37
Build 361541,958,706 - 41,958,931RGDNCBI36
Celera1521,060,872 - 21,061,097RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,994,140 - 20,994,365UniSTS
REN38023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,171,616 - 44,171,871UniSTSGRCh37
Build 361541,958,908 - 41,959,163RGDNCBI36
Celera1521,061,074 - 21,061,329RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,994,342 - 20,994,597UniSTS
REN38024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,171,830 - 44,172,083UniSTSGRCh37
Build 361541,959,122 - 41,959,375RGDNCBI36
Celera1521,061,288 - 21,061,541RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,994,556 - 20,994,809UniSTS
REN38025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,172,058 - 44,172,314UniSTSGRCh37
Build 361541,959,350 - 41,959,606RGDNCBI36
Celera1521,061,516 - 21,061,772RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,994,784 - 20,995,040UniSTS
REN38026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,172,309 - 44,172,535UniSTSGRCh37
Build 361541,959,601 - 41,959,827RGDNCBI36
Celera1521,061,767 - 21,061,993RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,995,035 - 20,995,261UniSTS
REN38027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,172,521 - 44,172,777UniSTSGRCh37
Build 361541,959,813 - 41,960,069RGDNCBI36
Celera1521,061,979 - 21,062,235RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,995,247 - 20,995,503UniSTS
REN38028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,172,768 - 44,173,025UniSTSGRCh37
Build 361541,960,060 - 41,960,317RGDNCBI36
Celera1521,062,226 - 21,062,483RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,995,494 - 20,995,751UniSTS
REN38029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,172,963 - 44,173,224UniSTSGRCh37
Build 361541,960,255 - 41,960,516RGDNCBI36
Celera1521,062,421 - 21,062,682RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,995,689 - 20,995,950UniSTS
REN38030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,173,201 - 44,173,447UniSTSGRCh37
Build 361541,960,493 - 41,960,739RGDNCBI36
Celera1521,062,659 - 21,062,905RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,995,927 - 20,996,173UniSTS
REN38031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,173,429 - 44,173,667UniSTSGRCh37
Build 361541,960,721 - 41,960,959RGDNCBI36
Celera1521,062,887 - 21,063,125RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,996,155 - 20,996,393UniSTS
REN38032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,173,664 - 44,173,888UniSTSGRCh37
Build 361541,960,956 - 41,961,180RGDNCBI36
Celera1521,063,122 - 21,063,346RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,996,390 - 20,996,614UniSTS
REN38033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,173,864 - 44,174,118UniSTSGRCh37
Build 361541,961,156 - 41,961,410RGDNCBI36
Celera1521,063,322 - 21,063,576RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,996,590 - 20,996,844UniSTS
REN38034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,174,103 - 44,174,354UniSTSGRCh37
Build 361541,961,395 - 41,961,646RGDNCBI36
Celera1521,063,561 - 21,063,812RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,996,829 - 20,997,080UniSTS
REN38035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,174,331 - 44,174,558UniSTSGRCh37
Build 361541,961,623 - 41,961,850RGDNCBI36
Celera1521,063,789 - 21,064,016RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,997,057 - 20,997,284UniSTS
REN38036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,174,932 - 44,175,160UniSTSGRCh37
Build 361541,962,224 - 41,962,452RGDNCBI36
Celera1521,064,390 - 21,064,618RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,997,658 - 20,997,886UniSTS
REN38037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,174,979 - 44,175,246UniSTSGRCh37
Build 361541,962,271 - 41,962,538RGDNCBI36
Celera1521,064,437 - 21,064,704RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,997,705 - 20,997,972UniSTS
REN38038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,175,226 - 44,175,454UniSTSGRCh37
Build 361541,962,518 - 41,962,746RGDNCBI36
Celera1521,064,684 - 21,064,912RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,997,952 - 20,998,180UniSTS
REN38039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,175,595 - 44,175,836UniSTSGRCh37
Build 361541,962,887 - 41,963,128RGDNCBI36
Celera1521,065,053 - 21,065,294RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,998,321 - 20,998,562UniSTS
REN38040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,175,822 - 44,176,068UniSTSGRCh37
Build 361541,963,114 - 41,963,360RGDNCBI36
Celera1521,065,280 - 21,065,526RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,998,548 - 20,998,794UniSTS
REN38041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,176,045 - 44,176,302UniSTSGRCh37
Build 361541,963,337 - 41,963,594RGDNCBI36
Celera1521,065,503 - 21,065,760RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,998,771 - 20,999,028UniSTS
REN38042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,176,275 - 44,176,523UniSTSGRCh37
Build 361541,963,567 - 41,963,815RGDNCBI36
Celera1521,065,733 - 21,065,981RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,999,001 - 20,999,249UniSTS
REN38043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,176,494 - 44,176,722UniSTSGRCh37
Build 361541,963,786 - 41,964,014RGDNCBI36
Celera1521,065,952 - 21,066,180RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,999,220 - 20,999,448UniSTS
REN38044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,176,693 - 44,176,943UniSTSGRCh37
Build 361541,963,985 - 41,964,235RGDNCBI36
Celera1521,066,151 - 21,066,401RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,999,419 - 20,999,669UniSTS
REN38045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,176,913 - 44,177,166UniSTSGRCh37
Build 361541,964,205 - 41,964,458RGDNCBI36
Celera1521,066,371 - 21,066,624RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,999,639 - 20,999,892UniSTS
REN38046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,177,147 - 44,177,401UniSTSGRCh37
Build 361541,964,439 - 41,964,693RGDNCBI36
Celera1521,066,605 - 21,066,859RGD
Cytogenetic Map15q15.3UniSTS
HuRef1520,999,873 - 21,000,127UniSTS
REN38047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,177,667 - 44,177,893UniSTSGRCh37
Build 361541,964,959 - 41,965,185RGDNCBI36
Celera1521,067,125 - 21,067,351RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,000,393 - 21,000,619UniSTS
REN38048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,177,888 - 44,178,134UniSTSGRCh37
Build 361541,965,180 - 41,965,426RGDNCBI36
Celera1521,067,346 - 21,067,592RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,000,614 - 21,000,860UniSTS
REN38049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,178,119 - 44,178,354UniSTSGRCh37
Build 361541,965,411 - 41,965,646RGDNCBI36
Celera1521,067,577 - 21,067,812RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,000,845 - 21,001,080UniSTS
REN38050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,178,333 - 44,178,592UniSTSGRCh37
Build 361541,965,625 - 41,965,884RGDNCBI36
Celera1521,067,791 - 21,068,050RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,001,059 - 21,001,318UniSTS
REN38051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,178,580 - 44,178,832UniSTSGRCh37
Build 361541,965,872 - 41,966,124RGDNCBI36
Celera1521,068,038 - 21,068,290RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,001,306 - 21,001,558UniSTS
REN38052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,178,824 - 44,179,067UniSTSGRCh37
Build 361541,966,116 - 41,966,359RGDNCBI36
Celera1521,068,282 - 21,068,525RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,001,550 - 21,001,793UniSTS
REN38053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,179,036 - 44,179,276UniSTSGRCh37
Build 361541,966,328 - 41,966,568RGDNCBI36
Celera1521,068,494 - 21,068,734RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,001,762 - 21,002,002UniSTS
REN38054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,179,253 - 44,179,481UniSTSGRCh37
Build 361541,966,545 - 41,966,773RGDNCBI36
Celera1521,068,711 - 21,068,939RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,001,979 - 21,002,207UniSTS
REN38055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,179,460 - 44,179,690UniSTSGRCh37
Build 361541,966,752 - 41,966,982RGDNCBI36
Celera1521,068,918 - 21,069,148RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,002,186 - 21,002,416UniSTS
REN38056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,179,661 - 44,179,911UniSTSGRCh37
Build 361541,966,953 - 41,967,203RGDNCBI36
Celera1521,069,119 - 21,069,369RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,002,387 - 21,002,637UniSTS
REN38057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,179,904 - 44,180,167UniSTSGRCh37
Build 361541,967,196 - 41,967,459RGDNCBI36
Celera1521,069,362 - 21,069,625RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,002,630 - 21,002,893UniSTS
REN38058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,180,154 - 44,180,405UniSTSGRCh37
Build 361541,967,446 - 41,967,697RGDNCBI36
Celera1521,069,612 - 21,069,863RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,002,880 - 21,003,131UniSTS
REN38059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,180,394 - 44,180,639UniSTSGRCh37
Build 361541,967,686 - 41,967,931RGDNCBI36
Celera1521,069,852 - 21,070,097RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,003,120 - 21,003,365UniSTS
REN38060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,180,605 - 44,180,831UniSTSGRCh37
Build 361541,967,897 - 41,968,123RGDNCBI36
Celera1521,070,063 - 21,070,289RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,003,331 - 21,003,557UniSTS
REN38061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,180,810 - 44,181,060UniSTSGRCh37
Build 361541,968,102 - 41,968,352RGDNCBI36
Celera1521,070,268 - 21,070,518RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,003,536 - 21,003,786UniSTS
REN38062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,181,059 - 44,181,308UniSTSGRCh37
Build 361541,968,351 - 41,968,600RGDNCBI36
Celera1521,070,517 - 21,070,766RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,003,785 - 21,004,034UniSTS
REN38063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,181,285 - 44,181,536UniSTSGRCh37
Build 361541,968,577 - 41,968,828RGDNCBI36
Celera1521,070,743 - 21,070,994RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,004,011 - 21,004,262UniSTS
REN38064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,181,511 - 44,181,758UniSTSGRCh37
Build 361541,968,803 - 41,969,050RGDNCBI36
Celera1521,070,969 - 21,071,216RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,004,237 - 21,004,484UniSTS
REN38065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,181,737 - 44,181,968UniSTSGRCh37
Build 361541,969,029 - 41,969,260RGDNCBI36
Celera1521,071,195 - 21,071,426RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,004,463 - 21,004,694UniSTS
REN38066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,181,966 - 44,182,210UniSTSGRCh37
Build 361541,969,258 - 41,969,502RGDNCBI36
Celera1521,071,424 - 21,071,668RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,004,692 - 21,004,936UniSTS
REN38067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,182,194 - 44,182,435UniSTSGRCh37
Build 361541,969,486 - 41,969,727RGDNCBI36
Celera1521,071,652 - 21,071,893RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,004,920 - 21,005,161UniSTS
REN38068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,182,412 - 44,182,661UniSTSGRCh37
Build 361541,969,704 - 41,969,953RGDNCBI36
Celera1521,071,870 - 21,072,119RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,005,138 - 21,005,387UniSTS
REN38069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,182,640 - 44,182,905UniSTSGRCh37
Build 361541,969,932 - 41,970,197RGDNCBI36
Celera1521,072,098 - 21,072,363RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,005,366 - 21,005,631UniSTS
REN38070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,182,894 - 44,183,143UniSTSGRCh37
Build 361541,970,186 - 41,970,435RGDNCBI36
Celera1521,072,352 - 21,072,601RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,005,620 - 21,005,869UniSTS
REN38071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,183,113 - 44,183,337UniSTSGRCh37
Build 361541,970,405 - 41,970,629RGDNCBI36
Celera1521,072,571 - 21,072,795RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,005,839 - 21,006,063UniSTS
REN38072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,183,309 - 44,183,556UniSTSGRCh37
Build 361541,970,601 - 41,970,848RGDNCBI36
Celera1521,072,767 - 21,073,014RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,006,035 - 21,006,282UniSTS
REN38073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,183,534 - 44,183,794UniSTSGRCh37
Build 361541,970,826 - 41,971,086RGDNCBI36
Celera1521,072,992 - 21,073,252RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,006,260 - 21,006,520UniSTS
REN38074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,183,788 - 44,184,028UniSTSGRCh37
Build 361541,971,080 - 41,971,320RGDNCBI36
Celera1521,073,246 - 21,073,486RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,006,514 - 21,006,754UniSTS
REN38075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,184,023 - 44,184,248UniSTSGRCh37
Build 361541,971,315 - 41,971,540RGDNCBI36
Celera1521,073,481 - 21,073,706RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,006,749 - 21,006,974UniSTS
REN38076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,184,215 - 44,184,439UniSTSGRCh37
Build 361541,971,507 - 41,971,731RGDNCBI36
Celera1521,073,673 - 21,073,897RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,006,941 - 21,007,165UniSTS
REN38077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,184,387 - 44,184,615UniSTSGRCh37
Build 361541,971,679 - 41,971,907RGDNCBI36
Celera1521,073,845 - 21,074,073RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,007,113 - 21,007,341UniSTS
REN38078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,184,589 - 44,184,825UniSTSGRCh37
Build 361541,971,881 - 41,972,117RGDNCBI36
Celera1521,074,047 - 21,074,283RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,007,315 - 21,007,551UniSTS
REN38079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,184,771 - 44,185,025UniSTSGRCh37
Build 361541,972,063 - 41,972,317RGDNCBI36
Celera1521,074,229 - 21,074,483RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,007,497 - 21,007,751UniSTS
REN38080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,185,391 - 44,185,628UniSTSGRCh37
Build 361541,972,683 - 41,972,920RGDNCBI36
Celera1521,074,849 - 21,075,086RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,008,117 - 21,008,354UniSTS
REN38081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,185,614 - 44,185,866UniSTSGRCh37
Build 361541,972,906 - 41,973,158RGDNCBI36
Celera1521,075,072 - 21,075,324RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,008,340 - 21,008,592UniSTS
REN38082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,185,856 - 44,186,113UniSTSGRCh37
Build 361541,973,148 - 41,973,405RGDNCBI36
Celera1521,075,314 - 21,075,571RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,008,582 - 21,008,839UniSTS
REN38083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,186,107 - 44,186,364UniSTSGRCh37
Build 361541,973,399 - 41,973,656RGDNCBI36
Celera1521,075,565 - 21,075,822RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,008,833 - 21,009,090UniSTS
REN38084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,186,346 - 44,186,588UniSTSGRCh37
Build 361541,973,638 - 41,973,880RGDNCBI36
Celera1521,075,804 - 21,076,046RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,009,072 - 21,009,314UniSTS
REN38085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,186,564 - 44,186,789UniSTSGRCh37
Build 361541,973,856 - 41,974,081RGDNCBI36
Celera1521,076,022 - 21,076,247RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,009,290 - 21,009,515UniSTS
REN38086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,186,775 - 44,187,023UniSTSGRCh37
Build 361541,974,067 - 41,974,315RGDNCBI36
Celera1521,076,233 - 21,076,481RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,009,501 - 21,009,749UniSTS
REN38087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,186,918 - 44,187,153UniSTSGRCh37
Build 361541,974,210 - 41,974,445RGDNCBI36
Celera1521,076,376 - 21,076,611RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,009,644 - 21,009,879UniSTS
REN38088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,187,181 - 44,187,428UniSTSGRCh37
Build 361541,974,473 - 41,974,720RGDNCBI36
Celera1521,076,639 - 21,076,886RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,009,907 - 21,010,154UniSTS
REN38089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,187,413 - 44,187,669UniSTSGRCh37
Build 361541,974,705 - 41,974,961RGDNCBI36
Celera1521,076,871 - 21,077,127RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,010,139 - 21,010,395UniSTS
REN38090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,187,666 - 44,187,912UniSTSGRCh37
Build 361541,974,958 - 41,975,204RGDNCBI36
Celera1521,077,124 - 21,077,370RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,010,392 - 21,010,638UniSTS
REN38091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,187,891 - 44,188,142UniSTSGRCh37
Build 361541,975,183 - 41,975,434RGDNCBI36
Celera1521,077,349 - 21,077,600RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,010,617 - 21,010,868UniSTS
REN38092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,188,120 - 44,188,357UniSTSGRCh37
Build 361541,975,412 - 41,975,649RGDNCBI36
Celera1521,077,578 - 21,077,815RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,010,846 - 21,011,083UniSTS
REN38093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,188,350 - 44,188,594UniSTSGRCh37
Build 361541,975,642 - 41,975,886RGDNCBI36
Celera1521,077,808 - 21,078,052RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,011,076 - 21,011,320UniSTS
REN38094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,188,586 - 44,188,850UniSTSGRCh37
Build 361541,975,878 - 41,976,142RGDNCBI36
Celera1521,078,044 - 21,078,308RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,011,312 - 21,011,576UniSTS
REN38095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,188,816 - 44,189,065UniSTSGRCh37
Build 361541,976,108 - 41,976,357RGDNCBI36
Celera1521,078,274 - 21,078,523RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,011,542 - 21,011,791UniSTS
REN38096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,189,045 - 44,189,299UniSTSGRCh37
Build 361541,976,337 - 41,976,591RGDNCBI36
Celera1521,078,503 - 21,078,757RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,011,771 - 21,012,025UniSTS
REN38097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,189,150 - 44,189,402UniSTSGRCh37
Build 361541,976,442 - 41,976,694RGDNCBI36
Celera1521,078,608 - 21,078,860RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,011,876 - 21,012,128UniSTS
REN38098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,189,710 - 44,189,952UniSTSGRCh37
Build 361541,977,002 - 41,977,244RGDNCBI36
Celera1521,079,168 - 21,079,410RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,012,437 - 21,012,679UniSTS
REN38099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,189,886 - 44,190,112UniSTSGRCh37
Build 361541,977,178 - 41,977,404RGDNCBI36
Celera1521,079,344 - 21,079,570RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,012,613 - 21,012,839UniSTS
REN38100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,190,087 - 44,190,341UniSTSGRCh37
Build 361541,977,379 - 41,977,633RGDNCBI36
Celera1521,079,545 - 21,079,799RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,012,814 - 21,013,068UniSTS
REN38101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,190,334 - 44,190,567UniSTSGRCh37
Build 361541,977,626 - 41,977,859RGDNCBI36
Celera1521,079,792 - 21,080,025RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,013,061 - 21,013,294UniSTS
REN38102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,190,558 - 44,190,805UniSTSGRCh37
Build 361541,977,850 - 41,978,097RGDNCBI36
Celera1521,080,016 - 21,080,263RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,013,285 - 21,013,532UniSTS
REN38103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,190,783 - 44,191,043UniSTSGRCh37
Build 361541,978,075 - 41,978,335RGDNCBI36
Celera1521,080,241 - 21,080,501RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,013,510 - 21,013,770UniSTS
REN38104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,191,021 - 44,191,258UniSTSGRCh37
Build 361541,978,313 - 41,978,550RGDNCBI36
Celera1521,080,479 - 21,080,716RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,013,748 - 21,013,985UniSTS
REN38105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,191,234 - 44,191,460UniSTSGRCh37
Build 361541,978,526 - 41,978,752RGDNCBI36
Celera1521,080,692 - 21,080,918RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,013,961 - 21,014,187UniSTS
REN38106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,191,427 - 44,191,679UniSTSGRCh37
Build 361541,978,719 - 41,978,971RGDNCBI36
Celera1521,080,885 - 21,081,137RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,014,154 - 21,014,406UniSTS
REN38107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,191,654 - 44,191,905UniSTSGRCh37
Build 361541,978,946 - 41,979,197RGDNCBI36
Celera1521,081,112 - 21,081,363RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,014,381 - 21,014,632UniSTS
REN38108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,191,888 - 44,192,135UniSTSGRCh37
Build 361541,979,180 - 41,979,427RGDNCBI36
Celera1521,081,346 - 21,081,593RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,014,615 - 21,014,862UniSTS
REN38109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,192,112 - 44,192,352UniSTSGRCh37
Build 361541,979,404 - 41,979,644RGDNCBI36
Celera1521,081,570 - 21,081,810RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,014,839 - 21,015,079UniSTS
REN38110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,192,330 - 44,192,592UniSTSGRCh37
Build 361541,979,622 - 41,979,884RGDNCBI36
Celera1521,081,788 - 21,082,050RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,015,057 - 21,015,319UniSTS
REN38111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,192,586 - 44,192,811UniSTSGRCh37
Build 361541,979,878 - 41,980,103RGDNCBI36
Celera1521,082,044 - 21,082,269RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,015,313 - 21,015,538UniSTS
REN38112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,192,676 - 44,192,921UniSTSGRCh37
Build 361541,979,968 - 41,980,213RGDNCBI36
Celera1521,082,134 - 21,082,379RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,015,403 - 21,015,648UniSTS
REN38113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,192,896 - 44,193,145UniSTSGRCh37
Build 361541,980,188 - 41,980,437RGDNCBI36
Celera1521,082,354 - 21,082,603RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,015,623 - 21,015,872UniSTS
REN38114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,193,128 - 44,193,383UniSTSGRCh37
Build 361541,980,420 - 41,980,675RGDNCBI36
Celera1521,082,586 - 21,082,841RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,015,855 - 21,016,110UniSTS
REN38115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,193,382 - 44,193,631UniSTSGRCh37
Build 361541,980,674 - 41,980,923RGDNCBI36
Celera1521,082,840 - 21,083,089RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,016,109 - 21,016,358UniSTS
REN38116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,193,613 - 44,193,866UniSTSGRCh37
Build 361541,980,905 - 41,981,158RGDNCBI36
Celera1521,083,071 - 21,083,324RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,016,340 - 21,016,593UniSTS
REN38117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,193,843 - 44,194,101UniSTSGRCh37
Build 361541,981,135 - 41,981,393RGDNCBI36
Celera1521,083,301 - 21,083,559RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,016,570 - 21,016,828UniSTS
REN38118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,194,086 - 44,194,342UniSTSGRCh37
Build 361541,981,378 - 41,981,634RGDNCBI36
Celera1521,083,544 - 21,083,800RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,016,813 - 21,017,069UniSTS
REN38119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,194,326 - 44,194,575UniSTSGRCh37
Build 361541,981,618 - 41,981,867RGDNCBI36
Celera1521,083,784 - 21,084,033RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,017,053 - 21,017,302UniSTS
REN38120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,194,547 - 44,194,773UniSTSGRCh37
Build 361541,981,839 - 41,982,065RGDNCBI36
Celera1521,084,005 - 21,084,231RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,017,274 - 21,017,500UniSTS
REN38121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,194,755 - 44,195,027UniSTSGRCh37
Build 361541,982,047 - 41,982,319RGDNCBI36
Celera1521,084,213 - 21,084,486RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,017,482 - 21,017,755UniSTS
REN38122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,195,004 - 44,195,239UniSTSGRCh37
Build 361541,982,296 - 41,982,531RGDNCBI36
Celera1521,084,463 - 21,084,698RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,017,732 - 21,017,967UniSTS
REN38123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,195,216 - 44,195,465UniSTSGRCh37
Build 361541,982,508 - 41,982,757RGDNCBI36
Celera1521,084,675 - 21,084,924RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,017,944 - 21,018,193UniSTS
REN38124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,195,441 - 44,195,701UniSTSGRCh37
Build 361541,982,733 - 41,982,993RGDNCBI36
Celera1521,084,900 - 21,085,160RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,018,169 - 21,018,429UniSTS
REN38125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,195,696 - 44,195,954UniSTSGRCh37
Build 361541,982,988 - 41,983,246RGDNCBI36
Celera1521,085,155 - 21,085,413RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,018,424 - 21,018,682UniSTS
REN38126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,195,932 - 44,196,198UniSTSGRCh37
Build 361541,983,224 - 41,983,490RGDNCBI36
Celera1521,085,391 - 21,085,657RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,018,660 - 21,018,926UniSTS
REN38127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,196,171 - 44,196,398UniSTSGRCh37
Build 361541,983,463 - 41,983,690RGDNCBI36
Celera1521,085,630 - 21,085,857RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,018,899 - 21,019,126UniSTS
REN38128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,196,375 - 44,196,641UniSTSGRCh37
Build 361541,983,667 - 41,983,933RGDNCBI36
Celera1521,085,834 - 21,086,100RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,019,103 - 21,019,369UniSTS
REN38129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,196,489 - 44,196,715UniSTSGRCh37
Build 361541,983,781 - 41,984,007RGDNCBI36
Celera1521,085,948 - 21,086,174RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,019,217 - 21,019,443UniSTS
REN38130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,196,685 - 44,196,930UniSTSGRCh37
Build 361541,983,977 - 41,984,222RGDNCBI36
Celera1521,086,144 - 21,086,389RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,019,413 - 21,019,658UniSTS
REN38131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,196,922 - 44,197,156UniSTSGRCh37
Build 361541,984,214 - 41,984,448RGDNCBI36
Celera1521,086,381 - 21,086,615RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,019,650 - 21,019,884UniSTS
REN38132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,197,109 - 44,197,337UniSTSGRCh37
Build 361541,984,401 - 41,984,629RGDNCBI36
Celera1521,086,568 - 21,086,796RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,019,837 - 21,020,065UniSTS
REN38133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,197,654 - 44,197,878UniSTSGRCh37
Build 361541,984,946 - 41,985,170RGDNCBI36
Celera1521,087,113 - 21,087,337RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,020,382 - 21,020,606UniSTS
REN38134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,197,849 - 44,198,110UniSTSGRCh37
Build 361541,985,141 - 41,985,402RGDNCBI36
Celera1521,087,308 - 21,087,569RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,020,577 - 21,020,838UniSTS
REN38135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,198,090 - 44,198,332UniSTSGRCh37
Build 361541,985,382 - 41,985,624RGDNCBI36
Celera1521,087,549 - 21,087,791RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,020,818 - 21,021,060UniSTS
REN38136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,198,315 - 44,198,545UniSTSGRCh37
Build 361541,985,607 - 41,985,837RGDNCBI36
Celera1521,087,774 - 21,088,004RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,021,043 - 21,021,273UniSTS
REN38137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,198,522 - 44,198,767UniSTSGRCh37
Build 361541,985,814 - 41,986,059RGDNCBI36
Celera1521,087,981 - 21,088,226RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,021,250 - 21,021,495UniSTS
REN38138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,198,554 - 44,198,792UniSTSGRCh37
Build 361541,985,846 - 41,986,084RGDNCBI36
Celera1521,088,013 - 21,088,251RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,021,282 - 21,021,520UniSTS
REN38139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,199,096 - 44,199,322UniSTSGRCh37
Build 361541,986,388 - 41,986,614RGDNCBI36
Celera1521,088,555 - 21,088,781RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,021,824 - 21,022,050UniSTS
REN38140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,199,318 - 44,199,554UniSTSGRCh37
Build 361541,986,610 - 41,986,846RGDNCBI36
Celera1521,088,777 - 21,089,013RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,022,046 - 21,022,282UniSTS
REN38141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,199,500 - 44,199,727UniSTSGRCh37
Build 361541,986,792 - 41,987,019RGDNCBI36
Celera1521,088,959 - 21,089,186RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,022,228 - 21,022,455UniSTS
REN38142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,199,711 - 44,199,946UniSTSGRCh37
Build 361541,987,003 - 41,987,238RGDNCBI36
Celera1521,089,170 - 21,089,405RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,022,439 - 21,022,675UniSTS
REN38143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,200,275 - 44,200,520UniSTSGRCh37
Build 361541,987,567 - 41,987,812RGDNCBI36
Celera1521,089,734 - 21,089,979RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,023,004 - 21,023,249UniSTS
REN38144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,200,499 - 44,200,750UniSTSGRCh37
Build 361541,987,791 - 41,988,042RGDNCBI36
Celera1521,089,958 - 21,090,207RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,023,228 - 21,023,477UniSTS
REN38145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,200,744 - 44,200,998UniSTSGRCh37
Build 361541,988,036 - 41,988,290RGDNCBI36
Celera1521,090,201 - 21,090,455RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,023,471 - 21,023,725UniSTS
REN38146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,200,997 - 44,201,251UniSTSGRCh37
Build 361541,988,289 - 41,988,543RGDNCBI36
Celera1521,090,454 - 21,090,708RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,023,724 - 21,023,978UniSTS
REN38147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,201,094 - 44,201,320UniSTSGRCh37
Build 361541,988,386 - 41,988,612RGDNCBI36
Celera1521,090,551 - 21,090,777RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,023,821 - 21,024,047UniSTS
REN38148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,201,563 - 44,201,800UniSTSGRCh37
Build 361541,988,855 - 41,989,092RGDNCBI36
Celera1521,091,020 - 21,091,257RGD
Cytogenetic Map15q15.3UniSTS
REN38149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,201,775 - 44,202,014UniSTSGRCh37
Build 361541,989,067 - 41,989,306RGDNCBI36
Celera1521,091,232 - 21,091,471RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,024,492 - 21,024,731UniSTS
REN38150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,201,991 - 44,202,235UniSTSGRCh37
Build 361541,989,283 - 41,989,527RGDNCBI36
Celera1521,091,448 - 21,091,692RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,024,708 - 21,024,952UniSTS
REN38151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,202,208 - 44,202,432UniSTSGRCh37
Build 361541,989,500 - 41,989,724RGDNCBI36
Celera1521,091,665 - 21,091,889RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,024,925 - 21,025,149UniSTS
REN38152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,202,428 - 44,202,670UniSTSGRCh37
Build 361541,989,720 - 41,989,962RGDNCBI36
Celera1521,091,885 - 21,092,127RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,025,145 - 21,025,387UniSTS
REN38153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,202,665 - 44,202,891UniSTSGRCh37
Build 361541,989,957 - 41,990,183RGDNCBI36
Celera1521,092,122 - 21,092,348RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,025,382 - 21,025,608UniSTS
REN38154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,202,887 - 44,203,133UniSTSGRCh37
Build 361541,990,179 - 41,990,425RGDNCBI36
Celera1521,092,344 - 21,092,590RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,025,604 - 21,025,850UniSTS
REN38155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,203,110 - 44,203,345UniSTSGRCh37
Build 361541,990,402 - 41,990,637RGDNCBI36
Celera1521,092,567 - 21,092,802RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,025,827 - 21,026,062UniSTS
REN38156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,203,308 - 44,203,544UniSTSGRCh37
Build 361541,990,600 - 41,990,836RGDNCBI36
Celera1521,092,765 - 21,093,001RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,026,025 - 21,026,261UniSTS
REN38157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,203,521 - 44,203,774UniSTSGRCh37
Build 361541,990,813 - 41,991,066RGDNCBI36
Celera1521,092,978 - 21,093,231RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,026,238 - 21,026,491UniSTS
REN38158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,203,757 - 44,203,990UniSTSGRCh37
Build 361541,991,049 - 41,991,282RGDNCBI36
Celera1521,093,214 - 21,093,447RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,026,474 - 21,026,707UniSTS
REN38159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,203,965 - 44,204,213UniSTSGRCh37
Build 361541,991,257 - 41,991,505RGDNCBI36
Celera1521,093,422 - 21,093,670RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,026,682 - 21,026,930UniSTS
REN38160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,204,194 - 44,204,453UniSTSGRCh37
Build 361541,991,486 - 41,991,745RGDNCBI36
Celera1521,093,651 - 21,093,910RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,026,911 - 21,027,170UniSTS
REN38161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,204,436 - 44,204,692UniSTSGRCh37
Build 361541,991,728 - 41,991,984RGDNCBI36
Celera1521,093,893 - 21,094,149RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,027,153 - 21,027,409UniSTS
REN38162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,204,682 - 44,204,925UniSTSGRCh37
Build 361541,991,974 - 41,992,217RGDNCBI36
Celera1521,094,139 - 21,094,382RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,027,399 - 21,027,642UniSTS
REN38163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,204,879 - 44,205,136UniSTSGRCh37
Build 361541,992,171 - 41,992,428RGDNCBI36
Celera1521,094,336 - 21,094,593RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,027,596 - 21,027,853UniSTS
REN38164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,205,112 - 44,205,360UniSTSGRCh37
Build 361541,992,404 - 41,992,652RGDNCBI36
Celera1521,094,569 - 21,094,817RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,027,829 - 21,028,077UniSTS
REN38165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,205,333 - 44,205,577UniSTSGRCh37
Build 361541,992,625 - 41,992,869RGDNCBI36
Celera1521,094,790 - 21,095,034RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,028,050 - 21,028,294UniSTS
REN38166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,205,554 - 44,205,817UniSTSGRCh37
Build 361541,992,846 - 41,993,109RGDNCBI36
Celera1521,095,011 - 21,095,274RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,028,271 - 21,028,534UniSTS
REN38167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,205,805 - 44,206,075UniSTSGRCh37
Build 361541,993,097 - 41,993,367RGDNCBI36
Celera1521,095,262 - 21,095,532RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,028,522 - 21,028,792UniSTS
REN38168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,206,052 - 44,206,299UniSTSGRCh37
Build 361541,993,344 - 41,993,591RGDNCBI36
Celera1521,095,509 - 21,095,756RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,028,769 - 21,029,016UniSTS
REN38169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,206,296 - 44,206,535UniSTSGRCh37
Build 361541,993,588 - 41,993,827RGDNCBI36
Celera1521,095,753 - 21,095,992RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,029,013 - 21,029,252UniSTS
REN38170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,206,512 - 44,206,773UniSTSGRCh37
Build 361541,993,804 - 41,994,065RGDNCBI36
Celera1521,095,969 - 21,096,230RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,029,229 - 21,029,490UniSTS
REN38171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,206,690 - 44,206,914UniSTSGRCh37
Build 361541,993,982 - 41,994,206RGDNCBI36
Celera1521,096,147 - 21,096,371RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,029,407 - 21,029,631UniSTS
REN38172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,207,220 - 44,207,455UniSTSGRCh37
Build 361541,994,512 - 41,994,747RGDNCBI36
Celera1521,096,701 - 21,096,936RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,029,937 - 21,030,172UniSTS
REN38173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,207,448 - 44,207,695UniSTSGRCh37
Build 361541,994,740 - 41,994,987RGDNCBI36
Celera1521,096,929 - 21,097,176RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,030,165 - 21,030,412UniSTS
REN38174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,207,672 - 44,207,923UniSTSGRCh37
Build 361541,994,964 - 41,995,215RGDNCBI36
Celera1521,097,153 - 21,097,404RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,030,389 - 21,030,640UniSTS
REN38175  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,207,911 - 44,208,170UniSTSGRCh37
Build 361541,995,203 - 41,995,462RGDNCBI36
Celera1521,097,392 - 21,097,651RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,030,628 - 21,030,887UniSTS
REN38176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,208,147 - 44,208,409UniSTSGRCh37
Build 361541,995,439 - 41,995,701RGDNCBI36
Celera1521,097,628 - 21,097,890RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,030,864 - 21,031,126UniSTS
REN38177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,208,385 - 44,208,615UniSTSGRCh37
Build 361541,995,677 - 41,995,907RGDNCBI36
Celera1521,097,866 - 21,098,096RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,031,102 - 21,031,332UniSTS
REN38178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,208,602 - 44,208,862UniSTSGRCh37
Build 361541,995,894 - 41,996,154RGDNCBI36
Celera1521,098,083 - 21,098,343RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,031,319 - 21,031,579UniSTS
REN38179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,208,738 - 44,208,962UniSTSGRCh37
Build 361541,996,030 - 41,996,254RGDNCBI36
Celera1521,098,219 - 21,098,443RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,031,455 - 21,031,679UniSTS
REN38180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,208,888 - 44,209,124UniSTSGRCh37
Build 361541,996,180 - 41,996,416RGDNCBI36
Celera1521,098,369 - 21,098,605RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,031,605 - 21,031,841UniSTS
REN38181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,209,101 - 44,209,325UniSTSGRCh37
Build 361541,996,393 - 41,996,617RGDNCBI36
Celera1521,098,582 - 21,098,806RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,031,818 - 21,032,042UniSTS
REN38182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,209,307 - 44,209,556UniSTSGRCh37
Build 361541,996,599 - 41,996,848RGDNCBI36
Celera1521,098,788 - 21,099,037RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,032,024 - 21,032,273UniSTS
REN38183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,209,521 - 44,209,752UniSTSGRCh37
Build 361541,996,813 - 41,997,044RGDNCBI36
Celera1521,099,002 - 21,099,233RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,032,238 - 21,032,469UniSTS
REN38184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,209,781 - 44,210,011UniSTSGRCh37
Build 361541,997,073 - 41,997,303RGDNCBI36
Celera1521,099,262 - 21,099,492RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,032,498 - 21,032,728UniSTS
REN38185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,209,989 - 44,210,235UniSTSGRCh37
Build 361541,997,281 - 41,997,527RGDNCBI36
Celera1521,099,470 - 21,099,716RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,032,706 - 21,032,952UniSTS
REN38186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,210,108 - 44,210,344UniSTSGRCh37
Build 361541,997,400 - 41,997,636RGDNCBI36
Celera1521,099,589 - 21,099,825RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,032,825 - 21,033,061UniSTS
REN38187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,210,258 - 44,210,519UniSTSGRCh37
Build 361541,997,550 - 41,997,811RGDNCBI36
Celera1521,099,739 - 21,100,000RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,032,975 - 21,033,236UniSTS
REN38188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,210,495 - 44,210,740UniSTSGRCh37
Build 361541,997,787 - 41,998,032RGDNCBI36
Celera1521,099,976 - 21,100,221RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,033,212 - 21,033,457UniSTS
REN38189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,210,722 - 44,210,971UniSTSGRCh37
Build 361541,998,014 - 41,998,263RGDNCBI36
Celera1521,100,203 - 21,100,452RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,033,439 - 21,033,688UniSTS
REN38190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,210,963 - 44,211,208UniSTSGRCh37
Build 361541,998,255 - 41,998,500RGDNCBI36
Celera1521,100,444 - 21,100,689RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,033,680 - 21,033,925UniSTS
REN38191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,211,187 - 44,211,427UniSTSGRCh37
Build 361541,998,479 - 41,998,719RGDNCBI36
Celera1521,100,668 - 21,100,908RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,033,904 - 21,034,144UniSTS
REN38192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,211,406 - 44,211,631UniSTSGRCh37
Build 361541,998,698 - 41,998,923RGDNCBI36
Celera1521,100,887 - 21,101,112RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,034,123 - 21,034,348UniSTS
REN38193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,211,602 - 44,211,836UniSTSGRCh37
Build 361541,998,894 - 41,999,128RGDNCBI36
Celera1521,101,083 - 21,101,317RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,034,319 - 21,034,553UniSTS
REN38194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,211,803 - 44,212,056UniSTSGRCh37
Build 361541,999,095 - 41,999,348RGDNCBI36
Celera1521,101,284 - 21,101,537RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,034,520 - 21,034,773UniSTS
REN38195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,212,033 - 44,212,270UniSTSGRCh37
Build 361541,999,325 - 41,999,562RGDNCBI36
Celera1521,101,514 - 21,101,751RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,034,750 - 21,034,987UniSTS
REN38196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,212,256 - 44,212,515UniSTSGRCh37
Build 361541,999,548 - 41,999,807RGDNCBI36
Celera1521,101,737 - 21,101,996RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,034,973 - 21,035,232UniSTS
REN38197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,212,497 - 44,212,734UniSTSGRCh37
Build 361541,999,789 - 42,000,026RGDNCBI36
Celera1521,101,978 - 21,102,215RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,035,214 - 21,035,451UniSTS
REN38198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,212,686 - 44,212,951UniSTSGRCh37
Build 361541,999,978 - 42,000,243RGDNCBI36
Celera1521,102,167 - 21,102,432RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,035,403 - 21,035,668UniSTS
REN38199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,212,947 - 44,213,201UniSTSGRCh37
Build 361542,000,239 - 42,000,493RGDNCBI36
Celera1521,102,428 - 21,102,682RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,035,664 - 21,035,918UniSTS
REN38200  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,213,188 - 44,213,436UniSTSGRCh37
Build 361542,000,480 - 42,000,728RGDNCBI36
Celera1521,102,669 - 21,102,917RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,035,905 - 21,036,153UniSTS
REN38201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,213,412 - 44,213,670UniSTSGRCh37
Build 361542,000,704 - 42,000,962RGDNCBI36
Celera1521,102,893 - 21,103,151RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,036,129 - 21,036,387UniSTS
REN38202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,213,662 - 44,213,909UniSTSGRCh37
Build 361542,000,954 - 42,001,201RGDNCBI36
Celera1521,103,143 - 21,103,390RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,036,379 - 21,036,626UniSTS
REN38203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,213,904 - 44,214,145UniSTSGRCh37
Build 361542,001,196 - 42,001,437RGDNCBI36
Celera1521,103,385 - 21,103,626RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,036,621 - 21,036,862UniSTS
REN38204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,214,105 - 44,214,343UniSTSGRCh37
Build 361542,001,397 - 42,001,635RGDNCBI36
Celera1521,103,586 - 21,103,824RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,036,822 - 21,037,060UniSTS
REN38205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,214,320 - 44,214,575UniSTSGRCh37
Build 361542,001,612 - 42,001,867RGDNCBI36
Celera1521,103,801 - 21,104,056RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,037,037 - 21,037,292UniSTS
REN38206  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,214,574 - 44,214,808UniSTSGRCh37
Build 361542,001,866 - 42,002,100RGDNCBI36
Celera1521,104,055 - 21,104,289RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,037,291 - 21,037,525UniSTS
REN38207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,214,640 - 44,214,867UniSTSGRCh37
Build 361542,001,932 - 42,002,159RGDNCBI36
Celera1521,104,121 - 21,104,348RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,037,357 - 21,037,584UniSTS
REN38208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,214,845 - 44,215,108UniSTSGRCh37
Build 361542,002,137 - 42,002,400RGDNCBI36
Celera1521,104,326 - 21,104,589RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,037,562 - 21,037,825UniSTS
REN38209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,214,961 - 44,215,218UniSTSGRCh37
Build 361542,002,253 - 42,002,510RGDNCBI36
Celera1521,104,442 - 21,104,699RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,037,678 - 21,037,935UniSTS
REN38210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,215,196 - 44,215,443UniSTSGRCh37
Build 361542,002,488 - 42,002,735RGDNCBI36
Celera1521,104,677 - 21,104,924RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,037,913 - 21,038,160UniSTS
REN38211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,215,424 - 44,215,673UniSTSGRCh37
Build 361542,002,716 - 42,002,965RGDNCBI36
Celera1521,104,905 - 21,105,154RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,038,141 - 21,038,390UniSTS
REN38212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,215,645 - 44,215,898UniSTSGRCh37
Build 361542,002,937 - 42,003,190RGDNCBI36
Celera1521,105,126 - 21,105,379RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,038,362 - 21,038,615UniSTS
REN38213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,215,875 - 44,216,116UniSTSGRCh37
Build 361542,003,167 - 42,003,408RGDNCBI36
Celera1521,105,356 - 21,105,597RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,038,592 - 21,038,833UniSTS
REN38214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,216,092 - 44,216,328UniSTSGRCh37
Build 361542,003,384 - 42,003,620RGDNCBI36
Celera1521,105,573 - 21,105,809RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,038,809 - 21,039,045UniSTS
REN38215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,216,304 - 44,216,553UniSTSGRCh37
Build 361542,003,596 - 42,003,845RGDNCBI36
Celera1521,105,785 - 21,106,034RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,039,021 - 21,039,270UniSTS
REN38216  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,216,537 - 44,216,796UniSTSGRCh37
Build 361542,003,829 - 42,004,088RGDNCBI36
Celera1521,106,018 - 21,106,277RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,039,254 - 21,039,513UniSTS
REN38217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,216,745 - 44,216,992UniSTSGRCh37
Build 361542,004,037 - 42,004,284RGDNCBI36
Celera1521,106,226 - 21,106,473RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,039,462 - 21,039,709UniSTS
REN38218  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,216,965 - 44,217,190UniSTSGRCh37
Build 361542,004,257 - 42,004,482RGDNCBI36
Celera1521,106,446 - 21,106,671RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,039,682 - 21,039,907UniSTS
REN38219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,217,058 - 44,217,308UniSTSGRCh37
Build 361542,004,350 - 42,004,600RGDNCBI36
Celera1521,106,539 - 21,106,789RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,039,775 - 21,040,025UniSTS
REN38220  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,217,496 - 44,217,731UniSTSGRCh37
Build 361542,004,788 - 42,005,023RGDNCBI36
Celera1521,106,977 - 21,107,212RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,040,213 - 21,040,448UniSTS
REN38221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,217,711 - 44,217,971UniSTSGRCh37
Build 361542,005,003 - 42,005,263RGDNCBI36
Celera1521,107,192 - 21,107,452RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,040,428 - 21,040,688UniSTS
REN38222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,217,949 - 44,218,210UniSTSGRCh37
Build 361542,005,241 - 42,005,502RGDNCBI36
Celera1521,107,430 - 21,107,691RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,040,666 - 21,040,927UniSTS
REN38223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,218,205 - 44,218,456UniSTSGRCh37
Build 361542,005,497 - 42,005,748RGDNCBI36
Celera1521,107,686 - 21,107,937RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,040,922 - 21,041,173UniSTS
REN38224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,218,433 - 44,218,688UniSTSGRCh37
Build 361542,005,725 - 42,005,980RGDNCBI36
Celera1521,107,914 - 21,108,169RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,041,150 - 21,041,405UniSTS
REN38225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,218,625 - 44,218,860UniSTSGRCh37
Build 361542,005,917 - 42,006,152RGDNCBI36
Celera1521,108,106 - 21,108,341RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,041,342 - 21,041,577UniSTS
REN38226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,218,837 - 44,219,071UniSTSGRCh37
Build 361542,006,129 - 42,006,363RGDNCBI36
Celera1521,108,318 - 21,108,552RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,041,554 - 21,041,788UniSTS
REN38227  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,219,055 - 44,219,305UniSTSGRCh37
Build 361542,006,347 - 42,006,597RGDNCBI36
Celera1521,108,536 - 21,108,786RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,041,772 - 21,042,022UniSTS
REN38228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,219,293 - 44,219,543UniSTSGRCh37
Build 361542,006,585 - 42,006,835RGDNCBI36
Celera1521,108,774 - 21,109,024RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,042,010 - 21,042,260UniSTS
REN38229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,219,520 - 44,219,764UniSTSGRCh37
Build 361542,006,812 - 42,007,056RGDNCBI36
Celera1521,109,001 - 21,109,245RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,042,237 - 21,042,481UniSTS
REN38230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,219,744 - 44,219,996UniSTSGRCh37
Build 361542,007,036 - 42,007,288RGDNCBI36
Celera1521,109,225 - 21,109,477RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,042,461 - 21,042,713UniSTS
REN38231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,219,982 - 44,220,230UniSTSGRCh37
Build 361542,007,274 - 42,007,522RGDNCBI36
Celera1521,109,463 - 21,109,711RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,042,699 - 21,042,947UniSTS
REN38232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,220,205 - 44,220,436UniSTSGRCh37
Build 361542,007,497 - 42,007,728RGDNCBI36
Celera1521,109,686 - 21,109,917RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,042,922 - 21,043,153UniSTS
REN38233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,220,412 - 44,220,654UniSTSGRCh37
Build 361542,007,704 - 42,007,946RGDNCBI36
Celera1521,109,893 - 21,110,135RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,043,129 - 21,043,371UniSTS
REN38234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,220,644 - 44,220,906UniSTSGRCh37
Build 361542,007,936 - 42,008,198RGDNCBI36
Celera1521,110,125 - 21,110,387RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,043,361 - 21,043,623UniSTS
REN38235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,220,886 - 44,221,146UniSTSGRCh37
Build 361542,008,178 - 42,008,438RGDNCBI36
Celera1521,110,367 - 21,110,627RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,043,603 - 21,043,863UniSTS
REN38236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,221,136 - 44,221,393UniSTSGRCh37
Build 361542,008,428 - 42,008,685RGDNCBI36
Celera1521,110,617 - 21,110,874RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,043,853 - 21,044,110UniSTS
REN38237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,221,384 - 44,221,631UniSTSGRCh37
Build 361542,008,676 - 42,008,923RGDNCBI36
Celera1521,110,865 - 21,111,112RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,044,101 - 21,044,348UniSTS
REN38238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,221,621 - 44,221,867UniSTSGRCh37
Build 361542,008,913 - 42,009,159RGDNCBI36
Celera1521,111,102 - 21,111,348RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,044,338 - 21,044,584UniSTS
REN38239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,221,837 - 44,222,071UniSTSGRCh37
Build 361542,009,129 - 42,009,363RGDNCBI36
Celera1521,111,318 - 21,111,552RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,044,554 - 21,044,788UniSTS
REN38240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,222,049 - 44,222,308UniSTSGRCh37
Build 361542,009,341 - 42,009,600RGDNCBI36
Celera1521,111,530 - 21,111,789RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,044,766 - 21,045,025UniSTS
REN38241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,222,307 - 44,222,558UniSTSGRCh37
Build 361542,009,599 - 42,009,850RGDNCBI36
Celera1521,111,788 - 21,112,039RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,045,024 - 21,045,275UniSTS
REN38242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,222,535 - 44,222,784UniSTSGRCh37
Build 361542,009,827 - 42,010,076RGDNCBI36
Celera1521,112,016 - 21,112,265RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,045,252 - 21,045,501UniSTS
REN38243  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,222,780 - 44,223,041UniSTSGRCh37
Build 361542,010,072 - 42,010,333RGDNCBI36
Celera1521,112,261 - 21,112,522RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,045,497 - 21,045,758UniSTS
REN38244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,223,018 - 44,223,244UniSTSGRCh37
Build 361542,010,310 - 42,010,536RGDNCBI36
Celera1521,112,499 - 21,112,725RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,045,735 - 21,045,961UniSTS
REN38245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,223,225 - 44,223,468UniSTSGRCh37
Build 361542,010,517 - 42,010,760RGDNCBI36
Celera1521,112,706 - 21,112,949RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,045,942 - 21,046,185UniSTS
REN38246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,223,445 - 44,223,689UniSTSGRCh37
Build 361542,010,737 - 42,010,981RGDNCBI36
Celera1521,112,926 - 21,113,170RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,046,162 - 21,046,406UniSTS
REN38247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,223,666 - 44,223,914UniSTSGRCh37
Build 361542,010,958 - 42,011,206RGDNCBI36
Celera1521,113,147 - 21,113,395RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,046,383 - 21,046,631UniSTS
REN38248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,223,911 - 44,224,160UniSTSGRCh37
Build 361542,011,203 - 42,011,452RGDNCBI36
Celera1521,113,392 - 21,113,641RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,046,628 - 21,046,877UniSTS
REN38249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,224,157 - 44,224,399UniSTSGRCh37
Build 361542,011,449 - 42,011,691RGDNCBI36
Celera1521,113,638 - 21,113,880RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,046,874 - 21,047,116UniSTS
REN38250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,224,366 - 44,224,590UniSTSGRCh37
Build 361542,011,658 - 42,011,882RGDNCBI36
Celera1521,113,847 - 21,114,071RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,047,083 - 21,047,307UniSTS
REN38251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,224,560 - 44,224,799UniSTSGRCh37
Build 361542,011,852 - 42,012,091RGDNCBI36
Celera1521,114,041 - 21,114,280RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,047,277 - 21,047,516UniSTS
REN38252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,224,773 - 44,225,004UniSTSGRCh37
Build 361542,012,065 - 42,012,296RGDNCBI36
Celera1521,114,254 - 21,114,485RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,047,490 - 21,047,721UniSTS
REN38253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,224,985 - 44,225,239UniSTSGRCh37
Build 361542,012,277 - 42,012,531RGDNCBI36
Celera1521,114,466 - 21,114,720RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,047,702 - 21,047,956UniSTS
REN38254  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,225,210 - 44,225,464UniSTSGRCh37
Build 361542,012,502 - 42,012,756RGDNCBI36
Celera1521,114,691 - 21,114,945RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,047,927 - 21,048,181UniSTS
REN38255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,225,402 - 44,225,649UniSTSGRCh37
Build 361542,012,694 - 42,012,941RGDNCBI36
Celera1521,114,883 - 21,115,130RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,048,119 - 21,048,366UniSTS
REN38256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,225,624 - 44,225,884UniSTSGRCh37
Build 361542,012,916 - 42,013,176RGDNCBI36
Celera1521,115,105 - 21,115,365RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,048,341 - 21,048,601UniSTS
REN38257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,225,860 - 44,226,090UniSTSGRCh37
Build 361542,013,152 - 42,013,382RGDNCBI36
Celera1521,115,341 - 21,115,571RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,048,577 - 21,048,807UniSTS
REN38258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,226,086 - 44,226,335UniSTSGRCh37
Build 361542,013,378 - 42,013,627RGDNCBI36
Celera1521,115,567 - 21,115,816RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,048,803 - 21,049,052UniSTS
REN38259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,226,306 - 44,226,578UniSTSGRCh37
Build 361542,013,598 - 42,013,870RGDNCBI36
Celera1521,115,787 - 21,116,059RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,049,023 - 21,049,295UniSTS
REN38260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,226,567 - 44,226,828UniSTSGRCh37
Build 361542,013,859 - 42,014,120RGDNCBI36
Celera1521,116,048 - 21,116,309RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,049,284 - 21,049,545UniSTS
REN38261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,226,804 - 44,227,064UniSTSGRCh37
Build 361542,014,096 - 42,014,356RGDNCBI36
Celera1521,116,285 - 21,116,545RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,049,521 - 21,049,781UniSTS
REN38262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,227,041 - 44,227,294UniSTSGRCh37
Build 361542,014,333 - 42,014,586RGDNCBI36
Celera1521,116,522 - 21,116,775RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,049,758 - 21,050,011UniSTS
REN38263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,227,179 - 44,227,403UniSTSGRCh37
Build 361542,014,471 - 42,014,695RGDNCBI36
Celera1521,116,660 - 21,116,884RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,049,896 - 21,050,120UniSTS
REN38264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,227,703 - 44,227,930UniSTSGRCh37
Build 361542,014,995 - 42,015,222RGDNCBI36
Celera1521,117,184 - 21,117,411RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,050,420 - 21,050,647UniSTS
REN38265  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,227,903 - 44,228,147UniSTSGRCh37
Build 361542,015,195 - 42,015,439RGDNCBI36
Celera1521,117,384 - 21,117,628RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,050,620 - 21,050,864UniSTS
REN38266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,228,105 - 44,228,346UniSTSGRCh37
Build 361542,015,397 - 42,015,638RGDNCBI36
Celera1521,117,586 - 21,117,827RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,050,822 - 21,051,063UniSTS
REN38267  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,228,306 - 44,228,533UniSTSGRCh37
Build 361542,015,598 - 42,015,825RGDNCBI36
Celera1521,117,787 - 21,118,014RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,051,023 - 21,051,250UniSTS
REN38268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,228,505 - 44,228,770UniSTSGRCh37
Build 361542,015,797 - 42,016,062RGDNCBI36
Celera1521,117,986 - 21,118,251RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,051,222 - 21,051,487UniSTS
REN38269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,228,747 - 44,228,994UniSTSGRCh37
Build 361542,016,039 - 42,016,286RGDNCBI36
Celera1521,118,228 - 21,118,475RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,051,464 - 21,051,711UniSTS
REN38270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,228,970 - 44,229,218UniSTSGRCh37
Build 361542,016,262 - 42,016,510RGDNCBI36
Celera1521,118,451 - 21,118,699RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,051,687 - 21,051,935UniSTS
REN38271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,229,189 - 44,229,438UniSTSGRCh37
Build 361542,016,481 - 42,016,730RGDNCBI36
Celera1521,118,670 - 21,118,919RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,051,906 - 21,052,155UniSTS
REN38272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,229,292 - 44,229,543UniSTSGRCh37
Build 361542,016,584 - 42,016,835RGDNCBI36
Celera1521,118,773 - 21,119,024RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,052,009 - 21,052,260UniSTS
REN38273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,229,472 - 44,229,718UniSTSGRCh37
Build 361542,016,764 - 42,017,010RGDNCBI36
Celera1521,118,953 - 21,119,199RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,052,189 - 21,052,435UniSTS
REN38274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,229,871 - 44,230,097UniSTSGRCh37
Build 361542,017,163 - 42,017,389RGDNCBI36
Celera1521,119,352 - 21,119,578RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,052,588 - 21,052,814UniSTS
REN38275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,229,944 - 44,230,183UniSTSGRCh37
Build 361542,017,236 - 42,017,475RGDNCBI36
Celera1521,119,425 - 21,119,664RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,052,661 - 21,052,900UniSTS
REN38276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,230,119 - 44,230,364UniSTSGRCh37
Build 361542,017,411 - 42,017,656RGDNCBI36
Celera1521,119,600 - 21,119,845RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,052,836 - 21,053,081UniSTS
REN38277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,230,338 - 44,230,588UniSTSGRCh37
Build 361542,017,630 - 42,017,880RGDNCBI36
Celera1521,119,819 - 21,120,069RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,053,055 - 21,053,305UniSTS
REN38278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,230,551 - 44,230,810UniSTSGRCh37
Build 361542,017,843 - 42,018,102RGDNCBI36
Celera1521,120,032 - 21,120,291RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,053,268 - 21,053,527UniSTS
REN38279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,230,780 - 44,231,012UniSTSGRCh37
Build 361542,018,072 - 42,018,304RGDNCBI36
Celera1521,120,261 - 21,120,493RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,053,497 - 21,053,729UniSTS
REN38280  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,230,918 - 44,231,171UniSTSGRCh37
Build 361542,018,210 - 42,018,463RGDNCBI36
Celera1521,120,399 - 21,120,652RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,053,635 - 21,053,888UniSTS
REN38281  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,231,392 - 44,231,637UniSTSGRCh37
Build 361542,018,684 - 42,018,929RGDNCBI36
Celera1521,120,873 - 21,121,118RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,054,109 - 21,054,354UniSTS
REN38282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,231,595 - 44,231,840UniSTSGRCh37
Build 361542,018,887 - 42,019,132RGDNCBI36
Celera1521,121,076 - 21,121,321RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,054,312 - 21,054,557UniSTS
REN38283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,231,651 - 44,231,912UniSTSGRCh37
Build 361542,018,943 - 42,019,204RGDNCBI36
Celera1521,121,132 - 21,121,393RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,054,368 - 21,054,629UniSTS
REN38284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,231,876 - 44,232,104UniSTSGRCh37
Build 361542,019,168 - 42,019,396RGDNCBI36
Celera1521,121,357 - 21,121,585RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,054,593 - 21,054,821UniSTS
REN38285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,232,079 - 44,232,303UniSTSGRCh37
Build 361542,019,371 - 42,019,595RGDNCBI36
Celera1521,121,560 - 21,121,784RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,054,796 - 21,055,020UniSTS
REN38286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,232,274 - 44,232,515UniSTSGRCh37
Build 361542,019,566 - 42,019,807RGDNCBI36
Celera1521,121,755 - 21,121,996RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,054,991 - 21,055,232UniSTS
REN38287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,232,489 - 44,232,733UniSTSGRCh37
Build 361542,019,781 - 42,020,025RGDNCBI36
Celera1521,121,970 - 21,122,214RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,055,206 - 21,055,450UniSTS
REN38288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,232,695 - 44,232,950UniSTSGRCh37
Build 361542,019,987 - 42,020,242RGDNCBI36
Celera1521,122,176 - 21,122,431RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,055,412 - 21,055,667UniSTS
REN38289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,232,836 - 44,233,088UniSTSGRCh37
Build 361542,020,128 - 42,020,380RGDNCBI36
Celera1521,122,317 - 21,122,569RGD
Cytogenetic Map15q15.3UniSTS
HuRef1521,055,553 - 21,055,805UniSTS
D15S487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,204,067 - 44,204,168UniSTSGRCh37
Build 361541,991,359 - 41,991,460RGDNCBI36
Celera1521,093,524 - 21,093,625RGD
HuRef1521,026,784 - 21,026,885UniSTS
D15S495  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,305,829 - 44,305,958UniSTSGRCh37
Build 361542,093,121 - 42,093,250RGDNCBI36
Celera1521,195,334 - 21,195,463RGD
HuRef1521,128,935 - 21,129,064UniSTS
stSG628009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,165,354 - 44,166,434UniSTSGRCh37
Build 361541,952,646 - 41,953,726RGDNCBI36
Celera1521,054,812 - 21,055,892RGD
HuRef1520,988,081 - 20,989,161UniSTS
stSG628015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,171,916 - 44,173,155UniSTSGRCh37
Build 361541,959,208 - 41,960,447RGDNCBI36
Celera1521,061,374 - 21,062,613RGD
HuRef1520,994,642 - 20,995,881UniSTS
stSG628016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,173,136 - 44,174,378UniSTSGRCh37
Build 361541,960,428 - 41,961,670RGDNCBI36
Celera1521,062,594 - 21,063,836RGD
HuRef1520,995,862 - 20,997,104UniSTS
stSG628017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,174,359 - 44,175,700UniSTSGRCh37
Build 361541,961,651 - 41,962,992RGDNCBI36
Celera1521,063,817 - 21,065,158RGD
HuRef1520,997,085 - 20,998,426UniSTS
stSG628018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,175,681 - 44,176,813UniSTSGRCh37
Build 361541,962,973 - 41,964,105RGDNCBI36
Celera1521,065,139 - 21,066,271RGD
HuRef1520,998,407 - 20,999,539UniSTS
stSG628019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,176,795 - 44,177,949UniSTSGRCh37
Build 361541,964,087 - 41,965,241RGDNCBI36
Celera1521,066,253 - 21,067,407RGD
HuRef1520,999,521 - 21,000,675UniSTS
stSG628020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,177,930 - 44,179,025UniSTSGRCh37
Build 361541,965,222 - 41,966,317RGDNCBI36
Celera1521,067,388 - 21,068,483RGD
HuRef1521,000,656 - 21,001,751UniSTS
stSG628021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,179,006 - 44,180,188UniSTSGRCh37
Build 361541,966,298 - 41,967,480RGDNCBI36
Celera1521,068,464 - 21,069,646RGD
HuRef1521,001,732 - 21,002,914UniSTS
stSG628022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,180,169 - 44,181,459UniSTSGRCh37
Build 361541,967,461 - 41,968,751RGDNCBI36
Celera1521,069,627 - 21,070,917RGD
HuRef1521,002,895 - 21,004,185UniSTS
stSG628023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,181,494 - 44,182,868UniSTSGRCh37
Build 361541,968,786 - 41,970,160RGDNCBI36
Celera1521,070,952 - 21,072,326RGD
HuRef1521,004,220 - 21,005,594UniSTS
stSG628024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,182,851 - 44,184,283UniSTSGRCh37
Build 361541,970,143 - 41,971,575RGDNCBI36
Celera1521,072,309 - 21,073,741RGD
HuRef1521,005,577 - 21,007,009UniSTS
stSG628025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,184,264 - 44,185,587UniSTSGRCh37
Build 361541,971,556 - 41,972,879RGDNCBI36
Celera1521,073,722 - 21,075,045RGD
HuRef1521,006,990 - 21,008,313UniSTS
stSG628026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,185,567 - 44,186,832UniSTSGRCh37
Build 361541,972,859 - 41,974,124RGDNCBI36
Celera1521,075,025 - 21,076,290RGD
HuRef1521,008,293 - 21,009,558UniSTS
stSG628028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,188,266 - 44,189,269UniSTSGRCh37
Build 361541,975,558 - 41,976,561RGDNCBI36
Celera1521,077,724 - 21,078,727RGD
HuRef1521,010,992 - 21,011,995UniSTS
stSG628029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,189,250 - 44,190,510UniSTSGRCh37
GRCh371544,189,250 - 44,190,482UniSTSGRCh37
Build 361541,976,542 - 41,977,774RGDNCBI36
Celera1521,078,708 - 21,079,968UniSTS
Celera1521,078,708 - 21,079,940RGD
HuRef1521,011,976 - 21,013,237UniSTS
HuRef1521,011,976 - 21,013,209UniSTS
stSG628030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,190,491 - 44,191,942UniSTSGRCh37
Build 361541,977,783 - 41,979,234RGDNCBI36
Celera1521,079,949 - 21,081,400RGD
HuRef1521,013,218 - 21,014,669UniSTS
HuRef1521,013,189 - 21,014,669UniSTS
stSG628031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,191,816 - 44,192,817UniSTSGRCh37
Build 361541,979,108 - 41,980,109RGDNCBI36
Celera1521,081,274 - 21,082,275RGD
HuRef1521,014,543 - 21,015,544UniSTS
stSG628032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,192,798 - 44,194,236UniSTSGRCh37
Build 361541,980,090 - 41,981,528RGDNCBI36
Celera1521,082,256 - 21,083,694RGD
HuRef1521,015,525 - 21,016,963UniSTS
stSG628033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,194,217 - 44,195,335UniSTSGRCh37
Build 361541,981,509 - 41,982,627RGDNCBI36
Celera1521,083,675 - 21,084,794RGD
HuRef1521,016,944 - 21,018,063UniSTS
stSG628034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,195,316 - 44,196,471UniSTSGRCh37
Build 361541,982,608 - 41,983,763RGDNCBI36
Celera1521,084,775 - 21,085,930RGD
HuRef1521,018,044 - 21,019,199UniSTS
stSG628035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,196,452 - 44,197,702UniSTSGRCh37
Build 361541,983,744 - 41,984,994RGDNCBI36
Celera1521,085,911 - 21,087,161RGD
HuRef1521,019,180 - 21,020,430UniSTS
stSG628036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,197,683 - 44,198,753UniSTSGRCh37
Build 361541,984,975 - 41,986,045RGDNCBI36
Celera1521,087,142 - 21,088,212RGD
HuRef1521,020,411 - 21,021,481UniSTS
stSG628037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,198,743 - 44,200,201UniSTSGRCh37
Build 361541,986,035 - 41,987,493RGDNCBI36
Celera1521,088,202 - 21,089,660RGD
HuRef1521,021,471 - 21,022,930UniSTS
stSG628038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,200,264 - 44,201,295UniSTSGRCh37
Build 361541,987,556 - 41,988,587RGDNCBI36
Celera1521,089,723 - 21,090,752RGD
HuRef1521,022,993 - 21,024,022UniSTS
stSG628040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,202,667 - 44,203,884UniSTSGRCh37
Build 361541,989,959 - 41,991,176RGDNCBI36
Celera1521,092,124 - 21,093,341RGD
HuRef1521,025,384 - 21,026,601UniSTS
stSG628041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,203,984 - 44,205,334UniSTSGRCh37
Build 361541,991,276 - 41,992,626RGDNCBI36
Celera1521,093,441 - 21,094,791RGD
HuRef1521,026,701 - 21,028,051UniSTS
stSG628042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,205,332 - 44,206,437UniSTSGRCh37
Build 361541,992,624 - 41,993,729RGDNCBI36
Celera1521,094,789 - 21,095,894RGD
HuRef1521,028,049 - 21,029,154UniSTS
stSG628043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,206,418 - 44,207,596UniSTSGRCh37
Build 361541,993,710 - 41,994,888RGDNCBI36
Celera1521,095,875 - 21,097,077RGD
HuRef1521,029,135 - 21,030,313UniSTS
stSG628044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,207,577 - 44,208,745UniSTSGRCh37
Build 361541,994,869 - 41,996,037RGDNCBI36
Celera1521,097,058 - 21,098,226RGD
HuRef1521,030,294 - 21,031,462UniSTS
stSG628045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,208,726 - 44,210,201UniSTSGRCh37
Build 361541,996,018 - 41,997,493RGDNCBI36
Celera1521,098,207 - 21,099,682RGD
HuRef1521,031,443 - 21,032,918UniSTS
stSG628046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,210,182 - 44,211,359UniSTSGRCh37
Build 361541,997,474 - 41,998,651RGDNCBI36
Celera1521,099,663 - 21,100,840RGD
HuRef1521,032,899 - 21,034,076UniSTS
stSG628047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,211,342 - 44,211,553UniSTSGRCh37
Build 361541,998,634 - 41,998,845RGDNCBI36
Celera1521,100,823 - 21,101,034RGD
HuRef1521,034,059 - 21,034,270UniSTS
stSG628048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,211,557 - 44,212,705UniSTSGRCh37
Build 361541,998,849 - 41,999,997RGDNCBI36
Celera1521,101,038 - 21,102,186RGD
HuRef1521,034,274 - 21,035,422UniSTS
stSG628049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,212,686 - 44,214,042UniSTSGRCh37
Build 361541,999,978 - 42,001,334RGDNCBI36
Celera1521,102,167 - 21,103,523RGD
HuRef1521,035,403 - 21,036,759UniSTS
stSG628050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,214,205 - 44,215,345UniSTSGRCh37
Build 361542,001,497 - 42,002,637RGDNCBI36
Celera1521,103,686 - 21,104,826RGD
HuRef1521,036,922 - 21,038,062UniSTS
stSG628051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,215,326 - 44,216,696UniSTSGRCh37
Build 361542,002,618 - 42,003,988RGDNCBI36
Celera1521,104,807 - 21,106,177RGD
HuRef1521,038,043 - 21,039,413UniSTS
stSG628052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,216,613 - 44,217,628UniSTSGRCh37
Build 361542,003,905 - 42,004,920RGDNCBI36
Celera1521,106,094 - 21,107,109RGD
HuRef1521,039,330 - 21,040,345UniSTS
stSG628053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,217,623 - 44,218,753UniSTSGRCh37
Build 361542,004,915 - 42,006,045RGDNCBI36
Celera1521,107,104 - 21,108,234RGD
HuRef1521,040,340 - 21,041,470UniSTS
stSG628054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,218,748 - 44,219,769UniSTSGRCh37
Build 361542,006,040 - 42,007,061RGDNCBI36
Celera1521,108,229 - 21,109,250RGD
HuRef1521,041,465 - 21,042,486UniSTS
stSG628055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,219,757 - 44,221,023UniSTSGRCh37
Build 361542,007,049 - 42,008,315RGDNCBI36
Celera1521,109,238 - 21,110,504RGD
HuRef1521,042,474 - 21,043,740UniSTS
stSG628056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,221,004 - 44,222,396UniSTSGRCh37
Build 361542,008,296 - 42,009,688RGDNCBI36
Celera1521,110,485 - 21,111,877RGD
HuRef1521,043,721 - 21,045,113UniSTS
stSG628057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,222,377 - 44,223,822UniSTSGRCh37
Build 361542,009,669 - 42,011,114RGDNCBI36
Celera1521,111,858 - 21,113,303RGD
HuRef1521,045,094 - 21,046,539UniSTS
stSG628058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,223,823 - 44,225,244UniSTSGRCh37
Build 361542,011,115 - 42,012,536RGDNCBI36
Celera1521,113,304 - 21,114,725RGD
HuRef1521,046,540 - 21,047,961UniSTS
stSG628059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,225,226 - 44,226,241UniSTSGRCh37
Build 361542,012,518 - 42,013,533RGDNCBI36
Celera1521,114,707 - 21,115,722RGD
HuRef1521,047,943 - 21,048,958UniSTS
stSG628060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,226,222 - 44,227,312UniSTSGRCh37
Build 361542,013,514 - 42,014,604RGDNCBI36
Celera1521,115,703 - 21,116,793RGD
HuRef1521,048,939 - 21,050,029UniSTS
stSG628061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,227,293 - 44,228,334UniSTSGRCh37
Build 361542,014,585 - 42,015,626RGDNCBI36
Celera1521,116,774 - 21,117,815RGD
HuRef1521,050,010 - 21,051,051UniSTS
stSG628062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371544,228,315 - 44,229,475UniSTSGRCh37
Build 361542,015,607 - 42,016,767RGDNCBI36
Celera1521,117,796 - 21,118,956RGD
HuRef1521,051,032 - 21,052,192UniSTS


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 61 81 82 10 3 14 286 65 1320 10 85 102 5 140
Low 2010 943 695 47 404 23 971 1089 2391 133 877 422 28 159 617
Below cutoff 360 1825 760 383 1331 246 2924 863 20 191 480 1078 138 1036 1863 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001286490 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001286491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322949 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001411124 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_104455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433195 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054379029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054379030 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054379031 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008489026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_931927 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC023356 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC073940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC090513 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC090516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK090572 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK123018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC007796 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC020191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC043486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA276649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY049131 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000402883   ⟹   ENSP00000384142
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,870,767 - 44,195,210 (-)Ensembl
RefSeq Acc Id: ENST00000417257   ⟹   ENSP00000403067
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,870,764 - 44,195,271 (-)Ensembl
RefSeq Acc Id: ENST00000421674   ⟹   ENSP00000401635
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,873,275 - 44,195,193 (-)Ensembl
RefSeq Acc Id: ENST00000449926   ⟹   ENSP00000399684
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,873,275 - 43,924,309 (-)Ensembl
RefSeq Acc Id: ENST00000451277   ⟹   ENSP00000392786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,873,535 - 44,195,252 (-)Ensembl
RefSeq Acc Id: ENST00000458630   ⟹   ENSP00000404496
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,873,275 - 44,195,040 (-)Ensembl
RefSeq Acc Id: ENST00000473965
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,874,360 - 43,885,106 (-)Ensembl
RefSeq Acc Id: ENST00000479319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,901,914 - 43,909,927 (-)Ensembl
RefSeq Acc Id: ENST00000484674   ⟹   ENSP00000452968
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,873,275 - 44,194,446 (-)Ensembl
RefSeq Acc Id: ENST00000558108   ⟹   ENSP00000454031
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,873,533 - 43,919,502 (-)Ensembl
RefSeq Acc Id: ENST00000618556   ⟹   ENSP00000479575
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,870,761 - 43,924,314 (-)Ensembl
RefSeq Acc Id: ENST00000636859   ⟹   ENSP00000490339
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1543,873,853 - 43,879,846 (-)Ensembl
RefSeq Acc Id: NM_001286490   ⟹   NP_001273419
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,194,446 (-)NCBI
HuRef1520,985,686 - 21,310,838 (-)NCBI
CHM1_11544,281,210 - 44,604,906 (-)NCBI
T2T-CHM13v2.01541,678,124 - 42,001,880 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001286491   ⟹   NP_001273420
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,195,271 (-)NCBI
HuRef1520,985,686 - 21,310,838 (-)NCBI
CHM1_11544,281,210 - 44,605,754 (-)NCBI
T2T-CHM13v2.01541,678,124 - 42,002,705 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322949   ⟹   NP_001309878
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,195,271 (-)NCBI
CHM1_11544,281,210 - 44,605,754 (-)NCBI
T2T-CHM13v2.01541,678,124 - 42,002,705 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322950   ⟹   NP_001309879
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,195,271 (-)NCBI
CHM1_11544,281,210 - 44,605,754 (-)NCBI
T2T-CHM13v2.01541,678,124 - 42,002,705 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001322951   ⟹   NP_001309880
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,195,271 (-)NCBI
CHM1_11544,281,210 - 44,605,754 (-)NCBI
T2T-CHM13v2.01541,678,124 - 42,002,705 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001411124   ⟹   NP_001398053
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,195,271 (-)NCBI
T2T-CHM13v2.01541,678,124 - 42,002,705 (-)NCBI
RefSeq Acc Id: NM_032892   ⟹   NP_116281
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,195,271 (-)NCBI
GRCh371544,162,962 - 44,487,429 (-)NCBI
Build 361541,953,022 - 42,274,721 (-)NCBI Archive
Celera1521,055,188 - 21,376,921 (-)RGD
HuRef1520,985,686 - 21,310,838 (-)NCBI
CHM1_11544,281,210 - 44,605,754 (-)NCBI
T2T-CHM13v2.01541,678,124 - 42,002,705 (-)NCBI
Sequence:
RefSeq Acc Id: NR_104455
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,195,271 (-)NCBI
HuRef1520,985,686 - 21,310,838 (-)NCBI
CHM1_11544,281,210 - 44,605,754 (-)NCBI
T2T-CHM13v2.01541,678,124 - 42,002,705 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047433193   ⟹   XP_047289149
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,194,446 (-)NCBI
RefSeq Acc Id: XM_047433194   ⟹   XP_047289150
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,199,473 (-)NCBI
RefSeq Acc Id: XM_047433195   ⟹   XP_047289151
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 43,918,989 (-)NCBI
RefSeq Acc Id: XM_054379029   ⟹   XP_054235004
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01541,678,124 - 42,002,289 (-)NCBI
RefSeq Acc Id: XM_054379030   ⟹   XP_054235005
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01541,678,124 - 42,006,910 (-)NCBI
RefSeq Acc Id: XM_054379031   ⟹   XP_054235006
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01541,678,124 - 41,726,347 (-)NCBI
RefSeq Acc Id: XR_008489026
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01541,678,124 - 42,002,705 (-)NCBI
RefSeq Acc Id: XR_931927
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381543,870,764 - 44,195,271 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001273419 (Get FASTA)   NCBI Sequence Viewer  
  NP_001273420 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309878 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309879 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309880 (Get FASTA)   NCBI Sequence Viewer  
  NP_001398053 (Get FASTA)   NCBI Sequence Viewer  
  NP_116281 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289149 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289150 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289151 (Get FASTA)   NCBI Sequence Viewer  
  XP_054235004 (Get FASTA)   NCBI Sequence Viewer  
  XP_054235005 (Get FASTA)   NCBI Sequence Viewer  
  XP_054235006 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH53647 (Get FASTA)   NCBI Sequence Viewer  
  BAC03480 (Get FASTA)   NCBI Sequence Viewer  
  BAF82702 (Get FASTA)   NCBI Sequence Viewer  
  BAG53851 (Get FASTA)   NCBI Sequence Viewer  
  EAW77249 (Get FASTA)   NCBI Sequence Viewer  
  EAW77250 (Get FASTA)   NCBI Sequence Viewer  
  EAW77251 (Get FASTA)   NCBI Sequence Viewer  
  EAW77252 (Get FASTA)   NCBI Sequence Viewer  
  EAW77253 (Get FASTA)   NCBI Sequence Viewer  
  EAW77254 (Get FASTA)   NCBI Sequence Viewer  
  EAW77255 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000384142
  ENSP00000384142.1
  ENSP00000392786.1
  ENSP00000399684
  ENSP00000399684.1
  ENSP00000401635.1
  ENSP00000403067
  ENSP00000403067.1
  ENSP00000404496.1
  ENSP00000452968
  ENSP00000452968.1
  ENSP00000454031.2
  ENSP00000479575
  ENSP00000479575.1
  ENSP00000490339.1
GenBank Protein Q7Z6J6 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_116281   ⟸   NM_032892
- Peptide Label: isoform 2
- UniProtKB: Q8NBG4 (UniProtKB/Swiss-Prot),   Q7Z6J6 (UniProtKB/Swiss-Prot),   H0Y5N1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001273420   ⟸   NM_001286491
- Peptide Label: isoform 4
- UniProtKB: A0A087WVP2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001273419   ⟸   NM_001286490
- Peptide Label: isoform 3
- UniProtKB: B3KVN9 (UniProtKB/TrEMBL),   H0YKW6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309880   ⟸   NM_001322951
- Peptide Label: isoform 8
- UniProtKB: H0Y5N1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309878   ⟸   NM_001322949
- Peptide Label: isoform 6
- UniProtKB: H0Y5N1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309879   ⟸   NM_001322950
- Peptide Label: isoform 7
- UniProtKB: H0Y5N1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000454031   ⟸   ENST00000558108
RefSeq Acc Id: ENSP00000392786   ⟸   ENST00000451277
RefSeq Acc Id: ENSP00000490339   ⟸   ENST00000636859
RefSeq Acc Id: ENSP00000384142   ⟸   ENST00000402883
RefSeq Acc Id: ENSP00000403067   ⟸   ENST00000417257
RefSeq Acc Id: ENSP00000404496   ⟸   ENST00000458630
RefSeq Acc Id: ENSP00000452968   ⟸   ENST00000484674
RefSeq Acc Id: ENSP00000479575   ⟸   ENST00000618556
RefSeq Acc Id: ENSP00000401635   ⟸   ENST00000421674
RefSeq Acc Id: ENSP00000399684   ⟸   ENST00000449926
RefSeq Acc Id: XP_047289150   ⟸   XM_047433194
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047289149   ⟸   XM_047433193
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047289151   ⟸   XM_047433195
- Peptide Label: isoform X2
- UniProtKB: A8K1U8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001398053   ⟸   NM_001411124
- Peptide Label: isoform 9
- UniProtKB: B5MC67 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054235005   ⟸   XM_054379030
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054235004   ⟸   XM_054379029
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054235006   ⟸   XM_054379031
- Peptide Label: isoform X2
- UniProtKB: A8K1U8 (UniProtKB/TrEMBL)
Protein Domains
FERM   FERM adjacent   FERM C-terminal PH-like

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q7Z6J6-F1-model_v2 AlphaFold Q7Z6J6 1-570 view protein structure

Promoters
RGD ID:6792349
Promoter ID:HG_KWN:21240
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Jurkat,   Lymphoblastoid
Transcripts:OTTHUMT00000315942
Position:
Human AssemblyChrPosition (strand)Source
Build 361541,964,411 - 41,965,502 (-)MPROMDB
RGD ID:6792271
Promoter ID:HG_KWN:21244
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   Lymphoblastoid
Transcripts:ENST00000402883,   OTTHUMT00000133879,   OTTHUMT00000133883,   OTTHUMT00000332218,   OTTHUMT00000332219,   UC001ZTM.1,   UC001ZTN.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361542,274,589 - 42,275,089 (-)MPROMDB
RGD ID:7229329
Promoter ID:EPDNEW_H20409
Type:initiation region
Name:FRMD5_2
Description:FERM domain containing 5
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20410  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381544,195,100 - 44,195,160EPDNEW
RGD ID:7229327
Promoter ID:EPDNEW_H20410
Type:initiation region
Name:FRMD5_1
Description:FERM domain containing 5
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20409  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381544,195,271 - 44,195,331EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:28214 AgrOrtholog
COSMIC FRMD5 COSMIC
Ensembl Genes ENSG00000171877 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000402883 ENTREZGENE
  ENST00000402883.5 UniProtKB/TrEMBL
  ENST00000417257 ENTREZGENE
  ENST00000417257.6 UniProtKB/Swiss-Prot
  ENST00000421674.5 UniProtKB/TrEMBL
  ENST00000449926 ENTREZGENE
  ENST00000449926.5 UniProtKB/TrEMBL
  ENST00000451277.5 UniProtKB/TrEMBL
  ENST00000458630.5 UniProtKB/TrEMBL
  ENST00000484674 ENTREZGENE
  ENST00000484674.5 UniProtKB/TrEMBL
  ENST00000558108.6 UniProtKB/TrEMBL
  ENST00000618556 ENTREZGENE
  ENST00000618556.4 UniProtKB/TrEMBL
  ENST00000636859.1 UniProtKB/TrEMBL
Gene3D-CATH 1.20.80.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.30.29.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000171877 GTEx
HGNC ID HGNC:28214 ENTREZGENE
Human Proteome Map FRMD5 Human Proteome Map
InterPro Band_41_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ez/rad/moesin-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM-adjacent UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM/acyl-CoA-bd_prot_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_central UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_PH-like_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ubiquitin-like_domsf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:84978 UniProtKB/Swiss-Prot
NCBI Gene 84978 ENTREZGENE
OMIM 616309 OMIM
PANTHER 4.1 G PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM DOMAIN-CONTAINING PROTEIN 5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam FERM_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_M UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF08736 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142671751 PharmGKB
PRINTS BAND41 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ERMFAMILY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE FERM_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART B41 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FERM_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM01195 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP PH domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF47031 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF54236 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WVP2 ENTREZGENE, UniProtKB/TrEMBL
  A0A1B0GV18_HUMAN UniProtKB/TrEMBL
  A8K1U8 ENTREZGENE, UniProtKB/TrEMBL
  B3KVN9 ENTREZGENE, UniProtKB/TrEMBL
  B5MC67 ENTREZGENE, UniProtKB/TrEMBL
  F8WCI0_HUMAN UniProtKB/TrEMBL
  F8WEJ8_HUMAN UniProtKB/TrEMBL
  FRMD5_HUMAN UniProtKB/Swiss-Prot
  H0Y5N1 ENTREZGENE, UniProtKB/TrEMBL
  H0YKW6 ENTREZGENE, UniProtKB/TrEMBL
  H0YNI9_HUMAN UniProtKB/TrEMBL
  H7C282_HUMAN UniProtKB/TrEMBL
  Q7Z6J6 ENTREZGENE
  Q8NBG4 ENTREZGENE
UniProt Secondary Q8NBG4 UniProtKB/Swiss-Prot