P4HA2 (prolyl 4-hydroxylase subunit alpha 2) - Rat Genome Database

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Gene: P4HA2 (prolyl 4-hydroxylase subunit alpha 2) Homo sapiens
Analyze
Symbol: P4HA2
Name: prolyl 4-hydroxylase subunit alpha 2
RGD ID: 1320142
HGNC Page HGNC:8547
Description: Enables procollagen-proline 4-dioxygenase activity. Located in cytosol; endoplasmic reticulum; and nucleoplasm. Implicated in myopia.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: 4-PH alpha 2; 4-PH alpha-2; C-P4Halpha(II); collagen prolyl 4-hydroxylase alpha(II); lncRNA promotes epithelial-mesenchymal transition; lncRNA-PE; MYP25; procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide II; procollagen-proline,2-oxoglutarate-4-dioxygenase subunit alpha-2; prolyl 4-hydroxylase subunit alpha-2; prolyl 4-hydroxylase, alpha polypeptide II
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
GRCh385132,190,147 - 132,227,853 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5132,190,147 - 132,295,315 (-)EnsemblGRCh38hg38GRCh38
GRCh375131,525,840 - 131,563,546 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 365131,556,202 - 131,591,455 (-)NCBINCBI36Build 36hg18NCBI36
Build 345131,556,201 - 131,590,458NCBI
Celera5127,658,410 - 127,693,660 (-)NCBICelera
Cytogenetic Map5q31.1NCBI
HuRef5126,720,651 - 126,756,017 (-)NCBIHuRef
CHM1_15130,961,055 - 130,996,320 (-)NCBICHM1_1
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(1->4)-beta-D-glucan  (ISO)
1,10-phenanthroline  (EXP)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,4-dinitrotoluene  (ISO)
2,6-dinitrotoluene  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
5-aza-2'-deoxycytidine  (EXP)
5-chloro-7-iodoquinolin-8-ol  (EXP)
acrylamide  (EXP)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
atrazine  (EXP,ISO)
benzo[a]pyrene  (EXP)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (EXP,ISO)
Bisphenol B  (EXP)
bisphenol F  (EXP,ISO)
cadmium dichloride  (EXP,ISO)
calciol  (ISO)
calcium silicate  (ISO)
carbon nanotube  (ISO)
CGP 52608  (EXP)
choline  (ISO)
cisplatin  (EXP)
cobalt dichloride  (EXP,ISO)
cyclosporin A  (EXP)
cytarabine  (EXP)
dexamethasone  (EXP)
diclofenac  (EXP)
dioxygen  (EXP,ISO)
diquat  (ISO)
dorsomorphin  (EXP)
entinostat  (EXP)
ethanol  (EXP,ISO)
fluoranthene  (ISO)
folic acid  (EXP,ISO)
ivermectin  (EXP)
L-ascorbic acid  (EXP)
L-methionine  (ISO)
lead(0)  (EXP)
methamphetamine  (ISO)
N(4)-hydroxycytidine  (ISO)
nickel dichloride  (ISO)
nickel subsulfide  (ISO)
nickel sulfate  (EXP)
oxaliplatin  (EXP,ISO)
paracetamol  (EXP,ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (EXP)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
potassium dichromate  (ISO)
progesterone  (ISO)
propiconazole  (ISO)
SB 431542  (EXP)
SCH 23390  (ISO)
serpentine asbestos  (EXP)
sodium arsenite  (EXP,ISO)
sunitinib  (EXP)
tamoxifen  (ISO)
temozolomide  (EXP)
tetrachloromethane  (ISO)
thifluzamide  (EXP)
titanium dioxide  (ISO)
topotecan  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
triptonide  (ISO)
valproic acid  (EXP)
vancomycin  (ISO)
vinclozolin  (ISO)
zinc atom  (EXP)
zinc dichloride  (EXP)
zinc(0)  (EXP)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

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

Human Phenotype
Abdominal aortic aneurysm  (IAGP)
Abdominal pain  (IAGP)
Abnormal pleura morphology  (IAGP)
Abnormality of thrombocytes  (IAGP)
Alopecia  (IAGP)
Amaurosis fugax  (IAGP)
Anorexia  (IAGP)
Aortic dissection  (IAGP)
Arrhythmia  (IAGP)
Arterial thrombosis  (IAGP)
Arthralgia  (IAGP)
Arthritis  (IAGP)
Ataxia  (IAGP)
Autosomal dominant inheritance  (IAGP)
Cerebral ischemia  (IAGP)
Conductive hearing impairment  (IAGP)
Cough  (IAGP)
Depression  (IAGP)
Diabetes insipidus  (IAGP)
Diplopia  (IAGP)
Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis  (IAGP)
Elevated erythrocyte sedimentation rate  (IAGP)
Epistaxis  (IAGP)
Fatigue  (IAGP)
Fever  (IAGP)
Gangrene  (IAGP)
Gastrointestinal infarctions  (IAGP)
Glossitis  (IAGP)
Headache  (IAGP)
Hearing impairment  (IAGP)
Hematuria  (IAGP)
Hepatic failure  (IAGP)
High myopia  (IAGP)
Hyperhidrosis  (IAGP)
Impaired mastication  (IAGP)
Joint stiffness  (IAGP)
Juvenile onset  (IAGP)
Mediastinal lymphadenopathy  (IAGP)
Meningitis  (IAGP)
Muscle weakness  (IAGP)
Myalgia  (IAGP)
Nystagmus  (IAGP)
Ophthalmoparesis  (IAGP)
Optic atrophy  (IAGP)
Paresthesia  (IAGP)
Pericarditis  (IAGP)
Peripheral neuropathy  (IAGP)
Ptosis  (IAGP)
Recurrent pharyngitis  (IAGP)
Renal insufficiency  (IAGP)
Retinal detachment  (IAGP)
Schizophrenia  (IAGP)
Skin ulcer  (IAGP)
Sudden cardiac death  (IAGP)
Vasculitis  (IAGP)
Vertigo  (IAGP)
Visual field defect  (IAGP)
Visual impairment  (IAGP)
Visual loss  (IAGP)
Weight loss  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9211872   PMID:11606192   PMID:12477932   PMID:12824157   PMID:14500733   PMID:14667819   PMID:15489334   PMID:16344560   PMID:16877351   PMID:16885164   PMID:16917063   PMID:17213842  
PMID:18457437   PMID:19131452   PMID:19615732   PMID:20000738   PMID:20628624   PMID:21516116   PMID:21859152   PMID:21873635   PMID:22190034   PMID:22412388   PMID:22813596   PMID:23686814  
PMID:24383403   PMID:25036637   PMID:25416956   PMID:25741866   PMID:25814554   PMID:26186194   PMID:26344197   PMID:26496610   PMID:27173435   PMID:27633981   PMID:28041642   PMID:28093469  
PMID:28380382   PMID:28514442   PMID:29180619   PMID:29364500   PMID:29437589   PMID:30021884   PMID:30410060   PMID:30880498   PMID:31278071   PMID:31536960   PMID:31586073   PMID:32149426  
PMID:32572027   PMID:32622013   PMID:32707033   PMID:32994395   PMID:33001583   PMID:33545068   PMID:33961781   PMID:34079125   PMID:34387118   PMID:34471235   PMID:34732716   PMID:35256949  
PMID:35271311   PMID:35338135   PMID:35379950   PMID:35384245   PMID:35509820   PMID:35563538   PMID:35673909   PMID:35696571   PMID:35831314   PMID:35944360   PMID:36215168   PMID:36403427  
PMID:36724073   PMID:36906285   PMID:36943397  


Genomics

Comparative Map Data
P4HA2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385132,190,147 - 132,227,853 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5132,190,147 - 132,295,315 (-)EnsemblGRCh38hg38GRCh38
GRCh375131,525,840 - 131,563,546 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 365131,556,202 - 131,591,455 (-)NCBINCBI36Build 36hg18NCBI36
Build 345131,556,201 - 131,590,458NCBI
Celera5127,658,410 - 127,693,660 (-)NCBICelera
Cytogenetic Map5q31.1NCBI
HuRef5126,720,651 - 126,756,017 (-)NCBIHuRef
CHM1_15130,961,055 - 130,996,320 (-)NCBICHM1_1
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBIT2T-CHM13v2.0
P4ha2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391153,991,750 - 54,022,494 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1153,990,921 - 54,022,491 (+)EnsemblGRCm39 Ensembl
GRCm381154,100,924 - 54,131,668 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1154,100,095 - 54,131,665 (+)EnsemblGRCm38mm10GRCm38
MGSCv371153,914,426 - 53,945,169 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361153,944,939 - 53,975,071 (+)NCBIMGSCv36mm8
Celera1158,688,554 - 58,719,297 (+)NCBICelera
Cytogenetic Map11B1.3NCBI
cM Map1132.13NCBI
P4ha2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81038,743,894 - 38,772,741 (+)NCBIGRCr8
mRatBN7.21038,243,136 - 38,271,983 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1038,243,139 - 38,287,314 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1042,928,504 - 42,957,355 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01042,418,604 - 42,447,453 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01037,922,310 - 37,951,165 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01039,435,227 - 39,464,134 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1039,435,227 - 39,464,188 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01039,214,791 - 39,243,698 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41039,522,157 - 39,551,063 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11039,535,833 - 39,564,271 (+)NCBI
Celera1037,584,460 - 37,613,368 (+)NCBICelera
Cytogenetic Map10q22NCBI
P4ha2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554083,574,860 - 3,607,015 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554083,574,860 - 3,607,015 (-)NCBIChiLan1.0ChiLan1.0
P4HA2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v24127,447,132 - 127,546,038 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan15125,583,719 - 125,685,655 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v05127,613,037 - 127,650,647 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.15133,778,520 - 133,813,779 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl5133,778,520 - 133,813,779 (-)Ensemblpanpan1.1panPan2
P4HA2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11120,514,982 - 20,548,261 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1120,514,978 - 20,549,541 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1119,310,369 - 19,350,017 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01121,300,346 - 21,333,655 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1121,300,356 - 21,333,637 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11120,019,425 - 20,052,694 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01119,867,545 - 19,900,820 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01120,509,393 - 20,542,685 (-)NCBIUU_Cfam_GSD_1.0
P4ha2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213115,927,933 - 115,960,406 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366472,930,494 - 2,964,550 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366472,930,748 - 2,963,168 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
P4HA2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl2134,502,212 - 134,595,430 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.12134,502,210 - 134,595,444 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.22139,853,792 - 139,886,023 (-)NCBISscrofa10.2Sscrofa10.2susScr3
P4HA2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12335,022,675 - 35,058,128 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2335,020,535 - 35,058,009 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603442,885,975 - 42,923,550 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
P4ha2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473339,871,180 - 39,903,377 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473339,871,156 - 39,902,266 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in P4HA2
59 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3 copy number gain See cases [RCV000051193] Chr5:130860928..155321811 [GRCh38]
Chr5:130196621..154701371 [GRCh37]
Chr5:130224520..154681564 [NCBI36]
Chr5:5q23.3-33.2		 pathogenic
GRCh38/hg38 5q23.2-31.1(chr5:126438406-132873967)x1 copy number loss See cases [RCV000052109] Chr5:126438406..132873967 [GRCh38]
Chr5:125774098..132209659 [GRCh37]
Chr5:125801997..132237558 [NCBI36]
Chr5:5q23.2-31.1		 pathogenic
GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1 copy number loss See cases [RCV000053524] Chr5:106619588..156124387 [GRCh38]
Chr5:105955289..155551397 [GRCh37]
Chr5:105983188..155483975 [NCBI36]
Chr5:5q21.3-33.2		 pathogenic
GRCh38/hg38 5q23.1-31.1(chr5:116677122-132686163)x1 copy number loss See cases [RCV000053525] Chr5:116677122..132686163 [GRCh38]
Chr5:116012818..132021855 [GRCh37]
Chr5:116040717..132049754 [NCBI36]
Chr5:5q23.1-31.1		 pathogenic
NM_001017973.1(P4HA2):c.704C>T (p.Ser235Phe) single nucleotide variant Malignant melanoma [RCV000066625] Chr5:132210289 [GRCh38]
Chr5:131545982 [GRCh37]
Chr5:131573881 [NCBI36]
Chr5:5q31.1		 not provided
GRCh38/hg38 5q31.1(chr5:131626503-135815054)x1 copy number loss See cases [RCV000135442] Chr5:131626503..135815054 [GRCh38]
Chr5:130962196..135150743 [GRCh37]
Chr5:130990095..135178642 [NCBI36]
Chr5:5q31.1		 pathogenic
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3 copy number gain See cases [RCV000138808] Chr5:129847794..153353546 [GRCh38]
Chr5:129183487..152733106 [GRCh37]
Chr5:129211386..152713299 [NCBI36]
Chr5:5q23.3-33.2		 pathogenic
GRCh38/hg38 5q31.1(chr5:132180822-132235177)x3 copy number gain See cases [RCV000140364] Chr5:132180822..132235177 [GRCh38]
Chr5:131516515..131570870 [GRCh37]
Chr5:131544414..131598769 [NCBI36]
Chr5:5q31.1		 likely benign
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 copy number gain not provided [RCV000487658] Chr5:94844077..178830410 [GRCh37]
Chr5:5q15-35.3		 likely benign
NM_001365677.2(P4HA2):c.1352_1353del (p.Val451fs) microsatellite Myopia 25, autosomal dominant [RCV000412535] Chr5:132198224..132198225 [GRCh38]
Chr5:131533917..131533918 [GRCh37]
Chr5:5q31.1		 pathogenic
NM_001017974.2(P4HA2):c.871G>A (p.Glu291Lys) single nucleotide variant Myopia 25, autosomal dominant [RCV000412575] Chr5:132209170 [GRCh38]
Chr5:131544863 [GRCh37]
Chr5:5q31.1		 pathogenic
NM_001017974.2(P4HA2):c.419A>G (p.Gln140Arg) single nucleotide variant Myopia 25, autosomal dominant [RCV000412662] Chr5:132213966 [GRCh38]
Chr5:131549659 [GRCh37]
Chr5:5q31.1		 pathogenic
NM_001017974.2(P4HA2):c.940C>T (p.His314Tyr) single nucleotide variant Inborn genetic diseases [RCV002536423]|not provided [RCV000729166] Chr5:132207848 [GRCh38]
Chr5:131543541 [GRCh37]
Chr5:5q31.1		 uncertain significance
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 copy number gain See cases [RCV000449349] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3		 pathogenic
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 copy number gain See cases [RCV000448245] Chr5:106716357..180687338 [GRCh37]
Chr5:5q21.3-35.3		 pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
NM_001017974.2(P4HA2):c.674G>A (p.Arg225His) single nucleotide variant Inborn genetic diseases [RCV003281237] Chr5:132210319 [GRCh38]
Chr5:131546012 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001365677.2(P4HA2):c.1349G>A (p.Arg450His) single nucleotide variant Inborn genetic diseases [RCV003259360] Chr5:132198228 [GRCh38]
Chr5:131533921 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1580G>A (p.Cys527Tyr) single nucleotide variant Inborn genetic diseases [RCV003281739] Chr5:132193032 [GRCh38]
Chr5:131528725 [GRCh37]
Chr5:5q31.1		 uncertain significance
NC_000005.9:g.(?_86400000)_(154000000_?)del deletion Familial adenomatous polyposis 1 [RCV002231249]|Hereditary cancer-predisposing syndrome [RCV000554476] Chr5:86400000..154000000 [GRCh37]
Chr5:5q14.3-33.2		 pathogenic
GRCh37/hg19 5q31.1(chr5:131484039-132998360)x3 copy number gain Blepharophimosis [RCV000677199] Chr5:131484039..132998360 [GRCh37]
Chr5:5q31.1		 uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
NC_000005.10:g.(?_131428263)_(132208822_?)del deletion Schizophrenia [RCV000754294] Chr5:131428263..132208822 [GRCh38]
Chr5:5q31.1		 likely pathogenic
NM_001017974.2(P4HA2):c.63C>T (p.Ala21=) single nucleotide variant not provided [RCV000894994] Chr5:132218564 [GRCh38]
Chr5:131554257 [GRCh37]
Chr5:5q31.1		 likely benign
GRCh37/hg19 5q23.2-31.2(chr5:126377719-136270989)x1 copy number loss not provided [RCV000762739] Chr5:126377719..136270989 [GRCh37]
Chr5:5q23.2-31.2		 likely pathogenic
NM_001365677.2(P4HA2):c.1371+1G>A single nucleotide variant not provided [RCV000883767] Chr5:132198205 [GRCh38]
Chr5:131533898 [GRCh37]
Chr5:5q31.1		 pathogenic|likely benign
NM_001017974.2(P4HA2):c.645T>C (p.Tyr215=) single nucleotide variant P4HA2-related condition [RCV003960596]|not provided [RCV000948707] Chr5:132210348 [GRCh38]
Chr5:131546041 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001017974.2(P4HA2):c.1230A>G (p.Val410=) single nucleotide variant not provided [RCV000906393] Chr5:132203769 [GRCh38]
Chr5:131539462 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001017974.2(P4HA2):c.1068C>T (p.Ile356=) single nucleotide variant not provided [RCV000922373] Chr5:132207720 [GRCh38]
Chr5:131543413 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001365677.2(P4HA2):c.1307A>G (p.Asn436Ser) single nucleotide variant P4HA2-related condition [RCV003940385]|not provided [RCV000879684] Chr5:132198270 [GRCh38]
Chr5:131533963 [GRCh37]
Chr5:5q31.1		 benign|likely benign
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32		 uncertain significance
GRCh37/hg19 5q31.1(chr5:131504297-131673288)x1 copy number loss not provided [RCV000849530] Chr5:131504297..131673288 [GRCh37]
Chr5:5q31.1		 uncertain significance
GRCh37/hg19 5q31.1(chr5:131107107-131528744)x3 copy number gain not provided [RCV000846701] Chr5:131107107..131528744 [GRCh37]
Chr5:5q31.1		 uncertain significance
GRCh37/hg19 5q23.3-31.1(chr5:127800418-134002686) copy number loss Neurodevelopmental disorder and language delay with or without structural brain abnormalities [RCV003236718] Chr5:127800418..134002686 [GRCh37]
Chr5:5q23.3-31.1		 pathogenic
NM_001017974.2(P4HA2):c.25C>A (p.Leu9Met) single nucleotide variant Inborn genetic diseases [RCV003241102] Chr5:132218602 [GRCh38]
Chr5:131554295 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.226G>T (p.Ala76Ser) single nucleotide variant Myopia 25, autosomal dominant [RCV002489426]|P4HA2-related condition [RCV003936191]|not provided [RCV000974564] Chr5:132217302 [GRCh38]
Chr5:131552995 [GRCh37]
Chr5:5q31.1		 benign|likely benign
NM_001017974.2(P4HA2):c.82+4C>T single nucleotide variant not provided [RCV000974064] Chr5:132218541 [GRCh38]
Chr5:131554234 [GRCh37]
Chr5:5q31.1		 benign
NM_001017974.2(P4HA2):c.331+9C>T single nucleotide variant not provided [RCV000923338] Chr5:132217188 [GRCh38]
Chr5:131552881 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001017974.2(P4HA2):c.654C>G (p.Phe218Leu) single nucleotide variant not provided [RCV000907409] Chr5:132210339 [GRCh38]
Chr5:131546032 [GRCh37]
Chr5:5q31.1		 benign
NM_001017974.2(P4HA2):c.1128C>T (p.Val376=) single nucleotide variant not provided [RCV000909508] Chr5:132204105 [GRCh38]
Chr5:131539798 [GRCh37]
Chr5:5q31.1		 likely benign
NC_000005.9:g.(?_130497712)_(131729974_?)del deletion Renal carnitine transport defect [RCV001031175] Chr5:130497712..131729974 [GRCh37]
Chr5:5q23.3-31.1		 pathogenic
NC_000005.9:g.(?_131436897)_(131729974_?)del deletion Renal carnitine transport defect [RCV001033393] Chr5:131436897..131729974 [GRCh37]
Chr5:5q31.1		 pathogenic
NM_001017974.2(P4HA2):c.269T>A (p.Val90Glu) single nucleotide variant not provided [RCV001786689] Chr5:132217259 [GRCh38]
Chr5:131552952 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1201C>T (p.Arg401Trp) single nucleotide variant Inborn genetic diseases [RCV003295270] Chr5:132203798 [GRCh38]
Chr5:131539491 [GRCh37]
Chr5:5q31.1		 uncertain significance
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910) copy number gain not specified [RCV002053526] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3		 pathogenic
NM_001017974.2(P4HA2):c.179+16_179+17insT insertion not provided [RCV002226019] Chr5:132217735..132217736 [GRCh38]
Chr5:131553428..131553429 [GRCh37]
Chr5:5q31.1		 benign
NM_001017974.2(P4HA2):c.164T>C (p.Leu55Pro) single nucleotide variant not provided [RCV002300851] Chr5:132217767 [GRCh38]
Chr5:131553460 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1096G>A (p.Val366Ile) single nucleotide variant Inborn genetic diseases [RCV002749185] Chr5:132204137 [GRCh38]
Chr5:131539830 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001365677.2(P4HA2):c.1314G>C (p.Glu438Asp) single nucleotide variant Inborn genetic diseases [RCV002882634] Chr5:132198263 [GRCh38]
Chr5:131533956 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.121G>A (p.Val41Met) single nucleotide variant Inborn genetic diseases [RCV002858924] Chr5:132217810 [GRCh38]
Chr5:131553503 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1180G>A (p.Val394Ile) single nucleotide variant Inborn genetic diseases [RCV002859672] Chr5:132203819 [GRCh38]
Chr5:131539512 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.182G>C (p.Trp61Ser) single nucleotide variant Inborn genetic diseases [RCV002745057] Chr5:132217346 [GRCh38]
Chr5:131553039 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.695G>A (p.Arg232His) single nucleotide variant Inborn genetic diseases [RCV002709273] Chr5:132210298 [GRCh38]
Chr5:131545991 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.728C>T (p.Ala243Val) single nucleotide variant Inborn genetic diseases [RCV002744799] Chr5:132209313 [GRCh38]
Chr5:131545006 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1471G>A (p.Gly491Arg) single nucleotide variant Inborn genetic diseases [RCV002789882] Chr5:132194986 [GRCh38]
Chr5:131530679 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1129G>T (p.Ala377Ser) single nucleotide variant Inborn genetic diseases [RCV002674237] Chr5:132204104 [GRCh38]
Chr5:131539797 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.725G>A (p.Arg242Gln) single nucleotide variant Inborn genetic diseases [RCV002855359] Chr5:132209316 [GRCh38]
Chr5:131545009 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.692G>A (p.Arg231His) single nucleotide variant Inborn genetic diseases [RCV002807675] Chr5:132210301 [GRCh38]
Chr5:131545994 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1538A>G (p.Asn513Ser) single nucleotide variant Inborn genetic diseases [RCV002674204] Chr5:132193074 [GRCh38]
Chr5:131528767 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.910C>T (p.Arg304Cys) single nucleotide variant Inborn genetic diseases [RCV002678746] Chr5:132207878 [GRCh38]
Chr5:131543571 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.782C>A (p.Thr261Lys) single nucleotide variant Myopia 25, autosomal dominant [RCV003131866] Chr5:132209259 [GRCh38]
Chr5:131544952 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.64G>A (p.Glu22Lys) single nucleotide variant Inborn genetic diseases [RCV003184951] Chr5:132218563 [GRCh38]
Chr5:131554256 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.917A>G (p.Gln306Arg) single nucleotide variant Inborn genetic diseases [RCV003210692] Chr5:132207871 [GRCh38]
Chr5:131543564 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.742C>T (p.Arg248Trp) single nucleotide variant Inborn genetic diseases [RCV003202270] Chr5:132209299 [GRCh38]
Chr5:131544992 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.345C>A (p.Asn115Lys) single nucleotide variant Inborn genetic diseases [RCV003212562] Chr5:132214040 [GRCh38]
Chr5:131549733 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.14T>C (p.Val5Ala) single nucleotide variant Inborn genetic diseases [RCV003178531] Chr5:132218613 [GRCh38]
Chr5:131554306 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.886G>C (p.Gly296Arg) single nucleotide variant Inborn genetic diseases [RCV003204262] Chr5:132209155 [GRCh38]
Chr5:131544848 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.776A>G (p.Glu259Gly) single nucleotide variant Inborn genetic diseases [RCV003197685] Chr5:132209265 [GRCh38]
Chr5:131544958 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.346C>G (p.Leu116Val) single nucleotide variant Inborn genetic diseases [RCV003342150] Chr5:132214039 [GRCh38]
Chr5:131549732 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1103A>G (p.Asp368Gly) single nucleotide variant Inborn genetic diseases [RCV003352542] Chr5:132204130 [GRCh38]
Chr5:131539823 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1487G>A (p.Arg496Gln) single nucleotide variant Inborn genetic diseases [RCV003370189] Chr5:132194970 [GRCh38]
Chr5:131530663 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.476A>G (p.Lys159Arg) single nucleotide variant P4HA2-related condition [RCV003402541] Chr5:132210517 [GRCh38]
Chr5:131546210 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1434+8C>A single nucleotide variant P4HA2-related condition [RCV003929141]|not provided [RCV003428602] Chr5:132195404 [GRCh38]
Chr5:131531097 [GRCh37]
Chr5:5q31.1		 benign|likely benign
NM_001017974.2(P4HA2):c.267G>T (p.Leu89=) single nucleotide variant not provided [RCV003429762] Chr5:132217261 [GRCh38]
Chr5:131552954 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001017974.2(P4HA2):c.520C>T (p.Arg174Cys) single nucleotide variant P4HA2-related condition [RCV003408751] Chr5:132210473 [GRCh38]
Chr5:131546166 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1263T>A (p.Tyr421Ter) single nucleotide variant not provided [RCV003443909] Chr5:132198921 [GRCh38]
Chr5:131534614 [GRCh37]
Chr5:5q31.1		 uncertain significance
GRCh37/hg19 5q31.1(chr5:131502885-131673154)x1 copy number loss not specified [RCV003986554] Chr5:131502885..131673154 [GRCh37]
Chr5:5q31.1		 uncertain significance
NM_001017974.2(P4HA2):c.1026C>T (p.Tyr342=) single nucleotide variant P4HA2-related condition [RCV003914276] Chr5:132207762 [GRCh38]
Chr5:131543455 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001017974.2(P4HA2):c.731G>C (p.Gly244Ala) single nucleotide variant P4HA2-related condition [RCV003909559] Chr5:132209310 [GRCh38]
Chr5:131545003 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001017974.2(P4HA2):c.648T>G (p.Ala216=) single nucleotide variant P4HA2-related condition [RCV003933965] Chr5:132210345 [GRCh38]
Chr5:131546038 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001017974.2(P4HA2):c.339C>T (p.Ile113=) single nucleotide variant P4HA2-related condition [RCV003909566] Chr5:132214046 [GRCh38]
Chr5:131549739 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001017974.2(P4HA2):c.1252-5C>T single nucleotide variant P4HA2-related condition [RCV003929489] Chr5:132198937 [GRCh38]
Chr5:131534630 [GRCh37]
Chr5:5q31.1		 likely benign
NM_001017974.2(P4HA2):c.1347A>G (p.Leu449=) single nucleotide variant P4HA2-related condition [RCV003967301] Chr5:132198339 [GRCh38]
Chr5:131534032 [GRCh37]
Chr5:5q31.1		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4614
Count of miRNA genes:1056
Interacting mature miRNAs:1310
Transcripts:ENST00000166534, ENST00000360568, ENST00000379086, ENST00000379100, ENST00000379104, ENST00000395164, ENST00000401867, ENST00000416053, ENST00000417528, ENST00000418055, ENST00000428369, ENST00000428841, ENST00000431054, ENST00000439698, ENST00000453286, ENST00000467587, ENST00000471826, ENST00000474628, ENST00000478055, ENST00000481636
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
RH47156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,342 - 131,528,464UniSTSGRCh37
Build 365131,556,241 - 131,556,363RGDNCBI36
Celera5127,658,449 - 127,658,571RGD
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5q31UniSTS
HuRef5126,720,690 - 126,720,812UniSTS
GeneMap99-GB4 RH Map5503.48UniSTS
bac5078S  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,529,878 - 131,530,071UniSTSGRCh37
Build 365131,557,777 - 131,557,970RGDNCBI36
Celera5127,659,985 - 127,660,178RGD
Cytogenetic Map5q31UniSTS
HuRef5126,722,391 - 126,722,584UniSTS
ECD00566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,554,095 - 131,554,994UniSTSGRCh37
Build 365131,581,994 - 131,582,893RGDNCBI36
Celera5127,684,199 - 127,685,098RGD
Cytogenetic Map5q31UniSTS
HuRef5126,746,556 - 126,747,455UniSTS
ECD00897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,555,181 - 131,556,066UniSTSGRCh37
Build 365131,583,080 - 131,583,965RGDNCBI36
Celera5127,685,285 - 127,686,170RGD
Cytogenetic Map5q31UniSTS
HuRef5126,747,642 - 126,748,527UniSTS
ECD00926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,553,143 - 131,554,027UniSTSGRCh37
Build 365131,581,042 - 131,581,926RGDNCBI36
Celera5127,683,247 - 127,684,131RGD
Cytogenetic Map5q31UniSTS
HuRef5126,745,603 - 126,746,488UniSTS
ECD00947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,533,712 - 131,534,595UniSTSGRCh37
Build 365131,561,611 - 131,562,494RGDNCBI36
Celera5127,663,820 - 127,664,703RGD
Cytogenetic Map5q31UniSTS
HuRef5126,726,225 - 126,727,108UniSTS
ECD00979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,534,668 - 131,535,550UniSTSGRCh37
Build 365131,562,567 - 131,563,449RGDNCBI36
Celera5127,664,776 - 127,665,658RGD
Cytogenetic Map5q31UniSTS
HuRef5126,727,181 - 126,728,063UniSTS
ECD01132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,541,374 - 131,542,250UniSTSGRCh37
Build 365131,569,273 - 131,570,149RGDNCBI36
Celera5127,671,482 - 127,672,358RGD
Cytogenetic Map5q31UniSTS
HuRef5126,733,887 - 126,734,763UniSTS
ECD01284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,552,213 - 131,553,083UniSTSGRCh37
Build 365131,580,112 - 131,580,982RGDNCBI36
Celera5127,682,317 - 127,683,187RGD
Cytogenetic Map5q31UniSTS
HuRef5126,744,673 - 126,745,543UniSTS
ECD01400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,556,075 - 131,556,941UniSTSGRCh37
Build 365131,583,974 - 131,584,840RGDNCBI36
Celera5127,686,179 - 127,687,045RGD
Cytogenetic Map5q31UniSTS
HuRef5126,748,536 - 126,749,402UniSTS
ECD01427  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,546,494 - 131,547,359UniSTSGRCh37
Build 365131,574,393 - 131,575,258RGDNCBI36
Celera5127,676,602 - 127,677,467RGD
Cytogenetic Map5q31UniSTS
HuRef5126,738,958 - 126,739,823UniSTS
ECD01528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,545,504 - 131,546,366UniSTSGRCh37
Build 365131,573,403 - 131,574,265RGDNCBI36
Celera5127,675,612 - 127,676,474RGD
Cytogenetic Map5q31UniSTS
HuRef5126,737,968 - 126,738,830UniSTS
ECD05138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,562,342 - 131,563,086UniSTSGRCh37
Build 365131,590,241 - 131,590,985RGDNCBI36
Celera5127,692,446 - 127,693,190RGD
Cytogenetic Map5q31UniSTS
HuRef5126,754,803 - 126,755,547UniSTS
ECD05969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,564,013 - 131,564,734UniSTSGRCh37
Build 365131,591,912 - 131,592,633RGDNCBI36
Celera5127,694,117 - 127,694,838RGD
Cytogenetic Map5q31UniSTS
HuRef5126,756,474 - 126,757,195UniSTS
ECD06294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,537,116 - 131,537,828UniSTSGRCh37
Build 365131,565,015 - 131,565,727RGDNCBI36
Celera5127,667,224 - 127,667,936RGD
Cytogenetic Map5q31UniSTS
HuRef5126,729,629 - 126,730,341UniSTS
ECD06373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,791 - 131,529,501UniSTSGRCh37
Build 365131,556,690 - 131,557,400RGDNCBI36
Celera5127,658,898 - 127,659,608RGD
Cytogenetic Map5q31UniSTS
HuRef5126,721,139 - 126,722,014UniSTS
ECD06602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,537,843 - 131,538,547UniSTSGRCh37
Build 365131,565,742 - 131,566,446RGDNCBI36
Celera5127,667,951 - 127,668,655RGD
Cytogenetic Map5q31UniSTS
HuRef5126,730,356 - 126,731,060UniSTS
ECD06716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,062 - 131,528,763UniSTSGRCh37
Build 365131,555,961 - 131,556,662RGDNCBI36
Celera5127,658,169 - 127,658,870RGD
Cytogenetic Map5q31UniSTS
HuRef5126,720,410 - 126,721,111UniSTS
ECD07080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,539,267 - 131,539,958UniSTSGRCh37
Build 365131,567,166 - 131,567,857RGDNCBI36
Celera5127,669,375 - 127,670,066RGD
Cytogenetic Map5q31UniSTS
HuRef5126,731,780 - 126,732,471UniSTS
ECD07121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,536,401 - 131,537,091UniSTSGRCh37
Build 365131,564,300 - 131,564,990RGDNCBI36
Celera5127,666,509 - 127,667,199RGD
Cytogenetic Map5q31UniSTS
HuRef5126,728,914 - 126,729,604UniSTS
ECD07371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,549,241 - 131,549,924UniSTSGRCh37
Build 365131,577,140 - 131,577,823RGDNCBI36
Celera5127,679,349 - 127,680,032RGD
Cytogenetic Map5q31UniSTS
HuRef5126,741,705 - 126,742,388UniSTS
ECD07406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,540,042 - 131,540,724UniSTSGRCh37
Build 365131,567,941 - 131,568,623RGDNCBI36
Celera5127,670,150 - 127,670,832RGD
Cytogenetic Map5q31UniSTS
HuRef5126,732,555 - 126,733,237UniSTS
ECD07554  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,549,955 - 131,550,633UniSTSGRCh37
Build 365131,577,854 - 131,578,532RGDNCBI36
Celera5127,680,063 - 127,680,741RGD
Cytogenetic Map5q31UniSTS
HuRef5126,742,419 - 126,743,097UniSTS
ECD08087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,563,280 - 131,563,944UniSTSGRCh37
Build 365131,591,179 - 131,591,843RGDNCBI36
Celera5127,693,384 - 127,694,048RGD
Cytogenetic Map5q31UniSTS
HuRef5126,755,741 - 126,756,405UniSTS
ECD08237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,550,712 - 131,551,372UniSTSGRCh37
Build 365131,578,611 - 131,579,271RGDNCBI36
Celera5127,680,820 - 127,681,480RGD
Cytogenetic Map5q31UniSTS
HuRef5126,743,176 - 126,743,836UniSTS
ECD08366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,561,482 - 131,562,138UniSTSGRCh37
Build 365131,589,381 - 131,590,037RGDNCBI36
Celera5127,691,586 - 127,692,242RGD
Cytogenetic Map5q31UniSTS
HuRef5126,753,943 - 126,754,599UniSTS
ECD08771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,557,331 - 131,557,977UniSTSGRCh37
Build 365131,585,230 - 131,585,876RGDNCBI36
Celera5127,687,435 - 127,688,081RGD
Cytogenetic Map5q31UniSTS
HuRef5126,749,792 - 126,750,438UniSTS
ECD08843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,530,034 - 131,530,678UniSTSGRCh37
Build 365131,557,933 - 131,558,577RGDNCBI36
Celera5127,660,141 - 127,660,785RGD
Cytogenetic Map5q31UniSTS
HuRef5126,722,547 - 126,723,191UniSTS
ECD09224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,530,706 - 131,531,340UniSTSGRCh37
Build 365131,558,605 - 131,559,239RGDNCBI36
Celera5127,660,813 - 127,661,447RGD
Cytogenetic Map5q31UniSTS
HuRef5126,723,219 - 126,723,853UniSTS
ECD09385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,560,778 - 131,561,408UniSTSGRCh37
Build 365131,588,677 - 131,589,307RGDNCBI36
Celera5127,690,882 - 127,691,512RGD
Cytogenetic Map5q31UniSTS
HuRef5126,753,239 - 126,753,869UniSTS
ECD09535  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,531,392 - 131,532,018UniSTSGRCh37
Build 365131,559,291 - 131,559,917RGDNCBI36
Celera5127,661,499 - 127,662,125RGD
Cytogenetic Map5q31UniSTS
HuRef5126,723,905 - 126,724,531UniSTS
ECD09618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,560,118 - 131,560,742UniSTSGRCh37
Build 365131,588,017 - 131,588,641RGDNCBI36
Celera5127,690,222 - 127,690,846RGD
Cytogenetic Map5q31UniSTS
HuRef5126,752,579 - 126,753,203UniSTS
ECD10009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,558,023 - 131,558,636UniSTSGRCh37
Build 365131,585,922 - 131,586,535RGDNCBI36
Celera5127,688,127 - 127,688,740RGD
Cytogenetic Map5q31UniSTS
HuRef5126,750,484 - 126,751,097UniSTS
ECD13769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,547,599 - 131,548,108UniSTSGRCh37
Build 365131,575,498 - 131,576,007RGDNCBI36
Celera5127,677,707 - 127,678,216RGD
Cytogenetic Map5q31UniSTS
HuRef5126,740,063 - 126,740,572UniSTS
ECD13819  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,544,680 - 131,545,188UniSTSGRCh37
Build 365131,572,579 - 131,573,087RGDNCBI36
Celera5127,674,788 - 127,675,296RGD
Cytogenetic Map5q31UniSTS
HuRef5126,737,144 - 126,737,652UniSTS
ECD15188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,544,181 - 131,544,657UniSTSGRCh37
Build 365131,572,080 - 131,572,556RGDNCBI36
Celera5127,674,289 - 127,674,765RGD
Cytogenetic Map5q31UniSTS
HuRef5126,736,645 - 126,737,121UniSTS
ECD16158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,543,274 - 131,543,725UniSTSGRCh37
Build 365131,571,173 - 131,571,624RGDNCBI36
Celera5127,673,382 - 127,673,833RGD
Cytogenetic Map5q31UniSTS
HuRef5126,735,787 - 126,736,238UniSTS
ECD20217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,532,725 - 131,533,017UniSTSGRCh37
Build 365131,560,624 - 131,560,916RGDNCBI36
Celera5127,662,833 - 127,663,125RGD
Cytogenetic Map5q31UniSTS
HuRef5126,725,239 - 126,725,531UniSTS
ECD20350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,559,578 - 131,559,865UniSTSGRCh37
Build 365131,587,477 - 131,587,764RGDNCBI36
Celera5127,689,682 - 127,689,969RGD
Cytogenetic Map5q31UniSTS
HuRef5126,752,039 - 126,752,326UniSTS
ECD20638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,535,916 - 131,536,193UniSTSGRCh37
Build 365131,563,815 - 131,564,092RGDNCBI36
Celera5127,666,024 - 127,666,301RGD
Cytogenetic Map5q31UniSTS
HuRef5126,728,429 - 126,728,706UniSTS
ECD21105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,548,465 - 131,548,726UniSTSGRCh37
Build 365131,576,364 - 131,576,625RGDNCBI36
Celera5127,678,573 - 127,678,834RGD
Cytogenetic Map5q31UniSTS
HuRef5126,740,929 - 126,741,190UniSTS
REN69218  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,527,923 - 131,528,172UniSTSGRCh37
Build 365131,555,822 - 131,556,071RGDNCBI36
Celera5127,658,030 - 127,658,279RGD
Cytogenetic Map5q31UniSTS
HuRef5126,720,271 - 126,720,520UniSTS
REN69219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,171 - 131,528,436UniSTSGRCh37
Build 365131,556,070 - 131,556,335RGDNCBI36
Celera5127,658,278 - 127,658,543RGD
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5q31UniSTS
HuRef5126,720,519 - 126,720,784UniSTS
REN69220  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,399 - 131,528,661UniSTSGRCh37
Build 365131,556,298 - 131,556,560RGDNCBI36
Celera5127,658,506 - 127,658,768RGD
Cytogenetic Map5q31UniSTS
HuRef5126,720,747 - 126,721,009UniSTS
REN69221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,633 - 131,528,892UniSTSGRCh37
Build 365131,556,532 - 131,556,791RGDNCBI36
Celera5127,658,740 - 127,658,999RGD
Cytogenetic Map5q31UniSTS
HuRef5126,720,981 - 126,721,240UniSTS
REN69222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,890 - 131,529,135UniSTSGRCh37
Build 365131,556,789 - 131,557,034RGDNCBI36
Celera5127,658,997 - 127,659,242RGD
Cytogenetic Map5q31UniSTS
HuRef5126,721,238 - 126,721,648UniSTS
REN69223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,529,101 - 131,529,341UniSTSGRCh37
Build 365131,557,000 - 131,557,240RGDNCBI36
Celera5127,659,208 - 127,659,448RGD
Cytogenetic Map5q31UniSTS
HuRef5126,721,614 - 126,721,854UniSTS
REN69224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,529,300 - 131,529,555UniSTSGRCh37
Build 365131,557,199 - 131,557,454RGDNCBI36
Celera5127,659,407 - 127,659,662RGD
Cytogenetic Map5q31UniSTS
HuRef5126,721,813 - 126,722,068UniSTS
REN69225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,529,534 - 131,529,776UniSTSGRCh37
Build 365131,557,433 - 131,557,675RGDNCBI36
Celera5127,659,641 - 127,659,883RGD
Cytogenetic Map5q31UniSTS
HuRef5126,722,047 - 126,722,289UniSTS
REN69226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,529,755 - 131,530,003UniSTSGRCh37
Build 365131,557,654 - 131,557,902RGDNCBI36
Celera5127,659,862 - 127,660,110RGD
Cytogenetic Map5q31UniSTS
HuRef5126,722,268 - 126,722,516UniSTS
REN69227  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,529,965 - 131,530,219UniSTSGRCh37
Build 365131,557,864 - 131,558,118RGDNCBI36
Celera5127,660,072 - 127,660,326RGD
Cytogenetic Map5q31UniSTS
HuRef5126,722,478 - 126,722,732UniSTS
REN69228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,530,192 - 131,530,431UniSTSGRCh37
Build 365131,558,091 - 131,558,330RGDNCBI36
Celera5127,660,299 - 127,660,538RGD
Cytogenetic Map5q31UniSTS
HuRef5126,722,705 - 126,722,944UniSTS
REN69229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,530,388 - 131,530,620UniSTSGRCh37
Build 365131,558,287 - 131,558,519RGDNCBI36
Celera5127,660,495 - 127,660,727RGD
Cytogenetic Map5q31UniSTS
HuRef5126,722,901 - 126,723,133UniSTS
REN69230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,530,604 - 131,530,855UniSTSGRCh37
Build 365131,558,503 - 131,558,754RGDNCBI36
Celera5127,660,711 - 127,660,962RGD
Cytogenetic Map5q31UniSTS
HuRef5126,723,117 - 126,723,368UniSTS
REN69231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,530,847 - 131,531,078UniSTSGRCh37
Build 365131,558,746 - 131,558,977RGDNCBI36
Celera5127,660,954 - 127,661,185RGD
Cytogenetic Map5q31UniSTS
HuRef5126,723,360 - 126,723,591UniSTS
REN69232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,531,055 - 131,531,307UniSTSGRCh37
Build 365131,558,954 - 131,559,206RGDNCBI36
Celera5127,661,162 - 127,661,414RGD
Cytogenetic Map5q31UniSTS
HuRef5126,723,568 - 126,723,820UniSTS
REN69233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,531,282 - 131,531,538UniSTSGRCh37
Build 365131,559,181 - 131,559,437RGDNCBI36
Celera5127,661,389 - 127,661,645RGD
Cytogenetic Map5q31UniSTS
HuRef5126,723,795 - 126,724,051UniSTS
REN69234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,531,486 - 131,531,735UniSTSGRCh37
Build 365131,559,385 - 131,559,634RGDNCBI36
Celera5127,661,593 - 127,661,842RGD
Cytogenetic Map5q31UniSTS
HuRef5126,723,999 - 126,724,248UniSTS
REN69235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,531,702 - 131,531,927UniSTSGRCh37
Build 365131,559,601 - 131,559,826RGDNCBI36
Celera5127,661,809 - 127,662,034RGD
Cytogenetic Map5q31UniSTS
HuRef5126,724,215 - 126,724,440UniSTS
REN69236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,531,904 - 131,532,154UniSTSGRCh37
Build 365131,559,803 - 131,560,053RGDNCBI36
Celera5127,662,011 - 127,662,261RGD
Cytogenetic Map5q31UniSTS
HuRef5126,724,417 - 126,724,667UniSTS
REN69237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,532,029 - 131,532,278UniSTSGRCh37
Build 365131,559,928 - 131,560,177RGDNCBI36
Celera5127,662,136 - 127,662,385RGD
Cytogenetic Map5q31UniSTS
HuRef5126,724,542 - 126,724,791UniSTS
REN69238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,532,594 - 131,532,818UniSTSGRCh37
Build 365131,560,493 - 131,560,717RGDNCBI36
Celera5127,662,702 - 127,662,926RGD
Cytogenetic Map5q31UniSTS
HuRef5126,725,108 - 126,725,332UniSTS
REN69239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,532,800 - 131,533,024UniSTSGRCh37
Build 365131,560,699 - 131,560,923RGDNCBI36
Celera5127,662,908 - 127,663,132RGD
Cytogenetic Map5q31UniSTS
HuRef5126,725,314 - 126,725,538UniSTS
REN69240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,532,969 - 131,533,217UniSTSGRCh37
Build 365131,560,868 - 131,561,116RGDNCBI36
Celera5127,663,077 - 127,663,325RGD
Cytogenetic Map5q31UniSTS
HuRef5126,725,483 - 126,725,731UniSTS
REN69241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,533,195 - 131,533,453UniSTSGRCh37
Build 365131,561,094 - 131,561,352RGDNCBI36
Celera5127,663,303 - 127,663,561RGD
Cytogenetic Map5q31UniSTS
HuRef5126,725,709 - 126,725,966UniSTS
REN69242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,533,440 - 131,533,704UniSTSGRCh37
Build 365131,561,339 - 131,561,603RGDNCBI36
Celera5127,663,548 - 127,663,812RGD
Cytogenetic Map5q31UniSTS
HuRef5126,725,953 - 126,726,217UniSTS
REN69243  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,533,689 - 131,533,928UniSTSGRCh37
Build 365131,561,588 - 131,561,827RGDNCBI36
Celera5127,663,797 - 127,664,036RGD
Cytogenetic Map5q31UniSTS
HuRef5126,726,202 - 126,726,441UniSTS
REN69244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,533,903 - 131,534,151UniSTSGRCh37
Build 365131,561,802 - 131,562,050RGDNCBI36
Celera5127,664,011 - 127,664,259RGD
Cytogenetic Map5q31UniSTS
HuRef5126,726,416 - 126,726,664UniSTS
REN69245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,534,128 - 131,534,371UniSTSGRCh37
Build 365131,562,027 - 131,562,270RGDNCBI36
Celera5127,664,236 - 127,664,479RGD
Cytogenetic Map5q31UniSTS
HuRef5126,726,641 - 126,726,884UniSTS
REN69246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,534,346 - 131,534,600UniSTSGRCh37
Build 365131,562,245 - 131,562,499RGDNCBI36
Celera5127,664,454 - 127,664,708RGD
Cytogenetic Map5q31UniSTS
HuRef5126,726,859 - 126,727,113UniSTS
REN69247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,534,593 - 131,534,833UniSTSGRCh37
Build 365131,562,492 - 131,562,732RGDNCBI36
Celera5127,664,701 - 127,664,941RGD
Cytogenetic Map5q31UniSTS
HuRef5126,727,106 - 126,727,346UniSTS
REN69248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,534,783 - 131,535,030UniSTSGRCh37
Build 365131,562,682 - 131,562,929RGDNCBI36
Celera5127,664,891 - 127,665,138RGD
Cytogenetic Map5q31UniSTS
HuRef5126,727,296 - 126,727,543UniSTS
REN69249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,535,016 - 131,535,266UniSTSGRCh37
Build 365131,562,915 - 131,563,165RGDNCBI36
Celera5127,665,124 - 127,665,374RGD
Cytogenetic Map5q31UniSTS
HuRef5126,727,529 - 126,727,779UniSTS
REN69250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,535,223 - 131,535,470UniSTSGRCh37
Build 365131,563,122 - 131,563,369RGDNCBI36
Celera5127,665,331 - 127,665,578RGD
Cytogenetic Map5q31UniSTS
HuRef5126,727,736 - 126,727,983UniSTS
REN69251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,535,389 - 131,535,617UniSTSGRCh37
Build 365131,563,288 - 131,563,516RGDNCBI36
Celera5127,665,497 - 127,665,725RGD
Cytogenetic Map5q31UniSTS
HuRef5126,727,902 - 126,728,130UniSTS
REN69252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,535,495 - 131,535,739UniSTSGRCh37
Build 365131,563,394 - 131,563,638RGDNCBI36
Celera5127,665,603 - 127,665,847RGD
Cytogenetic Map5q31UniSTS
HuRef5126,728,008 - 126,728,252UniSTS
REN69253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,535,712 - 131,535,941UniSTSGRCh37
Build 365131,563,611 - 131,563,840RGDNCBI36
Celera5127,665,820 - 127,666,049RGD
Cytogenetic Map5q31UniSTS
HuRef5126,728,225 - 126,728,454UniSTS
REN69254  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,535,919 - 131,536,179UniSTSGRCh37
Build 365131,563,818 - 131,564,078RGDNCBI36
Celera5127,666,027 - 127,666,287RGD
Cytogenetic Map5q31UniSTS
HuRef5126,728,432 - 126,728,692UniSTS
REN69255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,536,173 - 131,536,424UniSTSGRCh37
Build 365131,564,072 - 131,564,323RGDNCBI36
Celera5127,666,281 - 127,666,532RGD
Cytogenetic Map5q31UniSTS
HuRef5126,728,686 - 126,728,937UniSTS
REN69256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,536,411 - 131,536,654UniSTSGRCh37
Build 365131,564,310 - 131,564,553RGDNCBI36
Celera5127,666,519 - 127,666,762RGD
Cytogenetic Map5q31UniSTS
HuRef5126,728,924 - 126,729,167UniSTS
REN69257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,536,599 - 131,536,864UniSTSGRCh37
Build 365131,564,498 - 131,564,763RGDNCBI36
Celera5127,666,707 - 127,666,972RGD
Cytogenetic Map5q31UniSTS
HuRef5126,729,112 - 126,729,377UniSTS
REN69258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,536,841 - 131,537,091UniSTSGRCh37
Build 365131,564,740 - 131,564,990RGDNCBI36
Celera5127,666,949 - 127,667,199RGD
Cytogenetic Map5q31UniSTS
HuRef5126,729,354 - 126,729,604UniSTS
REN69259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,537,068 - 131,537,327UniSTSGRCh37
Build 365131,564,967 - 131,565,226RGDNCBI36
Celera5127,667,176 - 127,667,435RGD
Cytogenetic Map5q31UniSTS
HuRef5126,729,581 - 126,729,840UniSTS
REN69260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,537,306 - 131,537,536UniSTSGRCh37
Build 365131,565,205 - 131,565,435RGDNCBI36
Celera5127,667,414 - 127,667,644RGD
Cytogenetic Map5q31UniSTS
HuRef5126,729,819 - 126,730,049UniSTS
REN69261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,537,520 - 131,537,777UniSTSGRCh37
Build 365131,565,419 - 131,565,676RGDNCBI36
Celera5127,667,628 - 127,667,885RGD
Cytogenetic Map5q31UniSTS
HuRef5126,730,033 - 126,730,290UniSTS
REN69262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,537,776 - 131,538,019UniSTSGRCh37
Build 365131,565,675 - 131,565,918RGDNCBI36
Celera5127,667,884 - 127,668,127RGD
Cytogenetic Map5q31UniSTS
HuRef5126,730,289 - 126,730,532UniSTS
REN69263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,538,003 - 131,538,262UniSTSGRCh37
Build 365131,565,902 - 131,566,161RGDNCBI36
Celera5127,668,111 - 127,668,370RGD
Cytogenetic Map5q31UniSTS
HuRef5126,730,516 - 126,730,775UniSTS
REN69264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,538,255 - 131,538,505UniSTSGRCh37
Build 365131,566,154 - 131,566,404RGDNCBI36
Celera5127,668,363 - 127,668,613RGD
Cytogenetic Map5q31UniSTS
HuRef5126,730,768 - 126,731,018UniSTS
REN69265  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,538,491 - 131,538,740UniSTSGRCh37
Build 365131,566,390 - 131,566,639RGDNCBI36
Celera5127,668,599 - 127,668,848RGD
Cytogenetic Map5q31UniSTS
HuRef5126,731,004 - 126,731,253UniSTS
REN69266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,538,717 - 131,538,964UniSTSGRCh37
Build 365131,566,616 - 131,566,863RGDNCBI36
Celera5127,668,825 - 127,669,072RGD
Cytogenetic Map5q31UniSTS
HuRef5126,731,230 - 126,731,477UniSTS
REN69267  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,538,961 - 131,539,208UniSTSGRCh37
Build 365131,566,860 - 131,567,107RGDNCBI36
Celera5127,669,069 - 127,669,316RGD
Cytogenetic Map5q31UniSTS
HuRef5126,731,474 - 126,731,721UniSTS
REN69268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,539,183 - 131,539,432UniSTSGRCh37
Build 365131,567,082 - 131,567,331RGDNCBI36
Celera5127,669,291 - 127,669,540RGD
Cytogenetic Map5q31UniSTS
HuRef5126,731,696 - 126,731,945UniSTS
REN69269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,539,397 - 131,539,647UniSTSGRCh37
Build 365131,567,296 - 131,567,546RGDNCBI36
Celera5127,669,505 - 127,669,755RGD
Cytogenetic Map5q31UniSTS
HuRef5126,731,910 - 126,732,160UniSTS
REN69270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,539,626 - 131,539,882UniSTSGRCh37
Build 365131,567,525 - 131,567,781RGDNCBI36
Celera5127,669,734 - 127,669,990RGD
Cytogenetic Map5q31UniSTS
HuRef5126,732,139 - 126,732,395UniSTS
REN69271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,539,854 - 131,540,094UniSTSGRCh37
Build 365131,567,753 - 131,567,993RGDNCBI36
Celera5127,669,962 - 127,670,202RGD
Cytogenetic Map5q31UniSTS
HuRef5126,732,367 - 126,732,607UniSTS
REN69272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,540,073 - 131,540,307UniSTSGRCh37
Build 365131,567,972 - 131,568,206RGDNCBI36
Celera5127,670,181 - 127,670,415RGD
Cytogenetic Map5q31UniSTS
HuRef5126,732,586 - 126,732,820UniSTS
REN69273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,540,282 - 131,540,542UniSTSGRCh37
Build 365131,568,181 - 131,568,441RGDNCBI36
Celera5127,670,390 - 127,670,650RGD
Cytogenetic Map5q31UniSTS
HuRef5126,732,795 - 126,733,055UniSTS
REN69274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,540,535 - 131,540,792UniSTSGRCh37
Build 365131,568,434 - 131,568,691RGDNCBI36
Celera5127,670,643 - 127,670,900RGD
Cytogenetic Map5q31UniSTS
HuRef5126,733,048 - 126,733,305UniSTS
REN69275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,540,757 - 131,540,995UniSTSGRCh37
Build 365131,568,656 - 131,568,894RGDNCBI36
Celera5127,670,865 - 127,671,103RGD
Cytogenetic Map5q31UniSTS
HuRef5126,733,270 - 126,733,508UniSTS
REN69276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,540,972 - 131,541,224UniSTSGRCh37
Build 365131,568,871 - 131,569,123RGDNCBI36
Celera5127,671,080 - 127,671,332RGD
Cytogenetic Map5q31UniSTS
HuRef5126,733,485 - 126,733,737UniSTS
REN69277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,541,209 - 131,541,456UniSTSGRCh37
Build 365131,569,108 - 131,569,355RGDNCBI36
Celera5127,671,317 - 127,671,564RGD
Cytogenetic Map5q31UniSTS
HuRef5126,733,722 - 126,733,969UniSTS
REN69278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,541,426 - 131,541,668UniSTSGRCh37
Build 365131,569,325 - 131,569,567RGDNCBI36
Celera5127,671,534 - 127,671,776RGD
Cytogenetic Map5q31UniSTS
HuRef5126,733,939 - 126,734,181UniSTS
REN69279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,541,667 - 131,541,916UniSTSGRCh37
Build 365131,569,566 - 131,569,815RGDNCBI36
Celera5127,671,775 - 127,672,024RGD
Cytogenetic Map5q31UniSTS
HuRef5126,734,180 - 126,734,429UniSTS
REN69280  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,541,906 - 131,542,159UniSTSGRCh37
Build 365131,569,805 - 131,570,058RGDNCBI36
Celera5127,672,014 - 127,672,267RGD
Cytogenetic Map5q31UniSTS
HuRef5126,734,419 - 126,734,672UniSTS
REN69281  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,542,135 - 131,542,377UniSTSGRCh37
Build 365131,570,034 - 131,570,276RGDNCBI36
Celera5127,672,243 - 127,672,485RGD
Cytogenetic Map5q31UniSTS
HuRef5126,734,648 - 126,734,890UniSTS
REN69282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,542,369 - 131,542,629UniSTSGRCh37
Build 365131,570,268 - 131,570,528RGDNCBI36
Celera5127,672,477 - 127,672,737RGD
Cytogenetic Map5q31UniSTS
HuRef5126,734,882 - 126,735,142UniSTS
REN69283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,542,558 - 131,542,805UniSTSGRCh37
Build 365131,570,457 - 131,570,704RGDNCBI36
Celera5127,672,666 - 127,672,913RGD
Cytogenetic Map5q31UniSTS
HuRef5126,735,071 - 126,735,318UniSTS
REN69284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,542,776 - 131,543,027UniSTSGRCh37
Build 365131,570,675 - 131,570,926RGDNCBI36
Celera5127,672,884 - 127,673,135RGD
Cytogenetic Map5q31UniSTS
HuRef5126,735,289 - 126,735,540UniSTS
REN69285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,543,002 - 131,543,251UniSTSGRCh37
Build 365131,570,901 - 131,571,150RGDNCBI36
Celera5127,673,110 - 127,673,359RGD
Cytogenetic Map5q31UniSTS
HuRef5126,735,515 - 126,735,764UniSTS
REN69286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,543,244 - 131,543,503UniSTSGRCh37
Build 365131,571,143 - 131,571,402RGDNCBI36
Celera5127,673,352 - 127,673,611RGD
Cytogenetic Map5q31UniSTS
HuRef5126,735,757 - 126,736,016UniSTS
REN69287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,543,483 - 131,543,712UniSTSGRCh37
Build 365131,571,382 - 131,571,611RGDNCBI36
Celera5127,673,591 - 127,673,820RGD
Cytogenetic Map5q31UniSTS
HuRef5126,735,996 - 126,736,225UniSTS
REN69288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,543,687 - 131,543,922UniSTSGRCh37
Build 365131,571,586 - 131,571,821RGDNCBI36
Celera5127,673,795 - 127,674,030RGD
Cytogenetic Map5q31UniSTS
HuRef5126,736,200 - 126,736,435UniSTS
REN69289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,543,965 - 131,544,195UniSTSGRCh37
Build 365131,571,864 - 131,572,094RGDNCBI36
Celera5127,674,073 - 127,674,303RGD
Cytogenetic Map5q31UniSTS
HuRef5126,736,478 - 126,736,659UniSTS
REN69290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,544,182 - 131,544,426UniSTSGRCh37
Build 365131,572,081 - 131,572,325RGDNCBI36
Celera5127,674,290 - 127,674,534RGD
Cytogenetic Map5q31UniSTS
HuRef5126,736,646 - 126,736,890UniSTS
REN69291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,544,400 - 131,544,634UniSTSGRCh37
Build 365131,572,299 - 131,572,533RGDNCBI36
Celera5127,674,508 - 127,674,742RGD
Cytogenetic Map5q31UniSTS
HuRef5126,736,864 - 126,737,098UniSTS
REN69292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,544,592 - 131,544,841UniSTSGRCh37
Build 365131,572,491 - 131,572,740RGDNCBI36
Celera5127,674,700 - 127,674,949RGD
Cytogenetic Map5q31UniSTS
HuRef5126,737,056 - 126,737,305UniSTS
REN69293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,544,818 - 131,545,068UniSTSGRCh37
Build 365131,572,717 - 131,572,967RGDNCBI36
Celera5127,674,926 - 127,675,176RGD
Cytogenetic Map5q31UniSTS
HuRef5126,737,282 - 126,737,532UniSTS
REN69294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,544,975 - 131,545,201UniSTSGRCh37
Build 365131,572,874 - 131,573,100RGDNCBI36
Celera5127,675,083 - 127,675,309RGD
Cytogenetic Map5q31UniSTS
HuRef5126,737,439 - 126,737,665UniSTS
REN69295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,545,097 - 131,545,338UniSTSGRCh37
Build 365131,572,996 - 131,573,237RGDNCBI36
Celera5127,675,205 - 127,675,446RGD
Cytogenetic Map5q31UniSTS
HuRef5126,737,561 - 126,737,802UniSTS
REN69296  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,545,330 - 131,545,557UniSTSGRCh37
Build 365131,573,229 - 131,573,456RGDNCBI36
Celera5127,675,438 - 127,675,665RGD
Cytogenetic Map5q31UniSTS
HuRef5126,737,794 - 126,738,021UniSTS
REN69297  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,545,529 - 131,545,773UniSTSGRCh37
Build 365131,573,428 - 131,573,672RGDNCBI36
Celera5127,675,637 - 127,675,881RGD
Cytogenetic Map5q31UniSTS
HuRef5126,737,993 - 126,738,237UniSTS
REN69298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,545,751 - 131,545,983UniSTSGRCh37
Build 365131,573,650 - 131,573,882RGDNCBI36
Celera5127,675,859 - 127,676,091RGD
Cytogenetic Map5q31UniSTS
HuRef5126,738,215 - 126,738,447UniSTS
REN69299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,545,964 - 131,546,220UniSTSGRCh37
Build 365131,573,863 - 131,574,119RGDNCBI36
Celera5127,676,072 - 127,676,328RGD
Cytogenetic Map5q31UniSTS
HuRef5126,738,428 - 126,738,684UniSTS
REN69300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,546,218 - 131,546,451UniSTSGRCh37
Build 365131,574,117 - 131,574,350RGDNCBI36
Celera5127,676,326 - 127,676,559RGD
Cytogenetic Map5q31UniSTS
HuRef5126,738,682 - 126,738,915UniSTS
REN69301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,546,429 - 131,546,683UniSTSGRCh37
Build 365131,574,328 - 131,574,582RGDNCBI36
Celera5127,676,537 - 127,676,791RGD
Cytogenetic Map5q31UniSTS
HuRef5126,738,893 - 126,739,147UniSTS
REN69302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,546,660 - 131,546,918UniSTSGRCh37
Build 365131,574,559 - 131,574,817RGDNCBI36
Celera5127,676,768 - 127,677,026RGD
Cytogenetic Map5q31UniSTS
HuRef5126,739,124 - 126,739,382UniSTS
REN69303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,546,895 - 131,547,154UniSTSGRCh37
Build 365131,574,794 - 131,575,053RGDNCBI36
Celera5127,677,003 - 127,677,262RGD
Cytogenetic Map5q31UniSTS
HuRef5126,739,359 - 126,739,618UniSTS
REN69304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,547,136 - 131,547,400UniSTSGRCh37
Build 365131,575,035 - 131,575,299RGDNCBI36
Celera5127,677,244 - 127,677,508RGD
Cytogenetic Map5q31UniSTS
HuRef5126,739,600 - 126,739,864UniSTS
REN69305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,547,389 - 131,547,655UniSTSGRCh37
Build 365131,575,288 - 131,575,554RGDNCBI36
Celera5127,677,497 - 127,677,763RGD
Cytogenetic Map5q31UniSTS
HuRef5126,739,853 - 126,740,119UniSTS
REN69306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,547,649 - 131,547,894UniSTSGRCh37
Build 365131,575,548 - 131,575,793RGDNCBI36
Celera5127,677,757 - 127,678,002RGD
Cytogenetic Map5q31UniSTS
HuRef5126,740,113 - 126,740,358UniSTS
REN69307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,547,873 - 131,548,123UniSTSGRCh37
Build 365131,575,772 - 131,576,022RGDNCBI36
Celera5127,677,981 - 127,678,231RGD
Cytogenetic Map5q31UniSTS
HuRef5126,740,337 - 126,740,587UniSTS
REN69308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,548,102 - 131,548,369UniSTSGRCh37
Build 365131,576,001 - 131,576,268RGDNCBI36
Celera5127,678,210 - 127,678,477RGD
Cytogenetic Map5q31UniSTS
HuRef5126,740,566 - 126,740,833UniSTS
REN69309  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,548,339 - 131,548,588UniSTSGRCh37
Build 365131,576,238 - 131,576,487RGDNCBI36
Celera5127,678,447 - 127,678,696RGD
Cytogenetic Map5q31UniSTS
HuRef5126,740,803 - 126,741,052UniSTS
REN69310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,548,568 - 131,548,807UniSTSGRCh37
Build 365131,576,467 - 131,576,706RGDNCBI36
Celera5127,678,676 - 127,678,915RGD
Cytogenetic Map5q31UniSTS
HuRef5126,741,032 - 126,741,271UniSTS
REN69311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,548,785 - 131,549,042UniSTSGRCh37
Build 365131,576,684 - 131,576,941RGDNCBI36
Celera5127,678,893 - 127,679,150RGD
Cytogenetic Map5q31UniSTS
HuRef5126,741,249 - 126,741,506UniSTS
REN69312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,549,020 - 131,549,268UniSTSGRCh37
Build 365131,576,919 - 131,577,167RGDNCBI36
Celera5127,679,128 - 127,679,376RGD
Cytogenetic Map5q31UniSTS
HuRef5126,741,484 - 126,741,732UniSTS
REN69313  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,549,250 - 131,549,498UniSTSGRCh37
Build 365131,577,149 - 131,577,397RGDNCBI36
Celera5127,679,358 - 127,679,606RGD
Cytogenetic Map5q31UniSTS
HuRef5126,741,714 - 126,741,962UniSTS
REN69314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,549,468 - 131,549,716UniSTSGRCh37
Build 365131,577,367 - 131,577,615RGDNCBI36
Celera5127,679,576 - 127,679,824RGD
Cytogenetic Map5q31UniSTS
HuRef5126,741,932 - 126,742,180UniSTS
REN69315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,549,685 - 131,549,936UniSTSGRCh37
Build 365131,577,584 - 131,577,835RGDNCBI36
Celera5127,679,793 - 127,680,044RGD
Cytogenetic Map5q31UniSTS
HuRef5126,742,149 - 126,742,400UniSTS
REN69316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,549,921 - 131,550,168UniSTSGRCh37
Build 365131,577,820 - 131,578,067RGDNCBI36
Celera5127,680,029 - 127,680,276RGD
Cytogenetic Map5q31UniSTS
HuRef5126,742,385 - 126,742,632UniSTS
REN69317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,550,158 - 131,550,386UniSTSGRCh37
Build 365131,578,057 - 131,578,285RGDNCBI36
Celera5127,680,266 - 127,680,494RGD
Cytogenetic Map5q31UniSTS
HuRef5126,742,622 - 126,742,850UniSTS
REN69318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,550,370 - 131,550,631UniSTSGRCh37
Build 365131,578,269 - 131,578,530RGDNCBI36
Celera5127,680,478 - 127,680,739RGD
Cytogenetic Map5q31UniSTS
HuRef5126,742,834 - 126,743,095UniSTS
REN69319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,550,610 - 131,550,860UniSTSGRCh37
Build 365131,578,509 - 131,578,759RGDNCBI36
Celera5127,680,718 - 127,680,968RGD
Cytogenetic Map5q31UniSTS
HuRef5126,743,074 - 126,743,324UniSTS
REN69320  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,550,840 - 131,551,090UniSTSGRCh37
Build 365131,578,739 - 131,578,989RGDNCBI36
Celera5127,680,948 - 127,681,198RGD
Cytogenetic Map5q31UniSTS
HuRef5126,743,304 - 126,743,554UniSTS
REN69321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,551,073 - 131,551,329UniSTSGRCh37
Build 365131,578,972 - 131,579,228RGDNCBI36
Celera5127,681,181 - 127,681,437RGD
Cytogenetic Map5q31UniSTS
HuRef5126,743,537 - 126,743,793UniSTS
REN69322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,551,316 - 131,551,542UniSTSGRCh37
Build 365131,579,215 - 131,579,441RGDNCBI36
Celera5127,681,424 - 127,681,650RGD
Cytogenetic Map5q31UniSTS
HuRef5126,743,780 - 126,744,006UniSTS
REN69323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,551,647 - 131,551,899UniSTSGRCh37
Build 365131,579,546 - 131,579,798RGDNCBI36
Celera5127,681,752 - 127,682,003RGD
Cytogenetic Map5q31UniSTS
HuRef5126,744,108 - 126,744,359UniSTS
REN69324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,551,939 - 131,552,163UniSTSGRCh37
Build 365131,579,838 - 131,580,062RGDNCBI36
Celera5127,682,043 - 127,682,267RGD
Cytogenetic Map5q31UniSTS
HuRef5126,744,399 - 126,744,623UniSTS
REN69325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,552,140 - 131,552,382UniSTSGRCh37
Build 365131,580,039 - 131,580,281RGDNCBI36
Celera5127,682,244 - 127,682,486RGD
Cytogenetic Map5q31UniSTS
HuRef5126,744,600 - 126,744,842UniSTS
REN69326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,552,357 - 131,552,597UniSTSGRCh37
Build 365131,580,256 - 131,580,496RGDNCBI36
Celera5127,682,461 - 127,682,701RGD
Cytogenetic Map5q31UniSTS
HuRef5126,744,817 - 126,745,057UniSTS
REN69327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,552,577 - 131,552,831UniSTSGRCh37
Build 365131,580,476 - 131,580,730RGDNCBI36
Celera5127,682,681 - 127,682,935RGD
Cytogenetic Map5q31UniSTS
HuRef5126,745,037 - 126,745,291UniSTS
REN69328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,552,778 - 131,553,034UniSTSGRCh37
Build 365131,580,677 - 131,580,933RGDNCBI36
Celera5127,682,882 - 127,683,138RGD
Cytogenetic Map5q31UniSTS
HuRef5126,745,238 - 126,745,494UniSTS
REN69329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,553,006 - 131,553,255UniSTSGRCh37
Build 365131,580,905 - 131,581,154RGDNCBI36
Celera5127,683,110 - 127,683,359RGD
Cytogenetic Map5q31UniSTS
HuRef5126,745,466 - 126,745,715UniSTS
REN69330  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,553,230 - 131,553,489UniSTSGRCh37
Build 365131,581,129 - 131,581,388RGDNCBI36
Celera5127,683,334 - 127,683,593RGD
Cytogenetic Map5q31UniSTS
HuRef5126,745,690 - 126,745,950UniSTS
REN69331  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,553,482 - 131,553,736UniSTSGRCh37
Build 365131,581,381 - 131,581,635RGDNCBI36
Celera5127,683,586 - 127,683,840RGD
Cytogenetic Map5q31UniSTS
HuRef5126,745,943 - 126,746,197UniSTS
REN69332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,553,713 - 131,553,952UniSTSGRCh37
Build 365131,581,612 - 131,581,851RGDNCBI36
Celera5127,683,817 - 127,684,056RGD
Cytogenetic Map5q31UniSTS
HuRef5126,746,174 - 126,746,413UniSTS
REN69333  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,553,927 - 131,554,174UniSTSGRCh37
Build 365131,581,826 - 131,582,073RGDNCBI36
Celera5127,684,031 - 127,684,278RGD
Cytogenetic Map5q31UniSTS
HuRef5126,746,388 - 126,746,635UniSTS
REN69334  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,554,142 - 131,554,379UniSTSGRCh37
Build 365131,582,041 - 131,582,278RGDNCBI36
Celera5127,684,246 - 127,684,483RGD
Cytogenetic Map5q31UniSTS
HuRef5126,746,603 - 126,746,840UniSTS
REN69335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,554,350 - 131,554,612UniSTSGRCh37
Build 365131,582,249 - 131,582,511RGDNCBI36
Celera5127,684,454 - 127,684,716RGD
Cytogenetic Map5q31UniSTS
HuRef5126,746,811 - 126,747,073UniSTS
REN69336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,554,589 - 131,554,855UniSTSGRCh37
Build 365131,582,488 - 131,582,754RGDNCBI36
Celera5127,684,693 - 127,684,959RGD
Cytogenetic Map5q31UniSTS
HuRef5126,747,050 - 126,747,316UniSTS
REN69337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,554,832 - 131,555,082UniSTSGRCh37
Build 365131,582,731 - 131,582,981RGDNCBI36
Celera5127,684,936 - 127,685,186RGD
Cytogenetic Map5q31UniSTS
HuRef5126,747,293 - 126,747,543UniSTS
REN69338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,555,057 - 131,555,286UniSTSGRCh37
Build 365131,582,956 - 131,583,185RGDNCBI36
Celera5127,685,161 - 127,685,390RGD
Cytogenetic Map5q31UniSTS
HuRef5126,747,518 - 126,747,747UniSTS
REN69339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,555,285 - 131,555,532UniSTSGRCh37
Build 365131,583,184 - 131,583,431RGDNCBI36
Celera5127,685,389 - 127,685,636RGD
Cytogenetic Map5q31UniSTS
HuRef5126,747,746 - 126,747,993UniSTS
REN69340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,555,503 - 131,555,751UniSTSGRCh37
Build 365131,583,402 - 131,583,650RGDNCBI36
Celera5127,685,607 - 127,685,855RGD
Cytogenetic Map5q31UniSTS
HuRef5126,747,964 - 126,748,212UniSTS
REN69341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,555,729 - 131,555,983UniSTSGRCh37
Build 365131,583,628 - 131,583,882RGDNCBI36
Celera5127,685,833 - 127,686,087RGD
Cytogenetic Map5q31UniSTS
HuRef5126,748,190 - 126,748,444UniSTS
REN69342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,555,975 - 131,556,222UniSTSGRCh37
Build 365131,583,874 - 131,584,121RGDNCBI36
Celera5127,686,079 - 127,686,326RGD
Cytogenetic Map5q31UniSTS
HuRef5126,748,436 - 126,748,683UniSTS
REN69343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,556,217 - 131,556,498UniSTSGRCh37
GRCh375131,556,217 - 131,556,465UniSTSGRCh37
Build 365131,584,116 - 131,584,364RGDNCBI36
Celera5127,686,321 - 127,686,602UniSTS
Celera5127,686,321 - 127,686,569RGD
Cytogenetic Map5q31UniSTS
HuRef5126,748,678 - 126,748,926UniSTS
HuRef5126,748,678 - 126,748,959UniSTS
REN69344  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,556,399 - 131,556,661UniSTSGRCh37
Build 365131,584,298 - 131,584,560RGDNCBI36
Celera5127,686,503 - 127,686,765RGD
Cytogenetic Map5q31UniSTS
HuRef5126,748,860 - 126,749,122UniSTS
REN69345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,556,628 - 131,556,888UniSTSGRCh37
Build 365131,584,527 - 131,584,787RGDNCBI36
Celera5127,686,732 - 127,686,992RGD
Cytogenetic Map5q31UniSTS
HuRef5126,749,089 - 126,749,349UniSTS
REN69346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,556,860 - 131,557,084UniSTSGRCh37
Build 365131,584,759 - 131,584,983RGDNCBI36
Celera5127,686,964 - 127,687,188RGD
Cytogenetic Map5q31UniSTS
HuRef5126,749,321 - 126,749,545UniSTS
REN69347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,557,053 - 131,557,277UniSTSGRCh37
Build 365131,584,952 - 131,585,176RGDNCBI36
Celera5127,687,157 - 127,687,381RGD
Cytogenetic Map5q31UniSTS
HuRef5126,749,514 - 126,749,738UniSTS
REN69348  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,557,245 - 131,557,493UniSTSGRCh37
Build 365131,585,144 - 131,585,392RGDNCBI36
Celera5127,687,349 - 127,687,597RGD
Cytogenetic Map5q31UniSTS
HuRef5126,749,706 - 126,749,954UniSTS
REN69349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,557,469 - 131,557,698UniSTSGRCh37
Build 365131,585,368 - 131,585,597RGDNCBI36
Celera5127,687,573 - 127,687,802RGD
Cytogenetic Map5q31UniSTS
HuRef5126,749,930 - 126,750,159UniSTS
REN69350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,557,674 - 131,557,923UniSTSGRCh37
Build 365131,585,573 - 131,585,822RGDNCBI36
Celera5127,687,778 - 127,688,027RGD
Cytogenetic Map5q31UniSTS
HuRef5126,750,135 - 126,750,384UniSTS
REN69351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,557,898 - 131,558,149UniSTSGRCh37
Build 365131,585,797 - 131,586,048RGDNCBI36
Celera5127,688,002 - 127,688,253RGD
Cytogenetic Map5q31UniSTS
HuRef5126,750,359 - 126,750,610UniSTS
REN69352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,558,126 - 131,558,365UniSTSGRCh37
Build 365131,586,025 - 131,586,264RGDNCBI36
Celera5127,688,230 - 127,688,469RGD
Cytogenetic Map5q31UniSTS
HuRef5126,750,587 - 126,750,826UniSTS
REN69353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,558,348 - 131,558,585UniSTSGRCh37
Build 365131,586,247 - 131,586,484RGDNCBI36
Celera5127,688,452 - 127,688,689RGD
Cytogenetic Map5q31UniSTS
HuRef5126,750,809 - 126,751,046UniSTS
REN69354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,558,555 - 131,558,825UniSTSGRCh37
Build 365131,586,454 - 131,586,724RGDNCBI36
Celera5127,688,659 - 127,688,929RGD
Cytogenetic Map5q31UniSTS
HuRef5126,751,016 - 126,751,286UniSTS
REN69355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,558,736 - 131,558,960UniSTSGRCh37
Build 365131,586,635 - 131,586,859RGDNCBI36
Celera5127,688,840 - 127,689,064RGD
Cytogenetic Map5q31UniSTS
HuRef5126,751,197 - 126,751,421UniSTS
REN69356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,559,015 - 131,559,279UniSTSGRCh37
Build 365131,586,914 - 131,587,178RGDNCBI36
Celera5127,689,119 - 127,689,383RGD
Cytogenetic Map5q31UniSTS
HuRef5126,751,476 - 126,751,740UniSTS
REN69357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,559,256 - 131,559,498UniSTSGRCh37
Build 365131,587,155 - 131,587,397RGDNCBI36
Celera5127,689,360 - 127,689,602RGD
Cytogenetic Map5q31UniSTS
HuRef5126,751,717 - 126,751,959UniSTS
REN69358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,559,484 - 131,559,723UniSTSGRCh37
Build 365131,587,383 - 131,587,622RGDNCBI36
Celera5127,689,588 - 127,689,827RGD
Cytogenetic Map5q31UniSTS
HuRef5126,751,945 - 126,752,184UniSTS
REN69359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,559,700 - 131,559,955UniSTSGRCh37
Build 365131,587,599 - 131,587,854RGDNCBI36
Celera5127,689,804 - 127,690,059RGD
Cytogenetic Map5q31UniSTS
HuRef5126,752,161 - 126,752,416UniSTS
REN69360  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,559,939 - 131,560,205UniSTSGRCh37
Build 365131,587,838 - 131,588,104RGDNCBI36
Celera5127,690,043 - 127,690,309RGD
Cytogenetic Map5q31UniSTS
HuRef5126,752,400 - 126,752,666UniSTS
REN69361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,560,184 - 131,560,408UniSTSGRCh37
Build 365131,588,083 - 131,588,307RGDNCBI36
Celera5127,690,288 - 127,690,512RGD
Cytogenetic Map5q31UniSTS
HuRef5126,752,645 - 126,752,869UniSTS
REN69362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,560,384 - 131,560,639UniSTSGRCh37
Build 365131,588,283 - 131,588,538RGDNCBI36
Celera5127,690,488 - 127,690,743RGD
Cytogenetic Map5q31UniSTS
HuRef5126,752,845 - 126,753,100UniSTS
REN69363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,560,625 - 131,560,865UniSTSGRCh37
Build 365131,588,524 - 131,588,764RGDNCBI36
Celera5127,690,729 - 127,690,969RGD
Cytogenetic Map5q31UniSTS
HuRef5126,753,086 - 126,753,326UniSTS
REN69364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,560,857 - 131,561,102UniSTSGRCh37
Build 365131,588,756 - 131,589,001RGDNCBI36
Celera5127,690,961 - 127,691,206RGD
Cytogenetic Map5q31UniSTS
HuRef5126,753,318 - 126,753,563UniSTS
REN69365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,561,090 - 131,561,316UniSTSGRCh37
Build 365131,588,989 - 131,589,215RGDNCBI36
Celera5127,691,194 - 127,691,420RGD
Cytogenetic Map5q31UniSTS
HuRef5126,753,551 - 126,753,777UniSTS
REN69366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,561,293 - 131,561,549UniSTSGRCh37
Build 365131,589,192 - 131,589,448RGDNCBI36
Celera5127,691,397 - 127,691,653RGD
Cytogenetic Map5q31UniSTS
HuRef5126,753,754 - 126,754,010UniSTS
REN69367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,561,525 - 131,561,757UniSTSGRCh37
Build 365131,589,424 - 131,589,656RGDNCBI36
Celera5127,691,629 - 127,691,861RGD
Cytogenetic Map5q31UniSTS
HuRef5126,753,986 - 126,754,218UniSTS
REN69368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,561,735 - 131,561,988UniSTSGRCh37
Build 365131,589,634 - 131,589,887RGDNCBI36
Celera5127,691,839 - 127,692,092RGD
Cytogenetic Map5q31UniSTS
HuRef5126,754,196 - 126,754,449UniSTS
REN69369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,561,939 - 131,562,167UniSTSGRCh37
Build 365131,589,838 - 131,590,066RGDNCBI36
Celera5127,692,043 - 127,692,271RGD
Cytogenetic Map5q31UniSTS
HuRef5126,754,400 - 126,754,628UniSTS
REN69370  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,562,145 - 131,562,384UniSTSGRCh37
Build 365131,590,044 - 131,590,283RGDNCBI36
Celera5127,692,249 - 127,692,488RGD
Cytogenetic Map5q31UniSTS
HuRef5126,754,606 - 126,754,845UniSTS
REN69371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,562,341 - 131,562,593UniSTSGRCh37
Build 365131,590,240 - 131,590,492RGDNCBI36
Celera5127,692,445 - 127,692,697RGD
Cytogenetic Map5q31UniSTS
HuRef5126,754,802 - 126,755,054UniSTS
REN69372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,562,570 - 131,562,817UniSTSGRCh37
Build 365131,590,469 - 131,590,716RGDNCBI36
Celera5127,692,674 - 127,692,921RGD
Cytogenetic Map5q31UniSTS
HuRef5126,755,031 - 126,755,278UniSTS
REN69373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,562,797 - 131,563,038UniSTSGRCh37
Build 365131,590,696 - 131,590,937RGDNCBI36
Celera5127,692,901 - 127,693,142RGD
Cytogenetic Map5q31UniSTS
HuRef5126,755,258 - 126,755,499UniSTS
REN69374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,562,985 - 131,563,246UniSTSGRCh37
Build 365131,590,884 - 131,591,145RGDNCBI36
Celera5127,693,089 - 127,693,350RGD
Cytogenetic Map5q31UniSTS
HuRef5126,755,446 - 126,755,707UniSTS
REN69375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,563,226 - 131,563,463UniSTSGRCh37
Build 365131,591,125 - 131,591,362RGDNCBI36
Celera5127,693,330 - 127,693,567RGD
Cytogenetic Map5q31UniSTS
HuRef5126,755,687 - 126,755,924UniSTS
REN69376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,563,274 - 131,563,498UniSTSGRCh37
Build 365131,591,173 - 131,591,397RGDNCBI36
Celera5127,693,378 - 127,693,602RGD
Cytogenetic Map5q31UniSTS
HuRef5126,755,735 - 126,755,959UniSTS
REN69377  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,563,925 - 131,564,152UniSTSGRCh37
Build 365131,591,824 - 131,592,051RGDNCBI36
Celera5127,694,029 - 127,694,256RGD
Cytogenetic Map5q31UniSTS
HuRef5126,756,386 - 126,756,613UniSTS
REN69378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,564,128 - 131,564,370UniSTSGRCh37
Build 365131,592,027 - 131,592,269RGDNCBI36
Celera5127,694,232 - 127,694,474RGD
Cytogenetic Map5q31UniSTS
HuRef5126,756,589 - 126,756,831UniSTS
REN69379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,564,348 - 131,564,587UniSTSGRCh37
Build 365131,592,247 - 131,592,486RGDNCBI36
Celera5127,694,452 - 127,694,691RGD
Cytogenetic Map5q31UniSTS
HuRef5126,756,809 - 126,757,048UniSTS
REN69380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,564,568 - 131,564,820UniSTSGRCh37
Build 365131,592,467 - 131,592,719RGDNCBI36
Celera5127,694,672 - 127,694,924RGD
Cytogenetic Map5q31UniSTS
HuRef5126,757,029 - 126,757,281UniSTS
REN69381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,564,817 - 131,565,048UniSTSGRCh37
Build 365131,592,716 - 131,592,947RGDNCBI36
Celera5127,694,921 - 127,695,152RGD
Cytogenetic Map5q31UniSTS
HuRef5126,757,278 - 126,757,509UniSTS
REN69382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,565,047 - 131,565,296UniSTSGRCh37
Build 365131,592,946 - 131,593,195RGDNCBI36
Celera5127,695,151 - 127,695,400RGD
Cytogenetic Map5q31UniSTS
HuRef5126,757,508 - 126,757,757UniSTS
REN69383  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,565,289 - 131,565,539UniSTSGRCh37
Build 365131,593,188 - 131,593,438RGDNCBI36
Celera5127,695,393 - 127,695,643RGD
Cytogenetic Map5q31UniSTS
HuRef5126,757,750 - 126,758,000UniSTS
stSG601097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,067 - 131,529,183UniSTSGRCh37
Build 365131,555,966 - 131,557,082RGDNCBI36
Celera5127,658,174 - 127,659,290RGD
HuRef5126,720,415 - 126,721,696UniSTS
stSG601098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,529,207 - 131,530,529UniSTSGRCh37
Build 365131,557,106 - 131,558,428RGDNCBI36
Celera5127,659,314 - 127,660,636RGD
HuRef5126,721,720 - 126,723,042UniSTS
stSG601099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,530,562 - 131,531,583UniSTSGRCh37
Build 365131,558,461 - 131,559,482RGDNCBI36
Celera5127,660,669 - 127,661,690RGD
HuRef5126,723,075 - 126,724,096UniSTS
stSG601100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,531,564 - 131,532,903UniSTSGRCh37
Build 365131,559,463 - 131,560,802RGDNCBI36
Celera5127,661,671 - 127,663,011RGD
HuRef5126,724,077 - 126,725,417UniSTS
stSG601101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,532,884 - 131,534,212UniSTSGRCh37
Build 365131,560,783 - 131,562,111RGDNCBI36
Celera5127,662,992 - 127,664,320RGD
HuRef5126,725,398 - 126,726,725UniSTS
stSG601102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,534,193 - 131,535,550UniSTSGRCh37
Build 365131,562,092 - 131,563,449RGDNCBI36
Celera5127,664,301 - 127,665,658RGD
HuRef5126,726,706 - 126,728,063UniSTS
stSG601103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,535,537 - 131,536,909UniSTSGRCh37
Build 365131,563,436 - 131,564,808RGDNCBI36
Celera5127,665,645 - 127,667,017RGD
HuRef5126,728,050 - 126,729,422UniSTS
stSG601104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,536,908 - 131,538,093UniSTSGRCh37
Build 365131,564,807 - 131,565,992RGDNCBI36
Celera5127,667,016 - 127,668,201RGD
HuRef5126,729,421 - 126,730,606UniSTS
stSG601105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,538,074 - 131,539,514UniSTSGRCh37
Build 365131,565,973 - 131,567,413RGDNCBI36
Celera5127,668,182 - 127,669,622RGD
HuRef5126,730,587 - 126,732,027UniSTS
stSG601106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,539,495 - 131,540,518UniSTSGRCh37
Build 365131,567,394 - 131,568,417RGDNCBI36
Celera5127,669,603 - 127,670,626RGD
HuRef5126,732,008 - 126,733,031UniSTS
stSG601107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,540,499 - 131,541,569UniSTSGRCh37
Build 365131,568,398 - 131,569,468RGDNCBI36
Celera5127,670,607 - 127,671,677RGD
HuRef5126,733,012 - 126,734,082UniSTS
stSG601108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,541,584 - 131,542,986UniSTSGRCh37
Build 365131,569,483 - 131,570,885RGDNCBI36
Celera5127,671,692 - 127,673,094RGD
HuRef5126,734,097 - 126,735,499UniSTS
stSG601110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,544,329 - 131,545,534UniSTSGRCh37
Build 365131,572,228 - 131,573,433RGDNCBI36
Celera5127,674,437 - 127,675,642RGD
HuRef5126,736,793 - 126,737,998UniSTS
stSG601111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,545,531 - 131,546,577UniSTSGRCh37
Build 365131,573,430 - 131,574,476RGDNCBI36
Celera5127,675,639 - 127,676,685RGD
HuRef5126,737,995 - 126,739,041UniSTS
stSG601112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,546,558 - 131,547,931UniSTSGRCh37
Build 365131,574,457 - 131,575,830RGDNCBI36
Celera5127,676,666 - 127,678,039RGD
HuRef5126,739,022 - 126,740,395UniSTS
stSG601113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,547,913 - 131,549,248UniSTSGRCh37
Build 365131,575,812 - 131,577,147RGDNCBI36
Celera5127,678,021 - 127,679,356RGD
HuRef5126,740,377 - 126,741,712UniSTS
stSG601114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,549,241 - 131,550,431UniSTSGRCh37
Build 365131,577,140 - 131,578,330RGDNCBI36
Celera5127,679,349 - 127,680,539RGD
HuRef5126,741,705 - 126,742,895UniSTS
stSG601115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,550,458 - 131,551,915UniSTSGRCh37
Build 365131,578,357 - 131,579,814RGDNCBI36
Celera5127,680,566 - 127,682,019RGD
HuRef5126,742,922 - 126,744,375UniSTS
stSG601116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,551,903 - 131,553,083UniSTSGRCh37
Build 365131,579,802 - 131,580,982RGDNCBI36
Celera5127,682,007 - 127,683,187RGD
HuRef5126,744,363 - 126,745,543UniSTS
stSG601117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,553,064 - 131,554,126UniSTSGRCh37
Build 365131,580,963 - 131,582,025RGDNCBI36
Celera5127,683,168 - 127,684,230RGD
HuRef5126,745,524 - 126,746,587UniSTS
stSG601118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,554,106 - 131,555,200UniSTSGRCh37
Build 365131,582,005 - 131,583,099RGDNCBI36
Celera5127,684,210 - 127,685,304RGD
HuRef5126,746,567 - 126,747,661UniSTS
stSG601119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,555,181 - 131,556,557UniSTSGRCh37
Build 365131,583,080 - 131,584,456RGDNCBI36
Celera5127,685,285 - 127,686,661RGD
HuRef5126,747,642 - 126,749,018UniSTS
stSG601120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,556,556 - 131,557,618UniSTSGRCh37
Build 365131,584,455 - 131,585,517RGDNCBI36
Celera5127,686,660 - 127,687,722RGD
HuRef5126,749,017 - 126,750,079UniSTS
stSG601121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,557,601 - 131,558,624UniSTSGRCh37
Build 365131,585,500 - 131,586,523RGDNCBI36
Celera5127,687,705 - 127,688,728RGD
HuRef5126,750,062 - 126,751,085UniSTS
stSG601122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,558,605 - 131,559,785UniSTSGRCh37
Build 365131,586,504 - 131,587,684RGDNCBI36
Celera5127,688,709 - 127,689,889RGD
HuRef5126,751,066 - 126,752,246UniSTS
stSG601123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,559,766 - 131,561,056UniSTSGRCh37
Build 365131,587,665 - 131,588,955RGDNCBI36
Celera5127,689,870 - 127,691,160RGD
HuRef5126,752,227 - 126,753,517UniSTS
stSG601124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,561,037 - 131,562,138UniSTSGRCh37
Build 365131,588,936 - 131,590,037RGDNCBI36
Celera5127,691,141 - 127,692,242RGD
HuRef5126,753,498 - 126,754,599UniSTS
RH18422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,531,722 - 131,531,896UniSTSGRCh37
Build 365131,559,621 - 131,559,795RGDNCBI36
Celera5127,661,829 - 127,662,003RGD
Cytogenetic Map5q31UniSTS
HuRef5126,724,235 - 126,724,409UniSTS
GeneMap99-GB4 RH Map5509.47UniSTS
RH18238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,377 - 131,528,599UniSTSGRCh37
Build 365131,556,276 - 131,556,498RGDNCBI36
Celera5127,658,484 - 127,658,706RGD
Cytogenetic Map5q31UniSTS
HuRef5126,720,725 - 126,720,947UniSTS
GeneMap99-GB4 RH Map5509.47UniSTS
WI-14188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,338 - 131,528,463UniSTSGRCh37
Build 365131,556,237 - 131,556,362RGDNCBI36
Celera5127,658,445 - 127,658,570RGD
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5q31UniSTS
HuRef5126,720,686 - 126,720,811UniSTS
GeneMap99-GB4 RH Map5504.3UniSTS
Whitehead-RH Map5416.9UniSTS
P4HA2__5805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375131,528,271 - 131,528,719UniSTSGRCh37
Build 365131,556,170 - 131,556,618RGDNCBI36
Celera5127,658,378 - 127,658,826RGD
HuRef5126,720,619 - 126,721,067UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High
Medium 1182 1465 505 183 216 83 1325 566 630 241 617 988 114 254 1015 2
Low 1248 928 1204 432 990 374 3031 1624 2975 176 831 621 58 1 950 1773 2
Below cutoff 3 588 17 7 678 8 3 110 2 5 3 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_052887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001017974 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142599 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001365677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001365678 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001365679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001365680 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001365681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_004199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005272117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005272118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005272119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005272120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006714728 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC034220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC063976 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ314859 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AU117989 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY358970 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC017062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC025960 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC035813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI758477 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647924 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA544450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U90441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000166534   ⟹   ENSP00000166534
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,192,610 - 132,227,857 (-)Ensembl
RefSeq Acc Id: ENST00000360568   ⟹   ENSP00000353772
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,190,147 - 132,227,853 (-)Ensembl
RefSeq Acc Id: ENST00000379086   ⟹   ENSP00000368379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,192,610 - 132,227,819 (-)Ensembl
RefSeq Acc Id: ENST00000379100   ⟹   ENSP00000368394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,192,613 - 132,227,835 (-)Ensembl
RefSeq Acc Id: ENST00000379104   ⟹   ENSP00000368398
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,190,147 - 132,227,853 (-)Ensembl
RefSeq Acc Id: ENST00000395164   ⟹   ENSP00000378593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,210,490 - 132,222,091 (-)Ensembl
RefSeq Acc Id: ENST00000401867   ⟹   ENSP00000384999
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,191,838 - 132,227,815 (-)Ensembl
RefSeq Acc Id: ENST00000416053   ⟹   ENSP00000394953
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,217,223 - 132,277,600 (-)Ensembl
RefSeq Acc Id: ENST00000417528   ⟹   ENSP00000389523
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,210,380 - 132,227,794 (-)Ensembl
RefSeq Acc Id: ENST00000418055   ⟹   ENSP00000403883
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,214,041 - 132,227,835 (-)Ensembl
RefSeq Acc Id: ENST00000428369   ⟹   ENSP00000396495
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,192,709 - 132,227,561 (-)Ensembl
RefSeq Acc Id: ENST00000428841   ⟹   ENSP00000395956
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,217,779 - 132,228,258 (-)Ensembl
RefSeq Acc Id: ENST00000431054   ⟹   ENSP00000391257
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,210,381 - 132,295,271 (-)Ensembl
RefSeq Acc Id: ENST00000439698   ⟹   ENSP00000405406
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,210,441 - 132,277,855 (-)Ensembl
RefSeq Acc Id: ENST00000453286   ⟹   ENSP00000413542
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,213,924 - 132,227,839 (-)Ensembl
RefSeq Acc Id: ENST00000467587
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,193,041 - 132,195,730 (-)Ensembl
RefSeq Acc Id: ENST00000471826
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,248,907 - 132,295,315 (-)Ensembl
RefSeq Acc Id: ENST00000474628
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,192,671 - 132,195,258 (-)Ensembl
RefSeq Acc Id: ENST00000478055
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,217,197 - 132,227,262 (-)Ensembl
RefSeq Acc Id: ENST00000481636
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,277,209 - 132,277,922 (-)Ensembl
RefSeq Acc Id: ENST00000506807
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5132,192,986 - 132,193,568 (-)Ensembl
RefSeq Acc Id: NM_001017974   ⟹   NP_001017974
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,190,147 - 132,227,853 (-)NCBI
GRCh375131,528,299 - 131,563,556 (-)NCBI
Build 365131,556,202 - 131,591,455 (-)NCBI Archive
Celera5127,658,410 - 127,693,660 (-)RGD
HuRef5126,720,651 - 126,756,017 (-)ENTREZGENE
CHM1_15130,961,055 - 130,996,320 (-)NCBI
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142598   ⟹   NP_001136070
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,190,147 - 132,227,853 (-)NCBI
GRCh375131,528,299 - 131,563,556 (-)NCBI
Celera5127,658,410 - 127,693,660 (-)RGD
HuRef5126,720,651 - 126,756,017 (-)ENTREZGENE
CHM1_15130,961,055 - 130,996,320 (-)NCBI
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142599   ⟹   NP_001136071
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,190,147 - 132,227,853 (-)NCBI
GRCh375131,528,299 - 131,563,556 (-)NCBI
Celera5127,658,410 - 127,693,660 (-)RGD
HuRef5126,720,651 - 126,756,017 (-)ENTREZGENE
CHM1_15130,961,055 - 130,996,320 (-)NCBI
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001365677   ⟹   NP_001352606
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,190,147 - 132,227,853 (-)NCBI
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001365678   ⟹   NP_001352607
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,190,147 - 132,227,853 (-)NCBI
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001365679   ⟹   NP_001352608
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,190,147 - 132,227,853 (-)NCBI
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001365680   ⟹   NP_001352609
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,190,147 - 132,227,853 (-)NCBI
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001365681   ⟹   NP_001352610
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,190,147 - 132,227,853 (-)NCBI
T2T-CHM13v2.05132,710,021 - 132,747,731 (-)NCBI
Sequence:
RefSeq Acc Id: NM_004199   ⟹   NP_004190
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,190,147 - 132,227,091 (-)NCBI
GRCh375131,528,299 - 131,563,556 (-)NCBI
Build 365131,556,202 - 131,590,834 (-)NCBI Archive
Celera5127,658,410 - 127,693,660 (-)RGD
HuRef5126,720,651 - 126,756,017 (-)ENTREZGENE
CHM1_15130,961,055 - 130,995,699 (-)NCBI
T2T-CHM13v2.05132,710,021 - 132,746,969 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001017974 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136070 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136071 (Get FASTA)   NCBI Sequence Viewer  
  NP_001352606 (Get FASTA)   NCBI Sequence Viewer  
  NP_001352607 (Get FASTA)   NCBI Sequence Viewer  
  NP_001352608 (Get FASTA)   NCBI Sequence Viewer  
  NP_001352609 (Get FASTA)   NCBI Sequence Viewer  
  NP_001352610 (Get FASTA)   NCBI Sequence Viewer  
  NP_004190 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB71339 (Get FASTA)   NCBI Sequence Viewer  
  AAH17062 (Get FASTA)   NCBI Sequence Viewer  
  AAH35813 (Get FASTA)   NCBI Sequence Viewer  
  AAQ89329 (Get FASTA)   NCBI Sequence Viewer  
  CAC85688 (Get FASTA)   NCBI Sequence Viewer  
  CAC85689 (Get FASTA)   NCBI Sequence Viewer  
  CAI46066 (Get FASTA)   NCBI Sequence Viewer  
  EAW62341 (Get FASTA)   NCBI Sequence Viewer  
  EAW62342 (Get FASTA)   NCBI Sequence Viewer  
  EAW62343 (Get FASTA)   NCBI Sequence Viewer  
  EAW62344 (Get FASTA)   NCBI Sequence Viewer  
  EAW62345 (Get FASTA)   NCBI Sequence Viewer  
  EAW62346 (Get FASTA)   NCBI Sequence Viewer  
  EAW62347 (Get FASTA)   NCBI Sequence Viewer  
  EAW62348 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000166534
  ENSP00000166534.4
  ENSP00000353772
  ENSP00000353772.3
  ENSP00000368379
  ENSP00000368379.1
  ENSP00000368394
  ENSP00000368394.2
  ENSP00000368398
  ENSP00000368398.2
  ENSP00000378593.1
  ENSP00000384999
  ENSP00000384999.1
  ENSP00000389523.1
  ENSP00000391257.1
  ENSP00000394953.1
  ENSP00000395956.1
  ENSP00000396495.1
  ENSP00000403883.1
  ENSP00000405406.1
  ENSP00000413542.1
GenBank Protein O15460 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001136070   ⟸   NM_001142598
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5HYD8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136071   ⟸   NM_001142599
- Peptide Label: isoform 1 precursor
- UniProtKB: D3DQ86 (UniProtKB/Swiss-Prot),   D3DQ85 (UniProtKB/Swiss-Prot),   Q8WWN0 (UniProtKB/Swiss-Prot),   O15460 (UniProtKB/Swiss-Prot),   Q5HYD8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001017974   ⟸   NM_001017974
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5HYD8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_004190   ⟸   NM_004199
- Peptide Label: isoform 1 precursor
- UniProtKB: D3DQ86 (UniProtKB/Swiss-Prot),   D3DQ85 (UniProtKB/Swiss-Prot),   Q8WWN0 (UniProtKB/Swiss-Prot),   O15460 (UniProtKB/Swiss-Prot),   Q5HYD8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001352610   ⟸   NM_001365681
- Peptide Label: isoform 3 precursor
- UniProtKB: Q5HYD8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001352606   ⟸   NM_001365677
- Peptide Label: isoform 1 precursor
- UniProtKB: O15460 (UniProtKB/Swiss-Prot),   D3DQ86 (UniProtKB/Swiss-Prot),   D3DQ85 (UniProtKB/Swiss-Prot),   Q8WWN0 (UniProtKB/Swiss-Prot),   Q5HYD8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001352609   ⟸   NM_001365680
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5HYD8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001352607   ⟸   NM_001365678
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5HYD8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001352608   ⟸   NM_001365679
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5HYD8 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000405406   ⟸   ENST00000439698
RefSeq Acc Id: ENSP00000353772   ⟸   ENST00000360568
RefSeq Acc Id: ENSP00000395956   ⟸   ENST00000428841
RefSeq Acc Id: ENSP00000396495   ⟸   ENST00000428369
RefSeq Acc Id: ENSP00000413542   ⟸   ENST00000453286
RefSeq Acc Id: ENSP00000384999   ⟸   ENST00000401867
RefSeq Acc Id: ENSP00000166534   ⟸   ENST00000166534
RefSeq Acc Id: ENSP00000394953   ⟸   ENST00000416053
RefSeq Acc Id: ENSP00000389523   ⟸   ENST00000417528
RefSeq Acc Id: ENSP00000403883   ⟸   ENST00000418055
RefSeq Acc Id: ENSP00000368379   ⟸   ENST00000379086
RefSeq Acc Id: ENSP00000368398   ⟸   ENST00000379104
RefSeq Acc Id: ENSP00000368394   ⟸   ENST00000379100
RefSeq Acc Id: ENSP00000391257   ⟸   ENST00000431054
RefSeq Acc Id: ENSP00000378593   ⟸   ENST00000395164
Protein Domains
Fe2OG dioxygenase   Prolyl 4-hydroxylase alpha-subunit N-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O15460-F1-model_v2 AlphaFold O15460 1-535 view protein structure

Promoters
RGD ID:6851602
Promoter ID:EP73603
Type:initiation region
Name:HS_P4HA2
Description:Procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline4-hydroxylase), alpha polypeptide II.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:NEDO full length human cDNA sequencing project.; Oligo-capping
Position:
Human AssemblyChrPosition (strand)Source
Build 365131,591,440 - 131,591,500EPD
RGD ID:6803041
Promoter ID:HG_KWN:51026
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:ENST00000166534,   ENST00000358760,   ENST00000379086,   ENST00000401867,   NM_001017973,   NM_004199,   OTTHUMT00000132654,   OTTHUMT00000132657,   OTTHUMT00000132658,   OTTHUMT00000157390,   OTTHUMT00000157391,   OTTHUMT00000315750,   OTTHUMT00000315752,   UC003KWI.1,   UC003KWK.1
Position:
Human AssemblyChrPosition (strand)Source
Build 365131,591,446 - 131,592,322 (-)MPROMDB
RGD ID:6870498
Promoter ID:EPDNEW_H8414
Type:initiation region
Name:P4HA2_1
Description:prolyl 4-hydroxylase subunit alpha 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8418  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh385132,227,851 - 132,227,911EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8547 AgrOrtholog
COSMIC P4HA2 COSMIC
Ensembl Genes ENSG00000072682 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000166534 ENTREZGENE
  ENST00000166534.8 UniProtKB/Swiss-Prot
  ENST00000360568 ENTREZGENE
  ENST00000360568.8 UniProtKB/Swiss-Prot
  ENST00000379086 ENTREZGENE
  ENST00000379086.5 UniProtKB/Swiss-Prot
  ENST00000379100 ENTREZGENE
  ENST00000379100.7 UniProtKB/Swiss-Prot
  ENST00000379104 ENTREZGENE
  ENST00000379104.7 UniProtKB/Swiss-Prot
  ENST00000395164.5 UniProtKB/TrEMBL
  ENST00000401867 ENTREZGENE
  ENST00000401867.5 UniProtKB/Swiss-Prot
  ENST00000416053.5 UniProtKB/TrEMBL
  ENST00000417528.5 UniProtKB/TrEMBL
  ENST00000418055.5 UniProtKB/TrEMBL
  ENST00000428369.6 UniProtKB/TrEMBL
  ENST00000428841.1 UniProtKB/TrEMBL
  ENST00000431054.5 UniProtKB/TrEMBL
  ENST00000439698.5 UniProtKB/TrEMBL
  ENST00000453286.5 UniProtKB/TrEMBL
Gene3D-CATH 1.25.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  6.10.140.1460 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  q2cbj1_9rhob like domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000072682 GTEx
HGNC ID HGNC:8547 ENTREZGENE
Human Proteome Map P4HA2 Human Proteome Map
InterPro Oxoglu/Fe-dep_dioxygenase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P4HA-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pro_4_hyd_alph UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pro_4_hyd_alph_FE2OG_OXY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pro_4_hyd_alph_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TPR-like_helical_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TPR_repeat UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8974 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 8974 ENTREZGENE
OMIM 600608 OMIM
PANTHER PROLYL 4-HYDROXYLASE SUBUNIT ALPHA-2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10869 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 2OG-FeII_Oxy_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P4Ha_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32875 PharmGKB
PROSITE FE2OG_OXY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROKAR_LIPOPROTEIN UniProtKB/TrEMBL
  TPR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TPR_REGION UniProtKB/Swiss-Prot
SMART P4Hc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48452 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8MXE0_HUMAN UniProtKB/TrEMBL
  C9JCP0_HUMAN UniProtKB/TrEMBL
  C9JFJ1_HUMAN UniProtKB/TrEMBL
  C9JIG4_HUMAN UniProtKB/TrEMBL
  C9JN43_HUMAN UniProtKB/TrEMBL
  C9JX45_HUMAN UniProtKB/TrEMBL
  D3DQ85 ENTREZGENE
  D3DQ86 ENTREZGENE
  E7ENX0_HUMAN UniProtKB/TrEMBL
  E7EPI9_HUMAN UniProtKB/TrEMBL
  E7ERI1_HUMAN UniProtKB/TrEMBL
  O15460 ENTREZGENE, UniProtKB/Swiss-Prot
  Q05DA4_HUMAN UniProtKB/TrEMBL
  Q5HYD8 ENTREZGENE, UniProtKB/TrEMBL
  Q8WWN0 ENTREZGENE
UniProt Secondary D3DQ85 UniProtKB/Swiss-Prot
  D3DQ86 UniProtKB/Swiss-Prot
  Q8WWN0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-02 P4HA2  prolyl 4-hydroxylase subunit alpha 2  P4HA2  prolyl 4-hydroxylase, alpha polypeptide II  Symbol and/or name change 5135510 APPROVED