FLVCR2 (FLVCR heme transporter 2) - Rat Genome Database

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Gene: FLVCR2 (FLVCR heme transporter 2) Homo sapiens
Analyze
Symbol: FLVCR2
Name: FLVCR heme transporter 2
RGD ID: 1352163
HGNC Page HGNC
Description: Exhibits heme binding activity and heme transmembrane transporter activity. Predicted to be involved in heme export. Predicted to localize to integral component of membrane and plasma membrane. Implicated in proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: C14orf58; calcium-chelate transporter; CCT; EPV; feline leukemia virus subgroup C cellular receptor 2; feline leukemia virus subgroup C cellular receptor family member 2; feline leukemia virus subgroup C cellular receptor family, member 2; feline leukemia virus subgroup C receptor-related protein 2; feline virus subgoup C receptor 2; FLJ20371; FLVCRL14q; MFSD7C; PVHH; SLC49A2
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
GRCh38.p13 Ensembl1475,578,620 - 75,663,214 (+)EnsemblGRCh38hg38GRCh38
GRCh381475,578,620 - 75,648,167 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371476,044,963 - 76,114,510 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361475,114,745 - 75,184,263 (+)NCBINCBI36hg18NCBI36
Build 341475,114,744 - 75,184,260NCBI
Celera1456,083,035 - 56,152,616 (+)NCBI
Cytogenetic Map14q24.3NCBI
HuRef1456,212,884 - 56,282,462 (+)NCBIHuRef
CHM1_11475,982,702 - 76,052,275 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

Additional References at PubMed
PMID:55640   PMID:10737800   PMID:12477932   PMID:12508121   PMID:14702039   PMID:14729055   PMID:15489334   PMID:16344560   PMID:16439531   PMID:20206334   PMID:20690116   PMID:20823265  
PMID:20967262   PMID:21873635   PMID:22658674   PMID:25131804   PMID:25677735   PMID:25906927   PMID:28514442   PMID:32973183  


Genomics

Comparative Map Data
FLVCR2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1475,578,620 - 75,663,214 (+)EnsemblGRCh38hg38GRCh38
GRCh381475,578,620 - 75,648,167 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371476,044,963 - 76,114,510 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361475,114,745 - 75,184,263 (+)NCBINCBI36hg18NCBI36
Build 341475,114,744 - 75,184,260NCBI
Celera1456,083,035 - 56,152,616 (+)NCBI
Cytogenetic Map14q24.3NCBI
HuRef1456,212,884 - 56,282,462 (+)NCBIHuRef
CHM1_11475,982,702 - 76,052,275 (+)NCBICHM1_1
Flvcr2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391285,793,313 - 85,860,359 (+)NCBIGRCm39mm39
GRCm39 Ensembl1285,793,313 - 85,860,359 (+)Ensembl
GRCm381285,746,539 - 85,813,586 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1285,746,539 - 85,813,585 (+)EnsemblGRCm38mm10GRCm38
MGSCv371287,087,489 - 87,154,535 (+)NCBIGRCm37mm9NCBIm37
MGSCv361286,635,642 - 86,702,688 (+)NCBImm8
Celera1287,206,720 - 87,273,824 (+)NCBICelera
Cytogenetic Map12D2NCBI
Flvcr2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.26105,408,355 - 105,472,355 (+)NCBI
Rnor_6.0 Ensembl6109,617,355 - 109,681,495 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.06109,617,348 - 109,681,495 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.06118,926,062 - 118,989,790 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.46109,853,763 - 109,933,029 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.16109,857,466 - 109,935,200 (+)NCBI
Celera6103,235,369 - 103,299,032 (+)NCBICelera
Cytogenetic Map6q31NCBI
Flvcr2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495561246,724 - 97,729 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495561246,723 - 99,012 (+)NCBIChiLan1.0ChiLan1.0
FLVCR2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11474,975,027 - 75,045,971 (+)NCBIpanpan1.1PanPan1.1panPan2
Mhudiblu_PPA_v01456,132,370 - 56,209,882 (+)NCBIMhudiblu_PPA_v0panPan3
FLVCR2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1848,588,294 - 48,640,339 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl848,587,863 - 48,653,488 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha848,266,908 - 48,323,256 (+)NCBI
ROS_Cfam_1.0848,808,288 - 48,864,727 (+)NCBI
UMICH_Zoey_3.1848,481,173 - 48,537,580 (+)NCBI
UNSW_CanFamBas_1.0848,502,591 - 48,559,009 (+)NCBI
UU_Cfam_GSD_1.0848,898,900 - 48,955,237 (+)NCBI
Flvcr2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864027,356,714 - 27,415,105 (-)NCBI
SpeTri2.0NW_0049364884,653,891 - 4,713,982 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FLVCR2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl798,718,095 - 98,823,839 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1798,718,319 - 98,772,196 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.27104,423,885 - 104,479,246 (+)NCBISscrofa10.2Sscrofa10.2susScr3
FLVCR2
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12452,820,221 - 52,892,367 (+)NCBI
ChlSab1.1 Ensembl2452,820,592 - 52,890,667 (+)Ensembl
Flvcr2
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473426,033,790 - 26,085,027 (-)NCBI

Position Markers
SHGC-34049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371476,067,829 - 76,067,978UniSTSGRCh37
Build 361475,137,582 - 75,137,731RGDNCBI36
Celera1456,105,925 - 56,106,074RGD
Cytogenetic Map14q24.3UniSTS
HuRef1456,235,775 - 56,235,924UniSTS
Stanford-G3 RH Map142781.0UniSTS
GeneMap99-GB4 RH Map14201.29UniSTS
Whitehead-RH Map14268.9UniSTS
NCBI RH Map14847.9UniSTS
GeneMap99-G3 RH Map142829.0UniSTS
RH75673  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371476,088,791 - 76,089,036UniSTSGRCh37
Build 361475,158,544 - 75,158,789RGDNCBI36
Celera1456,126,903 - 56,127,148RGD
Cytogenetic Map14q24.3UniSTS
HuRef1456,256,749 - 56,256,994UniSTS
A004T16  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371476,114,276 - 76,114,486UniSTSGRCh37
Build 361475,184,029 - 75,184,239RGDNCBI36
Celera1456,152,380 - 56,152,590RGD
Cytogenetic Map14q24.3UniSTS
HuRef1456,282,226 - 56,282,436UniSTS
GeneMap99-GB4 RH Map14201.09UniSTS
Whitehead-RH Map14268.5UniSTS
STS-T79170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371476,113,200 - 76,113,448UniSTSGRCh37
Build 361475,182,953 - 75,183,201RGDNCBI36
Celera1456,151,304 - 56,151,552RGD
Cytogenetic Map14q24.3UniSTS
HuRef1456,281,150 - 56,281,398UniSTS
GeneMap99-GB4 RH Map14201.29UniSTS
GDB:434012  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q31.2-q33.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map10p11.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map14q31UniSTS
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
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Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
RH91415  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q24.3UniSTS
HuRef1456,282,161 - 56,282,283UniSTS
GeneMap99-GB4 RH Map14200.99UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3034
Count of miRNA genes:1007
Interacting mature miRNAs:1254
Transcripts:ENST00000238667, ENST00000539311, ENST00000553341, ENST00000553587, ENST00000554496, ENST00000554580, ENST00000555027, ENST00000555058, ENST00000555385, ENST00000556241, ENST00000556409, ENST00000556745, ENST00000556856
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.


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 285 198 524 216 515 170 1158 142 678 59 437 530 46 72 965 4
Low 2034 2591 1191 406 1306 293 3136 1939 2196 349 987 992 123 1132 1778 1
Below cutoff 113 196 6 1 78 1 58 111 827 11 24 58 3 1 45 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000238667   ⟹   ENSP00000238667
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,578,620 - 75,648,167 (+)Ensembl
RefSeq Acc Id: ENST00000539311   ⟹   ENSP00000443439
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,605,462 - 75,646,618 (+)Ensembl
RefSeq Acc Id: ENST00000553341   ⟹   ENSP00000452584
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,622,058 - 75,641,897 (+)Ensembl
RefSeq Acc Id: ENST00000553587   ⟹   ENSP00000451603
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,622,060 - 75,663,164 (+)Ensembl
RefSeq Acc Id: ENST00000554496
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,579,456 - 75,646,655 (+)Ensembl
RefSeq Acc Id: ENST00000554580   ⟹   ENSP00000451781
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,631,714 - 75,641,898 (+)Ensembl
RefSeq Acc Id: ENST00000555027   ⟹   ENSP00000452453
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,632,610 - 75,646,633 (+)Ensembl
RefSeq Acc Id: ENST00000555058   ⟹   ENSP00000451104
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,605,815 - 75,633,697 (+)Ensembl
RefSeq Acc Id: ENST00000555385
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,579,584 - 75,663,214 (+)Ensembl
RefSeq Acc Id: ENST00000556241
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,622,058 - 75,663,164 (+)Ensembl
RefSeq Acc Id: ENST00000556409
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,632,627 - 75,639,462 (+)Ensembl
RefSeq Acc Id: ENST00000556745
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,640,732 - 75,641,976 (+)Ensembl
RefSeq Acc Id: ENST00000556856   ⟹   ENSP00000452468
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,622,092 - 75,647,150 (+)Ensembl
RefSeq Acc Id: NM_001195283   ⟹   NP_001182212
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,605,540 - 75,648,167 (+)NCBI
GRCh371476,044,940 - 76,114,512 (+)ENTREZGENE
HuRef1456,212,884 - 56,282,462 (+)ENTREZGENE
CHM1_11476,009,568 - 76,052,275 (+)NCBI
Sequence:
RefSeq Acc Id: NM_017791   ⟹   NP_060261
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,578,620 - 75,648,167 (+)NCBI
GRCh371476,044,940 - 76,114,512 (+)RGD
Build 361475,114,745 - 75,184,263 (+)NCBI Archive
Celera1456,083,035 - 56,152,616 (+)RGD
HuRef1456,212,884 - 56,282,462 (+)ENTREZGENE
CHM1_11475,982,702 - 76,052,275 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_060261   ⟸   NM_017791
- Peptide Label: isoform 1
- UniProtKB: Q9UPI3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001182212   ⟸   NM_001195283
- Peptide Label: isoform 2
- UniProtKB: Q9UPI3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000452453   ⟸   ENST00000555027
RefSeq Acc Id: ENSP00000451104   ⟸   ENST00000555058
RefSeq Acc Id: ENSP00000452468   ⟸   ENST00000556856
RefSeq Acc Id: ENSP00000443439   ⟸   ENST00000539311
RefSeq Acc Id: ENSP00000238667   ⟸   ENST00000238667
RefSeq Acc Id: ENSP00000452584   ⟸   ENST00000553341
RefSeq Acc Id: ENSP00000451603   ⟸   ENST00000553587
RefSeq Acc Id: ENSP00000451781   ⟸   ENST00000554580
Protein Domains
MFS

Promoters
RGD ID:6791588
Promoter ID:HG_KWN:19822
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid,   NB4
Transcripts:NM_017791
Position:
Human AssemblyChrPosition (strand)Source
Build 361475,114,501 - 75,115,001 (+)MPROMDB
RGD ID:7228193
Promoter ID:EPDNEW_H19842
Type:initiation region
Name:FLVCR2_1
Description:feline leukemia virus subgroup C cellular receptor family member2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,578,625 - 75,578,685EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_017791.3(FLVCR2):c.402C>G (p.Tyr134Ter) single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000023841] Chr14:75579374 [GRCh38]
Chr14:76045717 [GRCh37]
Chr14:14q24.3
pathogenic
NM_017791.3(FLVCR2):c.1289C>G (p.Thr430Arg) single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000001145] Chr14:75641008 [GRCh38]
Chr14:76107351 [GRCh37]
Chr14:14q24.3
pathogenic
NM_017791.2(FLVCR2):c.329_334delACATCT (p.Asn110_Phe112delinsIle) deletion Posterior column ataxia-retinitis pigmentosa syndrome [RCV000778098]|Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000001146] Chr14:75579301..75579306 [GRCh38]
Chr14:76045644..76045649 [GRCh37]
Chr14:14q24.3
pathogenic|uncertain significance
NM_017791.3(FLVCR2):c.1192C>G (p.Leu398Val) single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000001147] Chr14:75639419 [GRCh38]
Chr14:76105762 [GRCh37]
Chr14:14q24.3
pathogenic
NM_017791.3(FLVCR2):c.473C>A (p.Ser158Ter) single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000001148] Chr14:75579445 [GRCh38]
Chr14:76045788 [GRCh37]
Chr14:14q24.3
pathogenic
NM_017791.3(FLVCR2):c.839C>G (p.Pro280Arg) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000778099]|Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000001149] Chr14:75624639 [GRCh38]
Chr14:76090982 [GRCh37]
Chr14:14q24.3
pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_017791.3(FLVCR2):c.977C>T (p.Ala326Val) single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000001150] Chr14:75633653 [GRCh38]
Chr14:76099996 [GRCh37]
Chr14:14q24.3
pathogenic
NM_017791.3(FLVCR2):c.1341+2T>C single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000001151] Chr14:75641062 [GRCh38]
Chr14:76107405 [GRCh37]
Chr14:14q24.3
pathogenic
GRCh38/hg38 14q24.3(chr14:73877072-78042422)x1 copy number loss See cases [RCV000051548] Chr14:73877072..78042422 [GRCh38]
Chr14:74343775..78508765 [GRCh37]
Chr14:73413528..77578518 [NCBI36]
Chr14:14q24.3
pathogenic
GRCh38/hg38 14q24.3-31.1(chr14:75489052-79610332)x1 copy number loss See cases [RCV000051549] Chr14:75489052..79610332 [GRCh38]
Chr14:75955395..80076675 [GRCh37]
Chr14:75025148..79146428 [NCBI36]
Chr14:14q24.3-31.1
pathogenic
GRCh38/hg38 14q24.2-32.2(chr14:72787506-99596719)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|See cases [RCV000052293] Chr14:72787506..99596719 [GRCh38]
Chr14:73254214..100063056 [GRCh37]
Chr14:72323967..99132809 [NCBI36]
Chr14:14q24.2-32.2
pathogenic
GRCh38/hg38 14q24.3(chr14:75489052-75967965)x3 copy number gain See cases [RCV000052084] Chr14:75489052..75967965 [GRCh38]
Chr14:75955395..76434308 [GRCh37]
Chr14:75025148..75504061 [NCBI36]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.376C>T (p.Leu126=) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000377875]|not specified [RCV000081863] Chr14:75579348 [GRCh38]
Chr14:76045691 [GRCh37]
Chr14:14q24.3
benign|likely benign
NM_017791.3(FLVCR2):c.47T>C (p.Val16Ala) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000326404]|not specified [RCV000081864] Chr14:75579019 [GRCh38]
Chr14:76045362 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.543G>A (p.Val181=) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000373082]|not specified [RCV000081865] Chr14:75579515 [GRCh38]
Chr14:76045858 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.648C>G (p.Ser216=) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000338326]|not specified [RCV000081866] Chr14:75579620 [GRCh38]
Chr14:76045963 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.998G>A (p.Arg333His) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120376]|not provided [RCV000171224] Chr14:75633674 [GRCh38]
Chr14:76100017 [GRCh37]
Chr14:14q24.3
likely pathogenic|uncertain significance
GRCh37/hg19 14q24.2-q24.3(chr14:73152115..77698582) deletion Intellectual disability, mild [RCV000190520] Chr14:73152115..77698582 [GRCh37]
Chr14:14q24.2-24.3
pathogenic|likely pathogenic
GRCh38/hg38 14q24.1-31.1(chr14:69562099-81975384)x1 copy number loss See cases [RCV000134154] Chr14:69562099..81975384 [GRCh38]
Chr14:70028816..82441728 [GRCh37]
Chr14:69098569..81511481 [NCBI36]
Chr14:14q24.1-31.1
pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3 copy number gain See cases [RCV000134000] Chr14:73655772..106879298 [GRCh38]
Chr14:74122475..107287505 [GRCh37]
Chr14:73192228..106358550 [NCBI36]
Chr14:14q24.3-32.33
pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33
pathogenic
GRCh38/hg38 14q24.3(chr14:74986195-76399258)x1 copy number loss See cases [RCV000137114] Chr14:74986195..76399258 [GRCh38]
Chr14:75452898..76865601 [GRCh37]
Chr14:74522651..75935354 [NCBI36]
Chr14:14q24.3
uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33
pathogenic
GRCh38/hg38 14q24.3-31.1(chr14:73343213-78835059)x1 copy number loss See cases [RCV000143265] Chr14:73343213..78835059 [GRCh38]
Chr14:73809921..79301402 [GRCh37]
Chr14:72879674..78371155 [NCBI36]
Chr14:14q24.3-31.1
pathogenic|likely pathogenic
NM_017791.3(FLVCR2):c.*756A>G single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000282376] Chr14:75647228 [GRCh38]
Chr14:76113571 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*155C>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000265331] Chr14:75646627 [GRCh38]
Chr14:76112970 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.2(FLVCR2):c.329_334delACATCT (p.Asn110_Phe112delinsIle) deletion Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000285703] Chr14:75579301..75579306 [GRCh38]
Chr14:76045644..76045649 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.-71C>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000268956] Chr14:75578902 [GRCh38]
Chr14:76045245 [GRCh37]
Chr14:14q24.3
benign|likely benign
NM_017791.3(FLVCR2):c.1474C>T (p.Arg492Trp) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000271118] Chr14:75641863 [GRCh38]
Chr14:76108206 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*18C>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000309739] Chr14:75646490 [GRCh38]
Chr14:76112833 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.164C>T (p.Pro55Leu) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000272925] Chr14:75579136 [GRCh38]
Chr14:76045479 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.-121_-120CT[1] microsatellite Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000274666] Chr14:75578851..75578852 [GRCh38]
Chr14:76045194..76045195 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.953-15C>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000406478] Chr14:75633614 [GRCh38]
Chr14:76099957 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*517C>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000259478] Chr14:75646989 [GRCh38]
Chr14:76113332 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1098C>A single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000295206] Chr14:75647570 [GRCh38]
Chr14:76113913 [GRCh37]
Chr14:14q24.3
benign|likely benign
NM_017791.3(FLVCR2):c.*573C>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000317676] Chr14:75647045 [GRCh38]
Chr14:76113388 [GRCh37]
Chr14:14q24.3
benign|uncertain significance
NM_017791.3(FLVCR2):c.421G>A (p.Val141Met) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000343023] Chr14:75579393 [GRCh38]
Chr14:76045736 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.604G>A (p.Ala202Thr) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000280822] Chr14:75579576 [GRCh38]
Chr14:76045919 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.286A>G (p.Met96Val) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000320971] Chr14:75579258 [GRCh38]
Chr14:76045601 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.2(FLVCR2):c.-356G>C single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000366974] Chr14:75578617 [GRCh38]
Chr14:76044960 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.*187T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000322740] Chr14:75646659 [GRCh38]
Chr14:76113002 [GRCh37]
Chr14:14q24.3
likely benign|uncertain significance
NM_017791.3(FLVCR2):c.-96T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000370479] Chr14:75578877 [GRCh38]
Chr14:76045220 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.*1633A>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000346913] Chr14:75648105 [GRCh38]
Chr14:76114448 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1040C>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000348982] Chr14:75647512 [GRCh38]
Chr14:76113855 [GRCh37]
Chr14:14q24.3
benign|likely benign
NM_017791.3(FLVCR2):c.947C>G (p.Thr316Ser) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000350901] Chr14:75624747 [GRCh38]
Chr14:76091090 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*734del deletion Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000374637] Chr14:75647206 [GRCh38]
Chr14:76113549 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1588A>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000308490] Chr14:75648060 [GRCh38]
Chr14:76114403 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1411_*1412del deletion Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000352311] Chr14:75647883..75647884 [GRCh38]
Chr14:76114226..76114227 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.-111T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000332196] Chr14:75578862 [GRCh38]
Chr14:76045205 [GRCh37]
Chr14:14q24.3
benign|uncertain significance
NM_017791.3(FLVCR2):c.905C>A (p.Ala302Asp) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000312386] Chr14:75624705 [GRCh38]
Chr14:76091048 [GRCh37]
Chr14:14q24.3
likely benign|uncertain significance
NM_017791.3(FLVCR2):c.78C>A (p.Ser26Arg) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000383377] Chr14:75579050 [GRCh38]
Chr14:76045393 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.1441G>A (p.Ala481Thr) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000363359]|not provided [RCV000947581] Chr14:75641281 [GRCh38]
Chr14:76107624 [GRCh37]
Chr14:14q24.3
benign|likely benign
NM_017791.3(FLVCR2):c.1326C>T (p.Leu442=) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000306678] Chr14:75641045 [GRCh38]
Chr14:76107388 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1085T>G single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000387155] Chr14:75647557 [GRCh38]
Chr14:76113900 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1413_*1414GT[9] microsatellite Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000392116] Chr14:75647883..75647884 [GRCh38]
Chr14:76114226..76114227 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*98T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000357580] Chr14:75646570 [GRCh38]
Chr14:76112913 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*379T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000379782] Chr14:75646851 [GRCh38]
Chr14:76113194 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1070T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120180] Chr14:75647542 [GRCh38]
Chr14:76113885 [GRCh37]
Chr14:14q24.3
uncertain significance
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3 copy number gain See cases [RCV000448557] Chr14:62493932..107285437 [GRCh37]
Chr14:14q23.2-32.33
pathogenic
NM_017791.3(FLVCR2):c.1011del (p.Trp337fs) deletion not provided [RCV000482956] Chr14:75633686 [GRCh38]
Chr14:76100029 [GRCh37]
Chr14:14q24.3
pathogenic|likely pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q24.3(chr14:76082940-78372356)x1 copy number loss See cases [RCV000511668] Chr14:76082940..78372356 [GRCh37]
Chr14:14q24.3
uncertain significance
GRCh37/hg19 14q24.3(chr14:76105695-76107636) copy number loss High palate [RCV000626566] Chr14:76105695..76107636 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.1289C>T (p.Thr430Met) single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000626319] Chr14:75641008 [GRCh38]
Chr14:76107351 [GRCh37]
Chr14:14q24.3
pathogenic
GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3 copy number gain See cases [RCV000512497] Chr14:73750741..107285437 [GRCh37]
Chr14:14q24.2-32.33
pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33
pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
NM_017791.3(FLVCR2):c.69G>A (p.Ala23=) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001115388] Chr14:75579041 [GRCh38]
Chr14:76045384 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.903C>T (p.Ile301=) single nucleotide variant not provided [RCV000970271] Chr14:75624703 [GRCh38]
Chr14:76091046 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.84_101GGTCCATCCCAGCGTCTC[1] (p.29_34VHPSVS[1]) microsatellite not provided [RCV000949581] Chr14:75579045..75579062 [GRCh38]
Chr14:76045388..76045405 [GRCh37]
Chr14:14q24.3
likely benign
NM_017791.3(FLVCR2):c.732C>T (p.Asp244=) single nucleotide variant not provided [RCV000901282] Chr14:75622141 [GRCh38]
Chr14:76088484 [GRCh37]
Chr14:14q24.3
likely benign
NM_017791.3(FLVCR2):c.670C>G (p.Leu224Val) single nucleotide variant not provided [RCV000925566] Chr14:75622079 [GRCh38]
Chr14:76088422 [GRCh37]
Chr14:14q24.3
likely benign
GRCh37/hg19 14q24.3(chr14:74040231-76368547) copy number loss not provided [RCV000767572] Chr14:74040231..76368547 [GRCh37]
Chr14:14q24.3
likely pathogenic
NM_017791.3(FLVCR2):c.1157_1158del (p.Leu386fs) deletion Posterior column ataxia-retinitis pigmentosa syndrome [RCV000778411] Chr14:75639384..75639385 [GRCh38]
Chr14:76105727..76105728 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.1580G>T (p.Ter527Leu) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000778412] Chr14:75646471 [GRCh38]
Chr14:76112814 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.1581A>C (p.Ter527Cys) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV000778413] Chr14:75646472 [GRCh38]
Chr14:76112815 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.840C>T (p.Pro280=) single nucleotide variant not provided [RCV000940377] Chr14:75624640 [GRCh38]
Chr14:76090983 [GRCh37]
Chr14:14q24.3
likely benign
NM_017791.3(FLVCR2):c.135C>T (p.Val45=) single nucleotide variant not provided [RCV000918357] Chr14:75579107 [GRCh38]
Chr14:76045450 [GRCh37]
Chr14:14q24.3
likely benign
NM_017791.3(FLVCR2):c.391dup (p.Met131fs) duplication Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV000826106] Chr14:75579362..75579363 [GRCh38]
Chr14:76045705..76045706 [GRCh37]
Chr14:14q24.3
likely pathogenic
NM_017791.3(FLVCR2):c.*644G>A single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001116894] Chr14:75647116 [GRCh38]
Chr14:76113459 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*856T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001116896] Chr14:75647328 [GRCh38]
Chr14:76113671 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1517T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120481] Chr14:75647989 [GRCh38]
Chr14:76114332 [GRCh37]
Chr14:14q24.3
likely benign
NM_017791.3(FLVCR2):c.*1672G>A single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120483] Chr14:75648144 [GRCh38]
Chr14:76114487 [GRCh37]
Chr14:14q24.3
uncertain significance
GRCh37/hg19 14q24.3(chr14:76057971-76576494)x3 copy number gain not provided [RCV000846916] Chr14:76057971..76576494 [GRCh37]
Chr14:14q24.3
uncertain significance
GRCh37/hg19 14q24.3(chr14:75938193-76098127)x3 copy number gain not provided [RCV000846794] Chr14:75938193..76098127 [GRCh37]
Chr14:14q24.3
uncertain significance
GRCh37/hg19 14q24.3(chr14:75938193-76104307)x3 copy number gain not provided [RCV000849520] Chr14:75938193..76104307 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*510A>G single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001115480] Chr14:75646982 [GRCh38]
Chr14:76113325 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.835C>T (p.Pro279Ser) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120067]|not provided [RCV000954477] Chr14:75624635 [GRCh38]
Chr14:76090978 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.766A>G (p.Ile256Val) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120066] Chr14:75622175 [GRCh38]
Chr14:76088518 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1003G>A single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120179] Chr14:75647475 [GRCh38]
Chr14:76113818 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*254T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001115479] Chr14:75646726 [GRCh38]
Chr14:76113069 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.*513A>G single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001115481] Chr14:75646985 [GRCh38]
Chr14:76113328 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*675A>G single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001116895] Chr14:75647147 [GRCh38]
Chr14:76113490 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*910C>A single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001116898] Chr14:75647382 [GRCh38]
Chr14:76113725 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.*952T>G single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001116899] Chr14:75647424 [GRCh38]
Chr14:76113767 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.360C>G (p.Ala120=) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001118540] Chr14:75579332 [GRCh38]
Chr14:76045675 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.669+8G>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120064] Chr14:75579649 [GRCh38]
Chr14:76045992 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.727C>T (p.Arg243Trp) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120065] Chr14:75622136 [GRCh38]
Chr14:76088479 [GRCh37]
Chr14:14q24.3
likely benign
NM_017791.3(FLVCR2):c.*1071G>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120181] Chr14:75647543 [GRCh38]
Chr14:76113886 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1319C>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120182] Chr14:75647791 [GRCh38]
Chr14:76114134 [GRCh37]
Chr14:14q24.3
likely benign
NM_017791.3(FLVCR2):c.953-14G>A single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120375] Chr14:75633615 [GRCh38]
Chr14:76099958 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.1278T>C (p.Ala426=) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120377] Chr14:75640997 [GRCh38]
Chr14:76107340 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*1613C>T single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120482] Chr14:75648085 [GRCh38]
Chr14:76114428 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*991T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120178] Chr14:75647463 [GRCh38]
Chr14:76113806 [GRCh37]
Chr14:14q24.3
benign
NM_017791.3(FLVCR2):c.*1322G>A single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001120183] Chr14:75647794 [GRCh38]
Chr14:76114137 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.277T>C (p.Cys93Arg) single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001118539] Chr14:75579249 [GRCh38]
Chr14:76045592 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.*893T>C single nucleotide variant Posterior column ataxia-retinitis pigmentosa syndrome [RCV001116897] Chr14:75647365 [GRCh38]
Chr14:76113708 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_017791.3(FLVCR2):c.733G>T (p.Glu245Ter) single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV001334950] Chr14:75622142 [GRCh38]
Chr14:76088485 [GRCh37]
Chr14:14q24.3
pathogenic
NM_017791.3(FLVCR2):c.1019C>T (p.Pro340Leu) single nucleotide variant Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome [RCV001334949] Chr14:75633695 [GRCh38]
Chr14:76100038 [GRCh37]
Chr14:14q24.3
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20105 AgrOrtholog
COSMIC FLVCR2 COSMIC
Ensembl Genes ENSG00000119686 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000238667 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000443439 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000451104 UniProtKB/TrEMBL
  ENSP00000451603 UniProtKB/TrEMBL
  ENSP00000451781 UniProtKB/TrEMBL
  ENSP00000452453 UniProtKB/TrEMBL
  ENSP00000452468 UniProtKB/TrEMBL
  ENSP00000452584 UniProtKB/TrEMBL
Ensembl Transcript ENST00000238667 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000539311 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000553341 UniProtKB/TrEMBL
  ENST00000553587 UniProtKB/TrEMBL
  ENST00000554580 UniProtKB/TrEMBL
  ENST00000555027 UniProtKB/TrEMBL
  ENST00000555058 UniProtKB/TrEMBL
  ENST00000556856 UniProtKB/TrEMBL
GTEx ENSG00000119686 GTEx
HGNC ID HGNC:20105 ENTREZGENE
Human Proteome Map FLVCR2 Human Proteome Map
InterPro MFS UniProtKB/Swiss-Prot
  MFS_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_trans_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:55640 UniProtKB/Swiss-Prot
NCBI Gene 55640 ENTREZGENE
OMIM 225790 OMIM
  610865 OMIM
Pfam MFS_1 UniProtKB/Swiss-Prot
PharmGKB PA162388720 PharmGKB
PROSITE MFS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF103473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt FLVC2_HUMAN UniProtKB/Swiss-Prot
  G3V391_HUMAN UniProtKB/TrEMBL
  G3V458_HUMAN UniProtKB/TrEMBL
  G3V4G2_HUMAN UniProtKB/TrEMBL
  G3V5P5_HUMAN UniProtKB/TrEMBL
  G3V5Q8_HUMAN UniProtKB/TrEMBL
  G3V5Y3_HUMAN UniProtKB/TrEMBL
  Q9UPI3 ENTREZGENE
UniProt Secondary B7Z485 UniProtKB/Swiss-Prot
  Q53ZT9 UniProtKB/Swiss-Prot
  Q96JY3 UniProtKB/Swiss-Prot
  Q9NX90 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-10-08 FLVCR2  FLVCR heme transporter 2  FLVCR2  feline leukemia virus subgroup C cellular receptor family member 2  Symbol and/or name change 5135510 APPROVED
2015-11-24 FLVCR2  feline leukemia virus subgroup C cellular receptor family member 2    feline leukemia virus subgroup C cellular receptor family, member 2  Symbol and/or name change 5135510 APPROVED