RANBP17 (RAN binding protein 17) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: RANBP17 (RAN binding protein 17) Homo sapiens
Analyze
Symbol: RANBP17
Name: RAN binding protein 17
RGD ID: 1345238
HGNC Page HGNC:14428
Description: Predicted to enable nuclear export signal receptor activity. Predicted to be involved in protein export from nucleus. Predicted to be located in nucleus. Predicted to be part of nuclear pore. Predicted to be active in cytoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ32916; ran-binding protein 17
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
GRCh385170,862,018 - 171,300,015 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5170,861,870 - 171,300,015 (+)EnsemblGRCh38hg38GRCh38
GRCh375170,289,022 - 170,727,019 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365170,221,600 - 170,659,624 (+)NCBINCBI36Build 36hg18NCBI36
Build 345170,221,599 - 170,659,623NCBI
Celera5166,321,110 - 166,759,577 (+)NCBICelera
Cytogenetic Map5q35.1NCBI
HuRef5165,386,841 - 165,824,900 (+)NCBIHuRef
CHM1_15169,721,527 - 170,159,603 (+)NCBICHM1_1
T2T-CHM13v2.05171,402,331 - 171,840,355 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IBA,IEA)
nuclear pore  (IBA,IEA,NAS)
nucleus  (IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:11024021   PMID:11071879   PMID:12477932   PMID:14702039   PMID:18854154   PMID:19913121   PMID:20503194   PMID:20628086   PMID:21873635   PMID:22589738   PMID:22658674   PMID:22939629  
PMID:28514442   PMID:28611215   PMID:33637726   PMID:33961781   PMID:35256949   PMID:35271311   PMID:35850701  


Genomics

Comparative Map Data
RANBP17
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385170,862,018 - 171,300,015 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5170,861,870 - 171,300,015 (+)EnsemblGRCh38hg38GRCh38
GRCh375170,289,022 - 170,727,019 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365170,221,600 - 170,659,624 (+)NCBINCBI36Build 36hg18NCBI36
Build 345170,221,599 - 170,659,623NCBI
Celera5166,321,110 - 166,759,577 (+)NCBICelera
Cytogenetic Map5q35.1NCBI
HuRef5165,386,841 - 165,824,900 (+)NCBIHuRef
CHM1_15169,721,527 - 170,159,603 (+)NCBICHM1_1
T2T-CHM13v2.05171,402,331 - 171,840,355 (+)NCBIT2T-CHM13v2.0
Ranbp17
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391133,161,794 - 33,463,789 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1133,161,795 - 33,463,746 (-)EnsemblGRCm39 Ensembl
GRCm381133,211,794 - 33,513,784 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1133,211,795 - 33,513,746 (-)EnsemblGRCm38mm10GRCm38
MGSCv371133,111,794 - 33,413,746 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361133,112,419 - 33,413,635 (-)NCBIMGSCv36mm8
Celera1135,623,919 - 35,926,644 (-)NCBICelera
Cytogenetic Map11A4NCBI
cM Map1119.21NCBI
Ranbp17
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81018,304,634 - 18,607,162 (-)NCBIGRCr8
mRatBN7.21017,800,406 - 18,102,947 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1017,800,999 - 18,102,831 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1022,549,092 - 22,857,795 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01022,037,685 - 22,346,389 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01017,525,836 - 17,827,317 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01018,139,763 - 18,445,347 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1018,139,766 - 18,443,964 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01018,023,823 - 18,330,481 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41018,111,581 - 18,413,103 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1017,441,300 - 17,740,782 (-)NCBICelera
Cytogenetic Map10q12NCBI
Ranbp17
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540823,777,698 - 24,092,682 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540823,777,501 - 24,092,993 (+)NCBIChiLan1.0ChiLan1.0
RANBP17
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v24166,017,542 - 166,440,272 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan15164,157,093 - 164,575,563 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v05166,220,228 - 166,649,006 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.15172,979,949 - 173,402,987 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl5172,980,121 - 173,401,395 (+)Ensemblpanpan1.1panPan2
RANBP17
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1440,828,393 - 41,126,981 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl440,828,395 - 41,127,268 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha440,778,918 - 41,079,709 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0441,208,134 - 41,509,345 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl441,208,137 - 41,509,291 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1441,022,717 - 41,323,476 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0441,213,065 - 41,513,833 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0441,723,475 - 42,024,572 (-)NCBIUU_Cfam_GSD_1.0
Ranbp17
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440721395,059,513 - 95,343,778 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366093,782,193 - 4,066,266 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366093,880,389 - 4,065,145 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RANBP17
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1652,836,297 - 53,160,162 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11652,836,291 - 53,160,156 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21657,033,539 - 57,353,878 (-)NCBISscrofa10.2Sscrofa10.2susScr3
RANBP17
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12373,073,889 - 73,475,803 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2373,073,871 - 73,476,689 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660345,176,076 - 5,599,921 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ranbp17
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473318,771,144 - 19,121,060 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473318,772,283 - 19,120,506 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in RANBP17
91 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q32-35.3(chr5:149714592-181272151)x3 copy number gain See cases [RCV000051863] Chr5:149714592..181272151 [GRCh38]
Chr5:149094155..180699152 [GRCh37]
Chr5:149074348..180631758 [NCBI36]
Chr5:5q32-35.3
pathogenic
GRCh38/hg38 5q33.3-35.3(chr5:160029980-181269805)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051865]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051865]|See cases [RCV000051865] Chr5:160029980..181269805 [GRCh38]
Chr5:159456987..180696806 [GRCh37]
Chr5:159389565..180629412 [NCBI36]
Chr5:5q33.3-35.3
pathogenic
GRCh38/hg38 5q34-35.3(chr5:168689326-181269946)x3 copy number gain See cases [RCV000051866] Chr5:168689326..181269946 [GRCh38]
Chr5:168116331..180696947 [GRCh37]
Chr5:168048909..180629553 [NCBI36]
Chr5:5q34-35.3
pathogenic
GRCh38/hg38 5q34-35.1(chr5:166371405-171390034)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052148]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052148]|See cases [RCV000052148] Chr5:166371405..171390034 [GRCh38]
Chr5:165798410..170817038 [GRCh37]
Chr5:165730988..170749643 [NCBI36]
Chr5:5q34-35.1
pathogenic
NM_022897.4(RANBP17):c.594+21A>G single nucleotide variant Malignant melanoma [RCV000066843] Chr5:170909786 [GRCh38]
Chr5:170336790 [GRCh37]
Chr5:170269368 [NCBI36]
Chr5:5q35.1
not provided
NM_022897.4(RANBP17):c.2961G>A (p.Met987Ile) single nucleotide variant Malignant melanoma [RCV000066844] Chr5:171293900 [GRCh38]
Chr5:170720904 [GRCh37]
Chr5:170653509 [NCBI36]
Chr5:5q35.1
not provided
NM_022897.4(RANBP17):c.1710+39497A>G single nucleotide variant Lung cancer [RCV000095561] Chr5:171007874 [GRCh38]
Chr5:170434878 [GRCh37]
Chr5:5q35.1
uncertain significance
GRCh38/hg38 5q33.3-35.3(chr5:156825512-181269805)x3 copy number gain See cases [RCV000133847] Chr5:156825512..181269805 [GRCh38]
Chr5:156252523..180696806 [GRCh37]
Chr5:156185101..180629412 [NCBI36]
Chr5:5q33.3-35.3
pathogenic
GRCh38/hg38 5q34-35.3(chr5:164386701-181269805)x3 copy number gain See cases [RCV000135546] Chr5:164386701..181269805 [GRCh38]
Chr5:163813707..180696806 [GRCh37]
Chr5:163746285..180629412 [NCBI36]
Chr5:5q34-35.3
pathogenic
GRCh38/hg38 5q35.1(chr5:170226622-171028731)x3 copy number gain See cases [RCV000137321] Chr5:170226622..171028731 [GRCh38]
Chr5:169653626..170455735 [GRCh37]
Chr5:169586204..170388340 [NCBI36]
Chr5:5q35.1
likely benign
GRCh38/hg38 5q35.1-35.3(chr5:169334755-181285301)x3 copy number gain See cases [RCV000141249] Chr5:169334755..181285301 [GRCh38]
Chr5:168761759..180712302 [GRCh37]
Chr5:168694337..180644908 [NCBI36]
Chr5:5q35.1-35.3
pathogenic
GRCh38/hg38 5q34-35.1(chr5:168433412-171417179)x1 copy number loss See cases [RCV000140907] Chr5:168433412..171417179 [GRCh38]
Chr5:167860417..170844183 [GRCh37]
Chr5:167792995..170776788 [NCBI36]
Chr5:5q34-35.1
uncertain significance
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
GRCh37/hg19 5q34-35.1(chr5:164207156-172799124)x1 copy number loss See cases [RCV000447112] Chr5:164207156..172799124 [GRCh37]
Chr5:5q34-35.1
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
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 5q35.1(chr5:168955293-170432136)x1 copy number loss See cases [RCV000511893] Chr5:168955293..170432136 [GRCh37]
Chr5:5q35.1
uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NM_022897.5(RANBP17):c.2046T>A (p.Asp682Glu) single nucleotide variant Inborn genetic diseases [RCV003294780] Chr5:171199677 [GRCh38]
Chr5:170626681 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2041G>A (p.Glu681Lys) single nucleotide variant Inborn genetic diseases [RCV003275616] Chr5:171199672 [GRCh38]
Chr5:170626676 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2582A>G (p.Asn861Ser) single nucleotide variant Inborn genetic diseases [RCV003250026] Chr5:171241087 [GRCh38]
Chr5:170668091 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2675T>C (p.Leu892Pro) single nucleotide variant Inborn genetic diseases [RCV003285201] Chr5:171242719 [GRCh38]
Chr5:170669723 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1247G>T (p.Arg416Leu) single nucleotide variant Inborn genetic diseases [RCV003256791] Chr5:170919586 [GRCh38]
Chr5:170346590 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2044G>A (p.Asp682Asn) single nucleotide variant Inborn genetic diseases [RCV003279394] Chr5:171199675 [GRCh38]
Chr5:170626679 [GRCh37]
Chr5:5q35.1
uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5q33.2-35.3(chr5:155344802-180693344)x3 copy number gain not provided [RCV000745284] Chr5:155344802..180693344 [GRCh37]
Chr5:5q33.2-35.3
pathogenic
GRCh37/hg19 5q35.1(chr5:170491870-170553290)x3 copy number gain not provided [RCV000745331] Chr5:170491870..170553290 [GRCh37]
Chr5:5q35.1
benign
GRCh37/hg19 5q33.3-35.1(chr5:156597181-171166353)x3 copy number gain not provided [RCV000845588] Chr5:156597181..171166353 [GRCh37]
Chr5:5q33.3-35.1
pathogenic
GRCh37/hg19 5q35.1(chr5:169923301-170592803)x3 copy number gain not provided [RCV000847787] Chr5:169923301..170592803 [GRCh37]
Chr5:5q35.1
uncertain significance
GRCh37/hg19 5q34-35.2(chr5:166421173-173324843)x1 copy number loss Atrial septal defect 7 [RCV000853560] Chr5:166421173..173324843 [GRCh37]
Chr5:5q34-35.2
pathogenic
NM_022897.5(RANBP17):c.1284A>T (p.Leu428Phe) single nucleotide variant Inborn genetic diseases [RCV003240065] Chr5:170924366 [GRCh38]
Chr5:170351370 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2854G>A (p.Gly952Ser) single nucleotide variant Inborn genetic diseases [RCV003239695] Chr5:171265758 [GRCh38]
Chr5:170692762 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.955G>A (p.Gly319Ser) single nucleotide variant Inborn genetic diseases [RCV003295100] Chr5:170918713 [GRCh38]
Chr5:170345717 [GRCh37]
Chr5:5q35.1
uncertain significance
GRCh37/hg19 5q32-35.3(chr5:149010383-180719789) copy number gain Hunter-McAlpine craniosynostosis [RCV002280612] Chr5:149010383..180719789 [GRCh37]
Chr5:5q32-35.3
pathogenic
NC_000005.9:g.170591818_170713790dup duplication Congenital hydrocephalus [RCV000845239] Chr5:170591818..170713790 [GRCh37]
Chr5:5q35.1
uncertain significance
GRCh37/hg19 5q34-35.1(chr5:164207156-172799124) copy number loss not specified [RCV002053537] Chr5:164207156..172799124 [GRCh37]
Chr5:5q34-35.1
pathogenic
NM_022897.5(RANBP17):c.1710+75929A>G single nucleotide variant Autism spectrum disorder [RCV001839104] Chr5:171044306 [GRCh38]
Chr5:170471310 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2997G>A (p.Trp999Ter) single nucleotide variant See cases [RCV002253001] Chr5:171293936 [GRCh38]
Chr5:170720940 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1910T>G (p.Phe637Cys) single nucleotide variant Inborn genetic diseases [RCV003297540] Chr5:171183211 [GRCh38]
Chr5:170610215 [GRCh37]
Chr5:5q35.1
uncertain significance
GRCh37/hg19 5q35.1-35.3(chr5:170350336-180719789)x3 copy number gain See cases [RCV002292398] Chr5:170350336..180719789 [GRCh37]
Chr5:5q35.1-35.3
pathogenic
NM_022897.5(RANBP17):c.1589T>C (p.Ile530Thr) single nucleotide variant Inborn genetic diseases [RCV003281580] Chr5:170968256 [GRCh38]
Chr5:170395260 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2573A>T (p.His858Leu) single nucleotide variant Inborn genetic diseases [RCV003260475] Chr5:171241078 [GRCh38]
Chr5:170668082 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1790C>G (p.Thr597Arg) single nucleotide variant Inborn genetic diseases [RCV003285628] Chr5:171171211 [GRCh38]
Chr5:170598215 [GRCh37]
Chr5:5q35.1
uncertain significance
GRCh37/hg19 5q33.1-35.2(chr5:150535183-172906793)x3 copy number gain not provided [RCV002474507] Chr5:150535183..172906793 [GRCh37]
Chr5:5q33.1-35.2
pathogenic
NM_022897.5(RANBP17):c.1160T>C (p.Val387Ala) single nucleotide variant Inborn genetic diseases [RCV002771838] Chr5:170919499 [GRCh38]
Chr5:170346503 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.896G>T (p.Arg299Leu) single nucleotide variant Inborn genetic diseases [RCV002684109] Chr5:170916526 [GRCh38]
Chr5:170343530 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.3014T>A (p.Leu1005His) single nucleotide variant Inborn genetic diseases [RCV002907497] Chr5:171293953 [GRCh38]
Chr5:170720957 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.3154G>A (p.Val1052Ile) single nucleotide variant Inborn genetic diseases [RCV002992140] Chr5:171295998 [GRCh38]
Chr5:170723002 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.2917C>A (p.Gln973Lys) single nucleotide variant Inborn genetic diseases [RCV002818126] Chr5:171265821 [GRCh38]
Chr5:170692825 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.301C>A (p.Pro101Thr) single nucleotide variant Inborn genetic diseases [RCV002784924] Chr5:170892431 [GRCh38]
Chr5:170319435 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.3134G>A (p.Gly1045Glu) single nucleotide variant Inborn genetic diseases [RCV002691624] Chr5:171295978 [GRCh38]
Chr5:170722982 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2555A>G (p.Lys852Arg) single nucleotide variant Inborn genetic diseases [RCV002925986] Chr5:171241060 [GRCh38]
Chr5:170668064 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1052A>G (p.Tyr351Cys) single nucleotide variant Inborn genetic diseases [RCV002844322] Chr5:170918810 [GRCh38]
Chr5:170345814 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.251A>G (p.Asp84Gly) single nucleotide variant Inborn genetic diseases [RCV002823350] Chr5:170881891 [GRCh38]
Chr5:170308895 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1333T>G (p.Leu445Val) single nucleotide variant Inborn genetic diseases [RCV002870637] Chr5:170924415 [GRCh38]
Chr5:170351419 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1246C>T (p.Arg416Trp) single nucleotide variant Inborn genetic diseases [RCV002845794] Chr5:170919585 [GRCh38]
Chr5:170346589 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2161G>A (p.Ala721Thr) single nucleotide variant Inborn genetic diseases [RCV002886878] Chr5:171205542 [GRCh38]
Chr5:170632546 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1669C>T (p.Arg557Cys) single nucleotide variant Inborn genetic diseases [RCV002743873] Chr5:170968336 [GRCh38]
Chr5:170395340 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1567T>C (p.Ser523Pro) single nucleotide variant Inborn genetic diseases [RCV002768029] Chr5:170953695 [GRCh38]
Chr5:170380699 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2348G>A (p.Arg783His) single nucleotide variant Inborn genetic diseases [RCV002744069] Chr5:171221766 [GRCh38]
Chr5:170648770 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1016A>G (p.Asn339Ser) single nucleotide variant Inborn genetic diseases [RCV002708847] Chr5:170918774 [GRCh38]
Chr5:170345778 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.3233A>G (p.Asn1078Ser) single nucleotide variant Inborn genetic diseases [RCV002985914] Chr5:171298824 [GRCh38]
Chr5:170725828 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.2009C>T (p.Ala670Val) single nucleotide variant Inborn genetic diseases [RCV002652155] Chr5:171183401 [GRCh38]
Chr5:170610405 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2818A>G (p.Ile940Val) single nucleotide variant Inborn genetic diseases [RCV002719082] Chr5:171265722 [GRCh38]
Chr5:170692726 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.422A>G (p.Gln141Arg) single nucleotide variant Inborn genetic diseases [RCV002940228] Chr5:170892552 [GRCh38]
Chr5:170319556 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1522A>G (p.Thr508Ala) single nucleotide variant Inborn genetic diseases [RCV002965482] Chr5:170953650 [GRCh38]
Chr5:170380654 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.3221G>A (p.Arg1074His) single nucleotide variant Inborn genetic diseases [RCV002669344] Chr5:171298812 [GRCh38]
Chr5:170725816 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.950C>G (p.Pro317Arg) single nucleotide variant Inborn genetic diseases [RCV002963459] Chr5:170916580 [GRCh38]
Chr5:170343584 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2542T>C (p.Phe848Leu) single nucleotide variant Inborn genetic diseases [RCV002959643] Chr5:171241047 [GRCh38]
Chr5:170668051 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2273G>A (p.Arg758Gln) single nucleotide variant Inborn genetic diseases [RCV002988288] Chr5:171213672 [GRCh38]
Chr5:170640676 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.60A>G (p.Ile20Met) single nucleotide variant Inborn genetic diseases [RCV002989558] Chr5:170878138 [GRCh38]
Chr5:170305142 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1000G>C (p.Ala334Pro) single nucleotide variant Inborn genetic diseases [RCV002897017] Chr5:170918758 [GRCh38]
Chr5:170345762 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.977A>G (p.Tyr326Cys) single nucleotide variant Inborn genetic diseases [RCV002718725] Chr5:170918735 [GRCh38]
Chr5:170345739 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2212A>G (p.Thr738Ala) single nucleotide variant Inborn genetic diseases [RCV002669545] Chr5:171205593 [GRCh38]
Chr5:170632597 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1873C>T (p.Leu625Phe) single nucleotide variant Inborn genetic diseases [RCV002719022] Chr5:171183174 [GRCh38]
Chr5:170610178 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.10C>T (p.His4Tyr) single nucleotide variant Inborn genetic diseases [RCV002648230] Chr5:170862043 [GRCh38]
Chr5:170289047 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2240C>T (p.Thr747Met) single nucleotide variant Inborn genetic diseases [RCV002669952] Chr5:171213639 [GRCh38]
Chr5:170640643 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.731C>T (p.Thr244Met) single nucleotide variant Inborn genetic diseases [RCV003197077] Chr5:170911105 [GRCh38]
Chr5:170338109 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2821G>A (p.Val941Ile) single nucleotide variant Inborn genetic diseases [RCV003207806] Chr5:171265725 [GRCh38]
Chr5:170692729 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2987G>A (p.Arg996Gln) single nucleotide variant Inborn genetic diseases [RCV003183082] Chr5:171293926 [GRCh38]
Chr5:170720930 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.80G>C (p.Arg27Thr) single nucleotide variant Inborn genetic diseases [RCV003185084] Chr5:170878158 [GRCh38]
Chr5:170305162 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1015A>G (p.Asn339Asp) single nucleotide variant Inborn genetic diseases [RCV003185781] Chr5:170918773 [GRCh38]
Chr5:170345777 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1664A>G (p.Gln555Arg) single nucleotide variant Inborn genetic diseases [RCV003379355] Chr5:170968331 [GRCh38]
Chr5:170395335 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1544A>G (p.His515Arg) single nucleotide variant Inborn genetic diseases [RCV003347642] Chr5:170953672 [GRCh38]
Chr5:170380676 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1270G>A (p.Val424Met) single nucleotide variant Inborn genetic diseases [RCV003347238] Chr5:170919609 [GRCh38]
Chr5:170346613 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2275T>G (p.Trp759Gly) single nucleotide variant Inborn genetic diseases [RCV003349774] Chr5:171213674 [GRCh38]
Chr5:170640678 [GRCh37]
Chr5:5q35.1
uncertain significance
GRCh37/hg19 5q35.1(chr5:170417259-170695484)x1 copy number loss not provided [RCV003485491] Chr5:170417259..170695484 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.506C>G (p.Pro169Arg) single nucleotide variant not provided [RCV003430002] Chr5:170909677 [GRCh38]
Chr5:170336681 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.692T>C (p.Ile231Thr) single nucleotide variant not provided [RCV003428716] Chr5:170911066 [GRCh38]
Chr5:170338070 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.559G>A (p.Asp187Asn) single nucleotide variant RANBP17-related condition [RCV003408325] Chr5:170909730 [GRCh38]
Chr5:170336734 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.2777-6G>A single nucleotide variant not provided [RCV003430003] Chr5:171265675 [GRCh38]
Chr5:170692679 [GRCh37]
Chr5:5q35.1
likely benign
GRCh37/hg19 5q34-35.1(chr5:165763259-170909410)x1 copy number loss not specified [RCV003986566] Chr5:165763259..170909410 [GRCh37]
Chr5:5q34-35.1
pathogenic
NM_022897.5(RANBP17):c.1767G>A (p.Glu589=) single nucleotide variant RANBP17-related condition [RCV003976403] Chr5:171170186 [GRCh38]
Chr5:170597190 [GRCh37]
Chr5:5q35.1
benign
NM_022897.5(RANBP17):c.-2A>G single nucleotide variant RANBP17-related condition [RCV003944110] Chr5:170862032 [GRCh38]
Chr5:170289036 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.13T>C (p.Phe5Leu) single nucleotide variant RANBP17-related condition [RCV003979099] Chr5:170862046 [GRCh38]
Chr5:170289050 [GRCh37]
Chr5:5q35.1
benign
NM_022897.5(RANBP17):c.2555A>C (p.Lys852Thr) single nucleotide variant RANBP17-related condition [RCV003944563] Chr5:171241060 [GRCh38]
Chr5:170668064 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.2291C>T (p.Thr764Ile) single nucleotide variant RANBP17-related condition [RCV003962004] Chr5:171213690 [GRCh38]
Chr5:170640694 [GRCh37]
Chr5:5q35.1
benign
NM_022897.5(RANBP17):c.1953C>T (p.Gly651=) single nucleotide variant RANBP17-related condition [RCV003964555] Chr5:171183345 [GRCh38]
Chr5:170610349 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.529G>A (p.Ala177Thr) single nucleotide variant RANBP17-related condition [RCV003927356] Chr5:170909700 [GRCh38]
Chr5:170336704 [GRCh37]
Chr5:5q35.1
benign
NM_022897.5(RANBP17):c.161G>A (p.Gly54Glu) single nucleotide variant RANBP17-related condition [RCV003957101] Chr5:170878239 [GRCh38]
Chr5:170305243 [GRCh37]
Chr5:5q35.1
uncertain significance
NM_022897.5(RANBP17):c.1057G>C (p.Glu353Gln) single nucleotide variant RANBP17-related condition [RCV003941778] Chr5:170918815 [GRCh38]
Chr5:170345819 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.547A>T (p.Thr183Ser) single nucleotide variant RANBP17-related condition [RCV003959212] Chr5:170909718 [GRCh38]
Chr5:170336722 [GRCh37]
Chr5:5q35.1
benign
NM_022897.5(RANBP17):c.-9C>A single nucleotide variant RANBP17-related condition [RCV003932151] Chr5:170862025 [GRCh38]
Chr5:170289029 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.272A>G (p.Asn91Ser) single nucleotide variant RANBP17-related condition [RCV003968942] Chr5:170892402 [GRCh38]
Chr5:170319406 [GRCh37]
Chr5:5q35.1
likely benign
NM_022897.5(RANBP17):c.2100A>G (p.Val700=) single nucleotide variant RANBP17-related condition [RCV003972097] Chr5:171199731 [GRCh38]
Chr5:170626735 [GRCh37]
Chr5:5q35.1
benign
NM_022897.5(RANBP17):c.290C>T (p.Pro97Leu) single nucleotide variant Inborn genetic diseases [RCV003345705] Chr5:170892420 [GRCh38]
Chr5:170319424 [GRCh37]
Chr5:5q35.1
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:8322
Count of miRNA genes:1336
Interacting mature miRNAs:1776
Transcripts:ENST00000389118, ENST00000443155, ENST00000517629, ENST00000518492, ENST00000519130, ENST00000519256, ENST00000519944, ENST00000519949, ENST00000520586, ENST00000520864, ENST00000520879, ENST00000521165, ENST00000521759, ENST00000521834, ENST00000522066, ENST00000522380, ENST00000522533, ENST00000522734, ENST00000523189, ENST00000523665, ENST00000523727, ENST00000524364
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
D5S653  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,507,163 - 170,507,312UniSTSGRCh37
GRCh375170,507,163 - 170,507,299UniSTSGRCh37
Build 365170,439,768 - 170,439,904RGDNCBI36
Celera5166,539,714 - 166,539,846RGD
Celera5166,539,714 - 166,539,859UniSTS
HuRef5165,605,067 - 165,605,199UniSTS
HuRef5165,605,067 - 165,605,212UniSTS
Marshfield Genetic Map5177.92RGD
Stanford-G3 RH Map56048.0UniSTS
Whitehead-RH Map5535.8UniSTS
Whitehead-YAC Contig Map5 UniSTS
NCBI RH Map5973.0UniSTS
NCBI RH Map5978.7UniSTS
GeneMap99-G3 RH Map56136.0UniSTS
D5S1910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,376,250 - 170,376,406UniSTSGRCh37
Build 365170,308,855 - 170,309,011RGDNCBI36
Celera5166,408,323 - 166,408,479RGD
Cytogenetic Map5q34UniSTS
HuRef5165,474,089 - 165,474,245UniSTS
Whitehead-YAC Contig Map5 UniSTS
bac51036S  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,630,613 - 170,630,759UniSTSGRCh37
Build 365170,563,218 - 170,563,364RGDNCBI36
Celera5166,663,169 - 166,663,315RGD
Cytogenetic Map5q34UniSTS
HuRef5165,728,548 - 165,728,694UniSTS
bac51036T  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,467,897 - 170,468,097UniSTSGRCh37
Build 365170,400,502 - 170,400,702RGDNCBI36
Celera5166,500,408 - 166,500,608RGD
Cytogenetic Map5q34UniSTS
HuRef5165,565,766 - 165,565,966UniSTS
bac52067T  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,720,401 - 170,720,601UniSTSGRCh37
Build 365170,653,006 - 170,653,206RGDNCBI36
Celera5166,752,959 - 166,753,159RGD
Cytogenetic Map5q34UniSTS
HuRef5165,818,281 - 165,818,481UniSTS
SHGC-141902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,689,928 - 170,690,243UniSTSGRCh37
Build 365170,622,533 - 170,622,848RGDNCBI36
Celera5166,722,484 - 166,722,799RGD
Cytogenetic Map5q34UniSTS
HuRef5165,787,821 - 165,788,136UniSTS
G20312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,725,995 - 170,726,095UniSTSGRCh37
Build 365170,658,600 - 170,658,700RGDNCBI36
Celera5166,758,553 - 166,758,653RGD
Cytogenetic Map5q34UniSTS
HuRef5165,823,876 - 165,823,976UniSTS
A005L27  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,725,995 - 170,726,095UniSTSGRCh37
Build 365170,658,600 - 170,658,700RGDNCBI36
Celera5166,758,553 - 166,758,653RGD
Cytogenetic Map5q34UniSTS
HuRef5165,823,876 - 165,823,976UniSTS
GeneMap99-GB4 RH Map5635.09UniSTS
NCBI RH Map5973.0UniSTS
RH35915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,577,212 - 170,577,369UniSTSGRCh37
Build 365170,509,817 - 170,509,974RGDNCBI36
Celera5166,609,773 - 166,609,930RGD
Cytogenetic Map5q34UniSTS
HuRef5165,675,146 - 165,675,303UniSTS
GeneMap99-GB4 RH Map5634.89UniSTS
NCBI RH Map5973.0UniSTS
WI-11325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,410,909 - 170,411,044UniSTSGRCh37
Build 365170,343,514 - 170,343,649RGDNCBI36
Celera5166,442,976 - 166,443,111RGD
Cytogenetic Map5q34UniSTS
HuRef5165,508,792 - 165,508,927UniSTS
GeneMap99-GB4 RH Map5632.26UniSTS
Whitehead-RH Map5535.9UniSTS
D5S2399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,612,893 - 170,613,132UniSTSGRCh37
Build 365170,545,498 - 170,545,737RGDNCBI36
Celera5166,645,449 - 166,645,688RGD
Cytogenetic Map5q34UniSTS
HuRef5165,710,821 - 165,711,060UniSTS
A009Y40  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,577,172 - 170,577,362UniSTSGRCh37
Build 365170,509,777 - 170,509,967RGDNCBI36
Celera5166,609,733 - 166,609,923RGD
Cytogenetic Map5q34UniSTS
HuRef5165,675,106 - 165,675,296UniSTS
GeneMap99-GB4 RH Map5632.67UniSTS
G32995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375170,577,172 - 170,577,362UniSTSGRCh37
Celera5166,609,733 - 166,609,923UniSTS
Cytogenetic Map5q34UniSTS
HuRef5165,675,106 - 165,675,296UniSTS
D5S653  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5q34UniSTS
Marshfield Genetic Map5177.92UniSTS
Whitehead-RH Map5535.8UniSTS
Whitehead-YAC Contig Map5 UniSTS
NCBI RH Map5973.0UniSTS
D5S653  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5q34UniSTS
Stanford-G3 RH Map56048.0UniSTS
NCBI RH Map5978.7UniSTS
GeneMap99-G3 RH Map56136.0UniSTS


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 1 1 2 14 3 68 13 1
Low 2258 1484 1509 405 339 260 2482 912 2431 252 1247 1549 154 1 824 1515 5 1
Below cutoff 159 1371 190 194 1077 181 1859 1265 1242 144 136 26 14 380 1270

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_022897 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534627 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009738 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009739 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009740 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009742 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009744 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009746 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009747 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417532 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353164 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353165 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353167 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353168 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353169 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353170 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353172 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353173 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001742202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007058628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007058629 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007058630 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008487154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008487155 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008487156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008487157 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_941108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC008514 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC016574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC018753 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC021077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC091980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF222747 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ271459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ288952 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ288953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ288954 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ288955 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027880 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK057478 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298785 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC030953 (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
  DC365649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC404010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF584202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC877158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000389118   ⟹   ENSP00000373770
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,861,932 - 171,298,858 (+)Ensembl
RefSeq Acc Id: ENST00000443155
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,861,870 - 170,911,409 (+)Ensembl
RefSeq Acc Id: ENST00000517629
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,924,356 - 170,924,918 (+)Ensembl
RefSeq Acc Id: ENST00000518492   ⟹   ENSP00000427980
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,968,256 - 171,029,200 (+)Ensembl
RefSeq Acc Id: ENST00000519130
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,862,023 - 170,911,342 (+)Ensembl
RefSeq Acc Id: ENST00000519256   ⟹   ENSP00000429298
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,862,018 - 171,243,064 (+)Ensembl
RefSeq Acc Id: ENST00000519944   ⟹   ENSP00000429609
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,863,486 - 170,892,490 (+)Ensembl
RefSeq Acc Id: ENST00000519949   ⟹   ENSP00000430444
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,862,018 - 171,300,015 (+)Ensembl
RefSeq Acc Id: ENST00000520586
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5171,143,272 - 171,205,607 (+)Ensembl
RefSeq Acc Id: ENST00000520864   ⟹   ENSP00000429845
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,862,035 - 171,207,903 (+)Ensembl
RefSeq Acc Id: ENST00000520879
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,918,171 - 170,953,668 (+)Ensembl
RefSeq Acc Id: ENST00000521165
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,953,621 - 170,968,506 (+)Ensembl
RefSeq Acc Id: ENST00000521759
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5171,143,267 - 171,299,177 (+)Ensembl
RefSeq Acc Id: ENST00000521834
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5171,241,033 - 171,271,619 (+)Ensembl
RefSeq Acc Id: ENST00000522066   ⟹   ENSP00000430958
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,862,018 - 171,300,015 (+)Ensembl
RefSeq Acc Id: ENST00000522380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,919,451 - 170,970,658 (+)Ensembl
RefSeq Acc Id: ENST00000522533   ⟹   ENSP00000430599
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,862,018 - 171,300,015 (+)Ensembl
RefSeq Acc Id: ENST00000522734   ⟹   ENSP00000430577
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,911,028 - 170,924,407 (+)Ensembl
RefSeq Acc Id: ENST00000523189   ⟹   ENSP00000427975
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,862,018 - 171,300,015 (+)Ensembl
RefSeq Acc Id: ENST00000523665
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5171,143,312 - 171,205,579 (+)Ensembl
RefSeq Acc Id: ENST00000523727
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5170,881,839 - 170,896,238 (+)Ensembl
RefSeq Acc Id: ENST00000524364
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5171,143,321 - 171,213,682 (+)Ensembl
RefSeq Acc Id: NM_022897   ⟹   NP_075048
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,300,015 (+)NCBI
GRCh375170,288,880 - 170,727,454 (+)NCBI
Build 365170,221,600 - 170,659,624 (+)NCBI Archive
Celera5166,321,110 - 166,759,577 (+)RGD
HuRef5165,386,841 - 165,824,900 (+)ENTREZGENE
CHM1_15169,721,517 - 170,159,603 (+)NCBI
T2T-CHM13v2.05171,402,331 - 171,840,355 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011534627   ⟹   XP_011532929
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,300,015 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011534636   ⟹   XP_011532938
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,158,480 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011534637   ⟹   XP_011532939
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,024,565 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009736   ⟹   XP_016865225
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,300,015 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009738   ⟹   XP_016865227
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,300,015 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009739   ⟹   XP_016865228
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,300,015 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009740   ⟹   XP_016865229
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,300,015 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009741   ⟹   XP_016865230
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,271,618 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009742   ⟹   XP_016865231
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,271,618 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009744   ⟹   XP_016865233
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,207,903 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009745   ⟹   XP_016865234
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,910,976 - 171,300,015 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009746   ⟹   XP_016865235
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 170,986,682 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009747   ⟹   XP_016865236
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385171,158,361 - 171,300,015 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047417530   ⟹   XP_047273486
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,300,015 (+)NCBI
RefSeq Acc Id: XM_047417531   ⟹   XP_047273487
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,207,903 (+)NCBI
RefSeq Acc Id: XM_047417532   ⟹   XP_047273488
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,207,903 (+)NCBI
RefSeq Acc Id: XM_047417533   ⟹   XP_047273489
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,924,098 - 171,300,015 (+)NCBI
RefSeq Acc Id: XM_054353158   ⟹   XP_054209133
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,840,355 (+)NCBI
RefSeq Acc Id: XM_054353159   ⟹   XP_054209134
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,840,355 (+)NCBI
RefSeq Acc Id: XM_054353160   ⟹   XP_054209135
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,840,355 (+)NCBI
RefSeq Acc Id: XM_054353161   ⟹   XP_054209136
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,840,355 (+)NCBI
RefSeq Acc Id: XM_054353162   ⟹   XP_054209137
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,840,355 (+)NCBI
RefSeq Acc Id: XM_054353163   ⟹   XP_054209138
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,840,355 (+)NCBI
RefSeq Acc Id: XM_054353164   ⟹   XP_054209139
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,817,211 (+)NCBI
RefSeq Acc Id: XM_054353165   ⟹   XP_054209140
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,817,210 (+)NCBI
RefSeq Acc Id: XM_054353166   ⟹   XP_054209141
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,751,650 (+)NCBI
RefSeq Acc Id: XM_054353167   ⟹   XP_054209142
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,451,289 - 171,840,355 (+)NCBI
RefSeq Acc Id: XM_054353168   ⟹   XP_054209143
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,751,648 (+)NCBI
RefSeq Acc Id: XM_054353169   ⟹   XP_054209144
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,698,821 (+)NCBI
RefSeq Acc Id: XM_054353170   ⟹   XP_054209145
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,541,995 (+)NCBI
RefSeq Acc Id: XM_054353171   ⟹   XP_054209146
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,564,907 (+)NCBI
RefSeq Acc Id: XM_054353172   ⟹   XP_054209147
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,464,438 - 171,840,355 (+)NCBI
RefSeq Acc Id: XM_054353173   ⟹   XP_054209148
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,698,702 - 171,840,355 (+)NCBI
RefSeq Acc Id: XR_007058628
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,295,992 (+)NCBI
RefSeq Acc Id: XR_007058629
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 170,986,682 (+)NCBI
RefSeq Acc Id: XR_007058630
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,032,926 (+)NCBI
RefSeq Acc Id: XR_008487154
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,836,332 (+)NCBI
RefSeq Acc Id: XR_008487155
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,541,995 (+)NCBI
RefSeq Acc Id: XR_008487156
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,612,011 (+)NCBI
RefSeq Acc Id: XR_008487157
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.05171,402,331 - 171,612,011 (+)NCBI
RefSeq Acc Id: XR_941108
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,018 - 171,032,926 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_075048 (Get FASTA)   NCBI Sequence Viewer  
  XP_011532929 (Get FASTA)   NCBI Sequence Viewer  
  XP_011532938 (Get FASTA)   NCBI Sequence Viewer  
  XP_011532939 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865225 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865227 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865228 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865229 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865230 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865231 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865233 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865234 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865235 (Get FASTA)   NCBI Sequence Viewer  
  XP_016865236 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273486 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273487 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273488 (Get FASTA)   NCBI Sequence Viewer  
  XP_047273489 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209133 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209134 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209135 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209136 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209137 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209138 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209139 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209140 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209141 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209142 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209143 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209144 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209145 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209146 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209147 (Get FASTA)   NCBI Sequence Viewer  
  XP_054209148 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAG44255 (Get FASTA)   NCBI Sequence Viewer  
  BAB55427 (Get FASTA)   NCBI Sequence Viewer  
  BAB71504 (Get FASTA)   NCBI Sequence Viewer  
  BAG60924 (Get FASTA)   NCBI Sequence Viewer  
  CAC81055 (Get FASTA)   NCBI Sequence Viewer  
  CAC81806 (Get FASTA)   NCBI Sequence Viewer  
  CAC81807 (Get FASTA)   NCBI Sequence Viewer  
  CAC81808 (Get FASTA)   NCBI Sequence Viewer  
  CAC81809 (Get FASTA)   NCBI Sequence Viewer  
  CAH56326 (Get FASTA)   NCBI Sequence Viewer  
  CCQ43699 (Get FASTA)   NCBI Sequence Viewer  
  EAW61454 (Get FASTA)   NCBI Sequence Viewer  
  EAW61455 (Get FASTA)   NCBI Sequence Viewer  
  EAW61456 (Get FASTA)   NCBI Sequence Viewer  
  EAW61457 (Get FASTA)   NCBI Sequence Viewer  
  EAW61458 (Get FASTA)   NCBI Sequence Viewer  
  EAW61459 (Get FASTA)   NCBI Sequence Viewer  
  EAW61460 (Get FASTA)   NCBI Sequence Viewer  
  EAW61461 (Get FASTA)   NCBI Sequence Viewer  
  EAW61462 (Get FASTA)   NCBI Sequence Viewer  
  EAW61463 (Get FASTA)   NCBI Sequence Viewer  
  EAW61464 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000373770
  ENSP00000373770.4
  ENSP00000427975
  ENSP00000427975.1
  ENSP00000427980.1
  ENSP00000429298
  ENSP00000429298.1
  ENSP00000429609.1
  ENSP00000429845.1
  ENSP00000430444.1
  ENSP00000430577.1
  ENSP00000430599.1
  ENSP00000430958
  ENSP00000430958.1
GenBank Protein Q9H2T7 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_075048   ⟸   NM_022897
- UniProtKB: Q8IU74 (UniProtKB/Swiss-Prot),   Q9H2T7 (UniProtKB/Swiss-Prot),   Q546R4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011532929   ⟸   XM_011534627
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011532938   ⟸   XM_011534636
- Peptide Label: isoform X12
- UniProtKB: Q658U9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011532939   ⟸   XM_011534637
- Peptide Label: isoform X14
- UniProtKB: Q658U9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016865227   ⟸   XM_017009738
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016865228   ⟸   XM_017009739
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_016865225   ⟸   XM_017009736
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016865229   ⟸   XM_017009740
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016865230   ⟸   XM_017009741
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_016865231   ⟸   XM_017009742
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_016865233   ⟸   XM_017009744
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_016865235   ⟸   XM_017009746
- Peptide Label: isoform X13
- UniProtKB: Q8IVM9 (UniProtKB/TrEMBL),   Q658U9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016865234   ⟸   XM_017009745
- Peptide Label: isoform X10
- Sequence:
RefSeq Acc Id: XP_016865236   ⟸   XM_017009747
- Peptide Label: isoform X16
- Sequence:
RefSeq Acc Id: ENSP00000427980   ⟸   ENST00000518492
RefSeq Acc Id: ENSP00000429298   ⟸   ENST00000519256
RefSeq Acc Id: ENSP00000429609   ⟸   ENST00000519944
RefSeq Acc Id: ENSP00000430444   ⟸   ENST00000519949
RefSeq Acc Id: ENSP00000373770   ⟸   ENST00000389118
RefSeq Acc Id: ENSP00000429845   ⟸   ENST00000520864
RefSeq Acc Id: ENSP00000430958   ⟸   ENST00000522066
RefSeq Acc Id: ENSP00000430599   ⟸   ENST00000522533
RefSeq Acc Id: ENSP00000430577   ⟸   ENST00000522734
RefSeq Acc Id: ENSP00000427975   ⟸   ENST00000523189
RefSeq Acc Id: XP_047273486   ⟸   XM_047417530
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047273487   ⟸   XM_047417531
- Peptide Label: isoform X9
RefSeq Acc Id: XP_047273488   ⟸   XM_047417532
- Peptide Label: isoform X11
RefSeq Acc Id: XP_047273489   ⟸   XM_047417533
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054209133   ⟸   XM_054353158
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054209136   ⟸   XM_054353161
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054209137   ⟸   XM_054353162
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054209134   ⟸   XM_054353159
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054209135   ⟸   XM_054353160
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054209138   ⟸   XM_054353163
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054209139   ⟸   XM_054353164
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054209140   ⟸   XM_054353165
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054209141   ⟸   XM_054353166
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054209143   ⟸   XM_054353168
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054209144   ⟸   XM_054353169
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054209146   ⟸   XM_054353171
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054209145   ⟸   XM_054353170
- Peptide Label: isoform X13
- UniProtKB: Q8IVM9 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054209142   ⟸   XM_054353167
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054209147   ⟸   XM_054353172
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054209148   ⟸   XM_054353173
- Peptide Label: isoform X16
Protein Domains
Importin N-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9H2T7-F1-model_v2 AlphaFold Q9H2T7 1-1088 view protein structure

Promoters
RGD ID:6803508
Promoter ID:HG_KWN:51769
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:NM_022897,   UC003MAW.2,   UC003MAX.1,   UC003MAY.1,   UC003MAZ.1,   UC010JJR.1
Position:
Human AssemblyChrPosition (strand)Source
Build 365170,221,456 - 170,221,956 (+)MPROMDB
RGD ID:6871526
Promoter ID:EPDNEW_H8928
Type:initiation region
Name:RANBP17_2
Description:RAN binding protein 17
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8929  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,861,860 - 170,861,920EPDNEW
RGD ID:6871528
Promoter ID:EPDNEW_H8929
Type:initiation region
Name:RANBP17_1
Description:RAN binding protein 17
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8928  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh385170,862,026 - 170,862,086EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14428 AgrOrtholog
COSMIC RANBP17 COSMIC
Ensembl Genes ENSG00000204764 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000389118 ENTREZGENE
  ENST00000389118.8 UniProtKB/Swiss-Prot
  ENST00000518492.1 UniProtKB/TrEMBL
  ENST00000519256 ENTREZGENE
  ENST00000519256.5 UniProtKB/Swiss-Prot
  ENST00000519944.1 UniProtKB/TrEMBL
  ENST00000519949.5 UniProtKB/Swiss-Prot
  ENST00000520864.5 UniProtKB/TrEMBL
  ENST00000522066 ENTREZGENE
  ENST00000522066.5 UniProtKB/TrEMBL
  ENST00000522533.5 UniProtKB/Swiss-Prot
  ENST00000522734.1 UniProtKB/TrEMBL
  ENST00000523189 ENTREZGENE
  ENST00000523189.6 UniProtKB/Swiss-Prot
Gene3D-CATH 1.25.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000204764 GTEx
HGNC ID HGNC:14428 ENTREZGENE
Human Proteome Map RANBP17 Human Proteome Map
InterPro ARM-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ARM-type_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Importin-beta_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  XPO4/7-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:64901 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 64901 ENTREZGENE
OMIM 606141 OMIM
PANTHER PTHR12596 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RAN-BINDING PROTEIN 17 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam IBN_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34208 PharmGKB
SMART IBN_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48371 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt E5RHX1_HUMAN UniProtKB/TrEMBL
  H0YAS2_HUMAN UniProtKB/TrEMBL
  H0YBM6_HUMAN UniProtKB/TrEMBL
  H0YBY7_HUMAN UniProtKB/TrEMBL
  L8E953_HUMAN UniProtKB/TrEMBL
  Q546R4 ENTREZGENE, UniProtKB/TrEMBL
  Q658U9 ENTREZGENE, UniProtKB/TrEMBL
  Q8IU74 ENTREZGENE
  Q8IVM9 ENTREZGENE, UniProtKB/TrEMBL
  Q9H2T7 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary Q8IU74 UniProtKB/Swiss-Prot