RAB11FIP4 (RAB11 family interacting protein 4) - Rat Genome Database

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Gene: RAB11FIP4 (RAB11 family interacting protein 4) Homo sapiens
Analyze
Symbol: RAB11FIP4
Name: RAB11 family interacting protein 4
RGD ID: 1348691
HGNC Page HGNC:30267
Description: Enables protein homodimerization activity and small GTPase binding activity. Involved in regulation of cytokinesis. Located in cleavage furrow; cytoplasmic vesicle; and midbody.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: arfophilin-2; FIP4-Rab11; FLJ00131; KIAA1821; MGC11316; MGC126566; RAB11 family interacting protein 4 (class II); rab11 family-interacting protein 4; RAB11-FIP4
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
GRCh381731,391,675 - 31,538,211 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1731,391,675 - 31,538,211 (+)EnsemblGRCh38hg38GRCh38
GRCh371729,718,693 - 29,865,230 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361726,742,768 - 26,889,352 (+)NCBINCBI36Build 36hg18NCBI36
Build 341726,742,767 - 26,889,352NCBI
Celera1726,666,452 - 26,785,001 (+)NCBICelera
Cytogenetic Map17q11.2NCBI
HuRef1725,912,539 - 26,075,598 (+)NCBIHuRef
CHM1_11729,764,889 - 29,927,838 (+)NCBICHM1_1
T2T-CHM13v2.01732,337,033 - 32,483,971 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
1,1-dichloroethene  (ISO)
1,2-dichloroethane  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-hydroxypropanoic acid  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
4-hydroxyphenyl retinamide  (ISO)
6-propyl-2-thiouracil  (ISO)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (ISO)
amitrole  (ISO)
amphetamine  (ISO)
antirheumatic drug  (EXP)
avobenzone  (EXP)
azathioprine  (EXP)
benzene  (EXP)
benzo[a]pyrene  (EXP)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[e]pyrene  (EXP)
bisphenol A  (EXP,ISO)
butanal  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
clotrimazole  (ISO)
copper(II) sulfate  (EXP)
cyclosporin A  (EXP)
dibutyl phthalate  (ISO)
dorsomorphin  (EXP)
entinostat  (EXP)
ethanol  (ISO)
fulvestrant  (EXP)
gentamycin  (ISO)
GW 4064  (ISO)
hydrogen peroxide  (EXP)
lead(0)  (EXP)
lipopolysaccharide  (EXP)
menadione  (EXP)
methapyrilene  (EXP)
methimazole  (ISO)
methoxychlor  (ISO)
N-methyl-4-phenylpyridinium  (EXP)
oxaliplatin  (ISO)
ozone  (ISO)
panobinostat  (EXP)
paracetamol  (ISO)
pentanal  (EXP)
perfluorohexanesulfonic acid  (EXP,ISO)
perfluorononanoic acid  (EXP)
perfluorooctane-1-sulfonic acid  (EXP)
perfluorooctanoic acid  (EXP)
quercetin  (EXP)
rac-lactic acid  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (ISO)
sotorasib  (EXP)
sulfadimethoxine  (ISO)
sunitinib  (EXP)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
trametinib  (EXP)
trichloroethene  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
triptonide  (ISO)
trovafloxacin  (ISO)
uranium atom  (EXP)
urethane  (EXP)
valproic acid  (EXP)
vancomycin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
centrosome  (IEA)
cleavage furrow  (IBA,IDA,IEA)
cytoplasm  (IEA)
cytoskeleton  (IEA)
endocytic vesicle  (IBA,IDA)
endosome  (IDA,IEA)
extracellular space  (HDA)
membrane  (IEA)
midbody  (IBA,IDA,IEA)
recycling endosome membrane  (IBA,IDA,IEA)
spindle  (IEA)

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
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. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10843809   PMID:11347906   PMID:11468690   PMID:11495908   PMID:12470645   PMID:12477932   PMID:12696059   PMID:12857874   PMID:14702039   PMID:15489334   PMID:15601896   PMID:16148947  
PMID:16344560   PMID:16713569   PMID:17030804   PMID:17632510   PMID:20379614   PMID:20682791   PMID:21873635   PMID:22348143   PMID:22522702   PMID:22664934   PMID:25745995   PMID:28035375  
PMID:28514442   PMID:29257314   PMID:29507755   PMID:32296183   PMID:33961781   PMID:35914814  


Genomics

Comparative Map Data
RAB11FIP4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381731,391,675 - 31,538,211 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1731,391,675 - 31,538,211 (+)EnsemblGRCh38hg38GRCh38
GRCh371729,718,693 - 29,865,230 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361726,742,768 - 26,889,352 (+)NCBINCBI36Build 36hg18NCBI36
Build 341726,742,767 - 26,889,352NCBI
Celera1726,666,452 - 26,785,001 (+)NCBICelera
Cytogenetic Map17q11.2NCBI
HuRef1725,912,539 - 26,075,598 (+)NCBIHuRef
CHM1_11729,764,889 - 29,927,838 (+)NCBICHM1_1
T2T-CHM13v2.01732,337,033 - 32,483,971 (+)NCBIT2T-CHM13v2.0
Rab11fip4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391179,481,847 - 79,588,842 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1179,482,038 - 79,588,849 (+)EnsemblGRCm39 Ensembl
GRCm381179,591,021 - 79,698,016 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1179,591,212 - 79,698,023 (+)EnsemblGRCm38mm10GRCm38
MGSCv371179,404,714 - 79,507,514 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361179,407,407 - 79,510,207 (+)NCBIMGSCv36mm8
Celera1189,223,898 - 89,326,618 (+)NCBICelera
Cytogenetic Map11B5NCBI
cM Map1146.88NCBI
Rab11fip4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81065,048,070 - 65,156,086 (+)NCBIGRCr8
mRatBN7.21064,550,109 - 64,658,123 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1064,550,177 - 64,654,759 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1069,176,576 - 69,282,868 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01068,681,960 - 68,788,261 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01064,151,473 - 64,252,234 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01066,942,363 - 67,051,672 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1066,942,398 - 67,048,308 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01064,598,379 - 64,705,864 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41065,780,123 - 65,883,833 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11065,863,324 - 65,896,402 (+)NCBI
Celera1063,520,873 - 63,623,693 (+)NCBICelera
Cytogenetic Map10q25NCBI
Rab11fip4
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554816,469,286 - 6,548,919 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554816,501,704 - 6,554,448 (+)NCBIChiLan1.0ChiLan1.0
RAB11FIP4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21932,947,881 - 33,094,468 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11734,826,949 - 34,973,445 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01725,265,176 - 25,411,124 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11726,001,073 - 26,146,941 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1726,006,251 - 26,146,947 (-)Ensemblpanpan1.1panPan2
RAB11FIP4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1941,336,537 - 41,416,230 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl941,341,877 - 41,416,176 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha940,498,477 - 40,616,083 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0942,157,076 - 42,274,857 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl942,157,087 - 42,274,857 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1940,940,966 - 41,058,478 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0941,236,011 - 41,353,380 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0941,311,847 - 41,429,386 (-)NCBIUU_Cfam_GSD_1.0
Rab11fip4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560240,387,162 - 40,504,353 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365383,269,336 - 3,382,304 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365383,269,317 - 3,382,298 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RAB11FIP4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1243,364,140 - 43,474,241 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11243,360,758 - 43,474,235 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21245,195,241 - 45,303,103 (-)NCBISscrofa10.2Sscrofa10.2susScr3
RAB11FIP4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11624,851,474 - 24,991,482 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1624,851,595 - 24,991,361 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660755,082,170 - 5,224,352 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Rab11fip4
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248753,972,765 - 4,098,853 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248753,972,765 - 4,103,150 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in RAB11FIP4
36 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q11.2(chr17:30706864-31999939)x3 copy number gain See cases [RCV000050717] Chr17:30706864..31999939 [GRCh38]
Chr17:29033882..30326958 [GRCh37]
Chr17:26058008..27351071 [NCBI36]
Chr17:17q11.2
pathogenic|uncertain significance|conflicting data from submitters
GRCh38/hg38 17q11.2(chr17:30706864-31999939)x1 copy number loss Abnormality of head and neck [RCV000050718]|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050719]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050719]|See cases [RCV000050718] Chr17:30706864..31999939 [GRCh38]
Chr17:29033882..30326958 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30706864-32099761)x3 copy number gain See cases [RCV000050616] Chr17:30706864..32099761 [GRCh38]
Chr17:29033882..30426780 [GRCh37]
Chr17:26058008..27450893 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30630734-32088380)x3 copy number gain See cases [RCV000051881] Chr17:30630734..32088380 [GRCh38]
Chr17:28957752..30415399 [GRCh37]
Chr17:25981878..27439512 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30667972-32023858)x3 copy number gain See cases [RCV000051884] Chr17:30667972..32023858 [GRCh38]
Chr17:28994990..30350877 [GRCh37]
Chr17:26019116..27374990 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30613848-31875279)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054360]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054360]|See cases [RCV000054360] Chr17:30613848..31875279 [GRCh38]
Chr17:28940866..30202298 [GRCh37]
Chr17:25964992..27226411 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30672816-31999939)x1 copy number loss See cases [RCV000054361] Chr17:30672816..31999939 [GRCh38]
Chr17:28999834..30326958 [GRCh37]
Chr17:26023960..27351071 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30706863-31994624)x1 copy number loss See cases [RCV000054362] Chr17:30706863..31994624 [GRCh38]
Chr17:29033881..30321643 [GRCh37]
Chr17:26058007..27345756 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30767194-31937486)x1 copy number loss See cases [RCV000054363] Chr17:30767194..31937486 [GRCh38]
Chr17:29094212..30264505 [GRCh37]
Chr17:26118338..27288618 [NCBI36]
Chr17:17q11.2
pathogenic
NM_032932.5(RAB11FIP4):c.1008C>T (p.Cys336=) single nucleotide variant Malignant melanoma [RCV000063184] Chr17:31523590 [GRCh38]
Chr17:29850608 [GRCh37]
Chr17:26874728 [NCBI36]
Chr17:17q11.2
not provided
NM_032932.6(RAB11FIP4):c.1901A>T (p.Glu634Val) single nucleotide variant Malignant tumor of prostate [RCV000149321] Chr17:31531719 [GRCh38]
Chr17:29858737 [GRCh37]
Chr17:17q11.2
uncertain significance
GRCh38/hg38 17q11.2(chr17:30706864-31999939)x1 copy number loss See cases [RCV000050718] Chr17:30706864..31999939 [GRCh38]
Chr17:29033882..30326958 [GRCh37]
Chr17:26058008..27351071 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:31441351-32005206)x1 copy number loss See cases [RCV000137707] Chr17:31441351..32005206 [GRCh38]
Chr17:29768369..30332225 [GRCh37]
Chr17:26792495..27356338 [NCBI36]
Chr17:17q11.2
uncertain significance
GRCh38/hg38 17q11.2(chr17:30706845-31999933)x1 copy number loss See cases [RCV000139159] Chr17:30706845..31999933 [GRCh38]
Chr17:29033863..30326952 [GRCh37]
Chr17:26057989..27351065 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30684919-32021402)x1 copy number loss See cases [RCV000140221] Chr17:30684919..32021402 [GRCh38]
Chr17:29011937..30348421 [GRCh37]
Chr17:26036063..27372534 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:31354282-31441410)x3 copy number gain See cases [RCV000140944] Chr17:31354282..31441410 [GRCh38]
Chr17:29681300..29768428 [GRCh37]
Chr17:26705426..26792554 [NCBI36]
Chr17:17q11.2
uncertain significance
GRCh38/hg38 17q11.2(chr17:30666018-32085769)x1 copy number loss See cases [RCV000141687] Chr17:30666018..32085769 [GRCh38]
Chr17:28993036..30412788 [GRCh37]
Chr17:26017162..27436901 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30677603-32071701)x3 copy number gain See cases [RCV000142123] Chr17:30677603..32071701 [GRCh38]
Chr17:29004621..30398720 [GRCh37]
Chr17:26028747..27422833 [NCBI36]
Chr17:17q11.2
uncertain significance
GRCh38/hg38 17q11.2(chr17:30625268-32059496)x1 copy number loss See cases [RCV000142020] Chr17:30625268..32059496 [GRCh38]
Chr17:28952286..30386515 [GRCh37]
Chr17:25976412..27410628 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:28947825-32490020)x1 copy number loss See cases [RCV000143027] Chr17:28947825..32490020 [GRCh38]
Chr17:27274843..30817038 [GRCh37]
Chr17:24298969..27841151 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30678153-32073866)x1 copy number loss See cases [RCV000143278] Chr17:30678153..32073866 [GRCh38]
Chr17:29005171..30400885 [GRCh37]
Chr17:26029297..27424998 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh38/hg38 17q11.2(chr17:30706864-31999939)x3 copy number gain See cases [RCV000148149] Chr17:30706864..31999939 [GRCh38]
Chr17:29033882..30326958 [GRCh37]
Chr17:26058008..27351071 [NCBI36]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.1-11.2(chr17:25403446-31685464)x3 copy number gain not provided [RCV000762776] Chr17:25403446..31685464 [GRCh37]
Chr17:17q11.1-11.2
likely pathogenic
GRCh37/hg19 17q11.2(chr17:29782998-30651260)x1 copy number loss See cases [RCV000240147] Chr17:29782998..30651260 [GRCh37]
Chr17:17q11.2
uncertain significance
Single allele duplication Global developmental delay [RCV000414764] Chr17:29111368..30183819 [GRCh37]
Chr17:17q11.2
likely pathogenic
GRCh37/hg19 17q11.2(chr17:28997893-30408615)x1 copy number loss See cases [RCV000447440] Chr17:28997893..30408615 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:28959760-30367155)x1 copy number loss See cases [RCV000445869] Chr17:28959760..30367155 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:29103348-30298773)x1 copy number loss See cases [RCV000510513] Chr17:29103348..30298773 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:28997791-30386515)x1 copy number loss See cases [RCV000510597] Chr17:28997791..30386515 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:28993036-30386515)x1 copy number loss See cases [RCV000511944] Chr17:28993036..30386515 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17q11.2-12(chr17:29578241-32142196)x1 copy number loss See cases [RCV000511107] Chr17:29578241..32142196 [GRCh37]
Chr17:17q11.2-12
pathogenic
NM_032932.6(RAB11FIP4):c.1238G>A (p.Arg413Lys) single nucleotide variant Inborn genetic diseases [RCV003274378] Chr17:31525194 [GRCh38]
Chr17:29852212 [GRCh37]
Chr17:17q11.2
uncertain significance
GRCh37/hg19 17q11.2(chr17:29033882-30326958) copy number loss Cafe au lait spots, multiple [RCV000626517] Chr17:29033882..30326958 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:29033882-30326958) copy number loss Cafe au lait spots, multiple [RCV000626518] Chr17:29033882..30326958 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17q11.1-11.2(chr17:25248166-30645676)x1 copy number loss Mitogen-activated protein kinase kinase inhibitor response [RCV000626439] Chr17:25248166..30645676 [GRCh37]
Chr17:17q11.1-11.2
drug response
GRCh37/hg19 17q11.2(chr17:29003358-30412788)x1 copy number loss not provided [RCV000683915] Chr17:29003358..30412788 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:28997893-30391813)x1 copy number loss not provided [RCV000683914] Chr17:28997893..30391813 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17q11.2(chr17:29015932-30298437)x1 copy number loss not provided [RCV000739455] Chr17:29015932..30298437 [GRCh37]
Chr17:17q11.2
likely pathogenic
GRCh37/hg19 17q11.2(chr17:29830490-29830898)x0 copy number loss not provided [RCV000751998] Chr17:29830490..29830898 [GRCh37]
Chr17:17q11.2
benign
GRCh37/hg19 17q11.2(chr17:29830490-29839696)x1 copy number loss not provided [RCV000751999] Chr17:29830490..29839696 [GRCh37]
Chr17:17q11.2
benign
GRCh37/hg19 17q11.2(chr17:29373189-30412788)x1 copy number loss not provided [RCV001006890] Chr17:29373189..30412788 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:29111368-30183819) copy number gain not provided [RCV000767739] Chr17:29111368..30183819 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:28941066-30326958)x1 copy number loss Chromosome 17q11.2 deletion syndrome, 1.4Mb [RCV000856639] Chr17:28941066..30326958 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17p11.2-q21.2(chr17:21690653-38772647)x3 copy number gain not provided [RCV000846852] Chr17:21690653..38772647 [GRCh37]
Chr17:17p11.2-q21.2
pathogenic
GRCh37/hg19 17q11.2(chr17:29393104-30427403)x1 copy number loss See cases [RCV001194568] Chr17:29393104..30427403 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:29054315-30391711)x3 copy number gain not provided [RCV000848806] Chr17:29054315..30391711 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:29054315-30409336)x1 copy number loss not provided [RCV000847727] Chr17:29054315..30409336 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:28999903-30409337)x1 copy number loss not provided [RCV000846363] Chr17:28999903..30409337 [GRCh37]
Chr17:17q11.2
pathogenic
NM_032932.6(RAB11FIP4):c.1473G>T (p.Lys491Asn) single nucleotide variant Inborn genetic diseases [RCV003249073] Chr17:31528522 [GRCh38]
Chr17:29855540 [GRCh37]
Chr17:17q11.2
uncertain significance
GRCh37/hg19 17q11.2(chr17:29088218-30159137)x1 copy number loss not provided [RCV001006889] Chr17:29088218..30159137 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:29039844-30412788)x1 copy number loss not provided [RCV001259329] Chr17:29039844..30412788 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:28993036-30412788) copy number loss Chromosome 17q11.2 deletion syndrome, 1.4Mb [RCV002280633]|Neurofibromatosis, type 1 [RCV002280632] Chr17:28993036..30412788 [GRCh37]
Chr17:17q11.2
pathogenic
Single allele deletion Cerebral palsy [RCV001796573] Chr17:28992701..30408700 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:29076232-30043725)x1 copy number loss not provided [RCV002291543] Chr17:29076232..30043725 [GRCh37]
Chr17:17q11.2
pathogenic
NM_032932.6(RAB11FIP4):c.296C>T (p.Thr99Met) single nucleotide variant Inborn genetic diseases [RCV002685074] Chr17:31434082 [GRCh38]
Chr17:29761100 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.1612C>T (p.Arg538Cys) single nucleotide variant Inborn genetic diseases [RCV002968901] Chr17:31528737 [GRCh38]
Chr17:29855755 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.31C>T (p.Pro11Ser) single nucleotide variant Inborn genetic diseases [RCV002818527] Chr17:31391883 [GRCh38]
Chr17:29718901 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.1415T>C (p.Met472Thr) single nucleotide variant Inborn genetic diseases [RCV002997081] Chr17:31528464 [GRCh38]
Chr17:29855482 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.1292A>G (p.Glu431Gly) single nucleotide variant Inborn genetic diseases [RCV002707671] Chr17:31527859 [GRCh38]
Chr17:29854877 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.508G>T (p.Gly170Trp) single nucleotide variant Inborn genetic diseases [RCV002925843] Chr17:31517822 [GRCh38]
Chr17:29844840 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.93C>G (p.Asp31Glu) single nucleotide variant Inborn genetic diseases [RCV002782907] Chr17:31391945 [GRCh38]
Chr17:29718963 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.411C>A (p.Asp137Glu) single nucleotide variant Inborn genetic diseases [RCV002911487] Chr17:31517725 [GRCh38]
Chr17:29844743 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.1175C>T (p.Thr392Met) single nucleotide variant Inborn genetic diseases [RCV002887220] Chr17:31525131 [GRCh38]
Chr17:29852149 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.64C>T (p.Arg22Cys) single nucleotide variant Inborn genetic diseases [RCV002702031] Chr17:31391916 [GRCh38]
Chr17:29718934 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.1186G>T (p.Ala396Ser) single nucleotide variant Inborn genetic diseases [RCV002874125] Chr17:31525142 [GRCh38]
Chr17:29852160 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.1656G>C (p.Glu552Asp) single nucleotide variant Inborn genetic diseases [RCV002987337] Chr17:31530328 [GRCh38]
Chr17:29857346 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.127G>A (p.Ala43Thr) single nucleotide variant Inborn genetic diseases [RCV002836095] Chr17:31391979 [GRCh38]
Chr17:29718997 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.22T>G (p.Ser8Ala) single nucleotide variant Inborn genetic diseases [RCV003255787] Chr17:31391874 [GRCh38]
Chr17:29718892 [GRCh37]
Chr17:17q11.2
likely benign
NM_032932.6(RAB11FIP4):c.1487C>T (p.Thr496Met) single nucleotide variant Inborn genetic diseases [RCV003184216] Chr17:31528536 [GRCh38]
Chr17:29855554 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.1753G>A (p.Ala585Thr) single nucleotide variant Inborn genetic diseases [RCV003202183] Chr17:31530425 [GRCh38]
Chr17:29857443 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.343G>A (p.Glu115Lys) single nucleotide variant Inborn genetic diseases [RCV003214628] Chr17:31517657 [GRCh38]
Chr17:29844675 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.1229A>G (p.Lys410Arg) single nucleotide variant Inborn genetic diseases [RCV003384953] Chr17:31525185 [GRCh38]
Chr17:29852203 [GRCh37]
Chr17:17q11.2
uncertain significance
NM_032932.6(RAB11FIP4):c.1838G>A (p.Arg613Gln) single nucleotide variant Inborn genetic diseases [RCV003386601] Chr17:31531656 [GRCh38]
Chr17:29858674 [GRCh37]
Chr17:17q11.2
uncertain significance
GRCh37/hg19 17q11.2(chr17:28387597-30812008)x1 copy number loss not provided [RCV003483317] Chr17:28387597..30812008 [GRCh37]
Chr17:17q11.2
pathogenic
Single allele deletion not provided [RCV003448706] Chr17:29000371..30367382 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:29305509-31246638)x3 copy number gain not specified [RCV003987238] Chr17:29305509..31246638 [GRCh37]
Chr17:17q11.2
pathogenic
GRCh37/hg19 17q11.2(chr17:28277040-30903559)x1 copy number loss not specified [RCV003987216] Chr17:28277040..30903559 [GRCh37]
Chr17:17q11.2
pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:6799
Count of miRNA genes:1449
Interacting mature miRNAs:1989
Transcripts:ENST00000325874, ENST00000394744, ENST00000578148, ENST00000578694, ENST00000579589, ENST00000579908, ENST00000581280, ENST00000581460, ENST00000582009, ENST00000583755, ENST00000585058
Prediction methods:Microtar, Miranda, Pita, Pita,Targetscan, 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
Cda0zg05  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,859,881 - 29,859,980UniSTSGRCh37
Build 361726,884,001 - 26,884,100RGDNCBI36
Celera1726,779,651 - 26,779,750RGD
Cytogenetic Map17q11.2UniSTS
HuRef1726,070,248 - 26,070,347UniSTS
GeneMap99-GB4 RH Map17278.96UniSTS
WIAF-1519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,858,878 - 29,859,059UniSTSGRCh37
Build 361726,882,998 - 26,883,179RGDNCBI36
Celera1726,778,648 - 26,778,829RGD
Cytogenetic Map17q11.2UniSTS
HuRef1726,069,245 - 26,069,426UniSTS
GeneMap99-GB4 RH Map17269.91UniSTS
RH91562  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,704,149 - 29,704,336UniSTSGRCh37
Build 361726,728,275 - 26,728,462RGDNCBI36
Celera1726,624,465 - 26,624,652RGD
Cytogenetic Map17q11.2UniSTS
HuRef1725,914,637 - 25,914,824UniSTS
GeneMap99-GB4 RH Map17280.88UniSTS
SHGC-83604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,786,770 - 29,787,104UniSTSGRCh37
Build 361726,810,896 - 26,811,230RGDNCBI36
Celera1726,706,531 - 26,706,865RGD
Cytogenetic Map17q11.2UniSTS
HuRef1725,997,205 - 25,997,539UniSTS
TNG Radiation Hybrid Map1712481.0UniSTS
G60284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,858,847 - 29,859,069UniSTSGRCh37
Build 361726,882,967 - 26,883,189RGDNCBI36
Celera1726,778,617 - 26,778,839RGD
Cytogenetic Map17q11.2UniSTS
HuRef1726,069,214 - 26,069,436UniSTS
TNG Radiation Hybrid Map1712510.0UniSTS
D17S145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,720,195 - 29,720,646UniSTSGRCh37
Build 361726,744,321 - 26,744,772RGDNCBI36
Celera1726,639,964 - 26,640,415RGD
Cytogenetic Map17q11.2UniSTS
HuRef1725,930,623 - 25,931,074UniSTS
D5S1621E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,865,075 - 29,865,173UniSTSGRCh37
Build 361726,889,195 - 26,889,293RGDNCBI36
Celera1726,784,844 - 26,784,942RGD
Cytogenetic Map17q11.2UniSTS
HuRef1726,075,441 - 26,075,539UniSTS
RH78318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,864,902 - 29,865,048UniSTSGRCh37
Build 361726,889,022 - 26,889,168RGDNCBI36
Celera1726,784,671 - 26,784,817RGD
Cytogenetic Map17q11.2UniSTS
HuRef1726,075,268 - 26,075,414UniSTS
GeneMap99-GB4 RH Map17279.06UniSTS
WI-18876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,701,219 - 29,701,345UniSTSGRCh37
Build 361726,725,345 - 26,725,471RGDNCBI36
Celera1726,621,545 - 26,621,671RGD
Cytogenetic Map17q11.2UniSTS
HuRef1725,911,707 - 25,911,833UniSTS
GeneMap99-GB4 RH Map17273.17UniSTS
Whitehead-RH Map17300.5UniSTS
D17S1681  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,859,808 - 29,860,062UniSTSGRCh37
Build 361726,883,928 - 26,884,182RGDNCBI36
Celera1726,779,578 - 26,779,832RGD
Cytogenetic Map17q11.2UniSTS
HuRef1726,070,175 - 26,070,429UniSTS
GeneMap99-GB4 RH Map17280.88UniSTS
Whitehead-RH Map17306.1UniSTS
Whitehead-YAC Contig Map17 UniSTS
D17S1972  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,701,254 - 29,701,459UniSTSGRCh37
Build 361726,725,380 - 26,725,585RGDNCBI36
Celera1726,621,580 - 26,621,785RGD
Cytogenetic Map17q11.2UniSTS
HuRef1725,911,742 - 25,911,947UniSTS
Stanford-G3 RH Map171213.0UniSTS
Whitehead-YAC Contig Map17 UniSTS
GeneMap99-G3 RH Map171714.0UniSTS
STS-M79255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,864,244 - 29,864,327UniSTSGRCh37
Build 361726,888,364 - 26,888,447RGDNCBI36
Celera1726,784,013 - 26,784,096RGD
Cytogenetic Map17q11.2UniSTS
HuRef1726,074,610 - 26,074,693UniSTS
GeneMap99-GB4 RH Map17267.1UniSTS
SHGC-57602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,703,888 - 29,704,008UniSTSGRCh37
Build 361726,728,014 - 26,728,134RGDNCBI36
Celera1726,624,204 - 26,624,324RGD
Cytogenetic Map17q11.2UniSTS
HuRef1725,914,376 - 25,914,496UniSTS
TNG Radiation Hybrid Map1712454.0UniSTS
RH18392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,702,918 - 29,703,063UniSTSGRCh37
Build 361726,727,044 - 26,727,189RGDNCBI36
Celera1726,623,242 - 26,623,387RGD
Cytogenetic Map17q11.2UniSTS
HuRef1725,913,406 - 25,913,551UniSTS
GeneMap99-GB4 RH Map17277.73UniSTS
RH78102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,704,381 - 29,704,503UniSTSGRCh37
Build 361726,728,507 - 26,728,629RGDNCBI36
Celera1726,624,697 - 26,624,819RGD
Cytogenetic Map17q11.2UniSTS
HuRef1725,914,869 - 25,914,991UniSTS
GeneMap99-GB4 RH Map17280.88UniSTS
IB518  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,859,794 - 29,859,971UniSTSGRCh37
Build 361726,883,914 - 26,884,091RGDNCBI36
Celera1726,779,564 - 26,779,741RGD
Cytogenetic Map17q11.2UniSTS
HuRef1726,070,161 - 26,070,338UniSTS
GeneMap99-GB4 RH Map17275.0UniSTS
Whitehead-RH Map17301.9UniSTS
SGC30494  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,708,992 - 29,709,132UniSTSGRCh37
Build 361726,733,118 - 26,733,258RGDNCBI36
Celera1726,629,308 - 26,629,448RGD
Cytogenetic Map17q11.2UniSTS
HuRef1725,919,480 - 25,919,620UniSTS
GeneMap99-GB4 RH Map17280.88UniSTS
Whitehead-RH Map17304.8UniSTS
SHGC-8060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,859,794 - 29,859,968UniSTSGRCh37
Build 361726,883,914 - 26,884,088RGDNCBI36
Celera1726,779,564 - 26,779,738RGD
Cytogenetic Map17q11.2UniSTS
HuRef1726,070,161 - 26,070,335UniSTS
GeneMap99-G3 RH Map171714.0UniSTS
RAB11-FIP4__5629  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,859,469 - 29,860,111UniSTSGRCh37
Build 361726,883,589 - 26,884,231RGDNCBI36
Celera1726,779,239 - 26,779,881RGD
HuRef1726,069,836 - 26,070,478UniSTS
NF1__6237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371729,701,074 - 29,701,463UniSTSGRCh37
Build 361726,725,200 - 26,725,589RGDNCBI36
Celera1726,621,400 - 26,621,789RGD
HuRef1725,911,562 - 25,911,951UniSTS
D1S1423  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p22.3-p21.32UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map9q12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map10p14-p13UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map11q23-q24UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map22cen-q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map4q28UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map1q41-q42UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map11q24.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3q13UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map9p21.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq27.2UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map20q11.21-q11.23UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map15q26UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p15.1-p14UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map7q32.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21-q24UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map8q24.12UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map6q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map20pter-p12UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map14q22.2UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p22-p21UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map10q22.3-q23.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map3p12.3UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map3q11.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6p24.2UniSTS
Cytogenetic Map20q13.33UniSTS
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
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Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
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
RH69351  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17q11.2UniSTS
HuRef1725,944,804 - 25,944,949UniSTS
GeneMap99-GB4 RH Map17280.88UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High
Medium 486 415 111 29 767 33 574 7 2668 53 497 195 2 200 3
Low 1539 1369 1458 577 1147 416 1963 939 1048 347 886 1387 170 1 741 1171 1
Below cutoff 410 1200 156 16 34 15 1815 1243 18 17 65 26 2 463 1416

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_051977 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001303542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346747 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346748 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346749 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB058724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC003101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC135724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ314646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097424 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL359563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL831830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY169244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC004515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC023618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC047674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC093914 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC094803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC101517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC131530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI461640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA956442 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DR000701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC877637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC877646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000394744   ⟹   ENSP00000378227
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,488,000 - 31,531,849 (+)Ensembl
RefSeq Acc Id: ENST00000578148
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,530,972 - 31,531,852 (+)Ensembl
RefSeq Acc Id: ENST00000578694   ⟹   ENSP00000463616
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,488,192 - 31,521,184 (+)Ensembl
RefSeq Acc Id: ENST00000579589   ⟹   ENSP00000466538
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,488,118 - 31,517,708 (+)Ensembl
RefSeq Acc Id: ENST00000579908
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,431,813 - 31,448,495 (+)Ensembl
RefSeq Acc Id: ENST00000581280
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,391,935 - 31,392,658 (+)Ensembl
RefSeq Acc Id: ENST00000581460
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,521,866 - 31,527,893 (+)Ensembl
RefSeq Acc Id: ENST00000582009   ⟹   ENSP00000463206
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,431,559 - 31,521,223 (+)Ensembl
RefSeq Acc Id: ENST00000583755   ⟹   ENSP00000465929
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,488,108 - 31,525,116 (+)Ensembl
RefSeq Acc Id: ENST00000585058
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,520,906 - 31,527,593 (+)Ensembl
RefSeq Acc Id: ENST00000621161   ⟹   ENSP00000482620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1731,391,675 - 31,538,211 (+)Ensembl
RefSeq Acc Id: NM_001303542   ⟹   NP_001290471
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381731,488,108 - 31,538,211 (+)NCBI
CHM1_11729,877,616 - 29,927,842 (+)NCBI
T2T-CHM13v2.01732,433,454 - 32,483,971 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346747   ⟹   NP_001333676
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381731,488,108 - 31,538,211 (+)NCBI
T2T-CHM13v2.01732,433,454 - 32,483,971 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346748   ⟹   NP_001333677
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381731,488,108 - 31,538,211 (+)NCBI
T2T-CHM13v2.01732,433,454 - 32,483,971 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346749   ⟹   NP_001333678
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381731,488,108 - 31,538,211 (+)NCBI
T2T-CHM13v2.01732,433,454 - 32,483,971 (+)NCBI
Sequence:
RefSeq Acc Id: NM_032932   ⟹   NP_116321
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381731,391,675 - 31,538,211 (+)NCBI
GRCh371729,718,642 - 29,865,232 (+)RGD
Build 361726,742,768 - 26,889,352 (+)NCBI Archive
Celera1726,666,452 - 26,785,001 (+)RGD
HuRef1725,912,539 - 26,075,598 (+)ENTREZGENE
CHM1_11729,764,889 - 29,927,842 (+)NCBI
T2T-CHM13v2.01732,337,033 - 32,483,971 (+)NCBI
Sequence:
RefSeq Acc Id: NP_116321   ⟸   NM_032932
- Peptide Label: isoform 1
- UniProtKB: Q8NDT7 (UniProtKB/Swiss-Prot),   Q8N829 (UniProtKB/Swiss-Prot),   Q52LI1 (UniProtKB/Swiss-Prot),   Q969D8 (UniProtKB/Swiss-Prot),   Q86YS3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001290471   ⟸   NM_001303542
- Peptide Label: isoform 2
- UniProtKB: Q86YS3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001333677   ⟸   NM_001346748
- Peptide Label: isoform 4
- UniProtKB: Q86YS3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001333676   ⟸   NM_001346747
- Peptide Label: isoform 3
- Sequence:
RefSeq Acc Id: NP_001333678   ⟸   NM_001346749
- Peptide Label: isoform 5
- UniProtKB: Q86YS3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000463206   ⟸   ENST00000582009
RefSeq Acc Id: ENSP00000482620   ⟸   ENST00000621161
RefSeq Acc Id: ENSP00000465929   ⟸   ENST00000583755
RefSeq Acc Id: ENSP00000463616   ⟸   ENST00000578694
RefSeq Acc Id: ENSP00000466538   ⟸   ENST00000579589
RefSeq Acc Id: ENSP00000378227   ⟸   ENST00000394744
Protein Domains
EF-hand   FIP-RBD

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q86YS3-F1-model_v2 AlphaFold Q86YS3 1-637 view protein structure

Promoters
RGD ID:6794463
Promoter ID:HG_KWN:25707
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:UC002HGO.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361726,838,841 - 26,839,341 (+)MPROMDB
RGD ID:7234547
Promoter ID:EPDNEW_H23018
Type:initiation region
Name:RAB11FIP4_1
Description:RAB11 family interacting protein 4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381731,391,675 - 31,391,735EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30267 AgrOrtholog
COSMIC RAB11FIP4 COSMIC
Ensembl Genes ENSG00000131242 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000394744 ENTREZGENE
  ENST00000394744.6 UniProtKB/Swiss-Prot
  ENST00000578694.1 UniProtKB/TrEMBL
  ENST00000579589.1 UniProtKB/TrEMBL
  ENST00000582009.5 UniProtKB/TrEMBL
  ENST00000583755.1 UniProtKB/TrEMBL
  ENST00000621161 ENTREZGENE
  ENST00000621161.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.5.2440 UniProtKB/Swiss-Prot
  EF-hand UniProtKB/Swiss-Prot
GTEx ENSG00000131242 GTEx
HGNC ID HGNC:30267 ENTREZGENE
Human Proteome Map RAB11FIP4 Human Proteome Map
InterPro EF-hand-dom_pair UniProtKB/Swiss-Prot
  EF_hand_dom UniProtKB/Swiss-Prot
  FIP-RBD_C_sf UniProtKB/Swiss-Prot
  Rab-bd_FIP-RBD UniProtKB/Swiss-Prot
KEGG Report hsa:84440 UniProtKB/Swiss-Prot
NCBI Gene 84440 ENTREZGENE
OMIM 611999 OMIM
PANTHER RAB11 FAMILY-INTERACTING PROTEIN 4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RAB11-FAMILY INTERACTING PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam RBD-FIP UniProtKB/Swiss-Prot
PharmGKB PA134978007 PharmGKB
PROSITE EF_HAND_2 UniProtKB/Swiss-Prot
  FIP_RBD UniProtKB/Swiss-Prot
Superfamily-SCOP SSF144270 UniProtKB/Swiss-Prot
  SSF47473 UniProtKB/Swiss-Prot
UniProt J3QKR9_HUMAN UniProtKB/TrEMBL
  J3QLM3_HUMAN UniProtKB/TrEMBL
  K7EL58_HUMAN UniProtKB/TrEMBL
  K7EMK3_HUMAN UniProtKB/TrEMBL
  L8ECL7_HUMAN UniProtKB/TrEMBL
  Q52LI1 ENTREZGENE
  Q86YS3 ENTREZGENE
  Q8N829 ENTREZGENE
  Q8NDT7 ENTREZGENE
  Q969D8 ENTREZGENE
  RFIP4_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q52LI1 UniProtKB/Swiss-Prot
  Q8N829 UniProtKB/Swiss-Prot
  Q8NDT7 UniProtKB/Swiss-Prot
  Q969D8 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-05-03 RAB11FIP4  RAB11 family interacting protein 4    RAB11 family interacting protein 4 (class II)  Symbol and/or name change 5135510 APPROVED