DOCK4 (dedicator of cytokinesis 4) - Rat Genome Database

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Gene: DOCK4 (dedicator of cytokinesis 4) Homo sapiens
Analyze
Symbol: DOCK4
Name: dedicator of cytokinesis 4
RGD ID: 1350295
HGNC Page HGNC:19192
Description: Enables PDZ domain binding activity; enzyme binding activity; and guanyl-nucleotide exchange factor activity. Involved in cell chemotaxis; negative regulation of vascular associated smooth muscle contraction; and positive regulation of vascular associated smooth muscle cell migration. Located in several cellular components, including Golgi apparatus; cytosol; and nucleolus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: dedicator of cytokinesis protein 4; FLJ34238; KIAA0716; MGC134911; MGC134912
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387111,726,110 - 112,206,399 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7111,726,110 - 112,206,407 (-)EnsemblGRCh38hg38GRCh38
GRCh377111,366,166 - 111,846,454 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367111,153,400 - 111,633,698 (-)NCBINCBI36Build 36hg18NCBI36
Build 347110,962,280 - 111,440,144NCBI
Celera7106,178,467 - 106,658,751 (-)NCBICelera
Cytogenetic Map7q31.1NCBI
HuRef7105,734,071 - 106,214,221 (-)NCBIHuRef
CHM1_17111,300,360 - 111,780,666 (-)NCBICHM1_1
T2T-CHM13v2.07113,044,415 - 113,524,706 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27110,734,721 - 111,215,001 (-)NCBI
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
(-)-demecolcine  (EXP)
(1->4)-beta-D-glucan  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
17beta-estradiol 3-benzoate  (ISO)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
acrolein  (EXP)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
alpha-pinene  (EXP)
antirheumatic drug  (EXP)
aristolochic acid A  (EXP)
arsenite(3-)  (EXP)
atrazine  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[e]pyrene  (EXP)
beta-lapachone  (EXP)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP)
cadmium dichloride  (EXP)
caffeine  (EXP)
calcitriol  (EXP)
carbon nanotube  (ISO)
chloroprene  (ISO)
chlorpyrifos  (ISO)
choline  (ISO)
cisplatin  (EXP)
crocidolite asbestos  (EXP)
Cuprizon  (ISO)
cyclosporin A  (EXP)
DDE  (EXP)
diazinon  (EXP)
Dibutyl phosphate  (EXP)
diquat  (ISO)
disodium selenite  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
ethyl methanesulfonate  (EXP)
flutamide  (ISO)
folic acid  (ISO)
FR900359  (EXP)
hydrogen peroxide  (EXP)
ivermectin  (EXP)
kojic acid  (EXP)
L-methionine  (ISO)
lead diacetate  (ISO)
lead(0)  (ISO)
methapyrilene  (EXP)
methoxychlor  (ISO)
methylmercury chloride  (EXP)
mono(2-ethylhexyl) phthalate  (EXP)
N,N-diethyl-m-toluamide  (ISO)
ozone  (EXP,ISO)
PD 0325901  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
permethrin  (ISO)
phenobarbital  (ISO)
pirinixic acid  (EXP)
potassium chromate  (EXP)
potassium dichromate  (ISO)
progesterone  (EXP)
propanal  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
rotenone  (ISO)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium dichromate  (EXP)
sulforaphane  (EXP)
tert-butyl hydroperoxide  (EXP)
testosterone  (ISO)
theophylline  (EXP)
thimerosal  (EXP)
thioacetamide  (ISO)
titanium dioxide  (ISO)
trichostatin A  (EXP)
triphenyl phosphate  (EXP)
valproic acid  (EXP)
vincristine  (EXP)
vorinostat  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cell projection  (IEA)
cytoplasm  (IBA,IEA)
cytosol  (IDA,IEA,TAS)
glutamatergic synapse  (IEA,ISO)
Golgi apparatus  (IDA)
membrane  (IDA)
nucleolus  (IDA)
plasma membrane  (IBA,IDA,IEA)
postsynapse  (IEA,ISO)
stereocilium  (IEA,ISS)
stereocilium bundle  (IEA,ISS)

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. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI 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:9872452   PMID:12432077   PMID:12477932   PMID:12628187   PMID:12853948   PMID:14702039   PMID:15324660   PMID:16213364   PMID:16344560   PMID:16464467   PMID:17027967   PMID:17353931  
PMID:18271526   PMID:18459162   PMID:18641688   PMID:19383911   PMID:19401682   PMID:19528233   PMID:19807924   PMID:20346443   PMID:20379614   PMID:20679435   PMID:21532034   PMID:21682944  
PMID:21706016   PMID:21873635   PMID:21930703   PMID:21988832   PMID:22158624   PMID:22315970   PMID:22747683   PMID:22788528   PMID:22890011   PMID:22952844   PMID:23084401   PMID:23402259  
PMID:23720743   PMID:24324551   PMID:24599690   PMID:25644601   PMID:25754235   PMID:25921289   PMID:26129894   PMID:26186194   PMID:26578796   PMID:28380382   PMID:28514442   PMID:28718761  
PMID:28925399   PMID:29331416   PMID:29395067   PMID:29507755   PMID:29540532   PMID:30021884   PMID:31019307   PMID:31091453   PMID:31678930   PMID:31871319   PMID:31980649   PMID:32203420  
PMID:32296183   PMID:32576693   PMID:33541421   PMID:33559155   PMID:33961781   PMID:33968925   PMID:34079125   PMID:34186245   PMID:34349018   PMID:34591612   PMID:35302184   PMID:35944360  
PMID:36215168   PMID:36543142   PMID:36822513   PMID:36931259   PMID:37689310   PMID:38113892   PMID:38443923   PMID:38526744   PMID:38580884  


Genomics

Comparative Map Data
DOCK4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387111,726,110 - 112,206,399 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7111,726,110 - 112,206,407 (-)EnsemblGRCh38hg38GRCh38
GRCh377111,366,166 - 111,846,454 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367111,153,400 - 111,633,698 (-)NCBINCBI36Build 36hg18NCBI36
Build 347110,962,280 - 111,440,144NCBI
Celera7106,178,467 - 106,658,751 (-)NCBICelera
Cytogenetic Map7q31.1NCBI
HuRef7105,734,071 - 106,214,221 (-)NCBIHuRef
CHM1_17111,300,360 - 111,780,666 (-)NCBICHM1_1
T2T-CHM13v2.07113,044,415 - 113,524,706 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27110,734,721 - 111,215,001 (-)NCBI
Dock4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391240,495,956 - 40,896,873 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1240,495,951 - 40,896,873 (+)EnsemblGRCm39 Ensembl
GRCm381240,445,957 - 40,846,874 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1240,445,952 - 40,846,874 (+)EnsemblGRCm38mm10GRCm38
MGSCv371241,172,640 - 41,573,082 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361240,956,476 - 41,356,918 (+)NCBIMGSCv36mm8
Celera1241,872,490 - 42,274,555 (+)NCBICelera
Cytogenetic Map12B1NCBI
cM Map1218.06NCBI
Dock4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8663,240,050 - 63,629,772 (+)NCBIGRCr8
mRatBN7.2657,512,929 - 57,902,597 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl657,512,908 - 57,901,855 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.0660,374,839 - 60,782,648 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl660,566,196 - 60,782,556 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0670,333,585 - 70,369,177 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.0669,962,956 - 70,320,855 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4659,903,426 - 60,136,543 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera656,552,544 - 56,940,868 (+)NCBICelera
Cytogenetic Map6q21NCBI
Dock4
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541015,550,235 - 15,777,103 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541015,548,041 - 15,835,382 (-)NCBIChiLan1.0ChiLan1.0
DOCK4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26148,562,897 - 149,034,110 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan17573,151 - 1,044,254 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v07103,697,418 - 104,169,469 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.17116,400,535 - 116,872,055 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7116,400,535 - 116,871,755 (-)Ensemblpanpan1.1panPan2
DOCK4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11451,448,910 - 51,859,366 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1451,451,059 - 51,859,040 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1450,903,465 - 51,313,338 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01451,494,893 - 51,905,212 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1451,497,038 - 51,905,147 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11451,512,246 - 51,919,885 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01451,195,473 - 51,603,462 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01451,565,830 - 51,975,770 (-)NCBIUU_Cfam_GSD_1.0
Dock4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511871,124,923 - 71,564,210 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367951,009,634 - 1,260,358 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936795823,730 - 1,262,584 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
DOCK4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1833,423,221 - 33,879,366 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11833,423,199 - 33,879,368 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21836,256,470 - 36,652,374 (+)NCBISscrofa10.2Sscrofa10.2susScr3
DOCK4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12180,548,079 - 81,022,410 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2180,547,655 - 80,812,702 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604222,793,912 - 23,269,122 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Dock4
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473917,705,769 - 18,152,858 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473917,705,893 - 18,152,679 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in DOCK4
130 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_014705.3(DOCK4):c.5013+116G>T single nucleotide variant Lung cancer [RCV000105414] Chr7:111740978 [GRCh38]
Chr7:111381034 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_014705.3(DOCK4):c.1481-1712G>A single nucleotide variant Lung cancer [RCV000105415] Chr7:111897430 [GRCh38]
Chr7:111537486 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh38/hg38 7q22.1-31.1(chr7:101807149-112414850)x1 copy number loss See cases [RCV000050924] Chr7:101807149..112414850 [GRCh38]
Chr7:101450429..112054905 [GRCh37]
Chr7:101237149..111842141 [NCBI36]
Chr7:7q22.1-31.1		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q31.1(chr7:111693844-112286237)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052718]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052718]|See cases [RCV000052718] Chr7:111693844..112286237 [GRCh38]
Chr7:111333900..111926292 [GRCh37]
Chr7:111121136..111713528 [NCBI36]
Chr7:7q31.1		 uncertain significance
GRCh38/hg38 7q31.1-31.31(chr7:110524677-118306203)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054159]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054159]|See cases [RCV000054159] Chr7:110524677..118306203 [GRCh38]
Chr7:110164734..117946257 [GRCh37]
Chr7:109951970..117733493 [NCBI36]
Chr7:7q31.1-31.31		 pathogenic
GRCh38/hg38 7q31.1(chr7:111693844-112335449)x3 copy number gain See cases [RCV000133852] Chr7:111693844..112335449 [GRCh38]
Chr7:111333900..111975504 [GRCh37]
Chr7:111121136..111762740 [NCBI36]
Chr7:7q31.1		 uncertain significance
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q31.1(chr7:112092584-112144255)x1 copy number loss See cases [RCV000135135] Chr7:112092584..112144255 [GRCh38]
Chr7:111732639..111784310 [GRCh37]
Chr7:111519875..111571546 [NCBI36]
Chr7:7q31.1		 benign
GRCh38/hg38 7q31.1(chr7:111771934-112414850)x3 copy number gain See cases [RCV000135752] Chr7:111771934..112414850 [GRCh38]
Chr7:111411990..112054905 [GRCh37]
Chr7:111199226..111842141 [NCBI36]
Chr7:7q31.1		 likely benign
GRCh38/hg38 7q31.1(chr7:111889459-112144314)x1 copy number loss See cases [RCV000136605] Chr7:111889459..112144314 [GRCh38]
Chr7:111529515..111784369 [GRCh37]
Chr7:111316751..111571605 [NCBI36]
Chr7:7q31.1		 uncertain significance
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3		 pathogenic
GRCh38/hg38 7q22.1-31.31(chr7:102196924-121278641)x1 copy number loss See cases [RCV000137522] Chr7:102196924..121278641 [GRCh38]
Chr7:101912320..120918695 [GRCh37]
Chr7:101626924..120705931 [NCBI36]
Chr7:7q22.1-31.31		 pathogenic
GRCh38/hg38 7q31.1(chr7:111465095-111830755)x1 copy number loss See cases [RCV000138175] Chr7:111465095..111830755 [GRCh38]
Chr7:111105151..111470811 [GRCh37]
Chr7:110892387..111258047 [NCBI36]
Chr7:7q31.1		 uncertain significance
GRCh38/hg38 7q31.1(chr7:111452375-111771993)x1 copy number loss See cases [RCV000140806] Chr7:111452375..111771993 [GRCh38]
Chr7:111092431..111412049 [GRCh37]
Chr7:110879667..111199285 [NCBI36]
Chr7:7q31.1		 uncertain significance
GRCh38/hg38 7q31.1(chr7:111482147-111855998)x1 copy number loss See cases [RCV000141897] Chr7:111482147..111855998 [GRCh38]
Chr7:111122203..111496054 [GRCh37]
Chr7:110909439..111283290 [NCBI36]
Chr7:7q31.1		 uncertain significance
NC_000007.13:g.111433419_111630024del deletion Normal pregnancy [RCV000161497] Chr7:111433419..111630024 [GRCh37]
Chr7:7q31.1		 not provided
GRCh37/hg19 7q31.1-32.1(chr7:111613396-127897316)x1 copy number loss See cases [RCV000240177] Chr7:111613396..127897316 [GRCh37]
Chr7:7q31.1-32.1		 pathogenic
GRCh37/hg19 7q31.1(chr7:111647224-112063278)x1 copy number loss See cases [RCV000449376] Chr7:111647224..112063278 [GRCh37]
Chr7:7q31.1		 uncertain significance
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q31.1(chr7:111201819-111835830)x3 copy number gain See cases [RCV000446892] Chr7:111201819..111835830 [GRCh37]
Chr7:7q31.1		 likely benign
GRCh37/hg19 7q31.1(chr7:111554114-111805855)x1 copy number loss See cases [RCV000446699] Chr7:111554114..111805855 [GRCh37]
Chr7:7q31.1		 likely benign
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
NC_000007.13:g.(?_110151471)_(112422581_?)dup duplication Schizophrenia [RCV000416690] Chr7:110151471..112422581 [GRCh37]
Chr7:109938707..112209817 [NCBI36]
Chr7:7q31.1		 likely pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q31.1-31.2(chr7:111642645-115770275)x1 copy number loss See cases [RCV000511505] Chr7:111642645..115770275 [GRCh37]
Chr7:7q31.1-31.2		 pathogenic
GRCh37/hg19 7q31.1(chr7:111054068-111372900)x1 copy number loss See cases [RCV000511920] Chr7:111054068..111372900 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q31.1(chr7:110322161-112423237)x3 copy number gain See cases [RCV000510770] Chr7:110322161..112423237 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1153A>T (p.Ile385Leu) single nucleotide variant not specified [RCV004316558] Chr7:111915818 [GRCh38]
Chr7:111555873 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1979T>C (p.Val660Ala) single nucleotide variant not specified [RCV004311969] Chr7:111872038 [GRCh38]
Chr7:111512094 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:110992183-111387739)x1 copy number loss See cases [RCV000512507] Chr7:110992183..111387739 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111303344-111922531)x1 copy number loss not provided [RCV000682858] Chr7:111303344..111922531 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111092450-111610938)x1 copy number loss not provided [RCV000682853] Chr7:111092450..111610938 [GRCh37]
Chr7:7q31.1		 likely benign
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
GRCh37/hg19 7q31.1(chr7:111069891-111778727)x3 copy number gain not provided [RCV000682865] Chr7:111069891..111778727 [GRCh37]
Chr7:7q31.1		 likely benign
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Childhood apraxia of speech [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1		 pathogenic
NC_000007.14:g.(?_111777402)_(111865491_?)del deletion Autism [RCV000754325] Chr7:111777402..111865491 [GRCh38]
Chr7:7q31.1		 likely pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
Single allele duplication Schizophrenia [RCV000754324] Chr7:110509840..112783102 [GRCh38]
Chr7:7q31.1		 likely pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q31.1(chr7:111092478-112140506)x3 copy number gain not provided [RCV000746997] Chr7:111092478..112140506 [GRCh37]
Chr7:7q31.1		 benign
GRCh37/hg19 7q31.1(chr7:111235377-111435243)x1 copy number loss not provided [RCV000747002] Chr7:111235377..111435243 [GRCh37]
Chr7:7q31.1		 benign
GRCh37/hg19 7q31.1(chr7:111309224-111952443)x1 copy number loss not provided [RCV000747003] Chr7:111309224..111952443 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.732C>T (p.Asn244=) single nucleotide variant not provided [RCV000919630] Chr7:111945768 [GRCh38]
Chr7:111585823 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.1603A>G (p.Asn535Asp) single nucleotide variant not provided [RCV000951096] Chr7:111877171 [GRCh38]
Chr7:111517227 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.4215G>A (p.Gln1405=) single nucleotide variant not provided [RCV000900260] Chr7:111758738 [GRCh38]
Chr7:111398794 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.576C>T (p.Asp192=) single nucleotide variant not provided [RCV000905585] Chr7:111977257 [GRCh38]
Chr7:111617312 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.2028-9G>A single nucleotide variant not provided [RCV000921786] Chr7:111869664 [GRCh38]
Chr7:111509720 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.1083A>G (p.Leu361=) single nucleotide variant not provided [RCV000905922] Chr7:111915888 [GRCh38]
Chr7:111555943 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.3792G>T (p.Leu1264=) single nucleotide variant not provided [RCV000880611] Chr7:111769565 [GRCh38]
Chr7:111409621 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.1416A>G (p.Lys472=) single nucleotide variant not provided [RCV000967065] Chr7:111900438 [GRCh38]
Chr7:111540494 [GRCh37]
Chr7:7q31.1		 benign
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q31.1(chr7:111366166-111682388)x1 copy number loss not provided [RCV003312706] Chr7:111366166..111682388 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:110968770-111390462)x3 copy number gain See cases [RCV000790580] Chr7:110968770..111390462 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2412G>A (p.Leu804=) single nucleotide variant not provided [RCV000939939] Chr7:111863433 [GRCh38]
Chr7:111503489 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.423C>T (p.Asp141=) single nucleotide variant not provided [RCV000975164] Chr7:111989056 [GRCh38]
Chr7:111629111 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.317G>A (p.Arg106His) single nucleotide variant not provided [RCV000982208] Chr7:111989162 [GRCh38]
Chr7:111629217 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.3083C>A (p.Ser1028Tyr) single nucleotide variant not provided [RCV000896642] Chr7:111809325 [GRCh38]
Chr7:111449381 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.3167G>A (p.Gly1056Glu) single nucleotide variant not provided [RCV000881737] Chr7:111790605 [GRCh38]
Chr7:111430661 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.550-8T>C single nucleotide variant not provided [RCV000897957] Chr7:111977291 [GRCh38]
Chr7:111617346 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.4074A>G (p.Gln1358=) single nucleotide variant not provided [RCV000895014] Chr7:111760269 [GRCh38]
Chr7:111400325 [GRCh37]
Chr7:7q31.1		 likely benign
GRCh37/hg19 7q31.1(chr7:111823490-111938673)x1 copy number loss not provided [RCV001005999] Chr7:111823490..111938673 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:109939104-113649529)x1 copy number loss not provided [RCV000849707] Chr7:109939104..113649529 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111580450-111715471)x1 copy number loss not provided [RCV000849715] Chr7:111580450..111715471 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111558284-111759659)x3 copy number gain not provided [RCV000847259] Chr7:111558284..111759659 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111188513-111395987)x1 copy number loss not provided [RCV000848950] Chr7:111188513..111395987 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1-31.31(chr7:107410314-117825549)x1 copy number loss not provided [RCV000846765] Chr7:107410314..117825549 [GRCh37]
Chr7:7q31.1-31.31		 pathogenic
Single allele duplication Neurodevelopmental disorder [RCV000787437] Chr7:111303881..114362948 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5491C>A (p.Gln1831Lys) single nucleotide variant not provided [RCV000963641] Chr7:111728711 [GRCh38]
Chr7:111368767 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.1095C>T (p.His365=) single nucleotide variant not provided [RCV000897909] Chr7:111915876 [GRCh38]
Chr7:111555931 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.784-7T>G single nucleotide variant not provided [RCV000917177] Chr7:111944878 [GRCh38]
Chr7:111584933 [GRCh37]
Chr7:7q31.1		 benign
GRCh37/hg19 7q22.3-31.32(chr7:106617406-123217914)x1 copy number loss not provided [RCV001005991] Chr7:106617406..123217914 [GRCh37]
Chr7:7q22.3-31.32		 pathogenic
GRCh37/hg19 7q31.1(chr7:107786826-112356275)x1 copy number loss not provided [RCV000847183] Chr7:107786826..112356275 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111772148-111869174)x1 copy number loss not provided [RCV000849386] Chr7:111772148..111869174 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111339228-111473040)x3 copy number gain not provided [RCV003233262] Chr7:111339228..111473040 [GRCh37]
Chr7:7q31.1		 not provided
NM_001363540.2(DOCK4):c.2771G>A (p.Arg924Gln) single nucleotide variant not specified [RCV004302475] Chr7:111834652 [GRCh38]
Chr7:111474708 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2937T>C (p.Ile979=) single nucleotide variant not provided [RCV000905584] Chr7:111811943 [GRCh38]
Chr7:111451999 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.5777C>T (p.Pro1926Leu) single nucleotide variant not provided [RCV000892273] Chr7:111728425 [GRCh38]
Chr7:111368481 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.4736G>A (p.Arg1579Lys) single nucleotide variant not provided [RCV000907349] Chr7:111742074 [GRCh38]
Chr7:111382130 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.316C>T (p.Arg106Cys) single nucleotide variant not provided [RCV000892511] Chr7:111989163 [GRCh38]
Chr7:111629218 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.4545T>C (p.Asn1515=) single nucleotide variant not provided [RCV000955380] Chr7:111747315 [GRCh38]
Chr7:111387371 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.121+10C>G single nucleotide variant not provided [RCV000908922] Chr7:112004038 [GRCh38]
Chr7:111644093 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.2878C>A (p.Arg960Ser) single nucleotide variant DOCK4-related disorder [RCV003910575]|not provided [RCV000890360] Chr7:111822414 [GRCh38]
Chr7:111462470 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.3030C>T (p.Leu1010=) single nucleotide variant not provided [RCV000911643] Chr7:111809378 [GRCh38]
Chr7:111449434 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.5814C>T (p.Pro1938=) single nucleotide variant not provided [RCV000913818] Chr7:111728388 [GRCh38]
Chr7:111368444 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.61G>A (p.Val21Ile) single nucleotide variant not provided [RCV000912615] Chr7:112004108 [GRCh38]
Chr7:111644163 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.2081G>T (p.Arg694Leu) single nucleotide variant not specified [RCV004304862] Chr7:111869602 [GRCh38]
Chr7:111509658 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111284148-111676080)x1 copy number loss not provided [RCV002473857] Chr7:111284148..111676080 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3 copy number gain not provided [RCV001005994] Chr7:109251060..159119707 [GRCh37]
Chr7:7q31.1-36.3		 pathogenic
GRCh37/hg19 7q31.1(chr7:109594999-113885203)x3 copy number gain not provided [RCV001005995] Chr7:109594999..113885203 [GRCh37]
Chr7:7q31.1		 likely pathogenic
GRCh37/hg19 7q31.1(chr7:111642645-111873378)x1 copy number loss not provided [RCV001005998] Chr7:111642645..111873378 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111724684-112064238)x3 copy number gain not provided [RCV001258814] Chr7:111724684..112064238 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111227710-111427735)x3 copy number gain not provided [RCV001258816] Chr7:111227710..111427735 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111237776-111464082)x1 copy number loss not provided [RCV001258818] Chr7:111237776..111464082 [GRCh37]
Chr7:7q31.1		 uncertain significance
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q31.1(chr7:111324658-111538227)x1 copy number loss not provided [RCV001832982] Chr7:111324658..111538227 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111609961-113375421)x3 copy number gain not provided [RCV001827681] Chr7:111609961..113375421 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111642646-111704409)x1 copy number loss not provided [RCV001834424] Chr7:111642646..111704409 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q22.1-31.1(chr7:99417471-111586308) copy number loss not specified [RCV002053711] Chr7:99417471..111586308 [GRCh37]
Chr7:7q22.1-31.1		 pathogenic
GRCh37/hg19 7q22.1-31.31(chr7:100676872-119156160) copy number loss not specified [RCV002053712] Chr7:100676872..119156160 [GRCh37]
Chr7:7q22.1-31.31		 pathogenic
GRCh37/hg19 7q22.3-32.1(chr7:106984287-128949489) copy number gain not specified [RCV002053715] Chr7:106984287..128949489 [GRCh37]
Chr7:7q22.3-32.1		 pathogenic
NM_014705.4(DOCK4):c.2027+14T>A single nucleotide variant not provided [RCV002221727]   benign
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3		 uncertain significance
NM_001363540.2(DOCK4):c.3879G>C (p.Glu1293Asp) single nucleotide variant not specified [RCV004295408] Chr7:111767068 [GRCh38]
Chr7:111407124 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5567A>G (p.Tyr1856Cys) single nucleotide variant not specified [RCV004288136] Chr7:111728635 [GRCh38]
Chr7:111368691 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111753333-112016056)x1 copy number loss not provided [RCV002465359] Chr7:111753333..112016056 [GRCh37]
Chr7:7q31.1		 not provided
GRCh37/hg19 7q31.1(chr7:111168726-111653169)x1 copy number loss not provided [RCV002475821] Chr7:111168726..111653169 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4330A>G (p.Ser1444Gly) single nucleotide variant not specified [RCV004192065] Chr7:111755601 [GRCh38]
Chr7:111395657 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.305A>T (p.Gln102Leu) single nucleotide variant not specified [RCV004138928] Chr7:111994145 [GRCh38]
Chr7:111634200 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.752A>C (p.Asp251Ala) single nucleotide variant not specified [RCV004154032] Chr7:111945748 [GRCh38]
Chr7:111585803 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3176A>G (p.Lys1059Arg) single nucleotide variant not specified [RCV004210404] Chr7:111790596 [GRCh38]
Chr7:111430652 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2342G>A (p.Arg781Gln) single nucleotide variant not specified [RCV004244266] Chr7:111863503 [GRCh38]
Chr7:111503559 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2063G>A (p.Arg688Gln) single nucleotide variant not specified [RCV004125862] Chr7:111869620 [GRCh38]
Chr7:111509676 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4459A>C (p.Asn1487His) single nucleotide variant not specified [RCV004102792] Chr7:111747401 [GRCh38]
Chr7:111387457 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1697C>T (p.Ser566Phe) single nucleotide variant not specified [RCV004242221] Chr7:111877077 [GRCh38]
Chr7:111517133 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5366C>T (p.Ser1789Leu) single nucleotide variant not specified [RCV004183704] Chr7:111735107 [GRCh38]
Chr7:111375163 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2247G>C (p.Glu749Asp) single nucleotide variant not specified [RCV004236923] Chr7:111868017 [GRCh38]
Chr7:111508073 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2882C>T (p.Pro961Leu) single nucleotide variant not specified [RCV004175604] Chr7:111822410 [GRCh38]
Chr7:111462466 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2851A>G (p.Ile951Val) single nucleotide variant not specified [RCV004229685] Chr7:111822441 [GRCh38]
Chr7:111462497 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5187G>C (p.Glu1729Asp) single nucleotide variant not specified [RCV004171643] Chr7:111739179 [GRCh38]
Chr7:111379235 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1280C>T (p.Thr427Met) single nucleotide variant not specified [RCV004241243] Chr7:111901714 [GRCh38]
Chr7:111541770 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2935A>G (p.Ile979Val) single nucleotide variant not specified [RCV004227529] Chr7:111811945 [GRCh38]
Chr7:111452001 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.205G>A (p.Val69Ile) single nucleotide variant not specified [RCV004121646] Chr7:111998461 [GRCh38]
Chr7:111638516 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.916C>G (p.Leu306Val) single nucleotide variant not specified [RCV004210506] Chr7:111940171 [GRCh38]
Chr7:111580226 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5438C>T (p.Thr1813Met) single nucleotide variant not specified [RCV004199658] Chr7:111732269 [GRCh38]
Chr7:111372325 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.570G>T (p.Lys190Asn) single nucleotide variant not specified [RCV004143061] Chr7:111977263 [GRCh38]
Chr7:111617318 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5908C>T (p.Arg1970Cys) single nucleotide variant not specified [RCV004167388] Chr7:111728294 [GRCh38]
Chr7:111368350 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3449G>A (p.Arg1150Gln) single nucleotide variant not specified [RCV004086219] Chr7:111783932 [GRCh38]
Chr7:111423988 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3873G>T (p.Gln1291His) single nucleotide variant not specified [RCV004108319] Chr7:111767074 [GRCh38]
Chr7:111407130 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5314C>T (p.Pro1772Ser) single nucleotide variant not specified [RCV004152225] Chr7:111735159 [GRCh38]
Chr7:111375215 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2980T>C (p.Phe994Leu) single nucleotide variant not specified [RCV004173948] Chr7:111811900 [GRCh38]
Chr7:111451956 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4771G>A (p.Val1591Met) single nucleotide variant not specified [RCV004073884] Chr7:111742039 [GRCh38]
Chr7:111382095 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5873G>A (p.Arg1958Lys) single nucleotide variant not specified [RCV004212595] Chr7:111728329 [GRCh38]
Chr7:111368385 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.148A>T (p.Asn50Tyr) single nucleotide variant not specified [RCV004228199] Chr7:112000508 [GRCh38]
Chr7:111640563 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3675T>G (p.Phe1225Leu) single nucleotide variant not specified [RCV004073803] Chr7:111778280 [GRCh38]
Chr7:111418336 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3647A>G (p.Tyr1216Cys) single nucleotide variant not specified [RCV004259001] Chr7:111778308 [GRCh38]
Chr7:111418364 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.826G>A (p.Val276Met) single nucleotide variant not specified [RCV004261160] Chr7:111944829 [GRCh38]
Chr7:111584884 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4063G>C (p.Glu1355Gln) single nucleotide variant not specified [RCV004272143] Chr7:111760280 [GRCh38]
Chr7:111400336 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3225G>T (p.Leu1075Phe) single nucleotide variant not specified [RCV004249215] Chr7:111790547 [GRCh38]
Chr7:111430603 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4241A>G (p.Lys1414Arg) single nucleotide variant not specified [RCV004268017] Chr7:111758712 [GRCh38]
Chr7:111398768 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2966C>G (p.Ala989Gly) single nucleotide variant not specified [RCV004269252] Chr7:111811914 [GRCh38]
Chr7:111451970 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5389C>T (p.Pro1797Ser) single nucleotide variant not specified [RCV004320993] Chr7:111735084 [GRCh38]
Chr7:111375140 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5462C>T (p.Ala1821Val) single nucleotide variant not specified [RCV004312375] Chr7:111732245 [GRCh38]
Chr7:111372301 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1715T>C (p.Phe572Ser) single nucleotide variant not specified [RCV004299968] Chr7:111877059 [GRCh38]
Chr7:111517115 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4286G>A (p.Arg1429Gln) single nucleotide variant DOCK4-related disorder [RCV003397280] Chr7:111758667 [GRCh38]
Chr7:111398723 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.702T>C (p.Ser234=) single nucleotide variant not specified [RCV004350083] Chr7:111945798 [GRCh38]
Chr7:111585853 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.5869C>T (p.Arg1957Trp) single nucleotide variant not specified [RCV004334685] Chr7:111728333 [GRCh38]
Chr7:111368389 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5350G>C (p.Glu1784Gln) single nucleotide variant not specified [RCV004362268] Chr7:111735123 [GRCh38]
Chr7:111375179 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5450C>A (p.Ser1817Tyr) single nucleotide variant not specified [RCV004352139] Chr7:111732257 [GRCh38]
Chr7:111372313 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5315C>T (p.Pro1772Leu) single nucleotide variant not specified [RCV004363779] Chr7:111735158 [GRCh38]
Chr7:111375214 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5732C>T (p.Pro1911Leu) single nucleotide variant not specified [RCV004346351] Chr7:111728470 [GRCh38]
Chr7:111368526 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.380G>A (p.Arg127Gln) single nucleotide variant not specified [RCV004346428] Chr7:111989099 [GRCh38]
Chr7:111629154 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1-31.2(chr7:108967155-116850770)x1 copy number loss not provided [RCV003482979] Chr7:108967155..116850770 [GRCh37]
Chr7:7q31.1-31.2		 pathogenic
NM_001363540.2(DOCK4):c.1238T>A (p.Phe413Tyr) single nucleotide variant not provided [RCV003423750] Chr7:111901756 [GRCh38]
Chr7:111541812 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5504C>T (p.Pro1835Leu) single nucleotide variant DOCK4-related disorder [RCV003418883] Chr7:111728698 [GRCh38]
Chr7:111368754 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3200T>C (p.Ile1067Thr) single nucleotide variant Neurodevelopmental disorder [RCV003388867] Chr7:111790572 [GRCh38]
Chr7:111430628 [GRCh37]
Chr7:7q31.1		 likely pathogenic
NM_001363540.2(DOCK4):c.758C>T (p.Pro253Leu) single nucleotide variant Neurodevelopmental disorder [RCV003388874] Chr7:111945742 [GRCh38]
Chr7:111585797 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4040G>A (p.Arg1347Gln) single nucleotide variant Neurodevelopmental disorder [RCV003388868] Chr7:111760303 [GRCh38]
Chr7:111400359 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2689C>T (p.Pro897Ser) single nucleotide variant Autism spectrum disorder [RCV003447827] Chr7:111844810 [GRCh38]
Chr7:111484866 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.892C>T (p.Arg298Ter) single nucleotide variant Neurodevelopmental disorder [RCV003388870] Chr7:111940195 [GRCh38]
Chr7:111580250 [GRCh37]
Chr7:7q31.1		 likely pathogenic|uncertain significance
NM_001363540.2(DOCK4):c.3937del (p.Asp1313fs) deletion Neurodevelopmental disorder [RCV003388872] Chr7:111765201 [GRCh38]
Chr7:111405257 [GRCh37]
Chr7:7q31.1		 likely pathogenic|uncertain significance
NM_001363540.2(DOCK4):c.3125T>C (p.Val1042Ala) single nucleotide variant Neurodevelopmental disorder [RCV003388873] Chr7:111808862 [GRCh38]
Chr7:111448918 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5913G>T (p.Lys1971Asn) single nucleotide variant Neurodevelopmental disorder [RCV003388869] Chr7:111728289 [GRCh38]
Chr7:111368345 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2770C>T (p.Arg924Ter) single nucleotide variant Neurodevelopmental disorder [RCV003388871] Chr7:111834653 [GRCh38]
Chr7:111474709 [GRCh37]
Chr7:7q31.1		 likely pathogenic|uncertain significance
NM_001363540.2(DOCK4):c.1258G>A (p.Val420Met) single nucleotide variant Neurodevelopmental disorder [RCV003388875] Chr7:111901736 [GRCh38]
Chr7:111541792 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2945C>T (p.Thr982Ile) single nucleotide variant Neurodevelopmental disorder [RCV003388865] Chr7:111811935 [GRCh38]
Chr7:111451991 [GRCh37]
Chr7:7q31.1		 likely pathogenic
NM_001363540.2(DOCK4):c.3131T>C (p.Met1044Thr) single nucleotide variant Neurodevelopmental disorder [RCV003388866] Chr7:111808856 [GRCh38]
Chr7:111448912 [GRCh37]
Chr7:7q31.1		 likely pathogenic
NM_001363540.2(DOCK4):c.550-1G>T single nucleotide variant not provided [RCV003490710] Chr7:111977284 [GRCh38]
Chr7:111617339 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:111340222-113515460)x3 copy number gain not specified [RCV003986681] Chr7:111340222..113515460 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3112G>A (p.Gly1038Ser) single nucleotide variant DOCK4-related disorder [RCV003892270] Chr7:111808875 [GRCh38]
Chr7:111448931 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3778C>T (p.Arg1260Cys) single nucleotide variant DOCK4-related disorder [RCV003909297] Chr7:111769579 [GRCh38]
Chr7:111409635 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5418T>A (p.Thr1806=) single nucleotide variant DOCK4-related disorder [RCV003981566] Chr7:111735055 [GRCh38]
Chr7:111375111 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.5738G>A (p.Ser1913Asn) single nucleotide variant DOCK4-related disorder [RCV003902096] Chr7:111728464 [GRCh38]
Chr7:111368520 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001363540.2(DOCK4):c.4417-2A>G single nucleotide variant DOCK4-related disorder [RCV003926854] Chr7:111747445 [GRCh38]
Chr7:111387501 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5804C>T (p.Ser1935Leu) single nucleotide variant DOCK4-related disorder [RCV003976645] Chr7:111728398 [GRCh38]
Chr7:111368454 [GRCh37]
Chr7:7q31.1		 benign
NM_001363540.2(DOCK4):c.23A>C (p.Glu8Ala) single nucleotide variant not specified [RCV004381878] Chr7:112206116 [GRCh38]
Chr7:111846171 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1649G>T (p.Gly550Val) single nucleotide variant not specified [RCV004381873] Chr7:111877125 [GRCh38]
Chr7:111517181 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3731G>A (p.Arg1244Gln) single nucleotide variant not specified [RCV004381882] Chr7:111769626 [GRCh38]
Chr7:111409682 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4385C>G (p.Ser1462Cys) single nucleotide variant not specified [RCV004381884] Chr7:111755546 [GRCh38]
Chr7:111395602 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5464G>A (p.Gly1822Arg) single nucleotide variant not specified [RCV004381887] Chr7:111732243 [GRCh38]
Chr7:111372299 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.340C>T (p.Arg114Trp) single nucleotide variant not specified [RCV004381881] Chr7:111989139 [GRCh38]
Chr7:111629194 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2867G>A (p.Arg956Gln) single nucleotide variant not specified [RCV004381880] Chr7:111822425 [GRCh38]
Chr7:111462481 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1327T>G (p.Ser443Ala) single nucleotide variant not specified [RCV004381872] Chr7:111900527 [GRCh38]
Chr7:111540583 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4421A>G (p.Glu1474Gly) single nucleotide variant not specified [RCV004381885] Chr7:111747439 [GRCh38]
Chr7:111387495 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2190G>C (p.Glu730Asp) single nucleotide variant not specified [RCV004381876] Chr7:111868074 [GRCh38]
Chr7:111508130 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4853G>A (p.Arg1618His) single nucleotide variant not specified [RCV004381886] Chr7:111741606 [GRCh38]
Chr7:111381662 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2831T>A (p.Leu944Gln) single nucleotide variant not specified [RCV004381879] Chr7:111834592 [GRCh38]
Chr7:111474648 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5506T>C (p.Ser1836Pro) single nucleotide variant not specified [RCV004381888] Chr7:111728696 [GRCh38]
Chr7:111368752 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.2336A>G (p.Asp779Gly) single nucleotide variant not specified [RCV004381877] Chr7:111863509 [GRCh38]
Chr7:111503565 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1699T>C (p.Phe567Leu) single nucleotide variant not specified [RCV004381874] Chr7:111877075 [GRCh38]
Chr7:111517131 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3689A>G (p.Tyr1230Cys) single nucleotide variant not specified [RCV004624427] Chr7:111769668 [GRCh38]
Chr7:111409724 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.411C>G (p.Asp137Glu) single nucleotide variant not specified [RCV004624429] Chr7:111989068 [GRCh38]
Chr7:111629123 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5738G>T (p.Ser1913Ile) single nucleotide variant not specified [RCV004624430] Chr7:111728464 [GRCh38]
Chr7:111368520 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1637C>A (p.Pro546His) single nucleotide variant not specified [RCV004624431] Chr7:111877137 [GRCh38]
Chr7:111517193 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.379C>T (p.Arg127Trp) single nucleotide variant not specified [RCV004624432] Chr7:111989100 [GRCh38]
Chr7:111629155 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3593A>G (p.Tyr1198Cys) single nucleotide variant not specified [RCV004624433] Chr7:111778362 [GRCh38]
Chr7:111418418 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5374G>A (p.Gly1792Arg) single nucleotide variant not specified [RCV004624434] Chr7:111735099 [GRCh38]
Chr7:111375155 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.953A>G (p.Asp318Gly) single nucleotide variant not specified [RCV004624435] Chr7:111940134 [GRCh38]
Chr7:111580189 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.785A>G (p.Asp262Gly) single nucleotide variant not specified [RCV004624436] Chr7:111944870 [GRCh38]
Chr7:111584925 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4891G>T (p.Asp1631Tyr) single nucleotide variant not specified [RCV004624437] Chr7:111741568 [GRCh38]
Chr7:111381624 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3668A>G (p.Gln1223Arg) single nucleotide variant not specified [RCV004624439] Chr7:111778287 [GRCh38]
Chr7:111418343 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3229C>G (p.Pro1077Ala) single nucleotide variant not specified [RCV004624440] Chr7:111790543 [GRCh38]
Chr7:111430599 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.1774A>G (p.Thr592Ala) single nucleotide variant not specified [RCV004624441] Chr7:111872535 [GRCh38]
Chr7:111512591 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3941A>G (p.Lys1314Arg) single nucleotide variant not specified [RCV004624442] Chr7:111765197 [GRCh38]
Chr7:111405253 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5071A>G (p.Thr1691Ala) single nucleotide variant not specified [RCV004624443] Chr7:111739447 [GRCh38]
Chr7:111379503 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.878G>A (p.Cys293Tyr) single nucleotide variant not specified [RCV004624444] Chr7:111940209 [GRCh38]
Chr7:111580264 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.4492C>T (p.Gln1498Ter) single nucleotide variant DOCK4-related disorder [RCV004740140] Chr7:111747368 [GRCh38]
Chr7:111387424 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.3316-10T>G single nucleotide variant DOCK4-related disorder [RCV004729852] Chr7:111788757 [GRCh38]
Chr7:111428813 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001363540.2(DOCK4):c.5398C>T (p.Pro1800Ser) single nucleotide variant DOCK4-related disorder [RCV004728371] Chr7:111735075 [GRCh38]
Chr7:111375131 [GRCh37]
Chr7:7q31.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2904
Count of miRNA genes:1101
Interacting mature miRNAs:1324
Transcripts:ENST00000417165, ENST00000423057, ENST00000428053, ENST00000428084, ENST00000437129, ENST00000437633, ENST00000445943, ENST00000450156, ENST00000464338, ENST00000468571, ENST00000469898, ENST00000476846, ENST00000486186, ENST00000492436, ENST00000492532, ENST00000494651, ENST00000494769
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407104195GWAS753171_Hprotein measurement QTL GWAS753171 (human)2e-08protein measurement7112036530112036531Human
407325383GWAS974359_Htestosterone measurement QTL GWAS974359 (human)7e-10testosterone measurementserum testosterone level (CMO:0000568)7112010597112010598Human
406928320GWAS577296_HAstigmatism QTL GWAS577296 (human)0.000002Astigmatism7111988366111988367Human
407282308GWAS931284_Hdehydroepiandrosterone sulphate measurement QTL GWAS931284 (human)0.000003dehydroepiandrosterone sulphate measurementblood progesterone level (CMO:0000514)7112134457112134458Human
407120135GWAS769111_Hprotein measurement QTL GWAS769111 (human)6e-09protein measurement7112036530112036531Human
406905029GWAS554005_HR-warfarin measurement QTL GWAS554005 (human)0.000008R-warfarin measurement7111935203111935204Human
407226816GWAS875792_Hconcentration dose ratio, response to antidepressant QTL GWAS875792 (human)0.0000003concentration dose ratio, response to antidepressant7111871082111871083Human
407362498GWAS1011474_Htype 2 diabetes mellitus QTL GWAS1011474 (human)8e-08type 2 diabetes mellitus7111746160111746161Human
407037065GWAS686041_Hprotein measurement QTL GWAS686041 (human)9e-10protein measurement7111859525111859526Human
407001166GWAS650142_Hsex hormone-binding globulin measurement QTL GWAS650142 (human)2e-08sex hormone-binding globulin measurement7111984034111984035Human
407027663GWAS676639_Hbreast size QTL GWAS676639 (human)0.000006breast sizemammary gland morphological measurement (CMO:0000414)7112002591112002592Human
407234312GWAS883288_Hbone density QTL GWAS883288 (human)1e-300bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)7111811293111811294Human
407004439GWAS653415_Hprotein measurement QTL GWAS653415 (human)1e-08protein measurement7112036530112036531Human
407028503GWAS677479_HC-reactive protein measurement QTL GWAS677479 (human)7e-11C-reactive protein measurementblood C-reactive protein level (CMO:0003160)7111887504111887505Human
407047253GWAS696229_Hprotein measurement QTL GWAS696229 (human)2e-08protein measurement7112045209112045210Human
407368912GWAS1017888_HAlzheimer disease, diastolic blood pressure QTL GWAS1017888 (human)8e-08Alzheimer disease, diastolic blood pressurediastolic blood pressure (CMO:0000005)7111940111111940112Human
407317663GWAS966639_Htestosterone measurement QTL GWAS966639 (human)3e-09testosterone measurementserum testosterone level (CMO:0000568)7112048267112048268Human
407419025GWAS1068001_Hdiastolic blood pressure QTL GWAS1068001 (human)0.000001diastolic blood pressurediastolic blood pressure (CMO:0000005)7111940111111940112Human
406980504GWAS629480_Hintracranial volume measurement QTL GWAS629480 (human)0.000007intracranial volume measurement7111745615111745616Human
407314968GWAS963944_Htestosterone measurement QTL GWAS963944 (human)3e-09testosterone measurementserum testosterone level (CMO:0000568)7112010597112010598Human
407080227GWAS729203_HPR interval QTL GWAS729203 (human)0.000003PR intervalPR interval (CMO:0000233)7111811603111811604Human
407029152GWAS678128_Hresponse to fenofibrate QTL GWAS678128 (human)0.0000001response to fenofibrate7112037851112037852Human
407326821GWAS975797_Htestosterone measurement QTL GWAS975797 (human)1e-09testosterone measurementserum testosterone level (CMO:0000568)7112022774112022775Human
407336484GWAS985460_Hinsomnia QTL GWAS985460 (human)4e-08insomnia7111761945111761946Human
407037094GWAS686070_Hprotein measurement QTL GWAS686070 (human)2e-09protein measurement7112036530112036531Human
407336483GWAS985459_Hinsomnia QTL GWAS985459 (human)3e-08insomnia7111745615111745616Human
407194221GWAS843197_Hpost-traumatic stress disorder QTL GWAS843197 (human)0.000003post-traumatic stress disorder7111734005111734006Human
407153133GWAS802109_Hgut microbiome measurement QTL GWAS802109 (human)0.000006gut microbiome measurement7111901636111901637Human
407289261GWAS938237_Hserum albumin measurement QTL GWAS938237 (human)5e-11serum albumin measurementserum albumin level (CMO:0000550)7111984034111984035Human
407360556GWAS1009532_Hdiastolic blood pressure QTL GWAS1009532 (human)5e-09diastolic blood pressurediastolic blood pressure (CMO:0000005)7111940111111940112Human
407035827GWAS684803_Hprotein measurement QTL GWAS684803 (human)7e-09protein measurement7112036530112036531Human
407038833GWAS687809_Hlongitudinal BMI measurement QTL GWAS687809 (human)0.000005longitudinal BMI measurementbody mass index (BMI) (CMO:0000105)7112058053112058054Human
407325940GWAS974916_Htestosterone measurement QTL GWAS974916 (human)2e-08testosterone measurementserum testosterone level (CMO:0000568)7112048267112048268Human
407363006GWAS1011982_Hdiastolic blood pressure QTL GWAS1011982 (human)3e-08diastolic blood pressurediastolic blood pressure (CMO:0000005)7111940111111940112Human
407227391GWAS876367_Hbody height QTL GWAS876367 (human)8e-10body height (VT:0001253)body height (CMO:0000106)7112123424112123425Human
407019001GWAS667977_Hsex hormone-binding globulin measurement QTL GWAS667977 (human)4e-08sex hormone-binding globulin measurement7111984034111984035Human
407373940GWAS1022916_Hserum albumin measurement QTL GWAS1022916 (human)2e-10serum albumin measurementserum albumin level (CMO:0000550)7111940111111940112Human

Markers in Region
D7S523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,701,727 - 111,701,958UniSTSGRCh37
GRCh377111,701,890 - 111,701,958UniSTSGRCh37
GRCh377111,701,726 - 111,701,910UniSTSGRCh37
Build 367111,488,962 - 111,489,146RGDNCBI36
Celera7106,514,020 - 106,514,253UniSTS
Celera7106,514,185 - 106,514,253UniSTS
Celera7106,514,019 - 106,514,205RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,069,515 - 106,069,750UniSTS
HuRef7106,069,682 - 106,069,750UniSTS
HuRef7106,069,514 - 106,069,702UniSTS
CRA_TCAGchr7v27111,070,455 - 111,070,523UniSTS
CRA_TCAGchr7v27111,070,287 - 111,070,475UniSTS
CRA_TCAGchr7v27111,070,288 - 111,070,523UniSTS
Marshfield Genetic Map7123.01UniSTS
Marshfield Genetic Map7123.01RGD
Genethon Genetic Map7123.9UniSTS
TNG Radiation Hybrid Map749272.0UniSTS
Stanford-G3 RH Map75560.0UniSTS
GeneMap99-GB4 RH Map7541.09UniSTS
Whitehead-YAC Contig Map7 UniSTS
NCBI RH Map71108.2UniSTS
GeneMap99-G3 RH Map75560.0UniSTS
GDB:3754623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,611,967 - 111,612,061UniSTSGRCh37
Build 367111,399,203 - 111,399,297RGDNCBI36
Celera7106,424,276 - 106,424,370RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,979,768 - 105,979,862UniSTS
CRA_TCAGchr7v27110,980,536 - 110,980,630UniSTS
GDB:1234268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,649,666 - 111,649,855UniSTSGRCh37
Build 367111,436,902 - 111,437,091RGDNCBI36
Celera7106,461,967 - 106,462,156RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,017,458 - 106,017,647UniSTS
CRA_TCAGchr7v27111,018,234 - 111,018,423UniSTS
RH94189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,366,200 - 111,366,334UniSTSGRCh37
Build 367111,153,436 - 111,153,570RGDNCBI36
Celera7106,178,503 - 106,178,637RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,734,107 - 105,734,241UniSTS
CRA_TCAGchr7v27110,734,757 - 110,734,891UniSTS
GeneMap99-GB4 RH Map7537.91UniSTS
RH93151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,763,154 - 111,763,307UniSTSGRCh37
Build 367111,550,390 - 111,550,543RGDNCBI36
Celera7106,575,446 - 106,575,599RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,130,917 - 106,131,070UniSTS
CRA_TCAGchr7v27111,131,699 - 111,131,852UniSTS
GeneMap99-GB4 RH Map7542.09UniSTS
G42167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,750,494 - 111,751,029UniSTSGRCh37
Build 367111,537,730 - 111,538,265RGDNCBI36
Celera7106,562,789 - 106,563,324RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,118,269 - 106,118,804UniSTS
CRA_TCAGchr7v27111,119,043 - 111,119,578UniSTS
G42169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,654,497 - 111,654,705UniSTSGRCh37
Build 367111,441,733 - 111,441,941RGDNCBI36
Celera7106,466,798 - 106,467,006RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,022,289 - 106,022,497UniSTS
CRA_TCAGchr7v27111,023,065 - 111,023,273UniSTS
G49158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,374,545 - 111,374,835UniSTSGRCh37
Build 367111,161,781 - 111,162,071RGDNCBI36
Celera7106,186,851 - 106,187,141RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,742,455 - 105,742,745UniSTS
CRA_TCAGchr7v27110,743,105 - 110,743,395UniSTS
TNG Radiation Hybrid Map749076.0UniSTS
G49159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,471,922 - 111,472,235UniSTSGRCh37
Build 367111,259,158 - 111,259,471RGDNCBI36
Celera7106,284,221 - 106,284,534RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,839,748 - 105,840,061UniSTS
CRA_TCAGchr7v27110,840,476 - 110,840,789UniSTS
TNG Radiation Hybrid Map749166.0UniSTS
SHGC-81329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,429,050 - 111,429,359UniSTSGRCh37
Build 367111,216,286 - 111,216,595RGDNCBI36
Celera7106,241,348 - 106,241,657RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,796,868 - 105,797,177UniSTS
CRA_TCAGchr7v27110,797,604 - 110,797,913UniSTS
TNG Radiation Hybrid Map749147.0UniSTS
RH119391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,639,748 - 111,640,076UniSTSGRCh37
Build 367111,426,984 - 111,427,312RGDNCBI36
Celera7106,452,049 - 106,452,377RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,007,545 - 106,007,873UniSTS
CRA_TCAGchr7v27111,008,316 - 111,008,644UniSTS
TNG Radiation Hybrid Map749235.0UniSTS
RH119803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,370,047 - 111,370,332UniSTSGRCh37
Build 367111,157,283 - 111,157,568RGDNCBI36
Celera7106,182,350 - 106,182,635RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,737,954 - 105,738,239UniSTS
CRA_TCAGchr7v27110,738,604 - 110,738,889UniSTS
TNG Radiation Hybrid Map749099.0UniSTS
RH118992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,787,455 - 111,787,732UniSTSGRCh37
Build 367111,574,691 - 111,574,968RGDNCBI36
Celera7106,599,748 - 106,600,025RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,155,216 - 106,155,493UniSTS
CRA_TCAGchr7v27111,156,001 - 111,156,278UniSTS
TNG Radiation Hybrid Map749313.0UniSTS
RH68519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,820,730 - 111,820,936UniSTSGRCh37
Build 367111,607,966 - 111,608,172RGDNCBI36
Celera7106,633,016 - 106,633,222RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,188,485 - 106,188,691UniSTS
CRA_TCAGchr7v27111,189,269 - 111,189,475UniSTS
GeneMap99-GB4 RH Map7541.09UniSTS
NCBI RH Map71108.2UniSTS
SHGC-173129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,623,030 - 111,623,304UniSTSGRCh37
Build 367111,410,266 - 111,410,540RGDNCBI36
Celera7106,435,337 - 106,435,611RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,990,828 - 105,991,102UniSTS
CRA_TCAGchr7v27110,991,602 - 110,991,876UniSTS
TNG Radiation Hybrid Map749223.0UniSTS
L29706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,566,768 - 111,567,104UniSTSGRCh37
Build 367111,354,004 - 111,354,340RGDNCBI36
Celera7106,379,075 - 106,379,411RGD
HuRef7105,934,566 - 105,934,902UniSTS
CRA_TCAGchr7v27110,935,335 - 110,935,671UniSTS
RH48305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,367,258 - 111,367,378UniSTSGRCh37
Build 367111,154,494 - 111,154,614RGDNCBI36
Celera7106,179,561 - 106,179,681RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,735,165 - 105,735,285UniSTS
CRA_TCAGchr7v27110,735,815 - 110,735,935UniSTS
GeneMap99-GB4 RH Map7537.91UniSTS
NCBI RH Map71105.0UniSTS
D7S1424  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,445,767 - 111,445,926UniSTSGRCh37
Build 367111,233,003 - 111,233,162RGDNCBI36
Celera7106,258,065 - 106,258,224RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,813,589 - 105,813,748UniSTS
CRA_TCAGchr7v27110,814,321 - 110,814,480UniSTS
GDB:4585517  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,824,062 - 111,824,149UniSTSGRCh37
Build 367111,611,298 - 111,611,385RGDNCBI36
Celera7106,636,350 - 106,636,437RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,191,819 - 106,191,906UniSTS
CRA_TCAGchr7v27111,192,603 - 111,192,690UniSTS
GDB:1317590  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,637,505 - 111,637,671UniSTSGRCh37
Build 367111,424,741 - 111,424,907RGDNCBI36
Celera7106,449,806 - 106,449,972RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,005,301 - 106,005,467UniSTS
CRA_TCAGchr7v27111,006,073 - 111,006,239UniSTS
GDB:1317986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,786,946 - 111,787,221UniSTSGRCh37
Build 367111,574,182 - 111,574,457RGDNCBI36
Celera7106,599,239 - 106,599,514RGD
Cytogenetic Map7q31.1UniSTS
HuRef7106,154,707 - 106,154,982UniSTS
CRA_TCAGchr7v27111,155,492 - 111,155,767UniSTS
A009E05  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,419,163 - 111,419,262UniSTSGRCh37
Build 367111,206,399 - 111,206,498RGDNCBI36
Celera7106,231,461 - 106,231,560RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,786,981 - 105,787,080UniSTS
CRA_TCAGchr7v27110,787,717 - 110,787,816UniSTS
GeneMap99-GB4 RH Map7541.09UniSTS
NCBI RH Map71107.0UniSTS
RH66687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,586,359 - 111,586,524UniSTSGRCh37
Build 367111,373,595 - 111,373,760RGDNCBI36
Celera7106,398,666 - 106,398,831RGD
Cytogenetic Map7q31.1UniSTS
HuRef7105,954,156 - 105,954,321UniSTS
CRA_TCAGchr7v27110,954,926 - 110,955,091UniSTS
GeneMap99-GB4 RH Map7541.09UniSTS
NCBI RH Map71107.0UniSTS
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map10q11.1-q24UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic MapXq13.1-q21.1UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map9p23UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map6p12UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map22q12.3-q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map19q11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map1p32.2-p32.1UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map4q13.2UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map14q24.2UniSTS
G32465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377111,419,163 - 111,419,262UniSTSGRCh37
Celera7106,231,461 - 106,231,560UniSTS
Cytogenetic Map7q31.1UniSTS
HuRef7105,786,981 - 105,787,080UniSTS
CRA_TCAGchr7v27110,787,717 - 110,787,816UniSTS
D7S523  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7q31.1UniSTS
D7S523  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7q31.1UniSTS
TNG Radiation Hybrid Map749272.0UniSTS
Stanford-G3 RH Map75560.0UniSTS
GeneMap99-GB4 RH Map7541.09UniSTS
NCBI RH Map71108.2UniSTS
GeneMap99-G3 RH Map75560.0UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1204 2434 2788 2247 4968 1724 2345 4 622 1922 464 2269 7259 6431 52 3731 847 1732 1612 171

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_028060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014705 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716189 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421079 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359408 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359411 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359414 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359415 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359416 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054359419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB018259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC003077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC003080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005047 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF085922 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055497 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK098050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294722 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY233380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC117688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC117689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC117694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM126591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM545903 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA646980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458551 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458553 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458554 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458555 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510967 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LS482367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000417165   ⟹   ENSP00000403504
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,769,657 - 111,789,024 (-)Ensembl
Ensembl Acc Id: ENST00000423057   ⟹   ENSP00000412834
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,726,110 - 111,877,128 (-)Ensembl
Ensembl Acc Id: ENST00000428053   ⟹   ENSP00000393486
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,760,224 - 111,784,426 (-)Ensembl
Ensembl Acc Id: ENST00000428084   ⟹   ENSP00000410746
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,726,110 - 112,206,399 (-)Ensembl
Ensembl Acc Id: ENST00000437129   ⟹   ENSP00000406298
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,765,155 - 111,784,428 (-)Ensembl
Ensembl Acc Id: ENST00000437633   ⟹   ENSP00000404179
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,726,110 - 112,206,399 (-)Ensembl
Ensembl Acc Id: ENST00000445943   ⟹   ENSP00000397412
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,728,274 - 112,004,131 (-)Ensembl
Ensembl Acc Id: ENST00000450156   ⟹   ENSP00000406468
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,726,691 - 111,784,479 (-)Ensembl
Ensembl Acc Id: ENST00000468571
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,976,538 - 111,994,173 (-)Ensembl
Ensembl Acc Id: ENST00000469898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,788,501 - 111,822,424 (-)Ensembl
Ensembl Acc Id: ENST00000476846
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,862,883 - 112,206,394 (-)Ensembl
Ensembl Acc Id: ENST00000486186
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,726,747 - 111,740,214 (-)Ensembl
Ensembl Acc Id: ENST00000492436
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,767,081 - 111,789,260 (-)Ensembl
Ensembl Acc Id: ENST00000492532
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,869,460 - 111,872,347 (-)Ensembl
Ensembl Acc Id: ENST00000494651   ⟹   ENSP00000440944
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,801,686 - 112,004,132 (-)Ensembl
Ensembl Acc Id: ENST00000494769
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,728,421 - 111,732,514 (-)Ensembl
Ensembl Acc Id: ENST00000658652   ⟹   ENSP00000499282
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,726,154 - 111,809,321 (-)Ensembl
Ensembl Acc Id: ENST00000661654
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,935,108 - 112,206,407 (-)Ensembl
Ensembl Acc Id: ENST00000664131   ⟹   ENSP00000499490
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7111,726,824 - 111,784,426 (-)Ensembl
RefSeq Acc Id: NM_001363540   ⟹   NP_001350469
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,399 (-)NCBI
T2T-CHM13v2.07113,044,415 - 113,524,706 (-)NCBI
Sequence:
RefSeq Acc Id: NM_014705   ⟹   NP_055520
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,399 (-)NCBI
GRCh377111,366,164 - 111,846,462 (-)ENTREZGENE
Build 367111,153,400 - 111,633,698 (-)NCBI Archive
HuRef7105,734,071 - 106,214,221 (-)ENTREZGENE
CHM1_17111,300,360 - 111,780,666 (-)NCBI
T2T-CHM13v2.07113,044,415 - 113,524,706 (-)NCBI
CRA_TCAGchr7v27110,734,721 - 111,215,001 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: XM_006716189   ⟹   XP_006716252
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,399 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012819   ⟹   XP_016868308
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,067 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012820   ⟹   XP_016868309
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,066 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012821   ⟹   XP_016868310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,068 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012822   ⟹   XP_016868311
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,047,464 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012823   ⟹   XP_016868312
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,068 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012824   ⟹   XP_016868313
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,067 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012825   ⟹   XP_016868314
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,068 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024447006   ⟹   XP_024302774
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,066 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047421078   ⟹   XP_047277034
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,067 (-)NCBI
RefSeq Acc Id: XM_047421079   ⟹   XP_047277035
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,047,463 (-)NCBI
RefSeq Acc Id: XM_047421081   ⟹   XP_047277037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387111,726,110 - 112,206,399 (-)NCBI
RefSeq Acc Id: XM_054359408   ⟹   XP_054215383
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,374 (-)NCBI
RefSeq Acc Id: XM_054359409   ⟹   XP_054215384
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,373 (-)NCBI
RefSeq Acc Id: XM_054359410   ⟹   XP_054215385
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,375 (-)NCBI
RefSeq Acc Id: XM_054359411   ⟹   XP_054215386
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,365,779 (-)NCBI
RefSeq Acc Id: XM_054359412   ⟹   XP_054215387
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,374 (-)NCBI
RefSeq Acc Id: XM_054359413   ⟹   XP_054215388
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,365,778 (-)NCBI
RefSeq Acc Id: XM_054359414   ⟹   XP_054215389
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,375 (-)NCBI
RefSeq Acc Id: XM_054359415   ⟹   XP_054215390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,374 (-)NCBI
RefSeq Acc Id: XM_054359416   ⟹   XP_054215391
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,375 (-)NCBI
RefSeq Acc Id: XM_054359417   ⟹   XP_054215392
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,706 (-)NCBI
RefSeq Acc Id: XM_054359418   ⟹   XP_054215393
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,706 (-)NCBI
RefSeq Acc Id: XM_054359419   ⟹   XP_054215394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07113,044,415 - 113,524,373 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001350469 (Get FASTA)   NCBI Sequence Viewer  
  NP_055520 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716252 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868308 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868309 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868310 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868311 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868312 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868313 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868314 (Get FASTA)   NCBI Sequence Viewer  
  XP_024302774 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277034 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277035 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277037 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215383 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215384 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215385 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215386 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215387 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215388 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215389 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215390 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215391 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215392 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215393 (Get FASTA)   NCBI Sequence Viewer  
  XP_054215394 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB83946 (Get FASTA)   NCBI Sequence Viewer  
  AAI17689 (Get FASTA)   NCBI Sequence Viewer  
  AAI17690 (Get FASTA)   NCBI Sequence Viewer  
  AAI17695 (Get FASTA)   NCBI Sequence Viewer  
  AAO73565 (Get FASTA)   NCBI Sequence Viewer  
  AAS07431 (Get FASTA)   NCBI Sequence Viewer  
  BAA34436 (Get FASTA)   NCBI Sequence Viewer  
  BAC03696 (Get FASTA)   NCBI Sequence Viewer  
  BAC05221 (Get FASTA)   NCBI Sequence Viewer  
  BAH11861 (Get FASTA)   NCBI Sequence Viewer  
  BAH11895 (Get FASTA)   NCBI Sequence Viewer  
  EAL24377 (Get FASTA)   NCBI Sequence Viewer  
  EAW83451 (Get FASTA)   NCBI Sequence Viewer  
  EAW83452 (Get FASTA)   NCBI Sequence Viewer  
  EAW83453 (Get FASTA)   NCBI Sequence Viewer  
  EAW83454 (Get FASTA)   NCBI Sequence Viewer  
  EAW83455 (Get FASTA)   NCBI Sequence Viewer  
  EAW83456 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000393486.1
  ENSP00000397412.1
  ENSP00000403504.1
  ENSP00000404179
  ENSP00000404179.1
  ENSP00000406298.1
  ENSP00000406468.2
  ENSP00000410746
  ENSP00000410746.1
  ENSP00000412834.1
  ENSP00000499282.1
  ENSP00000499490.1
GenBank Protein Q8N1I0 (Get FASTA)   NCBI Sequence Viewer  
  SPT35744 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_055520   ⟸   NM_014705
- Peptide Label: isoform 1
- UniProtKB: O94824 (UniProtKB/Swiss-Prot),   O14584 (UniProtKB/Swiss-Prot),   Q8NB45 (UniProtKB/Swiss-Prot),   Q8N1I0 (UniProtKB/Swiss-Prot),   Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006716252   ⟸   XM_006716189
- Peptide Label: isoform X11
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868313   ⟸   XM_017012824
- Peptide Label: isoform X8
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868314   ⟸   XM_017012825
- Peptide Label: isoform X9
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868310   ⟸   XM_017012821
- Peptide Label: isoform X3
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868308   ⟸   XM_017012819
- Peptide Label: isoform X1
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868309   ⟸   XM_017012820
- Peptide Label: isoform X2
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868312   ⟸   XM_017012823
- Peptide Label: isoform X7
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868311   ⟸   XM_017012822
- Peptide Label: isoform X4
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024302774   ⟸   XM_024447006
- Peptide Label: isoform X12
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001350469   ⟸   NM_001363540
- Peptide Label: isoform 2
- UniProtKB: Q149N6 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000412834   ⟸   ENST00000423057
Ensembl Acc Id: ENSP00000404179   ⟸   ENST00000437633
Ensembl Acc Id: ENSP00000406468   ⟸   ENST00000450156
Ensembl Acc Id: ENSP00000410746   ⟸   ENST00000428084
Ensembl Acc Id: ENSP00000393486   ⟸   ENST00000428053
Ensembl Acc Id: ENSP00000499490   ⟸   ENST00000664131
Ensembl Acc Id: ENSP00000440944   ⟸   ENST00000494651
Ensembl Acc Id: ENSP00000403504   ⟸   ENST00000417165
Ensembl Acc Id: ENSP00000397412   ⟸   ENST00000445943
Ensembl Acc Id: ENSP00000499282   ⟸   ENST00000658652
Ensembl Acc Id: ENSP00000406298   ⟸   ENST00000437129
RefSeq Acc Id: XP_047277037   ⟸   XM_047421081
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047277034   ⟸   XM_047421078
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047277035   ⟸   XM_047421079
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054215392   ⟸   XM_054359417
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054215393   ⟸   XM_054359418
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054215391   ⟸   XM_054359416
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054215385   ⟸   XM_054359410
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054215389   ⟸   XM_054359414
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054215387   ⟸   XM_054359412
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054215390   ⟸   XM_054359415
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054215383   ⟸   XM_054359408
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054215394   ⟸   XM_054359419
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054215384   ⟸   XM_054359409
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054215386   ⟸   XM_054359411
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054215388   ⟸   XM_054359413
- Peptide Label: isoform X6
Protein Domains
C2 DOCK-type   DOCKER   SH3

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8N1I0-F1-model_v2 AlphaFold Q8N1I0 1-1966 view protein structure

Promoters
RGD ID:6806443
Promoter ID:HG_KWN:59313
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_014705,   NM_021994,   OTTHUMT00000338469,   OTTHUMT00000338472,   OTTHUMT00000338473,   OTTHUMT00000338940,   OTTHUMT00000338943,   UC003VFY.1,   UC003VGA.1,   UC003VGC.2,   UC003VGD.2,   UC003VGF.2,   UC010LJT.1
Position:
Human AssemblyChrPosition (strand)Source
Build 367111,632,401 - 111,634,057 (+)MPROMDB
RGD ID:7211681
Promoter ID:EPDNEW_H11583
Type:initiation region
Name:DOCK4_1
Description:dedicator of cytokinesis 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
GRCh387112,206,394 - 112,206,454EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:19192 AgrOrtholog
COSMIC DOCK4 COSMIC
Ensembl Genes ENSG00000128512 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000417165.1 UniProtKB/TrEMBL
  ENST00000423057.6 UniProtKB/TrEMBL
  ENST00000428053.5 UniProtKB/TrEMBL
  ENST00000428084 ENTREZGENE
  ENST00000428084.6 UniProtKB/Swiss-Prot
  ENST00000437129.5 UniProtKB/TrEMBL
  ENST00000437633 ENTREZGENE
  ENST00000437633.6 UniProtKB/Swiss-Prot
  ENST00000445943.5 UniProtKB/TrEMBL
  ENST00000450156.6 UniProtKB/TrEMBL
  ENST00000658652.1 UniProtKB/TrEMBL
  ENST00000664131.1 UniProtKB/TrEMBL
Gene3D-CATH 1.20.1270.350 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.20.58.740 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.25.40.410 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.60.40.150 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3 Domains UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000128512 GTEx
HGNC ID HGNC:19192 ENTREZGENE
Human Proteome Map DOCK4 Human Proteome Map
InterPro C2_Dock-B UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  C2_domain_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DHR-1_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DHR-2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCK UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCK4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCK4_SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCK_C_lobe_A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCK_C_lobe_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCK_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCK_N_sub1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCKER_Lobe_A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCKER_Lobe_B UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCKER_Lobe_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9732 UniProtKB/Swiss-Prot
NCBI Gene 9732 ENTREZGENE
OMIM 607679 OMIM
PANTHER PTHR45653 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR45653:SF7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DHR-2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DHR-2_Lobe_B UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DHR-2_Lobe_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCK-C2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOCK_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134939318 PharmGKB
PROSITE DHR_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DHR_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50044 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A2X0SFR8_HUMAN UniProtKB/TrEMBL
  A0A590UJ51_HUMAN UniProtKB/TrEMBL
  A0A590UJM5_HUMAN UniProtKB/TrEMBL
  A4D0S8_HUMAN UniProtKB/TrEMBL
  C9J637_HUMAN UniProtKB/TrEMBL
  C9J7D9_HUMAN UniProtKB/TrEMBL
  C9JDB3_HUMAN UniProtKB/TrEMBL
  DOCK4_HUMAN UniProtKB/Swiss-Prot
  F8WES4_HUMAN UniProtKB/TrEMBL
  H0Y599_HUMAN UniProtKB/TrEMBL
  H0Y7H7_HUMAN UniProtKB/TrEMBL
  O14584 ENTREZGENE
  O94824 ENTREZGENE
  Q149N2_HUMAN UniProtKB/TrEMBL
  Q149N5_HUMAN UniProtKB/TrEMBL
  Q149N6 ENTREZGENE, UniProtKB/TrEMBL
  Q75MU6_HUMAN UniProtKB/TrEMBL
  Q8N1I0 ENTREZGENE
  Q8NB45 ENTREZGENE
UniProt Secondary O14584 UniProtKB/Swiss-Prot
  O94824 UniProtKB/Swiss-Prot
  Q8NB45 UniProtKB/Swiss-Prot