THBS4 (thrombospondin 4) - Rat Genome Database

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Gene: THBS4 (thrombospondin 4) Homo sapiens
Analyze
Symbol: THBS4
Name: thrombospondin 4
RGD ID: 735475
HGNC Page HGNC:11788
Description: Enables calcium ion binding activity; heparin binding activity; and integrin binding activity. Involved in several processes, including endothelial cell-cell adhesion; myoblast migration; and positive regulation of neutrophil chemotaxis. Located in basement membrane and extracellular space.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: thrombospondin-4; TSP-4; TSP4
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38579,991,332 - 80,083,287 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl579,991,311 - 80,083,287 (+)EnsemblGRCh38hg38GRCh38
GRCh37579,287,155 - 79,379,110 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36579,366,747 - 79,414,866 (+)NCBINCBI36Build 36hg18NCBI36
Build 34579,366,746 - 79,414,861NCBI
Celera575,232,509 - 75,280,442 (+)NCBICelera
Cytogenetic Map5q14.1NCBI
HuRef574,539,053 - 74,586,983 (+)NCBIHuRef
CHM1_1578,764,258 - 78,812,159 (+)NCBICHM1_1
T2T-CHM13v2.0580,475,183 - 80,567,137 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(E)-thiamethoxam  (ISO)
1,2-dimethylhydrazine  (ISO)
1-chloro-2,4-dinitrobenzene  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4,6-tribromophenol  (EXP)
2,6-dinitrotoluene  (ISO)
2-amino-2-deoxy-D-glucopyranose  (ISO)
3,3',5,5'-tetrabromobisphenol A  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
3,7-dihydropurine-6-thione  (ISO)
4,4'-sulfonyldiphenol  (EXP)
5-aza-2'-deoxycytidine  (EXP)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acrylamide  (EXP,ISO)
aflatoxin B1  (EXP)
Aflatoxin B2 alpha  (EXP)
aldehydo-D-glucosamine  (ISO)
all-trans-retinoic acid  (EXP)
alpha-hexylcinnamaldehyde  (ISO)
amitrole  (ISO)
ammonium chloride  (ISO)
arsenite(3-)  (ISO)
atrazine  (EXP,ISO)
benzo[a]pyrene  (EXP)
beta-D-glucosamine  (ISO)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (EXP,ISO)
bromobenzene  (ISO)
butanal  (EXP)
C60 fullerene  (ISO)
cadmium dichloride  (EXP)
carbamazepine  (EXP)
carbon nanotube  (ISO)
chlorpyrifos  (ISO)
cisplatin  (EXP)
copper(II) sulfate  (EXP)
Cuprizon  (ISO)
decabromodiphenyl ether  (EXP)
dextran sulfate  (ISO)
dibutyl phthalate  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP,ISO)
enalapril  (ISO)
ethanol  (ISO)
etoposide  (EXP)
flavonoids  (ISO)
furan  (ISO)
furosemide  (ISO)
isotretinoin  (EXP)
lidocaine  (ISO)
lipopolysaccharide  (EXP)
mercaptopurine  (ISO)
mercury dichloride  (ISO)
methyl salicylate  (ISO)
metoprolol  (ISO)
milrinone  (ISO)
niclosamide  (EXP)
ozone  (ISO)
paracetamol  (ISO)
pentane-2,3-dione  (ISO)
perfluorohexanesulfonic acid  (ISO)
phenylmercury acetate  (EXP)
phthalaldehyde  (ISO)
pirinixic acid  (ISO)
potassium dichromate  (ISO)
purine-6-thiol  (ISO)
rotenone  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
sodium arsenite  (EXP)
streptozocin  (ISO)
testosterone enanthate  (EXP)
tetrachloromethane  (ISO)
thiamethoxam  (ISO)
titanium dioxide  (ISO)
triazines  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
trimellitic anhydride  (ISO)
valproic acid  (EXP)
vanadyl sulfate  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. Epigenetic profiling of cutaneous T-cell lymphoma: promoter hypermethylation of multiple tumor suppressor genes including BCL7a, PTPRG, and p73. van Doorn R, etal., J Clin Oncol. 2005 Jun 10;23(17):3886-96. Epub 2005 May 16.
Additional References at PubMed
PMID:6338048   PMID:7490284   PMID:7519904   PMID:7852353   PMID:8350346   PMID:8432726   PMID:10501972   PMID:11137453   PMID:11967953   PMID:12477932   PMID:12482844   PMID:12952849  
PMID:14674882   PMID:15121769   PMID:15131549   PMID:15474480   PMID:15489334   PMID:16099885   PMID:16148025   PMID:16246837   PMID:16923428   PMID:17182969   PMID:17202846   PMID:17709521  
PMID:17927980   PMID:18178577   PMID:18802666   PMID:19420105   PMID:19578796   PMID:19834535   PMID:19913121   PMID:20227257   PMID:20452482   PMID:20485444   PMID:20628086   PMID:20628624  
PMID:20673868   PMID:20846368   PMID:21244100   PMID:21701537   PMID:21873635   PMID:22011848   PMID:22380695   PMID:22682248   PMID:22745497   PMID:23420636   PMID:23533145   PMID:23637781  
PMID:23801863   PMID:23874812   PMID:23942617   PMID:24787432   PMID:24941943   PMID:25234833   PMID:25436638   PMID:25976449   PMID:26186194   PMID:27160021   PMID:27357608   PMID:28177895  
PMID:28514442   PMID:29138119   PMID:29336258   PMID:29676528   PMID:29807011   PMID:30132849   PMID:30464261   PMID:30669608   PMID:30746617   PMID:30802535   PMID:31227875   PMID:31703077  
PMID:32421868   PMID:32567740   PMID:33910854   PMID:33961781   PMID:33971315   PMID:34390328   PMID:35563538   PMID:36566568  


Genomics

Comparative Map Data
THBS4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38579,991,332 - 80,083,287 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl579,991,311 - 80,083,287 (+)EnsemblGRCh38hg38GRCh38
GRCh37579,287,155 - 79,379,110 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36579,366,747 - 79,414,866 (+)NCBINCBI36Build 36hg18NCBI36
Build 34579,366,746 - 79,414,861NCBI
Celera575,232,509 - 75,280,442 (+)NCBICelera
Cytogenetic Map5q14.1NCBI
HuRef574,539,053 - 74,586,983 (+)NCBIHuRef
CHM1_1578,764,258 - 78,812,159 (+)NCBICHM1_1
T2T-CHM13v2.0580,475,183 - 80,567,137 (+)NCBIT2T-CHM13v2.0
Thbs4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391392,888,094 - 92,931,326 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1392,888,098 - 92,931,326 (-)EnsemblGRCm39 Ensembl
GRCm381392,751,586 - 92,794,818 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1392,751,590 - 92,794,818 (-)EnsemblGRCm38mm10GRCm38
MGSCv371393,521,541 - 93,564,773 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361393,852,339 - 93,895,511 (-)NCBIMGSCv36mm8
Celera1396,355,385 - 96,398,324 (-)NCBICelera
Cytogenetic Map13C3NCBI
cM Map1347.75NCBI
Thbs4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8225,718,219 - 25,760,345 (-)NCBIGRCr8
mRatBN7.2223,983,158 - 24,025,289 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl223,983,158 - 24,026,313 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx231,012,074 - 31,054,079 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0229,112,424 - 29,154,423 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0223,940,916 - 23,982,917 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0222,343,727 - 22,385,855 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl222,343,727 - 22,385,855 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0241,549,115 - 41,591,101 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4223,010,823 - 23,053,527 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1222,931,199 - 22,973,881 (-)NCBI
Celera220,070,701 - 20,112,733 (-)NCBICelera
Cytogenetic Map2q12NCBI
Thbs4
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542521,069,855 - 21,117,061 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495542521,072,873 - 21,117,061 (-)NCBIChiLan1.0ChiLan1.0
THBS4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2435,218,007 - 35,315,815 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1533,377,268 - 33,469,098 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0535,232,459 - 35,324,613 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1535,505,370 - 35,553,040 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl535,505,375 - 35,553,040 (-)Ensemblpanpan1.1panPan2
THBS4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1326,945,001 - 26,982,224 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl326,945,081 - 26,988,597 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha328,184,781 - 28,226,829 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0326,864,062 - 26,906,077 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl326,864,144 - 26,906,081 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1326,803,818 - 26,845,793 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0326,780,744 - 26,822,700 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0327,060,242 - 27,102,310 (-)NCBIUU_Cfam_GSD_1.0
Thbs4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213183,030,397 - 183,077,597 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365497,780,842 - 7,829,379 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365497,781,214 - 7,828,569 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
THBS4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl288,726,687 - 88,780,751 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1288,729,531 - 88,780,759 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2290,502,359 - 90,549,528 (+)NCBISscrofa10.2Sscrofa10.2susScr3
THBS4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1474,195,487 - 74,275,723 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl474,234,261 - 74,275,775 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604923,076,969 - 23,123,257 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Thbs4
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248694,553,194 - 4,601,587 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248694,553,192 - 4,601,076 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in THBS4
59 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q13.3-22.1(chr5:74163186-110809453)x3 copy number gain See cases [RCV000051839] Chr5:74163186..110809453 [GRCh38]
Chr5:73459011..110145153 [GRCh37]
Chr5:73494767..110173052 [NCBI36]
Chr5:5q13.3-22.1		 pathogenic
GRCh38/hg38 5q14.1(chr5:79665668-81197686)x1 copy number loss See cases [RCV000052576] Chr5:79665668..81197686 [GRCh38]
Chr5:78961491..80493505 [GRCh37]
Chr5:78997247..80529261 [NCBI36]
Chr5:5q14.1		 uncertain significance
NM_003248.4(THBS4):c.715G>A (p.Asp239Asn) single nucleotide variant Malignant melanoma [RCV000067015] Chr5:80058773 [GRCh38]
Chr5:79354596 [GRCh37]
Chr5:79390352 [NCBI36]
Chr5:5q14.1		 not provided
NM_003248.4(THBS4):c.942C>T (p.Pro314=) single nucleotide variant Malignant melanoma [RCV000067016] Chr5:80059860 [GRCh38]
Chr5:79355683 [GRCh37]
Chr5:79391439 [NCBI36]
Chr5:5q14.1		 not provided
NM_003248.4(THBS4):c.1537G>A (p.Gly513Arg) single nucleotide variant Malignant melanoma [RCV000128473] Chr5:80070727 [GRCh38]
Chr5:79366550 [GRCh37]
Chr5:79402306 [NCBI36]
Chr5:5q14.1		 not provided
NM_003248.6(THBS4):c.1885C>T (p.Gln629Ter) single nucleotide variant Hirschsprung disease, susceptibility to, 1 [RCV000201285] Chr5:80073320 [GRCh38]
Chr5:79369143 [GRCh37]
Chr5:5q14.1		 uncertain significance
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
NM_003248.6(THBS4):c.2239G>A (p.Asp747Asn) single nucleotide variant Inborn genetic diseases [RCV003261280] Chr5:80078201 [GRCh38]
Chr5:79374024 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.539A>G (p.Gln180Arg) single nucleotide variant Inborn genetic diseases [RCV003281504] Chr5:80056031 [GRCh38]
Chr5:79351854 [GRCh37]
Chr5:5q14.1		 uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32		 uncertain significance
NM_003248.6(THBS4):c.2728G>A (p.Val910Ile) single nucleotide variant not provided [RCV000926620] Chr5:80082449 [GRCh38]
Chr5:79378272 [GRCh37]
Chr5:5q14.1		 likely benign
NM_003248.6(THBS4):c.1936G>A (p.Val646Ile) single nucleotide variant not provided [RCV000965686] Chr5:80076898 [GRCh38]
Chr5:79372721 [GRCh37]
Chr5:5q14.1		 benign
NM_003248.6(THBS4):c.2877C>T (p.Phe959=) single nucleotide variant not provided [RCV000901325] Chr5:80083132 [GRCh38]
Chr5:79378955 [GRCh37]
Chr5:5q14.1		 likely benign
NM_003248.6(THBS4):c.1259C>T (p.Ala420Val) single nucleotide variant not provided [RCV000960254] Chr5:80068037 [GRCh38]
Chr5:79363860 [GRCh37]
Chr5:5q14.1		 benign
NM_003248.6(THBS4):c.1561G>A (p.Asp521Asn) single nucleotide variant Inborn genetic diseases [RCV003240183] Chr5:80071021 [GRCh38]
Chr5:79366844 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.423A>G (p.Leu141=) single nucleotide variant not provided [RCV000964983] Chr5:80055915 [GRCh38]
Chr5:79351738 [GRCh37]
Chr5:5q14.1		 benign
GRCh37/hg19 5q13.2-15(chr5:72790061-97478870)x3 copy number gain not provided [RCV001005683] Chr5:72790061..97478870 [GRCh37]
Chr5:5q13.2-15		 pathogenic
GRCh37/hg19 5q14.1(chr5:79153777-79683363) copy number loss not specified [RCV002053506] Chr5:79153777..79683363 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.806C>T (p.Pro269Leu) single nucleotide variant Inborn genetic diseases [RCV003276459] Chr5:80059724 [GRCh38]
Chr5:79355547 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2458T>C (p.Tyr820His) single nucleotide variant Inborn genetic diseases [RCV003286272] Chr5:80079205 [GRCh38]
Chr5:79375028 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.146T>C (p.Val49Ala) single nucleotide variant Inborn genetic diseases [RCV003286073] Chr5:80040134 [GRCh38]
Chr5:79335957 [GRCh37]
Chr5:5q14.1		 uncertain significance
GRCh37/hg19 5q14.1(chr5:79153778-79683392)x1 copy number loss not provided [RCV002474876] Chr5:79153778..79683392 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1357G>A (p.Gly453Ser) single nucleotide variant Inborn genetic diseases [RCV002729639] Chr5:80070315 [GRCh38]
Chr5:79366138 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1838A>G (p.Gln613Arg) single nucleotide variant Inborn genetic diseases [RCV002859816] Chr5:80072395 [GRCh38]
Chr5:79368218 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1742A>G (p.Asn581Ser) single nucleotide variant Inborn genetic diseases [RCV002973625] Chr5:80072299 [GRCh38]
Chr5:79368122 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1981G>A (p.Asp661Asn) single nucleotide variant Inborn genetic diseases [RCV002687177] Chr5:80076943 [GRCh38]
Chr5:79372766 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2089G>A (p.Asp697Asn) single nucleotide variant Inborn genetic diseases [RCV002739315] Chr5:80078051 [GRCh38]
Chr5:79373874 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.83C>G (p.Pro28Arg) single nucleotide variant Inborn genetic diseases [RCV002692876] Chr5:80035620 [GRCh38]
Chr5:79331443 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1160C>T (p.Ala387Val) single nucleotide variant Inborn genetic diseases [RCV002821829] Chr5:80065443 [GRCh38]
Chr5:79361266 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.895G>T (p.Val299Phe) single nucleotide variant Inborn genetic diseases [RCV002822826] Chr5:80059813 [GRCh38]
Chr5:79355636 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.301C>T (p.Arg101Cys) single nucleotide variant Inborn genetic diseases [RCV002821759] Chr5:80055793 [GRCh38]
Chr5:79351616 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.679A>G (p.Met227Val) single nucleotide variant Inborn genetic diseases [RCV002978119] Chr5:80058737 [GRCh38]
Chr5:79354560 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.200A>G (p.Gln67Arg) single nucleotide variant Inborn genetic diseases [RCV002823617] Chr5:80040188 [GRCh38]
Chr5:79336011 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.622A>T (p.Ser208Cys) single nucleotide variant Inborn genetic diseases [RCV002978254] Chr5:80058287 [GRCh38]
Chr5:79354110 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1039G>C (p.Gly347Arg) single nucleotide variant Inborn genetic diseases [RCV002853867] Chr5:80061746 [GRCh38]
Chr5:79357569 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.91T>C (p.Phe31Leu) single nucleotide variant Inborn genetic diseases [RCV002805077] Chr5:80040079 [GRCh38]
Chr5:79335902 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2428G>A (p.Val810Met) single nucleotide variant Inborn genetic diseases [RCV002850338] Chr5:80079175 [GRCh38]
Chr5:79374998 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.388A>G (p.Arg130Gly) single nucleotide variant Inborn genetic diseases [RCV002930690] Chr5:80055880 [GRCh38]
Chr5:79351703 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1771C>T (p.Arg591Trp) single nucleotide variant Inborn genetic diseases [RCV002788962] Chr5:80072328 [GRCh38]
Chr5:79368151 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.881C>T (p.Pro294Leu) single nucleotide variant Inborn genetic diseases [RCV002673441] Chr5:80059799 [GRCh38]
Chr5:79355622 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1120A>G (p.Lys374Glu) single nucleotide variant Inborn genetic diseases [RCV002652174] Chr5:80061827 [GRCh38]
Chr5:79357650 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2065C>A (p.Pro689Thr) single nucleotide variant Inborn genetic diseases [RCV002921653] Chr5:80077027 [GRCh38]
Chr5:79372850 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2791A>C (p.Ile931Leu) single nucleotide variant Inborn genetic diseases [RCV002713962] Chr5:80082512 [GRCh38]
Chr5:79378335 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2869G>A (p.Asp957Asn) single nucleotide variant Inborn genetic diseases [RCV002669146] Chr5:80083124 [GRCh38]
Chr5:79378947 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.158C>T (p.Pro53Leu) single nucleotide variant Inborn genetic diseases [RCV002944599] Chr5:80040146 [GRCh38]
Chr5:79335969 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1555G>A (p.Glu519Lys) single nucleotide variant Inborn genetic diseases [RCV002679931] Chr5:80070745 [GRCh38]
Chr5:79366568 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2320A>G (p.Thr774Ala) single nucleotide variant Inborn genetic diseases [RCV003188364] Chr5:80079067 [GRCh38]
Chr5:79374890 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.133G>A (p.Ala45Thr) single nucleotide variant Inborn genetic diseases [RCV003173255] Chr5:80040121 [GRCh38]
Chr5:79335944 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2095G>A (p.Val699Met) single nucleotide variant Inborn genetic diseases [RCV003205212] Chr5:80078057 [GRCh38]
Chr5:79373880 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1625C>T (p.Ala542Val) single nucleotide variant Inborn genetic diseases [RCV003263676] Chr5:80071085 [GRCh38]
Chr5:79366908 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.295A>G (p.Ile99Val) single nucleotide variant Inborn genetic diseases [RCV003196268] Chr5:80055787 [GRCh38]
Chr5:79351610 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.718C>T (p.Leu240Phe) single nucleotide variant Inborn genetic diseases [RCV003206262] Chr5:80058776 [GRCh38]
Chr5:79354599 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2125C>G (p.Gln709Glu) single nucleotide variant Inborn genetic diseases [RCV003186634] Chr5:80078087 [GRCh38]
Chr5:79373910 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.1192T>G (p.Leu398Val) single nucleotide variant Inborn genetic diseases [RCV003287563] Chr5:80065475 [GRCh38]
Chr5:79361298 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2880T>A (p.Asp960Glu) single nucleotide variant Inborn genetic diseases [RCV003343437] Chr5:80083135 [GRCh38]
Chr5:79378958 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.475G>A (p.Ala159Thr) single nucleotide variant Inborn genetic diseases [RCV003360372] Chr5:80055967 [GRCh38]
Chr5:79351790 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2092G>A (p.Gly698Arg) single nucleotide variant Inborn genetic diseases [RCV003384406] Chr5:80078054 [GRCh38]
Chr5:79373877 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.2407C>G (p.Gln803Glu) single nucleotide variant Inborn genetic diseases [RCV003354916] Chr5:80079154 [GRCh38]
Chr5:79374977 [GRCh37]
Chr5:5q14.1		 uncertain significance
NM_003248.6(THBS4):c.785-3T>G single nucleotide variant not provided [RCV003885716] Chr5:80059700 [GRCh38]
Chr5:79355523 [GRCh37]
Chr5:5q14.1		 benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1165
Count of miRNA genes:583
Interacting mature miRNAs:659
Transcripts:ENST00000350881, ENST00000504720, ENST00000510218, ENST00000511733, ENST00000511888, ENST00000513310, ENST00000515510
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
SHGC-12514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37579,378,972 - 79,379,098UniSTSGRCh37
Build 36579,414,728 - 79,414,854RGDNCBI36
Celera575,280,304 - 75,280,430RGD
Cytogenetic Map5q13UniSTS
HuRef574,586,845 - 74,586,971UniSTS
Stanford-G3 RH Map52967.0UniSTS
GeneMap99-GB4 RH Map5377.98UniSTS
Whitehead-RH Map5277.4UniSTS
NCBI RH Map5398.9UniSTS
GeneMap99-G3 RH Map52962.0UniSTS
MARC_15765-15766:1041972257:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37579,354,082 - 79,354,593UniSTSGRCh37
Build 36579,389,838 - 79,390,349RGDNCBI36
Celera575,255,416 - 75,255,927RGD
HuRef574,561,964 - 74,562,475UniSTS
THBS4  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37579,366,178 - 79,366,519UniSTSGRCh37
Celera575,267,510 - 75,267,851UniSTS
HuRef574,574,059 - 74,574,400UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 5 1 1 1 3 1
Medium 1565 900 467 170 59 25 2171 1977 1958 45 534 211 149 1 879 1562
Low 611 1534 919 143 901 127 2067 211 1759 281 848 1262 19 322 1205 2 1
Below cutoff 236 556 333 303 961 306 111 8 14 93 64 125 6 20 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_047084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001306212 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001306213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001306214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417678 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054353384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956176 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007058633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008487159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC012636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC112184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY566253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC050456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC310687 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC342285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC376500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z19585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000350881   ⟹   ENSP00000339730
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl580,035,348 - 80,083,287 (+)Ensembl
RefSeq Acc Id: ENST00000504720
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl580,078,835 - 80,083,287 (+)Ensembl
RefSeq Acc Id: ENST00000510218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl579,991,332 - 80,055,967 (+)Ensembl
RefSeq Acc Id: ENST00000511733   ⟹   ENSP00000422298
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl580,036,023 - 80,083,282 (+)Ensembl
RefSeq Acc Id: ENST00000511888
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl580,082,004 - 80,083,188 (+)Ensembl
RefSeq Acc Id: ENST00000513310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl579,991,311 - 80,055,906 (+)Ensembl
RefSeq Acc Id: ENST00000515510
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl580,073,272 - 80,076,879 (+)Ensembl
RefSeq Acc Id: NM_001306212   ⟹   NP_001293141
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38579,991,332 - 80,083,287 (+)NCBI
CHM1_1578,720,207 - 78,812,159 (+)NCBI
T2T-CHM13v2.0580,475,183 - 80,567,137 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001306213   ⟹   NP_001293142
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38579,991,332 - 80,083,287 (+)NCBI
CHM1_1578,720,207 - 78,812,159 (+)NCBI
T2T-CHM13v2.0580,475,183 - 80,567,137 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001306214   ⟹   NP_001293143
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38580,036,023 - 80,083,287 (+)NCBI
CHM1_1578,764,934 - 78,812,159 (+)NCBI
T2T-CHM13v2.0580,519,873 - 80,567,137 (+)NCBI
Sequence:
RefSeq Acc Id: NM_003248   ⟹   NP_003239
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38580,035,348 - 80,083,287 (+)NCBI
GRCh37579,331,170 - 79,379,111 (+)NCBI
Build 36579,366,747 - 79,414,866 (+)NCBI Archive
HuRef574,539,053 - 74,586,983 (+)ENTREZGENE
CHM1_1578,764,210 - 78,812,159 (+)NCBI
T2T-CHM13v2.0580,519,198 - 80,567,137 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009799   ⟹   XP_016865288
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38580,035,348 - 80,074,258 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047417678   ⟹   XP_047273634
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38580,035,348 - 80,074,301 (+)NCBI
RefSeq Acc Id: XM_054353383   ⟹   XP_054209358
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0580,519,198 - 80,558,108 (+)NCBI
RefSeq Acc Id: XM_054353384   ⟹   XP_054209359
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0580,519,198 - 80,558,151 (+)NCBI
RefSeq Acc Id: XR_007058633
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38580,035,348 - 80,076,867 (+)NCBI
RefSeq Acc Id: XR_008487159
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0580,519,198 - 80,560,717 (+)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_003239   ⟸   NM_003248
- Peptide Label: isoform a precursor
- UniProtKB: B2R909 (UniProtKB/Swiss-Prot),   Q86TG2 (UniProtKB/Swiss-Prot),   P35443 (UniProtKB/Swiss-Prot),   B7Z832 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001293142   ⟸   NM_001306213
- Peptide Label: isoform b
- UniProtKB: E7ES19 (UniProtKB/TrEMBL),   B7Z832 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001293141   ⟸   NM_001306212
- Peptide Label: isoform b
- UniProtKB: E7ES19 (UniProtKB/TrEMBL),   B7Z832 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001293143   ⟸   NM_001306214
- Peptide Label: isoform b
- UniProtKB: B7Z832 (UniProtKB/TrEMBL),   E7ES19 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016865288   ⟸   XM_017009799
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000339730   ⟸   ENST00000350881
RefSeq Acc Id: ENSP00000422298   ⟸   ENST00000511733
RefSeq Acc Id: XP_047273634   ⟸   XM_047417678
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054209359   ⟸   XM_054353384
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054209358   ⟸   XM_054353383
- Peptide Label: isoform X1
Protein Domains
EGF-like   Laminin G-like   TSP C-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P35443-F1-model_v2 AlphaFold P35443 1-961 view protein structure

Promoters
RGD ID:6869992
Promoter ID:EPDNEW_H8161
Type:initiation region
Name:THBS4_2
Description:thrombospondin 4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8162  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38579,991,332 - 79,991,392EPDNEW
RGD ID:6869994
Promoter ID:EPDNEW_H8162
Type:initiation region
Name:THBS4_1
Description:thrombospondin 4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8161  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38580,035,348 - 80,035,408EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11788 AgrOrtholog
COSMIC THBS4 COSMIC
Ensembl Genes ENSG00000113296 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000350881 ENTREZGENE
  ENST00000350881.6 UniProtKB/Swiss-Prot
  ENST00000511733 ENTREZGENE
  ENST00000511733.1 UniProtKB/TrEMBL
Gene3D-CATH 1.20.5.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.60.120.200 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  4.10.1080.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Laminin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000113296 GTEx
HGNC ID HGNC:11788 ENTREZGENE
Human Proteome Map THBS4 Human Proteome Map
InterPro ConA-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF-like_Ca-bd_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF_Ca-bd_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Thbs/COMP_coiled-coil UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Thrombospondin_3-like_rpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Thrombospondin_3_rpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Thrombospondin_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP/COMP_coiled-coil_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP_type-3_rpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSPN-like_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:7060 UniProtKB/Swiss-Prot
NCBI Gene 7060 ENTREZGENE
OMIM 600715 OMIM
PANTHER THROMBOSPONDIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  THROMBOSPONDIN-4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam COMP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA36500 PharmGKB
PROSITE EGF_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF_CA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP_CTER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART EGF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF_CA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSPN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Assembly domain of cartilage oligomeric matrix protein UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EGF/Laminin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF103647 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF49899 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B2R909 ENTREZGENE
  B7Z832 ENTREZGENE, UniProtKB/TrEMBL
  E7ES19 ENTREZGENE, UniProtKB/TrEMBL
  P35443 ENTREZGENE
  Q86TG2 ENTREZGENE
  TSP4_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B2R909 UniProtKB/Swiss-Prot
  Q86TG2 UniProtKB/Swiss-Prot