TPBGL (trophoblast glycoprotein like) - Rat Genome Database

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Gene: TPBGL (trophoblast glycoprotein like) Homo sapiens
Analyze
Symbol: TPBGL
Name: trophoblast glycoprotein like
RGD ID: 6770651
HGNC Page HGNC:44159
Description: Predicted to be involved in negative regulation of canonical Wnt signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: trophoblast glycoprotein-like; uncharacterized protein LOC100507050
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
GRCh381175,240,774 - 75,243,704 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1175,240,774 - 75,243,704 (+)EnsemblGRCh38hg38GRCh38
GRCh371174,951,819 - 74,954,749 (+)NCBIGRCh37GRCh37hg19GRCh37
Celera1172,257,978 - 72,259,799 (+)NCBICelera
Cytogenetic Map11q13.4NCBI
HuRef1171,250,303 - 71,252,377 (+)NCBIHuRef
CHM1_11174,835,553 - 74,838,352 (+)NCBICHM1_1
T2T-CHM13v2.01175,170,381 - 75,173,311 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:21873635  


Genomics

Comparative Map Data
TPBGL
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381175,240,774 - 75,243,704 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1175,240,774 - 75,243,704 (+)EnsemblGRCh38hg38GRCh38
GRCh371174,951,819 - 74,954,749 (+)NCBIGRCh37GRCh37hg19GRCh37
Celera1172,257,978 - 72,259,799 (+)NCBICelera
Cytogenetic Map11q13.4NCBI
HuRef1171,250,303 - 71,252,377 (+)NCBIHuRef
CHM1_11174,835,553 - 74,838,352 (+)NCBICHM1_1
T2T-CHM13v2.01175,170,381 - 75,173,311 (+)NCBIT2T-CHM13v2.0
Tpbgl
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39799,273,274 - 99,276,310 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl799,273,289 - 99,276,310 (-)EnsemblGRCm39 Ensembl
GRCm38799,624,067 - 99,627,103 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl799,624,082 - 99,627,103 (-)EnsemblGRCm38mm10GRCm38
MGSCv377106,772,591 - 106,774,849 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv367106,772,343 - 106,777,643 (-)NCBIMGSCv36mm8
Celera799,949,700 - 99,951,957 (-)NCBICelera
Cytogenetic Map7E1NCBI
cM Map754.11NCBI
Tpbgl
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81163,335,851 - 163,338,677 (-)NCBIGRCr8
mRatBN7.21153,923,722 - 153,926,548 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1153,925,098 - 153,926,252 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1161,919,369 - 161,922,195 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01169,099,496 - 169,102,322 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01161,973,047 - 161,975,873 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01164,588,032 - 164,591,872 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1164,589,408 - 164,590,562 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01170,791,702 - 170,794,758 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41156,958,302 - 156,958,973 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1152,009,093 - 152,012,933 (-)NCBICelera
Cytogenetic Map1q32NCBI
Tpbgl
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541416,582,232 - 16,583,481 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541416,580,847 - 16,583,930 (-)NCBIChiLan1.0ChiLan1.0
TPBGL
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2976,171,015 - 76,174,184 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11177,213,698 - 77,216,872 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01170,300,350 - 70,303,524 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
TPBGL
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12123,312,723 - 23,317,887 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2123,314,357 - 23,315,535 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2123,077,805 - 23,081,082 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02123,515,137 - 23,518,413 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.12123,313,629 - 23,316,921 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02123,509,726 - 23,513,016 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02123,427,704 - 23,430,996 (-)NCBIUU_Cfam_GSD_1.0
Tpbgl
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494762,476,008 - 62,479,035 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364984,076,084 - 4,077,253 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364984,074,869 - 4,079,796 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TPBGL
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.199,502,193 - 9,507,470 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
TPBGL
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1166,463,987 - 66,467,860 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl166,465,198 - 66,466,349 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604359,343,749 - 59,347,611 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tpbgl
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248171,849,056 - 1,850,225 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248171,846,286 - 1,850,672 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TPBGL
27 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11q13.4-14.1(chr11:71923251-79662025)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052684]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052684]|See cases [RCV000052684] Chr11:71923251..79662025 [GRCh38]
Chr11:71634297..79373069 [GRCh37]
Chr11:71311945..79050717 [NCBI36]
Chr11:11q13.4-14.1		 pathogenic
GRCh38/hg38 11q13.4-13.5(chr11:71928796-77064521)x1 copy number loss See cases [RCV000052708] Chr11:71928796..77064521 [GRCh38]
Chr11:71639842..76751808 [GRCh37]
Chr11:71317490..76453216 [NCBI36]
Chr11:11q13.4-13.5		 pathogenic
GRCh38/hg38 11q13.4-14.1(chr11:71969881-78232895)x1 copy number loss See cases [RCV000052709] Chr11:71969881..78232895 [GRCh38]
Chr11:71680927..77943941 [GRCh37]
Chr11:71358575..77621589 [NCBI36]
Chr11:11q13.4-14.1		 pathogenic
GRCh37/hg19 11q13.4(chr11:74580424-75099464)x3 copy number gain See cases [RCV000448058] Chr11:74580424..75099464 [GRCh37]
Chr11:11q13.4		 uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_001195528.2(TPBGL):c.248G>C (p.Gly83Ala) single nucleotide variant Inborn genetic diseases [RCV003255849] Chr11:75241297 [GRCh38]
Chr11:74952342 [GRCh37]
Chr11:11q13.4		 likely benign
NM_001195528.2(TPBGL):c.259C>G (p.Gln87Glu) single nucleotide variant Inborn genetic diseases [RCV003255850] Chr11:75241308 [GRCh38]
Chr11:74952353 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.290G>C (p.Ser97Thr) single nucleotide variant Inborn genetic diseases [RCV003255851] Chr11:75241339 [GRCh38]
Chr11:74952384 [GRCh37]
Chr11:11q13.4		 likely benign
GRCh37/hg19 11q13.4-23.3(chr11:71588805-116680918)x3 copy number gain not provided [RCV000683374] Chr11:71588805..116680918 [GRCh37]
Chr11:11q13.4-23.3		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_001195528.2(TPBGL):c.395C>T (p.Ala132Val) single nucleotide variant Inborn genetic diseases [RCV003288793] Chr11:75241444 [GRCh38]
Chr11:74952489 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.258C>G (p.Asp86Glu) single nucleotide variant Inborn genetic diseases [RCV003245992] Chr11:75241307 [GRCh38]
Chr11:74952352 [GRCh37]
Chr11:11q13.4		 uncertain significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
GRCh37/hg19 11q13.4-13.5(chr11:74839014-75366449) copy number gain not specified [RCV002052937] Chr11:74839014..75366449 [GRCh37]
Chr11:11q13.4-13.5		 uncertain significance
NC_000011.9:g.(?_71146421)_(75283128_?)dup duplication 3-methylglutaconic aciduria, type VIIB [RCV003122786] Chr11:71146421..75283128 [GRCh37]
Chr11:11q13.4-13.5		 uncertain significance
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
NM_001195528.2(TPBGL):c.424C>T (p.Pro142Ser) single nucleotide variant Inborn genetic diseases [RCV002753770] Chr11:75241473 [GRCh38]
Chr11:74952518 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.403G>A (p.Gly135Ser) single nucleotide variant Inborn genetic diseases [RCV002946372] Chr11:75241452 [GRCh38]
Chr11:74952497 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.23C>G (p.Pro8Arg) single nucleotide variant Inborn genetic diseases [RCV002844310] Chr11:75241072 [GRCh38]
Chr11:74952117 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.779G>C (p.Arg260Pro) single nucleotide variant Inborn genetic diseases [RCV002659990] Chr11:75241828 [GRCh38]
Chr11:74952873 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.845G>T (p.Arg282Leu) single nucleotide variant Inborn genetic diseases [RCV002783952] Chr11:75241894 [GRCh38]
Chr11:74952939 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.838G>A (p.Gly280Arg) single nucleotide variant Inborn genetic diseases [RCV002758259] Chr11:75241887 [GRCh38]
Chr11:74952932 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.799C>T (p.Pro267Ser) single nucleotide variant Inborn genetic diseases [RCV002737045] Chr11:75241848 [GRCh38]
Chr11:74952893 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.46G>T (p.Val16Leu) single nucleotide variant Inborn genetic diseases [RCV002952302] Chr11:75241095 [GRCh38]
Chr11:74952140 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.247G>C (p.Gly83Arg) single nucleotide variant Inborn genetic diseases [RCV002976995] Chr11:75241296 [GRCh38]
Chr11:74952341 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.1017C>G (p.Asn339Lys) single nucleotide variant Inborn genetic diseases [RCV002665696] Chr11:75242066 [GRCh38]
Chr11:74953111 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.862A>G (p.Ser288Gly) single nucleotide variant Inborn genetic diseases [RCV002699653] Chr11:75241911 [GRCh38]
Chr11:74952956 [GRCh37]
Chr11:11q13.4		 likely benign
NM_001195528.2(TPBGL):c.821C>A (p.Pro274Gln) single nucleotide variant Inborn genetic diseases [RCV002900909] Chr11:75241870 [GRCh38]
Chr11:74952915 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.1012C>T (p.Arg338Cys) single nucleotide variant Inborn genetic diseases [RCV002673332] Chr11:75242061 [GRCh38]
Chr11:74953106 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.355A>T (p.Ser119Cys) single nucleotide variant Inborn genetic diseases [RCV002855428] Chr11:75241404 [GRCh38]
Chr11:74952449 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.313C>A (p.His105Asn) single nucleotide variant Inborn genetic diseases [RCV003255852] Chr11:75241362 [GRCh38]
Chr11:74952407 [GRCh37]
Chr11:11q13.4		 likely benign
NM_001195528.2(TPBGL):c.859G>C (p.Asp287His) single nucleotide variant Inborn genetic diseases [RCV003193483] Chr11:75241908 [GRCh38]
Chr11:74952953 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.916G>A (p.Ala306Thr) single nucleotide variant Inborn genetic diseases [RCV003212256] Chr11:75241965 [GRCh38]
Chr11:74953010 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.177C>A (p.Asp59Glu) single nucleotide variant Inborn genetic diseases [RCV003197090] Chr11:75241226 [GRCh38]
Chr11:74952271 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.578G>C (p.Arg193Pro) single nucleotide variant Inborn genetic diseases [RCV003207874] Chr11:75241627 [GRCh38]
Chr11:74952672 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.831C>G (p.Asp277Glu) single nucleotide variant Inborn genetic diseases [RCV003258594] Chr11:75241880 [GRCh38]
Chr11:74952925 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.384C>A (p.Asn128Lys) single nucleotide variant Inborn genetic diseases [RCV003197984] Chr11:75241433 [GRCh38]
Chr11:74952478 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_001195528.2(TPBGL):c.568G>C (p.Ala190Pro) single nucleotide variant Inborn genetic diseases [RCV003183836] Chr11:75241617 [GRCh38]
Chr11:74952662 [GRCh37]
Chr11:11q13.4		 uncertain significance
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3 copy number gain not provided [RCV003484842] Chr11:59923608..76272324 [GRCh37]
Chr11:11q12.2-13.5		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:827
Count of miRNA genes:479
Interacting mature miRNAs:514
Transcripts:ENST00000562197
Prediction methods: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
SGC38123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371174,954,479 - 74,954,731UniSTSGRCh37
Build 361174,632,127 - 74,632,379RGDNCBI36
Celera1172,261,035 - 72,261,287RGD
Cytogenetic Map11q13.4UniSTS
HuRef1171,252,107 - 71,252,359UniSTS
GeneMap99-GB4 RH Map11273.98UniSTS
Whitehead-RH Map11371.8UniSTS
NCBI RH Map11631.8UniSTS


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 adipose tissue appendage entire extraembryonic component
High
Medium 4 12 2 2 12 63 3 248 15
Low 932 240 698 93 267 58 1358 386 2638 106 669 703 37 601 761
Below cutoff 1420 2463 923 449 914 324 2693 1554 956 261 492 833 130 597 1760 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000562197   ⟹   ENSP00000474988
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1175,240,774 - 75,243,704 (+)Ensembl
RefSeq Acc Id: NM_001195528   ⟹   NP_001182457
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381175,240,774 - 75,243,704 (+)NCBI
GRCh371174,951,950 - 74,954,749 (+)NCBI
HuRef1171,250,303 - 71,252,377 (+)NCBI
CHM1_11174,835,553 - 74,838,352 (+)NCBI
T2T-CHM13v2.01175,170,381 - 75,173,311 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001182457 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000474988
  ENSP00000474988.1
GenBank Protein P0DKB5 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001182457   ⟸   NM_001195528
- Peptide Label: precursor
- UniProtKB: P0DKB5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000474988   ⟸   ENST00000562197

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P0DKB5-F1-model_v2 AlphaFold P0DKB5 1-382 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:44159 AgrOrtholog
COSMIC TPBGL COSMIC
Ensembl Genes ENSG00000261594 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000562197 ENTREZGENE
  ENST00000562197.3 UniProtKB/Swiss-Prot
Gene3D-CATH 3.80.10.10 UniProtKB/Swiss-Prot
GTEx ENSG00000261594 GTEx
HGNC ID HGNC:44159 ENTREZGENE
Human Proteome Map TPBGL Human Proteome Map
InterPro Cys-rich_flank_reg_C UniProtKB/Swiss-Prot
  Leu-rich_rpt UniProtKB/Swiss-Prot
  Leu-rich_rpt_typical-subtyp UniProtKB/Swiss-Prot
  LRR_dom_sf UniProtKB/Swiss-Prot
KEGG Report hsa:100507050 UniProtKB/Swiss-Prot
NCBI Gene TPBGL ENTREZGENE
PANTHER LP06937P UniProtKB/Swiss-Prot
  TROPHOBLAST GLYCOPROTEIN-LIKE UniProtKB/Swiss-Prot
Pfam LRR_8 UniProtKB/Swiss-Prot
PharmGKB PA166049109 PharmGKB
SMART LRR_TYP UniProtKB/Swiss-Prot
  LRRCT UniProtKB/Swiss-Prot
Superfamily-SCOP L domain-like UniProtKB/Swiss-Prot
UniProt P0DKB5 ENTREZGENE, UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-02-28 TPBGL  trophoblast glycoprotein like    trophoblast glycoprotein-like  Symbol and/or name change 5135510 APPROVED