THUMPD2 (THUMP domain containing 2) - Rat Genome Database

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Gene: THUMPD2 (THUMP domain containing 2) Homo sapiens
Analyze
Symbol: THUMPD2
Name: THUMP domain containing 2
RGD ID: 1315745
HGNC Page HGNC:14890
Description: Predicted to enable tRNA (guanine) methyltransferase activity. Predicted to be involved in tRNA methylation.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C2orf8; MGC2454; SAM-dependent methyltransferase; THUMP domain-containing protein 2
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
GRCh38239,736,060 - 39,779,276 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl239,736,060 - 39,779,267 (-)EnsemblGRCh38hg38GRCh38
GRCh37239,963,200 - 40,006,416 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36239,816,949 - 39,859,881 (-)NCBINCBI36Build 36hg18NCBI36
Build 34239,875,095 - 39,918,028NCBI
Celera239,804,157 - 39,847,379 (-)NCBICelera
Cytogenetic Map2p22.1NCBI
HuRef239,702,624 - 39,745,816 (-)NCBIHuRef
CHM1_1239,893,491 - 39,936,707 (-)NCBICHM1_1
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)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
methylation  (IEA)
tRNA methylation  (IBA,IEA)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:12063391   PMID:12477932   PMID:14702039   PMID:15489334   PMID:18957941   PMID:21873635   PMID:22939629   PMID:26465331   PMID:28514442   PMID:30021884   PMID:31536960  
PMID:32814053   PMID:33961781   PMID:34948388   PMID:35831314  


Genomics

Comparative Map Data
THUMPD2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38239,736,060 - 39,779,276 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl239,736,060 - 39,779,267 (-)EnsemblGRCh38hg38GRCh38
GRCh37239,963,200 - 40,006,416 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36239,816,949 - 39,859,881 (-)NCBINCBI36Build 36hg18NCBI36
Build 34239,875,095 - 39,918,028NCBI
Celera239,804,157 - 39,847,379 (-)NCBICelera
Cytogenetic Map2p22.1NCBI
HuRef239,702,624 - 39,745,816 (-)NCBIHuRef
CHM1_1239,893,491 - 39,936,707 (-)NCBICHM1_1
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBIT2T-CHM13v2.0
Thumpd2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391781,331,676 - 81,372,542 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1781,333,761 - 81,372,511 (-)EnsemblGRCm39 Ensembl
GRCm381781,024,247 - 81,065,113 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1781,026,332 - 81,065,082 (-)EnsemblGRCm38mm10GRCm38
MGSCv371781,425,667 - 81,464,425 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361780,934,653 - 80,973,411 (-)NCBIMGSCv36mm8
Celera1785,358,226 - 85,398,858 (-)NCBICelera
Cytogenetic Map17E3NCBI
cM Map1751.04NCBI
Thumpd2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8619,677,039 - 19,728,947 (+)NCBIGRCr8
mRatBN7.2613,924,742 - 13,976,657 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl613,924,765 - 13,976,657 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx614,228,394 - 14,280,284 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0614,551,389 - 14,596,793 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0614,041,656 - 14,093,548 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.063,743,080 - 3,794,512 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl63,743,074 - 3,794,501 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.063,710,777 - 3,762,198 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.463,974,995 - 4,026,884 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.163,974,998 - 4,026,884 (-)NCBI
Celera613,611,109 - 13,658,637 (+)NCBICelera
Cytogenetic Map6q12NCBI
Thumpd2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554417,329,093 - 7,369,782 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554417,329,468 - 7,369,957 (-)NCBIChiLan1.0ChiLan1.0
THUMPD2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21286,690,167 - 86,732,755 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12A86,694,147 - 86,737,375 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02A39,768,913 - 39,816,471 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12A40,526,774 - 40,569,226 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A40,526,774 - 40,571,909 (-)Ensemblpanpan1.1panPan2
THUMPD2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11731,701,025 - 31,738,451 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1731,701,475 - 31,738,478 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1731,460,906 - 31,498,263 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01732,359,635 - 32,397,274 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1732,359,660 - 32,397,265 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11731,580,931 - 31,618,257 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01731,650,259 - 31,687,785 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01731,864,590 - 31,902,483 (-)NCBIUU_Cfam_GSD_1.0
Thumpd2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440629240,140,558 - 40,182,653 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493650811,569,170 - 11,611,609 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493650811,569,195 - 11,611,264 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
THUMPD2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl3100,557,016 - 100,597,671 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.13100,557,168 - 100,597,664 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.23106,694,190 - 106,734,643 (-)NCBISscrofa10.2Sscrofa10.2susScr3
THUMPD2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11467,589,985 - 67,632,144 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604544,305,947 - 44,375,406 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Thumpd2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473821,237,709 - 21,287,551 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473821,238,535 - 21,287,491 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in THUMPD2
31 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2p25.3-16.1(chr2:66097-55570637)x3 copy number gain See cases [RCV000052933] Chr2:66097..55570637 [GRCh38]
Chr2:66097..55797773 [GRCh37]
Chr2:56097..55651277 [NCBI36]
Chr2:2p25.3-16.1		 pathogenic
GRCh38/hg38 2p22.3-21(chr2:32849247-45016061)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052942]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052942]|See cases [RCV000052942] Chr2:32849247..45016061 [GRCh38]
Chr2:33074314..45243200 [GRCh37]
Chr2:32927818..45096704 [NCBI36]
Chr2:2p22.3-21		 pathogenic
NM_025264.4(THUMPD2):c.1284C>T (p.Ser428=) single nucleotide variant Malignant melanoma [RCV000060567] Chr2:39736963 [GRCh38]
Chr2:39964103 [GRCh37]
Chr2:39817607 [NCBI36]
Chr2:2p22.1		 not provided
inv(2)(p21p23.2) inversion Endometrial carcinoma [RCV000659263] Chr2:29447680..42554394 [GRCh37]
Chr2:2p23.2-21		 likely pathogenic
GRCh38/hg38 2p22.2-21(chr2:37000557-41954686)x1 copy number loss See cases [RCV000139443] Chr2:37000557..41954686 [GRCh38]
Chr2:37227700..42181826 [GRCh37]
Chr2:37081204..42035330 [NCBI36]
Chr2:2p22.2-21		 pathogenic
GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3 copy number gain See cases [RCV000141494] Chr2:7495123..87705899 [GRCh38]
Chr2:7635254..88005418 [GRCh37]
Chr2:7552705..87786533 [NCBI36]
Chr2:2p25.1-11.2		 benign
GRCh38/hg38 2p25.3-21(chr2:236816-45983232)x3 copy number gain See cases [RCV000143682] Chr2:236816..45983232 [GRCh38]
Chr2:236816..46210371 [GRCh37]
Chr2:226816..46063875 [NCBI36]
Chr2:2p25.3-21		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p23.3-16.1(chr2:27861707-60790985)x3 copy number gain See cases [RCV000454271] Chr2:27861707..60790985 [GRCh37]
Chr2:2p23.3-16.1		 pathogenic
GRCh37/hg19 2p23.2-21(chr2:28069882-43543420)x3 copy number gain See cases [RCV000447397] Chr2:28069882..43543420 [GRCh37]
Chr2:2p23.2-21		 pathogenic
GRCh37/hg19 2p22.1(chr2:39987132-40349524)x1 copy number loss See cases [RCV000445771] Chr2:39987132..40349524 [GRCh37]
Chr2:2p22.1		 uncertain significance
GRCh37/hg19 2p22.1(chr2:39987132-40347064)x1 copy number loss See cases [RCV000445709] Chr2:39987132..40347064 [GRCh37]
Chr2:2p22.1		 uncertain significance
GRCh37/hg19 2p22.1(chr2:39982433-40037717) copy number loss Abnormal esophagus morphology [RCV000416688] Chr2:39982433..40037717 [GRCh37]
Chr2:2p22.1		 likely benign
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NC_000002.11:g.38121110_47669522inv inversion Hereditary nonpolyposis colorectal neoplasms [RCV002231155] Chr2:38121110..47669522 [GRCh37]
Chr2:2p22.2-21		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_025264.5(THUMPD2):c.160A>T (p.Thr54Ser) single nucleotide variant Inborn genetic diseases [RCV003277247] Chr2:39771607 [GRCh38]
Chr2:39998747 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.107C>T (p.Ala36Val) single nucleotide variant Inborn genetic diseases [RCV003291904] Chr2:39779133 [GRCh38]
Chr2:40006273 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.743A>C (p.Gln248Pro) single nucleotide variant Inborn genetic diseases [RCV003271159] Chr2:39768431 [GRCh38]
Chr2:39995571 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.342T>G (p.Asn114Lys) single nucleotide variant Inborn genetic diseases [RCV003261206] Chr2:39770040 [GRCh38]
Chr2:39997180 [GRCh37]
Chr2:2p22.1		 uncertain significance
t(2;2)(p23;p21)(hg19 chr2:g.42552694::ochr2:g.29446394) inversion Small cell lung carcinoma [RCV000576833] Chr2:29446394..42552694 [GRCh37]
Chr2:2p23.2-21		 pathogenic
GRCh37/hg19 2p22.3-16.1(chr2:34792916-56676541)x3 copy number gain not provided [RCV000682169] Chr2:34792916..56676541 [GRCh37]
Chr2:2p22.3-16.1		 pathogenic
GRCh37/hg19 2p24.1-16.3(chr2:22665048-52850368)x3 copy number gain not provided [RCV000752875] Chr2:22665048..52850368 [GRCh37]
Chr2:2p24.1-16.3		 pathogenic
GRCh37/hg19 2p23.3-21(chr2:24881528-43460021)x3 copy number gain not provided [RCV001532444] Chr2:24881528..43460021 [GRCh37]
Chr2:2p23.3-21		 likely pathogenic
NM_025264.5(THUMPD2):c.1306C>A (p.Pro436Thr) single nucleotide variant Inborn genetic diseases [RCV003245884] Chr2:39736941 [GRCh38]
Chr2:39964081 [GRCh37]
Chr2:2p22.1		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NC_000002.11:g.39053852_42501893dup duplication Neurodevelopmental disorder [RCV000787462] Chr2:39053852..42501893 [GRCh37]
Chr2:2p22.1-21		 likely pathogenic
GRCh37/hg19 2p22.1(chr2:39578669-40167082)x3 copy number gain not provided [RCV001005251] Chr2:39578669..40167082 [GRCh37]
Chr2:2p22.1		 uncertain significance
GRCh37/hg19 2p23.3-21(chr2:24601818-43466284)x3 copy number gain See cases [RCV001581099] Chr2:24601818..43466284 [GRCh37]
Chr2:2p23.3-21		 pathogenic
GRCh37/hg19 2p22.1-21(chr2:39751028-43437611) copy number loss not specified [RCV002052471] Chr2:39751028..43437611 [GRCh37]
Chr2:2p22.1-21		 uncertain significance
GRCh37/hg19 2p22.1(chr2:39987132-40349524) copy number loss not specified [RCV002052482] Chr2:39987132..40349524 [GRCh37]
Chr2:2p22.1		 uncertain significance
GRCh37/hg19 2p23.2-21(chr2:29899368-42441440) copy number loss not specified [RCV002053089] Chr2:29899368..42441440 [GRCh37]
Chr2:2p23.2-21		 pathogenic
NC_000002.11:g.(?_38121051)_(47710088_?)dup duplication Hereditary nonpolyposis colorectal neoplasms [RCV003122260] Chr2:38121051..47710088 [GRCh37]
Chr2:2p22.2-21		 uncertain significance
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1 copy number loss See cases [RCV002287563] Chr2:11504318..111365996 [GRCh37]
Chr2:2p25.1-q13		 pathogenic
NM_025264.5(THUMPD2):c.46G>C (p.Ala16Pro) single nucleotide variant Inborn genetic diseases [RCV002969914] Chr2:39779194 [GRCh38]
Chr2:40006334 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.172T>A (p.Leu58Met) single nucleotide variant Inborn genetic diseases [RCV002794667] Chr2:39771595 [GRCh38]
Chr2:39998735 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.235C>T (p.Pro79Ser) single nucleotide variant Inborn genetic diseases [RCV003001171] Chr2:39771532 [GRCh38]
Chr2:39998672 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.35C>T (p.Pro12Leu) single nucleotide variant Inborn genetic diseases [RCV003000572] Chr2:39779205 [GRCh38]
Chr2:40006345 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.974A>G (p.Tyr325Cys) single nucleotide variant Inborn genetic diseases [RCV002798435] Chr2:39755399 [GRCh38]
Chr2:39982539 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.868A>G (p.Met290Val) single nucleotide variant Inborn genetic diseases [RCV002952146] Chr2:39761354 [GRCh38]
Chr2:39988494 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.1171C>A (p.Leu391Ile) single nucleotide variant Inborn genetic diseases [RCV002821196] Chr2:39744386 [GRCh38]
Chr2:39971526 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.1302T>A (p.Asp434Glu) single nucleotide variant Inborn genetic diseases [RCV002761786] Chr2:39736945 [GRCh38]
Chr2:39964085 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.883G>C (p.Asp295His) single nucleotide variant Inborn genetic diseases [RCV002789846] Chr2:39761339 [GRCh38]
Chr2:39988479 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.835A>G (p.Thr279Ala) single nucleotide variant Inborn genetic diseases [RCV002986451] Chr2:39761387 [GRCh38]
Chr2:39988527 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.1364C>T (p.Ser455Leu) single nucleotide variant Inborn genetic diseases [RCV002915585] Chr2:39736883 [GRCh38]
Chr2:39964023 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.49C>G (p.Arg17Gly) single nucleotide variant Inborn genetic diseases [RCV002930235] Chr2:39779191 [GRCh38]
Chr2:40006331 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.768T>G (p.Asn256Lys) single nucleotide variant Inborn genetic diseases [RCV002768268] Chr2:39766092 [GRCh38]
Chr2:39993232 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.929G>A (p.Gly310Glu) single nucleotide variant Inborn genetic diseases [RCV002793100] Chr2:39755923 [GRCh38]
Chr2:39983063 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.5C>T (p.Ser2Leu) single nucleotide variant Inborn genetic diseases [RCV002675109] Chr2:39779235 [GRCh38]
Chr2:40006375 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.1391A>G (p.Lys464Arg) single nucleotide variant Inborn genetic diseases [RCV003215882] Chr2:39736856 [GRCh38]
Chr2:39963996 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.16G>A (p.Gly6Arg) single nucleotide variant Inborn genetic diseases [RCV003205525] Chr2:39779224 [GRCh38]
Chr2:40006364 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.893C>G (p.Ala298Gly) single nucleotide variant Inborn genetic diseases [RCV003205146] Chr2:39755959 [GRCh38]
Chr2:39983099 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.199G>T (p.Ala67Ser) single nucleotide variant Inborn genetic diseases [RCV003357315] Chr2:39771568 [GRCh38]
Chr2:39998708 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.374T>A (p.Leu125His) single nucleotide variant Inborn genetic diseases [RCV003358905] Chr2:39770008 [GRCh38]
Chr2:39997148 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.1496A>T (p.His499Leu) single nucleotide variant Inborn genetic diseases [RCV003347897] Chr2:39736751 [GRCh38]
Chr2:39963891 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.587C>T (p.Ala196Val) single nucleotide variant Inborn genetic diseases [RCV003384812] Chr2:39769795 [GRCh38]
Chr2:39996935 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.1102G>A (p.Val368Ile) single nucleotide variant Inborn genetic diseases [RCV003367685] Chr2:39744455 [GRCh38]
Chr2:39971595 [GRCh37]
Chr2:2p22.1		 uncertain significance
NM_025264.5(THUMPD2):c.854C>T (p.Thr285Ile) single nucleotide variant Inborn genetic diseases [RCV003362087] Chr2:39761368 [GRCh38]
Chr2:39988508 [GRCh37]
Chr2:2p22.1		 uncertain significance
GRCh37/hg19 2p23.1-21(chr2:30814984-42798684)x1 copy number loss not specified [RCV003986376] Chr2:30814984..42798684 [GRCh37]
Chr2:2p23.1-21		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2002
Count of miRNA genes:772
Interacting mature miRNAs:870
Transcripts:ENST00000260619, ENST00000378727, ENST00000403537, ENST00000454352, ENST00000460072, ENST00000505747, ENST00000510781, ENST00000527689, ENST00000530095, ENST00000530522, ENST00000531687
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
G62651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37239,989,500 - 39,989,802UniSTSGRCh37
Build 36239,843,004 - 39,843,306RGDNCBI36
Celera239,830,463 - 39,830,765RGD
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map2p22.1UniSTS
HuRef239,728,941 - 39,729,243UniSTS
TNG Radiation Hybrid Map227768.0UniSTS
SHGC-112290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37239,987,244 - 39,987,537UniSTSGRCh37
Build 36239,840,748 - 39,841,041RGDNCBI36
Celera239,828,207 - 39,828,500RGD
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map2p22.1UniSTS
HuRef239,726,685 - 39,726,978UniSTS
TNG Radiation Hybrid Map227768.0UniSTS
D11S2268E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37119,302,246 - 9,302,395UniSTSGRCh37
GRCh37239,983,888 - 39,984,037UniSTSGRCh37
Build 36239,837,392 - 39,837,541RGDNCBI36
Celera239,824,850 - 39,824,999RGD
Celera119,423,504 - 9,423,653UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map11p15.4UniSTS
HuRef239,723,328 - 39,723,477UniSTS
HuRef118,974,939 - 8,975,088UniSTS
GeneMap99-GB4 RH Map1148.79UniSTS
NCBI RH Map1131.3UniSTS
WI-18232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37239,963,501 - 39,963,634UniSTSGRCh37
Build 36239,817,005 - 39,817,138RGDNCBI36
Celera239,804,458 - 39,804,591RGD
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map2p22.1UniSTS
HuRef239,702,925 - 39,703,058UniSTS
GeneMap99-GB4 RH Map2126.4UniSTS
Whitehead-RH Map2193.8UniSTS
RH78734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37239,963,600 - 39,963,746UniSTSGRCh37
Build 36239,817,104 - 39,817,250RGDNCBI36
Celera239,804,557 - 39,804,703RGD
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map2p22.1UniSTS
HuRef239,703,024 - 39,703,170UniSTS
D2S2923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37239,978,931 - 39,979,075UniSTSGRCh37
Build 36239,832,435 - 39,832,579RGDNCBI36
Celera239,819,892 - 39,820,036RGD
HuRef239,718,365 - 39,718,509UniSTS
D10S16   No map positions available.
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1372 1366 1009 154 950 44 3346 729 1524 137 1195 1373 123 1 881 2005 3 1
Low 1067 1570 716 469 946 420 1011 1466 2209 282 262 240 51 323 783 3 1
Below cutoff 55 1 1 55 1 2 1 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001321468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321470 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321474 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321477 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321478 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321479 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_025264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_028102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135659 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135660 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135661 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135662 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135664 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011533119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054344077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054344078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054344079 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001738966 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001738967 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001738968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC007246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC007253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF380577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF380578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF380579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH011179 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK057801 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK226034 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292002 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301353 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC004163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC379776 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ891427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HH961786 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584661 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000378727   ⟹   ENSP00000368001
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl239,736,307 - 39,779,267 (-)Ensembl
RefSeq Acc Id: ENST00000403537
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl239,768,903 - 39,779,239 (-)Ensembl
RefSeq Acc Id: ENST00000460072
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl239,736,060 - 39,770,013 (-)Ensembl
RefSeq Acc Id: ENST00000505747   ⟹   ENSP00000423933
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl239,736,061 - 39,779,258 (-)Ensembl
RefSeq Acc Id: ENST00000510781   ⟹   ENSP00000426202
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl239,761,332 - 39,779,152 (-)Ensembl
RefSeq Acc Id: ENST00000527689
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl239,761,365 - 39,766,212 (-)Ensembl
RefSeq Acc Id: ENST00000530095
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl239,736,683 - 39,744,654 (-)Ensembl
RefSeq Acc Id: ENST00000530522   ⟹   ENSP00000434844
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl239,736,610 - 39,779,221 (-)Ensembl
RefSeq Acc Id: ENST00000531687
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl239,770,017 - 39,779,240 (-)Ensembl
RefSeq Acc Id: NM_001321468   ⟹   NP_001308397
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321469   ⟹   NP_001308398
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321470   ⟹   NP_001308399
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321474   ⟹   NP_001308403
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321475   ⟹   NP_001308404
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321477   ⟹   NP_001308406
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321478   ⟹   NP_001308407
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321479   ⟹   NP_001308408
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321480   ⟹   NP_001308409
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321481   ⟹   NP_001308410
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NM_025264   ⟹   NP_079540
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,061 - 39,779,258 (-)NCBI
GRCh37239,963,200 - 40,006,416 (-)RGD
Build 36239,816,949 - 39,859,881 (-)NCBI Archive
Celera239,804,157 - 39,847,379 (-)RGD
HuRef239,702,624 - 39,745,816 (-)RGD
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,057 - 39,788,255 (-)NCBI
Sequence:
RefSeq Acc Id: NR_028102
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
GRCh37239,963,200 - 40,006,416 (-)RGD
Celera239,804,157 - 39,847,379 (-)RGD
HuRef239,702,624 - 39,745,816 (-)RGD
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135659
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135660
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135661
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135662
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135663
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135664
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
CHM1_1239,893,491 - 39,936,707 (-)NCBI
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011533119   ⟹   XP_011531421
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017005050   ⟹   XP_016860539
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,736,060 - 39,779,276 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017005053   ⟹   XP_016860542
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38239,768,492 - 39,779,276 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054344077   ⟹   XP_054200052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
RefSeq Acc Id: XM_054344078   ⟹   XP_054200053
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0239,745,056 - 39,788,273 (-)NCBI
RefSeq Acc Id: XM_054344079   ⟹   XP_054200054
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0239,777,493 - 39,788,273 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001308397 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308398 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308399 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308403 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308404 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308406 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308407 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308408 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308409 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308410 (Get FASTA)   NCBI Sequence Viewer  
  NP_079540 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531421 (Get FASTA)   NCBI Sequence Viewer  
  XP_016860539 (Get FASTA)   NCBI Sequence Viewer  
  XP_016860542 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200052 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200053 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200054 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH04163 (Get FASTA)   NCBI Sequence Viewer  
  AAH13299 (Get FASTA)   NCBI Sequence Viewer  
  AAL18604 (Get FASTA)   NCBI Sequence Viewer  
  AAL18605 (Get FASTA)   NCBI Sequence Viewer  
  AAL18606 (Get FASTA)   NCBI Sequence Viewer  
  AAL26317 (Get FASTA)   NCBI Sequence Viewer  
  AAL26318 (Get FASTA)   NCBI Sequence Viewer  
  AAX93065 (Get FASTA)   NCBI Sequence Viewer  
  AAY14769 (Get FASTA)   NCBI Sequence Viewer  
  ADO22289 (Get FASTA)   NCBI Sequence Viewer  
  BAB71581 (Get FASTA)   NCBI Sequence Viewer  
  BAF84691 (Get FASTA)   NCBI Sequence Viewer  
  BAG52741 (Get FASTA)   NCBI Sequence Viewer  
  BAG60449 (Get FASTA)   NCBI Sequence Viewer  
  BAG62898 (Get FASTA)   NCBI Sequence Viewer  
  CBX51366 (Get FASTA)   NCBI Sequence Viewer  
  EAX00339 (Get FASTA)   NCBI Sequence Viewer  
  EAX00340 (Get FASTA)   NCBI Sequence Viewer  
  EAX00341 (Get FASTA)   NCBI Sequence Viewer  
  EAX00342 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000368001.4
  ENSP00000423933
  ENSP00000423933.1
  ENSP00000434844.1
GenBank Protein Q9BTF0 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_079540   ⟸   NM_025264
- Peptide Label: isoform 1
- UniProtKB: Q53TT8 (UniProtKB/Swiss-Prot),   A8K7I7 (UniProtKB/Swiss-Prot),   Q53TV0 (UniProtKB/Swiss-Prot),   Q9BTF0 (UniProtKB/Swiss-Prot),   A0A384ME97 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011531421   ⟸   XM_011533119
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: NP_001308399   ⟸   NM_001321470
- Peptide Label: isoform 4
- UniProtKB: B4DP37 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001308398   ⟸   NM_001321469
- Peptide Label: isoform 3
- UniProtKB: B4DP37 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001308404   ⟸   NM_001321475
- Peptide Label: isoform 6
- Sequence:
RefSeq Acc Id: NP_001308406   ⟸   NM_001321477
- Peptide Label: isoform 7
- Sequence:
RefSeq Acc Id: NP_001308409   ⟸   NM_001321480
- Peptide Label: isoform 7
- Sequence:
RefSeq Acc Id: NP_001308408   ⟸   NM_001321479
- Peptide Label: isoform 7
- Sequence:
RefSeq Acc Id: NP_001308403   ⟸   NM_001321474
- Peptide Label: isoform 5
- Sequence:
RefSeq Acc Id: NP_001308397   ⟸   NM_001321468
- Peptide Label: isoform 2
- Sequence:
RefSeq Acc Id: NP_001308410   ⟸   NM_001321481
- Peptide Label: isoform 7
- Sequence:
RefSeq Acc Id: NP_001308407   ⟸   NM_001321478
- Peptide Label: isoform 7
- Sequence:
RefSeq Acc Id: XP_016860539   ⟸   XM_017005050
- Peptide Label: isoform X1
- UniProtKB: A0A384ME97 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016860542   ⟸   XM_017005053
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000423933   ⟸   ENST00000505747
RefSeq Acc Id: ENSP00000434844   ⟸   ENST00000530522
RefSeq Acc Id: ENSP00000368001   ⟸   ENST00000378727
RefSeq Acc Id: ENSP00000426202   ⟸   ENST00000510781
RefSeq Acc Id: XP_054200053   ⟸   XM_054344078
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054200052   ⟸   XM_054344077
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054200054   ⟸   XM_054344079
- Peptide Label: isoform X3
Protein Domains
THUMP   UPF0020

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9BTF0-F1-model_v2 AlphaFold Q9BTF0 1-503 view protein structure

Promoters
RGD ID:6860160
Promoter ID:EPDNEW_H3245
Type:initiation region
Name:THUMPD2_1
Description:THUMP domain containing 2
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
GRCh38239,779,247 - 39,779,307EPDNEW
RGD ID:6798317
Promoter ID:HG_KWN:32351
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000403537,   NM_025264,   NR_028102
Position:
Human AssemblyChrPosition (strand)Source
Build 36239,859,584 - 39,860,084 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14890 AgrOrtholog
COSMIC THUMPD2 COSMIC
Ensembl Genes ENSG00000138050 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000378727 ENTREZGENE
  ENST00000378727.8 UniProtKB/Swiss-Prot
  ENST00000505747 ENTREZGENE
  ENST00000505747.6 UniProtKB/Swiss-Prot
  ENST00000530522.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.2130.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.150 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000138050 GTEx
HGNC ID HGNC:14890 ENTREZGENE
Human Proteome Map THUMPD2 Human Proteome Map
InterPro RNA_methylase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SAM-dependent_MTases UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  THUMP_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:80745 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 80745 ENTREZGENE
OMIM 611751 OMIM
PANTHER THUMP DOMAIN-CONTAINING UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  THUMP DOMAIN-CONTAINING PROTEIN 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam THUMP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UPF0020 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134976355 PharmGKB
PROSITE THUMP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART THUMP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF53335 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  THUMP domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A384ME97 ENTREZGENE, UniProtKB/TrEMBL
  A8K7I7 ENTREZGENE
  B4DP37 ENTREZGENE, UniProtKB/TrEMBL
  H0YE26_HUMAN UniProtKB/TrEMBL
  Q53TT8 ENTREZGENE
  Q53TV0 ENTREZGENE
  Q969Z2_HUMAN UniProtKB/TrEMBL
  Q9BTF0 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A8K7I7 UniProtKB/Swiss-Prot
  Q53TT8 UniProtKB/Swiss-Prot
  Q53TV0 UniProtKB/Swiss-Prot