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Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | TPST2 | Human | autism spectrum disorder | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:35663546 | |
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Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | TPST2 | Human | autism spectrum disorder | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:35663546 | |
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# | Reference Title | Reference Citation |
1. | GOAs Human GO annotations | GOA_HUMAN data from the GO Consortium |
2. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:9733778 | PMID:9736702 | PMID:10089882 | PMID:10497246 | PMID:10591208 | PMID:11230166 | PMID:11256614 | PMID:12056800 | PMID:12169668 | PMID:12477932 | PMID:14702039 | PMID:15461802 |
PMID:15489334 | PMID:16303743 | PMID:17558413 | PMID:18672380 | PMID:19343046 | PMID:19402700 | PMID:20460947 | PMID:21873635 | PMID:23376485 | PMID:23481380 | PMID:24569807 | PMID:26108987 |
PMID:26186194 | PMID:28514442 | PMID:28821720 | PMID:32287057 | PMID:32393512 | PMID:33951064 | PMID:33961781 | PMID:34473204 | PMID:35420441 | PMID:35696571 | PMID:35748872 |
TPST2 (Homo sapiens - human) |
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Tpst2 (Mus musculus - house mouse) |
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Tpst2 (Rattus norvegicus - Norway rat) |
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Tpst2 (Chinchilla lanigera - long-tailed chinchilla) |
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TPST2 (Pan paniscus - bonobo/pygmy chimpanzee) |
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TPST2 (Canis lupus familiaris - dog) |
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Tpst2 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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TPST2 (Sus scrofa - pig) |
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TPST2 (Chlorocebus sabaeus - green monkey) |
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Tpst2 (Heterocephalus glaber - naked mole-rat) |
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Variants in TPST2
27 total Variants ![]() |
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 22q11.21-12.3(chr22:18178957-31821193)x3 | copy number gain | See cases [RCV000050768] | Chr22:18178957..31821193 [GRCh38] Chr22:18661724..32217179 [GRCh37] Chr22:17041724..30547179 [NCBI36] Chr22:22q11.21-12.3 |
pathogenic |
GRCh38/hg38 22q12.1-12.2(chr22:26221273-29477543)x1 | copy number loss | See cases [RCV000052869] | Chr22:26221273..29477543 [GRCh38] Chr22:26617239..29873532 [GRCh37] Chr22:24947239..28203532 [NCBI36] Chr22:22q12.1-12.2 |
pathogenic |
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3 | copy number gain | See cases [RCV000133646] | Chr22:16916608..50739836 [GRCh38] Chr22:17397498..51178264 [GRCh37] Chr22:15777498..49525130 [NCBI36] Chr22:22q11.1-13.33 |
pathogenic |
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3 | copy number gain | See cases [RCV000134730] | Chr22:16916743..50739785 [GRCh38] Chr22:17397633..51178213 [GRCh37] Chr22:15777633..49525079 [NCBI36] Chr22:22q11.1-13.33 |
pathogenic |
GRCh38/hg38 22q11.23-12.1(chr22:25003092-28634004)x1 | copy number loss | See cases [RCV000134954] | Chr22:25003092..28634004 [GRCh38] Chr22:25399059..29029992 [GRCh37] Chr22:23729059..27359992 [NCBI36] Chr22:22q11.23-12.1 |
likely pathogenic |
GRCh38/hg38 22q12.1(chr22:25685148-28217405)x1 | copy number loss | See cases [RCV000136530] | Chr22:25685148..28217405 [GRCh38] Chr22:26081115..28613393 [GRCh37] Chr22:24411115..26943393 [NCBI36] Chr22:22q12.1 |
uncertain significance |
GRCh38/hg38 22q11.23-12.3(chr22:23279231-36247369)x3 | copy number gain | See cases [RCV000138172] | Chr22:23279231..36247369 [GRCh38] Chr22:23621418..36643415 [GRCh37] Chr22:21951418..34973361 [NCBI36] Chr22:22q11.23-12.3 |
pathogenic |
GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3 | copy number gain | See cases [RCV000137926] | Chr22:20907226..37187347 [GRCh38] Chr22:21261514..37583387 [GRCh37] Chr22:19591514..35913333 [NCBI36] Chr22:22q11.21-12.3 |
pathogenic |
GRCh38/hg38 22q12.1(chr22:26535859-27296063)x1 | copy number loss | See cases [RCV000139801] | Chr22:26535859..27296063 [GRCh38] Chr22:26931825..27692024 [GRCh37] Chr22:25261825..26022024 [NCBI36] Chr22:22q12.1 |
uncertain significance |
GRCh38/hg38 22q12.1-12.2(chr22:26451042-31451926)x1 | copy number loss | See cases [RCV000143415] | Chr22:26451042..31451926 [GRCh38] Chr22:26847008..31847912 [GRCh37] Chr22:25177008..30177912 [NCBI36] Chr22:22q12.1-12.2 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3 | copy number gain | See cases [RCV000240091] | Chr22:16054691..51237518 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.1-12.1(chr22:16054691-27296513)x3 | copy number gain | See cases [RCV000240348] | Chr22:16054691..27296513 [GRCh37] Chr22:22q11.1-12.1 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3 | copy number gain | See cases [RCV000446956] | Chr22:16054691..51220902 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3 | copy number gain | See cases [RCV000448847] | Chr22:16054691..51237463 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838) | copy number gain | See cases [RCV000510873] | Chr22:16888900..51197838 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.23-12.3(chr22:23637907-36614412)x3 | copy number gain | See cases [RCV000511098] | Chr22:23637907..36614412 [GRCh37] Chr22:22q11.23-12.3 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3 | copy number gain | See cases [RCV000512333] | Chr22:16888900..51197838 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.22-12.3(chr22:22460754-35198232)x3 | copy number gain | not provided [RCV000684530] | Chr22:22460754..35198232 [GRCh37] Chr22:22q11.22-12.3 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16054667-51243435)x3 | copy number gain | not provided [RCV000741689] | Chr22:16054667..51243435 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51195728)x3 | copy number gain | not provided [RCV000741691] | Chr22:16114244..51195728 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51211392)x3 | copy number gain | not provided [RCV000741692] | Chr22:16114244..51211392 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
NM_003595.5(TPST2):c.124C>T (p.Arg42Trp) | single nucleotide variant | not specified [RCV004301883] | Chr22:26541507 [GRCh38] Chr22:26937473 [GRCh37] Chr22:22q12.1 |
uncertain significance |
GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3 | copy number gain | not provided [RCV000846344] | Chr22:16888899..51197838 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
NC_000022.10:g.(?_26142492)_(27026451_?)del | deletion | Cataract 23 [RCV003107531] | Chr22:26142492..27026451 [GRCh37] Chr22:22q12.1 |
uncertain significance |
GRCh37/hg19 22q12.1(chr22:26337910-28489947)x1 | copy number loss | not provided [RCV001007180] | Chr22:26337910..28489947 [GRCh37] Chr22:22q12.1 |
pathogenic |
GRCh37/hg19 22q11.1-12.1(chr22:16888899-27657507)x3 | copy number gain | not provided [RCV001007163] | Chr22:16888899..27657507 [GRCh37] Chr22:22q11.1-12.1 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3 | copy number gain | See cases [RCV001263056] | Chr22:16197005..51224252 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q12.1-12.2(chr22:26614429-29847680)x1 | copy number loss | not provided [RCV002472563] | Chr22:26614429..29847680 [GRCh37] Chr22:22q12.1-12.2 |
pathogenic |
NM_003595.5(TPST2):c.1039C>T (p.Arg347Trp) | single nucleotide variant | not specified [RCV004222557] | Chr22:26536290 [GRCh38] Chr22:26932256 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.1040G>A (p.Arg347Gln) | single nucleotide variant | not specified [RCV004223727] | Chr22:26536289 [GRCh38] Chr22:26932255 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.787G>T (p.Ala263Ser) | single nucleotide variant | not specified [RCV004170646] | Chr22:26540844 [GRCh38] Chr22:26936810 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.739C>T (p.Arg247Cys) | single nucleotide variant | not specified [RCV004100569] | Chr22:26540892 [GRCh38] Chr22:26936858 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.847G>A (p.Glu283Lys) | single nucleotide variant | not specified [RCV004129518] | Chr22:26536482 [GRCh38] Chr22:26932448 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.898A>C (p.Lys300Gln) | single nucleotide variant | not specified [RCV004211311] | Chr22:26536431 [GRCh38] Chr22:26932397 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.890C>T (p.Ala297Val) | single nucleotide variant | not specified [RCV004179077] | Chr22:26536439 [GRCh38] Chr22:26932405 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.277G>C (p.Glu93Gln) | single nucleotide variant | not specified [RCV004080366] | Chr22:26541354 [GRCh38] Chr22:26937320 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.130G>A (p.Ala44Thr) | single nucleotide variant | not specified [RCV004268034] | Chr22:26541501 [GRCh38] Chr22:26937467 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.854C>T (p.Ser285Phe) | single nucleotide variant | not specified [RCV004261678] | Chr22:26536475 [GRCh38] Chr22:26932441 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.107C>T (p.Ala36Val) | single nucleotide variant | not specified [RCV004263312] | Chr22:26541524 [GRCh38] Chr22:26937490 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.868A>G (p.Ile290Val) | single nucleotide variant | not specified [RCV004349297] | Chr22:26536461 [GRCh38] Chr22:26932427 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.73G>A (p.Gly25Arg) | single nucleotide variant | not specified [RCV004471037] | Chr22:26541558 [GRCh38] Chr22:26937524 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.749A>G (p.Lys250Arg) | single nucleotide variant | not specified [RCV004471039] | Chr22:26540882 [GRCh38] Chr22:26936848 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.769G>A (p.Gly257Ser) | single nucleotide variant | not specified [RCV004471040] | Chr22:26540862 [GRCh38] Chr22:26936828 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.989A>T (p.Asn330Ile) | single nucleotide variant | not specified [RCV004471041] | Chr22:26536340 [GRCh38] Chr22:26932306 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.646A>G (p.Lys216Glu) | single nucleotide variant | not specified [RCV004471036] | Chr22:26540985 [GRCh38] Chr22:26936951 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.188G>A (p.Arg63His) | single nucleotide variant | not specified [RCV004677367] | Chr22:26541443 [GRCh38] Chr22:26937409 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.125G>A (p.Arg42Gln) | single nucleotide variant | not specified [RCV004677368] | Chr22:26541506 [GRCh38] Chr22:26937472 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.5G>A (p.Arg2His) | single nucleotide variant | not specified [RCV004687612] | Chr22:26541626 [GRCh38] Chr22:26937592 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.512G>A (p.Arg171His) | single nucleotide variant | not specified [RCV004677370] | Chr22:26541119 [GRCh38] Chr22:26937085 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.1070C>A (p.Ala357Asp) | single nucleotide variant | not specified [RCV004677371] | Chr22:26532717 [GRCh38] Chr22:26928683 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.302G>T (p.Arg101Leu) | single nucleotide variant | not specified [RCV004878290] | Chr22:26541329 [GRCh38] Chr22:26937295 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.157G>T (p.Val53Leu) | single nucleotide variant | not specified [RCV004878291] | Chr22:26541474 [GRCh38] Chr22:26937440 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.377C>T (p.Ala126Val) | single nucleotide variant | not specified [RCV004878292] | Chr22:26541254 [GRCh38] Chr22:26937220 [GRCh37] Chr22:22q12.1 |
uncertain significance |
NM_003595.5(TPST2):c.485C>T (p.Thr162Met) | single nucleotide variant | not specified [RCV004878293] | Chr22:26541146 [GRCh38] Chr22:26937112 [GRCh37] Chr22:22q12.1 |
uncertain significance |
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. |
The following QTLs overlap with this region. | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer | ![]() | Gviewer |
SHGC-37519 |
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G49193 |
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G49244 |
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WI-14070 |
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WI-19497 |
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adipose tissue
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alimentary part of gastrointestinal system
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appendage
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circulatory system
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ectoderm
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endocrine system
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endoderm
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entire extraembryonic component
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exocrine system
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hemolymphoid system
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hepatobiliary system
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integumental system
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mesenchyme
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mesoderm
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musculoskeletal system
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nervous system
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pharyngeal arch
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renal system
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reproductive system
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respiratory system
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sensory system
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visual system
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1204 | 2439 | 2788 | 2253 | 4974 | 1726 | 2351 | 6 | 624 | 1951 | 465 | 2270 | 7306 | 6472 | 53 | 3734 | 1 | 852 | 1744 | 1617 | 175 | 1 |
RefSeq Transcripts | NM_001008566 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001362922 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001362923 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_003595 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_024452294 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047441549 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_007067981 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AA531491 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AF049891 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AF061254 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AJ006198 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK057171 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK074538 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK075139 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK093872 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK304545 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL136623 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL708491 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC001057 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC017509 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471095 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068256 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CQ782485 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CQ783200 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CR456597 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CR533528 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
HI573878 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
HI573880 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KF511430 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KF511431 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
Z95115 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
Ensembl Acc Id: | ENST00000338754 ⟹ ENSP00000339813 | ||||||||
Type: | CODING | ||||||||
Position: |
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Ensembl Acc Id: | ENST00000398110 ⟹ ENSP00000381180 | ||||||||
Type: | CODING | ||||||||
Position: |
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Ensembl Acc Id: | ENST00000403880 ⟹ ENSP00000385192 | ||||||||
Type: | CODING | ||||||||
Position: |
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Ensembl Acc Id: | ENST00000440953 ⟹ ENSP00000416791 | ||||||||
Type: | CODING | ||||||||
Position: |
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Ensembl Acc Id: | ENST00000442495 ⟹ ENSP00000403875 | ||||||||
Type: | CODING | ||||||||
Position: |
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Ensembl Acc Id: | ENST00000445720 ⟹ ENSP00000403758 | ||||||||
Type: | CODING | ||||||||
Position: |
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Ensembl Acc Id: | ENST00000450022 ⟹ ENSP00000414809 | ||||||||
Type: | CODING | ||||||||
Position: |
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Ensembl Acc Id: | ENST00000453117 ⟹ ENSP00000401134 | ||||||||
Type: | CODING | ||||||||
Position: |
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Ensembl Acc Id: | ENST00000454778 ⟹ ENSP00000400357 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | NM_001008566 ⟹ NP_001008566 | ||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001362922 ⟹ NP_001349851 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001362923 ⟹ NP_001349852 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_003595 ⟹ NP_003586 | ||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XM_024452294 ⟹ XP_024308062 | ||||||||
Type: | CODING | ||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XM_047441549 ⟹ XP_047297505 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XR_007067981 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
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Protein RefSeqs | NP_001008566 | (Get FASTA) | NCBI Sequence Viewer |
NP_001349851 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001349852 | (Get FASTA) | NCBI Sequence Viewer | |
NP_003586 | (Get FASTA) | NCBI Sequence Viewer | |
XP_024308062 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047297505 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAC34296 | (Get FASTA) | NCBI Sequence Viewer |
AAC36061 | (Get FASTA) | NCBI Sequence Viewer | |
AAH01057 | (Get FASTA) | NCBI Sequence Viewer | |
AAH17509 | (Get FASTA) | NCBI Sequence Viewer | |
BAG51969 | (Get FASTA) | NCBI Sequence Viewer | |
BAG52071 | (Get FASTA) | NCBI Sequence Viewer | |
BAH14212 | (Get FASTA) | NCBI Sequence Viewer | |
CAA06906 | (Get FASTA) | NCBI Sequence Viewer | |
CAB66558 | (Get FASTA) | NCBI Sequence Viewer | |
CAF85772 | (Get FASTA) | NCBI Sequence Viewer | |
CAF86406 | (Get FASTA) | NCBI Sequence Viewer | |
CAG30483 | (Get FASTA) | NCBI Sequence Viewer | |
CAG38559 | (Get FASTA) | NCBI Sequence Viewer | |
CBX47428 | (Get FASTA) | NCBI Sequence Viewer | |
CBX47429 | (Get FASTA) | NCBI Sequence Viewer | |
EAW59726 | (Get FASTA) | NCBI Sequence Viewer | |
EAW59727 | (Get FASTA) | NCBI Sequence Viewer | |
EAW59728 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000339813 | ||
ENSP00000339813.4 | |||
ENSP00000381180 | |||
ENSP00000381180.2 | |||
ENSP00000385192.1 | |||
ENSP00000400357.2 | |||
ENSP00000401134.1 | |||
ENSP00000403758.1 | |||
ENSP00000403875.1 | |||
ENSP00000414809.1 | |||
ENSP00000416791.1 | |||
GenBank Protein | O60704 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_003586 ⟸ NM_003595 |
- Peptide Label: | isoform 1 |
- UniProtKB: | Q6FI98 (UniProtKB/Swiss-Prot), B3KQA7 (UniProtKB/Swiss-Prot), Q9H0V4 (UniProtKB/Swiss-Prot), O60704 (UniProtKB/Swiss-Prot), B7Z976 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001008566 ⟸ NM_001008566 |
- Peptide Label: | isoform 1 |
- UniProtKB: | Q6FI98 (UniProtKB/Swiss-Prot), B3KQA7 (UniProtKB/Swiss-Prot), Q9H0V4 (UniProtKB/Swiss-Prot), O60704 (UniProtKB/Swiss-Prot), B7Z976 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_024308062 ⟸ XM_024452294 |
- Peptide Label: | isoform X1 |
- Sequence: |
RefSeq Acc Id: | NP_001349851 ⟸ NM_001362922 |
- Peptide Label: | isoform 1 |
- UniProtKB: | Q6FI98 (UniProtKB/Swiss-Prot), O60704 (UniProtKB/Swiss-Prot), B3KQA7 (UniProtKB/Swiss-Prot), Q9H0V4 (UniProtKB/Swiss-Prot), B7Z976 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | NP_001349852 ⟸ NM_001362923 |
- Peptide Label: | isoform 2 |
Ensembl Acc Id: | ENSP00000381180 ⟸ ENST00000398110 |
Ensembl Acc Id: | ENSP00000414809 ⟸ ENST00000450022 |
Ensembl Acc Id: | ENSP00000401134 ⟸ ENST00000453117 |
Ensembl Acc Id: | ENSP00000416791 ⟸ ENST00000440953 |
Ensembl Acc Id: | ENSP00000400357 ⟸ ENST00000454778 |
Ensembl Acc Id: | ENSP00000339813 ⟸ ENST00000338754 |
Ensembl Acc Id: | ENSP00000385192 ⟸ ENST00000403880 |
Ensembl Acc Id: | ENSP00000403875 ⟸ ENST00000442495 |
Ensembl Acc Id: | ENSP00000403758 ⟸ ENST00000445720 |
RefSeq Acc Id: | XP_047297505 ⟸ XM_047441549 |
- Peptide Label: | isoform X2 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-O60704-F1-model_v2 | AlphaFold | O60704 | 1-377 | view protein structure |
RGD ID: | 6851656 | ||||||||
Promoter ID: | EP73630 | ||||||||
Type: | initiation region | ||||||||
Name: | HS_TPST2 | ||||||||
Description: | Tyrosylprotein sulfotransferase 2. | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Experiment Methods: | NEDO full length human cDNA sequencing project.; Oligo-capping | ||||||||
Position: |
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RGD ID: | 6800430 | ||||||||
Promoter ID: | HG_KWN:42140 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4 | ||||||||
Transcripts: | OTTHUMT00000320820, OTTHUMT00000320823, OTTHUMT00000320824, OTTHUMT00000320825 | ||||||||
Position: |
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RGD ID: | 13603568 | ||||||||
Promoter ID: | EPDNEW_H27968 | ||||||||
Type: | initiation region | ||||||||
Name: | TPST2_2 | ||||||||
Description: | tyrosylprotein sulfotransferase 2 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H27969 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
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RGD ID: | 13603570 | ||||||||
Promoter ID: | EPDNEW_H27969 | ||||||||
Type: | initiation region | ||||||||
Name: | TPST2_1 | ||||||||
Description: | tyrosylprotein sulfotransferase 2 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H27968 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:12021 | AgrOrtholog |
COSMIC | TPST2 | COSMIC |
Ensembl Genes | ENSG00000128294 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000338754 | ENTREZGENE |
ENST00000338754.9 | UniProtKB/Swiss-Prot | |
ENST00000398110 | ENTREZGENE | |
ENST00000398110.6 | UniProtKB/Swiss-Prot | |
ENST00000403880.5 | UniProtKB/Swiss-Prot | |
ENST00000440953.5 | UniProtKB/TrEMBL | |
ENST00000442495.5 | UniProtKB/TrEMBL | |
ENST00000445720.1 | UniProtKB/TrEMBL | |
ENST00000450022.1 | UniProtKB/TrEMBL | |
ENST00000453117.1 | UniProtKB/TrEMBL | |
ENST00000454778.6 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Gene3D-CATH | 3.40.50.300 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
GTEx | ENSG00000128294 | GTEx |
HGNC ID | HGNC:12021 | ENTREZGENE |
Human Proteome Map | TPST2 | Human Proteome Map |
InterPro | P-loop_NTPase | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
TPST | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KEGG Report | hsa:8459 | UniProtKB/Swiss-Prot |
NCBI Gene | 8459 | ENTREZGENE |
OMIM | 603126 | OMIM |
PANTHER | PROTEIN-TYROSINE SULFOTRANSFERASE 2 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PTHR12788 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Pfam | Sulfotransfer_3 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PharmGKB | PA36700 | PharmGKB |
Superfamily-SCOP | SSF52540 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
UniProt | B1AHJ5_HUMAN | UniProtKB/TrEMBL |
B1AHJ6_HUMAN | UniProtKB/TrEMBL | |
B1AHJ7_HUMAN | UniProtKB/TrEMBL | |
B1AHJ8_HUMAN | UniProtKB/TrEMBL | |
B1AHJ9_HUMAN | UniProtKB/TrEMBL | |
B1AHK0_HUMAN | UniProtKB/TrEMBL | |
B3KQA7 | ENTREZGENE | |
B7Z976 | ENTREZGENE, UniProtKB/TrEMBL | |
O60704 | ENTREZGENE | |
Q6FI98 | ENTREZGENE | |
Q9H0V4 | ENTREZGENE | |
TPST2_HUMAN | UniProtKB/Swiss-Prot | |
UniProt Secondary | B3KQA7 | UniProtKB/Swiss-Prot |
Q6FI98 | UniProtKB/Swiss-Prot | |
Q9H0V4 | UniProtKB/Swiss-Prot |