Homo sapiens (human): 5612
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Entry
5612 CDS
T01001
Symbol
THAP12, DAP4, P52rIPK, PRKRIR, THAP0
Name
(RefSeq) THAP domain containing 12
Organism
hsa
Homo sapiens (human)
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
THAP
Dimer_Tnp_hAT
DUF4371
Ribosomal_uL24m-like
Motif
Other DBs
NCBI-GeneID:
5612
NCBI-ProteinID:
NP_004696
OMIM:
607374
HGNC:
9440
Ensembl:
ENSG00000137492
UniProt:
O43422
A0A140VJQ7
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All DBs
Position
11:complement(76349956..76381132)
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AA seq
761 aa
AA seq
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MPNFCAAPNCTRKSTQSDLAFFRFPRDPARCQKWVENCRRADLEDKTPDQLNKHYRLCAK
HFETSMICRTSPYRTVLRDNAIPTIFDLTSHLNNPHSRHRKRIKELSEDEIRTLKQKKID
ETSEQEQKHKETNNSNAQNPSEEEGEGQDEDILPLTLEEKENKEYLKSLFEILILMGKQN
IPLDGHEADEIPEGLFTPDNFQALLECRINSGEEVLRKRFETTAVNTLFCSKTQQRQMLE
ICESCIREETLREVRDSHFFSIITDDVVDIAGEEHLPVLVRFVDESHNLREEFIGFLPYE
ADAEILAVKFHTMITEKWGLNMEYCRGQAYIVSSGFSSKMKVVASRLLEKYPQAIYTLCS
SCALNMWLAKSVPVMGVSVALGTIEEVCSFFHRSPQLLLELDNVISVLFQNSKERGKELK
EICHSQWTGRHDAFEILVELLQALVLCLDGINSDTNIRWNNYIAGRAFVLCSAVSDFDFI
VTIVVLKNVLSFTRAFGKNLQGQTSDVFFAAGSLTAVLHSLNEVMENIEVYHEFWFEEAT
NLATKLDIQMKLPGKFRRAHQGNLESQLTSESYYKETLSVPTVEHIIQELKDIFSEQHLK
ALKCLSLVPSVMGQLKFNTSEEHHADMYRSDLPNPDTLSAELHCWRIKWKHRGKDIELPS
TIYEALHLPDIKFFPNVYALLKVLCILPVMKVENERYENGRKRLKAYLRNTLTDQRSSNL
ALLNINFDIKHDLDLMVDTYIKLYTSKSELPTDNSETVENT
NT seq
2286 nt
NT seq
+upstream
nt +downstream
nt
atgccgaacttctgcgctgcccccaactgcacgcggaagagcacgcagtccgacttggcc
ttcttcaggttcccgcgggaccctgccagatgccagaagtgggtggagaactgtaggaga
gcagacttagaagataaaacacctgatcagctaaataaacattatcgattatgtgccaaa
cattttgagacctctatgatctgtagaactagtccttataggacagttcttcgagataat
gcaataccaacaatatttgatcttaccagtcatttgaacaacccacatagtagacacaga
aaacgaataaaagaactgagtgaagatgaaatcaggacactgaaacagaaaaaaattgat
gaaacttctgagcaggaacaaaaacataaagaaaccaacaatagcaatgctcagaacccc
agcgaagaagagggtgaagggcaagatgaggacattttacctctaacccttgaagagaag
gaaaacaaagaatacctaaaatctctatttgaaatcttgattctgatgggaaagcaaaac
atacctctggatggacatgaggctgatgaaatcccagaaggtctctttactccagataac
tttcaggcactgctggagtgtcggataaattctggtgaagaggttctgagaaagcggttt
gagacaacagcagttaacacgttgttttgttcaaaaacacagcagaggcagatgctagag
atctgtgagagctgtattcgagaagaaactctcagggaagtgagagactcacacttcttt
tccattatcactgacgatgtagtggacatagcaggggaagagcacctacctgtgttggtg
aggtttgttgatgaatctcataacctaagagaggaatttataggcttcctgccttatgaa
gccgatgcagaaattttggctgtgaaatttcacactatgataactgagaagtggggatta
aatatggagtattgtcgtggccaggcttacattgtctctagtggattttcttccaaaatg
aaagttgttgcttctagacttttagagaaatatccccaagctatctacacactctgctct
tcctgtgccttaaatatgtggttggcaaaatcagtacctgttatgggagtatctgttgca
ttaggaacaattgaggaagtttgttcttttttccatcgatcaccacaactgcttttagaa
cttgacaacgtaatttctgttctttttcagaacagtaaagaaaggggtaaagaactgaag
gaaatctgccattctcagtggacaggcaggcatgatgcttttgaaattttagtggaactc
ctgcaagcacttgttttatgtttagatggtataaatagtgacacaaatattagatggaat
aactatatagctggccgagcatttgtactctgcagtgcagtgtcagattttgatttcatt
gttactattgttgttcttaaaaatgtcctatcttttacaagagcctttgggaaaaacctc
caggggcaaacctctgatgtcttctttgcggccggtagcttgactgcagtactgcattca
ctcaacgaagtgatggaaaatattgaagtttatcatgaattttggtttgaggaagccaca
aatttggcaaccaaacttgatattcaaatgaaactccctgggaaattccgcagagctcac
cagggtaacttggaatctcagctaacctctgagagttactataaagaaaccctaagtgtc
ccaacagtggagcacattattcaggaacttaaagatatattctcagaacagcacctcaaa
gctcttaaatgcttatctctggtaccctcagtcatgggacaactcaaattcaatacgtcg
gaggaacaccatgctgacatgtatagaagtgacttacccaatcctgacacgctgtcagct
gagcttcattgttggagaatcaaatggaaacacagggggaaagatatagagcttccgtcc
accatctatgaagccctccacctgcctgacatcaagttttttcctaatgtgtatgcattg
ctgaaggtcctgtgtattcttcctgtgatgaaggttgagaatgagcggtatgaaaatgga
cgaaagcgtcttaaagcatatttgaggaacactttgacagaccaaaggtcaagtaacttg
gctttgcttaacataaattttgatataaaacacgacctggatttaatggtggacacatat
attaaactctatacaagtaagtcagagcttcctacagataattccgaaactgtggaaaat
acctaa
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