Homo sapiens (human): 124907513
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Entry
124907513 CDS
T01001
Name
(RefSeq) uncharacterized LOC124907513
Organism
hsa
Homo sapiens (human)
SSDB
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Paralog
Gene cluster
GFIT
Motif
Pfam:
GED
Motif
Other DBs
NCBI-GeneID:
124907513
NCBI-ProteinID:
XP_047302484
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Position
15
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AA seq
901 aa
AA seq
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MEESAEQAQRRDETRVGRRRHSWRSRQSRQTKEFIFSELLSNLYSRRNLQTLVEESAEQA
QRCDKMLLLRAAVQPALAWEREDTRGGVGRAGRPRSSSSQSCCPTCPRVGTRRHSWRRRQ
SRQTKEFIFSELLSNLHSRPRSSSSQSCCPNCTRVGTRRHSWRSRQSRHRGVTRLAWEEE
DTPGGVGRAGRPRSSSSRSCCPTCTRVGTCRHLWRSRQSRHSGATRCCFSELLSNLHSLG
NKKTLVEASAEQADQGVHLLRAAVQPVLTWERADTRGGVGRAGRPRSSSSQSCCPTCTHV
GTSRHSWRRRQSRQTKEFIFSELLSNLHSRGNEKTLVKASAEKADQGVHLLRAAVQPALA
WEREDTRGGVGRAGRPRSSSSQSCCPNCTRVGTRRHSWRSRQSRHRGVTRLAWEEEDTPG
GVGRAGRPRSSSSRSCCPTCTRVGTCRHLWRSRQSRHSGATRCCFSELLSNLHWRGNEKT
LVEASAEQADQGVHLLRAAVQPVLAWERADTRGGVGRAGRPRSSSSQSCCPTCTRVGTRR
HSWRRRQSRQTKEFIFSELLSKLHSRGNEKTLMEESAEQAQRCDETRVGRRRHSWRSRQS
RQTKEFIFSELLSNLYSRRNLQTLVEASAEQADQGVHLLRASVQPVLAWEREDTRGGVGR
AGRPRSSSSQSCCPTCTRVGTRRHSWRRRQSRQTKEFIFSELLSNLHSRGNEKTLMEESA
EQAQRRDETRVGRRRHSWRSRQSRQTKEFIFSELLSNLYSRGNLQTLVEESAEQAQRCDE
MLLLRAAVQPALAWEREDTRGGVGRAGRPRSSSSQSCCPTCTRVGTSRHSWRRWQSRQTK
EFIFSELLSNLHSRGNEKTLVEASAEQADQGVHLLRAAVQTALAWEREDTHGGVGRAGTE
V
NT seq
2706 nt
NT seq
+upstream
nt +downstream
nt
atggaggagtcggccgagcaggcacagcggcgtgacgagactcgcgtgggaagaagaaga
cactcctggaggagtcggcagagcaggcagaccaaggagttcatcttctcggagctgctg
tccaacctgtactcgcgtcggaacctgcagacacttgtggaggagtcggcagagcaggca
cagcggtgcgacaagatgctgcttctcagagctgctgtccaacctgcactcgcgtgggaa
cgagaagacactcgtggaggcgtcggcagagcaggcagaccaaggagttcatcttctcag
agctgctgtccaacctgtcctcgcgtgggaacgagaagacactcgtggaggcgtcggcag
agcaggcagaccaaggagttcatcttctcagagctgctgtccaacctgcactcgcgacca
aggagttcatcttctcagagctgctgtccaaactgcactcgcgtgggaacgagaagacac
tcatggaggagtcggcagagcaggcacagaggtgtgacgagactcgcgtgggaagaagaa
gacactcctggaggagtcggcagagcaggcagaccaaggagttcatcttctcggagctgc
tgtccaacctgtactcgcgtcggaacctgcagacacttgtggaggagtcggcagagcagg
cacagcggtgcgacgagatgctgcttctcagagctgctgtccaacctgcactcgcttggg
aacaagaagacactcgtggaggcgtcggcagagcaggcagaccaaggagttcatcttctc
agagctgctgtccaacctgtactcacgtgggaacgagcagacactcgtggaggcgtcggc
agagcaggcagaccaaggagttcatcttctcagagctgctgtccaacctgtactcacgtg
ggaacgagcagacactcgtggaggcgtcggcagagcaggcagaccaaggagttcatcttc
tcagagctgctgtccaacctgcactcgcgtgggaatgagaagacactcgtgaaggcgtcg
gcagagaaggcagaccaaggagttcatcttctcagagctgctgtccaacctgcactcgcg
tgggaacgagaagacactcgtggaggcgtcggcagagcaggcagaccaaggagttcatct
tctcagagctgctgtccaaactgcactcgcgtgggaacgagaagacactcatggaggagt
cggcagagcaggcacagaggtgtgacgagactcgcgtgggaagaagaagacactcctgga
ggagtcggcagagcaggcagaccaaggagttcatcttctcggagctgctgtccaacctgt
actcgcgtcggaacctgcagacacttgtggaggagtcggcagagcaggcacagcggtgcg
acgagatgctgcttctcagagctgctgtccaacctgcactggcgtggcaacgagaagaca
ctcgtggaggcgtcggcagagcaggcagaccaaggagttcatcttctcagagctgctgtc
caacctgtactcgcgtgggaacgagcagacactcgtggaggcgttggcagagcaggcaga
ccaaggagttcatcttctcagagctgctgtccaacctgcactcgcgtgggaacgagaaga
cactcgtggaggcgtcggcagagcaggcagaccaaggagttcatcttctcagagctgctg
tccaaactgcactcgcgtgggaacgagaagacactcatggaggagtcggcagagcaggca
cagaggtgtgacgagactcgcgtgggaagaagaagacactcctggaggagtcggcagagc
aggcagaccaaggagttcatcttctcggagctgctgtccaacctgtactcgcgtcggaac
ctgcagacactcgtggaggcgtcggcagagcaggcagaccaaggagttcatcttctcaga
gcttctgtccaacctgtactcgcgtgggaacgagaagacactcgtggaggcgtcggcaga
gcaggcagaccaaggagttcatcttctcagagctgctgtccaacctgtactcgcgtggga
acgagaagacactcgtggaggcgtcggcagagcaggcagaccaaggagttcatcttctca
gagctgctgtccaacctgcactcgcgtgggaacgagaagacactcatggaggagtcggcc
gagcaggcacagcggcgtgacgagactcgcgtgggaagaagaagacactcctggaggagt
cggcagagcaggcagaccaaggagttcatcttctcggagctgctgtccaacctgtactcg
cgtgggaacctgcagacacttgtggaggagtcggcagagcaggcacagcggtgcgacgag
atgctgcttctcagagctgctgtccaacctgcactggcgtgggaacgagaagacactcgt
ggaggcgttggcagagcaggcagaccaaggagttcatcttctcagagctgctgtccaacc
tgtactcgcgtgggaacgagcagacactcgtggaggcgttggcagagcaggcagaccaag
gagttcatcttctcagagctgctgtccaacctgcactcgcgtgggaacgagaagacactc
gtggaggcgtcggcagagcaggcagaccaaggagttcatcttctcagagctgctgtccaa
actgcactcgcgtgggaacgagaagacactcatggaggagtcggcagagcaggcacagag
gtgtga
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