Homo sapiens (human): 79669
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Entry
79669 CDS
T01001
Symbol
C3orf52, HYPT15, TTMP
Name
(RefSeq) chromosome 3 open reading frame 52
KO
K26953
TPA-induced transmembrane protein
Organism
hsa
Homo sapiens (human)
Disease
H00786
Hypotrichosis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99995 Signaling proteins
79669 (C3orf52)
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Gene cluster
GFIT
Motif
Pfam:
SEA
Motif
Other DBs
NCBI-GeneID:
79669
NCBI-ProteinID:
NP_078892
OMIM:
611956
HGNC:
26255
Ensembl:
ENSG00000114529
UniProt:
Q5BVD1
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All DBs
Position
3:112086389..112136381
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AA seq
217 aa
AA seq
DB search
MDLAQPSQPVDELELSVLERQPEENTPLNGADKVFPSLDEEVPPAEANKESPWSSCNKNV
VGRCKLWMIITSIFLGVITVIIIGLCLAAVTYVDEDENEILELSSNKTFFIMLKIPEECV
AEEELPHLLTERLTDVYSTSPSLGRYFTSVEIVDFSGENATVTYDLQFGVPSDDENFMKY
MMSEELVLGILLQDFRDQNIPGCESLGLDPTSLLLYE
NT seq
654 nt
NT seq
+upstream
nt +downstream
nt
atggacctggcccaaccctcacagccagtagacgagctggagctctcggtgctcgagcgg
cagccagaagagaacacgcctctcaatggtgccgacaaggtcttcccttctttggacgag
gaggtccccccggccgaggctaacaaggaaagcccctggagctcctgtaataagaatgtg
gttggaagatgcaaactgtggatgatcatcacctccattttcctaggtgtcattacagtg
atcatcataggcttatgtcttgctgcagtaacttatgttgatgaagatgaaaatgaaata
cttgaattatcatcaaacaaaacattcttcatcatgctgaagattccagaggagtgtgtt
gctgaagaggaattgcctcacctgctcaccgaaaggctcacagatgtgtacagtacatcg
ccctctctgggtcgttattttacttcagttgaaatagtggacttcagtggtgaaaatgcc
acagtaacgtatgacctgcaatttggggttccatcagatgatgaaaattttatgaagtat
atgatgagtgaggagttggtgctgggcattttgctacaggatttccgtgatcagaatata
cctggttgtgagagtctggggcttgatccaacatccctcttgctctatgaatga
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