Homo sapiens (human): 83723
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Entry
83723 CDS
T01001
Symbol
TLCD3B, CORD22, FAM57B, FP1188
Name
(RefSeq) TLC domain containing 3B
KO
K26600
TLC domain-containing protein 3
Organism
hsa
Homo sapiens (human)
Disease
H00481
Cone-rod dystrophy and cone dystrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09191 Unclassified: metabolism
99983 Lipid metabolism
83723 (TLCD3B)
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Gene cluster
GFIT
Motif
Pfam:
TRAM_LAG1_CLN8
Motif
Other DBs
NCBI-GeneID:
83723
NCBI-ProteinID:
NP_113666
OMIM:
615175
HGNC:
25295
Ensembl:
ENSG00000149926
UniProt:
Q71RH2
F1T0F5
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All DBs
Position
16:complement(30024427..30053040)
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AA seq
274 aa
AA seq
DB search
MLTPMVAGGVVFPGLFLLSKNTLQRLPQLRWEEADAVIVSARLVSSVQAIMASTAGYIVS
TSCKHIIDDQHWLSSAYTQFAVPYFIYDIYAMFLCHWHKHQVKGHGGDDGAARAPGSTWA
IARGYLHKEFLMVLHHAAMVLVCFPLSVVWRQGKGDFFLGCMLMAEVSTPFVCLGKILIQ
YKQQHTLLHKVNGALMLLSFLCCRVLLFPYLYWAYGRHAGLPLLAVPLAIPAHVNLGAAL
LLAPQLYWFFLICRGACRLFWPRSRPPPACQAQD
NT seq
825 nt
NT seq
+upstream
nt +downstream
nt
atgctgaccccgatggtggccgggggggtggtgttccccggactcttcctcctctccaag
aacacgctccagcggctgccccagctacgctgggaggaggccgacgcagtcattgtctca
gccaggctggtgtcctctgtccaggccatcatggcctccactgccggctacatcgtctcc
acctcctgcaagcacatcattgatgaccaacactggctgtcctctgcctacacgcaattt
gctgtgccctacttcatctacgacatctacgccatgttcctctgtcactggcacaagcac
caggtcaaagggcatggaggggacgacggagcggccagagccccgggcagcacgtgggcc
atagcgcgtggctacctgcacaaggagttcctcatggtgctccaccatgccgccatggtg
ctggtgtgcttcccactctcagtggtgtggcgacagggtaagggagacttctttctgggt
tgcatgttgatggcagaggtcagcacgcccttcgtctgccttggcaagatcctcatccag
tacaagcagcagcacacactgctgcacaaggtgaacggggccctgatgctgctcagcttc
ctctgctgccgggtgctgctctttccctacctgtactgggcctacgggcgccatgccggc
ctgcccctgctggccgtgcccctggccatccctgcccacgtcaacctgggcgctgcgctg
ctcctggcccctcagctctactggttcttcctcatctgccgtggggcctgccgcctcttc
tggccccgctcccggccgcccccggcctgccaggcccaggactga
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