KEGG   Homo sapiens (human): 83723
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)
SSDB
Motif
Pfam: TRAM_LAG1_CLN8
Other DBs
NCBI-GeneID: 83723
NCBI-ProteinID: NP_113666
OMIM: 615175
HGNC: 25295
Ensembl: ENSG00000149926
UniProt: Q71RH2 F1T0F5
Position
16:complement(30024427..30053040)
AA seq 274 aa
MLTPMVAGGVVFPGLFLLSKNTLQRLPQLRWEEADAVIVSARLVSSVQAIMASTAGYIVS
TSCKHIIDDQHWLSSAYTQFAVPYFIYDIYAMFLCHWHKHQVKGHGGDDGAARAPGSTWA
IARGYLHKEFLMVLHHAAMVLVCFPLSVVWRQGKGDFFLGCMLMAEVSTPFVCLGKILIQ
YKQQHTLLHKVNGALMLLSFLCCRVLLFPYLYWAYGRHAGLPLLAVPLAIPAHVNLGAAL
LLAPQLYWFFLICRGACRLFWPRSRPPPACQAQD
NT seq 825 nt   +upstreamnt  +downstreamnt
atgctgaccccgatggtggccgggggggtggtgttccccggactcttcctcctctccaag
aacacgctccagcggctgccccagctacgctgggaggaggccgacgcagtcattgtctca
gccaggctggtgtcctctgtccaggccatcatggcctccactgccggctacatcgtctcc
acctcctgcaagcacatcattgatgaccaacactggctgtcctctgcctacacgcaattt
gctgtgccctacttcatctacgacatctacgccatgttcctctgtcactggcacaagcac
caggtcaaagggcatggaggggacgacggagcggccagagccccgggcagcacgtgggcc
atagcgcgtggctacctgcacaaggagttcctcatggtgctccaccatgccgccatggtg
ctggtgtgcttcccactctcagtggtgtggcgacagggtaagggagacttctttctgggt
tgcatgttgatggcagaggtcagcacgcccttcgtctgccttggcaagatcctcatccag
tacaagcagcagcacacactgctgcacaaggtgaacggggccctgatgctgctcagcttc
ctctgctgccgggtgctgctctttccctacctgtactgggcctacgggcgccatgccggc
ctgcccctgctggccgtgcccctggccatccctgcccacgtcaacctgggcgctgcgctg
ctcctggcccctcagctctactggttcttcctcatctgccgtggggcctgccgcctcttc
tggccccgctcccggccgcccccggcctgccaggcccaggactga

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