KEGG   Homo sapiens (human): 83938
Entry
83938             CDS       T01001                                 
Symbol
LRMDA, C10orf11, CDA017
Name
(RefSeq) leucine rich melanocyte differentiation associated
  KO
K24399  leucine-rich melanocyte differentiation-associated protein
Organism
hsa  Homo sapiens (human)
Disease
H00168  Oculocutaneous albinism
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09193 Unclassified: signaling and cellular processes
   99995 Signaling proteins
    83938 (LRMDA)
SSDB
Motif
Pfam: LRR_9 LRR_4 LRR_8
Other DBs
NCBI-GeneID: 83938
NCBI-ProteinID: NP_114413
OMIM: 614537
HGNC: 23405
Ensembl: ENSG00000148655
UniProt: Q9H2I8
Position
10:75431624..76560168
AA seq 198 aa
MEKYLSLSGNHSSNKRSLEGLSAFRSLEELILDNNQLGDDLVLPGLPRLHTLTLNKNRIT
DLENLLDHLAEVTPALEYLSLLGNVACPNELVSLEKDEEDYKRYRCFVLYKLPNLKFLDA
QKVTRQEREEALVRGVFMKVVKPKASSEDVASSPERHYTPLPSASRELTSHQGVLGKCRY
VYYGKNSEGNRFIRDDQL
NT seq 597 nt   +upstreamnt  +downstreamnt
atggaaaagtatttgtcactcagcggcaatcattcttcaaataaaaggtcactggaagga
ctgagcgcattcaggagcctggaggaactcatcttggacaacaatcagctgggggacgac
cttgtgttgccagggttacccagactgcataccttaaccctcaacaagaaccgaatcact
gatttggagaacctgctggatcacttggcagaagtgacaccagctctggagtacctcagt
ctgctgggcaacgtggcctgtcccaacgagctggtcagcttggaaaaggatgaggaagac
tacaagagatacagatgctttgttctgtacaagctgcccaacttgaaatttctggatgcc
cagaaagtaaccagacaagaacgagaggaggcgttggtcagaggagtcttcatgaaggtg
gtgaagcccaaggcttctagtgaggacgttgccagctccccggagcgccactacacgccc
ttgccttctgcttccagggaactcaccagtcaccaaggtgtcctggggaagtgtcgctac
gtttactatgggaaaaactcagagggcaacaggtttatccgagatgaccagctctga

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