Homo sapiens (human): 83938
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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)
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Gene cluster
GFIT
Motif
Pfam:
LRR_9
LRR_4
LRR_8
LRR_At5g56370
Sde2_N_Ubi_yeast
Motif
Other DBs
NCBI-GeneID:
83938
NCBI-ProteinID:
NP_114413
OMIM:
614537
HGNC:
23405
Ensembl:
ENSG00000148655
UniProt:
Q9H2I8
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Position
10:75431624..76560168
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AA seq
198 aa
AA seq
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MEKYLSLSGNHSSNKRSLEGLSAFRSLEELILDNNQLGDDLVLPGLPRLHTLTLNKNRIT
DLENLLDHLAEVTPALEYLSLLGNVACPNELVSLEKDEEDYKRYRCFVLYKLPNLKFLDA
QKVTRQEREEALVRGVFMKVVKPKASSEDVASSPERHYTPLPSASRELTSHQGVLGKCRY
VYYGKNSEGNRFIRDDQL
NT seq
597 nt
NT seq
+upstream
nt +downstream
nt
atggaaaagtatttgtcactcagcggcaatcattcttcaaataaaaggtcactggaagga
ctgagcgcattcaggagcctggaggaactcatcttggacaacaatcagctgggggacgac
cttgtgttgccagggttacccagactgcataccttaaccctcaacaagaaccgaatcact
gatttggagaacctgctggatcacttggcagaagtgacaccagctctggagtacctcagt
ctgctgggcaacgtggcctgtcccaacgagctggtcagcttggaaaaggatgaggaagac
tacaagagatacagatgctttgttctgtacaagctgcccaacttgaaatttctggatgcc
cagaaagtaaccagacaagaacgagaggaggcgttggtcagaggagtcttcatgaaggtg
gtgaagcccaaggcttctagtgaggacgttgccagctccccggagcgccactacacgccc
ttgccttctgcttccagggaactcaccagtcaccaaggtgtcctggggaagtgtcgctac
gtttactatgggaaaaactcagagggcaacaggtttatccgagatgaccagctctga
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