Homo sapiens (human): 10586
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Entry
10586 CDS
T01001
Symbol
MAB21L2, MCOPS14, MCSKS14
Name
(RefSeq) mab-21 like 2
Organism
hsa
Homo sapiens (human)
Disease
H02170
Microphthalmia, syndromic
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Mab-21
Mab-21_C
Motif
Other DBs
NCBI-GeneID:
10586
NCBI-ProteinID:
NP_006430
OMIM:
604357
HGNC:
6758
Ensembl:
ENSG00000181541
Pharos:
Q9Y586
(Tdark)
UniProt:
Q9Y586
LinkDB
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Position
4:150582151..150584693
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AA seq
359 aa
AA seq
DB search
MIAAQAKLVYQLNKYYTERCQARKAAIAKTIREVCKVVSDVLKEVEVQEPRFISSLSEID
ARYEGLEVISPTEFEVVLYLNQMGVFNFVDDGSLPGCAVLKLSDGRKRSMSLWVEFITAS
GYLSARKIRSRFQTLVAQAVDKCSYRDVVKMIADTSEVKLRIRERYVVQITPAFKCTGIW
PRSAAQWPMPHIPWPGPNRVAEVKAEGFNLLSKECYSLTGKQSSAESDAWVLQFGEAENR
LLMGGCRNKCLSVLKTLRDRHLELPGQPLNNYHMKTLLLYECEKHPRETDWDESCLGDRL
NGILLQLISCLQCRRCPHYFLPNLDLFQGKPHSALESAAKQTWRLAREILTNPKSLDKL
NT seq
1080 nt
NT seq
+upstream
nt +downstream
nt
atgatcgccgctcaggccaagctggtttaccagctcaataagtactacactgagcgctgt
caggcgcgcaaggcggccatcgccaaaaccatccgagaggtctgtaaggtggtctcggac
gtgctcaaggaagtggaggtgcaggagcctcgcttcatcagctccttgagcgagatcgat
gcccgctacgaggggctcgaggtcatttcgcccaccgaatttgaggtggtgctctaccta
aaccagatgggcgtcttcaacttcgtggacgacggctcgctgcccggctgcgcagtgctc
aaactgagcgatgggcggaagcggagcatgtctctctgggtcgagttcatcacggcgtcg
ggctatctctcagcgcgtaagatccgctcgcgtttccagacgctggtggcccaggcggtg
gacaagtgcagctatcgggatgtggtcaagatgatcgcggacaccagcgaggtcaagttg
cgcatcagggagcgctatgtggtgcaaatcactccggcgttcaagtgcaccgggatctgg
cctcgcagcgcggcacagtggcctatgccccacatcccttggcccggccccaatcgggtg
gccgaggtcaaggccgaagggttcaacttgctctcgaaggagtgctactcgctgaccggc
aagcagagctcggcagagagcgacgcctgggtgctacagttcggggaggcggagaaccgc
ctgctgatgggcggctgccgaaacaagtgcctctcagtgctgaagactctgcgggaccgc
cacctggagctacccggccagccgctcaacaactaccacatgaagacgctgctgctgtac
gagtgcgagaaacacccacgagaaacggactgggacgagtcgtgcctgggcgaccggctc
aacggcatcctgctgcagctcatctcctgcctgcagtgccgccgctgccctcactacttt
ctgcccaacctcgacctctttcagggcaagccccattcggccctggagagcgctgccaag
cagacctggaggttggccagggaaattctcaccaatcccaaaagcctggacaaactatag
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integrated database retrieval system