Homo sapiens (human): 4118
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Entry
4118 CDS
T01001
Symbol
MAL, HLD28, MVP17, VIP17
Name
(RefSeq) mal, T cell differentiation protein (MAL blood group)
KO
K28033
myelin and lymphocyte protein
Organism
hsa
Homo sapiens (human)
Disease
H00679
Hypomyelinating leukodystrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
4118 (MAL)
Membrane trafficking [BR:
hsa04131
]
Endocytosis
Clathrin-mediated endocytosis
Others
4118 (MAL)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MARVEL
Otopetrin
Motif
Other DBs
NCBI-GeneID:
4118
NCBI-ProteinID:
NP_002362
OMIM:
188860
HGNC:
6817
Ensembl:
ENSG00000172005
UniProt:
P21145
LinkDB
All DBs
Position
2:95025708..95053992
Genome browser
AA seq
153 aa
AA seq
DB search
MAPAAATGGSTLPSGFSVFTTLPDLLFIFEFIFGGLVWILVASSLVPWPLVQGWVMFVSV
FCFVATTTLIILYIIGAHGGETSWVTLDAAYHCTAALFYLSASVLEALATITMQDGFTYR
HYHENIAAVVFSYIATLLYVVHAVFSLIRWKSS
NT seq
462 nt
NT seq
+upstream
nt +downstream
nt
atggcccccgcagcggcgacggggggcagcaccctgcccagtggcttctcggtcttcacc
accttgcccgacttgctcttcatctttgagtttatcttcgggggcctggtgtggatcctg
gtggcctcctccctggtgccctggcccctggtccagggctgggtgatgttcgtgtctgtg
ttctgcttcgtggccaccaccaccttgatcatcctgtacataattggagcccacggtgga
gagacttcctgggtcaccttggacgcagcctaccactgcaccgctgccctcttttacctc
agcgcctcagtcctggaggccctggccaccatcacgatgcaagacggcttcacctacagg
cactaccatgaaaacattgctgccgtggtgttctcctacatagccactctgctctacgtg
gtccatgcggtgttctctttaatcagatggaagtcttcataa
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