Homo sapiens (human): 132001
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Entry
132001 CDS
T01001
Symbol
TAMM41, C3orf31, COXPD56, RAM41, TAM41
Name
(RefSeq) TAM41 mitochondrial translocator assembly and maintenance homolog
KO
K17807
mitochondrial translocator assembly and maintenance protein 41
Organism
hsa
Homo sapiens (human)
Disease
H00891
Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
132001 (TAMM41)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial protein import machinery
Matrix
Other matrix factors
132001 (TAMM41)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Tam41_Mmp37
T4_tail_cap
Motif
Other DBs
NCBI-GeneID:
132001
NCBI-ProteinID:
NP_001381403
OMIM:
614948
HGNC:
25187
Ensembl:
ENSG00000144559
UniProt:
Q96BW9
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All DBs
Position
3:complement(11721896..11846885)
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AA seq
452 aa
AA seq
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MALQTLQSSWVTFRKILSHFPEELSLAFVYGSGVYRQAGPSSDQKNAMLDFVFTVDDPVA
WHSKNLKKNWSHYSFLKVLGPKIITSIQNNYGAGVYYNSLIMCNGRLIKYGVISTNVLIE
DLLNWNNLYIAGRLQKPVKIISVNEDVTLRSALDRNLKSAVTAAFLMLPESFSEEDLFIE
IAGLSYSGDFRMVVGEDKTKVLNIVKPNIAHFRELYGSILQENPQVVYKSQQGWLEIDKS
PEGQFTQLMTLPKTLQQQINHIMDPPGKNRDVEETLFQVAHDPDCGDVVRLGLSAIVRPS
SIRQSTKGIFTAGKSFGNPCVTYLLTEWLPHSWLQCKALYLLGACEMLSFDGHKLGYCSK
VQTGITAAEPGGRTMSDHWQCCWKLYCPSEFSETLPVCRVFPSYCFIYQSYRCIGLQKQQ
HLCSPSSSPSLRQLLPSVLVGYFCCYCHFSKW
NT seq
1359 nt
NT seq
+upstream
nt +downstream
nt
atggcgctgcagacgctgcagagctcgtgggtgaccttccgcaagatcctgtctcacttc
cccgaggagctgagtctggctttcgtctacggctccggggtgtaccgccaggcagggccg
agttcagaccagaagaatgctatgctggactttgtgttcacagtagatgaccctgtcgca
tggcattcaaagaacctgaagaaaaattggagtcactactctttcctaaaagttttaggg
cccaagattatcacgtccatccagaataactatggcgctggagtttactacaattcattg
atcatgtgtaatggtaggcttatcaaatatggagttattagcactaacgttctgattgaa
gatctcctcaactggaataacttatacattgctggacgactccaaaaaccggtgaaaatt
atctcagtgaacgaggatgtcactcttagatcagccctcgatagaaatctgaagagtgct
gtgaccgctgctttcctcatgctccccgaaagcttttctgaagaagacctcttcatagag
attgccggtctctcctattcaggtgactttcggatggtggttggagaagataaaacaaaa
gtgttgaatattgtgaagcccaatatagcccactttcgagagctctatggcagcatacta
caggaaaatcctcaagtggtgtataaaagccagcaaggctggctggagatagataaaagc
ccagaaggacagttcactcagctgatgacattgcccaaaaccttacagcaacagataaat
catattatggaccctcctggaaaaaacagagatgtggaagaaactttattccaagtggct
catgatcccgactgtggagatgtggtgcgactagggctttcagcaatcgtgagaccgtct
agtataagacagagcacgaaaggcatttttactgctggtaagagctttggaaatccgtgt
gtaacatacctgctgactgagtggcttccacactcttggttacagtgtaaagctttgtat
cttttaggtgcttgtgaaatgctgagctttgatggccataaactgggatattgcagtaag
gtacaaacaggcataacagcagcagaacctggtggtcgaacaatgtcagaccattggcag
tgctgttggaagctttactgcccttctgaattttctgagacacttcctgtgtgcagggtt
tttccctcatattgttttatttatcaaagttacagatgcataggattgcaaaaacagcag
catctgtgctccccctcctcttccccttctctgagacaactgcttccatctgtcttagtg
ggttatttttgttgttactgccatttctctaaatggtaa
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