KEGG   Homo sapiens (human): 80256
Entry
80256             CDS       T01001                                 
Symbol
ATOSB, FAM214B, KIAA1539
Name
(RefSeq) atos homolog B
Organism
hsa  Homo sapiens (human)
SSDB
Motif
Pfam: Chromosome_seg DUF4210
Other DBs
NCBI-GeneID: 80256
NCBI-ProteinID: NP_001304920
OMIM: 620169
HGNC: 25666
Ensembl: ENSG00000005238
UniProt: Q7L5A3
Position
9:complement(35104117..35116380)
AA seq 538 aa
MRHVQAEPSPSSEPEAGPSQPPVRQGALQGGLLMGYSPAGGATSPGVYQVSIFSPPAGTS
EPHRALKRQAPSTEGPRELKRGPGLGAREGLPPEEPSTVGLLGPEGPGLGLGVASQHFSH
RGLCVVEQRSSVTSSWTSGAWSPPCPPSNASCNTLHTRDWASPDPGGQGSLGESPGPAPP
GQLHTLDTDLHSLAQIGGKSPVAGVGNGGSLWPRESPGTANGHSPEHTPPGPGPPGPCPT
KRRLLPAGEAPDVSSEEEGPAPRRRRGSLGHPTAANSSDAKATPFWSHLLPGPKEPVLDP
TDCGPMGRRLKGARRLKLSPLRSLRKGPGLLSPPSASPVPTPAVSRTLLGNFEESLLRGR
FAPSGHIEGFTAEIGASGSYCPQHVTLPVTVTFFDVSEQNAPAPFLGIVDLNPLGRKGYS
VPKVGTVQVTLFNPNQTVVKMFLVTFDFSDMPAAHMTFLRHRLFLVPVGEEGNANPTHRL
LCYLLHLRFRSSRSGRLSLHGDIRLLFSRRSLELDTGLPYELQAVTEAPHNPRYSPLP
NT seq 1617 nt   +upstreamnt  +downstreamnt
atgcgccacgtgcaggcggagccgtctccatcctcagagccggaggctggcccttcacag
cctccagtcaggcagggggccctccagggtggcctgctcatgggctacagcccagcaggg
ggggcgacatcccccggggtctaccaggtatccatcttttcccctccggctggtacctct
gagcctcatagggccctgaaacgacaagccccatccactgagggtccccgggagctgaag
agaggccctgggctgggggccagagagggactaccccctgaagaaccatctactgtgggg
ctcttaggcccagagggaccggggctgggactaggtgtggccagccagcatttctcccac
cgtggcctctgtgttgtggaacagagaagtagtgtcacctcatcttggacttcgggggcc
tggagtcccccctgccccccatcaaatgcttcctgcaatactttgcacaccagagactgg
gcctccccagatccagggggacaggggtccctgggggagtccccagggccagcccctcca
ggccagctgcacacacttgacactgatttgcacagtcttgcacaaatagggggtaagagc
ccagtggctggggtgggcaatgggggtagcctctggcctagggagtcccctggcactgcc
aatgggcacagtcccgagcacacaccccctggccctggacccccaggcccctgccccacc
aagcgaaggctgcttcctgctggagaagccccagatgtcagctctgaggaagaggggcca
gcccctcggaggcgccggggatccctgggccaccctactgctgccaacagttctgatgcc
aaagccacacccttctggagccacctgctgcctgggcccaaagagcctgttttggaccca
acagactgcggtcccatggggcggaggctgaaaggagcccgtcgcctgaagctgagcccc
cttcgaagcctccggaaggggccaggcctgctgagcccccccagtgcctcccctgttcct
acccctgctgtcagccgtaccctgctgggcaactttgaggaatcattgctgcgaggacgt
tttgcaccatctggccacattgagggcttcacagcagaaattggagctagtgggtcatac
tgcccccagcacgtcacgctgcctgtcactgtcacattctttgatgtttctgagcaaaat
gccccggctcccttcctgggcatcgtggatctgaaccccttggggaggaagggttacagc
gtgcccaaggtgggcaccgtccaagtgaccttatttaaccccaaccagactgtggtaaag
atgttccttgtgacctttgacttctcggacatgcctgctgcccacatgaccttcctgcgc
catcgcctctttttggtgcctgtgggtgaggagggaaatgctaaccccacccaccgcctc
ctctgctacttgctgcacctcaggttccggagctcccgctcaggccgcttaagcctgcat
ggagatatccgcctgcttttttcccgccggagcctggagctggacacagggctcccctac
gaactgcaggctgtgaccgaggcccctcataatccacgttattcacctttgccctga

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