Homo sapiens (human): 23259
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Entry
23259 CDS
T01001
Symbol
DDHD2, SAMWD1, SPG54, iPLA(1)gamma, iPLA1A, iPLA1gamma, p125B
Name
(RefSeq) DDHD domain containing 2
KO
K16545
phospholipase DDHD2 [EC:3.1.1.-]
Organism
hsa
Homo sapiens (human)
Disease
H00266
Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
23259 (DDHD2)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Pericentriolar materials (PCM)
Other PCM proteins
23259 (DDHD2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DDHD
WWE_3
WWE
SAM_1
WWE_2
SAM_TNK
Phage_gp53
Motif
Other DBs
NCBI-GeneID:
23259
NCBI-ProteinID:
NP_001157704
OMIM:
615003
HGNC:
29106
Ensembl:
ENSG00000085788
UniProt:
O94830
LinkDB
All DBs
Position
8:38231585..38273647
Genome browser
AA seq
711 aa
AA seq
DB search
MSSVQSQQEQLSQSDPSPSPNSCSSFELIDMDAGSLYEPVSPHWFYCKIIDSKETWIPFN
SEDSQQLEEAYSSGKGCNGRVVPTDGGRYDVHLGERMRYAVYWDELASEVRRCTWFYKGD
KDNKYVPYSESFSQVLEETYMLAVTLDEWKKKLESPNREIIILHNPKLMVHYQPVAGSDD
WGSTPTEQGRPRTVKRGVENISVDIHCGEPLQIDHLVFVVHGIGPACDLRFRSIVQCVND
FRSVSLNLLQTHFKKAQENQQIGRVEFLPVNWHSPLHSTGVDVDLQRITLPSINRLRHFT
NDTILDVFFYNSPTYCQTIVDTVASEMNRIYTLFLQRNPDFKGGVSIAGHSLGSLILFDI
LTNQKDSLGDIDSEKDSLNIVMDQGDTPTLEEDLKKLQLSEFFDIFEKEKVDKEALALCT
DRDLQEIGIPLGPRKKILNYFSTRKNSMGIKRPAPQPASGANIPKESEFCSSSNTRNGDY
LDVGIGQVSVKYPRLIYKPEIFFAFGSPIGMFLTVRGLKRIDPNYRFPTCKGFFNIYHPF
DPVAYRIEPMVVPGVEFEPMLIPHHKGRKRMHLELREGLTRMSMDLKNNLLGSLRMAWKS
FTRAPYPALQASETPEETEAEPESTSEKPSDVNTEETSVAVKEEVLPINVGMLNGGQRID
YVLQEKPIESFNEYLFALQSHLCYWESEDTVLLVLKEIYQTQGIFLDQPLQ
NT seq
2136 nt
NT seq
+upstream
nt +downstream
nt
atgtcatcagtgcagtcacaacaggagcagttgtcccagtcagatccatctccgtcacca
aactcatgtagttcctttgagctaatagacatggatgctggcagcttgtatgaaccagtt
tctccccattggttttattgtaagataatagattctaaggagacatggattcctttcaac
tctgaggattcacagcagctggaagaggcatatagctctggaaaaggttgtaatgggaga
gttgttcctactgatgggggcagatatgatgttcatttgggggagaggatgcggtatgct
gtatactgggatgaactggcatcggaagtgagacgatgtacgtggttttacaagggggac
aaagacaataagtatgttccctactcggagagcttcagccaagttttagaggaaacttac
atgcttgctgtaactttggatgaatggaaaaagaaactggaatctcccaacagagaaatt
attattttacacaatccaaagcttatggtgcattaccagccagttgcagggtctgatgat
tggggttcaacacccacggagcagggtcgaccaagaactgtgaagagaggagttgagaac
atctctgttgacattcattgtggagaacctttacaaatagatcacttggtttttgtagtc
catgggattggaccagcttgtgatctccgctttcgaagcattgtacagtgtgttaatgat
tttcgcagtgtttccttgaacttgctacagacacattttaagaaagcccaagaaaatcag
cagattgggagggtagaatttcttccagtcaactggcacagtcctttgcattctactggt
gtggatgtagatctgcagcgaataaccctgcccagcattaaccgcctcaggcacttcacc
aatgacacaattctggatgtcttcttctacaatagtcccacctactgtcagactattgtg
gacacagttgcttctgaaatgaaccgaatatacacactttttctacagaggaaccctgat
ttcaaagggggtgtatccattgctggtcatagtttaggttcgcttatattgtttgatatc
ctaacaaatcagaaagattctttgggggatattgacagtgaaaaggattcgctaaatatt
gtaatggatcaaggagatacacctacactagaggaagatttgaagaaacttcagctctct
gaattctttgatatctttgagaaggagaaagtagataaggaagctctggctttatgtaca
gaccgagatcttcaggaaataggaattcctttaggaccaagaaagaagatattaaactat
ttcagcaccagaaaaaactcaatgggtattaagagaccagccccgcagcctgcttcaggg
gcaaacatccccaaagaatctgagttctgcagtagcagtaatactagaaatggtgactat
ctggatgttggcattgggcaggtgtctgtgaaatacccccggctcatctataaaccagag
atattctttgcctttggatctcccattggaatgttccttactgtccgaggactaaaaaga
attgatcccaactacagatttccaacgtgcaaaggtttcttcaatatttatcaccctttt
gatcctgtggcctataggattgaaccaatggtggtcccaggagtggaatttgagccaatg
ctgatcccacatcataaaggcaggaagcggatgcacttagaactgagagagggcttgacc
aggatgagtatggaccttaagaacaacttgctaggttcgctgcggatggcctggaagtct
tttaccagagctccataccctgccttacaagcttcagaaacaccagaagaaactgaagca
gaacctgaatcaacttcagagaagcctagtgatgttaacacagaagagacctctgtggca
gttaaagaagaagtcctgcctatcaatgtggggatgctgaatggaggccaacgcattgac
tatgtgctacaggagaagcctattgaaagttttaatgagtatttatttgctttacaaagc
catctatgctactgggagtctgaagatacagtattgctcgtcctcaaagagatctaccaa
acccagggtatcttccttgatcagcctttacagtaa
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