Homo sapiens (human): 55325
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Entry
55325 CDS
T01001
Symbol
UFSP2, BHD, C4orf20, DEE106, SEMDDR
Name
(RefSeq) UFM1 specific peptidase 2
KO
K01376
Ufm1-specific protease 2 [EC:3.4.22.-]
Organism
hsa
Homo sapiens (human)
Disease
H00606
Early infantile epileptic encephalopathy
H01817
Beukes hip dysplasia
H02187
Spondyloepimetaphyseal dysplasia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hsa01002
]
55325 (UFSP2)
Peptidases and inhibitors [BR:
hsa01002
]
Cysteine peptidases
Family C78
55325 (UFSP2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
UfSP2_N
Peptidase_C78
Motif
Other DBs
NCBI-GeneID:
55325
NCBI-ProteinID:
NP_060829
OMIM:
611482
HGNC:
25640
Ensembl:
ENSG00000109775
UniProt:
Q9NUQ7
B3KRI4
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All DBs
Position
4:complement(185399537..185425964)
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AA seq
469 aa
AA seq
DB search
MVISESMDILFRIRGGLDLAFQLATPNEIFLKKALKHVLSDLSTKLSSNALVFRICHSSV
YIWPSSDINTIPGELTDASACKNILRFIQFEPEEDIKRKFMRKKDKKLSDMHQIVNIDLM
LEMSTSLAAVTPIIERESGGHHYVNMTLPVDAVISVAPEETWGKVRKLLVDAIHNQLTDM
EKCILKYMKGTSIVVPEPLHFLLPGKKNLVTISYPSGIPDGQLQAYRKELHDLFNLPHDR
PYFKRSNAYHFPDEPYKDGYIRNPHTYLNPPNMETGMIYVVQGIYGYHHYMQDRIDDNGW
GCAYRSLQTICSWFKHQGYTERSIPTHREIQQALVDAGDKPATFVGSRQWIGSIEVQLVL
NQLIGITSKILFVSQGSEIASQGRELANHFQSEGTPVMIGGGVLAHTILGVAWNEITGQI
KFLILDPHYTGAEDLQVILEKGWCGWKGPDFWNKDAYYNLCLPQRPNMI
NT seq
1410 nt
NT seq
+upstream
nt +downstream
nt
atggtgatttcagaaagtatggatatactcttcagaataagaggaggccttgatttggct
tttcagctagctactcctaatgaaatttttctcaagaaggcactgaaacatgtgttgagt
gacctgtcaactaagctgtcttcaaacgcccttgtgttcagaatttgccacagttcagtg
tatatatggcctagcagtgacataaacaccattcctggagaactgactgatgcttctgct
tgtaagaacatactgcgctttattcaatttgagccagaagaagatataaaaagaaaattc
atgagaaagaaggacaaaaagttatcagacatgcatcaaatagtaaatatagatcttatg
ctggaaatgtcaacctccctggcagctgtaacgcccatcattgaaagggaaagcggagga
caccattatgttaatatgactttacctgtcgatgcagttatatctgttgctccagaagaa
acatggggaaaagttcgtaaactcctggttgatgcaattcataatcaactaactgacatg
gaaaaatgtattttgaaatatatgaaaggaacatctattgtggtccctgaaccactgcac
tttttattaccagggaaaaaaaatcttgtaacaatttcatatccttcaggaataccagat
ggccagctgcaggcctataggaaggagttacatgatcttttcaatctgcctcacgacaga
ccctatttcaaaaggtctaatgcttatcactttccagatgagccatacaaagatggttac
attagaaatccacatacttaccttaatccacctaacatggagactggtatgatttatgtg
gtccagggcatatatggctatcatcattatatgcaggatcgcatagatgacaatggctgg
ggctgtgcttatcgatctctgcagactatctgctcttggttcaaacatcagggatacaca
gagaggtccattccaacacacagagaaattcagcaggctctagtcgatgccggggacaaa
ccagcaacatttgtcggatcgcggcaatggattggatctattgaggtgcagctggtacta
aaccaattgatcggtataacgtcaaaaatcctgtttgtcagccaaggttcagaaattgcc
tctcaaggacgggaactggctaatcatttccaaagtgaaggaactccagttatgatcggg
ggaggagttttggcccacacaatactaggagttgcatggaatgagattacagggcagata
aagtttctgattctagatccacattataccggtgctgaagacctgcaagttattttggaa
aagggctggtgcggatggaagggcccagatttttggaacaaggatgcatactataactta
tgtcttcctcagcgaccaaatatgatttaa
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