Homo sapiens (human): 81555
Help
Entry
81555 CDS
T01001
Symbol
YIPF5, FinGER5, MEDS2, SB140, SMAP-5, SMAP5, YIP1A, YIPFalpha1A
Name
(RefSeq) Yip1 domain family member 5
KO
K20363
protein YIPF5/7
Organism
hsa
Homo sapiens (human)
Disease
H02132
Microcephaly syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
81555 (YIPF5)
Membrane trafficking [BR:
hsa04131
]
Endoplasmic reticulum (ER) - Golgi transport
Others
YIPF proteins
81555 (YIPF5)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Yip1
Motif
Other DBs
NCBI-GeneID:
81555
NCBI-ProteinID:
NP_001020118
OMIM:
611483
HGNC:
24877
Ensembl:
ENSG00000145817
UniProt:
Q969M3
LinkDB
All DBs
Position
5:complement(144158162..144170659)
Genome browser
AA seq
257 aa
AA seq
DB search
MSGFENLNTDFYQTSYSIDDQSQQSYDYGGSGGPYSKQYAGYDYSQQGRFVPPDMMQPQQ
PYTGQIYQPTQAYTPASPQPFYGNNFEDEPPLLEELGINFDHIWQKTLTVLHPLKVADGS
IMNETDLAGPMVFCLAFGATLLLAGKIQFGYVYGISAIGCLGMFCLLNLMSMTGVSFGCV
ASVLGYCLLPMILLSSFAVIFSLQGMVGIILTAGIIGWCSFSASKIFISALAMEGQQLLV
AYPCALLYGVFALISVF
NT seq
774 nt
NT seq
+upstream
nt +downstream
nt
atgtcaggctttgaaaacttaaacacggatttctaccagacaagttacagcatcgatgat
cagtcacagcagtcctatgattatggaggaagtggaggaccctatagcaaacagtatgct
ggctatgactattcgcagcaaggcagatttgtccctccagacatgatgcagccacaacag
ccatacaccgggcagatttaccagccaactcaggcatatactccagcttcacctcagcct
ttctatggaaacaactttgaggatgagccacctttattagaagagttaggtatcaatttt
gaccacatctggcaaaaaacactaacagtattacatccgttaaaagtagcagatggcagc
atcatgaatgaaactgatttggcaggtccaatggttttttgccttgcttttggagccaca
ttgctactggctggcaaaatccagtttggctatgtatacgggatcagtgcaattggatgt
ctaggaatgttttgtttattaaacttaatgagtatgacaggtgtttcatttggttgtgtg
gcaagtgtccttggatattgtcttctgcccatgatcctactttccagctttgcagtgata
ttttctttgcaaggaatggtaggaatcattctcactgctgggattattggatggtgtagt
ttttctgcttccaaaatatttatttctgcattagccatggaaggacagcaacttttagta
gcatatccttgcgctttgttatatggagtctttgccctgatttccgtcttttga
DBGET
integrated database retrieval system
