Homo sapiens (human): 4034
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Entry
4034 CDS
T01001
Symbol
LRCH4, LRN, LRRN1, LRRN4, PP14183
Name
(RefSeq) leucine-rich repeat and calponin homology domain-containing protein 4 isoform 1
Organism
hsa
Homo sapiens (human)
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Paralog
GFIT
Motif
Pfam:
LRR_8
LRR_14
CH
LRR_4
LRR_1
LRR_LRWD1
CAMSAP_CH
LRR_Zer-1
Motif
Other DBs
NCBI-GeneID:
4034
NCBI-ProteinID:
NP_002310
OMIM:
620165
HGNC:
6691
Ensembl:
ENSP00000309689.6
UniProt:
O75427
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All DBs
Position
7:complement(100574011..100586129)
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AA seq
683 aa
AA seq
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MAAAVAAPLAAGGEEAAATTSVPGSPGLPGRRSAERALEEAVATGTLNLSNRRLKHFPRG
AARSYDLSDITQADLSRNRFPEVPEAACQLVSLEGLSLYHNCLRCLNPALGNLTALTYLN
LSRNQLSLLPPYICQLPLRVLIVSNNKLGALPPDIGTLGSLRQLDVSSNELQSLPSELCG
LSSLRDLNVRRNQLSTLPEELGDLPLVRLDFSCNRVSRIPVSFCRLRHLQVILLDSNPLQ
SPPAQVCLKGKLHIFKYLSTEAGQRGSALGDLAPSRPPSFSPCPAEDLFPGHRYDGGLDS
GFHSVDSGSKRWSGNESTDEFSELSFRISELAREPRGPRERKEDGSADGDPVQIDFIDSH
VPGEDEERGTVEEQRPPELSPGAGDRERAPSSRREEPAGEERRRPDTLQLWQERERRQQQ
QSGAWGAPRKDSLLKPGLRAVVGGAAAVSTQAMHNGSPKSSASQAGAAAGQGAPAPAPAS
QEPLPIAGPATAPAPRPLGSIQRPNSFLFRSSSQSGSGPSSPDSVLRPRRYPQVPDEKDL
MTQLRQVLESRLQRPLPEDLAEALASGVILCQLANQLRPRSVPFIHVPSPAVPKLSALKA
RKNVESFLEACRKMGVPEADLCSPSDLLQGTARGLRTALEAVKRVGGKALPPLWPPSGLG
GFVVFYVVLMLLLYVTYTRLLGS
NT seq
2052 nt
NT seq
+upstream
nt +downstream
nt
atggcggcggccgtagcggctccactcgccgccgggggtgaggaggcggcagccacgacc
tccgtgcccgggtctccaggtctgccggggagacgcagtgcagagcgggccctagaggag
gccgtggccaccgggaccctgaacctgtctaaccggcgcttgaagcacttcccccggggc
gcggcccgtagctacgacctgtcagacatcacccaggctgacctgtcccggaaccggttt
cccgaggtgcccgaggcggcgtgccagctggtgtccctggagggcctgagcctctaccac
aattgcctgagatgcctgaacccagccttggggaatctcacagccctcacctacctcaac
ctcagccgaaaccagctgtcgctgctgccaccctacatctgccagctgcccctgagggtc
ctcatcgtcagcaacaacaagctgggagccctgccccctgacatcggcaccctgggaagc
ctgcgacagcttgacgtgagcagcaacgagctccaatccctgccctcggaactgtgtggc
ctctcttccctgcgggacctcaatgtccggaggaaccagctcagtacgctgcccgaagag
ctgggggacctccctctggtccgcctggatttctcctgtaaccgcgtctcccgaatccca
gtctccttctgccgcctgaggcacctgcaggtcattctgctggacagcaaccctctgcag
agtccacctgcccaggtctgcctgaaggggaaacttcacatcttcaagtatttgtccaca
gaggccgggcagcgtgggtcggccctgggggacctggccccttctcggcccccgagtttc
agtccctgccctgcagaggatctatttccgggacatcggtacgatggtgggctggactca
ggcttccacagcgttgatagtggcagcaagaggtggtctggaaatgagtcaacagatgaa
ttttcagagctgtcattccggatctcagagctggcccgggagccccggggacccagagaa
cgcaaggaggatggctcagcggacggagaccctgtgcagattgacttcatcgacagccat
gtccccggggaggatgaagagcgaggcactgtggaggagcagcgaccacccgaattaagc
cctggggcaggggacagggagagggcaccaagcagcaggcgggaggagccggcaggggag
gagcggcggcgcccggacaccttgcagctgtggcaggagcgggaacggcggcagcagcag
cagagcggggcgtggggggccccgaggaaggatagcctcttgaagccagggctcagggct
gttgtgggaggggccgccgccgtgtccactcaagccatgcacaacggctcgcctaagtcc
agtgcctcccaagcaggggctgcagcggggcagggagcccccgcccctgcccctgcctcc
caagagccccttcccatagctggaccagcgacagcacctgctccacggccacttggctcc
attcagagaccaaacagcttcctcttccgttcctcctctcagagtggctcaggcccttcc
tcaccagactctgtcctgagacctcggcggtacccccaggttccagatgagaaggactta
atgactcagctgcgccaggtccttgagtcccggctgcagcggcccctgcctgaggacctg
gccgaggctctggccagtggggtcatcctgtgccagctggccaaccagctacggccgcgc
tccgtgcccttcatccatgtgccctcccctgctgtgccaaaactcagtgccctcaaggct
cggaagaatgtggagagttttctagaagcctgtcgaaaaatgggggtgcctgaggctgac
ctgtgctcgccctcggatctcctccagggcactgcccgggggctgcggaccgcgctggag
gccgtgaagcgggtggggggcaaggccctaccgcccctctggcccccctctggtctgggc
ggcttcgtcgtcttctacgtggtcctcatgctgctgctctatgtcacctacactcggctc
ctgggttcctag
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