Homo sapiens (human): 105371045
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Entry
105371045 CDS
T01001
Symbol
PERCC1, DIAR11, ICR, gs104
Name
(RefSeq) proline and glutamate rich with coiled coil 1
Organism
hsa
Homo sapiens (human)
Disease
H01174
Congenital diarrhea
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TEADIR3
Motif
Other DBs
NCBI-GeneID:
105371045
NCBI-ProteinID:
NP_001352239
OMIM:
618656
HGNC:
52293
Ensembl:
ENSG00000284395
UniProt:
A0A1W2PR82
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All DBs
Position
16:1431078..1434441
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AA seq
267 aa
AA seq
DB search
MAAGVIRPLCDFQLPLLRHHPFLPSDPEPPETSEEEEEEEEEEEEEEGEGEGLGGCGRIL
PSSGRAEATEEAAPEGPGSPETPLQLLRFSELISDDIRRYFGRKDKGQDPDACDVYADSR
PPRSTARELYYADLVRLARGGSLEDEDTPEPRVPQGQVCRPGLSGDRAQPLGPLAELFDY
GLQQYWGSRAAAGWSLTLERKYGHITPMAQRKLPPSFWKEPTPSPLGLLHPGTPDFSDLL
ASWSTEACPELPGRGTPALEGARPAEA
NT seq
804 nt
NT seq
+upstream
nt +downstream
nt
atggccgccggtgtgatccggcccctgtgcgacttccagctgcccctgctgcgccaccac
cccttcctgccctcagatccggagcccccagagacttcggaggaggaagaggaggaggag
gaggaggaggaggaggaggagggcgagggcgaggggctggggggctgcggccggatcctc
ccgagctcaggccgggcagaggccacggaggaagcagcccccgagggtcccggcagcccc
gagaccccgctgcagctgctacgcttttcagagctcatcagcgacgacatccggcggtac
tttggccgcaaggataaggggcaggacccagatgcctgcgacgtctacgccgacagccgc
ccaccccgcagcactgcccgggagctctactatgcggacctggtgcgcctggcccgtggc
gggtccctggaggacgaggacaccccggagcccagggtaccccaagggcaggtgtgcagg
ccgggcctcagcggggacagggcgcagcccctgggacccctggccgagctcttcgactac
gggctgcagcagtactgggggtccagggcagcggccggctggagcctgacgctggagcgg
aagtacggccacatcacccccatggcccagaggaagctgcccccatccttctggaaggag
ccgacccctagccccctgggcctgctgcaccctggcacgccggacttcagcgacctgctg
gccagctggtcaaccgaggcctgtcctgagctgcccggcaggggaaccccagccctggaa
ggggcacggccagccgaggcctag
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