Type | Description |
---|---|
Definition | orofacial cleft 1 candidate 1 |
Date | Results | Publications |
---|---|---|
2012-05-12 11:11:00 | Disruption of the Mrds1/Ofcc1 gene elicits asymptomatic hyper-gamma-glutamyl-transpeptidasemia in mice. | 22242126 |
2010-02-08 11:13:00 | Opo shows homology to human transcripts linked to a hereditary craniofacial malformation, orofacial cleft 1 (OFC1). The expression of mouse Opo in neural crest derivatives and skull elements further supports this link. | 19766735 |
Type | IDs |
---|---|
Synonymous | opo |
Gene |
UniProtKB-ID:
C3S7Q5_MOUSE
UniprotKB:
C3S7Q5
UniParc:
UPI00019DBC9C
EMBL:
AC155272,
AC154480,
AC123807,
EU683438
Ensembl:
ENSMUSG00000047094
KO:
mmu:218165
|
Nucleutide sequences |
EMBL-CDS:
ACG75917.1
Ensembl_TRS:
ENSMUST00000054635
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000062217
RefSeq:
XP_036013880.1,
NP_742155.2
|
Others |
UniRef100:
UniRef100_C3S7Q5
UniRef90:
UniRef90_C3S7Q5
UniRef50:
UniRef50_M3X7H2
UniGene:
Mm.364096
|
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Refseq |
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