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246102 Rttn

246102

Rttn

rotatin

protein-coding

Mus musculus

基因描述

Type Description
Definition rotatin

研究结论

Date Results Publications
2010-01-21 00:00:00 cloning and characterization of rotatin 11900971
2010-01-21 00:00:00 No turning (nt), a recessive lethal mutation causing left-right and axial patterning defects is likely elicited by deficiency of Rttn on chromosome 18. 17551791

名称对应

Type IDs
Synonymous 4921538A15Rik, AI666264, C530033I08Rik, D230040K24
Gene
UniProtKB-ID: RTTN_MOUSE
UniprotKB: Q8R4Y8
UniParc: UPI00000EB015, UPI00000E9E38, UPI00001D8C4C, UPI00000E936F
EMBL: AK032605, AK052059, AK083016, BC049935, AF265232, BC023916
Ensembl: ENSMUSG00000023066
KO: mmu:246102
Nucleutide sequences
EMBL-CDS: BAC38732.1, AAH49935.1, BAC27946.1, AAM02906.1, AAH23916.1, BAC34842.1
Ensembl_TRS: ENSMUST00000023828
Protein sequencees
Ensembl_PRO: ENSMUSP00000023828
RefSeq: XP_036017043.1, XP_036017042.1, XP_011245382.1, XP_030106323.1, NP_780751.2
Others
UniRef100: UniRef100_Q8R4Y8
UniRef90: UniRef90_Q8R4Y8
UniRef50: UniRef50_Q86VV8
UniGene: Mm.772
CCDS: CCDS29390.1

全选

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