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144347 RFLNA

144347

RFLNA

refilin A

protein-coding

Homo sapiens

基因描述

Type Description
Definition refilin A

研究结论

Date Results Publications
2019-04-20 11:23:00 The present study implies that RFLNA is an additional causative gene for spondylocarpotarsal synostosis syndrome in humans and a defect in forming actin bundles and perinuclear actin caps may be a critical mechanism for the development of spondylocarpotarsal synostosis syndrome. 30796325
2013-06-29 12:07:00 The candidate marker CORO2A rs1985859 and the putative marker FAM101A rs7955740 may be of value for the prediction of radiosensitivity to preoperative colorectal tumors. 23490283

名称对应

Type IDs
Synonymous CFM2, FAM101A
Gene
UniProtKB-ID: RFLA_HUMAN
UniprotKB: Q6ZTI6
UniParc: UPI00001FB96E, UPI000022912B
EMBL: BC141805, AK126577, AC073916
Ensembl: ENSG00000178882
KO: hsa:144347, hsa:100533183
Nucleutide sequences
EMBL-CDS: BAC86601.1, AAI41806.1
Ensembl_TRS: ENST00000546355, ENST00000324038, ENST00000338359, ENST00000389727
Protein sequencees
Ensembl_PRO: ENSP00000315626, ENSP00000374377, ENSP00000444080, ENSP00000345898
RefSeq: NP_001352085.1, NP_859060.3
Others
UniRef100: UniRef100_Q6ZTI6
UniRef90: UniRef90_Q6ZTI6
UniRef50: UniRef50_Q7TS73
UniGene: Hs.432901
CCDS: CCDS9258.1

全选

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研究热度

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