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6322 SCML1

6322

SCML1

Scm polycomb group protein like 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition Scm polycomb group protein like 1

研究结论

Date Results Publications
2018-06-02 11:47:00 Here, we report a microdeletion of 170,6 Kb at Xp22.13 (17.733.948-17.904.576) (GRCh37/hg19).The microdeletion harbors the NHS, SCLML1, and RAI2 genes and results in a phenotype consistent with Nance-Horan syndromesyndrome and developmental delay 28464487
2010-01-21 00:00:00 the molecular evolutionary pattern of SCML1 in diverse primate species showed a strong signature of adaptive evolution which is caused by Darwinian positive selection 18601738

名称对应

Type IDs
Gene
UniProtKB-ID: SCML1_HUMAN, A0A024RBZ7_HUMAN, A0A024RBY0_HUMAN
UniprotKB: Q9UN30, A0A024RBZ7, A0A024RBY0
UniParc: UPI000021244E, UPI0000418AC0, UPI00000437E7
EMBL: AK313993, BC105028, AF160728, EU370780, CH471074, Z93242, BC026159
Ensembl: ENSG00000047634
KO: hsa:6322
Nucleutide sequences
EMBL-CDS: AAH26159.2, AAI05029.1, BAG36705.1, EAW98929.1, ABY68575.1, AAD47635.1, EAW98930.1, EAW98931.1, EAW98932.1
Gene_ORFName: hCG_19296, hCG_19296
Ensembl_TRS: ENST00000380041, ENST00000380043, ENST00000398080, ENST00000380045
Protein sequencees
Ensembl_PRO: ENSP00000369380, ENSP00000381154, ENSP00000369382, ENSP00000369384
RefSeq: XP_005274635.1, NP_006737.2, XP_006724572.1, NP_001032625.1, NP_001032624.1, XP_016885212.1, NP_001032629.1, XP_011543866.1, XP_006724571.1, XP_005274636.1
Others
UniRef100: UniRef100_Q9UN30, UniRef100_A0A024RBZ7, UniRef100_A0A024RBY0
UniRef90: UniRef90_Q9UN30
UniRef50: UniRef50_Q9UN30
UniGene: Hs.109655
CCDS: CCDS35211.1, CCDS35210.1, CCDS14182.2

全选

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