• THAT   AND
  • THAT   AND


Sequence in raw or FASTA format:

Database:

Blast Method:

 
 


SALL4 spalt-like transcription factor 4 [Homo sapiens (human)]


Clone ID RefSeq Accession Definition Vector Stock Status *Turnaround time Price Order
OHu18258 NM_020436 Homo sapiens spalt-like transcription factor 4 (SALL4), mRNA. pcDNA3.1+-DYK On-demand 25 $1699.00
OHu53056 XM_005260467 PREDICTED: Homo sapiens spalt-like transcription factor 4 (SALL4), transcript variant X1, mRNA. pcDNA3.1+-DYK On-demand 12-14 $279.00
OHu53056 XM_006723834 PREDICTED: Homo sapiens spalt-like transcription factor 4 (SALL4), transcript variant X2, mRNA. pcDNA3.1+-DYK On-demand 12-14 $279.00
OHu53056 XM_006723835 PREDICTED: Homo sapiens spalt-like transcription factor 4 (SALL4), transcript variant X3, mRNA. pcDNA3.1+-DYK On-demand 12-14 $279.00
OHu18258C NM_020436 Homo sapiens spalt-like transcription factor 4 (SALL4), mRNA. Customized vector On-demand 25 $1699.00
OHu53056C XM_005260467 PREDICTED: Homo sapiens spalt-like transcription factor 4 (SALL4), transcript variant X1, mRNA. Customized vector On-demand 12-14 $329.00
OHu53056C XM_006723834 PREDICTED: Homo sapiens spalt-like transcription factor 4 (SALL4), transcript variant X2, mRNA. Customized vector On-demand 12-14 $329.00
OHu53056C XM_006723835 PREDICTED: Homo sapiens spalt-like transcription factor 4 (SALL4), transcript variant X3, mRNA. Customized vector On-demand 12-14 $329.00

*Business Day

Related Services

Gene Symbol SALL4
Entrez Gene ID 57167
Full Name spalt-like transcription factor 4
Synonyms DRRS, HSAL4, ZNF797, dJ1112F19.1
General protein information
Preferred Names
sal-like protein 4
Names
sal-like protein 4
zinc finger protein 797
zinc finger protein SALL4
Gene Type protein-coding
Organism Homo sapiens (human)
Genome

20

20q13.2

Summary The protein encoded by this gene may be a zinc finger transcription factor. Defects in this gene are a cause of Duane-radial ray syndrome (DRRS). [provided by RefSeq, Jul 2008].
Disorder

MIM: 607343

Duane-radial ray syndrome, 607323 (3); IVIC syndrome, 147750 (3)

mRNA Protein Product Sequence Price Select
NM_020436, 187173293 NP_065169, 10047144 sal-like protein 4 ORF Sequence $1500.00
XM_005260467, 530418219 XP_005260524, 530418220 sal-like protein 4 isoform X1 ORF Sequence $750.00
XM_006723834, 578836086 XP_006723897, 578836087 sal-like protein 4 isoform X2 ORF Sequence $750.00
XM_006723835, 578836088 XP_006723898, 578836089 sal-like protein 4 isoform X3 ORF Sequence $750.00
Pathway Interaction Database
wnt_beta_catenin_pathwayRegulation of Wnt-mediated beta catenin signaling and target gene transcription
Reactome
REACT_111045Developmental Biology
REACT_200812Transcriptional regulation of pluripotent stem cells
Homo sapiens (human)SALL4NP_065169.1
Pan troglodytes (chimpanzee)SALL4XP_514728.2
Macaca mulatta (Rhesus monkey)SALL4XP_001093669.1
Canis lupus familiaris (dog)SALL4XP_543055.2
Bos taurus (cattle)SALL4NP_001179765.1
Mus musculus (house mouse)Sall4NP_780512.2
Rattus norvegicus (Norway rat)Sall4XP_003749680.1
Gallus gallus (chicken)SALL4NP_001074341.1
Danio rerio (zebrafish)sall4NP_001074078.1
Xenopus (Silurana) tropicalis (western clawed frog)sall4NP_001001458.1
Process
IDNameEvidence
GO:0000122negative regulation of transcription from RNA polymerase II promoterIEA
GO:0001833inner cell mass cell proliferationIEA
GO:0001843neural tube closureIEA
GO:0003281ventricular septum developmentIEA
GO:0006351transcription, DNA-templatedIEA
GO:0019827stem cell maintenanceIEA
GO:0030326embryonic limb morphogenesisIEA
GO:0045944positive regulation of transcription from RNA polymerase II promoterIEA
Component
IDNameEvidence
GO:0000792heterochromatinIEA
GO:0005634nucleusIEA
GO:0005737cytoplasmIEA
GO:0043234protein complexIEA
Function
IDNameEvidence
GO:0003677DNA bindingIEA
GO:0046872metal ion bindingIEA
GeneCards SALL4
UniProt Q9UJQ4
Vega OTTHUMG00000032752
MIM 607343
Ensembl ENSG00000101115
HGNC 15924
HPRD 08458

GeneRIFs: Gene References Into Functions What's a GeneRIF?

Interactant

Our customer service representatives are available 24 hours a day, Monday through Friday; please contact us anytime for assistance.