AutismKB 2.0

Annotation Detail for SLC38A5


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Basic Information Top
Gene Symbol:SLC38A5 ( JM24,SN2,SNAT5,pp7194 )
Gene Full Name: solute carrier family 38, member 5
Band: Xp11.23
Quick LinksEntrez ID:92745; OMIM: 300649; Uniprot ID:S38A5_HUMAN; ENSEMBL ID: ENSG00000017483; HGNC ID: 18070
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
226N-linked (GlcNAc...) (Potential).
Location(AA) Modifications Resource
No data
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_033518
  • Location:chrX 48201871-48213508
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 48215912 48216218 306 2557
H3ac HepG2E 48214034 48215228 1194 1123
TAF k562GSE8489 48214186 48215228 1042 1199
TFAP2C MCF7GSE21234 48214931 48215295 364 1605
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 48186255 48186511 256 15489
CTCF G2GSE9613 48190993 48191137 144 10807
Myc K562GSE19551 48195070 48195403 333 6635
NRSF mAbJurkat 48185392 48186511 1119 15920
RUNX JurkatGSE17954 48199107 48199181 74 2728
hScc1 G2GSE9613 48201708 48201923 215 56
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 48212839 48212969 130 0
CTCF CD4SISSRdata 48212839 48212969 130 0
CTCF G2GSE9613 48201708 48202063 355 0
CTCF G2GSE9613 48203810 48205229 1419 0
CTCF G2GSE9613 48208276 48210861 2585 0
CTCF G2GSE9613 48211577 48211932 355 0
CTCF G2GSE9613 48212535 48214371 1836 0
H3ac HepG2E 48210550 48211714 1164 0
H3ac HepG2E 48212005 48213560 1555 0
NRSF mAbJurkat 48207404 48207799 395 0
Oct1 H2O2-HelaGSE14283 48210660 48210706 46 0
Oct1 HelaGSE14283 48210658 48210708 50 0
RARA MCF7GSE15244 48207261 48207799 538 0
TAF k562GSE8489 48207261 48207799 538 0
TAF k562GSE8489 48212869 48213314 445 0
TFAP2C MCF7GSE21234 48201738 48202131 393 0
hScc1 BcellGSE12603 48211577 48211932 355 0
hScc1 G2GSE9613 48203670 48204130 460 0
hScc1 G2GSE9613 48204468 48205229 761 0
hScc1 G2GSE9613 48208276 48208858 582 0
hScc1 G2GSE9613 48212498 48213622 1124 0
Validated miRNA targets Top
Micro RNA Name Stem Loop Name The chromosome that miRNA located Publication
hsa-let-7b hsa-let-7b 22 18668040
hsa-let-7b* hsa-let-7b 22 18668040
hsa-miR-1 hsa-mir-1-2 18 18668040
hsa-miR-1 hsa-mir-1-1 20 18668040
hsa-miR-155 hsa-mir-155 21 18668040
hsa-miR-155* hsa-mir-155 21 18668040
hsa-miR-16 hsa-mir-16-1 13 18668040
hsa-miR-16 hsa-mir-16-2 3 18668040
hsa-miR-30a hsa-mir-30a 6 18668040
hsa-miR-30a* hsa-mir-30a 6 18668040
hsa-miR-30b hsa-mir-30b 8 18668040
hsa-miR-30b* hsa-mir-30b 8 18668040
hsa-miR-30c hsa-mir-30c-2 6 18668040
hsa-miR-30c hsa-mir-30c-1 1 18668040
hsa-miR-30c-1* hsa-mir-30c-1 1 18668040
hsa-miR-30c-2* hsa-mir-30c-2 6 18668040
hsa-miR-30d hsa-mir-30d 8 18668040
hsa-miR-30d* hsa-mir-30d 8 18668040
hsa-miR-30e hsa-mir-30e 1 18668040
hsa-miR-30e* hsa-mir-30e 1 18668040
ID in Tarbase Data Type Support Type miRNA Gene Direct Support Publication
1099 Unknown pSILAC miR-16 SLC38A5 down 50-25% 18668040
Ensembl Protein Type Differentially expressed in Pathology or Event Mis Regulation Gene Expression Tumour Involvement
ENSG00000017483 n_a n_a n_a muscle cell "benign tumour, malignant tumour"
Cis-Nats regulation Top

Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018