AutismKB 2.0

Annotation Detail for GHRL


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Basic Information Top
Gene Symbol:GHRL ( MTLRP )
Gene Full Name: ghrelin/obestatin prepropeptide
Band: 3p25.3
Quick LinksEntrez ID:51738; OMIM: 605353; Uniprot ID:GHRL_HUMAN; ENSEMBL ID: ENSG00000157017; HGNC ID: 18129
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
98Leucine amide (By similarity).
Location(AA) Modifications Resource
26O-decanoyl serine; alternate.Swiss-Prot 53.0
26O-octanoyl serine; alternate.Swiss-Prot 53.0
98Leucine amide (G-99 provides amide group)(By similarity).Swiss-Prot 53.0
Location(AA) Modification Resource
26Phosphoserine(IKK)HMM predict
29Phosphoserine(CDK)HMM predict
41Phosphoserine(PKG)HMM predict
91Phosphotyrosine(Abl)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_016362
  • Location:chr3 10302433-10307408
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
NFkBII GM12878GSE19485 10308836 10310652 1816 2336
NFkBII GM12892GSE19485 10308829 10310326 1497 2169
NFkBII GM15510GSE19485 10308983 10310277 1294 2222
NFkBII GM18526GSE19485 10309019 10310311 1292 2257
hScc1 BcellGSE12603 10309355 10309610 255 2074
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 10303681 10303923 242 0
CTCF CD4SISSRdata 10303681 10303923 242 0
CTCF G2GSE9613 10303317 10303908 591 0
Nanog hESGSE18292 10303686 10304082 396 0
Oct1 HelaGSE14283 10305041 10305072 31 0
RARA MCF7GSE15244 10302877 10303353 476 0
Validated miRNA targets Top
Cis-Nats regulation Top
Cluster ID Plue Type Plus Gene Name Plus Chromosome Plus Start Plus End Overlap Length Minus Type Minus Gene Name Minus Chromosome Minus Star Minus End Type
17757 EST chr3 10302471 10309328 66 mRNA GHRL chr3 10302433 10307409Sense/Antisense (SA) pairs

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