AutismKB 2.0

Annotation Detail for NARF


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:NARF ( DKFZp434G0420,FLJ10067,IOP2 )
Gene Full Name: nuclear prelamin A recognition factor
Band: 17q25.3
Quick LinksEntrez ID:26502; OMIM: 605349; Uniprot ID:NARF_HUMAN; ENSEMBL ID: ENSG00000141562; HGNC ID: 29916
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
444Phosphoserine.
Location(AA) Modifications Resource
Location(AA) Modification Resource
17Phosphothreonine(CK2)HMM predict
147Phosphoserine(ATM)HMM predict
214N-linkedHMM predict
216Phosphoserine(ATM)HMM predict
216Phosphoserine(CDC2)HMM predict
320Phosphotyrosine(SRC)HMM predict
387Phosphothreonine(CDC2)HMM predict
387Phosphothreonine(MAPK)HMM predict
422SulfotyrosineHMM predict
431Phosphoserine(CDC2)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_001038618
  • Location:chr17 78009358-78039429
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
H3K4me2 HCT116GSE10453 78008958 78009207 249 276
H3ac HepG2E 78008958 78009314 356 223
Myc hESGSE17917 78009111 78009550 439 28
TAF k562GSE8489 78008958 78009141 183 309
TFAP2C MCF7GSE21234 78008978 78009448 470 146
USF1 HepG2E 78008958 78009430 472 165
USF2 HepG2E 78008958 78009386 428 187
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 78009279 78010189 910 0
ETS1 JurkatGSE17954 78008815 78010492 1677 0
Fos K562GSE19551 78009076 78010199 1123 0
HIF1 HypoHepG2 78008958 78009986 1028 0
PHF8 Hs68minusFBSGSE20725 78009003 78010027 1024 0
hScc1 BcellGSE12603 78009355 78009708 353 0
hScc1 CdLSGSE12603 78009242 78010268 1026 0
p130 QuiescentGSE19898 78009673 78010012 339 0
Validated miRNA targets Top
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