AutismKB 2.0

Annotation Detail for NINL


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Basic Information Top
Gene Symbol:NINL ( FLJ11792,KIAA0980,NLP,dJ691N24.1 )
Gene Full Name: ninein-like
Band: 20p11.21
Quick LinksEntrez ID:22981; OMIM: 609580; Uniprot ID:NINL_HUMAN; ENSEMBL ID: ENSG00000101004; HGNC ID: 29163
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
497KEN box.
641D-box.
Location(AA) Modifications Resource
No data
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_025176
  • Location:chr20 25381337-25514152
  • strand:-
No data
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 25398707 25398946 239 0
CTCF CD4SISSRdata 25398707 25398946 239 0
CTCF G2GSE9613 25398539 25399143 604 0
CTCF G2GSE9613 25423716 25424223 507 0
ER MCF7GSE19013 25436711 25437363 652 0
Fos K562GSE19551 25471791 25472730 939 0
H3ac HepG2E 25467898 25469234 1336 0
H3ac HepG2E 25477015 25477649 634 0
H3ac HepG2E 25507642 25507844 202 0
H3ac HepG2E 25513163 25513584 421 0
Myc K562GSE19551 25491114 25491278 164 0
Myc hESGSE17917 25513715 25514069 354 0
Oct4 ESGSE20650 25418193 25418458 265 0
P300 T0-glioblastomaGSE21026 25454316 25455268 952 0
P300 T30-glioblastomaGSE21026 25436467 25437360 893 0
PHF8 293TGSE20725 25513532 25514398 866 0
PHF8 HeLaGSE20725 25513232 25514555 1323 0
PHF8 Hs68minusFBSGSE20725 25513220 25514333 1113 0
RARA MCF7GSE15244 25478104 25478702 598 0
Rb GrowingGSE19898 25454662 25454761 99 0
Rb GrowingGSE19898 25513423 25513680 257 0
STAT1 IFNSISSRdata 25502972 25503490 518 0
TFAP2C MCF7GSE21234 25425350 25426372 1022 0
TFAP2C MCF7GSE21234 25497933 25498558 625 0
USF1 HepG2E 25467573 25468460 887 0
USF1 HepG2E 25507642 25508128 486 0
USF1 HepG2E 25513163 25513514 351 0
USF2 HepG2E 25513163 25513514 351 0
hScc1 BcellGSE12603 25386658 25387018 360 0
hScc1 BcellGSE12603 25388118 25389106 988 0
hScc1 BcellGSE12603 25389374 25389980 606 0
hScc1 BcellGSE12603 25393141 25393544 403 0
hScc1 BcellGSE12603 25397326 25398120 794 0
hScc1 BcellGSE12603 25398466 25399179 713 0
hScc1 BcellGSE12603 25404969 25406095 1126 0
hScc1 BcellGSE12603 25422651 25423096 445 0
hScc1 BcellGSE12603 25423716 25424259 543 0
hScc1 BcellGSE12603 25424928 25425365 437 0
hScc1 BcellGSE12603 25426252 25427232 980 0
hScc1 BcellGSE12603 25429727 25429970 243 0
hScc1 BcellGSE12603 25436688 25437123 435 0
hScc1 BcellGSE12603 25438775 25439077 302 0
hScc1 BcellGSE12603 25445683 25446068 385 0
hScc1 BcellGSE12603 25455193 25455364 171 0
hScc1 BcellGSE12603 25476679 25477649 970 0
hScc1 BcellGSE12603 25508092 25508343 251 0
hScc1 BcellGSE12603 25513623 25514529 906 0
hScc1 CdLSGSE12603 25398539 25399251 712 0
p130 SenescentGSE19898 25513262 25513846 584 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
16216 mRNA chr20 25461662 25462148 486 mRNA KIAA0980 chr20 25381337 25514153 Non-exonic Bidirectional (NOB) 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


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