AutismKB 2.0

Annotation Detail for GALNT14


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:GALNT14 ( FLJ12691,FLJ13977,GALNT15,GalNac-T10,GalNac-T14 )
Gene Full Name: UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 14 (GalNAc-T14)
Band: 2p23.1
Quick LinksEntrez ID:79623; OMIM: 608225; Uniprot ID:GLT14_HUMAN; ENSEMBL ID: ENSG00000158089; HGNC ID: 22946
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
5Phosphothreonine(PKA)HMM predict
41Phosphothreonine(MAPK)HMM predict
74Phosphotyrosine(Syk)HMM predict
88Phosphoserine(CK1)HMM predict
136N-linkedHMM predict
138Phosphothreonine(MAPK)HMM predict
220Phosphotyrosine(EGFR)HMM predict
370Phosphotyrosine(Syk)HMM predict
544Phosphoserine(ATM)HMM predict
544Phosphoserine(CK1)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_024572
  • Location:chr2 30986837-31215074
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
H3K27me3 colorectalcancer 31215260 31216560 1300 836
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 31005659 31006053 394 0
CTCF G2GSE9613 31025651 31025796 145 0
CTCF G2GSE9613 31026842 31027335 493 0
CTCF G2GSE9613 31028062 31028426 364 0
CTCF G2GSE9613 31030436 31030695 259 0
CTCF G2GSE9613 31039421 31039643 222 0
CTCF G2GSE9613 31042474 31042684 210 0
CTCF G2GSE9613 31055425 31055791 366 0
CTCF G2GSE9613 31056151 31056769 618 0
CTCF G2GSE9613 31064711 31065030 319 0
CTCF G2GSE9613 31080542 31080841 299 0
CTCF G2GSE9613 31100593 31100763 170 0
CTCF G2GSE9613 31101715 31102040 325 0
CTCF G2GSE9613 31121315 31121811 496 0
CTCF G2GSE9613 31128969 31129326 357 0
CTCF G2GSE9613 31133803 31134053 250 0
CTCF G2GSE9613 31142896 31143290 394 0
CTCF G2GSE9613 31147950 31148514 564 0
CTCF G2GSE9613 31156099 31156386 287 0
CTCF G2GSE9613 31158464 31158716 252 0
CTCF G2GSE9613 31163864 31164111 247 0
CTCF G2GSE9613 31184354 31184690 336 0
CTCF G2GSE9613 31187515 31187702 187 0
CTCF G2GSE9613 31213640 31215104 1464 0
ER E2-MCF7GSE14664 31130658 31130694 36 0
ER Fulvestrant-MCF7GSE14664 31093155 31093198 43 0
ER Fulvestrant-MCF7GSE14664 31103884 31103920 36 0
ER Fulvestrant-MCF7GSE14664 31104052 31104085 33 0
ER Fulvestrant-MCF7GSE14664 31104329 31104372 43 0
ER MCF7GSE19013 31020428 31021058 630 0
FoxA1 MCF7MACSdata 31066138 31066402 264 0
H3K27me3 colorectalcancer 31212102 31213894 1792 0
NRSF JurkatGSE13047 31183806 31184569 763 0
NRSF mAbJurkat 31183196 31187155 3959 0
NRSF-mono JurkatQuESTdata 31183927 31184607 680 0
NRSF-poly JurkatQuESTdata 31183968 31184598 630 0
Nanog hESGSE18292 31014796 31014985 189 0
Oct1 H2O2-HelaGSE14283 31041432 31041459 27 0
Oct1 H2O2-HelaGSE14283 31047803 31047850 47 0
Oct1 H2O2-HelaGSE14283 31107562 31107590 28 0
Oct1 H2O2-HelaGSE14283 31130653 31130679 26 0
Oct1 HelaGSE14283 31047801 31047852 51 0
Oct1 HelaGSE14283 31107554 31107592 38 0
Oct1 HelaGSE14283 31187088 31187118 30 0
RNAII Tamoxifen-MCF7GSE14664 31214552 31214651 99 0
Rb QuiescentGSE19898 31116796 31116924 128 0
Rb SenescentGSE19898 31214362 31214590 228 0
Sox2 hESGSE18292 31014601 31015192 591 0
TFAP2C MCF7GSE21234 31032015 31032559 544 0
TFAP2C MCF7GSE21234 31066137 31066874 737 0
hScc1 BcellGSE12603 31125086 31125359 273 0
hScc1 BcellGSE12603 31143016 31143327 311 0
hScc1 BcellGSE12603 31213894 31214464 570 0
p63 keratinocytesGSE17611 31088500 31089366 866 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
14107 EST chr2 31121455 31125943 4488 mRNA GALNT14 chr2 31044984 31273222 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


Copyright © 2017, Center for Bioinformatics , Peking University | All Rights Reserved