AutismKB 2.0

Annotation Detail for MYLIP


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Basic Information Top
Gene Symbol:MYLIP ( IDOL,MIR )
Gene Full Name: myosin regulatory light chain interacting protein
Band: 6p22.3
Quick LinksEntrez ID:29116; OMIM: 610082; Uniprot ID:MYLIP_HUMAN; ENSEMBL ID: ENSG00000007944; HGNC ID: 21155
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
138SulfotyrosineHMM predict
238Phosphotyrosine(Syk)HMM predict
343N-linkedHMM predict
349Phosphoserine(CDC2)HMM predict
349Phosphoserine(CDK)HMM predict
349PhosphoserineHMM predict
354Phosphoserine(IKK)HMM predict
359N-linkedHMM predict
396N-linkedHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_013262
  • Location:chr6 16237295-16256454
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Fos K562GSE19551 16236762 16237705 943 62
Gata2 K562GSE18868 16217104 16218274 1170 19607
TAFII hESGSE17917 16236842 16237507 665 121
TFAP2C MCF7GSE21234 16236675 16237158 483 379
hScc1 BcellGSE12603 16236890 16237290 400 206
hScc1 CdLSGSE12603 16236890 16237163 273 269
hScc1 G2GSE9613 16236890 16237485 595 108
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Myc K562GSE19551 16265742 16266580 838 9707
TFAP2C MCF7GSE21234 16256829 16257076 247 498
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 16236890 16238222 1332 0
CTCF G2GSE9613 16253194 16253482 288 0
H3K4me2 HCT116GSE10453 16238151 16238996 845 0
H3K4me3 colorectalcancer 16238012 16239070 1058 0
H3ac HepG2E 16238115 16239070 955 0
Myc hESGSE17917 16237553 16237934 381 0
P300 T30-glioblastomaGSE21026 16244643 16246085 1442 0
Pol2 GM12878GSE19551 16236863 16237756 893 0
RARA MCF7GSE15244 16238222 16239442 1220 0
RARG MCF7GSE15244 16238115 16239270 1155 0
TAF HelaGSE8489 16238187 16238889 702 0
TAF k562GSE8489 16238115 16239745 1630 0
Validated miRNA targets Top
Micro RNA Name Stem Loop Name The chromosome that miRNA located Publication
hsa-miR-106a hsa-mir-106a X 17575136
hsa-miR-106a* hsa-mir-106a X 17575136
hsa-miR-17 hsa-mir-17 13 17575136
hsa-miR-17* hsa-mir-17 13 17575136
hsa-miR-181b hsa-mir-181b-1 1 20347265
hsa-miR-181b hsa-mir-181b-2 9 20347265
hsa-miR-198 hsa-mir-198 0 20347265
hsa-miR-19a hsa-mir-19a 13 17575136
hsa-miR-19a* hsa-mir-19a 13 17575136
hsa-miR-19b hsa-mir-19b-2 X 17575136
hsa-miR-19b hsa-mir-19b-1 13 17575136
hsa-miR-19b-1* hsa-mir-19b-1 13 17575136
hsa-miR-19b-2* hsa-mir-19b-2 X 17575136
hsa-miR-206 hsa-mir-206 6 20347265
hsa-miR-20b hsa-mir-20b X 17575136
hsa-miR-20b* hsa-mir-20b X 17575136
hsa-miR-24 hsa-mir-24-1 9 20347265
hsa-miR-24 hsa-mir-24-2 19 20347265
hsa-miR-24-1* hsa-mir-24-1 9 20347265
hsa-miR-24-2* hsa-mir-24-2 19 20347265
hsa-miR-26b hsa-mir-26b 2 20347265
hsa-miR-26b* hsa-mir-26b 2 20347265
hsa-miR-30b hsa-mir-30b 8 20347265
hsa-miR-30b* hsa-mir-30b 8 20347265
hsa-miR-30e hsa-mir-30e 1 20347265
hsa-miR-30e* hsa-mir-30e 1 20347265
hsa-miR-92a hsa-mir-92a-1 13 20347265
hsa-miR-92a hsa-mir-92a-2 X 20347265
hsa-miR-92a hsa-mir-92a-1 13 17575136
hsa-miR-92a hsa-mir-92a-2 X 17575136
hsa-miR-92a-1* hsa-mir-92a-1 13 20347265
hsa-miR-92a-2* hsa-mir-92a-2 X 20347265
ID in Tarbase Data Type Support Type miRNA Gene Direct Support Publication
229 Unknown TRUE miR-106a MYLIP n_a 17575136
512 Unknown TRUE miR-19b-2 MYLIP n_a 17575136
529 Unknown TRUE miR-20b MYLIP n_a 17575136
713 Unknown TRUE miR-92-2 MYLIP n_a 17575136
Ensembl Protein Type Differentially expressed in Pathology or Event Mis Regulation Gene Expression Tumour Involvement
ENSG00000007944 n_a n_a n_a "epithelium, lymphocyte, muscle cell, macrophage" "benign tumour, malignant tumour, carcinoma, leukaemia, sarcoma"
ENSG00000007944 n_a n_a n_a "epithelium, lymphocyte, muscle cell, macrophage" "benign tumour, malignant tumour, carcinoma, leukaemia, sarcoma"
ENSG00000007944 mesenchymal-epithelial transition (MET) n_a n_a "epithelium, lymphocyte, muscle cell, macrophage" "benign tumour, malignant tumour, carcinoma, leukaemia, sarcoma"
ENSG00000007944 n_a n_a n_a "epithelium, lymphocyte, muscle cell, macrophage" "benign tumour, malignant tumour, carcinoma, leukaemia, sarcoma"
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


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