AutismKB 2.0

Annotation Detail for FAM89B


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Basic Information Top
Gene Symbol:FAM89B ( MTVR1 )
Gene Full Name: family with sequence similarity 89, member B
Band: 11q13.1
Quick LinksEntrez ID:23625; OMIM: NA; Uniprot ID:FA89B_HUMAN; ENSEMBL ID: ENSG00000176973; HGNC ID: 16708
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
32N-linkedHMM predict
123Phosphoserine(CK1)HMM predict
124Phosphoserine(CK1)HMM predict
127Phosphoserine(CK1)HMM predict
138Phosphoserine(CK2)HMM predict
138Phosphoserine(CK2)HMM predict
147O-linkedHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_152832
  • Location:chr11 65096395-65098236
  • strand:+
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
ER MCF7GSE19013 65098979 65099801 822 1154
FOXA1 MCF7GSE15244 65098935 65099859 924 1161
H3ac HepG2E 65099150 65099622 472 1150
H3ac HepG2E 65100608 65101098 490 2617
H3ac HepG2E 65106730 65107241 511 8749
NRSF pAbJurkat 65099859 65100509 650 1948
NRSF pAbJurkat 65101504 65102486 982 3759
RARA MCF7GSE15244 65099079 65099683 604 1145
RARG MCF7GSE15244 65099005 65099859 854 1196
Rb GrowingGSE19898 65098169 65098605 436 151
Rb QuiescentGSE19898 65098078 65098500 422 53
Rb SenescentGSE19898 65098429 65098607 178 282
TFAP2C MCF7GSE21234 65098251 65099995 1744 887
VDR GM10861-stimGSE22484 65095947 65101695 5748 585
hScc1 BcellGSE12603 65098047 65100281 2234 928
hScc1 CdLSGSE12603 65098093 65099114 1021 367
p130 shRbSenescentGSE19898 65098156 65098468 312 76
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
hScc1 BcellGSE12603 65095946 65096945 999 0
hScc1 BcellGSE12603 65097360 65097789 429 0
hScc1 G2GSE9613 65095874 65096981 1107 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