AutismKB 2.0

Annotation Detail for TRPM8


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Basic Information Top
Gene Symbol:TRPM8 ( LTRPC6,MGC2849,TRPP8 )
Gene Full Name: transient receptor potential cation channel, subfamily M, member 8
Band: 2q37.1
Quick LinksEntrez ID:79054; OMIM: 606678; Uniprot ID:TRPM8_HUMAN; ENSEMBL ID: ENSG00000144481; HGNC ID: 17961
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
15N-linkedHMM predict
17Phosphothreonine(PKA)HMM predict
27Phosphoserine(CDK)HMM predict
27O-linkedHMM predict
31Phosphoserine(PKA)HMM predict
31Phosphoserine(IKK)HMM predict
37Phosphoserine(CK2)HMM predict
37Phosphoserine(CK1)HMM predict
75Phosphoserine(ATM)HMM predict
117Phosphotyrosine(INSR)HMM predict
186Phosphotyrosine(INSR)HMM predict
204PhosphoserineHMM predict
256N-linkedHMM predict
272Phosphothreonine(PKC)HMM predict
312Phosphothreonine(PKC)HMM predict
367Phosphoserine(PKG)HMM predict
455Phosphoserine(PKA)HMM predict
577Phosphoserine(CK1)HMM predict
621Phosphotyrosine(Syk)HMM predict
634Phosphoserine(CK2)HMM predict
635Phosphoserine(CK2)HMM predict
762Phosphoserine(IKK)HMM predict
821N-linkedHMM predict
934N-linkedHMM predict
1031S-palmitoylHMM predict
1032S-palmitoylHMM predict
1033S-palmitoylHMM predict
1050N-linkedHMM predict
1063Phosphotyrosine(Jak)HMM predict
1072N-linkedHMM predict
1074Phosphothreonine(CK2)HMM predict
1099IsoleucineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_024080
  • Location:chr2 234490781-234592903
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 234488148 234488715 567 2350
NRSF JurkatGSE13047 234485839 234487215 1376 4255
NRSF mAbJurkat 234480452 234482885 2433 9113
NRSF mAbJurkat 234483145 234488939 5794 4740
NRSF-mono JurkatQuESTdata 234485876 234487208 1332 4240
NRSF-poly JurkatQuESTdata 234485959 234487514 1555 4045
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Fos K562GSE19551 234596771 234597261 490 4113
P300 T30-glioblastomaGSE21026 234605626 234606421 795 13120
p130 SenescentGSE19898 234605973 234606321 348 13244
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CBP T30-glioblastomaGSE21026 234547416 234548806 1390 0
CTCF G2GSE9613 234498835 234499021 186 0
CTCF G2GSE9613 234502651 234503171 520 0
CTCF G2GSE9613 234525901 234526155 254 0
CTCF G2GSE9613 234539892 234540037 145 0
CTCF G2GSE9613 234550002 234550495 493 0
CTCF G2GSE9613 234566034 234566210 176 0
CTCF G2GSE9613 234575456 234575785 329 0
NRSF JurkatGSE13047 234550724 234551256 532 0
NRSF JurkatSISSRdata 234550823 234551123 300 0
NRSF mAbJurkat 234551115 234551742 627 0
NRSF-mono JurkatQuESTdata 234550729 234551255 526 0
NRSF-poly JurkatQuESTdata 234550774 234551246 472 0
Nanog hESGSE18292 234550076 234550432 356 0
P300 T30-glioblastomaGSE21026 234537756 234538652 896 0
P300 T30-glioblastomaGSE21026 234547556 234548839 1283 0
P300 T30-glioblastomaGSE21026 234555506 234556624 1118 0
P300 T30-glioblastomaGSE21026 234577193 234578353 1160 0
Rb SenescentGSE19898 234577651 234577929 278 0
STAT1 HeLaGSE12783 234547826 234548575 749 0
Sox2 hESGSE18292 234550189 234550459 270 0
TFAP2C MCF7GSE21234 234572560 234573036 476 0
hScc1 CdLSGSE12603 234549715 234550598 883 0
hScc1 G2GSE9613 234521968 234522101 133 0
hScc1 G2GSE9613 234550179 234551046 867 0
p130 SenescentGSE19898 234547207 234547619 412 0
p130 SenescentGSE19898 234547893 234548109 216 0
p130 SenescentGSE19898 234555717 234556098 381 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
15821 mRNA TRPM8 chr2 234608042 234710165 119 EST chr2 234636789 234646079Sense/Antisense (SA) 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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