Details for: KCNQ4
Associated with
Other Information
Genular Protein ID: 2485744241
Symbol: KCNQ4_HUMAN
Name: Potassium voltage-gated channel subfamily KQT member 4
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 10025409
Title: KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness.
PubMed ID: 10025409
PubMed ID: 16710414
Title: The DNA sequence and biological annotation of human chromosome 1.
PubMed ID: 16710414
DOI: 10.1038/nature04727
PubMed ID: 10713961
Title: Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors.
PubMed ID: 10713961
PubMed ID: 11245603
Title: KCNQ4 channels expressed in mammalian cells: functional characteristics and pharmacology.
PubMed ID: 11245603
PubMed ID: 23431407
Title: Distinct roles of molecular chaperones HSP90alpha and HSP90beta in the biogenesis of KCNQ4 channels.
PubMed ID: 23431407
PubMed ID: 29358396
Title: Centipedes subdue giant prey by blocking KCNQ channels.
PubMed ID: 29358396
PubMed ID: 17329207
Title: Structural insight into KCNQ (Kv7) channel assembly and channelopathy.
PubMed ID: 17329207
PubMed ID: 10369879
Title: Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
PubMed ID: 10369879
DOI: 10.1093/hmg/8.7.1321
PubMed ID: 10571947
Title: Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.
PubMed ID: 10571947
DOI: 10.1002/(sici)1098-1004(199912)14:6<493::aid-humu8>3.0.co;2-p
PubMed ID: 10925378
Title: Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.
PubMed ID: 10925378
DOI: 10.1002/1096-8628(20000731)93:3<184::aid-ajmg4>3.0.co;2-5
PubMed ID: 21242547
Title: Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 gene.
PubMed ID: 21242547
Sequence Information:
- Length: 695
- Mass: 77101
- Checksum: 51390F5E00E8C157
- Sequence:
MAEAPPRRLG LGPPPGDAPR AELVALTAVQ SEQGEAGGGG SPRRLGLLGS PLPPGAPLPG PGSGSGSACG QRSSAAHKRY RRLQNWVYNV LERPRGWAFV YHVFIFLLVF SCLVLSVLST IQEHQELANE CLLILEFVMI VVFGLEYIVR VWSAGCCCRY RGWQGRFRFA RKPFCVIDFI VFVASVAVIA AGTQGNIFAT SALRSMRFLQ ILRMVRMDRR GGTWKLLGSV VYAHSKELIT AWYIGFLVLI FASFLVYLAE KDANSDFSSY ADSLWWGTIT LTTIGYGDKT PHTWLGRVLA AGFALLGISF FALPAGILGS GFALKVQEQH RQKHFEKRRM PAANLIQAAW RLYSTDMSRA YLTATWYYYD SILPSFRELA LLFEHVQRAR NGGLRPLEVR RAPVPDGAPS RYPPVATCHR PGSTSFCPGE SSRMGIKDRI RMGSSQRRTG PSKQHLAPPT MPTSPSSEQV GEATSPTKVQ KSWSFNDRTR FRASLRLKPR TSAEDAPSEE VAEEKSYQCE LTVDDIMPAV KTVIRSIRIL KFLVAKRKFK ETLRPYDVKD VIEQYSAGHL DMLGRIKSLQ TRVDQIVGRG PGDRKAREKG DKGPSDAEVV DEISMMGRVV KVEKQVQSIE HKLDLLLGFY SRCLRSGTSA SLGAVQVPLF DPDITSDYHS PVDHEDISVS AQTLSISRSV STNMD
Genular Protein ID: 1964407486
Symbol: B3KQH8_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Sequence Information:
- Length: 356
- Mass: 39774
- Checksum: D4E9C75A25EAD9E3
- Sequence:
MPAANLIQAA WRLYSTDMSR AYLTATWYYY DSILPSFREL ALLFEHVQRA RNGGLRPLEV RRAPVPDGAP SRYPPVATCH RPGSTSFCPG ESSRMGIKDR IRMGSSQRRT GPSKQHLAPP TMPTSPSSEQ VGEATSPTKV QKSWSFNDRT RFRASLRLKP RTSAEDAPSE EVAEEKSYQC ELTVDDIMPA VKTVIRSIRI LKFLVAKRKF KETLRPYDVK DVIEQYSAGH LDMLGRIKSL QTRVDQIVGR GPGDRKTREK GDKGPSDAEV VDEISMMGRV VKVEKQVQSI EHKLDLLLGF YSRCLRSGTS ASLGAVQVPL FDPDITSDYH SPVDHEDISV SAQTLSISRS VSTNMD
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.