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GZF1 (GDNF inducible zinc finger protein 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
64412
Gene nameGene Name - the full gene name approved by the HGNC.
GDNF inducible zinc finger protein 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
GZF1
SynonymsGene synonyms aliases
JLSM, ZBTB23, ZNF336
ChromosomeChromosome number
20
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20p11.21
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1555786618 G>T Pathogenic Stop gained, non coding transcript variant, coding sequence variant
rs1555786729 ->A Pathogenic Non coding transcript variant, coding sequence variant, frameshift variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT005048 hsa-let-7b-5p Microarray 17699775
MIRT047985 hsa-miR-30c-5p CLASH 23622248
MIRT1039045 hsa-miR-124 CLIP-seq
MIRT1039046 hsa-miR-1244 CLIP-seq
MIRT1039047 hsa-miR-1257 CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 16049025
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IMP 16049025
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA 21873635
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA 16049025
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IMP 16049025
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q9H116
Protein name GDNF-inducible zinc finger protein 1 (Zinc finger and BTB domain-containing protein 23) (Zinc finger protein 336)
Protein function Transcriptional repressor that binds the GZF1 responsive element (GRE) (consensus: 5'-TGCGCN[TG][CA]TATA-3'). May be regulating VSX2/HOX10 expression.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00651 BTB
21 133
BTB/POZ domain
Domain
PF00096 zf-C2H2
348 371
Zinc finger, C2H2 type
Domain
PF13894 zf-C2H2_4
377 400
Domain
PF13912 zf-C2H2_6
406 431
Domain
PF00096 zf-C2H2
435 457
Zinc finger, C2H2 type
Domain
PF13912 zf-C2H2_6
463 488
Domain
PF00096 zf-C2H2
491 513
Zinc finger, C2H2 type
Domain
PF00096 zf-C2H2
519 541
Zinc finger, C2H2 type
Domain
PF13912 zf-C2H2_6
547 572
Domain
PF00096 zf-C2H2
575 597
Zinc finger, C2H2 type
Domain
Sequence
MESGAVLLESKSSPFNLLHEMHELRLLGHLCDVTVSVEYQGVRKDFMAHKAVLAATSKFF
KEVFLNEKSVDGTRTNVYLNEVQVADFASFLEFVYTAKVQVEEDRVQRMLEVAEKLKCLD
LSETCFQLKKQML
ESVLLELQNFSESQEVEVSSGSQVSAAPAPRASVATDGPHPSGLTDS
LDYPGERASNGMSSDLPPKKSKDKLDKKKEVVKPPYPKIRRASGRLAGRKVFVEIPKKKY
TRRLREQQKTAEGDVGDYRCPQDQSPDRVGTEMEQVSKNEGCQAGAELEELSKKAGPEEE
EEEEEEDEEGEKKKSNFKCSICEKAFLYEKSFLKHSKHRHGVATEVVYRCDTCGQTFANR
CNLKSHQRHVH
SSERHFPCELCGKKFKRKKDVKRHVLQVHEGGGERHRCGQCGKGLSSKT
ALRLHERTHTG
DRPYGCTECGARFSQPSALKTHMRIHTGEKPFVCDECGARFTQNHMLIY
HKRCHTGE
RPFMCETCGKSFASKEYLKHHNRIHTGSKPFKCEVCFRTFAQRNSLYQHIKV
H
TGERPYCCDQCGKQFTQLNALQRHRRIHTGERPFMCNACGRTFTDKSTLRRHTSIHDKN
TPWKSFLVIVDGSPKNDDGHKTEQPDEEYVSSKLSDKLLSFAENGHFHNLAAVQDTVPTM
QENSSADTACKADDSVVSQDTLLATTISELSELTPQTDSMPTQLHSLSNME
Sequence length 711
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Glaucoma Glaucoma rs121918355, rs1566660365, rs1566635134, rs121918356, rs1566634475, rs28936700, rs55771538, rs28936701, rs104893622, rs55989760, rs72549387, rs104893628, rs2125316417, rs104893629, rs74315328, rs121909193, rs74315330, rs74315329, rs74315332, rs74315334, rs74315336, rs74315338, rs74315341, rs121909194, rs74315331, rs1558603396, rs387907175, rs587778873, rs587778875, rs104894979, rs137854895, rs766425037, rs72549380, rs148542782, rs541217363, rs753021890, rs771076928, rs56010818, rs777678299, rs1446110883, rs1573274915, rs1587545234, rs751768343, rs944452644
Joint laxity, short stature, and myopia JOINT LAXITY, SHORT STATURE, AND MYOPIA rs1555786618, rs1555786729 28475863
Larsen syndrome Larsen syndrome rs80356506, rs80356513, rs80356508, rs80356503, rs28933068, rs80356511, rs80356516, rs387906937, rs80356504, rs879255269, rs372487178, rs794727854, rs1553704446, rs377340567, rs868820857, rs1589510055 28475863
Myopia Severe myopia rs387907109, rs146936371, rs587776903, rs786205127, rs398122836, rs199624584, rs587777625, rs786205216, rs758872875, rs764211125, rs1135402746, rs765658563, rs1555941129, rs1555941116, rs199923805, rs782555528, rs1554862601, rs1586620121, rs1387950081, rs2051026773, rs1422332023
Unknown
Disease name Disease term dbSNP ID References
Acquired kyphoscoliosis Acquired Kyphoscoliosis
Congenital kyphoscoliosis Congenital kyphoscoliosis
Congenital pectus carinatum Congenital pectus carinatum
Dwarfism Dwarfism

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