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.
|
|
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 |
GO:0000981 |
Function |
DNA-binding transcription factor activity, RNA polymerase II-specific |
IBA |
21873635 |
GO:0001227 |
Function |
DNA-binding transcription repressor activity, RNA polymerase II-specific |
IDA |
16049025 |
GO:0001227 |
Function |
DNA-binding transcription repressor activity, RNA polymerase II-specific |
IMP |
16049025 |
GO:0001658 |
Process |
Branching involved in ureteric bud morphogenesis |
IEA |
|
GO:0005654 |
Component |
Nucleoplasm |
IDA |
|
GO:0005730 |
Component |
Nucleolus |
IDA |
|
GO:0005737 |
Component |
Cytoplasm |
IEA |
|
GO:0006355 |
Process |
Regulation of transcription, DNA-templated |
IBA |
21873635 |
GO:0043565 |
Function |
Sequence-specific DNA binding |
IDA |
16049025 |
GO:0045892 |
Process |
Negative regulation of transcription, DNA-templated |
IDA |
16049025 |
GO:0046872 |
Function |
Metal ion binding |
IEA |
|
|
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
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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 |
|
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 |
|
|
Myopia-joint laxity-short stature syndrome |
Severe myopia-generalized joint laxity-short stature syndrome |
|
|
Osteopenia |
Osteopenia |
|
|
Proptosis |
Exophthalmos |
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