Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
24145 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
Pannexin 1 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
PANX1 |
SynonymsGene synonyms aliases
|
MRS1, OOMD7, OZEMA7, PX1, UNQ2529 |
ChromosomeChromosome number
|
11 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
11q21 |
SummarySummary of gene provided in NCBI Entrez Gene.
|
The protein encoded by this gene belongs to the innexin family. Innexin family members are the structural components of gap junctions. This protein and pannexin 2 are abundantly expressed in central nerve system (CNS) and are coexpressed in various neuron |
SNPsSNP information provided by dbSNP.
|
SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs1212949833 |
G>C,T |
Pathogenic |
Missense variant, coding sequence variant |
rs1591499598 |
CGGAGCCCA>- |
Pathogenic |
Genic upstream transcript variant, coding sequence variant, 5 prime UTR variant, inframe deletion |
rs1591529130 |
A>G |
Pathogenic |
Coding sequence variant, missense variant |
rs1591529258 |
C>T |
Pathogenic |
Coding sequence variant, stop gained |
|
miRNAmiRNA information provided by mirtarbase database.
|
|
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
|
|
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|
Protein
|
UniProt ID |
Q96RD7 |
Protein name |
Pannexin-1 (PANX1) [Cleaved into: Caspase-activated pannexin-1 (Caspase-activated PANX1)] |
Protein function |
Ion channel involved in a variety of physiological functions such as blood pressure regulation, apoptotic cell clearance and oogenesis (PubMed:15304325, PubMed:16908669, PubMed:20829356, PubMed:20944749, PubMed:30918116). Forms anion-selective c |
PDB |
6LTN
,
6LTO
,
6M02
,
6M66
,
6M67
,
6M68
,
6V6D
,
6WBF
,
6WBG
,
6WBI
,
6WBK
,
6WBL
,
6WBM
,
6WBN
,
7DWB
,
7F8J
,
7F8N
,
7F8O
,
7WSV
,
8GTS
,
8GTT
,
8GYO
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00876 |
Innexin |
33 → 263 |
Innexin |
Family |
|
Sequence |
|
Sequence length |
426 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
|
|
Associated diseases
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Hypothyroidism |
Hypothyroidism |
rs869320723, rs121908862, rs121908863, rs121908865, rs121908866, rs121908867, rs121908870, rs121908871, rs121908872, rs2140110277, rs121908881, rs121908884, rs121908885, rs786205080, rs1586182912, rs121917847, rs104893655, rs104893657, rs104893658, rs104893659, rs104893660, rs104893656, rs121917719, rs786204790, rs189261858, rs879255608, rs868197660, rs879255609, rs1586744173, rs1586182837, rs771222349, rs1587618417, rs1601844140, rs760832986, rs780982673, rs1603336347, rs1691155605 |
30595370 |
Liver failure |
Liver Failure, Acute |
rs118203990, rs118203991, rs118203992, rs387907022, rs201861847, rs796065037, rs759315662, rs368196005, rs796052121, rs369437593, rs367683258, rs766314948, rs368085185, rs770446752, rs753039116, rs776797592, rs1490906786, rs1562849964, rs759960319, rs776597537, rs375350359, rs1573008071, rs1601977105, rs1174791046, rs1019313682 |
29246445 |
|
|
|
| © 2021, Biomedical Informatics Centre, NIRRH |
ICMR-National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400012
Tel: +91-22-24192104, Fax No: +91-22-24139412 |