PEX11B
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 1[12]
- Cytogenetic location
- 1q21.1[16]
- Expressed in
- prefrontal cortex, Brodmann area 9, internal globus pallidus, palpebral conjunctiva, cingulate gyrus, right frontal lobe, nucleus accumbens, anterior cingulate cortex, mucosa of transverse colon, caudate nucleus[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- Zellweger spectrum disorder, peroxisome biogenesis disorder 14B[13][14]
- HomoloGene ID
- 2852[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en peroxisomal biogenesis factor 11 beta
en PEX11B
en PEX11beta
en PEX11-BETA
en PEX14B
ar PEX١١B
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000131779
- Ensembl transcript ID
- ENST00000537888, ENST00000369306, ENST00000428634
- Entrez Gene ID
- 8799
- Exact match
- identifiers.org
- Freebase ID
- /m/03hmjzx
- HGNC ID
- 8853
- HGNC gene symbol
- PEX11B
- OMIM ID
- 603867
- RefSeq RNA ID
- NR_073493, NM_001184795, NM_003846, NR_073491, NR_073492
- UMLS CUI
- C1418472
🔗 Connections
Expressed in 6
Chromosome 1
Found in taxon 1
Instance of 1
Press Enter · cited answer in seconds
0 sources
Summary
PEX11B is a gene[1].