FBXO38

F-box only protein 38 (FBXO38) is a protein that in humans is encoded by the FBXO38 gene.

FBXO38
Identifiers
Aliases	FBXO38, Fbx38, HMN2D, MOKA, SP329, F-box protein 38, FBX38
External IDs	OMIM: 608533 MGI: 2444639 GeneCards: FBXO38
Gene location (Human) Chr. Chromosome 5 (human)[1] Band 5q32 Start 148,383,935 bp[1] End 148,442,836 bp[1]
Gene location (Mouse) Chr. Chromosome 18 (mouse)[2] Band 18|18 E1 Start 62,504,155 bp[2] End 62,548,695 bp[2]
Orthologs
Species	Human	Mouse
Entrez	81545	107035
Ensembl	ENSG00000145868	ENSMUSG00000042211
UniProt	Q6PIJ6	Q8BMI0
RefSeq (mRNA)	NM_001271723 NM_030793 NM_205836	NM_134136 NM_001361088 NM_001361089 NM_001361090 NM_001361091
RefSeq (protein)	NP_001258652 NP_110420 NP_995308	NP_598897 NP_001348017 NP_001348018 NP_001348019 NP_001348020
Location (UCSC)	Chr 5: 148.38 – 148.44 Mb	Chr 18: 62.5 – 62.55 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Mutations in the FBXO38 gene are associated with distal spinal muscular atrophy with calf predominance.

References

1. GRCh38: Ensembl release 89: ENSG00000145868 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000042211 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

External links

• FBXO38 human gene location in the UCSC Genome Browser.
• FBXO38 human gene details in the UCSC Genome Browser.