FBXO38

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]
End	148,442,836 bp[1]
Gene location (Mouse)
Chr.	Chromosome 18 (mouse)[2]
End	62,548,695 bp[2]
RNA expression pattern
	Top expressed in
	stomach; ; heart; ; lung; ; kidney; ; corpus callosum; ; Achilles tendon; ; colon;
	More reference expression data
	n/a
Orthologs
	81545
	107035
	ENSG00000145868
	ENSMUSG00000042211
	Q6PIJ6
	Q8BMI0
	NM_001271723; NM_030793; NM_205836
	NM_134136; NM_001361088; NM_001361089; NM_001361090; NM_001361091
	NP_001258652; NP_110420; NP_995308
	NP_598897; NP_001348017; NP_001348018; NP_001348019; NP_001348020
	Wikidata
View/Edit Human	View/Edit Mouse

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

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

References

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

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