FAM177B

FAM177B
Identifiers
Aliases	FAM177B, family with sequence similarity 177 member B
External IDs	HomoloGene: 90471 GeneCards: FAM177B
Gene location (Human)
Chr.	Chromosome 1 (human)[1]
End	222,751,004 bp[1]
RNA expression pattern
	Top expressed in
	gallbladder; ; rectum; ; body of stomach; ; lymph node; ; appendix; ; gastric mucosa; ; minor salivary gland; ; spleen; ; tibialis anterior muscle; ; islet of Langerhans;
	n/a
	More reference expression data
	n/a
Orthologs
	400823
	n/a
	ENSG00000197520
	n/a
	A6PVY3
	n/a
	NM_207468; NM_001324080; NM_001394345
	n/a
	NP_001311009; NP_997351
	n/a
	Wikidata
View/Edit Human

Family with sequence similarity 177 member B (FAM177B) is a protein that in humans is encoded by the FAM177B gene.[3] The other member of this family is FAM177A1.

References

GRCh38: Ensembl release 89: ENSG00000197520 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"FAM177B family with sequence similarity 177 member B [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2022-08-24.

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000197520 - Ensembl, May 2017

[2] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[3] "FAM177B family with sequence similarity 177 member B [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2022-08-24.