Gene Expression Literature Summary

• Symbol: Fgd1
• Name: FYVE, RhoGEF and PH domain containing 1
• ID: MGI:104566

5 matching records from 5 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.

Age	E7.5	E10.5	E14.5	E15	E15.5	E16	E16.5	E18.5	E	P
In situ RNA (section)		1	2		1		1	1	1	1
Northern blot										2
RT-PCR				1		1				1
cDNA clones	1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available

Fgd1  FYVE, RhoGEF and PH domain containing 1   (Synonyms: faciogenital dysplasia, ZFYVE3)
Results	Reference
1*	J:153498 Diez-Roux G, Banfi S, Sultan M, Geffers L, Anand S, Rozado D, Magen A, Canidio E, Pagani M, Peluso I, Lin-Marq N, Koch M, Bilio M, Cantiello I, Verde R, De Masi C, Bianchi SA, Cicchini J, Perroud E, Mehmeti S, Dagand E, Schrinner S, Nurnberger A, SchmidtK, Metz K, Zwingmann C, Brieske N, Springer C, Hernandez AM, Herzog S, Grabbe F, Sieverding C, Fischer B, Schrader K, Brockmeyer M, Dettmer S, Helbig C, Alunni V, Battaini MA, Mura C, Henrichsen CN, Garcia-Lopez R, Echevarria D, Puelles E, et al., A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol. 2011;9(1):e1000582
3*	J:46439 Freeman TC, Dixon AK, Campbell EA, Tait TM, Richardson PJ, Rice KM, Maslen GL, Metcalfe AD, Streuli CH, Bentley DR, Expression Mapping of Mouse Genes. MGI Direct Data Submission. 1998;
8	J:63717 Gorski JL, Estrada L, Hu C, Liu Z, Skeletal-specific expression of fgd1 during bone formation and skeletal defects in faciogenital dysplasia (FGDY; aarskog syndrome). Dev Dyn. 2000 Aug;218(4):573-86
1	J:26633 Pasteris NG, de Gouyon B, Cadle AB, Campbell K, Herman GE, Gorski JL, Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene. Mamm Genome. 1995 Sep;6(9):658-61
1*	J:60236 Pasteris NG, Nagata K, Hall A, Gorski JL, Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue. Gene. 2000 Jan 25;242(1-2):237-47