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Gene Expression Data
Assay Details
Assay
Reference: J:231784 Maass PG, et al., PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nat Genet. 2015 Jun;47(6):647-53
Assay type: RNA in situ
MGI Accession ID: MGI:5819078
Gene symbol: Pde3a
Gene name: phosphodiesterase 3A, cGMP inhibited
Probe: Pde3a cDNA2
Probe preparation: Antisense labelled with digoxigenin RNA
Assay notes: Two probes were described. Fig. 2 did not specify whether the coding sequence probe MGI:5819076 or the 3' untranslated region probe MGI:5819077 was used. The 3' untranslated region probe was used in Fig. S3.
Results
Specimen 2d 12.5 d: embryonic day 12.5 (more )
Structure Level Pattern Image Note
TS20: forelimb Present Regionally restricted 2d 12.5 d Expression was detected in domains involved in digit formation. Expression was consistent with a role in chondrogenesis.

Specimen 2d 13.5 d: embryonic day 13.5 (more )
Structure Level Pattern Image Note
TS21: forelimb Present Regionally restricted 2d 13.5 d Expression was detected in domains involved in digit formation. Expression was consistent with a role in chondrogenesis.

Specimen S3a 11.5d: embryonic day 11.5 (more )
Structure Level Pattern Image Note
TS19: forelimb bud Absent S3a 11.5d

Specimen S3a 12.5d: embryonic day 12.5 (more )
Structure Level Pattern Image Note
TS20: forelimb Weak S3a 12.5d Light expression was noted. Expression was consistent with a role in chondrogenesis.

Specimen S3a 13.5d: embryonic day 13.5 (more )
Structure Level Pattern Image Note
TS21: forelimb Weak S3a 13.5d Light expression was noted. Expression was consistent with a role in chondrogenesis.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory