Incidental Mutation 'IGL02308:Gdf11'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gdf11
Ensembl Gene ENSMUSG00000025352
Gene Namegrowth differentiation factor 11
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock #IGL02308
Quality Score
Chromosomal Location128882295-128891718 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 128885384 bp
Amino Acid Change Tyrosine to Histidine at position 314 (Y314H)
Ref Sequence ENSEMBL: ENSMUSP00000026408 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026408]
Predicted Effect probably damaging
Transcript: ENSMUST00000026408
AA Change: Y314H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000026408
Gene: ENSMUSG00000025352
AA Change: Y314H

signal peptide 1 24 N/A INTRINSIC
Pfam:TGFb_propeptide 57 298 4.6e-39 PFAM
TGFB 311 405 4.8e-48 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein plays a role in the development of the nervous and other organ systems, and may regulate aging. Mice lacking a functional copy of this gene exhibit impaired anteroposterior patterning and other developmental defects. [provided by RefSeq, Aug 2016]
PHENOTYPE: Homozygotes for a null allele die neonatally showing altered patterning of the axial skeleton and impaired renal, palate, stomach, spleen and pancreatic development. A second null allele also alters retinal and olfactory epithelium neurogenesis. A third null allele causes extra thoracic vertebrae. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933427D14Rik G A 11: 72,202,482 S8F probably damaging Het
Alpk1 T A 3: 127,729,282 Q37L probably damaging Het
Cfap43 T C 19: 47,748,024 T1343A probably benign Het
Cmbl C A 15: 31,585,408 P146Q possibly damaging Het
Cog2 A T 8: 124,533,212 probably null Het
Dgkh C A 14: 78,587,576 V880L probably benign Het
Dopey1 T C 9: 86,520,088 S1114P probably damaging Het
Eif5b T A 1: 38,041,747 V723D probably damaging Het
Gm10110 T C 14: 89,897,595 noncoding transcript Het
Gm960 T C 19: 4,663,555 K132E probably damaging Het
Gria1 G A 11: 57,236,924 V320I probably benign Het
H2-Q10 T A 17: 35,473,566 *326R probably null Het
Irx6 T A 8: 92,677,031 L128Q probably damaging Het
Kif21b T A 1: 136,159,757 L937Q probably damaging Het
Lama5 A G 2: 180,190,327 probably benign Het
Mios A G 6: 8,231,269 I718V probably benign Het
Mroh8 A G 2: 157,254,973 V318A probably damaging Het
Nags A G 11: 102,149,071 *528W probably null Het
Nom1 T A 5: 29,437,710 V403D probably damaging Het
Npffr2 C A 5: 89,583,451 N413K probably benign Het
Olfr394 A T 11: 73,888,295 Y26N probably benign Het
Olfr671 T A 7: 104,975,458 I176F possibly damaging Het
Olr1 C T 6: 129,499,897 R135K possibly damaging Het
Pkhd1 A G 1: 20,070,376 probably null Het
Ptpro A G 6: 137,454,700 M1158V probably benign Het
Sh3d19 A G 3: 86,093,710 K238E probably damaging Het
Smarcc2 G T 10: 128,482,772 R641L probably damaging Het
Th T C 7: 142,898,057 E75G possibly damaging Het
Tlr1 A T 5: 64,925,947 L429* probably null Het
Ttn G A 2: 76,894,361 R2107* probably null Het
Ubr2 A T 17: 46,934,193 C1636S probably damaging Het
Vmn2r100 T A 17: 19,521,335 I103K possibly damaging Het
Vmn2r88 A G 14: 51,417,980 M558V possibly damaging Het
Zzef1 G A 11: 72,886,747 M1801I probably benign Het
Other mutations in Gdf11
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0056:Gdf11 UTSW 10 128886425 missense probably benign 0.04
R1773:Gdf11 UTSW 10 128891294 missense probably damaging 0.99
R1858:Gdf11 UTSW 10 128886446 missense probably damaging 1.00
R1988:Gdf11 UTSW 10 128885242 missense probably benign 0.05
R2025:Gdf11 UTSW 10 128891445 missense probably damaging 1.00
R7875:Gdf11 UTSW 10 128886341 missense probably benign 0.31
X0067:Gdf11 UTSW 10 128886203 missense possibly damaging 0.91
Posted On2015-04-16