Incidental Mutation 'IGL02035:Gm9'
ID 184485
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9
Ensembl Gene ENSMUSG00000073243
Gene Name predicted gene 9
Synonyms LOC194854
Accession Numbers
Essential gene? Not available question?
Stock # IGL02035
Quality Score
Status
Chromosome X
Chromosomal Location 36473001-36474694 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 36474544 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Glutamine at position 3 (H3Q)
Ref Sequence ENSEMBL: ENSMUSP00000099160 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000101636] [ENSMUST00000115210]
AlphaFold Q3UKW5
Predicted Effect probably benign
Transcript: ENSMUST00000101636
AA Change: H3Q

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
Predicted Effect probably benign
Transcript: ENSMUST00000115210
SMART Domains Protein: ENSMUSP00000110865
Gene: ENSMUSG00000071773

DomainStartEndE-ValueType
low complexity region 91 111 N/A INTRINSIC
HOX 163 223 6.33e-6 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahctf1 A T 1: 179,593,579 (GRCm39) I1135N probably benign Het
Atl1 A G 12: 70,007,318 (GRCm39) probably benign Het
Atr A G 9: 95,748,735 (GRCm39) N427D probably benign Het
Chd2 T C 7: 73,091,375 (GRCm39) probably null Het
Cnot4 A T 6: 35,047,186 (GRCm39) V142D probably damaging Het
Ctnnd1 A T 2: 84,450,425 (GRCm39) V265E probably damaging Het
Ddx27 G T 2: 166,871,432 (GRCm39) V510F probably benign Het
Elac2 A G 11: 64,892,661 (GRCm39) S822G probably benign Het
Fat3 A T 9: 16,289,266 (GRCm39) F86I probably benign Het
Fbn1 T A 2: 125,177,282 (GRCm39) probably null Het
Fgd4 C T 16: 16,308,280 (GRCm39) probably benign Het
Furin T C 7: 80,040,735 (GRCm39) E701G probably benign Het
Fzd2 A G 11: 102,497,270 (GRCm39) *571W probably null Het
Jak2 T C 19: 29,263,808 (GRCm39) V441A probably benign Het
Kcnj3 T A 2: 55,327,590 (GRCm39) N126K probably damaging Het
Lca5 T C 9: 83,305,365 (GRCm39) E147G probably damaging Het
Magt1 G T X: 105,027,382 (GRCm39) probably null Het
Nkx6-2 A T 7: 139,161,601 (GRCm39) W195R probably damaging Het
Nt5c1a A T 4: 123,107,895 (GRCm39) S193C possibly damaging Het
Or6c216 A G 10: 129,678,659 (GRCm39) L84P possibly damaging Het
Os9 G A 10: 126,932,160 (GRCm39) P604S possibly damaging Het
Pecam1 C T 11: 106,586,685 (GRCm39) A277T probably benign Het
Polr1c A G 17: 46,557,085 (GRCm39) V66A possibly damaging Het
Proser1 T C 3: 53,386,251 (GRCm39) V711A probably benign Het
Prr35 G T 17: 26,166,136 (GRCm39) H384N probably benign Het
Sbp A G 17: 24,161,586 (GRCm39) N19S possibly damaging Het
Sh3bp4 A G 1: 89,071,412 (GRCm39) T87A probably benign Het
Vmn1r59 A T 7: 5,457,208 (GRCm39) I184N possibly damaging Het
Zcchc14 T C 8: 122,331,354 (GRCm39) probably benign Het
Other mutations in Gm9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02927:Gm9 APN X 36,474,207 (GRCm39) missense possibly damaging 0.46
Posted On 2014-05-07