Incidental Mutation 'IGL00508:Rhox2g'
ID 3137
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rhox2g
Ensembl Gene ENSMUSG00000079629
Gene Name reproductive homeobox 2G
Synonyms Rhox2.7, EG434766
Accession Numbers
Essential gene? Probably non essential (E-score: 0.023) question?
Stock # IGL00508
Quality Score
Status
Chromosome X
Chromosomal Location 36820768-36825123 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 36824463 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Isoleucine at position 152 (N152I)
Ref Sequence ENSEMBL: ENSMUSP00000110823 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115166] [ENSMUST00000115169]
AlphaFold L7MUB9
Predicted Effect probably benign
Transcript: ENSMUST00000115166
SMART Domains Protein: ENSMUSP00000110820
Gene: ENSMUSG00000079628

DomainStartEndE-ValueType
HOX 128 190 5.14e-6 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000115169
AA Change: N152I

PolyPhen 2 Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000110823
Gene: ENSMUSG00000079629
AA Change: N152I

DomainStartEndE-ValueType
low complexity region 33 44 N/A INTRINSIC
low complexity region 89 98 N/A INTRINSIC
HOX 130 190 3.62e-3 SMART
Predicted Effect unknown
Transcript: ENSMUST00000183888
AA Change: N79I
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrv1 A C 13: 81,654,306 (GRCm39) D2188E probably damaging Het
Atrx A G X: 104,867,405 (GRCm39) S2026P probably damaging Het
Cacna1b A C 2: 24,547,301 (GRCm39) probably null Het
Cfap46 C T 7: 139,240,605 (GRCm39) S56N probably damaging Het
Cfap57 C T 4: 118,438,367 (GRCm39) probably null Het
Ckap5 T G 2: 91,436,601 (GRCm39) V1567G probably damaging Het
Cyp2c38 A T 19: 39,449,169 (GRCm39) Y61* probably null Het
D130052B06Rik A G 11: 33,549,402 (GRCm39) E7G unknown Het
Dhx38 A G 8: 110,283,566 (GRCm39) L527P possibly damaging Het
Dnaaf5 A G 5: 139,163,701 (GRCm39) N653D probably benign Het
Dnah8 T G 17: 31,074,904 (GRCm39) M4541R probably damaging Het
Dpyd A T 3: 118,858,636 (GRCm39) T617S probably benign Het
Fpr2 A T 17: 18,113,034 (GRCm39) N10I probably damaging Het
Frmd4a A T 2: 4,599,545 (GRCm39) K524* probably null Het
Gpr45 C T 1: 43,071,452 (GRCm39) P32S possibly damaging Het
H2-Eb2 A T 17: 34,553,341 (GRCm39) I176F probably damaging Het
Hcrtr1 T A 4: 130,031,062 (GRCm39) N74I probably damaging Het
Ifi47 C T 11: 48,986,241 (GRCm39) Q3* probably null Het
Krt8 T A 15: 101,906,460 (GRCm39) M350L probably benign Het
Lilra6 A G 7: 3,914,553 (GRCm39) S533P probably benign Het
Map1b A T 13: 99,565,741 (GRCm39) S2327T unknown Het
Mcoln3 T A 3: 145,839,683 (GRCm39) I345N probably damaging Het
Mettl3 C A 14: 52,532,436 (GRCm39) probably benign Het
Mgat4a G A 1: 37,488,204 (GRCm39) R472* probably null Het
Micall1 A G 15: 79,014,768 (GRCm39) K715E probably damaging Het
Pak1 G T 7: 97,503,775 (GRCm39) G37C probably benign Het
Pomt2 T G 12: 87,166,401 (GRCm39) H426P probably damaging Het
Pou2f3 G A 9: 43,051,258 (GRCm39) P155S probably benign Het
Psg25 A G 7: 18,263,656 (GRCm39) Y56H probably benign Het
Rab9 G T X: 165,240,860 (GRCm39) Y150* probably null Het
Sema6d T C 2: 124,498,844 (GRCm39) probably benign Het
Simc1 C A 13: 54,672,989 (GRCm39) Q446K probably benign Het
Svs5 G T 2: 164,078,962 (GRCm39) T315K possibly damaging Het
Syt9 C T 7: 107,024,574 (GRCm39) R156* probably null Het
Tmem260 A T 14: 48,746,578 (GRCm39) Y618F probably damaging Het
Wdr44 A G X: 23,666,783 (GRCm39) I719V possibly damaging Het
Zfp518a T G 19: 40,901,914 (GRCm39) I614M probably damaging Het
Other mutations in Rhox2g
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1296:Rhox2g UTSW X 36,824,865 (GRCm39) unclassified probably benign
Posted On 2012-04-20