Incidental Mutation 'IGL02476:Rhox3f'
ID 294970
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rhox3f
Ensembl Gene ENSMUSG00000095510
Gene Name reproductive homeobox 3F
Synonyms OTTMUSG00000017155
Accession Numbers
Essential gene? Not available question?
Stock # IGL02476
Quality Score
Status
Chromosome X
Chromosomal Location 36763005-36767149 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 36763192 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000138815 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115172] [ENSMUST00000183696] [ENSMUST00000184451] [ENSMUST00000185008]
AlphaFold A2ANE1
Predicted Effect probably benign
Transcript: ENSMUST00000115172
SMART Domains Protein: ENSMUSP00000110826
Gene: ENSMUSG00000095510

DomainStartEndE-ValueType
HOX 154 214 1.89e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000183696
SMART Domains Protein: ENSMUSP00000139277
Gene: ENSMUSG00000095510

DomainStartEndE-ValueType
SCOP:d1ftt__ 111 141 2e-3 SMART
Blast:HOX 111 146 5e-13 BLAST
low complexity region 190 203 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000184451
SMART Domains Protein: ENSMUSP00000138833
Gene: ENSMUSG00000095510

DomainStartEndE-ValueType
HOX 154 214 1.89e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000185008
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aamp T A 1: 74,320,683 (GRCm39) probably benign Het
Birc6 A G 17: 75,003,386 (GRCm39) E4752G possibly damaging Het
Chd1 C T 17: 15,954,535 (GRCm39) P468S probably damaging Het
Cnot3 A G 7: 3,661,067 (GRCm39) D556G probably benign Het
Csnk1d A G 11: 120,863,338 (GRCm39) Y201H probably damaging Het
Dhtkd1 A G 2: 5,935,717 (GRCm39) S132P possibly damaging Het
Dhx58 G T 11: 100,593,090 (GRCm39) Q206K probably benign Het
Dio1 C A 4: 107,149,574 (GRCm39) V195F probably damaging Het
Dio3 T C 12: 110,245,916 (GRCm39) V84A probably benign Het
Dnai4 T A 4: 102,944,545 (GRCm39) I3L possibly damaging Het
Extl3 T C 14: 65,314,693 (GRCm39) K163R probably benign Het
Fat2 A T 11: 55,201,950 (GRCm39) S375T probably damaging Het
Fbrs A G 7: 127,086,841 (GRCm39) D73G probably damaging Het
Fnip1 A G 11: 54,390,393 (GRCm39) probably benign Het
Frmpd4 A G X: 166,280,851 (GRCm39) V343A probably damaging Het
Gcc1 T C 6: 28,420,468 (GRCm39) D283G probably benign Het
Ghr T C 15: 3,349,528 (GRCm39) D550G probably damaging Het
Glycam1 G A 15: 103,471,307 (GRCm39) probably benign Het
Gpatch8 A G 11: 102,369,417 (GRCm39) S1374P probably damaging Het
Grm1 A T 10: 10,565,197 (GRCm39) M1037K probably benign Het
Gtpbp3 T C 8: 71,945,242 (GRCm39) L438P probably damaging Het
Ifi205 G T 1: 173,842,627 (GRCm39) N356K probably damaging Het
Ifi206 A G 1: 173,309,132 (GRCm39) L288P probably benign Het
Ift57 T C 16: 49,584,252 (GRCm39) V291A probably benign Het
Kif13a A C 13: 46,938,772 (GRCm39) C166G probably damaging Het
Lypd6 A G 2: 50,080,740 (GRCm39) T143A possibly damaging Het
Mtus2 G A 5: 148,014,748 (GRCm39) A514T probably benign Het
Neu2 T C 1: 87,524,674 (GRCm39) W220R probably damaging Het
Notch3 T C 17: 32,377,612 (GRCm39) S155G possibly damaging Het
Nrxn2 A G 19: 6,505,015 (GRCm39) E286G probably damaging Het
Onecut3 A G 10: 80,349,724 (GRCm39) E406G probably benign Het
Oog2 T A 4: 143,921,799 (GRCm39) D236E probably benign Het
Pck1 A G 2: 173,000,075 (GRCm39) H502R probably benign Het
Pld1 A G 3: 28,102,188 (GRCm39) Y313C probably damaging Het
Rpl34 A G 3: 130,520,613 (GRCm39) probably benign Het
Sema4c T C 1: 36,595,031 (GRCm39) K31E probably damaging Het
Septin11 T C 5: 93,296,443 (GRCm39) probably null Het
Slc4a9 T A 18: 36,668,498 (GRCm39) probably null Het
Snrnp200 T A 2: 127,059,408 (GRCm39) S434T probably benign Het
Snx13 A T 12: 35,136,940 (GRCm39) I134F probably damaging Het
Syt2 T C 1: 134,675,369 (GRCm39) S407P probably benign Het
Tbc1d19 T C 5: 54,046,755 (GRCm39) probably null Het
Tbc1d32 G T 10: 56,074,638 (GRCm39) Q192K possibly damaging Het
Ubr4 T A 4: 139,148,560 (GRCm39) C1681* probably null Het
Vmn1r43 T A 6: 89,847,043 (GRCm39) I148F possibly damaging Het
Vwa8 T C 14: 79,162,781 (GRCm39) V187A possibly damaging Het
Other mutations in Rhox3f
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2365:Rhox3f UTSW X 36,763,672 (GRCm39) nonsense probably null
R4111:Rhox3f UTSW X 36,763,672 (GRCm39) nonsense probably null
R4112:Rhox3f UTSW X 36,763,672 (GRCm39) nonsense probably null
R4113:Rhox3f UTSW X 36,763,672 (GRCm39) nonsense probably null
Posted On 2015-04-16