Incidental Mutation 'IGL02476:Rhox3f'
ID294970
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rhox3f
Ensembl Gene ENSMUSG00000095510
Gene Namereproductive homeobox 3F
SynonymsOTTMUSG00000017155
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02476
Quality Score
Status
ChromosomeX
Chromosomal Location37580992-37585496 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to T at 37581539 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000138815 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115172] [ENSMUST00000183696] [ENSMUST00000184451] [ENSMUST00000185008]
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: 74,281,524 probably benign Het
Birc6 A G 17: 74,696,391 E4752G possibly damaging Het
Chd1 C T 17: 15,734,273 P468S probably damaging Het
Cnot3 A G 7: 3,658,068 D556G probably benign Het
Csnk1d A G 11: 120,972,512 Y201H probably damaging Het
Dhtkd1 A G 2: 5,930,906 S132P possibly damaging Het
Dhx58 G T 11: 100,702,264 Q206K probably benign Het
Dio1 C A 4: 107,292,377 V195F probably damaging Het
Dio3 T C 12: 110,279,482 V84A probably benign Het
Extl3 T C 14: 65,077,244 K163R probably benign Het
Fat2 A T 11: 55,311,124 S375T probably damaging Het
Fbrs A G 7: 127,487,669 D73G probably damaging Het
Fnip1 A G 11: 54,499,567 probably benign Het
Frmpd4 A G X: 167,497,855 V343A probably damaging Het
Gcc1 T C 6: 28,420,469 D283G probably benign Het
Ghr T C 15: 3,320,046 D550G probably damaging Het
Glycam1 G A 15: 103,562,880 probably benign Het
Gpatch8 A G 11: 102,478,591 S1374P probably damaging Het
Grm1 A T 10: 10,689,453 M1037K probably benign Het
Gtpbp3 T C 8: 71,492,598 L438P probably damaging Het
Ifi205 G T 1: 174,015,061 N356K probably damaging Het
Ifi206 A G 1: 173,481,566 L288P probably benign Het
Ift57 T C 16: 49,763,889 V291A probably benign Het
Kif13a A C 13: 46,785,296 C166G probably damaging Het
Lypd6 A G 2: 50,190,728 T143A possibly damaging Het
Mtus2 G A 5: 148,077,938 A514T probably benign Het
Neu2 T C 1: 87,596,952 W220R probably damaging Het
Notch3 T C 17: 32,158,638 S155G possibly damaging Het
Nrxn2 A G 19: 6,454,985 E286G probably damaging Het
Onecut3 A G 10: 80,513,890 E406G probably benign Het
Oog2 T A 4: 144,195,229 D236E probably benign Het
Pck1 A G 2: 173,158,282 H502R probably benign Het
Pld1 A G 3: 28,048,039 Y313C probably damaging Het
Rpl34 A G 3: 130,726,964 probably benign Het
Sema4c T C 1: 36,555,950 K31E probably damaging Het
Sept11 T C 5: 93,148,584 probably null Het
Slc4a9 T A 18: 36,535,445 probably null Het
Snrnp200 T A 2: 127,217,488 S434T probably benign Het
Snx13 A T 12: 35,086,941 I134F probably damaging Het
Syt2 T C 1: 134,747,631 S407P probably benign Het
Tbc1d19 T C 5: 53,889,413 probably null Het
Tbc1d32 G T 10: 56,198,542 Q192K possibly damaging Het
Ubr4 T A 4: 139,421,249 C1681* probably null Het
Vmn1r43 T A 6: 89,870,061 I148F possibly damaging Het
Vwa8 T C 14: 78,925,341 V187A possibly damaging Het
Wdr78 T A 4: 103,087,348 I3L possibly damaging Het
Other mutations in Rhox3f
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2365:Rhox3f UTSW X 37582019 nonsense probably null
R4111:Rhox3f UTSW X 37582019 nonsense probably null
R4112:Rhox3f UTSW X 37582019 nonsense probably null
R4113:Rhox3f UTSW X 37582019 nonsense probably null
Posted On2015-04-16