Incidental Mutation 'IGL00976:Rhox4f'
ID 29601
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rhox4f
Ensembl Gene ENSMUSG00000079630
Gene Name reproductive homeobox 4F
Synonyms Rhox4.6
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.072) question?
Stock # IGL00976
Quality Score
Chromosome X
Chromosomal Location 37602894-37607704 bp(-) (GRCm38)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 37604395 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000110824 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115170]
AlphaFold Q2MDF8
Predicted Effect probably benign
Transcript: ENSMUST00000115170
SMART Domains Protein: ENSMUSP00000110824
Gene: ENSMUSG00000079630

low complexity region 90 101 N/A INTRINSIC
HOX 128 190 5.14e-6 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183974
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930519F16Rik A G X: 103,183,262 probably benign Het
Aldob C A 4: 49,541,220 V151L probably damaging Het
Cacna1i G A 15: 80,355,645 M298I probably benign Het
Capn3 A G 2: 120,491,901 N414S possibly damaging Het
Ccdc186 G A 19: 56,797,500 T701M probably damaging Het
Ccdc190 A T 1: 169,933,740 H137L probably benign Het
Clhc1 G A 11: 29,561,389 D278N probably benign Het
Cntnap3 T C 13: 64,794,352 Y188C probably damaging Het
Dnah1 A C 14: 31,278,138 V2466G probably damaging Het
Dnah8 A G 17: 30,851,710 T4457A probably damaging Het
Gm13078 T A 4: 143,727,015 M231K probably damaging Het
Hectd4 A G 5: 121,349,106 Q3388R probably benign Het
Hecw1 T A 13: 14,318,972 D316V probably damaging Het
Il1rap T C 16: 26,698,839 V263A probably benign Het
Il6 G A 5: 30,014,841 G72S probably benign Het
Katnal2 T C 18: 77,017,493 Y86C probably damaging Het
Kdm7a G T 6: 39,144,398 S874R possibly damaging Het
Mybpc2 T C 7: 44,522,317 probably null Het
Nphs1 T G 7: 30,460,685 S130A possibly damaging Het
Ntrk3 C T 7: 78,450,953 V444I probably benign Het
Numbl T C 7: 27,268,810 V144A possibly damaging Het
Olfr952 T A 9: 39,426,657 Y138F probably benign Het
P2rx1 T C 11: 73,013,000 probably null Het
Pcdhb3 G A 18: 37,302,948 V656I probably benign Het
Pole A G 5: 110,323,572 Y1394C probably benign Het
Rbm47 A G 5: 66,026,738 V174A possibly damaging Het
Serpina12 T C 12: 104,032,528 Y317C probably damaging Het
Slc12a5 T A 2: 164,979,304 I236N probably damaging Het
Slc4a4 G A 5: 88,954,798 G32R probably damaging Het
Slco1a4 T C 6: 141,807,182 probably null Het
Sorcs3 A T 19: 48,767,103 N894I probably damaging Het
Stk38l A G 6: 146,775,402 E393G probably benign Het
Synpo A G 18: 60,603,419 I485T possibly damaging Het
Tenm3 T A 8: 48,256,841 M1687L probably benign Het
Ttc39c T C 18: 12,684,895 probably benign Het
Unc13d T C 11: 116,070,467 E378G probably damaging Het
Vmn2r118 T A 17: 55,593,204 N567Y probably damaging Het
Other mutations in Rhox4f
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0047:Rhox4f UTSW X 37607469 missense probably benign 0.00
R0090:Rhox4f UTSW X 37607469 missense probably benign 0.00
R0097:Rhox4f UTSW X 37607469 missense probably benign 0.00
Posted On 2013-04-17