Incidental Mutation 'R6978:Pou6f2'
ID 542581
Institutional Source Beutler Lab
Gene Symbol Pou6f2
Ensembl Gene ENSMUSG00000009734
Gene Name POU domain, class 6, transcription factor 2
Synonyms RPF-1, D130006K24Rik
MMRRC Submission 045086-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6978 (G1)
Quality Score 225.009
Status Validated
Chromosome 13
Chromosomal Location 18295683-18572271 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 18347063 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 10 (F10L)
Ref Sequence ENSEMBL: ENSMUSP00000138840 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000176795] [ENSMUST00000184299]
AlphaFold no structure available at present
Predicted Effect
SMART Domains Protein: ENSMUSP00000114173
Gene: ENSMUSG00000009734
AA Change: F266L

DomainStartEndE-ValueType
low complexity region 67 79 N/A INTRINSIC
coiled coil region 107 143 N/A INTRINSIC
low complexity region 248 266 N/A INTRINSIC
POU 422 532 9.61e-26 SMART
HOX 553 615 3.01e-21 SMART
Predicted Effect
Predicted Effect probably damaging
Transcript: ENSMUST00000176795
AA Change: F20L

PolyPhen 2 Score 0.965 (Sensitivity: 0.78; Specificity: 0.95)
Predicted Effect probably damaging
Transcript: ENSMUST00000184299
AA Change: F10L

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000138840
Gene: ENSMUSG00000009734
AA Change: F10L

DomainStartEndE-ValueType
low complexity region 135 157 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.5%
Validation Efficiency 96% (51/53)
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele are viable, fertile and of normal size with no apparent phenotypic abnormalities. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adprh C T 16: 38,266,171 (GRCm39) G324S probably damaging Het
Amfr T C 8: 94,727,015 (GRCm39) E140G probably damaging Het
Anapc1 G T 2: 128,511,820 (GRCm39) Q458K probably benign Het
Ap1g1 T C 8: 110,554,968 (GRCm39) probably null Het
Arhgap45 G T 10: 79,857,682 (GRCm39) V211F probably benign Het
Baz2b T C 2: 59,738,059 (GRCm39) E1750G possibly damaging Het
Cmpk2 A T 12: 26,527,018 (GRCm39) T336S probably damaging Het
Col6a3 C T 1: 90,735,192 (GRCm39) probably null Het
Cyp2c29 T C 19: 39,310,107 (GRCm39) L272P probably damaging Het
Cyp3a13 A T 5: 137,903,801 (GRCm39) S286T probably benign Het
Cyp4f18 T G 8: 72,756,340 (GRCm39) S79R probably benign Het
Dio1 T C 4: 107,164,030 (GRCm39) T96A probably benign Het
Dnah7a T C 1: 53,701,526 (GRCm39) I210V probably null Het
Epha4 A G 1: 77,354,220 (GRCm39) Y841H probably damaging Het
Gm12695 T C 4: 96,657,959 (GRCm39) D70G possibly damaging Het
Gtf3c1 G T 7: 125,244,706 (GRCm39) T1680K possibly damaging Het
Hnrnpul2 T C 19: 8,801,640 (GRCm39) V314A probably damaging Het
Irx3 G T 8: 92,527,356 (GRCm39) P116Q probably damaging Het
Lrp4 C T 2: 91,322,343 (GRCm39) R1060C probably damaging Het
Mark3 G A 12: 111,593,582 (GRCm39) V205I probably benign Het
Mchr1 T C 15: 81,121,997 (GRCm39) L249P possibly damaging Het
Med26 T C 8: 73,250,427 (GRCm39) N224S possibly damaging Het
Megf9 C T 4: 70,351,766 (GRCm39) V452I probably benign Het
Mki67 T C 7: 135,303,691 (GRCm39) R726G probably benign Het
Mst1r T A 9: 107,789,793 (GRCm39) L583Q probably benign Het
Mybpc1 A G 10: 88,358,886 (GRCm39) C1102R probably damaging Het
Nr6a1 T C 2: 38,762,631 (GRCm39) T55A probably benign Het
Nup210l G A 3: 90,061,873 (GRCm39) R684Q possibly damaging Het
Or13a24 A C 7: 140,154,200 (GRCm39) I45L probably damaging Het
Or4f7 T A 2: 111,644,155 (GRCm39) L305F probably benign Het
Or6x1 C T 9: 40,099,085 (GRCm39) R225W probably damaging Het
Pgbd1 A G 13: 21,607,432 (GRCm39) L254P probably damaging Het
Ppfia3 T A 7: 44,996,272 (GRCm39) T726S probably benign Het
Rab21 T A 10: 115,134,766 (GRCm39) M118L possibly damaging Het
Rbm6 T C 9: 107,729,774 (GRCm39) probably null Het
Rmc1 T C 18: 12,318,804 (GRCm39) Y430H probably benign Het
Rpp38 A G 2: 3,330,758 (GRCm39) L48P probably damaging Het
Sart3 A T 5: 113,883,807 (GRCm39) I735N probably damaging Het
Slc44a1 T A 4: 53,544,671 (GRCm39) Y461N probably damaging Het
Smok2b A T 17: 13,455,295 (GRCm39) *485L probably null Het
Speer4a2 C A 5: 26,291,454 (GRCm39) E117D probably damaging Het
Spink8 T C 9: 109,649,725 (GRCm39) V69A probably benign Het
Spred2 G A 11: 19,948,254 (GRCm39) R83Q possibly damaging Het
Tmc1 T C 19: 20,781,999 (GRCm39) N573S probably damaging Het
Tmem275 C T 4: 115,755,560 (GRCm39) Q120* probably null Het
Tox4 G T 14: 52,524,694 (GRCm39) probably null Het
Unc13c T C 9: 73,839,259 (GRCm39) S531G probably benign Het
Vmn2r56 C T 7: 12,449,333 (GRCm39) V302I probably benign Het
Ypel1 C T 16: 16,902,438 (GRCm39) A110V probably benign Het
Zfp395 G A 14: 65,623,882 (GRCm39) R117H probably benign Het
Zic5 T C 14: 122,696,960 (GRCm39) T552A unknown Het
Zic5 CGACGAGTAG C 14: 122,696,967 (GRCm39) probably benign Het
Other mutations in Pou6f2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00486:Pou6f2 APN 13 18,314,170 (GRCm39) missense probably damaging 1.00
IGL03046:Pou6f2 UTSW 13 18,303,612 (GRCm39) utr 3 prime probably benign
PIT4402001:Pou6f2 UTSW 13 18,299,931 (GRCm39) missense
PIT4519001:Pou6f2 UTSW 13 18,414,149 (GRCm39) missense unknown
R0349:Pou6f2 UTSW 13 18,326,589 (GRCm39) missense probably damaging 1.00
R0510:Pou6f2 UTSW 13 18,314,308 (GRCm39) splice site probably benign
R1449:Pou6f2 UTSW 13 18,347,000 (GRCm39) missense probably damaging 1.00
R1911:Pou6f2 UTSW 13 18,326,548 (GRCm39) missense probably damaging 0.98
R2971:Pou6f2 UTSW 13 18,556,552 (GRCm39) missense unknown
R5193:Pou6f2 UTSW 13 18,300,129 (GRCm39) utr 3 prime probably benign
R5218:Pou6f2 UTSW 13 18,326,586 (GRCm39) missense probably damaging 1.00
R6226:Pou6f2 UTSW 13 18,303,739 (GRCm39) missense possibly damaging 0.83
R6747:Pou6f2 UTSW 13 18,303,772 (GRCm39) missense probably benign 0.26
R6805:Pou6f2 UTSW 13 18,414,074 (GRCm39) missense
R7072:Pou6f2 UTSW 13 18,299,754 (GRCm39) missense
R7158:Pou6f2 UTSW 13 18,326,623 (GRCm39) missense
R7187:Pou6f2 UTSW 13 18,414,298 (GRCm39) missense
R7198:Pou6f2 UTSW 13 18,303,748 (GRCm39) missense probably damaging 0.97
R7203:Pou6f2 UTSW 13 18,414,379 (GRCm39) missense unknown
R7241:Pou6f2 UTSW 13 18,299,874 (GRCm39) missense
R7307:Pou6f2 UTSW 13 18,414,298 (GRCm39) missense
R7827:Pou6f2 UTSW 13 18,553,092 (GRCm39) missense
R7895:Pou6f2 UTSW 13 18,300,033 (GRCm39) missense
R8070:Pou6f2 UTSW 13 18,414,209 (GRCm39) missense unknown
R8207:Pou6f2 UTSW 13 18,414,158 (GRCm39) missense
R8334:Pou6f2 UTSW 13 18,299,991 (GRCm39) missense probably damaging 1.00
R8680:Pou6f2 UTSW 13 18,414,196 (GRCm39) missense unknown
R8830:Pou6f2 UTSW 13 18,553,083 (GRCm39) missense
R9203:Pou6f2 UTSW 13 18,303,615 (GRCm39) missense
R9462:Pou6f2 UTSW 13 18,314,189 (GRCm39) missense probably benign 0.03
R9632:Pou6f2 UTSW 13 18,299,848 (GRCm39) missense
R9709:Pou6f2 UTSW 13 18,414,389 (GRCm39) missense unknown
Z1176:Pou6f2 UTSW 13 18,553,220 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TCCTATTCTTGACGTTGCAGTAAAC -3'
(R):5'- AATCTCTTACTGGGACCCTGC -3'

Sequencing Primer
(F):5'- GCAGTAAACATTCTTTATTTGCCTC -3'
(R):5'- TTACTGGGACCCTGCAGTGG -3'
Posted On 2018-11-28