Incidental Mutation 'R3434:Fhl4'
ID 266354
Institutional Source Beutler Lab
Gene Symbol Fhl4
Ensembl Gene ENSMUSG00000050035
Gene Name four and a half LIM domains 4
Synonyms
MMRRC Submission 040652-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.096) question?
Stock # R3434 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 84932883-84938359 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 84934308 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 158 (T158A)
Ref Sequence ENSEMBL: ENSMUSP00000150570 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059383] [ENSMUST00000095383] [ENSMUST00000216771] [ENSMUST00000216889]
AlphaFold Q8CDC8
Predicted Effect probably benign
Transcript: ENSMUST00000059383
AA Change: T158A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000050054
Gene: ENSMUSG00000050035
AA Change: T158A

DomainStartEndE-ValueType
LIM 38 91 1.69e-12 SMART
LIM 99 152 1.1e-11 SMART
LIM 160 211 2e-14 SMART
LIM 219 275 9.31e-15 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000095383
SMART Domains Protein: ENSMUSP00000093030
Gene: ENSMUSG00000060935

DomainStartEndE-ValueType
Pfam:UPF0444 24 114 1.7e-48 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000216771
Predicted Effect probably benign
Transcript: ENSMUST00000216889
AA Change: T158A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.3%
Validation Efficiency 98% (54/55)
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca17 G A 17: 24,508,511 (GRCm39) A1008V probably damaging Het
Adora3 A G 3: 105,812,231 (GRCm39) K39R probably benign Het
Ankib1 A G 5: 3,742,760 (GRCm39) V1085A probably damaging Het
Atp7a G A X: 105,138,463 (GRCm39) R563K probably benign Het
Azin1 T C 15: 38,493,820 (GRCm39) I268V probably benign Het
Carm1 T C 9: 21,480,769 (GRCm39) F81S probably damaging Het
Ccnjl A G 11: 43,470,688 (GRCm39) Y152C probably damaging Het
Chrna3 T A 9: 54,931,610 (GRCm39) I61F possibly damaging Het
Clca3a2 G A 3: 144,514,522 (GRCm39) probably benign Het
Clstn2 T A 9: 97,336,768 (GRCm39) D903V probably benign Het
Dpysl3 C T 18: 43,494,126 (GRCm39) V70I probably benign Het
Drg2 A T 11: 60,352,218 (GRCm39) K180* probably null Het
Dync2h1 A C 9: 7,011,236 (GRCm39) H3659Q probably benign Het
Dysf A T 6: 84,047,870 (GRCm39) Y349F probably benign Het
Epb41l4b T C 4: 57,040,865 (GRCm39) N533D probably benign Het
Fam47e T A 5: 92,733,221 (GRCm39) V152D probably damaging Het
Fasn G A 11: 120,713,599 (GRCm39) A24V probably damaging Het
Fnbp1l C T 3: 122,339,955 (GRCm39) R499Q probably damaging Het
Hdlbp A T 1: 93,355,883 (GRCm39) M358K probably benign Het
Ift74 A G 4: 94,510,089 (GRCm39) probably null Het
Lhx4 A G 1: 155,578,147 (GRCm39) Y332H probably damaging Het
Mast2 A T 4: 116,165,292 (GRCm39) S1314T probably benign Het
Mast4 A G 13: 102,923,887 (GRCm39) I508T probably damaging Het
Mdn1 T C 4: 32,733,726 (GRCm39) probably null Het
Mrps23 A G 11: 88,100,940 (GRCm39) K44E probably damaging Het
Mslnl G A 17: 25,961,908 (GRCm39) V128M probably damaging Het
Mup6 G T 4: 60,004,116 (GRCm39) probably null Het
Notch3 A T 17: 32,377,592 (GRCm39) D161E possibly damaging Het
Or2ag13 A T 7: 106,472,976 (GRCm39) Y159N probably benign Het
Or4a67 T C 2: 88,598,413 (GRCm39) D82G probably damaging Het
Or5w11 T C 2: 87,459,418 (GRCm39) F204L probably benign Het
P2rx4 T A 5: 122,863,133 (GRCm39) I202K probably damaging Het
Phykpl A G 11: 51,489,482 (GRCm39) T363A probably benign Het
Pitpnm1 G A 19: 4,162,234 (GRCm39) A1047T probably damaging Het
Ppat A G 5: 77,065,912 (GRCm39) I402T probably damaging Het
Rpgr A G X: 10,042,841 (GRCm39) S656P probably benign Het
Rsbn1l T C 5: 21,110,928 (GRCm39) probably benign Het
Sacs A G 14: 61,449,752 (GRCm39) K3933E probably damaging Het
Scn7a T C 2: 66,505,847 (GRCm39) I1681V probably benign Het
Sel1l3 T C 5: 53,274,432 (GRCm39) D1016G probably benign Het
Sf3a3 C A 4: 124,618,870 (GRCm39) T277N possibly damaging Het
Slc35a5 A G 16: 44,964,396 (GRCm39) I279T probably benign Het
Slc39a10 T C 1: 46,874,877 (GRCm39) T142A probably benign Het
Tle3 T A 9: 61,321,376 (GRCm39) probably null Het
Tmem117 T C 15: 94,992,573 (GRCm39) I411T probably damaging Het
Ttn T C 2: 76,698,721 (GRCm39) T5A possibly damaging Het
Tubgcp3 T C 8: 12,708,381 (GRCm39) probably null Het
Ush2a C T 1: 188,465,955 (GRCm39) P2841L probably damaging Het
Vmn1r209 A T 13: 22,990,267 (GRCm39) M141K probably benign Het
Vmn2r91 A T 17: 18,330,370 (GRCm39) probably benign Het
Other mutations in Fhl4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01819:Fhl4 APN 10 84,934,734 (GRCm39) missense probably damaging 1.00
IGL02623:Fhl4 APN 10 84,934,035 (GRCm39) missense probably damaging 1.00
PIT4382001:Fhl4 UTSW 10 84,934,293 (GRCm39) missense possibly damaging 0.95
R0412:Fhl4 UTSW 10 84,934,680 (GRCm39) missense possibly damaging 0.75
R0514:Fhl4 UTSW 10 84,934,250 (GRCm39) missense probably damaging 1.00
R1953:Fhl4 UTSW 10 84,934,171 (GRCm39) missense probably benign 0.00
R2567:Fhl4 UTSW 10 84,934,644 (GRCm39) missense possibly damaging 0.91
R4489:Fhl4 UTSW 10 84,934,319 (GRCm39) missense possibly damaging 0.76
R4512:Fhl4 UTSW 10 84,934,578 (GRCm39) missense possibly damaging 0.93
R6588:Fhl4 UTSW 10 84,933,971 (GRCm39) missense possibly damaging 0.50
R7699:Fhl4 UTSW 10 84,934,379 (GRCm39) missense probably benign 0.09
R7699:Fhl4 UTSW 10 84,934,113 (GRCm39) missense probably damaging 0.96
R8197:Fhl4 UTSW 10 84,934,101 (GRCm39) missense probably damaging 1.00
R8371:Fhl4 UTSW 10 84,934,637 (GRCm39) missense probably benign 0.37
Predicted Primers PCR Primer
(F):5'- CCCAGCACACTTCTTGGCTATATAG -3'
(R):5'- ACAAGTGTGCCACTCGAGTC -3'

Sequencing Primer
(F):5'- GGCTATATAGTTCTTGTAGCAATCC -3'
(R):5'- TTCCCCAAGTGCAAAGGGTG -3'
Posted On 2015-02-18