Incidental Mutation 'R1912:Folh1'
ID 210394
Institutional Source Beutler Lab
Gene Symbol Folh1
Ensembl Gene ENSMUSG00000001773
Gene Name folate hydrolase 1
Synonyms GCP2, mopsm, glutamate carboxypeptidase II, prostate-specific membrane antigen
MMRRC Submission 039930-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1912 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 86368185-86425151 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 86412175 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 199 (S199P)
Ref Sequence ENSEMBL: ENSMUSP00000001824 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000001824] [ENSMUST00000107271]
AlphaFold O35409
Predicted Effect possibly damaging
Transcript: ENSMUST00000001824
AA Change: S199P

PolyPhen 2 Score 0.954 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000001824
Gene: ENSMUSG00000001773
AA Change: S199P

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
Pfam:PA 171 264 2.5e-16 PFAM
Pfam:Peptidase_M28 359 561 1.2e-18 PFAM
Pfam:TFR_dimer 629 749 1.6e-37 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000107271
AA Change: S199P

PolyPhen 2 Score 0.787 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000102892
Gene: ENSMUSG00000001773
AA Change: S199P

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
Pfam:PA 167 265 7e-18 PFAM
Pfam:Peptidase_M28 339 475 2.1e-15 PFAM
Pfam:TFR_dimer 595 718 1.1e-43 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209082
Coding Region Coverage
  • 1x: 97.3%
  • 3x: 96.8%
  • 10x: 95.3%
  • 20x: 92.8%
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous mutation of this gene results in protection from peripheral neuropathy and ischemic brain injury. Homozygotes for a null allele show increased food intake, anxiety-like behavior, smaller sciatic nerve axons, and impaired angiogenesis. Homozygotes for a different null allele show less neuron degeneration and astrocyte damage after traumatic brain injury. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 122 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2900092C05Rik A G 7: 12,288,582 (GRCm39) M132V probably benign Het
4921524L21Rik T A 18: 6,620,205 (GRCm39) I45N possibly damaging Het
Abcb6 A G 1: 75,156,599 (GRCm39) V55A probably benign Het
Adam28 A T 14: 68,881,780 (GRCm39) D105E probably benign Het
Ahnak T C 19: 8,995,245 (GRCm39) S5510P probably damaging Het
Aldh3b1 T G 19: 3,971,187 (GRCm39) D159A probably damaging Het
Alx1 A G 10: 102,861,222 (GRCm39) L102P probably damaging Het
Ankrd50 C T 3: 38,510,925 (GRCm39) V481I probably benign Het
Aox4 G T 1: 58,303,561 (GRCm39) G1200W probably damaging Het
Arhgap45 A C 10: 79,856,524 (GRCm39) D24A probably benign Het
Arhgef16 A T 4: 154,364,780 (GRCm39) probably null Het
Asic4 A T 1: 75,445,876 (GRCm39) Y235F possibly damaging Het
Asph T C 4: 9,453,335 (GRCm39) E646G probably damaging Het
Atg4d A G 9: 21,183,935 (GRCm39) D350G probably damaging Het
Auts2 T C 5: 131,472,412 (GRCm39) T347A probably damaging Het
Bsnd A T 4: 106,345,227 (GRCm39) L73* probably null Het
Cachd1 A T 4: 100,810,366 (GRCm39) S323C probably damaging Het
Cacna1e A G 1: 154,312,195 (GRCm39) I1290T probably damaging Het
Cdh8 T A 8: 99,825,502 (GRCm39) N498Y probably damaging Het
Cdkn3 A G 14: 47,007,291 (GRCm39) probably null Het
Celf2 A T 2: 6,620,564 (GRCm39) M40K probably damaging Het
Cfap57 A C 4: 118,472,207 (GRCm39) S57R probably damaging Het
Cfh A G 1: 140,063,879 (GRCm39) probably null Het
Chdh A G 14: 29,754,745 (GRCm39) S252G probably benign Het
Col8a1 T A 16: 57,448,287 (GRCm39) I408F unknown Het
Corin C T 5: 72,515,746 (GRCm39) C303Y probably damaging Het
Crlf2 C T 5: 109,705,007 (GRCm39) C66Y possibly damaging Het
Csmd1 C T 8: 16,284,012 (GRCm39) probably null Het
Cyp4f16 T C 17: 32,764,018 (GRCm39) V270A probably damaging Het
Defa29 T A 8: 21,816,028 (GRCm39) H113L possibly damaging Het
Dhx35 A T 2: 158,684,227 (GRCm39) N501Y probably damaging Het
Dipk1b A G 2: 26,522,716 (GRCm39) E55G probably damaging Het
Dst A G 1: 34,330,931 (GRCm39) R4690G probably damaging Het
Elac2 T A 11: 64,885,089 (GRCm39) D439E probably benign Het
Ercc6 A G 14: 32,298,760 (GRCm39) R1383G probably damaging Het
Fat3 T A 9: 15,881,284 (GRCm39) Y3196F probably damaging Het
Fbxw13 A T 9: 109,010,611 (GRCm39) D342E probably benign Het
Fmod A G 1: 133,968,458 (GRCm39) N166S possibly damaging Het
Fv1 A G 4: 147,954,235 (GRCm39) N267S possibly damaging Het
Fyn T C 10: 39,402,828 (GRCm39) V200A possibly damaging Het
Gfus A T 15: 75,797,498 (GRCm39) D278E possibly damaging Het
Ggnbp2 T C 11: 84,753,122 (GRCm39) N39S probably benign Het
Gm10509 A T 17: 21,909,831 (GRCm39) I53F possibly damaging Het
Gpr139 A T 7: 118,744,102 (GRCm39) I161N possibly damaging Het
Grhl2 C T 15: 37,358,651 (GRCm39) T148I probably damaging Het
Hmcn1 C A 1: 150,480,633 (GRCm39) M4514I probably benign Het
Igsf10 T G 3: 59,236,993 (GRCm39) T1063P probably benign Het
Itgav A G 2: 83,625,830 (GRCm39) Y792C possibly damaging Het
Itgb2l T C 16: 96,228,135 (GRCm39) Q456R probably benign Het
Jph4 G A 14: 55,345,818 (GRCm39) A613V probably benign Het
Kcna2 A G 3: 107,012,717 (GRCm39) T433A probably benign Het
Kmt2e A G 5: 23,697,393 (GRCm39) K97R probably benign Het
Krba1 C A 6: 48,392,699 (GRCm39) A871E probably benign Het
Loxhd1 T C 18: 77,427,833 (GRCm39) F468L probably benign Het
Lpin1 A G 12: 16,596,728 (GRCm39) V713A probably damaging Het
Ltbp2 T A 12: 84,832,637 (GRCm39) I67F probably damaging Het
Mdc1 G A 17: 36,155,430 (GRCm39) R35H probably benign Het
Mdc1 A G 17: 36,161,703 (GRCm39) D872G probably benign Het
Mgam C T 6: 40,741,119 (GRCm39) Q959* probably null Het
Mttp T A 3: 137,821,788 (GRCm39) T260S probably benign Het
Naalad2 A T 9: 18,287,831 (GRCm39) D266E probably benign Het
Nans T A 4: 46,500,162 (GRCm39) L182H probably damaging Het
Nbas T A 12: 13,616,145 (GRCm39) C2228S probably benign Het
Nfix A T 8: 85,448,306 (GRCm39) V407E probably damaging Het
Nktr T A 9: 121,579,306 (GRCm39) probably benign Het
Nlrp10 G A 7: 108,524,602 (GRCm39) R293* probably null Het
Nrxn3 T C 12: 88,762,112 (GRCm39) F53S probably damaging Het
Or11h4 G A 14: 50,974,235 (GRCm39) P128L probably damaging Het
Or12e7 T C 2: 87,287,727 (GRCm39) S73P probably damaging Het
Or1e21 A T 11: 73,344,820 (GRCm39) F73I probably damaging Het
Or2f2 T C 6: 42,767,411 (GRCm39) I146T probably benign Het
Or3a1c T C 11: 74,046,711 (GRCm39) C244R probably damaging Het
Or5ak24 T A 2: 85,260,604 (GRCm39) N190Y probably damaging Het
Or5p68 A G 7: 107,946,014 (GRCm39) L58P probably damaging Het
Or6d12 A G 6: 116,492,950 (GRCm39) T71A probably benign Het
Oxld1 A G 11: 120,347,732 (GRCm39) V155A probably damaging Het
Pamr1 T A 2: 102,472,645 (GRCm39) F648Y probably damaging Het
Parg T C 14: 31,932,497 (GRCm39) W446R probably damaging Het
Pate13 A T 9: 35,819,915 (GRCm39) T23S probably benign Het
Phf3 A T 1: 30,843,426 (GRCm39) H1844Q probably damaging Het
Phf7 T C 14: 30,962,281 (GRCm39) I175V possibly damaging Het
Pibf1 G A 14: 99,425,245 (GRCm39) probably null Het
Plcxd1 A G 5: 110,251,308 (GRCm39) I295V probably benign Het
Pole2 A C 12: 69,256,764 (GRCm39) Y254D probably damaging Het
Ppm1e T A 11: 87,135,196 (GRCm39) I225F probably benign Het
Pttg1ip2 C A 5: 5,502,019 (GRCm39) W144C probably benign Het
Rem1 G A 2: 152,476,455 (GRCm39) V238M probably damaging Het
Resf1 T A 6: 149,230,342 (GRCm39) D1129E possibly damaging Het
Rnase2b T G 14: 51,400,357 (GRCm39) V146G probably damaging Het
Rnf169 G A 7: 99,575,461 (GRCm39) T378I probably damaging Het
Rpf2 A G 10: 40,112,197 (GRCm39) F80L probably benign Het
Sec11c T A 18: 65,947,945 (GRCm39) D128E probably damaging Het
Septin12 A G 16: 4,806,417 (GRCm39) V248A probably damaging Het
Serinc1 T C 10: 57,401,547 (GRCm39) N82S probably benign Het
Serpina9 A C 12: 103,967,508 (GRCm39) W296G probably damaging Het
Sgo2b A C 8: 64,384,503 (GRCm39) D164E probably damaging Het
Slc15a3 A G 19: 10,825,977 (GRCm39) N223D probably damaging Het
Slc44a3 A G 3: 121,325,815 (GRCm39) Y12H probably benign Het
Slco3a1 A G 7: 74,154,359 (GRCm39) F42S probably damaging Het
Snrnp40 C G 4: 130,271,836 (GRCm39) probably null Het
Snx7 A T 3: 117,623,317 (GRCm39) probably null Het
Sorl1 A T 9: 41,993,246 (GRCm39) D259E probably damaging Het
Stpg2 G A 3: 139,228,742 (GRCm39) probably null Het
Strn T A 17: 78,991,824 (GRCm39) Y165F probably damaging Het
Sval2 T A 6: 41,841,254 (GRCm39) *106R probably null Het
Tcaf3 A G 6: 42,573,622 (GRCm39) S197P possibly damaging Het
Tespa1 C A 10: 130,190,592 (GRCm39) T73N probably benign Het
Tex10 C T 4: 48,456,800 (GRCm39) R637Q probably benign Het
Thoc5 C A 11: 4,865,561 (GRCm39) T380K probably benign Het
Tmprss7 T A 16: 45,476,911 (GRCm39) R784* probably null Het
Trank1 A T 9: 111,219,777 (GRCm39) L2171F probably benign Het
Trpm2 T G 10: 77,781,710 (GRCm39) K303T probably benign Het
Unc80 G A 1: 66,549,784 (GRCm39) V681M probably damaging Het
Usp40 A G 1: 87,874,368 (GRCm39) F1131L probably benign Het
Vmn1r215 A T 13: 23,260,673 (GRCm39) I238F possibly damaging Het
Vwa3a A T 7: 120,394,850 (GRCm39) Y890F probably damaging Het
Zdhhc18 A G 4: 133,341,171 (GRCm39) L234P probably damaging Het
Zfp109 A G 7: 23,927,676 (GRCm39) S578P probably damaging Het
Zfp704 T C 3: 9,674,418 (GRCm39) D121G unknown Het
Zgrf1 G T 3: 127,356,786 (GRCm39) V671L probably benign Het
Zkscan8 A T 13: 21,704,927 (GRCm39) C265* probably null Het
Zscan26 T C 13: 21,629,310 (GRCm39) I398V possibly damaging Het
Other mutations in Folh1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00504:Folh1 APN 7 86,383,351 (GRCm39) missense probably damaging 1.00
IGL00531:Folh1 APN 7 86,368,977 (GRCm39) missense possibly damaging 0.82
IGL00772:Folh1 APN 7 86,380,992 (GRCm39) missense probably damaging 1.00
IGL01339:Folh1 APN 7 86,375,306 (GRCm39) missense probably damaging 1.00
IGL01373:Folh1 APN 7 86,395,350 (GRCm39) missense probably benign 0.39
IGL01645:Folh1 APN 7 86,391,435 (GRCm39) missense probably damaging 1.00
IGL01736:Folh1 APN 7 86,391,444 (GRCm39) missense possibly damaging 0.96
IGL02104:Folh1 APN 7 86,393,638 (GRCm39) missense possibly damaging 0.93
IGL02124:Folh1 APN 7 86,374,626 (GRCm39) missense probably damaging 0.99
IGL02338:Folh1 APN 7 86,385,723 (GRCm39) splice site probably benign
IGL02440:Folh1 APN 7 86,383,312 (GRCm39) missense probably benign 0.09
IGL02689:Folh1 APN 7 86,412,253 (GRCm39) splice site probably null
IGL02976:Folh1 APN 7 86,412,126 (GRCm39) missense probably benign
IGL03022:Folh1 APN 7 86,395,379 (GRCm39) missense possibly damaging 0.76
R0090:Folh1 UTSW 7 86,375,076 (GRCm39) splice site probably benign
R0285:Folh1 UTSW 7 86,391,373 (GRCm39) splice site probably benign
R0482:Folh1 UTSW 7 86,395,309 (GRCm39) splice site probably benign
R0492:Folh1 UTSW 7 86,395,400 (GRCm39) missense probably damaging 1.00
R1079:Folh1 UTSW 7 86,421,089 (GRCm39) missense probably damaging 1.00
R1148:Folh1 UTSW 7 86,410,938 (GRCm39) missense probably damaging 1.00
R1148:Folh1 UTSW 7 86,410,938 (GRCm39) missense probably damaging 1.00
R1493:Folh1 UTSW 7 86,410,938 (GRCm39) missense probably damaging 1.00
R1778:Folh1 UTSW 7 86,410,907 (GRCm39) critical splice donor site probably null
R1865:Folh1 UTSW 7 86,375,114 (GRCm39) missense possibly damaging 0.65
R1878:Folh1 UTSW 7 86,420,950 (GRCm39) missense probably benign
R1906:Folh1 UTSW 7 86,391,374 (GRCm39) splice site probably null
R2263:Folh1 UTSW 7 86,368,973 (GRCm39) missense probably benign
R3001:Folh1 UTSW 7 86,372,519 (GRCm39) missense probably damaging 1.00
R3002:Folh1 UTSW 7 86,372,519 (GRCm39) missense probably damaging 1.00
R3883:Folh1 UTSW 7 86,424,864 (GRCm39) missense possibly damaging 0.48
R4061:Folh1 UTSW 7 86,406,170 (GRCm39) missense possibly damaging 0.49
R4277:Folh1 UTSW 7 86,412,123 (GRCm39) critical splice donor site probably null
R4507:Folh1 UTSW 7 86,406,216 (GRCm39) missense probably benign
R4627:Folh1 UTSW 7 86,422,460 (GRCm39) missense probably benign 0.00
R4652:Folh1 UTSW 7 86,393,633 (GRCm39) nonsense probably null
R4653:Folh1 UTSW 7 86,393,633 (GRCm39) nonsense probably null
R4745:Folh1 UTSW 7 86,372,482 (GRCm39) critical splice donor site probably null
R5571:Folh1 UTSW 7 86,383,328 (GRCm39) missense probably damaging 1.00
R6000:Folh1 UTSW 7 86,375,142 (GRCm39) missense probably benign 0.01
R6307:Folh1 UTSW 7 86,372,517 (GRCm39) missense probably damaging 1.00
R6474:Folh1 UTSW 7 86,424,964 (GRCm39) missense probably damaging 0.99
R7112:Folh1 UTSW 7 86,424,845 (GRCm39) critical splice donor site probably null
R7131:Folh1 UTSW 7 86,375,320 (GRCm39) missense probably damaging 1.00
R7449:Folh1 UTSW 7 86,380,956 (GRCm39) missense probably benign 0.00
R7494:Folh1 UTSW 7 86,368,907 (GRCm39) missense probably damaging 1.00
R7539:Folh1 UTSW 7 86,375,117 (GRCm39) missense probably benign 0.35
R7764:Folh1 UTSW 7 86,412,126 (GRCm39) missense probably benign
R7803:Folh1 UTSW 7 86,375,306 (GRCm39) missense probably damaging 1.00
R8105:Folh1 UTSW 7 86,395,354 (GRCm39) missense probably damaging 1.00
R8208:Folh1 UTSW 7 86,375,125 (GRCm39) missense probably damaging 0.98
R8347:Folh1 UTSW 7 86,378,326 (GRCm39) nonsense probably null
R9130:Folh1 UTSW 7 86,368,913 (GRCm39) missense probably benign 0.12
R9749:Folh1 UTSW 7 86,368,908 (GRCm39) missense probably damaging 1.00
R9764:Folh1 UTSW 7 86,406,158 (GRCm39) missense probably benign 0.03
RF007:Folh1 UTSW 7 86,424,895 (GRCm39) missense probably benign
Z1088:Folh1 UTSW 7 86,375,162 (GRCm39) missense probably benign 0.00
Z1177:Folh1 UTSW 7 86,411,030 (GRCm39) missense probably benign 0.00
Z1177:Folh1 UTSW 7 86,393,655 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGCGCATCACTCCTATTGATC -3'
(R):5'- GGTTCATGTGTCATGGCACTC -3'

Sequencing Primer
(F):5'- GCATCACTCCTATTGATCTGTGTATG -3'
(R):5'- CATGGCACTCGTGGTGTTTTAGC -3'
Posted On 2014-06-30