Incidental Mutation 'R4831:Farp1'
ID 372844
Institutional Source Beutler Lab
Gene Symbol Farp1
Ensembl Gene ENSMUSG00000025555
Gene Name FERM, ARH/RhoGEF and pleckstrin domain protein 1
Synonyms Cdep
MMRRC Submission 042447-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4831 (G1)
Quality Score 169
Status Validated
Chromosome 14
Chromosomal Location 121272612-121521156 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 121514469 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Threonine at position 933 (A933T)
Ref Sequence ENSEMBL: ENSMUSP00000026635 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026635]
AlphaFold F8VPU2
Predicted Effect probably damaging
Transcript: ENSMUST00000026635
AA Change: A933T

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000026635
Gene: ENSMUSG00000025555
AA Change: A933T

DomainStartEndE-ValueType
B41 36 230 3.27e-68 SMART
FERM_C 234 324 3.87e-32 SMART
FA 328 374 6.07e-16 SMART
RhoGEF 546 732 2.07e-47 SMART
PH 763 861 1.05e-16 SMART
PH 936 1034 1.55e-19 SMART
Meta Mutation Damage Score 0.1513 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.6%
  • 20x: 93.3%
Validation Efficiency 99% (96/97)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein containing a FERM (4.2, exrin, radixin, moesin) domain, a Dbl homology domain, and two pleckstrin homology domains. These domains are found in guanine nucleotide exchange factors and proteins that link the cytoskeleton to the cell membrane. The encoded protein functions in neurons to promote dendritic growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]
Allele List at MGI
Other mutations in this stock
Total: 92 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810408A11Rik C T 11: 69,791,403 (GRCm39) V59I possibly damaging Het
4930544M13Rik T G 13: 114,744,183 (GRCm39) noncoding transcript Het
Abca13 A T 11: 9,492,077 (GRCm39) K4373* probably null Het
Abtb2 A T 2: 103,513,820 (GRCm39) T410S probably benign Het
Adamts13 T C 2: 26,873,142 (GRCm39) probably null Het
Ahnak2 C G 12: 112,742,183 (GRCm39) D630H probably damaging Het
Aox3 T C 1: 58,191,725 (GRCm39) S426P probably damaging Het
Atxn10 C T 15: 85,271,260 (GRCm39) S266F probably benign Het
B4galnt4 G T 7: 140,647,634 (GRCm39) M407I probably damaging Het
B4galnt4 T A 7: 140,644,470 (GRCm39) probably null Het
Bclaf1 T A 10: 20,197,872 (GRCm39) probably benign Het
C4b C T 17: 34,955,864 (GRCm39) probably null Het
Cdc42bpg T C 19: 6,361,365 (GRCm39) F297S probably damaging Het
Cdh10 A T 15: 19,013,664 (GRCm39) T755S probably benign Het
Ceacam12 T A 7: 17,811,305 (GRCm39) probably null Het
Cfap65 C A 1: 74,956,454 (GRCm39) V1042F possibly damaging Het
Cfap77 T C 2: 28,875,844 (GRCm39) I89V probably benign Het
Cfh T C 1: 140,014,125 (GRCm39) D688G probably benign Het
Clip1 C G 5: 123,721,664 (GRCm39) A1182P probably damaging Het
Cyp2b10 T A 7: 25,614,921 (GRCm39) Y309* probably null Het
Dcaf5 T C 12: 80,385,858 (GRCm39) E756G probably benign Het
Dctn1 A T 6: 83,176,753 (GRCm39) Q1231L possibly damaging Het
Dennd1c T A 17: 57,373,428 (GRCm39) R682* probably null Het
Eml6 C A 11: 29,727,052 (GRCm39) E1319* probably null Het
Erap1 T C 13: 74,838,766 (GRCm39) I904T probably damaging Het
Eri1 A T 8: 35,943,673 (GRCm39) I207N possibly damaging Het
Fcna T A 2: 25,515,353 (GRCm39) Q210L probably benign Het
Fhad1 A T 4: 141,643,378 (GRCm39) probably null Het
Fut8 T G 12: 77,440,603 (GRCm39) Y197D probably damaging Het
Garem1 G A 18: 21,262,825 (GRCm39) T663I probably benign Het
Gfm2 T C 13: 97,301,546 (GRCm39) S450P probably damaging Het
Gstk1 T G 6: 42,222,938 (GRCm39) probably benign Het
Helz2 C T 2: 180,879,210 (GRCm39) A803T probably damaging Het
Igsf9 T A 1: 172,319,455 (GRCm39) I280N probably damaging Het
Klhl10 A G 11: 100,336,669 (GRCm39) K219E probably benign Het
L3mbtl4 T A 17: 68,768,558 (GRCm39) V222D probably damaging Het
Lrrc9 A T 12: 72,546,453 (GRCm39) N1214Y probably damaging Het
Ltbp2 C T 12: 84,840,414 (GRCm39) E1051K possibly damaging Het
Mettl17 T C 14: 52,122,440 (GRCm39) F13S probably benign Het
Mettl24 C A 10: 40,559,413 (GRCm39) A21D possibly damaging Het
Mfsd6l T A 11: 68,447,331 (GRCm39) C61S probably benign Het
Mob4 T G 1: 55,191,899 (GRCm39) D204E probably benign Het
Mtus1 C G 8: 41,536,189 (GRCm39) R509T probably damaging Het
Nlrp4a T A 7: 26,149,844 (GRCm39) F484I possibly damaging Het
Nsrp1 T C 11: 76,941,444 (GRCm39) N88S probably benign Het
Odad2 G T 18: 7,222,564 (GRCm39) H568Q possibly damaging Het
Or10d5 C T 9: 39,861,408 (GRCm39) V220I probably benign Het
Or2g25 T A 17: 37,970,969 (GRCm39) H85L probably benign Het
Or51b6b T C 7: 103,309,678 (GRCm39) T260A probably benign Het
Or6c2 T A 10: 129,362,449 (GRCm39) Y118N probably damaging Het
Parg A G 14: 31,924,408 (GRCm39) N69S probably benign Het
Pcdh9 A C 14: 94,125,377 (GRCm39) N264K probably damaging Het
Pcdhb22 G T 18: 37,653,615 (GRCm39) L694F probably damaging Het
Pcnt T C 10: 76,248,335 (GRCm39) E928G probably damaging Het
Pdzk1 G A 3: 96,775,751 (GRCm39) G373D probably benign Het
Pea15a A G 1: 172,026,740 (GRCm39) I89T probably damaging Het
Phc1 T A 6: 122,313,964 (GRCm39) probably benign Het
Pikfyve T A 1: 65,235,900 (GRCm39) C191S probably damaging Het
Pitpnm1 T A 19: 4,158,130 (GRCm39) D573E probably damaging Het
Pld5 A G 1: 176,102,450 (GRCm39) probably benign Het
Plscr2 A T 9: 92,173,130 (GRCm39) N89I possibly damaging Het
Pm20d2 A C 4: 33,179,293 (GRCm39) N315K probably damaging Het
Pnpla1 T A 17: 29,097,518 (GRCm39) M228K probably benign Het
Prim2 T C 1: 33,709,217 (GRCm39) probably benign Het
Ralgapa2 A G 2: 146,246,987 (GRCm39) probably benign Het
Rgs22 G T 15: 36,050,294 (GRCm39) H719N probably benign Het
Ror2 C T 13: 53,272,880 (GRCm39) D250N probably damaging Het
Saal1 A G 7: 46,349,071 (GRCm39) V281A probably benign Het
Selenof A T 3: 144,296,411 (GRCm39) K94N probably damaging Het
Slamf9 T A 1: 172,304,831 (GRCm39) C148* probably null Het
Slc4a7 T C 14: 14,772,699 (GRCm38) probably null Het
Slco1a5 A G 6: 142,180,431 (GRCm39) I657T probably benign Het
St3gal2 A T 8: 111,684,480 (GRCm39) H46L probably benign Het
Sucnr1 T G 3: 59,994,069 (GRCm39) M199R probably damaging Het
Taok1 T A 11: 77,444,500 (GRCm39) E525V probably null Het
Tbc1d10c T A 19: 4,235,445 (GRCm39) E298V probably damaging Het
Tll2 T A 19: 41,118,951 (GRCm39) H259L probably damaging Het
Tpcn1 A T 5: 120,691,554 (GRCm39) F300Y probably damaging Het
Uba6 T A 5: 86,279,197 (GRCm39) I642L probably benign Het
Ubqln5 T A 7: 103,778,829 (GRCm39) probably benign Het
Vmn1r27 A T 6: 58,192,827 (GRCm39) L9Q possibly damaging Het
Vmn2r100 C T 17: 19,741,672 (GRCm39) T128I probably benign Het
Vmn2r109 C T 17: 20,761,494 (GRCm39) G621D probably benign Het
Vmn2r49 C T 7: 9,720,352 (GRCm39) D380N probably benign Het
Vps13a C T 19: 16,655,356 (GRCm39) V1891I probably benign Het
Wbp2 G T 11: 115,971,463 (GRCm39) Y147* probably null Het
Wdr46 T A 17: 34,160,810 (GRCm39) N191K probably benign Het
Wdr46 T C 17: 34,168,373 (GRCm39) probably benign Het
Wnt2 A C 6: 18,023,285 (GRCm39) F121L probably benign Het
Xpnpep1 T A 19: 53,003,053 (GRCm39) D100V probably benign Het
Xpo4 T C 14: 57,827,559 (GRCm39) Y879C probably damaging Het
Zswim4 A T 8: 84,938,948 (GRCm39) V978D probably damaging Het
Other mutations in Farp1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00584:Farp1 APN 14 121,474,561 (GRCm39) missense probably damaging 1.00
IGL01017:Farp1 APN 14 121,510,186 (GRCm39) missense possibly damaging 0.64
IGL02309:Farp1 APN 14 121,480,928 (GRCm39) missense probably benign
IGL02376:Farp1 APN 14 121,510,268 (GRCm39) missense probably damaging 0.98
IGL03018:Farp1 APN 14 121,339,581 (GRCm39) missense probably benign
IGL03400:Farp1 APN 14 121,444,733 (GRCm39) missense probably damaging 1.00
R0034:Farp1 UTSW 14 121,492,841 (GRCm39) missense probably benign 0.00
R0046:Farp1 UTSW 14 121,492,925 (GRCm39) missense probably benign 0.00
R0046:Farp1 UTSW 14 121,492,925 (GRCm39) missense probably benign 0.00
R0219:Farp1 UTSW 14 121,481,012 (GRCm39) missense possibly damaging 0.88
R0359:Farp1 UTSW 14 121,492,808 (GRCm39) splice site probably benign
R0616:Farp1 UTSW 14 121,514,434 (GRCm39) missense probably damaging 1.00
R0653:Farp1 UTSW 14 121,471,258 (GRCm39) critical splice donor site probably null
R0710:Farp1 UTSW 14 121,474,555 (GRCm39) missense probably damaging 1.00
R1391:Farp1 UTSW 14 121,495,378 (GRCm39) nonsense probably null
R1791:Farp1 UTSW 14 121,494,157 (GRCm39) missense probably damaging 1.00
R1920:Farp1 UTSW 14 121,492,908 (GRCm39) missense probably benign 0.16
R1953:Farp1 UTSW 14 121,492,894 (GRCm39) missense probably benign
R1958:Farp1 UTSW 14 121,456,787 (GRCm39) critical splice acceptor site probably null
R2891:Farp1 UTSW 14 121,494,148 (GRCm39) missense probably damaging 1.00
R3121:Farp1 UTSW 14 121,460,138 (GRCm39) splice site probably benign
R4005:Farp1 UTSW 14 121,513,809 (GRCm39) missense probably damaging 0.99
R4257:Farp1 UTSW 14 121,492,891 (GRCm39) missense probably benign 0.00
R4559:Farp1 UTSW 14 121,510,213 (GRCm39) missense probably damaging 1.00
R4654:Farp1 UTSW 14 121,513,716 (GRCm39) missense possibly damaging 0.50
R4739:Farp1 UTSW 14 121,476,199 (GRCm39) missense probably damaging 1.00
R4988:Farp1 UTSW 14 121,513,019 (GRCm39) missense probably damaging 1.00
R5379:Farp1 UTSW 14 121,494,169 (GRCm39) missense possibly damaging 0.88
R5463:Farp1 UTSW 14 121,472,489 (GRCm39) missense probably damaging 1.00
R5466:Farp1 UTSW 14 121,472,489 (GRCm39) missense probably damaging 1.00
R5467:Farp1 UTSW 14 121,472,489 (GRCm39) missense probably damaging 1.00
R5511:Farp1 UTSW 14 121,474,584 (GRCm39) missense probably damaging 0.98
R5520:Farp1 UTSW 14 121,472,489 (GRCm39) missense probably damaging 1.00
R5635:Farp1 UTSW 14 121,513,716 (GRCm39) missense possibly damaging 0.96
R5639:Farp1 UTSW 14 121,512,794 (GRCm39) missense probably damaging 1.00
R5954:Farp1 UTSW 14 121,460,079 (GRCm39) missense probably damaging 0.99
R6765:Farp1 UTSW 14 121,460,066 (GRCm39) missense probably benign 0.00
R7469:Farp1 UTSW 14 121,512,833 (GRCm39) missense probably damaging 1.00
R7549:Farp1 UTSW 14 121,472,589 (GRCm39) missense possibly damaging 0.89
R7660:Farp1 UTSW 14 121,514,334 (GRCm39) missense probably benign 0.00
R7752:Farp1 UTSW 14 121,495,359 (GRCm39) missense probably damaging 1.00
R7788:Farp1 UTSW 14 121,513,665 (GRCm39) missense probably benign 0.12
R7911:Farp1 UTSW 14 121,479,818 (GRCm39) missense probably damaging 1.00
R8013:Farp1 UTSW 14 121,479,813 (GRCm39) missense probably damaging 1.00
R8078:Farp1 UTSW 14 121,513,712 (GRCm39) missense probably benign 0.04
R8113:Farp1 UTSW 14 121,513,008 (GRCm39) missense probably benign 0.35
R8116:Farp1 UTSW 14 121,471,232 (GRCm39) missense probably damaging 1.00
R8716:Farp1 UTSW 14 121,479,855 (GRCm39) missense probably benign
R9103:Farp1 UTSW 14 121,509,104 (GRCm39) missense possibly damaging 0.55
R9190:Farp1 UTSW 14 121,492,988 (GRCm39) missense probably damaging 0.97
R9193:Farp1 UTSW 14 121,518,281 (GRCm39) missense probably benign 0.34
R9581:Farp1 UTSW 14 121,480,841 (GRCm39) missense probably benign 0.09
RF024:Farp1 UTSW 14 121,474,560 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TAACCTTCTGCAGAGTCCCC -3'
(R):5'- ACAAGGGCAGAATCTTGCCC -3'

Sequencing Primer
(F):5'- TGCAGAGTCCCCGGATGAAG -3'
(R):5'- CAGGGAATCTGCACTGCATTTAC -3'
Posted On 2016-03-01