Incidental Mutation 'R1965:Fam151a'
ID 218269
Institutional Source Beutler Lab
Gene Symbol Fam151a
Ensembl Gene ENSMUSG00000034871
Gene Name family with sequence simliarity 151, member A
Synonyms
MMRRC Submission 039978-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1965 (G1)
Quality Score 148
Status Not validated
Chromosome 4
Chromosomal Location 106591112-106605489 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 106591112 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000119211 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047620] [ENSMUST00000148281]
AlphaFold Q8QZW3
Predicted Effect probably benign
Transcript: ENSMUST00000047620
SMART Domains Protein: ENSMUSP00000047860
Gene: ENSMUSG00000034871

DomainStartEndE-ValueType
transmembrane domain 12 34 N/A INTRINSIC
Pfam:DUF2181 70 310 2.9e-107 PFAM
Pfam:DUF2181 342 579 8e-47 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000148281
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.6%
  • 20x: 93.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 88 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aco1 T G 4: 40,175,730 (GRCm39) L157R probably damaging Het
Acot11 A T 4: 106,606,550 (GRCm39) L513Q probably damaging Het
Amd1 A G 10: 40,170,755 (GRCm39) I52T probably benign Het
Ap2b1 T C 11: 83,237,721 (GRCm39) I557T probably benign Het
Arel1 T A 12: 84,987,173 (GRCm39) probably null Het
Arg1 T A 10: 24,792,762 (GRCm39) probably null Het
Atf1 A T 15: 100,152,052 (GRCm39) M135L probably benign Het
Atf2 T C 2: 73,681,242 (GRCm39) E77G possibly damaging Het
Axin1 G T 17: 26,403,199 (GRCm39) A394S probably damaging Het
Axin1 A T 17: 26,409,202 (GRCm39) Q734L probably damaging Het
Brd8 G C 18: 34,735,819 (GRCm39) A886G probably damaging Het
Ccdc39 T C 3: 33,880,629 (GRCm39) K446R probably damaging Het
Celf3 T C 3: 94,392,634 (GRCm39) V35A probably damaging Het
Cfap299 T A 5: 98,494,093 (GRCm39) D32E probably damaging Het
Ckap2 T C 8: 22,665,803 (GRCm39) T415A possibly damaging Het
Crybg3 T C 16: 59,323,600 (GRCm39) Y1066C probably damaging Het
Csmd3 T C 15: 47,713,144 (GRCm39) H1506R probably benign Het
Dnah10 A G 5: 124,852,267 (GRCm39) D1808G probably damaging Het
Dsc3 C T 18: 20,113,729 (GRCm39) G398R probably damaging Het
Emc2 A G 15: 43,390,863 (GRCm39) Q293R probably damaging Het
Evc2 A G 5: 37,520,876 (GRCm39) N251D possibly damaging Het
Fbxw16 T A 9: 109,270,289 (GRCm39) I151F probably damaging Het
Fmnl2 A G 2: 53,004,880 (GRCm39) D658G probably damaging Het
Fnip2 G A 3: 79,400,779 (GRCm39) T314I probably benign Het
Foxc2 T A 8: 121,843,413 (GRCm39) S20R probably damaging Het
Fpr-rs6 C T 17: 20,402,918 (GRCm39) G148R probably damaging Het
Fsip2 T C 2: 82,823,124 (GRCm39) S6286P possibly damaging Het
Fyb2 A T 4: 104,770,846 (GRCm39) I54F probably benign Het
Gbf1 T C 19: 46,260,003 (GRCm39) F999L probably damaging Het
Gldc G A 19: 30,114,513 (GRCm39) R466* probably null Het
Gm12695 T A 4: 96,651,082 (GRCm39) S124C probably benign Het
Gm4846 A T 1: 166,314,533 (GRCm39) I370N possibly damaging Het
Gsdmc3 T C 15: 63,730,296 (GRCm39) T423A probably damaging Het
Hjurp GT GTT 1: 88,194,246 (GRCm39) probably null Het
Jarid2 T A 13: 45,059,752 (GRCm39) N661K probably damaging Het
Kcnmb3 T C 3: 32,526,492 (GRCm39) Y233C probably damaging Het
Kidins220 A G 12: 25,044,905 (GRCm39) D191G probably damaging Het
Kmt2a A G 9: 44,732,757 (GRCm39) probably benign Het
Krt1 T C 15: 101,757,427 (GRCm39) D261G probably benign Het
Lrba A G 3: 86,513,175 (GRCm39) probably null Het
Myo1f C T 17: 33,817,146 (GRCm39) R730* probably null Het
Ncoa7 C A 10: 30,530,426 (GRCm39) E30* probably null Het
Neurod4 T A 10: 130,106,918 (GRCm39) K119* probably null Het
Npy5r T C 8: 67,133,929 (GRCm39) D288G probably benign Het
Nr3c2 A T 8: 77,636,092 (GRCm39) I398L probably damaging Het
Or10a5 T C 7: 106,635,565 (GRCm39) S68P probably damaging Het
Or12j4 C A 7: 140,046,574 (GRCm39) F153L probably benign Het
Or4b1 T C 2: 89,979,748 (GRCm39) S201G probably damaging Het
Or4k35 T C 2: 111,099,938 (GRCm39) Y258C probably damaging Het
Or51v8 A T 7: 103,320,103 (GRCm39) I45N probably damaging Het
Or5g25 T C 2: 85,478,090 (GRCm39) T192A possibly damaging Het
Or5w8 A G 2: 87,687,759 (GRCm39) K80R probably benign Het
Or9m1b A G 2: 87,836,648 (GRCm39) F149S probably damaging Het
P3r3urf G A 4: 116,031,376 (GRCm39) C82Y probably damaging Het
Pcf11 A T 7: 92,310,809 (GRCm39) M393K probably benign Het
Pck2 T C 14: 55,779,964 (GRCm39) V71A probably benign Het
Pdzd8 G T 19: 59,288,554 (GRCm39) L949I probably benign Het
Pdzrn4 G A 15: 92,644,190 (GRCm39) probably null Het
Phospho1 A G 11: 95,721,705 (GRCm39) N125S probably damaging Het
Pirb A T 7: 3,720,637 (GRCm39) L287Q probably benign Het
Ppid A T 3: 79,509,606 (GRCm39) K308* probably null Het
Ppp1r1b A G 11: 98,246,189 (GRCm39) E57G probably damaging Het
Prtg T G 9: 72,755,604 (GRCm39) S269A probably benign Het
Rbbp5 T A 1: 132,422,035 (GRCm39) S312T probably damaging Het
Rbm11 T A 16: 75,395,656 (GRCm39) probably null Het
Retreg1 A G 15: 25,970,250 (GRCm39) T139A probably damaging Het
Riok3 T A 18: 12,270,019 (GRCm39) H120Q probably damaging Het
Rln1 A T 19: 29,311,995 (GRCm39) M1K probably null Het
Rpp30 C T 19: 36,066,549 (GRCm39) S94L probably damaging Het
Sccpdh C T 1: 179,511,879 (GRCm39) P117L probably damaging Het
Serac1 T C 17: 6,099,274 (GRCm39) K506E possibly damaging Het
Serping1 G T 2: 84,596,072 (GRCm39) T454K probably damaging Het
Slc1a2 T A 2: 102,570,245 (GRCm39) N174K probably damaging Het
Slc2a2 A G 3: 28,773,634 (GRCm39) Q313R probably damaging Het
Slc46a2 T A 4: 59,914,249 (GRCm39) S225C probably damaging Het
Smarcc2 G A 10: 128,310,627 (GRCm39) E419K probably damaging Het
Stkld1 T A 2: 26,836,744 (GRCm39) probably null Het
Szt2 A G 4: 118,241,162 (GRCm39) M1704T probably benign Het
Tasor T G 14: 27,164,511 (GRCm39) C272W probably damaging Het
Tfcp2l1 C T 1: 118,580,653 (GRCm39) Q116* probably null Het
Timm44 A G 8: 4,310,603 (GRCm39) M383T possibly damaging Het
Tnpo2 G A 8: 85,771,946 (GRCm39) probably null Het
Tnrc6b A G 15: 80,764,640 (GRCm39) K714R probably damaging Het
Wdfy3 A G 5: 102,099,178 (GRCm39) L290P probably damaging Het
Wdr59 A G 8: 112,177,709 (GRCm39) F898L probably damaging Het
Zfp120 A T 2: 149,959,318 (GRCm39) C335S probably damaging Het
Zfp518a T C 19: 40,901,954 (GRCm39) S628P probably benign Het
Zfp879 A T 11: 50,724,355 (GRCm39) C234S probably damaging Het
Other mutations in Fam151a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01303:Fam151a APN 4 106,604,790 (GRCm39) missense possibly damaging 0.56
IGL02095:Fam151a APN 4 106,605,072 (GRCm39) missense probably damaging 1.00
IGL02170:Fam151a APN 4 106,592,795 (GRCm39) critical splice donor site probably null
IGL02725:Fam151a APN 4 106,605,211 (GRCm39) missense probably damaging 0.99
R0025:Fam151a UTSW 4 106,605,371 (GRCm39) missense probably benign 0.16
R0114:Fam151a UTSW 4 106,591,201 (GRCm39) missense possibly damaging 0.63
R0620:Fam151a UTSW 4 106,605,128 (GRCm39) missense probably benign 0.06
R1345:Fam151a UTSW 4 106,599,491 (GRCm39) missense probably damaging 0.99
R1482:Fam151a UTSW 4 106,602,876 (GRCm39) missense probably damaging 1.00
R2086:Fam151a UTSW 4 106,592,760 (GRCm39) splice site probably null
R4078:Fam151a UTSW 4 106,604,954 (GRCm39) missense probably benign 0.31
R4677:Fam151a UTSW 4 106,605,456 (GRCm39) missense possibly damaging 0.72
R6110:Fam151a UTSW 4 106,605,395 (GRCm39) missense probably damaging 0.98
R6188:Fam151a UTSW 4 106,602,696 (GRCm39) missense possibly damaging 0.61
R6288:Fam151a UTSW 4 106,605,341 (GRCm39) missense probably damaging 0.99
R6526:Fam151a UTSW 4 106,591,201 (GRCm39) missense possibly damaging 0.63
R7298:Fam151a UTSW 4 106,592,725 (GRCm39) missense possibly damaging 0.80
R7341:Fam151a UTSW 4 106,592,707 (GRCm39) missense probably benign 0.00
R7363:Fam151a UTSW 4 106,602,681 (GRCm39) missense probably damaging 1.00
R7573:Fam151a UTSW 4 106,600,502 (GRCm39) missense probably damaging 1.00
R8368:Fam151a UTSW 4 106,604,190 (GRCm39) missense probably benign 0.03
R8464:Fam151a UTSW 4 106,605,102 (GRCm39) missense probably benign 0.04
R8503:Fam151a UTSW 4 106,603,377 (GRCm39) missense possibly damaging 0.78
R8822:Fam151a UTSW 4 106,602,842 (GRCm39) missense probably benign 0.12
R8840:Fam151a UTSW 4 106,602,819 (GRCm39) missense probably benign 0.06
R8927:Fam151a UTSW 4 106,603,242 (GRCm39) unclassified probably benign
R9062:Fam151a UTSW 4 106,605,306 (GRCm39) missense probably benign 0.01
R9076:Fam151a UTSW 4 106,603,254 (GRCm39) missense probably damaging 1.00
R9140:Fam151a UTSW 4 106,605,344 (GRCm39) nonsense probably null
R9663:Fam151a UTSW 4 106,604,894 (GRCm39) missense possibly damaging 0.84
Predicted Primers PCR Primer
(F):5'- CAACGTTCCCAAGTTCATTTGG -3'
(R):5'- TGGATACATGGGCAGAGCTC -3'

Sequencing Primer
(F):5'- CCAAGTTCATTTGGGAGGTGGC -3'
(R):5'- TGGGCAGAGCTCAGTGAG -3'
Posted On 2014-08-01