Incidental Mutation 'R5851:Fam174a'
ID 454645
Institutional Source Beutler Lab
Gene Symbol Fam174a
Ensembl Gene ENSMUSG00000051185
Gene Name family with sequence similarity 174, member A
Synonyms Tmem157, 2310044D20Rik
MMRRC Submission 044067-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # R5851 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 95241353-95263009 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 95252868 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Serine at position 157 (G157S)
Ref Sequence ENSEMBL: ENSMUSP00000139943 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059975] [ENSMUST00000186780]
AlphaFold Q9D3L0
Predicted Effect probably damaging
Transcript: ENSMUST00000059975
AA Change: G157S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000057670
Gene: ENSMUSG00000051185
AA Change: G157S

DomainStartEndE-ValueType
Pfam:DUF1180 10 190 1.9e-69 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000186780
AA Change: G157S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000139943
Gene: ENSMUSG00000051185
AA Change: G157S

DomainStartEndE-ValueType
Pfam:DUF1180 1 190 5.7e-72 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000193380
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.0%
  • 20x: 94.0%
Validation Efficiency 100% (75/75)
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca2 A G 2: 25,332,322 (GRCm39) N1452D possibly damaging Het
Abhd15 T C 11: 77,409,273 (GRCm39) L329P probably benign Het
Add3 T C 19: 53,225,205 (GRCm39) S442P probably damaging Het
Arhgef18 T C 8: 3,484,980 (GRCm39) F228L probably damaging Het
Bptf A T 11: 107,001,688 (GRCm39) Y475N probably damaging Het
C3 T C 17: 57,518,612 (GRCm39) N1257S probably null Het
Cdkl1 A T 12: 69,803,338 (GRCm39) Y179* probably null Het
Ceacam1 T C 7: 25,174,025 (GRCm39) N210S possibly damaging Het
Celf3 T A 3: 94,386,433 (GRCm39) I7N probably damaging Het
Clxn T A 16: 14,738,300 (GRCm39) L155H probably damaging Het
Cmpk1 A G 4: 114,844,167 (GRCm39) V55A possibly damaging Het
Csrnp1 C T 9: 119,802,144 (GRCm39) G305D possibly damaging Het
Dnah3 A G 7: 119,638,585 (GRCm39) S1266P possibly damaging Het
Edc4 T C 8: 106,617,499 (GRCm39) L1077P probably damaging Het
Fubp3 T A 2: 31,488,622 (GRCm39) D159E probably benign Het
Garem2 C T 5: 30,319,288 (GRCm39) T250M probably damaging Het
H2-Eb1 C T 17: 34,528,745 (GRCm39) P92L probably benign Het
Ifnl3 G T 7: 28,222,936 (GRCm39) C69F probably damaging Het
Itga2b C A 11: 102,348,427 (GRCm39) probably benign Het
Klhl33 A T 14: 51,130,335 (GRCm39) D386E probably damaging Het
Lin9 T A 1: 180,496,763 (GRCm39) L351I probably benign Het
Loricrin G A 3: 91,987,846 (GRCm39) A480V unknown Het
Msh3 G T 13: 92,352,030 (GRCm39) Q1041K probably benign Het
Mtrex G A 13: 113,045,486 (GRCm39) R349W probably damaging Het
Myo1e G A 9: 70,291,086 (GRCm39) G959E probably benign Het
Nfat5 G T 8: 108,074,359 (GRCm39) V338L probably damaging Het
Nrf1 A G 6: 30,089,975 (GRCm39) H18R possibly damaging Het
Nup160 A G 2: 90,537,382 (GRCm39) D752G probably benign Het
Obscn A T 11: 58,885,526 (GRCm39) L2489* probably null Het
Or4p22 A G 2: 88,317,204 (GRCm39) I43V possibly damaging Het
Or51q1c A G 7: 103,652,659 (GRCm39) E59G probably benign Het
Paip1 T C 13: 119,577,301 (GRCm39) S215P possibly damaging Het
Pate2 T A 9: 35,581,797 (GRCm39) Y26* probably null Het
Pcdhb10 A G 18: 37,545,811 (GRCm39) I296V probably benign Het
Pdzph1 T G 17: 59,280,741 (GRCm39) T514P probably benign Het
Pnlip G A 19: 58,662,224 (GRCm39) W123* probably null Het
Prmt2 C A 10: 76,072,574 (GRCm39) C9F possibly damaging Het
Rbl1 T A 2: 157,009,245 (GRCm39) K763N probably benign Het
Rfk C T 19: 17,372,562 (GRCm39) A28V probably damaging Het
Scart1 C T 7: 139,807,940 (GRCm39) P704S possibly damaging Het
Sdk1 G A 5: 141,948,424 (GRCm39) V590I probably benign Het
Sele A G 1: 163,877,143 (GRCm39) K140E probably benign Het
Sla G A 15: 66,655,572 (GRCm39) T189I probably damaging Het
Slc46a2 A G 4: 59,913,906 (GRCm39) V339A probably damaging Het
Slc5a9 A G 4: 111,742,797 (GRCm39) F432L probably benign Het
Slc6a19 A G 13: 73,839,859 (GRCm39) F141S possibly damaging Het
Tas2r123 T C 6: 132,824,271 (GRCm39) L56S probably damaging Het
Tektip1 A T 10: 81,200,711 (GRCm39) probably null Het
Tmem245 T C 4: 56,916,770 (GRCm39) I53V probably benign Het
Tor2a A T 2: 32,651,619 (GRCm39) Q278L probably benign Het
Trav6-3 A G 14: 53,667,572 (GRCm39) M15V probably benign Het
Ttc28 G A 5: 111,383,335 (GRCm39) probably benign Het
Ubap2 G A 4: 41,206,268 (GRCm39) Q534* probably null Het
Yju2 C T 17: 56,274,582 (GRCm39) S298F probably damaging Het
Zfp954 C A 7: 7,118,624 (GRCm39) E307* probably null Het
Zscan21 A G 5: 138,124,740 (GRCm39) K219E probably benign Het
Other mutations in Fam174a
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1866:Fam174a UTSW 1 95,241,620 (GRCm39) missense probably benign 0.00
R3761:Fam174a UTSW 1 95,241,971 (GRCm39) missense probably damaging 1.00
R4492:Fam174a UTSW 1 95,241,701 (GRCm39) missense probably benign
R4716:Fam174a UTSW 1 95,241,770 (GRCm39) missense probably benign 0.10
R5617:Fam174a UTSW 1 95,241,972 (GRCm39) missense probably damaging 1.00
R5893:Fam174a UTSW 1 95,252,884 (GRCm39) missense probably damaging 1.00
R6230:Fam174a UTSW 1 95,241,951 (GRCm39) missense probably damaging 1.00
R7053:Fam174a UTSW 1 95,252,953 (GRCm39) missense probably damaging 0.96
R8994:Fam174a UTSW 1 95,241,689 (GRCm39) missense possibly damaging 0.80
Predicted Primers PCR Primer
(F):5'- GGTTTCCAGGAATCCTTTGTGC -3'
(R):5'- CTGCTGGAATAAAGCCTGTAAAATG -3'

Sequencing Primer
(F):5'- CCAGGAATCCTTTGTGCTAAATTG -3'
(R):5'- GATAGTGTACTTCAACTGTCTGAGC -3'
Posted On 2017-02-10