Incidental Mutation 'R4030:Serpina3n'
ID313190
Institutional Source Beutler Lab
Gene Symbol Serpina3n
Ensembl Gene ENSMUSG00000021091
Gene Nameserine (or cysteine) peptidase inhibitor, clade A, member 3N
Synonymsantitrypsin, Spi2/eb.4, alpha-1 antiproteinase, Spi2.2, Spi2-2
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R4030 (G1)
Quality Score225
Status Not validated
Chromosome12
Chromosomal Location104406729-104414329 bp(+) (GRCm38)
Type of Mutationcritical splice donor site (1 bp from exon)
DNA Base Change (assembly) G to T at 104411401 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000021506 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021506]
Predicted Effect probably null
Transcript: ENSMUST00000021506
SMART Domains Protein: ENSMUSP00000021506
Gene: ENSMUSG00000021091

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
SERPIN 56 417 7.64e-194 SMART
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700019A02Rik A G 1: 53,182,509 S54P probably benign Het
2700062C07Rik C T 18: 24,475,658 P145L probably benign Het
Akap3 A T 6: 126,865,021 D201V probably damaging Het
Ank A G 15: 27,544,257 N35D probably damaging Het
Bpifb2 T C 2: 153,891,317 S400P probably benign Het
Brd7 A T 8: 88,332,931 I617N probably damaging Het
Cdhr2 C A 13: 54,717,861 P224Q probably damaging Het
Cdon A G 9: 35,491,906 N1104S probably damaging Het
Ceacam3 T C 7: 17,158,342 Y337H probably benign Het
Chrna5 T C 9: 54,998,086 W61R probably damaging Het
Cntnap2 C A 6: 46,856,128 F758L probably benign Het
Cpsf1 G A 15: 76,601,779 T397M possibly damaging Het
Crhr2 T C 6: 55,117,677 D32G probably benign Het
Dip2b A G 15: 100,186,172 Y892C probably damaging Het
Dpyd A G 3: 118,897,166 D308G probably benign Het
Dsp A G 13: 38,191,428 N1063S possibly damaging Het
E030030I06Rik C A 10: 22,149,000 G5C unknown Het
Ehbp1 T C 11: 22,285,498 T32A probably damaging Het
Fam159a G T 4: 108,383,215 C43* probably null Het
Fbxo9 C A 9: 78,098,341 probably null Het
Gm13101 T A 4: 143,965,784 T216S probably benign Het
Gpatch3 G A 4: 133,578,147 R231H possibly damaging Het
Gpr68 A G 12: 100,879,216 L23P probably damaging Het
H2-Q6 C A 17: 35,425,816 Q194K probably benign Het
Hmgb1 A G 5: 149,050,700 M13T probably benign Het
Kdm5a T A 6: 120,405,113 L706* probably null Het
Krt12 A T 11: 99,422,028 F63L unknown Het
Lefty1 T C 1: 180,937,781 S305P probably benign Het
Lgr4 T C 2: 109,989,751 S102P probably benign Het
Loxl4 A T 19: 42,608,359 V71E probably damaging Het
Lrrc36 A C 8: 105,426,807 N83T probably damaging Het
Med26 G A 8: 72,496,569 R229C probably damaging Het
Mgam G A 6: 40,754,902 R1351Q probably damaging Het
Mkl1 G A 15: 81,015,784 T729I probably benign Het
Mroh8 T A 2: 157,213,720 D986V probably damaging Het
Mrpl49 T C 19: 6,055,200 D77G probably benign Het
Mrps30 T C 13: 118,380,541 N381D probably damaging Het
Olfr1248 C A 2: 89,617,863 V110F probably damaging Het
Omd T A 13: 49,589,649 N58K probably benign Het
Oog4 A T 4: 143,440,200 N11K probably benign Het
Plpp5 T A 8: 25,720,604 L74Q probably damaging Het
Prex2 T A 1: 11,208,568 Y1374N probably benign Het
Rbak A T 5: 143,173,969 I443K probably damaging Het
Rhpn1 A T 15: 75,710,557 S195C probably damaging Het
Rnf115 T A 3: 96,785,983 I210N probably damaging Het
Rock2 G A 12: 16,975,479 V1234I probably damaging Het
Scube2 A G 7: 109,831,771 V407A probably benign Het
Slco2b1 A G 7: 99,682,825 L283P probably damaging Het
Spag1 G A 15: 36,234,301 V736M probably damaging Het
Srebf2 T A 15: 82,178,783 C434S probably damaging Het
Ston2 T C 12: 91,648,263 Q457R possibly damaging Het
Trhr2 T C 8: 122,360,699 M1V probably null Het
Tshz1 T C 18: 84,014,829 K485E possibly damaging Het
Ttn T A 2: 76,754,824 I22042F probably damaging Het
Vmn2r105 T C 17: 20,208,754 R687G probably damaging Het
Vmn2r73 T C 7: 85,871,836 Y308C possibly damaging Het
Wdr49 C A 3: 75,323,665 L563F probably benign Het
Zfyve9 A G 4: 108,719,701 V61A possibly damaging Het
Other mutations in Serpina3n
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00534:Serpina3n APN 12 104412345 missense probably benign 0.39
IGL01930:Serpina3n APN 12 104408972 missense probably damaging 1.00
IGL01989:Serpina3n APN 12 104413491 missense probably benign
IGL02419:Serpina3n APN 12 104413518 missense possibly damaging 0.95
R0098:Serpina3n UTSW 12 104413518 missense probably damaging 1.00
R0098:Serpina3n UTSW 12 104413518 missense probably damaging 1.00
R0149:Serpina3n UTSW 12 104411376 missense probably benign 0.03
R1872:Serpina3n UTSW 12 104408944 missense probably benign 0.33
R1879:Serpina3n UTSW 12 104408954 missense probably benign 0.16
R2018:Serpina3n UTSW 12 104409214 missense probably damaging 0.97
R2315:Serpina3n UTSW 12 104412368 missense possibly damaging 0.77
R2968:Serpina3n UTSW 12 104409074 missense probably benign 0.12
R2969:Serpina3n UTSW 12 104409074 missense probably benign 0.12
R2970:Serpina3n UTSW 12 104409074 missense probably benign 0.12
R3409:Serpina3n UTSW 12 104411277 missense possibly damaging 0.93
R3410:Serpina3n UTSW 12 104411277 missense possibly damaging 0.93
R3411:Serpina3n UTSW 12 104411277 missense possibly damaging 0.93
R4388:Serpina3n UTSW 12 104411357 missense probably benign 0.11
R4659:Serpina3n UTSW 12 104413493 missense probably benign 0.03
R4728:Serpina3n UTSW 12 104409163 missense probably benign
R4783:Serpina3n UTSW 12 104409110 missense possibly damaging 0.84
R5001:Serpina3n UTSW 12 104408739 missense probably benign 0.00
R5983:Serpina3n UTSW 12 104409029 missense probably damaging 1.00
R6767:Serpina3n UTSW 12 104409062 missense probably benign 0.01
R7001:Serpina3n UTSW 12 104408925 missense probably benign 0.00
R7468:Serpina3n UTSW 12 104411397 missense probably benign 0.16
X0027:Serpina3n UTSW 12 104411187 missense probably benign 0.00
X0067:Serpina3n UTSW 12 104411270 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ATGAGCATGGAGGACCTGAC -3'
(R):5'- TCTAGCTGAGCCCATCTTGTG -3'

Sequencing Primer
(F):5'- TGGAGGACCTGACCACAC -3'
(R):5'- GAGCCCATCTTGTGAACATTGACAG -3'
Posted On2015-04-30