Incidental Mutation 'R1405:Prl3a1'
ID262770
Institutional Source Beutler Lab
Gene Symbol Prl3a1
Ensembl Gene ENSMUSG00000038883
Gene Nameprolactin family 3, subfamily a, member 1
SynonymsPLP-I, 1600016E11Rik, Prlpi, Plpi, PLP-H
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.100) question?
Stock #R1405 (G1)
Quality Score138
Status Not validated
Chromosome13
Chromosomal Location27259436-27276667 bp(+) (GRCm38)
Type of Mutationintron
DNA Base Change (assembly) A to G at 27275068 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000046522 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049463]
Predicted Effect probably null
Transcript: ENSMUST00000049463
SMART Domains Protein: ENSMUSP00000046522
Gene: ENSMUSG00000038883

DomainStartEndE-ValueType
Pfam:Hormone_1 16 227 2.3e-59 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223739
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 96.7%
  • 10x: 83.5%
  • 20x: 53.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arap1 G A 7: 101,398,436 probably null Het
Asb8 G A 15: 98,141,367 H51Y possibly damaging Het
Capn10 T G 1: 92,945,022 V490G probably benign Het
Ccdc146 G A 5: 21,399,732 S36L probably benign Het
Celsr1 C T 15: 85,905,434 probably null Het
Clvs2 C A 10: 33,513,260 *328L probably null Het
Cul9 C G 17: 46,522,175 A1326P probably damaging Het
Dstn A G 2: 143,938,436 K19E probably damaging Het
Ehmt2 T A 17: 34,906,577 H134Q probably benign Het
Faah G A 4: 116,001,148 P411S probably damaging Het
Fn1 A G 1: 71,642,078 F364L probably damaging Het
Gm14124 T A 2: 150,267,700 Y103* probably null Het
Gmnc A T 16: 26,960,446 N270K possibly damaging Het
Grip2 A T 6: 91,788,152 probably null Het
Hmg20a A T 9: 56,477,303 Q119L possibly damaging Het
Ipo7 T C 7: 110,029,841 I106T probably benign Het
Ipo7 C T 7: 110,039,249 P241L probably damaging Het
Katnb1 T C 8: 95,098,173 Y574H probably damaging Het
Larp6 A C 9: 60,737,566 M330L probably benign Het
Lrrc8e T C 8: 4,231,754 Y30H probably damaging Het
Nop56 T C 2: 130,277,948 V420A probably benign Het
Nrg1 T C 8: 31,917,827 D126G probably benign Het
Prdm1 T A 10: 44,439,965 N725I probably damaging Het
Psmd2 T C 16: 20,652,284 L59P possibly damaging Het
Ptgdr2 T C 19: 10,941,031 V304A probably benign Het
Rasa3 A G 8: 13,588,027 V339A possibly damaging Het
Sec24c G A 14: 20,692,525 probably null Het
Serpinb9e A G 13: 33,260,026 D343G probably benign Het
Sfi1 TCGC TC 11: 3,146,254 probably null Het
Sfi1 CCTCTC CCTCTCTC 11: 3,177,419 probably benign Het
Stab1 A C 14: 31,149,001 V1297G probably benign Het
Stk4 C T 2: 164,100,528 T360M probably benign Het
Tmprss2 G A 16: 97,596,805 T57I probably benign Het
Tnrc6a A G 7: 123,171,078 D697G probably damaging Het
Vwa5b2 T A 16: 20,604,316 D1021E probably benign Het
Wdr46 C A 17: 33,949,083 P543Q probably damaging Het
Zfp287 T A 11: 62,728,311 D119V probably damaging Het
Zxdc A G 6: 90,384,243 S737G possibly damaging Het
Other mutations in Prl3a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02216:Prl3a1 APN 13 27270144 missense probably benign 0.13
IGL02648:Prl3a1 APN 13 27270235 missense probably benign 0.00
R1405:Prl3a1 UTSW 13 27275068 intron probably null
R1596:Prl3a1 UTSW 13 27259617 start gained probably benign
R1823:Prl3a1 UTSW 13 27270194 missense probably damaging 0.99
R1952:Prl3a1 UTSW 13 27270153 missense possibly damaging 0.91
R2059:Prl3a1 UTSW 13 27270144 missense probably benign 0.13
R5843:Prl3a1 UTSW 13 27270110 missense probably damaging 1.00
R6222:Prl3a1 UTSW 13 27276114 missense probably benign 0.05
R6664:Prl3a1 UTSW 13 27270211 nonsense probably null
R7077:Prl3a1 UTSW 13 27276103 missense probably benign 0.35
R7846:Prl3a1 UTSW 13 27272459 missense probably damaging 1.00
Predicted Primers
Posted On2015-02-04