Incidental Mutation 'R2121:Prl3c1'
Institutional Source Beutler Lab
Gene Symbol Prl3c1
Ensembl Gene ENSMUSG00000017922
Gene Nameprolactin family 3, subfamily c, member 1
SynonymsPrlpj, PLP-J, PLP I
MMRRC Submission 040125-MU
Accession Numbers

Genbank: NM_013766, NM_001163218

Is this an essential gene? Probably non essential (E-score: 0.066) question?
Stock #R2121 (G1)
Quality Score225
Status Validated
Chromosomal Location27196659-27203749 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to A at 27199342 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000136890 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000018066] [ENSMUST00000110364] [ENSMUST00000178072] [ENSMUST00000178072]
Predicted Effect probably null
Transcript: ENSMUST00000018066
AA Change: L17*
SMART Domains Protein: ENSMUSP00000018066
Gene: ENSMUSG00000017922
AA Change: L17*

Pfam:Hormone_1 16 212 1.5e-31 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000110364
SMART Domains Protein: ENSMUSP00000105993
Gene: ENSMUSG00000017922

Pfam:Hormone_1 2 192 2.9e-31 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000178072
SMART Domains Protein: ENSMUSP00000136890
Gene: ENSMUSG00000017922

Pfam:Hormone_1 2 192 2.9e-31 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000178072
SMART Domains Protein: ENSMUSP00000136890
Gene: ENSMUSG00000017922

Pfam:Hormone_1 2 192 2.9e-31 PFAM
Meta Mutation Damage Score 0.6336 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.2%
  • 20x: 95.1%
Validation Efficiency 100% (66/66)
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced female fertility and a male reproductive tract phenotype that includes enlarged testes and seminal vesicles, increased sperm count, increased serum testosterone and luteinizing hormone levels, and abnormal adult Leydig cell differentiation. [provided by MGI curators]
Allele List at MGI

All alleles(1) : Targeted, knock-out(1)

Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg5 T A 17: 84,671,147 E294D probably benign Het
Adnp2 A G 18: 80,129,170 F675L probably benign Het
Akna G A 4: 63,376,900 T1024I probably benign Het
Ambn T A 5: 88,460,758 probably benign Het
Aox3 T C 1: 58,152,549 probably benign Het
Arhgef10 A G 8: 14,934,820 D200G probably damaging Het
Arhgef26 A T 3: 62,340,283 N263Y probably damaging Het
Arpp21 A G 9: 112,136,670 S375P probably damaging Het
Bscl2 G T 19: 8,839,782 E25* probably null Het
Ccl12 T A 11: 82,101,950 S17R probably damaging Het
Cdh1 A G 8: 106,664,210 I653V probably benign Het
Ceacam9 T A 7: 16,722,003 F12I probably benign Het
Cldn23 A G 8: 35,826,235 V33A probably benign Het
Cog1 T C 11: 113,649,598 L13P probably damaging Het
Col20a1 G C 2: 180,996,456 A346P probably damaging Het
Col6a3 T C 1: 90,810,365 D537G probably damaging Het
Ctnnd2 G A 15: 30,669,514 R423H probably damaging Het
Cyp2a12 A G 7: 27,036,646 *493W probably null Het
Dcdc2a T G 13: 25,119,285 S266R possibly damaging Het
Diaph1 A T 18: 37,896,389 M330K unknown Het
Dnah5 C T 15: 28,297,005 probably benign Het
F13a1 T A 13: 37,025,679 Y104F probably benign Het
Fam78b G A 1: 167,078,709 V146M probably damaging Het
Fancl G T 11: 26,459,841 probably benign Het
Gm10477 A G X: 56,524,832 K31E probably damaging Het
Gm7173 T C X: 79,510,321 I267V probably benign Het
Gstm7 T C 3: 107,926,914 M175V probably benign Het
Hcn4 T C 9: 58,824,058 S183P unknown Het
Heatr1 T C 13: 12,403,264 V359A probably benign Het
Ikbkb T C 8: 22,667,217 probably benign Het
Ints6l T A X: 56,504,868 S718T probably benign Het
Kctd5 T C 17: 24,055,966 T212A probably benign Het
Kdm3b T C 18: 34,796,780 probably benign Het
Ltbp1 T A 17: 75,310,159 V1031E possibly damaging Het
Lyst A G 13: 13,660,971 Y1746C probably damaging Het
Mageb5 A G X: 91,780,095 I226T probably damaging Het
Mdc1 C T 17: 35,847,943 A405V probably benign Het
Mlc1 A G 15: 88,963,431 Y305H probably benign Het
Muc4 A G 16: 32,760,238 Y2474C unknown Het
Mybphl A C 3: 108,375,176 N175T probably damaging Het
Ncbp3 T C 11: 73,053,478 V102A possibly damaging Het
Neb A G 2: 52,264,064 F2345S probably damaging Het
Nlrp6 T C 7: 140,926,444 V766A probably benign Het
Olfr1045 T A 2: 86,197,996 Y252F possibly damaging Het
Olfr866 T G 9: 20,027,501 I146L probably benign Het
Palb2 T C 7: 122,127,781 T289A possibly damaging Het
Pde10a A T 17: 8,977,215 Q657L probably damaging Het
Ppp2r2a A T 14: 67,023,128 F234I probably damaging Het
Psg20 T A 7: 18,681,022 Y316F probably benign Het
Sap18 T A 14: 57,798,554 S66T probably damaging Het
Serpina3m A G 12: 104,389,682 M203V possibly damaging Het
Slc6a21 A T 7: 45,288,462 I726F probably benign Het
Soga1 T C 2: 157,033,325 E835G probably damaging Het
Syt10 C T 15: 89,790,776 D456N probably damaging Het
Tfdp2 T C 9: 96,295,014 S75P probably damaging Het
Thegl A T 5: 77,060,758 I378L probably benign Het
Tll1 T C 8: 64,085,557 E351G probably benign Het
Tmed11 G A 5: 108,795,332 probably benign Het
Tmem81 C A 1: 132,508,109 Q218K probably benign Het
Tnfsf11 G A 14: 78,299,893 T110I probably benign Het
Ttc25 T A 11: 100,567,011 probably null Het
Tub G A 7: 109,026,737 G232S probably damaging Het
Vmn2r121 A T X: 124,133,742 probably null Het
Vwa5b1 T C 4: 138,588,569 T621A probably benign Het
Ythdf3 T C 3: 16,205,192 F501S possibly damaging Het
Other mutations in Prl3c1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00337:Prl3c1 APN 13 27200763 missense probably damaging 0.97
IGL00567:Prl3c1 APN 13 27200712 missense possibly damaging 0.82
IGL01105:Prl3c1 APN 13 27202425 missense probably benign 0.04
IGL02985:Prl3c1 APN 13 27199387 missense probably damaging 0.99
IGL03013:Prl3c1 APN 13 27199366 missense probably benign 0.01
H8930:Prl3c1 UTSW 13 27200706 nonsense probably null
R0437:Prl3c1 UTSW 13 27199464 missense probably benign 0.09
R0630:Prl3c1 UTSW 13 27200691 splice site probably benign
R1277:Prl3c1 UTSW 13 27203572 missense probably damaging 1.00
R2064:Prl3c1 UTSW 13 27196737 critical splice donor site probably null
R4752:Prl3c1 UTSW 13 27203525 missense probably benign 0.11
R4959:Prl3c1 UTSW 13 27202488 splice site probably null
R5863:Prl3c1 UTSW 13 27203610 makesense probably null
Predicted Primers PCR Primer

Sequencing Primer
Posted On2014-09-18