Incidental Mutation 'IGL02216:Prl3a1'
ID 284903
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prl3a1
Ensembl Gene ENSMUSG00000038883
Gene Name prolactin family 3, subfamily a, member 1
Synonyms Prlpi, PLP-I, 1600016E11Rik, PLP-H, Plpi
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL02216
Quality Score
Status
Chromosome 13
Chromosomal Location 27443472-27460669 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 27454127 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 35 (D35G)
Ref Sequence ENSEMBL: ENSMUSP00000046522 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049463]
AlphaFold Q78Y73
Predicted Effect probably benign
Transcript: ENSMUST00000049463
AA Change: D35G

PolyPhen 2 Score 0.129 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000046522
Gene: ENSMUSG00000038883
AA Change: D35G

DomainStartEndE-ValueType
Pfam:Hormone_1 16 227 2.3e-59 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223739
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930544D05Rik T C 11: 70,507,005 (GRCm39) F48L possibly damaging Het
Adamts12 A G 15: 11,241,571 (GRCm39) N381S possibly damaging Het
Akp3 A T 1: 87,055,372 (GRCm39) Q473L probably damaging Het
Albfm1 T C 5: 90,727,438 (GRCm39) probably benign Het
Ap5s1 T A 2: 131,054,887 (GRCm39) probably benign Het
Atp10b T A 11: 43,150,616 (GRCm39) L1438Q probably damaging Het
B3galt4 G A 17: 34,169,539 (GRCm39) P233L probably damaging Het
Brd8 C T 18: 34,735,780 (GRCm39) S899N probably damaging Het
Cc2d1a C A 8: 84,865,942 (GRCm39) E393* probably null Het
Cd209a G T 8: 3,795,576 (GRCm39) T165N probably damaging Het
Chid1 T C 7: 141,076,506 (GRCm39) probably benign Het
Cln3 A T 7: 126,174,514 (GRCm39) probably null Het
Cped1 A T 6: 22,059,944 (GRCm39) R203S probably damaging Het
Dele1 A T 18: 38,385,913 (GRCm39) I102F probably damaging Het
Dnttip2 G T 3: 122,069,910 (GRCm39) W375L probably benign Het
Dync1h1 T C 12: 110,629,436 (GRCm39) F4280S probably damaging Het
Ephb4 A G 5: 137,370,332 (GRCm39) D844G possibly damaging Het
Fhl2 T A 1: 43,170,879 (GRCm39) E145V probably null Het
Gne T C 4: 44,044,761 (GRCm39) K458E probably benign Het
Grid2 G T 6: 64,322,650 (GRCm39) R550L probably damaging Het
Klhl1 T A 14: 96,360,658 (GRCm39) T731S probably benign Het
Kng1 T A 16: 22,877,283 (GRCm39) D30E probably damaging Het
Kyat1 A G 2: 30,077,264 (GRCm39) V158A probably benign Het
Mcm8 G T 2: 132,681,449 (GRCm39) V642F probably damaging Het
Mdn1 C T 4: 32,739,092 (GRCm39) H3638Y probably benign Het
Neb T G 2: 52,116,502 (GRCm39) T4158P probably benign Het
Neo1 T C 9: 58,824,336 (GRCm39) I697M probably damaging Het
Nfkb1 A T 3: 135,300,724 (GRCm39) V614D probably damaging Het
Or7e169 G A 9: 19,757,861 (GRCm39) S18L probably damaging Het
Otog T C 7: 45,950,892 (GRCm39) S2555P probably damaging Het
Pkd1l1 T A 11: 8,784,897 (GRCm39) R1962S probably damaging Het
Plxnb1 A G 9: 108,929,918 (GRCm39) Y258C probably damaging Het
Pramel12 T A 4: 143,144,298 (GRCm39) probably null Het
Rag1 A T 2: 101,473,726 (GRCm39) V472D possibly damaging Het
Rbpj-ps3 G A 6: 46,506,641 (GRCm39) probably benign Het
Rnf112 C T 11: 61,340,804 (GRCm39) V472M probably damaging Het
Rps18 A G 17: 34,171,015 (GRCm39) probably benign Het
Rptn T C 3: 93,303,080 (GRCm39) S138P possibly damaging Het
Sbpl A C 17: 24,172,690 (GRCm39) N76K probably benign Het
Sh3bp1 A T 15: 78,789,364 (GRCm39) M241L probably benign Het
Slc22a17 T C 14: 55,145,433 (GRCm39) *198W probably null Het
Smc3 C T 19: 53,610,275 (GRCm39) R221C probably damaging Het
Snai1 A G 2: 167,380,768 (GRCm39) E87G probably benign Het
Snx22 C A 9: 65,976,470 (GRCm39) A49S probably benign Het
Tas2r143 A T 6: 42,377,268 (GRCm39) R33* probably null Het
Try4 A G 6: 41,281,965 (GRCm39) I184V probably benign Het
Ttn T A 2: 76,584,896 (GRCm39) K20355* probably null Het
Ttn A G 2: 76,622,069 (GRCm39) V15491A probably benign Het
Tut7 T C 13: 59,948,237 (GRCm39) T293A probably benign Het
Vmn1r170 A G 7: 23,305,915 (GRCm39) T106A probably damaging Het
Vmn2r59 A T 7: 41,661,817 (GRCm39) V666E probably damaging Het
Vsx1 T C 2: 150,526,495 (GRCm39) N221S possibly damaging Het
Zfp846 A G 9: 20,499,905 (GRCm39) E45G probably damaging Het
Other mutations in Prl3a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02648:Prl3a1 APN 13 27,454,218 (GRCm39) missense probably benign 0.00
R1405:Prl3a1 UTSW 13 27,459,051 (GRCm39) splice site probably null
R1405:Prl3a1 UTSW 13 27,459,051 (GRCm39) splice site probably null
R1596:Prl3a1 UTSW 13 27,443,600 (GRCm39) start gained probably benign
R1823:Prl3a1 UTSW 13 27,454,177 (GRCm39) missense probably damaging 0.99
R1952:Prl3a1 UTSW 13 27,454,136 (GRCm39) missense possibly damaging 0.91
R2059:Prl3a1 UTSW 13 27,454,127 (GRCm39) missense probably benign 0.13
R5843:Prl3a1 UTSW 13 27,454,093 (GRCm39) missense probably damaging 1.00
R6222:Prl3a1 UTSW 13 27,460,097 (GRCm39) missense probably benign 0.05
R6664:Prl3a1 UTSW 13 27,454,194 (GRCm39) nonsense probably null
R7077:Prl3a1 UTSW 13 27,460,086 (GRCm39) missense probably benign 0.35
R7846:Prl3a1 UTSW 13 27,456,442 (GRCm39) missense probably damaging 1.00
R9049:Prl3a1 UTSW 13 27,460,167 (GRCm39) missense probably damaging 1.00
R9616:Prl3a1 UTSW 13 27,459,118 (GRCm39) missense
Posted On 2015-04-16