Incidental Mutation 'IGL01388:Prl7c1'
ID 79108
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prl7c1
Ensembl Gene ENSMUSG00000060738
Gene Name prolactin family 7, subfamily c, member 1
Synonyms 1600017N11Rik, Prlpo, PLP-O
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # IGL01388
Quality Score
Status
Chromosome 13
Chromosomal Location 27957583-27964829 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 27960198 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Serine at position 115 (A115S)
Ref Sequence ENSEMBL: ENSMUSP00000072712 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072943]
AlphaFold Q9CRB5
Predicted Effect probably damaging
Transcript: ENSMUST00000072943
AA Change: A115S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000072712
Gene: ENSMUSG00000060738
AA Change: A115S

DomainStartEndE-ValueType
Pfam:Hormone_1 17 242 8.1e-60 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap28 T G 17: 68,160,034 (GRCm39) probably benign Het
Ces2b A C 8: 105,561,236 (GRCm39) probably benign Het
Col20a1 T A 2: 180,645,264 (GRCm39) M924K probably benign Het
Commd4 G A 9: 57,063,273 (GRCm39) probably benign Het
Ctnna3 A G 10: 63,339,886 (GRCm39) E24G possibly damaging Het
Cyp2a22 C T 7: 26,637,217 (GRCm39) R189H probably benign Het
Gapdhrt T C 14: 11,281,836 (GRCm38) D33G probably damaging Het
Gm20426 T C 6: 90,155,694 (GRCm39) probably benign Het
Gm6802 T G 12: 19,540,546 (GRCm39) noncoding transcript Het
Igkv8-21 A G 6: 70,292,153 (GRCm39) S30P probably benign Het
Lig4 A G 8: 10,023,586 (GRCm39) Y65H probably damaging Het
Mpzl1 T C 1: 165,433,336 (GRCm39) D105G probably benign Het
Myo10 A G 15: 25,736,703 (GRCm39) I451V possibly damaging Het
Nos2 G T 11: 78,848,278 (GRCm39) V1062L probably damaging Het
Oas2 A G 5: 120,886,657 (GRCm39) S170P probably damaging Het
Or1j19 G T 2: 36,677,367 (GRCm39) V277L probably benign Het
Or5w11 T A 2: 87,458,973 (GRCm39) H55Q probably benign Het
Or8b3b A T 9: 38,584,379 (GRCm39) Y120* probably null Het
Or8g37 A G 9: 39,731,298 (GRCm39) D121G probably damaging Het
Pcdh7 T C 5: 57,877,546 (GRCm39) L367P probably damaging Het
Pde3a A G 6: 141,405,464 (GRCm39) T439A probably damaging Het
Plekhm2 T C 4: 141,369,312 (GRCm39) Y124C probably damaging Het
Ppp4r4 T A 12: 103,543,108 (GRCm39) W155R probably damaging Het
Psg25 T C 7: 18,263,590 (GRCm39) I78V possibly damaging Het
Ptpn9 T A 9: 56,944,002 (GRCm39) V292E probably benign Het
Ptprs G A 17: 56,728,261 (GRCm39) R908C probably damaging Het
Rps6ka1 C T 4: 133,599,275 (GRCm39) V51I probably damaging Het
Scube1 T C 15: 83,504,332 (GRCm39) I492V probably benign Het
Trappc2 G A X: 165,232,775 (GRCm39) probably benign Het
Ubr4 T C 4: 139,187,554 (GRCm39) V739A possibly damaging Het
Unc79 T C 12: 103,136,018 (GRCm39) probably benign Het
Vmn2r27 G A 6: 124,200,791 (GRCm39) P389S possibly damaging Het
Wipi2 T A 5: 142,646,798 (GRCm39) F212I possibly damaging Het
Other mutations in Prl7c1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03096:Prl7c1 APN 13 27,957,689 (GRCm39) missense probably damaging 0.96
PIT4458001:Prl7c1 UTSW 13 27,957,741 (GRCm39) missense probably benign
R0566:Prl7c1 UTSW 13 27,962,961 (GRCm39) missense probably damaging 1.00
R0856:Prl7c1 UTSW 13 27,957,717 (GRCm39) missense possibly damaging 0.84
R0908:Prl7c1 UTSW 13 27,957,717 (GRCm39) missense possibly damaging 0.84
R1585:Prl7c1 UTSW 13 27,962,838 (GRCm39) missense probably damaging 0.99
R4193:Prl7c1 UTSW 13 27,960,261 (GRCm39) missense probably benign 0.01
R4628:Prl7c1 UTSW 13 27,962,065 (GRCm39) missense probably benign
R4728:Prl7c1 UTSW 13 27,960,268 (GRCm39) missense probably benign 0.00
R4873:Prl7c1 UTSW 13 27,957,742 (GRCm39) missense probably benign 0.01
R4875:Prl7c1 UTSW 13 27,957,742 (GRCm39) missense probably benign 0.01
R5714:Prl7c1 UTSW 13 27,962,949 (GRCm39) nonsense probably null
R6353:Prl7c1 UTSW 13 27,957,709 (GRCm39) missense possibly damaging 0.64
R6505:Prl7c1 UTSW 13 27,957,776 (GRCm39) missense probably damaging 1.00
R6878:Prl7c1 UTSW 13 27,962,827 (GRCm39) missense possibly damaging 0.66
R7104:Prl7c1 UTSW 13 27,962,952 (GRCm39) nonsense probably null
R7879:Prl7c1 UTSW 13 27,962,817 (GRCm39) missense probably damaging 1.00
R7896:Prl7c1 UTSW 13 27,962,070 (GRCm39) missense possibly damaging 0.86
R8828:Prl7c1 UTSW 13 27,957,854 (GRCm39) missense probably benign 0.14
R9142:Prl7c1 UTSW 13 27,964,751 (GRCm39) start gained probably benign
R9215:Prl7c1 UTSW 13 27,960,204 (GRCm39) missense probably benign 0.32
R9296:Prl7c1 UTSW 13 27,962,812 (GRCm39) missense probably benign 0.06
R9453:Prl7c1 UTSW 13 27,957,870 (GRCm39) missense probably benign 0.44
Posted On 2013-11-05