Mutagenetix > Incidental Mutation

Incidental Mutation 'R6682:Prl3d3'

527550

Institutional Source

Beutler Lab

Gene Symbol

Prl3d3

Ensembl Gene

ENSMUSG00000062201

Gene Name

prolactin family 3, subfamily d, member 3

Synonyms

Plig, PL-Ig

MMRRC Submission

044801-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.057) question?

Stock #

R6682 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

27340777-27346576 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 27345023 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Lysine at position 132 (E132K)

Ref Sequence

ENSEMBL: ENSMUSP00000073286 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073601] [ENSMUST00000223958]

AlphaFold

A0A0M6L0J6

Predicted Effect

probably benign
Transcript: ENSMUST00000073601
AA Change: E132K

PolyPhen 2 Score 0.435 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000073286
Gene: ENSMUSG00000062201
AA Change: E132K

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	16	223	9.9e-72	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000223958
AA Change: E133K

PolyPhen 2 Score 0.304 (Sensitivity: 0.90; Specificity: 0.89)

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.4%
20x: 95.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aspm	T	C	1: 139,385,460 (GRCm39)	V368A	possibly damaging	Het
Bcl9l	A	G	9: 44,412,400 (GRCm39)	T92A	possibly damaging	Het
Celsr2	A	T	3: 108,307,817 (GRCm39)		probably null	Het
Cndp2	T	C	18: 84,695,455 (GRCm39)	K149E	probably benign	Het
Cnpy4	T	C	5: 138,185,984 (GRCm39)		probably null	Het
Cox6c	A	T	15: 35,938,319 (GRCm39)		probably null	Het
Cpt2	G	T	4: 107,761,627 (GRCm39)	S158R	probably damaging	Het
Dlgap1	A	G	17: 71,094,118 (GRCm39)	K813R	probably damaging	Het
Dock10	A	C	1: 80,490,338 (GRCm39)	L1927R	probably damaging	Het
Gak	T	A	5: 108,746,742 (GRCm39)	K430I	probably damaging	Het
Grik3	T	A	4: 125,544,259 (GRCm39)	Y327N	probably damaging	Het
Ldb3	T	A	14: 34,274,221 (GRCm39)	T334S	possibly damaging	Het
Ldlr	A	G	9: 21,643,671 (GRCm39)	D85G	probably benign	Het
Med26	T	A	8: 73,249,927 (GRCm39)	T391S	probably benign	Het
Mmp27	A	G	9: 7,573,606 (GRCm39)	T233A	probably benign	Het
Mob1a	A	G	6: 83,311,132 (GRCm39)	Y117C	possibly damaging	Het
Mrps35	A	T	6: 146,949,777 (GRCm39)	E97V	possibly damaging	Het
Msln	A	T	17: 25,971,993 (GRCm39)	S75T	probably damaging	Het
Myoz1	C	T	14: 20,703,687 (GRCm39)		probably null	Het
Nim1k	A	G	13: 120,173,724 (GRCm39)	I390T	probably benign	Het
Or10k2	A	G	8: 84,268,187 (GRCm39)	H138R	probably benign	Het
Or4k51	C	T	2: 111,584,980 (GRCm39)	P129S	probably damaging	Het
Pclo	A	C	5: 14,589,893 (GRCm39)	Q731P	unknown	Het
Pth1r	C	T	9: 110,556,319 (GRCm39)		probably null	Het
Ptpru	T	C	4: 131,548,093 (GRCm39)	M135V	probably benign	Het
Slc12a9	A	T	5: 137,325,663 (GRCm39)	L316Q	probably damaging	Het
Slc35f6	G	A	5: 30,814,764 (GRCm39)	M177I	possibly damaging	Het
Smc4	T	A	3: 68,914,574 (GRCm39)	S62R	probably damaging	Het
Tmem179	C	T	12: 112,469,714 (GRCm39)	D29N	probably benign	Het
Togaram2	A	T	17: 72,011,749 (GRCm39)	D476V	probably benign	Het
Trpc4ap	C	T	2: 155,479,687 (GRCm39)		probably null	Het
Trpm8	C	A	1: 88,254,224 (GRCm39)	T149K	probably damaging	Het
Uhmk1	C	T	1: 170,039,804 (GRCm39)		probably null	Het
Vmn2r79	C	A	7: 86,653,370 (GRCm39)	T545K	possibly damaging	Het
Vmn2r95	C	A	17: 18,660,489 (GRCm39)	N300K	probably damaging	Het
Wdr41	G	A	13: 95,149,639 (GRCm39)	G419D	probably damaging	Het
Zc3hav1	A	T	6: 38,302,130 (GRCm39)	H597Q	probably benign	Het
Zfp704	T	C	3: 9,630,253 (GRCm39)	E36G	probably benign	Het
Zfp9	A	G	6: 118,444,202 (GRCm39)	V47A	possibly damaging	Het

Other mutations in Prl3d3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00674:Prl3d3	APN	13	27,343,114 (GRCm39)	critical splice donor site	probably null
IGL01124:Prl3d3	APN	13	27,343,090 (GRCm39)	missense	possibly damaging	0.91
R0627:Prl3d3	UTSW	13	27,340,830 (GRCm39)	missense	probably damaging	0.97
R2063:Prl3d3	UTSW	13	27,346,304 (GRCm39)	missense	probably benign	0.00
R4989:Prl3d3	UTSW	13	27,343,072 (GRCm39)	missense	possibly damaging	0.91
R5665:Prl3d3	UTSW	13	27,343,064 (GRCm39)	splice site	probably null
R6254:Prl3d3	UTSW	13	27,341,453 (GRCm39)	missense	possibly damaging	0.93
R6727:Prl3d3	UTSW	13	27,341,147 (GRCm39)	splice site	probably null
R6793:Prl3d3	UTSW	13	27,345,044 (GRCm39)	missense	probably benign	0.01
R6953:Prl3d3	UTSW	13	27,345,029 (GRCm39)	missense	probably benign	0.17
R6979:Prl3d3	UTSW	13	27,341,545 (GRCm39)	missense	possibly damaging	0.92
R7503:Prl3d3	UTSW	13	27,345,096 (GRCm39)	missense	probably benign	0.01
R8872:Prl3d3	UTSW	13	27,346,324 (GRCm39)	missense	possibly damaging	0.63
R9258:Prl3d3	UTSW	13	27,344,931 (GRCm39)	missense	possibly damaging	0.80

Predicted Primers

PCR Primer
(F):5'- TTATCAAAGTGGAAATCGAGAGCTG -3'
(R):5'- ATTACTCTCAGGCACAGCAG -3'

Sequencing Primer
(F):5'- AAAATATACTGCTGTTTGCCTCC -3'
(R):5'- CAGCAGTTCTGTGGAGATTAATG -3'

Posted On

2018-07-23