Mutagenetix > Incidental Mutation

Incidental Mutation 'R8301:Prl3c1'

656517

Institutional Source

Beutler Lab

Gene Symbol

Prl3c1

Ensembl Gene

ENSMUSG00000017922

Gene Name

prolactin family 3, subfamily c, member 1

Synonyms

Prlpj, PLP I, PLP-J

MMRRC Submission

067789-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.051) question?

Stock #

R8301 (G1)

Quality Score

161.009

Status

Validated

Chromosome

Chromosomal Location

27380643-27387732 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

A to C at 27383168 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000136890 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000018066] [ENSMUST00000110364] [ENSMUST00000178072]

AlphaFold

Q9QUN5

Predicted Effect

probably benign
Transcript: ENSMUST00000018066

SMART Domains

Protein: ENSMUSP00000018066
Gene: ENSMUSG00000017922

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	16	212	1.5e-31	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000110364

SMART Domains

Protein: ENSMUSP00000105993
Gene: ENSMUSG00000017922

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	2	192	2.9e-31	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000178072

SMART Domains

Protein: ENSMUSP00000136890
Gene: ENSMUSG00000017922

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	2	192	2.9e-31	PFAM

Meta Mutation Damage Score

0.0846

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

100% (71/71)

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: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310003L06Rik	A	T	5: 88,120,364 (GRCm39)	I374F	probably benign	Het
Ak9	G	A	10: 41,300,712 (GRCm39)	V1108I		Het
Aldh16a1	C	T	7: 44,791,406 (GRCm39)	A790T	possibly damaging	Het
Anks1	A	T	17: 28,278,554 (GRCm39)		probably benign	Het
Antxr2	T	G	5: 98,125,538 (GRCm39)	T240P	probably benign	Het
Arfgef1	A	T	1: 10,250,058 (GRCm39)	M945K	probably damaging	Het
Arhgef17	T	C	7: 100,528,866 (GRCm39)	T1591A	probably benign	Het
Aurka	A	G	2: 172,198,850 (GRCm39)	S374P	probably damaging	Het
Bccip	T	C	7: 133,320,933 (GRCm39)	S236P	probably benign	Het
Cacna1s	T	A	1: 136,001,179 (GRCm39)		probably benign	Het
Calm1	A	G	12: 100,171,944 (GRCm39)	E132G	probably benign	Het
Casz1	A	G	4: 149,030,500 (GRCm39)	D1173G	probably damaging	Het
Cdh17	A	G	4: 11,795,659 (GRCm39)	D413G	probably damaging	Het
Cfap57	A	G	4: 118,450,271 (GRCm39)	I617T	possibly damaging	Het
Creb5	A	G	6: 53,658,018 (GRCm39)	D116G	possibly damaging	Het
Csnka2ip	A	C	16: 64,299,354 (GRCm39)	S337A	unknown	Het
Ddx60	A	G	8: 62,453,631 (GRCm39)	E1250G	probably benign	Het
Dlgap2	T	A	8: 14,873,577 (GRCm39)	S727T	probably benign	Het
Dpy19l1	T	C	9: 24,396,407 (GRCm39)		probably benign	Het
Ebf2	A	G	14: 67,476,431 (GRCm39)	T134A	possibly damaging	Het
Echdc2	A	T	4: 108,030,106 (GRCm39)	M136L	probably benign	Het
Enpp2	A	G	15: 54,714,803 (GRCm39)	F598S	probably benign	Het
Extl3	A	C	14: 65,313,733 (GRCm39)	L483R	probably damaging	Het
Gcat	T	C	15: 78,920,089 (GRCm39)	V227A	possibly damaging	Het
Hsf2	A	G	10: 57,381,442 (GRCm39)	D344G	probably damaging	Het
Ighm	C	T	12: 113,385,165 (GRCm39)	G265D		Het
Igsf9b	T	G	9: 27,246,035 (GRCm39)		probably benign	Het
Ints6	A	G	14: 62,939,902 (GRCm39)	V596A	probably benign	Het
Ints8	T	C	4: 11,246,120 (GRCm39)	E182G	probably damaging	Het
Iqgap2	A	G	13: 95,818,659 (GRCm39)		probably null	Het
Kalrn	G	T	16: 34,177,470 (GRCm39)	Q250K	probably benign	Het
Lrrc1	T	A	9: 77,451,770 (GRCm39)	N46Y	probably damaging	Het
Myl10	G	C	5: 136,726,825 (GRCm39)	V70L	probably benign	Het
Naa50	A	G	16: 43,977,494 (GRCm39)	N74S	probably benign	Het
Neb	T	C	2: 52,178,847 (GRCm39)	N1303S	probably benign	Het
Nfs1	A	T	2: 155,976,413 (GRCm39)	C160*	probably null	Het
Or11g7	T	A	14: 50,691,021 (GRCm39)	S171T	probably benign	Het
Or52s1b	T	G	7: 102,822,280 (GRCm39)	K188T	probably damaging	Het
Or5p52	A	G	7: 107,502,833 (GRCm39)	K303R	probably benign	Het
Or6c76	T	C	10: 129,612,709 (GRCm39)	S309P	probably benign	Het
Orm2	T	C	4: 63,281,263 (GRCm39)	F67S	possibly damaging	Het
Pex5	A	G	6: 124,382,142 (GRCm39)	S180P	probably benign	Het
Phf14	G	C	6: 11,992,061 (GRCm39)	G746R	probably damaging	Het
Pkm	T	A	9: 59,575,914 (GRCm39)	V110E	probably damaging	Het
Plekha6	T	G	1: 133,192,425 (GRCm39)	N78K	probably damaging	Het
Plxna2	G	A	1: 194,472,483 (GRCm39)	V1076I	probably benign	Het
Polq	C	A	16: 36,882,181 (GRCm39)	D1448E	probably damaging	Het
Pot1b	T	C	17: 55,994,895 (GRCm39)	T256A	probably benign	Het
Prkch	C	T	12: 73,749,538 (GRCm39)	T377I	possibly damaging	Het
Prl7b1	A	C	13: 27,786,755 (GRCm39)	V158G	possibly damaging	Het
Prss22	T	C	17: 24,212,955 (GRCm39)	S261G	probably damaging	Het
Psd	T	C	19: 46,309,541 (GRCm39)		probably benign	Het
Psg18	A	T	7: 18,087,302 (GRCm39)	Y119N	probably damaging	Het
Rbm6	T	G	9: 107,729,993 (GRCm39)	R218S	probably damaging	Het
Rnf213	T	A	11: 119,325,568 (GRCm39)	S1491T		Het
Rsf1	T	C	7: 97,311,132 (GRCm39)	S621P		Het
Runx1	C	A	16: 92,402,544 (GRCm39)	*466L	probably null	Het
Samd4	A	G	14: 47,254,135 (GRCm39)	I200V	probably benign	Het
Sdsl	C	T	5: 120,597,584 (GRCm39)	C241Y	probably benign	Het
Selenon	T	C	4: 134,278,725 (GRCm39)		probably benign	Het
Setx	C	T	2: 29,035,702 (GRCm39)	P729L	possibly damaging	Het
Sf1	C	T	19: 6,418,396 (GRCm39)	Q55*	probably null	Het
Slc12a5	A	T	2: 164,835,611 (GRCm39)	N833I	probably damaging	Het
Slc1a4	T	C	11: 20,282,286 (GRCm39)	R63G	probably damaging	Het
Tmeff2	G	T	1: 51,220,996 (GRCm39)	A324S	probably benign	Het
Tmem217	A	G	17: 29,745,466 (GRCm39)	I88T	possibly damaging	Het
Tnfsf8	A	T	4: 63,779,115 (GRCm39)	I61N	probably benign	Het
Tpbgl	G	T	7: 99,274,774 (GRCm39)	A361E	probably damaging	Het
Trhde	T	A	10: 114,322,911 (GRCm39)	E667V	probably benign	Het
Unc13b	A	G	4: 43,263,568 (GRCm39)	T1598A	probably benign	Het
Vmn2r73	A	T	7: 85,507,510 (GRCm39)	C601S	probably benign	Het
Zfp873	C	A	10: 81,896,713 (GRCm39)	H481Q	probably damaging	Het

Other mutations in Prl3c1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00337:Prl3c1	APN	13	27,384,746 (GRCm39)	missense	probably damaging	0.97
IGL00567:Prl3c1	APN	13	27,384,695 (GRCm39)	missense	possibly damaging	0.82
IGL01105:Prl3c1	APN	13	27,386,408 (GRCm39)	missense	probably benign	0.04
IGL02985:Prl3c1	APN	13	27,383,370 (GRCm39)	missense	probably damaging	0.99
IGL03013:Prl3c1	APN	13	27,383,349 (GRCm39)	missense	probably benign	0.01
G1Funyon:Prl3c1	UTSW	13	27,383,168 (GRCm39)	unclassified	probably benign
H8930:Prl3c1	UTSW	13	27,384,689 (GRCm39)	nonsense	probably null
R0437:Prl3c1	UTSW	13	27,383,447 (GRCm39)	missense	probably benign	0.09
R0630:Prl3c1	UTSW	13	27,384,674 (GRCm39)	splice site	probably benign
R1277:Prl3c1	UTSW	13	27,387,555 (GRCm39)	missense	probably damaging	1.00
R2064:Prl3c1	UTSW	13	27,380,720 (GRCm39)	critical splice donor site	probably null
R2121:Prl3c1	UTSW	13	27,383,325 (GRCm39)	splice site	probably null
R4752:Prl3c1	UTSW	13	27,387,508 (GRCm39)	missense	probably benign	0.11
R4959:Prl3c1	UTSW	13	27,386,471 (GRCm39)	splice site	probably null
R5863:Prl3c1	UTSW	13	27,387,593 (GRCm39)	makesense	probably null
R7912:Prl3c1	UTSW	13	27,383,367 (GRCm39)	missense	probably benign	0.02
R7913:Prl3c1	UTSW	13	27,383,393 (GRCm39)	missense	probably benign	0.00
R8157:Prl3c1	UTSW	13	27,383,330 (GRCm39)	missense	probably damaging	1.00
R8352:Prl3c1	UTSW	13	27,386,385 (GRCm39)	missense	probably benign	0.01
R8452:Prl3c1	UTSW	13	27,386,385 (GRCm39)	missense	probably benign	0.01
R8898:Prl3c1	UTSW	13	27,387,578 (GRCm39)	missense	possibly damaging	0.93
Z1177:Prl3c1	UTSW	13	27,387,484 (GRCm39)	missense	possibly damaging	0.86

Predicted Primers

PCR Primer
(F):5'- TTAAGTGCTCTTAACCACTGGGG -3'
(R):5'- AGGAACATGCATGACACCAACAG -3'

Sequencing Primer
(F):5'- GGCCAAGCAGTCCCTCTTATAG -3'
(R):5'- AGGAACAGACCCTTCCCTG -3'

Posted On

2020-12-09