Mutagenetix > Incidental Mutation

Incidental Mutation 'R0178:Prl2c5'

23776

Institutional Source

Beutler Lab

Gene Symbol

Prl2c5

Ensembl Gene

ENSMUSG00000055360

Gene Name

prolactin family 2, subfamily c, member 5

Synonyms

MRP-4, Mrpplf4, PLF-4

MMRRC Submission

038446-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.079) question?

Stock #

R0178 (G1)

Quality Score

213

Status

Validated (trace)

Chromosome

Chromosomal Location

13357300-13366508 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 13366390 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Valine at position 220 (D220V)

Ref Sequence

ENSEMBL: ENSMUSP00000021778 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021778] [ENSMUST00000126540] [ENSMUST00000151144]

AlphaFold

Q9JLV9

Predicted Effect

probably damaging
Transcript: ENSMUST00000021778
AA Change: D220V

PolyPhen 2 Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000021778
Gene: ENSMUSG00000055360
AA Change: D220V

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	16	222	2.7e-70	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000126540
AA Change: D223V

PolyPhen 2 Score 0.416 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000115024
Gene: ENSMUSG00000055360
AA Change: D223V

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	19	225	1.5e-73	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143335

Predicted Effect

probably benign
Transcript: ENSMUST00000151144

SMART Domains

Protein: ENSMUSP00000117522
Gene: ENSMUSG00000055360

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	16	172	3.5e-51	PFAM

Meta Mutation Damage Score

0.4267

Coding Region Coverage

1x: 98.9%
3x: 98.1%
10x: 95.5%
20x: 88.8%

Validation Efficiency

95% (69/73)

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930596D02Rik	T	G	14: 35,533,435 (GRCm39)	N111T	probably benign	Het
Abca1	T	C	4: 53,081,953 (GRCm39)	D769G	possibly damaging	Het
Adcy6	G	T	15: 98,502,096 (GRCm39)	Q173K	probably benign	Het
Amotl1	G	A	9: 14,460,069 (GRCm39)	A890V	probably benign	Het
Arfgap2	C	T	2: 91,097,706 (GRCm39)	A141V	probably benign	Het
Asb2	G	A	12: 103,291,811 (GRCm39)	P324L	probably damaging	Het
Brd10	A	G	19: 29,732,188 (GRCm39)	S342P	probably damaging	Het
Cacna1g	G	A	11: 94,354,309 (GRCm39)	T202I	probably damaging	Het
Capn5	A	G	7: 97,782,098 (GRCm39)	L214P	probably damaging	Het
Cdh20	A	T	1: 104,902,776 (GRCm39)	D489V	possibly damaging	Het
Cers5	C	A	15: 99,644,905 (GRCm39)		probably benign	Het
Chct1	A	G	11: 85,069,264 (GRCm39)	H94R	probably benign	Het
Chrnb3	T	A	8: 27,883,392 (GRCm39)	V111D	probably damaging	Het
Clec2m	T	C	6: 129,303,786 (GRCm39)	R60G	probably benign	Het
Colec12	C	T	18: 9,858,921 (GRCm39)	P568L	unknown	Het
Cyp2r1	T	C	7: 114,149,643 (GRCm39)	E248G	probably damaging	Het
Dnaaf11	A	C	15: 66,325,950 (GRCm39)	D208E	probably benign	Het
Dnmt3b	A	G	2: 153,516,938 (GRCm39)	T536A	probably benign	Het
Eef2	G	A	10: 81,016,126 (GRCm39)	V496M	possibly damaging	Het
Fam118a	T	C	15: 84,930,081 (GRCm39)		probably benign	Het
Fer1l6	T	A	15: 58,509,763 (GRCm39)		probably null	Het
Fhad1	A	C	4: 141,682,651 (GRCm39)	F497V	probably benign	Het
Gbe1	G	A	16: 70,275,274 (GRCm39)	G358D	probably damaging	Het
Gdf10	A	G	14: 33,646,058 (GRCm39)	D69G	probably damaging	Het
Ggt6	A	G	11: 72,327,644 (GRCm39)	H150R	possibly damaging	Het
Gm45713	A	T	7: 44,783,882 (GRCm39)	L110Q	probably damaging	Het
Gm9847	T	C	12: 14,544,649 (GRCm39)		noncoding transcript	Het
Grwd1	T	C	7: 45,480,054 (GRCm39)	E51G	probably damaging	Het
Gvin3	A	T	7: 106,201,028 (GRCm39)	Y739N	probably damaging	Het
H13	A	G	2: 152,522,987 (GRCm39)	Y100C	probably damaging	Het
Kcne1	A	C	16: 92,145,697 (GRCm39)	M49R	probably damaging	Het
Kcnma1	C	T	14: 23,576,835 (GRCm39)	R236H	probably damaging	Het
Knl1	T	A	2: 118,888,886 (GRCm39)		probably benign	Het
Krt40	T	C	11: 99,432,565 (GRCm39)	I150M	probably damaging	Het
Ldb2	A	T	5: 44,630,841 (GRCm39)	V300E	probably damaging	Het
Lrp1b	A	T	2: 40,615,919 (GRCm39)	C3606S	probably damaging	Het
Lrrc42	A	G	4: 107,104,917 (GRCm39)	I16T	probably damaging	Het
Mtus1	G	T	8: 41,455,398 (GRCm39)	L87I	possibly damaging	Het
Myot	T	C	18: 44,470,053 (GRCm39)	F10S	probably damaging	Het
Nrg3	A	T	14: 38,098,413 (GRCm39)	H480Q	probably damaging	Het
Or52b2	G	A	7: 104,986,129 (GRCm39)	R265C	probably benign	Het
Or5ac23	A	T	16: 59,149,783 (GRCm39)	F30I	probably damaging	Het
Rbm17	G	A	2: 11,592,590 (GRCm39)	S295L	probably benign	Het
Serpina6	A	G	12: 103,613,172 (GRCm39)	I376T	probably damaging	Het
Sh2d2a	A	T	3: 87,756,730 (GRCm39)	T192S	probably benign	Het
Slc27a1	T	C	8: 72,037,106 (GRCm39)	Y417H	possibly damaging	Het
Slc6a1	T	G	6: 114,281,813 (GRCm39)	I32S	possibly damaging	Het
Sntb1	T	C	15: 55,769,540 (GRCm39)	T150A	probably damaging	Het
Tanc1	T	A	2: 59,665,791 (GRCm39)	C1183*	probably null	Het
Tmprss7	C	A	16: 45,511,206 (GRCm39)	W57C	probably damaging	Het
Ubac1	A	T	2: 25,911,440 (GRCm39)	V36E	possibly damaging	Het
Zfc3h1	T	C	10: 115,242,630 (GRCm39)		probably benign	Het
Zfp644	C	T	5: 106,784,771 (GRCm39)	C592Y	probably damaging	Het

Other mutations in Prl2c5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00910:Prl2c5	APN	13	13,364,061 (GRCm39)	critical splice donor site	probably null
IGL01874:Prl2c5	APN	13	13,365,362 (GRCm39)	missense	probably benign
IGL01878:Prl2c5	APN	13	13,360,402 (GRCm39)	missense	probably benign	0.00
R0276:Prl2c5	UTSW	13	13,357,634 (GRCm39)	intron	probably benign
R0373:Prl2c5	UTSW	13	13,357,609 (GRCm39)	intron	probably benign
R0539:Prl2c5	UTSW	13	13,363,906 (GRCm39)	splice site	probably null
R1037:Prl2c5	UTSW	13	13,360,492 (GRCm39)	nonsense	probably null
R1296:Prl2c5	UTSW	13	13,364,009 (GRCm39)	missense	probably damaging	1.00
R1458:Prl2c5	UTSW	13	13,365,310 (GRCm39)	missense	probably benign	0.40
R1557:Prl2c5	UTSW	13	13,365,265 (GRCm39)	missense	possibly damaging	0.52
R1850:Prl2c5	UTSW	13	13,360,377 (GRCm39)	missense	probably benign	0.40
R1866:Prl2c5	UTSW	13	13,365,358 (GRCm39)	splice site	probably null
R1894:Prl2c5	UTSW	13	13,366,263 (GRCm39)	missense	probably benign	0.04
R2060:Prl2c5	UTSW	13	13,365,238 (GRCm39)	missense	probably damaging	0.99
R2330:Prl2c5	UTSW	13	13,366,378 (GRCm39)	missense	possibly damaging	0.67
R4755:Prl2c5	UTSW	13	13,363,970 (GRCm39)	missense	probably benign
R5229:Prl2c5	UTSW	13	13,360,441 (GRCm39)	missense	probably damaging	1.00
R5364:Prl2c5	UTSW	13	13,357,627 (GRCm39)	missense	probably benign	0.01
R6307:Prl2c5	UTSW	13	13,365,175 (GRCm39)	missense	probably benign	0.01
R6350:Prl2c5	UTSW	13	13,357,631 (GRCm39)	critical splice donor site	probably null
R6927:Prl2c5	UTSW	13	13,357,503 (GRCm39)	splice site	probably null
R7397:Prl2c5	UTSW	13	13,366,327 (GRCm39)	missense	probably benign	0.01
R7965:Prl2c5	UTSW	13	13,360,469 (GRCm39)	missense	probably benign	0.01
R8084:Prl2c5	UTSW	13	13,360,539 (GRCm39)	missense	probably benign	0.20
R8959:Prl2c5	UTSW	13	13,365,392 (GRCm39)	intron	probably benign
R8980:Prl2c5	UTSW	13	13,360,470 (GRCm39)	missense	probably benign	0.12
R9258:Prl2c5	UTSW	13	13,365,297 (GRCm39)	missense	probably damaging	0.97
R9465:Prl2c5	UTSW	13	13,360,531 (GRCm39)	missense	probably benign	0.42
RF020:Prl2c5	UTSW	13	13,360,497 (GRCm39)	missense	probably benign	0.28
X0025:Prl2c5	UTSW	13	13,366,339 (GRCm39)	missense	probably benign	0.03

Predicted Primers

PCR Primer
(F):5'- TGGAGATGAAGAAAATAAGAACCCTGCC -3'
(R):5'- CAAGTTGTGTGATCAGGAGTGTCTGTC -3'

Sequencing Primer
(F):5'- CTGGTTCTTGCAATCTGACAATG -3'
(R):5'- accttcctctgcctccc -3'

Posted On

2013-04-16