Mutagenetix > Incidental Mutation

Incidental Mutation 'R4111:Prl7a2'

317327

Institutional Source

Beutler Lab

Gene Symbol

Prl7a2

Ensembl Gene

ENSMUSG00000046899

Gene Name

prolactin family 7, subfamily a, member 2

Synonyms

Prlpf, PLP-F

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.050) question?

Stock #

R4111 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

27842567-27852019 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 27849050 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 80 (Y80N)

Ref Sequence

ENSEMBL: ENSMUSP00000006660 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000006660]

AlphaFold

O54831

Predicted Effect

possibly damaging
Transcript: ENSMUST00000006660
AA Change: Y80N

PolyPhen 2 Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000006660
Gene: ENSMUSG00000046899
AA Change: Y80N

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	17	244	6.9e-45	PFAM

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.5%
20x: 96.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700012B07Rik	G	T	11: 109,684,980 (GRCm39)	C172*	probably null	Het
Acot10	A	T	15: 20,666,612 (GRCm39)	L43Q	probably damaging	Het
Alms1	G	A	6: 85,597,870 (GRCm39)	V1368I	probably benign	Het
Ambra1	T	C	2: 91,730,903 (GRCm39)	S894P	probably damaging	Het
Arhgef12	C	A	9: 42,883,570 (GRCm39)	G1320C	probably damaging	Het
Atg7	G	C	6: 114,690,255 (GRCm39)	G596R	probably damaging	Het
Birc6	T	C	17: 74,873,010 (GRCm39)	V423A	probably damaging	Het
Bltp3a	T	A	17: 28,105,064 (GRCm39)	L586*	probably null	Het
Cdh17	T	C	4: 11,814,628 (GRCm39)	S728P	probably damaging	Het
Ctu2	G	A	8: 123,203,256 (GRCm39)	R24Q	possibly damaging	Het
Dclk3	T	C	9: 111,298,148 (GRCm39)	I564T	probably damaging	Het
Ddx39b	T	A	17: 35,462,340 (GRCm39)	I42N	possibly damaging	Het
Defa39	T	C	8: 22,192,679 (GRCm39)	T106A	possibly damaging	Het
Dip2c	G	T	13: 9,687,137 (GRCm39)	G1254C	probably damaging	Het
Dzip1	T	A	14: 119,114,645 (GRCm39)	K837*	probably null	Het
Epha1	G	A	6: 42,335,772 (GRCm39)	T955M	possibly damaging	Het
Etfbkmt	T	C	6: 149,046,089 (GRCm39)		probably benign	Het
Etfrf1	T	C	6: 145,161,098 (GRCm39)	Y23H	probably damaging	Het
Fat3	G	A	9: 15,909,567 (GRCm39)	S2145F	probably damaging	Het
Gm5611	T	A	9: 16,941,989 (GRCm39)		noncoding transcript	Het
Gpr37l1	T	C	1: 135,095,008 (GRCm39)	T79A	possibly damaging	Het
Hrh3	C	A	2: 179,744,643 (GRCm39)	R99L	possibly damaging	Het
Hyls1	T	A	9: 35,472,714 (GRCm39)	Y234F	probably damaging	Het
Ifnar1	C	A	16: 91,293,046 (GRCm39)	P230T	probably damaging	Het
Impact	T	C	18: 13,109,090 (GRCm39)		probably null	Het
Kcna6	G	C	6: 126,716,737 (GRCm39)	R51G	probably damaging	Het
Lrpprc	G	A	17: 85,033,766 (GRCm39)	T1037M	probably benign	Het
Or10g9	C	A	9: 39,912,194 (GRCm39)	E110*	probably null	Het
Or4a2	C	A	2: 89,248,444 (GRCm39)	L104F	probably benign	Het
Or5an6	T	C	19: 12,371,665 (GRCm39)	F13L	probably damaging	Het
Or6n2	T	A	1: 173,896,999 (GRCm39)	I45N	probably damaging	Het
Pask	A	G	1: 93,238,540 (GRCm39)	V1315A	probably damaging	Het
Pramel16	T	A	4: 143,676,475 (GRCm39)	I210F	possibly damaging	Het
Rhox3f	G	T	X: 36,763,672 (GRCm39)	E140*	probably null	Het
Rtn2	T	C	7: 19,020,769 (GRCm39)	S81P	probably damaging	Het
Sbf2	G	A	7: 110,027,449 (GRCm39)	P470S	probably damaging	Het
Sec31b	G	T	19: 44,512,968 (GRCm39)	T507N	possibly damaging	Het
Sox30	A	G	11: 45,908,041 (GRCm39)	Y736C	probably benign	Het
Srsf3-ps	A	T	11: 98,516,223 (GRCm39)	V50D	probably damaging	Het
Synj2	G	A	17: 6,058,240 (GRCm39)	G243S	probably benign	Het
Tbr1	C	T	2: 61,642,076 (GRCm39)	P184L	probably benign	Het
Tns1	T	C	1: 73,981,091 (GRCm39)	N1091S	probably damaging	Het
Trappc10	A	G	10: 78,032,264 (GRCm39)	F1008S	probably benign	Het
Ube4a	T	A	9: 44,860,247 (GRCm39)	I272F	probably damaging	Het
Vmn1r122	A	T	7: 20,867,438 (GRCm39)	S206T	probably damaging	Het
Vmn2r1	A	C	3: 63,997,176 (GRCm39)	K277N	probably benign	Het
Vps13a	T	C	19: 16,617,992 (GRCm39)	E2931G	probably damaging	Het
Wdr70	G	T	15: 8,006,472 (GRCm39)	Q360K	probably benign	Het
Wdr90	G	T	17: 26,068,342 (GRCm39)	Q1329K	possibly damaging	Het
Wrn	T	C	8: 33,842,183 (GRCm39)	N37S	probably benign	Het
Yap1	A	T	9: 7,938,432 (GRCm39)	*358K	probably null	Het
Zfp964	T	A	8: 70,116,754 (GRCm39)	S450R	probably benign	Het
Zkscan2	T	C	7: 123,081,907 (GRCm39)		probably benign	Het
Zmynd10	A	T	9: 107,426,251 (GRCm39)	K133*	probably null	Het

Other mutations in Prl7a2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01484:Prl7a2	APN	13	27,843,191 (GRCm39)	missense	probably damaging	0.98
IGL02424:Prl7a2	APN	13	27,851,953 (GRCm39)	missense	probably null	0.08
IGL02734:Prl7a2	APN	13	27,843,190 (GRCm39)	missense	probably benign	0.38
IGL02823:Prl7a2	APN	13	27,846,734 (GRCm39)	missense	possibly damaging	0.95
PIT4260001:Prl7a2	UTSW	13	27,843,259 (GRCm39)	nonsense	probably null
R0733:Prl7a2	UTSW	13	27,846,671 (GRCm39)	missense	probably damaging	1.00
R1371:Prl7a2	UTSW	13	27,846,750 (GRCm39)	missense	probably benign	0.01
R1778:Prl7a2	UTSW	13	27,843,254 (GRCm39)	missense	probably damaging	0.98
R1857:Prl7a2	UTSW	13	27,843,163 (GRCm39)	nonsense	probably null
R2063:Prl7a2	UTSW	13	27,844,870 (GRCm39)	missense	probably damaging	0.98
R2064:Prl7a2	UTSW	13	27,844,870 (GRCm39)	missense	probably damaging	0.98
R2065:Prl7a2	UTSW	13	27,844,870 (GRCm39)	missense	probably damaging	0.98
R2067:Prl7a2	UTSW	13	27,844,870 (GRCm39)	missense	probably damaging	0.98
R2068:Prl7a2	UTSW	13	27,844,870 (GRCm39)	missense	probably damaging	0.98
R2176:Prl7a2	UTSW	13	27,843,089 (GRCm39)	missense	probably benign	0.10
R2213:Prl7a2	UTSW	13	27,849,051 (GRCm39)	missense	probably benign	0.06
R4459:Prl7a2	UTSW	13	27,849,979 (GRCm39)	missense	probably benign	0.21
R4483:Prl7a2	UTSW	13	27,844,930 (GRCm39)	missense	possibly damaging	0.80
R4722:Prl7a2	UTSW	13	27,844,858 (GRCm39)	missense	probably damaging	1.00
R5360:Prl7a2	UTSW	13	27,843,143 (GRCm39)	missense	probably benign	0.22
R5778:Prl7a2	UTSW	13	27,844,983 (GRCm39)	nonsense	probably null
R6667:Prl7a2	UTSW	13	27,845,024 (GRCm39)	missense	probably benign	0.03
R7107:Prl7a2	UTSW	13	27,843,076 (GRCm39)	missense	possibly damaging	0.89
R7600:Prl7a2	UTSW	13	27,843,264 (GRCm39)	missense	possibly damaging	0.63
R8298:Prl7a2	UTSW	13	27,844,994 (GRCm39)	missense	probably benign	0.00
R8447:Prl7a2	UTSW	13	27,849,941 (GRCm39)	missense	possibly damaging	0.72
R9009:Prl7a2	UTSW	13	27,849,994 (GRCm39)	missense	probably damaging	1.00
R9331:Prl7a2	UTSW	13	27,849,062 (GRCm39)	missense	probably damaging	1.00
R9624:Prl7a2	UTSW	13	27,849,869 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- CCAGTGATTTGATGAAGCTGTC -3'
(R):5'- GAAGGGGTTCTCTGTTTCAAAGAG -3'

Sequencing Primer
(F):5'- TGATGAAGCTGTCCTCTGC -3'
(R):5'- CTGTTCAGTGTCAGTACATACCAAGG -3'

Posted On

2015-05-15