Mutagenetix > Incidental Mutation

Incidental Mutation 'R0625:Prl7d1'

57436

Institutional Source

Beutler Lab

Gene Symbol

Prl7d1

Ensembl Gene

ENSMUSG00000021348

Gene Name

prolactin family 7, subfamily d, member 1

Synonyms

Plfr, PRP, PLF-RP

MMRRC Submission

038814-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0625 (G1)

Quality Score

202

Status

Not validated

Chromosome

Chromosomal Location

27706337-27716736 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 27710140 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 149 (C149S)

Ref Sequence

ENSEMBL: ENSMUSP00000153033 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021776] [ENSMUST00000224026]

AlphaFold

P04769

Predicted Effect

probably benign
Transcript: ENSMUST00000021776
AA Change: C148S

PolyPhen 2 Score 0.083 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000021776
Gene: ENSMUSG00000021348
AA Change: C148S

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	17	240	1.1e-78	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000224026
AA Change: C149S

PolyPhen 2 Score 0.102 (Sensitivity: 0.93; Specificity: 0.86)

Coding Region Coverage

1x: 99.4%
3x: 98.9%
10x: 97.5%
20x: 95.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930550C14Rik	T	C	9: 53,408,065 (GRCm38)	S2P	probably benign	Het
Abca16	A	C	7: 120,435,893 (GRCm38)	T301P	probably damaging	Het
Acer2	A	G	4: 86,887,162 (GRCm38)	D121G	possibly damaging	Het
Adgrd1	T	C	5: 129,171,931 (GRCm38)		probably null	Het
Arhgap11a	T	C	2: 113,841,711 (GRCm38)	I249V	probably benign	Het
Arhgap22	A	G	14: 33,366,714 (GRCm38)	E219G	probably benign	Het
C2cd4b	T	A	9: 67,759,751 (GRCm38)	S10T	probably benign	Het
Cnot6	A	T	11: 49,683,171 (GRCm38)	I224N	probably damaging	Het
Ctrc	T	C	4: 141,841,518 (GRCm38)	T125A	probably damaging	Het
Cxxc5	T	G	18: 35,858,589 (GRCm38)	S14R	unknown	Het
Cyp4f37	T	G	17: 32,634,678 (GRCm38)	F445L	probably damaging	Het
Dcbld1	T	G	10: 52,312,850 (GRCm38)	I186S	probably benign	Het
Dmxl2	T	C	9: 54,382,702 (GRCm38)	T2510A	probably benign	Het
Dnah3	A	G	7: 120,071,887 (GRCm38)	I591T	possibly damaging	Het
Dock5	A	T	14: 67,841,163 (GRCm38)	I204N	probably benign	Het
Dysf	G	A	6: 84,111,987 (GRCm38)		probably null	Het
Erich5	A	G	15: 34,471,369 (GRCm38)	E248G	probably damaging	Het
Fhip1a	A	G	3: 85,730,500 (GRCm38)	V164A	possibly damaging	Het
Foxm1	A	G	6: 128,373,871 (GRCm38)	S712G	probably damaging	Het
Frmpd1	A	G	4: 45,284,055 (GRCm38)	T959A	probably benign	Het
Gfra4	C	T	2: 131,040,256 (GRCm38)	V277I	probably null	Het
Hacd4	T	C	4: 88,435,010 (GRCm38)	I82V	probably benign	Het
Itih2	C	T	2: 10,123,414 (GRCm38)	V159I	possibly damaging	Het
Itpr2	T	A	6: 146,166,651 (GRCm38)	M2410L	probably benign	Het
Marchf11	A	G	15: 26,311,043 (GRCm38)	I202V	probably damaging	Het
Marchf3	A	G	18: 56,811,830 (GRCm38)		probably null	Het
Med12l	G	A	3: 59,247,437 (GRCm38)	E1135K	probably damaging	Het
Mib2	C	T	4: 155,659,460 (GRCm38)	G42S	probably damaging	Het
Mlx	T	C	11: 101,087,782 (GRCm38)	L78P	possibly damaging	Het
Muc5b	T	C	7: 141,846,427 (GRCm38)	C473R	unknown	Het
N4bp2l1	T	A	5: 150,576,745 (GRCm38)	R66*	probably null	Het
Nes	A	G	3: 87,977,172 (GRCm38)	T913A	possibly damaging	Het
Oas1a	T	C	5: 120,899,259 (GRCm38)	E235G	probably damaging	Het
Or5p56	T	C	7: 107,991,189 (GRCm38)	S275P	probably damaging	Het
Or8b1c	T	C	9: 38,473,208 (GRCm38)	S154P	possibly damaging	Het
Or8i2	T	A	2: 87,021,620 (GRCm38)	H308L	probably benign	Het
Parn	C	T	16: 13,640,294 (GRCm38)	V286I	probably benign	Het
Paxip1	G	A	5: 27,765,942 (GRCm38)	Q470*	probably null	Het
Phc2	C	G	4: 128,723,710 (GRCm38)	H510D	possibly damaging	Het
Pla2g4f	T	A	2: 120,305,041 (GRCm38)	D384V	probably damaging	Het
Plpbp	A	T	8: 27,045,131 (GRCm38)	N68I	probably damaging	Het
Podxl2	G	A	6: 88,849,955 (GRCm38)	A123V	possibly damaging	Het
Pole	A	T	5: 110,325,550 (GRCm38)	T1737S	possibly damaging	Het
Ppp3cc	T	C	14: 70,225,027 (GRCm38)	E396G	probably damaging	Het
Pramel7	T	A	2: 87,491,008 (GRCm38)	I228F	probably benign	Het
Qtrt1	G	T	9: 21,418,288 (GRCm38)	M217I	probably benign	Het
Sec24a	T	A	11: 51,729,454 (GRCm38)	D456V	probably damaging	Het
Shox2	T	G	3: 66,981,544 (GRCm38)		probably null	Het
Skint2	T	A	4: 112,624,086 (GRCm38)	S49T	probably damaging	Het
Smarca5	A	G	8: 80,720,686 (GRCm38)		probably null	Het
Sorcs2	T	A	5: 36,024,572 (GRCm38)	D1068V	possibly damaging	Het
Tmem114	T	C	16: 8,412,102 (GRCm38)		probably null	Het
Ttc7b	T	A	12: 100,355,046 (GRCm38)	M24L	probably benign	Het
Ttll3	A	G	6: 113,408,903 (GRCm38)		probably null	Het
Usp7	C	T	16: 8,704,982 (GRCm38)	D102N	probably benign	Het

Other mutations in Prl7d1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01390:Prl7d1	APN	13	27,710,166 (GRCm38)	missense	possibly damaging	0.91
IGL01735:Prl7d1	APN	13	27,714,389 (GRCm38)	missense	possibly damaging	0.83
IGL02139:Prl7d1	APN	13	27,712,083 (GRCm38)	missense	probably damaging	1.00
PIT4305001:Prl7d1	UTSW	13	27,714,337 (GRCm38)	missense	possibly damaging	0.90
PIT4531001:Prl7d1	UTSW	13	27,710,178 (GRCm38)	missense	probably damaging	1.00
R0555:Prl7d1	UTSW	13	27,712,055 (GRCm38)	missense	probably benign	0.13
R0631:Prl7d1	UTSW	13	27,710,182 (GRCm38)	missense	probably benign	0.32
R0837:Prl7d1	UTSW	13	27,714,338 (GRCm38)	missense	probably benign	0.06
R1403:Prl7d1	UTSW	13	27,709,197 (GRCm38)	missense	possibly damaging	0.89
R1403:Prl7d1	UTSW	13	27,709,197 (GRCm38)	missense	possibly damaging	0.89
R1459:Prl7d1	UTSW	13	27,709,257 (GRCm38)	missense	possibly damaging	0.81
R1643:Prl7d1	UTSW	13	27,712,131 (GRCm38)	missense	possibly damaging	0.53
R1691:Prl7d1	UTSW	13	27,709,382 (GRCm38)	missense	probably damaging	0.97
R2016:Prl7d1	UTSW	13	27,710,173 (GRCm38)	missense	probably damaging	1.00
R3873:Prl7d1	UTSW	13	27,716,668 (GRCm38)	start codon destroyed	probably null	0.92
R3874:Prl7d1	UTSW	13	27,716,668 (GRCm38)	start codon destroyed	probably null	0.92
R5251:Prl7d1	UTSW	13	27,709,244 (GRCm38)	missense	probably benign	0.33
R5275:Prl7d1	UTSW	13	27,709,247 (GRCm38)	missense	probably damaging	0.99
R5295:Prl7d1	UTSW	13	27,709,247 (GRCm38)	missense	probably damaging	0.99
R5398:Prl7d1	UTSW	13	27,710,074 (GRCm38)	missense	probably damaging	1.00
R6798:Prl7d1	UTSW	13	27,709,397 (GRCm38)	critical splice acceptor site	probably null
R6818:Prl7d1	UTSW	13	27,714,471 (GRCm38)	missense	probably benign	0.07
R6825:Prl7d1	UTSW	13	27,710,142 (GRCm38)	missense	probably benign	0.01
R7478:Prl7d1	UTSW	13	27,710,185 (GRCm38)	nonsense	probably null
R7795:Prl7d1	UTSW	13	27,709,280 (GRCm38)	missense	probably damaging	1.00
R7995:Prl7d1	UTSW	13	27,710,071 (GRCm38)	missense	probably benign
R8193:Prl7d1	UTSW	13	27,709,247 (GRCm38)	missense
R9313:Prl7d1	UTSW	13	27,709,199 (GRCm38)	missense	probably benign
R9424:Prl7d1	UTSW	13	27,710,202 (GRCm38)	missense	probably benign	0.00
R9430:Prl7d1	UTSW	13	27,714,377 (GRCm38)	missense	possibly damaging	0.80
R9733:Prl7d1	UTSW	13	27,714,356 (GRCm38)	missense	probably benign	0.00
R9758:Prl7d1	UTSW	13	27,709,277 (GRCm38)	missense	possibly damaging	0.91

Predicted Primers

PCR Primer
(F):5'- GGGCAGTTCTTTCATGTAAGAAGCAGG -3'
(R):5'- TTGCAAACTACAGGTGACCAGTCTAAC -3'

Sequencing Primer
(F):5'- ACTTGAGGACTTGCTATGCTC -3'
(R):5'- GTGACCAGTCTAACTTATACACTGC -3'

Posted On

2013-07-11