Mutagenetix > Incidental Mutations

Incidental Mutation 'R0057:Prlr'

16376

Institutional Source

Beutler Lab

Gene Symbol

Prlr

Ensembl Gene

ENSMUSG00000005268

Gene Name

prolactin receptor

Synonyms

Prlr-rs1, Pr-1

MMRRC Submission

038351-MU

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.270) question?

Stock #

R0057 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

10177238-10349180 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 10328423 bp

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 328 (Y328C)

Ref Sequence

ENSEMBL: ENSMUSP00000122219 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000124470] [ENSMUST00000128450] [ENSMUST00000128921] [ENSMUST00000137867] [ENSMUST00000148257]

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000005400

Predicted Effect

probably damaging
Transcript: ENSMUST00000124470
AA Change: Y328C

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000122219
Gene: ENSMUSG00000005268
AA Change: Y328C

Domain	Start	End	E-Value	Type
FN3	23	107	3.78e0	SMART
FN3	122	210	2.5e-2	SMART
transmembrane domain	231	253	N/A	INTRINSIC
low complexity region	278	291	N/A	INTRINSIC
low complexity region	342	356	N/A	INTRINSIC
low complexity region	384	397	N/A	INTRINSIC
low complexity region	454	467	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000128450

SMART Domains

Protein: ENSMUSP00000122209
Gene: ENSMUSG00000005268

Domain	Start	End	E-Value	Type
FN3	23	107	3.78e0	SMART
FN3	122	210	2.5e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000128921

SMART Domains

Protein: ENSMUSP00000121280
Gene: ENSMUSG00000005268

Domain	Start	End	E-Value	Type
FN3	23	107	3.78e0	SMART
FN3	122	210	2.5e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000137867

SMART Domains

Protein: ENSMUSP00000121935
Gene: ENSMUSG00000005268

Domain	Start	End	E-Value	Type
FN3	23	107	3.78e0	SMART
FN3	122	210	2.5e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145428

Predicted Effect

probably benign
Transcript: ENSMUST00000148257

SMART Domains

Protein: ENSMUSP00000118355
Gene: ENSMUSG00000005268

Domain	Start	End	E-Value	Type
FN3	23	107	3.78e0	SMART
FN3	122	210	2.5e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000157020

SMART Domains

Protein: ENSMUSP00000120297
Gene: ENSMUSG00000094814

Domain	Start	End	E-Value	Type
transmembrane domain	20	41	N/A	INTRINSIC

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 90.1%
3x: 87.8%
10x: 82.7%
20x: 75.7%

Validation Efficiency

89% (65/73)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a receptor for the anterior pituitary hormone, prolactin, and belongs to the type I cytokine receptor family. Prolactin-dependent signaling occurs as the result of ligand-induced dimerization of the prolactin receptor. Several alternatively spliced transcript variants encoding different membrane-bound and soluble isoforms have been described for this gene, which may function to modulate the endocrine and autocrine effects of prolactin in normal tissue and cancer. [provided by RefSeq, Feb 2011]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit abnormal growth, hormone and glucose homeostasis, hair cycling, female reproductive behavior, morphology, and function, and thyroid, prostate, Hardarian, and lacrimal gland morphologies. Heterozygous mice exhibit defective neuron proliferation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca8b	A	T	11: 109,941,559	F1309L	possibly damaging	Het
Abcc6	C	T	7: 46,020,143	A163T	probably benign	Het
Adam23	T	A	1: 63,570,919	H693Q	probably damaging	Het
Afg3l2	A	G	18: 67,423,086	F392L	probably damaging	Het
Ak9	A	T	10: 41,392,728	T1055S	probably benign	Het
Ap5z1	T	C	5: 142,470,389		probably benign	Het
Arhgef10l	A	G	4: 140,611,218		probably benign	Het
Bloc1s6	T	A	2: 122,744,221		probably benign	Het
Caskin1	A	G	17: 24,504,896	N886S	probably damaging	Het
Celsr1	A	C	15: 86,030,762	S1003R	probably benign	Het
Ctse	G	T	1: 131,663,371	D97Y	probably damaging	Het
Cux1	T	A	5: 136,256,282	I505F	probably damaging	Het
Dcaf11	T	C	14: 55,569,310	V490A	probably benign	Het
Dscam	A	C	16: 96,673,736	W1209G	probably damaging	Het
Emc8	A	G	8: 120,659,083		probably benign	Het
Entpd6	A	G	2: 150,758,828	K152R	probably null	Het
Eps8l2	C	T	7: 141,342,971	T49I	probably benign	Het
Fuk	C	T	8: 110,893,768		probably benign	Het
Gm12251	C	A	11: 58,393,041		probably benign	Het
Gna11	A	G	10: 81,530,940	M312T	probably benign	Het
Hacd2	T	A	16: 35,075,627	V105D	probably damaging	Het
Il17a	T	A	1: 20,733,657	I92N	probably damaging	Het
Ino80	G	A	2: 119,382,960	R1249C	probably damaging	Het
Irak4	A	C	15: 94,553,872	R115S	probably benign	Het
Jarid2	C	T	13: 44,884,856	H77Y	probably damaging	Het
Kcnk6	A	T	7: 29,225,663	L176Q	probably damaging	Het
Kmt2b	A	T	7: 30,576,792		probably benign	Het
Kremen2	A	C	17: 23,743,228	I210S	possibly damaging	Het
Ldah	T	C	12: 8,238,432		probably benign	Het
Lgals9	A	T	11: 78,971,436		probably benign	Het
Mfsd13a	C	T	19: 46,366,504	T40I	probably benign	Het
Msh4	C	T	3: 153,869,681	A686T	probably benign	Het
Mycbp2	T	C	14: 103,152,142	N3411D	probably damaging	Het
Myt1l	A	G	12: 29,842,612		probably null	Het
Nmbr	A	G	10: 14,760,524	N79S	probably damaging	Het
Npsr1	A	T	9: 24,300,427	I84F	probably damaging	Het
Olfr1022	C	A	2: 85,869,253	Y220*	probably null	Het
Olfr1346	T	C	7: 6,474,680	L190P	probably damaging	Het
Olfr648	G	T	7: 104,180,329	H26Q	probably benign	Het
Rasal3	A	G	17: 32,391,383	S977P	probably benign	Het
Ros1	C	T	10: 52,180,191	V68I	probably benign	Het
RP24-170A20.3	T	A	10: 39,891,097		probably benign	Het
Shmt2	G	A	10: 127,521,048	T31M	possibly damaging	Het
Snapc1	C	T	12: 73,975,032	R81C	probably damaging	Het
Snrnp200	C	G	2: 127,237,907	L1899V	probably damaging	Het
Snrnp48	T	A	13: 38,216,380	C154*	probably null	Het
Tdrd6	G	A	17: 43,617,161		probably benign	Het
Tmem175	C	T	5: 108,639,562	H92Y	probably damaging	Het
Tom1l1	G	A	11: 90,685,149		probably benign	Het
Top3a	C	T	11: 60,740,684	A951T	probably benign	Het
Tram2	C	T	1: 21,006,154	R184Q	probably damaging	Het
Trpc4ap	T	C	2: 155,640,486	E528G	possibly damaging	Het
Vwa7	G	A	17: 35,024,547	S710N	possibly damaging	Het
Zfa-ps	A	T	10: 52,545,106		noncoding transcript	Het
Zfp770	T	A	2: 114,197,232	R119*	probably null	Het

Other mutations in Prlr

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00429:Prlr	APN	15	10328324	missense	probably benign	0.00
IGL00688:Prlr	APN	15	10322381	unclassified	probably benign
IGL01527:Prlr	APN	15	10329171	missense	probably benign	0.28
IGL01626:Prlr	APN	15	10328718	missense	probably benign	0.12
IGL01660:Prlr	APN	15	10317590	missense	probably damaging	1.00
IGL01835:Prlr	APN	15	10329043	missense	probably damaging	1.00
IGL01926:Prlr	APN	15	10314220	start codon destroyed	probably null	0.76
IGL01952:Prlr	APN	15	10328342	missense	possibly damaging	0.95
IGL02306:Prlr	APN	15	10328674	missense	probably benign	0.05
IGL02394:Prlr	APN	15	10328578	missense	probably benign	0.03
IGL02430:Prlr	APN	15	10325391	missense	probably damaging	1.00
IGL02695:Prlr	APN	15	10328365	missense	probably benign	0.20
IGL02745:Prlr	APN	15	10328594	missense	possibly damaging	0.50
IGL03193:Prlr	APN	15	10328290	missense	possibly damaging	0.57
IGL03277:Prlr	APN	15	10328801	missense	probably benign	0.01
IGL03379:Prlr	APN	15	10319317	missense	possibly damaging	0.80
PIT4434001:Prlr	UTSW	15	10328372	missense	probably damaging	1.00
R0057:Prlr	UTSW	15	10328423	missense	probably damaging	0.99
R0545:Prlr	UTSW	15	10317566	missense	probably damaging	1.00
R1236:Prlr	UTSW	15	10325281	missense	probably benign	0.13
R1352:Prlr	UTSW	15	10328786	missense	probably benign
R1524:Prlr	UTSW	15	10319333	missense	probably damaging	0.97
R1537:Prlr	UTSW	15	10328278	splice site	probably null
R1690:Prlr	UTSW	15	10317590	missense	probably damaging	1.00
R1773:Prlr	UTSW	15	10325318	nonsense	probably null
R1789:Prlr	UTSW	15	10322536	missense	probably benign	0.32
R2421:Prlr	UTSW	15	10319257	missense	probably damaging	1.00
R4518:Prlr	UTSW	15	10328999	missense	possibly damaging	0.53
R4621:Prlr	UTSW	15	10319376	intron	probably benign
R4855:Prlr	UTSW	15	10328797	missense	probably benign	0.01
R4957:Prlr	UTSW	15	10319195	missense	probably damaging	1.00
R5053:Prlr	UTSW	15	10325385	missense	probably benign	0.00
R5731:Prlr	UTSW	15	10314135	missense	probably benign	0.00
R5749:Prlr	UTSW	15	10328718	missense	probably benign	0.12
R5806:Prlr	UTSW	15	10319204	missense	probably damaging	1.00
R5927:Prlr	UTSW	15	10322446	missense	probably benign	0.42
R6170:Prlr	UTSW	15	10328849	missense	probably benign	0.05
R6911:Prlr	UTSW	15	10329184	missense	probably benign
R6935:Prlr	UTSW	15	10319302	missense	probably damaging	1.00
R7327:Prlr	UTSW	15	10346438	missense	probably benign	0.00
R7539:Prlr	UTSW	15	10329023	missense	probably benign	0.11
R7579:Prlr	UTSW	15	10328935	missense	probably benign	0.08
R7615:Prlr	UTSW	15	10325924	missense	probably damaging	1.00
R7651:Prlr	UTSW	15	10328378	missense	probably benign	0.26

Posted On

2013-01-20