Incidental Mutation 'R1537:Prlr'
| ID |
169622 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Prlr
|
| Ensembl Gene |
ENSMUSG00000005268 |
| Gene Name |
prolactin receptor |
| Synonyms |
Prlr-rs1, Pr-1 |
| MMRRC Submission |
039576-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.323)
|
| Stock # |
R1537 (G1)
|
| Quality Score |
165 |
|
Status
|
Not validated
|
| Chromosome |
15 |
| Chromosomal Location |
10177324-10349266 bp(+) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
T to G
at 10328364 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000122219
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000124470]
[ENSMUST00000124470]
[ENSMUST00000128450]
[ENSMUST00000128921]
[ENSMUST00000137867]
[ENSMUST00000148257]
|
| AlphaFold |
Q08501 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000005400
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000124470
|
| SMART Domains |
Protein: ENSMUSP00000122219
Gene: ENSMUSG00000005268
| 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 null
Transcript: ENSMUST00000124470
|
| SMART Domains |
Protein: ENSMUSP00000122219
Gene: ENSMUSG00000005268
| 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 |
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.2%
- 10x: 96.0%
- 20x: 91.7%
|
| Validation Efficiency |
|
| 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: 67 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700003H04Rik |
T |
A |
3: 124,372,124 (GRCm39) |
H86L |
possibly damaging |
Het |
| 4930519G04Rik |
A |
G |
5: 115,008,278 (GRCm39) |
T31A |
probably benign |
Het |
| Ahcyl1 |
A |
G |
3: 107,603,505 (GRCm39) |
F30S |
probably benign |
Het |
| Alox5ap |
G |
A |
5: 149,201,993 (GRCm39) |
|
probably null |
Het |
| Amtn |
A |
G |
5: 88,526,729 (GRCm39) |
S53G |
probably null |
Het |
| Arap3 |
A |
T |
18: 38,122,737 (GRCm39) |
|
probably null |
Het |
| Ash1l |
T |
A |
3: 88,979,783 (GRCm39) |
V2769E |
probably damaging |
Het |
| Atp8b1 |
C |
T |
18: 64,678,335 (GRCm39) |
V854M |
probably damaging |
Het |
| Bhlha9 |
C |
T |
11: 76,563,457 (GRCm39) |
S28L |
probably benign |
Het |
| Bltp2 |
T |
A |
11: 78,180,169 (GRCm39) |
Y2150N |
probably damaging |
Het |
| Bmpr2 |
A |
G |
1: 59,907,285 (GRCm39) |
T793A |
probably benign |
Het |
| Ccdc80 |
G |
A |
16: 44,916,299 (GRCm39) |
A352T |
probably benign |
Het |
| Chst2 |
A |
T |
9: 95,288,194 (GRCm39) |
F51I |
probably benign |
Het |
| Col14a1 |
A |
G |
15: 55,244,163 (GRCm39) |
N412S |
unknown |
Het |
| Dclk2 |
T |
C |
3: 86,713,491 (GRCm39) |
I451V |
probably damaging |
Het |
| Ddb2 |
A |
G |
2: 91,065,234 (GRCm39) |
S64P |
probably benign |
Het |
| Diaph1 |
A |
G |
18: 38,029,146 (GRCm39) |
|
probably null |
Het |
| Dnai3 |
T |
C |
3: 145,748,504 (GRCm39) |
E870G |
probably damaging |
Het |
| Dusp4 |
G |
T |
8: 35,285,570 (GRCm39) |
R277L |
probably benign |
Het |
| Fmnl2 |
A |
G |
2: 52,995,549 (GRCm39) |
E424G |
probably damaging |
Het |
| Garem1 |
A |
T |
18: 21,301,931 (GRCm39) |
|
probably null |
Het |
| Gnpat |
A |
G |
8: 125,597,555 (GRCm39) |
E39G |
probably damaging |
Het |
| Golgb1 |
A |
T |
16: 36,719,150 (GRCm39) |
Q352L |
possibly damaging |
Het |
| Hdlbp |
T |
C |
1: 93,345,096 (GRCm39) |
D803G |
probably benign |
Het |
| Hps1 |
A |
G |
19: 42,748,143 (GRCm39) |
|
probably null |
Het |
| Ilvbl |
G |
A |
10: 78,415,565 (GRCm39) |
R327H |
probably benign |
Het |
| Itpr3 |
A |
G |
17: 27,333,121 (GRCm39) |
D1911G |
possibly damaging |
Het |
| Lmo7 |
T |
A |
14: 102,166,700 (GRCm39) |
|
probably benign |
Het |
| Mcm10 |
G |
A |
2: 5,003,591 (GRCm39) |
T542I |
possibly damaging |
Het |
| Med1 |
A |
G |
11: 98,051,772 (GRCm39) |
V497A |
probably damaging |
Het |
| Mn1 |
G |
A |
5: 111,602,646 (GRCm39) |
A1295T |
probably damaging |
Het |
| Myh7b |
A |
C |
2: 155,473,707 (GRCm39) |
D1580A |
probably damaging |
Het |
| Naa20 |
A |
G |
2: 145,754,438 (GRCm39) |
I101V |
probably benign |
Het |
| Nav3 |
T |
C |
10: 109,702,846 (GRCm39) |
Y229C |
probably damaging |
Het |
| Obscn |
T |
C |
11: 58,891,575 (GRCm39) |
R6986G |
unknown |
Het |
| Or51h7 |
G |
A |
7: 102,591,547 (GRCm39) |
T79I |
probably damaging |
Het |
| Or8b4 |
A |
G |
9: 37,830,570 (GRCm39) |
I211V |
probably benign |
Het |
| P2rx3 |
A |
G |
2: 84,853,825 (GRCm39) |
|
probably null |
Het |
| Pcdhac2 |
G |
A |
18: 37,279,539 (GRCm39) |
G840R |
possibly damaging |
Het |
| Pclo |
A |
G |
5: 14,762,489 (GRCm39) |
N3654S |
unknown |
Het |
| Pcnx2 |
T |
A |
8: 126,604,188 (GRCm39) |
E689D |
possibly damaging |
Het |
| Pds5a |
A |
G |
5: 65,804,464 (GRCm39) |
S532P |
probably benign |
Het |
| Phf1 |
G |
A |
17: 27,154,372 (GRCm39) |
|
probably null |
Het |
| Pkp4 |
G |
A |
2: 59,045,147 (GRCm39) |
V41M |
probably damaging |
Het |
| Prr12 |
G |
T |
7: 44,678,366 (GRCm39) |
A1954D |
unknown |
Het |
| Prtg |
A |
G |
9: 72,717,039 (GRCm39) |
T127A |
probably benign |
Het |
| Ptprh |
A |
G |
7: 4,552,698 (GRCm39) |
L884P |
probably damaging |
Het |
| Rnf170 |
T |
A |
8: 26,629,076 (GRCm39) |
D183E |
probably benign |
Het |
| Rrp12 |
A |
T |
19: 41,875,242 (GRCm39) |
H339Q |
probably damaging |
Het |
| Rubcnl |
T |
G |
14: 75,278,267 (GRCm39) |
S350R |
possibly damaging |
Het |
| Sgo2b |
T |
A |
8: 64,379,536 (GRCm39) |
T1099S |
possibly damaging |
Het |
| Ska2 |
T |
C |
11: 87,006,945 (GRCm39) |
S17P |
probably damaging |
Het |
| Slc38a2 |
A |
G |
15: 96,591,034 (GRCm39) |
I243T |
possibly damaging |
Het |
| Sptan1 |
T |
A |
2: 29,916,034 (GRCm39) |
D2007E |
possibly damaging |
Het |
| Taar5 |
T |
A |
10: 23,846,620 (GRCm39) |
L6H |
probably benign |
Het |
| Tbata |
G |
T |
10: 61,019,270 (GRCm39) |
|
probably null |
Het |
| Tent2 |
C |
T |
13: 93,312,076 (GRCm39) |
G208D |
probably damaging |
Het |
| Tmem107 |
T |
C |
11: 68,963,284 (GRCm39) |
S98P |
probably damaging |
Het |
| Tpst2 |
A |
G |
5: 112,456,286 (GRCm39) |
D275G |
possibly damaging |
Het |
| Ttc28 |
G |
T |
5: 111,433,184 (GRCm39) |
G2073W |
probably damaging |
Het |
| Ttc7 |
T |
C |
17: 87,629,891 (GRCm39) |
V291A |
possibly damaging |
Het |
| Vps13b |
T |
A |
15: 35,792,327 (GRCm39) |
N2198K |
possibly damaging |
Het |
| Wdr37 |
A |
T |
13: 8,887,039 (GRCm39) |
D249E |
probably benign |
Het |
| Xirp2 |
G |
T |
2: 67,340,357 (GRCm39) |
C866F |
probably damaging |
Het |
| Zfp990 |
A |
G |
4: 145,263,566 (GRCm39) |
E188G |
possibly damaging |
Het |
| Zkscan2 |
A |
G |
7: 123,099,064 (GRCm39) |
S43P |
possibly damaging |
Het |
| Zscan5b |
A |
G |
7: 6,236,850 (GRCm39) |
R200G |
probably benign |
Het |
|
| Other mutations in Prlr |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00429:Prlr
|
APN |
15 |
10,328,410 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00688:Prlr
|
APN |
15 |
10,322,467 (GRCm39) |
unclassified |
probably benign |
|
|
IGL01527:Prlr
|
APN |
15 |
10,329,257 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL01626:Prlr
|
APN |
15 |
10,328,804 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL01660:Prlr
|
APN |
15 |
10,317,676 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01835:Prlr
|
APN |
15 |
10,329,129 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01926:Prlr
|
APN |
15 |
10,314,306 (GRCm39) |
start codon destroyed |
probably null |
0.76 |
|
IGL01952:Prlr
|
APN |
15 |
10,328,428 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02306:Prlr
|
APN |
15 |
10,328,760 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02394:Prlr
|
APN |
15 |
10,328,664 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02430:Prlr
|
APN |
15 |
10,325,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02695:Prlr
|
APN |
15 |
10,328,451 (GRCm39) |
missense |
probably benign |
0.20 |
|
IGL02745:Prlr
|
APN |
15 |
10,328,680 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
IGL03193:Prlr
|
APN |
15 |
10,328,376 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
IGL03277:Prlr
|
APN |
15 |
10,328,887 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03379:Prlr
|
APN |
15 |
10,319,403 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
PIT4434001:Prlr
|
UTSW |
15 |
10,328,458 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0057:Prlr
|
UTSW |
15 |
10,328,509 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0057:Prlr
|
UTSW |
15 |
10,328,509 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0545:Prlr
|
UTSW |
15 |
10,317,652 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1236:Prlr
|
UTSW |
15 |
10,325,367 (GRCm39) |
missense |
probably benign |
0.13 |
|
R1352:Prlr
|
UTSW |
15 |
10,328,872 (GRCm39) |
missense |
probably benign |
|
|
R1524:Prlr
|
UTSW |
15 |
10,319,419 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1690:Prlr
|
UTSW |
15 |
10,317,676 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1773:Prlr
|
UTSW |
15 |
10,325,404 (GRCm39) |
nonsense |
probably null |
|
|
R1789:Prlr
|
UTSW |
15 |
10,322,622 (GRCm39) |
missense |
probably benign |
0.32 |
|
R2421:Prlr
|
UTSW |
15 |
10,319,343 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4518:Prlr
|
UTSW |
15 |
10,329,085 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R4621:Prlr
|
UTSW |
15 |
10,319,462 (GRCm39) |
intron |
probably benign |
|
|
R4855:Prlr
|
UTSW |
15 |
10,328,883 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4957:Prlr
|
UTSW |
15 |
10,319,281 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5053:Prlr
|
UTSW |
15 |
10,325,471 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5731:Prlr
|
UTSW |
15 |
10,314,221 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5749:Prlr
|
UTSW |
15 |
10,328,804 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5806:Prlr
|
UTSW |
15 |
10,319,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5927:Prlr
|
UTSW |
15 |
10,322,532 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6170:Prlr
|
UTSW |
15 |
10,328,935 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6911:Prlr
|
UTSW |
15 |
10,329,270 (GRCm39) |
missense |
probably benign |
|
|
R6935:Prlr
|
UTSW |
15 |
10,319,388 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7327:Prlr
|
UTSW |
15 |
10,346,524 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7539:Prlr
|
UTSW |
15 |
10,329,109 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7579:Prlr
|
UTSW |
15 |
10,329,021 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7615:Prlr
|
UTSW |
15 |
10,326,010 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7651:Prlr
|
UTSW |
15 |
10,328,464 (GRCm39) |
missense |
probably benign |
0.26 |
|
R8213:Prlr
|
UTSW |
15 |
10,329,328 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8537:Prlr
|
UTSW |
15 |
10,314,266 (GRCm39) |
start gained |
probably benign |
|
|
R9015:Prlr
|
UTSW |
15 |
10,319,352 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9252:Prlr
|
UTSW |
15 |
10,326,550 (GRCm39) |
splice site |
probably benign |
|
|
R9335:Prlr
|
UTSW |
15 |
10,325,357 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9341:Prlr
|
UTSW |
15 |
10,328,988 (GRCm39) |
missense |
probably benign |
|
|
R9343:Prlr
|
UTSW |
15 |
10,328,988 (GRCm39) |
missense |
probably benign |
|
|
Z1176:Prlr
|
UTSW |
15 |
10,314,341 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
|
| Posted On |
2014-04-13 |
Incidental Mutation