Mutagenetix > Incidental Mutations

Incidental Mutation 'R6896:Oprd1'

538322

Institutional Source

Beutler Lab

Gene Symbol

Oprd1

Ensembl Gene

ENSMUSG00000050511

Gene Name

opioid receptor, delta 1

Synonyms

DOR, mDOR, Nbor, DOR-1

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.081) question?

Stock #

R6896 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

132110726-132144486 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 132117301 bp

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 132 (M132K)

Ref Sequence

ENSEMBL: ENSMUSP00000050077 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000056336]

PDB Structure

Structure of the delta opioid receptor bound to naltrindole [X-RAY DIFFRACTION]

Predicted Effect

probably damaging
Transcript: ENSMUST00000056336
AA Change: M132K

PolyPhen 2 Score 0.971 (Sensitivity: 0.77; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000050077
Gene: ENSMUSG00000050511
AA Change: M132K

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srx	58	288	8.2e-8	PFAM
Pfam:7TM_GPCR_Srsx	60	333	1.7e-11	PFAM
Pfam:7tm_1	66	318	4e-58	PFAM
Pfam:7TM_GPCR_Srv	69	335	3.7e-9	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.2%
20x: 97.3%

Validation Efficiency

98% (49/50)

MGI Phenotype

PHENOTYPE: Mice homozygous for one knock-out allele do not develop analgesic tolerance to morphine while mice homozygous for a different knock-out allele exhibit hyperactivity, increased anxiety, and decreased coping response. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcg2	T	C	6: 58,683,313	L454P	probably damaging	Het
Acadm	T	C	3: 153,936,320	I192V	probably damaging	Het
Acadsb	T	A	7: 131,443,646	Y436N	probably benign	Het
Ache	G	A	5: 137,291,734	V442M	probably damaging	Het
Adam39	A	T	8: 40,824,938	N122I	possibly damaging	Het
Akap6	A	T	12: 52,887,494	I590F	probably benign	Het
Akap8	T	C	17: 32,317,331	N36S	probably benign	Het
Asap2	T	C	12: 21,265,525	S933P	probably damaging	Het
C3	C	T	17: 57,220,864		probably null	Het
Cdon	T	A	9: 35,452,106	M1K	probably null	Het
Cemip	T	A	7: 83,998,576	I99F	probably damaging	Het
Cfap58	T	G	19: 47,944,187	L130R	probably damaging	Het
Clca3a2	T	C	3: 144,808,701	D415G	probably damaging	Het
Coch	A	G	12: 51,602,869	D321G	possibly damaging	Het
Efcab11	A	G	12: 99,883,415		probably benign	Het
Ermap	G	T	4: 119,187,131	S156*	probably null	Het
Fap	G	T	2: 62,504,600	Y620*	probably null	Het
Galntl5	T	C	5: 25,189,949		probably null	Het
Il21r	C	A	7: 125,626,956	H76N	probably damaging	Het
Itpr1	T	G	6: 108,481,394	Y2041D	probably damaging	Het
Megf8	T	A	7: 25,329,932	N300K	probably benign	Het
Muc2	G	A	7: 141,752,695	V285I	possibly damaging	Het
Myh15	A	T	16: 49,113,071	Q623L	probably benign	Het
Myh7b	T	C	2: 155,622,568		probably null	Het
Naaladl1	T	A	19: 6,109,305		probably null	Het
Nlrp9b	T	G	7: 20,023,245	F136V	probably damaging	Het
Olfr1006	A	G	2: 85,674,933	Y73H	probably damaging	Het
Olfr1193	A	G	2: 88,677,996	N47S	probably damaging	Het
Olfr516	T	C	7: 108,845,543	T156A	probably benign	Het
Olfr814	A	T	10: 129,874,754	M1K	probably null	Het
Patj	T	A	4: 98,426,050	V369D	possibly damaging	Het
Pcdhb3	T	C	18: 37,301,212	L77P	probably damaging	Het
Pcf11	T	C	7: 92,649,551	D1259G	probably damaging	Het
Pdcl	A	T	2: 37,352,179	H186Q	probably damaging	Het
Pdzd9	A	T	7: 120,662,872	*77R	probably null	Het
Reln	C	T	5: 21,899,179	E3265K	probably benign	Het
Smg8	T	C	11: 87,077,961	T990A	possibly damaging	Het
Smok2a	C	T	17: 13,225,871	H112Y	probably benign	Het
Spatc1l	G	A	10: 76,569,408	R208H	probably damaging	Het
Taf7	T	C	18: 37,642,680	D278G	possibly damaging	Het
Vipas39	T	C	12: 87,242,571	N373S	probably benign	Het
Vmn2r78	C	T	7: 86,922,350	T456I	probably benign	Het
Vwf	T	C	6: 125,566,194	S148P	probably damaging	Het
Wdr60	C	T	12: 116,229,671	G554R	possibly damaging	Het
Wdr66	A	G	5: 123,278,358	T565A	possibly damaging	Het
Xpot	A	C	10: 121,613,485		probably null	Het
Zdbf2	A	T	1: 63,308,872	R2137W	probably damaging	Het
Zfp462	T	A	4: 55,009,544	N503K	possibly damaging	Het
Zfp641	T	A	15: 98,293,803	M1L	probably benign	Het

Other mutations in Oprd1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02825:Oprd1	APN	4	132117359	missense	probably damaging	0.96
IGL03030:Oprd1	APN	4	132117385	missense	possibly damaging	0.94
R0066:Oprd1	UTSW	4	132113988	missense	probably benign	0.00
R0403:Oprd1	UTSW	4	132113768	missense	probably benign	0.18
R1857:Oprd1	UTSW	4	132113681	missense	probably damaging	1.00
R4808:Oprd1	UTSW	4	132117394	missense	probably damaging	1.00
R5176:Oprd1	UTSW	4	132113793	missense	probably benign	0.34
R5693:Oprd1	UTSW	4	132144410	start gained	probably benign
R5957:Oprd1	UTSW	4	132144163	missense	probably benign	0.02
R6264:Oprd1	UTSW	4	132114054	missense	possibly damaging	0.78
R7205:Oprd1	UTSW	4	132113801	missense	probably damaging	1.00
R7417:Oprd1	UTSW	4	132117452	missense	probably damaging	1.00
R7426:Oprd1	UTSW	4	132114067	missense	probably benign	0.02
R7480:Oprd1	UTSW	4	132117181	missense	possibly damaging	0.92
R7552:Oprd1	UTSW	4	132113781	missense	possibly damaging	0.80
Z1177:Oprd1	UTSW	4	132113729	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACTGCCATGACCATGATGGG -3'
(R):5'- CGATCTTTGAGCAAGTCCCTTCAC -3'

Sequencing Primer
(F):5'- CATGACCATGATGGGGACCC -3'
(R):5'- CCCCAGTTTGATGGAAGCTGAAATC -3'

Posted On

2018-11-06