Mutagenetix > Incidental Mutation

Incidental Mutation 'R1885:Adora3'

209417

Institutional Source

Beutler Lab

Gene Symbol

Adora3

Ensembl Gene

ENSMUSG00000000562

Gene Name

adenosine A3 receptor

Synonyms

A3R, 1700001D09Rik, 4930578J19Rik, AA3R, ARA3, A3AR, Gpcr 2

MMRRC Submission

039906-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.091) question?

Stock #

R1885 (G1)

Quality Score

207

Status

Not validated

Chromosome

Chromosomal Location

105811737-105816244 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 105812152 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Histidine at position 13 (N13H)

Ref Sequence

ENSEMBL: ENSMUSP00000143674 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000000574] [ENSMUST00000010279] [ENSMUST00000164730] [ENSMUST00000196748] [ENSMUST00000200482]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000000574
AA Change: N13H

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)

SMART Domains

Protein: ENSMUSP00000000574
Gene: ENSMUSG00000000562
AA Change: N13H

Domain	Start	End	E-Value	Type
Pfam:7tm_4	21	301	3.5e-12	PFAM
Pfam:7TM_GPCR_Srsx	24	298	5e-12	PFAM
Pfam:7tm_1	30	283	2.8e-47	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000010279

SMART Domains

Protein: ENSMUSP00000010279
Gene: ENSMUSG00000074344

Domain	Start	End	E-Value	Type
low complexity region	3	13	N/A	INTRINSIC
IG	20	115	3.94e0	SMART
transmembrane domain	151	173	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000164730

SMART Domains

Protein: ENSMUSP00000126710
Gene: ENSMUSG00000000562

Domain	Start	End	E-Value	Type
Pfam:7tm_1	1	137	6.6e-21	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000196748
AA Change: N13H

PolyPhen 2 Score 0.797 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000143674
Gene: ENSMUSG00000074344
AA Change: N13H

Domain	Start	End	E-Value	Type
Pfam:7tm_4	21	131	7.3e-9	PFAM
Pfam:7TM_GPCR_Srsx	24	123	1.3e-7	PFAM
Pfam:7tm_1	30	129	2.9e-19	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197613

Predicted Effect

probably benign
Transcript: ENSMUST00000200482

SMART Domains

Protein: ENSMUSP00000142695
Gene: ENSMUSG00000074344

Domain	Start	End	E-Value	Type
low complexity region	3	13	N/A	INTRINSIC
IG	20	115	1.6e-2	SMART

Coding Region Coverage

1x: 97.0%
3x: 96.1%
10x: 92.7%
20x: 85.1%

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes a protein that belongs to the family of adenosine receptors, which are G-protein-coupled receptors that are involved in a variety of intracellular signaling pathways and physiological functions. The receptor encoded by this gene mediates a sustained cardioprotective function during cardiac ischemia, it is involved in the inhibition of neutrophil degranulation in neutrophil-mediated tissue injury, it has been implicated in both neuroprotective and neurodegenerative effects, and it may also mediate both cell proliferation and cell death. This gene shares its 3' terminal exon with a transcript variant from overlapping GeneID:69296, which encodes an immunoglobulin domain-containing protein. [provided by RefSeq, Nov 2014]
PHENOTYPE: Mice homozygous for targeted mutations that inactivate the gene are phenotypically indistinguishable from wild-type mice. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700102P08Rik	T	A	9: 108,270,809 (GRCm39)	D124E	possibly damaging	Het
Aarsd1	T	C	11: 101,302,227 (GRCm39)	T278A	probably benign	Het
Acox2	C	T	14: 8,248,102 (GRCm38)	M393I	probably benign	Het
Adcy10	A	G	1: 165,398,377 (GRCm39)	I1491M	probably benign	Het
Adcy3	T	A	12: 4,184,951 (GRCm39)	V209E	probably damaging	Het
Ap2b1	T	A	11: 83,281,561 (GRCm39)	N822K	probably damaging	Het
Apobec3	A	T	15: 79,781,906 (GRCm39)	H82L	probably damaging	Het
Atg9b	A	T	5: 24,593,252 (GRCm39)	W384R	probably damaging	Het
Atp8a1	A	G	5: 67,904,661 (GRCm39)	V506A	possibly damaging	Het
Atxn1	G	T	13: 45,721,280 (GRCm39)	A205D	probably benign	Het
B4galnt3	T	C	6: 120,200,601 (GRCm39)	E223G	probably damaging	Het
Brip1	C	A	11: 86,029,641 (GRCm39)	G631V	probably damaging	Het
Cacna1i	A	G	15: 80,243,145 (GRCm39)	E434G	probably damaging	Het
Caprin2	A	T	6: 148,779,383 (GRCm39)		probably null	Het
Cblif	G	A	19: 11,729,688 (GRCm39)	A216T	probably benign	Het
Ccdc80	A	C	16: 44,917,083 (GRCm39)	D613A	probably benign	Het
Ccdc81	T	C	7: 89,515,819 (GRCm39)	E620G	possibly damaging	Het
Cdhr18	A	C	14: 13,828,607 (GRCm38)	Y718D	probably damaging	Het
Cebpz	A	T	17: 79,239,545 (GRCm39)	D625E	probably benign	Het
Coq6	C	A	12: 84,419,238 (GRCm39)	N388K	probably damaging	Het
Cracd	A	G	5: 77,004,589 (GRCm39)	T317A	unknown	Het
D430041D05Rik	T	C	2: 104,060,800 (GRCm39)	M1365V	probably benign	Het
Dab1	C	T	4: 104,588,948 (GRCm39)	A524V	probably benign	Het
Dap3	A	G	3: 88,838,281 (GRCm39)	L86P	probably damaging	Het
Dpysl4	T	G	7: 138,676,723 (GRCm39)	V391G	probably damaging	Het
Dyrk4	G	T	6: 126,854,144 (GRCm39)	Q550K	probably benign	Het
Epas1	A	G	17: 87,112,723 (GRCm39)	D107G	probably damaging	Het
Esrp2	A	G	8: 106,858,453 (GRCm39)	V636A	possibly damaging	Het
Etl4	T	A	2: 20,748,795 (GRCm39)	Y176N	probably damaging	Het
Etnppl	T	C	3: 130,423,111 (GRCm39)	V264A	probably benign	Het
Ezhip	GTCATCATCATCATC	GTCATCATCATCATCATC	X: 5,994,645 (GRCm39)		probably benign	Het
Fer	T	A	17: 64,445,909 (GRCm39)	V790D	probably damaging	Het
Gdpd5	G	A	7: 99,109,204 (GRCm39)	V575I	probably benign	Het
Gfus	G	T	15: 75,798,838 (GRCm39)	T123N	possibly damaging	Het
Gipc3	T	C	10: 81,177,181 (GRCm39)	I130V	probably benign	Het
Iqsec3	G	A	6: 121,405,326 (GRCm39)		probably benign	Het
Kdm5d	G	T	Y: 940,781 (GRCm39)		probably null	Het
Kl	A	G	5: 150,876,959 (GRCm39)	R260G	possibly damaging	Het
Kras	T	C	6: 145,177,843 (GRCm39)	E143G	probably damaging	Het
Ksr1	C	A	11: 78,911,204 (GRCm39)	V11F	probably null	Het
Ksr1	T	C	11: 78,927,347 (GRCm39)	T329A	probably damaging	Het
Marchf6	A	G	15: 31,502,952 (GRCm39)	V83A	probably benign	Het
Mettl2	T	C	11: 105,022,446 (GRCm39)	I212T	possibly damaging	Het
Mgat3	A	G	15: 80,095,820 (GRCm39)	I216V	probably benign	Het
Mkrn3	G	A	7: 62,068,486 (GRCm39)	A435V	probably benign	Het
Mlh1	C	A	9: 111,087,624 (GRCm39)	S24I	probably benign	Het
Mmel1	G	A	4: 154,975,333 (GRCm39)	R424Q	possibly damaging	Het
Mob3a	G	A	10: 80,527,068 (GRCm39)	Q86*	probably null	Het
Myh3	A	G	11: 66,977,453 (GRCm39)	K368E	probably benign	Het
Myo16	T	A	8: 10,372,656 (GRCm39)	N118K	probably damaging	Het
Myo5c	A	G	9: 75,157,043 (GRCm39)	S160G	probably damaging	Het
Nat1	A	T	8: 67,943,653 (GRCm39)	I13F	probably damaging	Het
Ncoa7	T	C	10: 30,524,448 (GRCm39)	N823S	possibly damaging	Het
Nwd1	T	C	8: 73,431,622 (GRCm39)	S1207P	probably benign	Het
Or2y17	T	C	11: 49,231,662 (GRCm39)	L101P	probably damaging	Het
Or4k49	G	T	2: 111,495,099 (GRCm39)	S176I	probably damaging	Het
Or5p57	T	C	7: 107,665,985 (GRCm39)	N7D	probably benign	Het
Or5w22	T	C	2: 87,363,168 (GRCm39)	S264P	probably damaging	Het
Paqr8	A	T	1: 21,005,704 (GRCm39)	H286L	probably damaging	Het
Pdzd4	G	A	X: 72,839,052 (GRCm39)	R419C	probably damaging	Het
Pes1	A	G	11: 3,919,482 (GRCm39)	K52E	probably damaging	Het
Ppp1r13l	T	C	7: 19,111,496 (GRCm39)	S774P	probably damaging	Het
Robo2	T	C	16: 73,713,033 (GRCm39)	D1283G	probably benign	Het
Rp1l1	T	C	14: 64,265,839 (GRCm39)	V475A	probably benign	Het
Scml4	A	G	10: 42,788,223 (GRCm39)	Y51C	probably damaging	Het
Skic3	A	T	13: 76,261,166 (GRCm39)	R112S	probably benign	Het
Skic3	A	G	13: 76,278,354 (GRCm39)	Q556R	probably benign	Het
Slc2a4	C	T	11: 69,835,833 (GRCm39)	V339I	probably benign	Het
Slc39a6	G	A	18: 24,734,539 (GRCm39)		probably null	Het
Slco1b2	A	T	6: 141,628,951 (GRCm39)	Y551F	probably damaging	Het
Snx33	T	C	9: 56,833,121 (GRCm39)	H316R	probably benign	Het
Spata31d1a	T	G	13: 59,849,821 (GRCm39)	D769A	probably damaging	Het
Stmn2	A	T	3: 8,606,964 (GRCm39)	E28V	probably damaging	Het
Syt9	A	G	7: 107,035,736 (GRCm39)	D251G	probably damaging	Het
Tjap1	T	C	17: 46,573,347 (GRCm39)	T37A	probably damaging	Het
Tmc7	A	T	7: 118,160,310 (GRCm39)	F176I	possibly damaging	Het
Tprg1	A	G	16: 25,231,641 (GRCm39)	T206A	probably benign	Het
Ubqlnl	A	T	7: 103,799,272 (GRCm39)	M75K	possibly damaging	Het
Vmn2r115	ATCTTCT	ATCT	17: 23,578,962 (GRCm39)		probably benign	Het
Vmn2r12	C	T	5: 109,239,942 (GRCm39)	G207E	probably damaging	Het
Xrn2	T	G	2: 146,891,281 (GRCm39)	L697*	probably null	Het
Zfp764	A	G	7: 127,004,211 (GRCm39)	F307L	probably benign	Het
Zfp804b	T	C	5: 6,820,376 (GRCm39)	R860G	probably damaging	Het
Zranb2	A	T	3: 157,248,793 (GRCm39)		probably null	Het

Other mutations in Adora3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02565:Adora3	APN	3	105,815,128 (GRCm39)	missense	probably benign	0.02
IGL03210:Adora3	APN	3	105,815,176 (GRCm39)	missense	probably benign	0.01
R1886:Adora3	UTSW	3	105,812,152 (GRCm39)	missense	possibly damaging	0.80
R1887:Adora3	UTSW	3	105,812,152 (GRCm39)	missense	possibly damaging	0.80
R3434:Adora3	UTSW	3	105,812,231 (GRCm39)	missense	probably benign	0.11
R4864:Adora3	UTSW	3	105,815,131 (GRCm39)	missense	probably damaging	1.00
R5328:Adora3	UTSW	3	105,814,619 (GRCm39)	missense	probably benign	0.00
R5746:Adora3	UTSW	3	105,815,126 (GRCm39)	missense	possibly damaging	0.49
R6322:Adora3	UTSW	3	105,814,760 (GRCm39)	missense	probably benign	0.10
R6432:Adora3	UTSW	3	105,814,991 (GRCm39)	nonsense	probably null
R7264:Adora3	UTSW	3	105,812,141 (GRCm39)	missense	probably benign	0.02
R7772:Adora3	UTSW	3	105,815,039 (GRCm39)	missense	probably benign
R9020:Adora3	UTSW	3	105,815,141 (GRCm39)	missense	probably damaging	1.00
R9350:Adora3	UTSW	3	105,814,613 (GRCm39)	missense	possibly damaging	0.80
Z1177:Adora3	UTSW	3	105,815,101 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CAGGCCCTTTCTGAGAAGAGTC -3'
(R):5'- ATGGCCAAAGGTGTGACCAG -3'

Sequencing Primer
(F):5'- AAGGAATGAGCAAGTTGTGAGTTCTC -3'
(R):5'- GCACCCCAACGGCAATGTC -3'

Posted On

2014-06-30