Mutagenetix > Incidental Mutation

Incidental Mutation 'R2165:Or51a10'

235428

Institutional Source

Beutler Lab

Gene Symbol

Or51a10

Ensembl Gene

ENSMUSG00000049797

Gene Name

olfactory receptor family 51 subfamily A member 10

Synonyms

MOR13-6, GA_x6K02T2PBJ9-6784380-6783436, Olfr642

MMRRC Submission

040168-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.077) question?

Stock #

R2165 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

103698615-103699559 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 103698845 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 239 (T239A)

Ref Sequence

ENSEMBL: ENSMUSP00000148961 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052660] [ENSMUST00000074064] [ENSMUST00000138055] [ENSMUST00000214299]

AlphaFold

Q924X8

Predicted Effect

probably benign
Transcript: ENSMUST00000052660
AA Change: T239A

PolyPhen 2 Score 0.220 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000061462
Gene: ENSMUSG00000049797
AA Change: T239A

Domain	Start	End	E-Value	Type
Pfam:7tm_4	33	312	8.5e-119	PFAM
Pfam:7TM_GPCR_Srsx	37	309	1.7e-7	PFAM
Pfam:7tm_1	43	294	4.1e-23	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000074064

SMART Domains

Protein: ENSMUSP00000073707
Gene: ENSMUSG00000090219

Domain	Start	End	E-Value	Type
Pfam:7tm_4	33	312	2.6e-124	PFAM
Pfam:7TM_GPCR_Srsx	37	255	3.1e-7	PFAM
Pfam:7tm_1	43	294	3.2e-21	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000138055

SMART Domains

Protein: ENSMUSP00000139240
Gene: ENSMUSG00000109824

Domain	Start	End	E-Value	Type
transmembrane domain	29	51	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000214299
AA Change: T239A

PolyPhen 2 Score 0.220 (Sensitivity: 0.91; Specificity: 0.88)

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.6%
20x: 96.0%

Validation Efficiency

99% (71/72)

MGI Phenotype

FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	A	G	3: 121,906,048 (GRCm39)	T806A	possibly damaging	Het
Adgre1	T	G	17: 57,726,338 (GRCm39)	L403R	probably damaging	Het
Alox12	A	T	11: 70,133,398 (GRCm39)		probably null	Het
Ankib1	A	T	5: 3,763,210 (GRCm39)	D506E	possibly damaging	Het
Ascc3	T	G	10: 50,597,935 (GRCm39)	Y1268D	probably damaging	Het
Bik	A	G	15: 83,425,624 (GRCm39)	M42V	probably benign	Het
Bola1	A	T	3: 96,104,517 (GRCm39)	S26T	probably benign	Het
Bub1	T	C	2: 127,643,201 (GRCm39)	I1048V	probably benign	Het
Cad	A	G	5: 31,219,564 (GRCm39)	N621S	probably damaging	Het
Camkv	C	A	9: 107,822,799 (GRCm39)	N69K	possibly damaging	Het
Ccdc110	T	C	8: 46,395,876 (GRCm39)	M589T	probably benign	Het
Ccdc154	T	A	17: 25,389,864 (GRCm39)	V498E	probably damaging	Het
Ccr1l1	A	G	9: 123,777,691 (GRCm39)	L252P	probably damaging	Het
Cdh1	T	C	8: 107,390,953 (GRCm39)	C690R	probably damaging	Het
Cfap157	T	G	2: 32,668,175 (GRCm39)		probably null	Het
Cux2	A	G	5: 122,025,540 (GRCm39)	S43P	possibly damaging	Het
Cyb5rl	C	T	4: 106,925,880 (GRCm39)	P21S	probably damaging	Het
Cyp51	T	G	5: 4,136,594 (GRCm39)	Q400P	probably damaging	Het
Dnah7b	T	C	1: 46,137,152 (GRCm39)		probably benign	Het
Efcab3	G	A	11: 104,642,688 (GRCm39)	V1104I	possibly damaging	Het
Ephb4	A	G	5: 137,352,688 (GRCm39)	I90M	probably benign	Het
Fam13c	A	G	10: 70,378,523 (GRCm39)	N269S	probably damaging	Het
Fam83c	T	A	2: 155,673,444 (GRCm39)	Y248F	possibly damaging	Het
Fat2	A	G	11: 55,194,542 (GRCm39)	F1166L	probably benign	Het
Fem1a	A	G	17: 56,564,686 (GRCm39)	N260D	probably benign	Het
Fnbp4	T	A	2: 90,597,743 (GRCm39)		probably null	Het
Fut9	T	A	4: 25,619,733 (GRCm39)	*360Y	probably null	Het
Fut9	T	A	4: 25,619,734 (GRCm39)	*360L	probably null	Het
Gm3727	T	A	14: 7,264,625 (GRCm38)	Q10L	probably damaging	Het
Gpat2	G	A	2: 127,270,211 (GRCm39)	V75M	probably damaging	Het
Haspin	A	C	11: 73,027,456 (GRCm39)	N544K	probably damaging	Het
Havcr1	A	G	11: 46,669,379 (GRCm39)	N286S	probably benign	Het
Lrp6	A	C	6: 134,436,246 (GRCm39)	C1307G	probably damaging	Het
Lrrc2	A	C	9: 110,808,645 (GRCm39)	H294P	possibly damaging	Het
Mettl25b	A	T	3: 87,834,360 (GRCm39)		probably null	Het
Mon2	A	C	10: 122,878,269 (GRCm39)		probably null	Het
Mrc2	G	A	11: 105,239,257 (GRCm39)		probably null	Het
Mrgprb1	T	C	7: 48,097,070 (GRCm39)	I281V	probably benign	Het
Muc4	A	G	16: 32,569,294 (GRCm39)	E118G	probably damaging	Het
Nefh	T	C	11: 4,893,872 (GRCm39)	D394G	probably damaging	Het
Neurl4	A	G	11: 69,794,047 (GRCm39)	T168A	probably benign	Het
Or10s1	A	G	9: 39,986,211 (GRCm39)	N207D	possibly damaging	Het
Or1j18	T	A	2: 36,624,713 (GRCm39)	C127S	probably damaging	Het
Or5ak4	A	T	2: 85,161,446 (GRCm39)	N265K	probably benign	Het
Oxsr1	A	C	9: 119,123,498 (GRCm39)	M92R	probably damaging	Het
Pde8a	T	C	7: 80,945,516 (GRCm39)		probably null	Het
Pex5l	T	A	3: 33,007,281 (GRCm39)		probably null	Het
Pik3r4	T	A	9: 105,549,984 (GRCm39)	M1025K	probably benign	Het
Plch1	C	T	3: 63,605,903 (GRCm39)	E1325K	probably benign	Het
Plin2	A	T	4: 86,586,669 (GRCm39)	V54E	probably damaging	Het
Prss47	A	T	13: 65,192,887 (GRCm39)	I298N	probably damaging	Het
Prune2	A	G	19: 17,097,546 (GRCm39)	R1017G	probably benign	Het
Psg19	T	A	7: 18,530,911 (GRCm39)	Y81F	possibly damaging	Het
Ptch1	T	G	13: 63,672,773 (GRCm39)	E944A	probably benign	Het
Serpinb1a	T	C	13: 33,034,397 (GRCm39)		probably benign	Het
Sh3pxd2a	A	T	19: 47,266,794 (GRCm39)	V265E	probably damaging	Het
Slc22a17	A	T	14: 55,146,282 (GRCm39)	Y337*	probably null	Het
Slc25a27	A	G	17: 43,968,663 (GRCm39)	V138A	probably benign	Het
Slc4a2	A	G	5: 24,636,314 (GRCm39)	Y220C	probably damaging	Het
Slc66a3	G	A	12: 17,039,840 (GRCm39)	L192F	probably damaging	Het
Stab1	A	T	14: 30,890,392 (GRCm39)	S20T	probably benign	Het
Tcstv2a	A	T	13: 120,725,633 (GRCm39)	Q99L	probably damaging	Het
Thsd1	G	T	8: 22,728,538 (GRCm39)		probably benign	Het
Tmem204	G	A	17: 25,299,566 (GRCm39)		probably benign	Het
Tom1l1	A	G	11: 90,540,721 (GRCm39)		probably benign	Het
Toporsl	T	A	4: 52,612,072 (GRCm39)	F655Y	possibly damaging	Het
Vmn2r98	A	G	17: 19,301,553 (GRCm39)	K852E	unknown	Het
Wdpcp	T	G	11: 21,641,884 (GRCm39)	L174R	probably damaging	Het
Zbbx	G	A	3: 75,019,414 (GRCm39)	P99S	probably damaging	Het
Zfhx4	C	T	3: 5,468,418 (GRCm39)	P2859S	probably benign	Het
Zfp600	A	T	4: 146,133,488 (GRCm39)	R719*	probably null	Het
Zfp697	C	A	3: 98,335,330 (GRCm39)	A365E	unknown	Het
Zfp957	A	C	14: 79,451,053 (GRCm39)	S249A	probably benign	Het

Other mutations in Or51a10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01457:Or51a10	APN	7	103,699,376 (GRCm39)	missense	probably damaging	1.00
IGL01933:Or51a10	APN	7	103,699,021 (GRCm39)	missense	probably damaging	1.00
IGL01980:Or51a10	APN	7	103,699,300 (GRCm39)	missense	probably benign	0.21
IGL02161:Or51a10	APN	7	103,698,797 (GRCm39)	missense	possibly damaging	0.66
IGL02639:Or51a10	APN	7	103,698,988 (GRCm39)	missense	probably damaging	0.99
I2289:Or51a10	UTSW	7	103,698,961 (GRCm39)	missense	probably damaging	1.00
R0418:Or51a10	UTSW	7	103,698,979 (GRCm39)	missense	probably benign	0.00
R1647:Or51a10	UTSW	7	103,699,376 (GRCm39)	missense	probably damaging	1.00
R1648:Or51a10	UTSW	7	103,699,376 (GRCm39)	missense	probably damaging	1.00
R1701:Or51a10	UTSW	7	103,699,402 (GRCm39)	missense	possibly damaging	0.95
R2142:Or51a10	UTSW	7	103,699,507 (GRCm39)	missense	probably damaging	1.00
R2655:Or51a10	UTSW	7	103,698,638 (GRCm39)	missense	probably benign	0.03
R6216:Or51a10	UTSW	7	103,698,902 (GRCm39)	missense	probably damaging	1.00
R6759:Or51a10	UTSW	7	103,699,334 (GRCm39)	missense	probably damaging	1.00
R6925:Or51a10	UTSW	7	103,698,947 (GRCm39)	missense	probably benign	0.16
R7243:Or51a10	UTSW	7	103,698,962 (GRCm39)	missense	probably damaging	1.00
R7684:Or51a10	UTSW	7	103,698,667 (GRCm39)	missense	probably damaging	0.99
R7699:Or51a10	UTSW	7	103,699,800 (GRCm39)	start gained	probably benign
R8316:Or51a10	UTSW	7	103,698,829 (GRCm39)	missense	probably damaging	1.00
R8458:Or51a10	UTSW	7	103,698,875 (GRCm39)	missense	possibly damaging	0.93
R8836:Or51a10	UTSW	7	103,699,055 (GRCm39)	missense	probably benign	0.07
R9161:Or51a10	UTSW	7	103,699,725 (GRCm39)	start gained	probably benign
R9519:Or51a10	UTSW	7	103,698,636 (GRCm39)	missense	probably benign	0.00
Z1176:Or51a10	UTSW	7	103,699,480 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TGGTACCCAGTAACATCTTGTGC -3'
(R):5'- CTACTGCTTACACCCAGACCTG -3'

Sequencing Primer
(F):5'- AGTAACATCTTGTGCAGTCTCCTACG -3'
(R):5'- AGACCTGATACGCTTGCCCTG -3'

Posted On

2014-10-01