Mutagenetix > Incidental Mutation

Incidental Mutation 'R6996:Or7c70'

544222

Institutional Source

Beutler Lab

Gene Symbol

Or7c70

Ensembl Gene

ENSMUSG00000051190

Gene Name

olfactory receptor family 7 subfamily C member 70

Synonyms

MOR142-2_p, Olfr1356, MOR142-1, GA_x6K02T2QGN0-2962025-2962987

MMRRC Submission

045102-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.236) question?

Stock #

R6996 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

78682785-78683747 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 78683351 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Leucine at position 133 (V133L)

Ref Sequence

ENSEMBL: ENSMUSP00000144815 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000061289] [ENSMUST00000205100]

AlphaFold

Q7TQU8

Predicted Effect

probably benign
Transcript: ENSMUST00000061289
AA Change: V133L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000054345
Gene: ENSMUSG00000051190
AA Change: V133L

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	3.6e-58	PFAM
Pfam:7TM_GPCR_Srsx	35	305	1.4e-5	PFAM
Pfam:7tm_1	41	290	6.5e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000205100
AA Change: V133L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000144815
Gene: ENSMUSG00000051190
AA Change: V133L

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	3.6e-58	PFAM
Pfam:7TM_GPCR_Srsx	35	305	1.4e-5	PFAM
Pfam:7tm_1	41	290	6.5e-22	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

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: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam5	G	A	8: 25,296,517 (GRCm39)	S310L	probably damaging	Het
Adamts16	C	T	13: 70,946,157 (GRCm39)		probably null	Het
Arrb1	C	A	7: 99,240,569 (GRCm39)	D194E	probably benign	Het
Atp1a3	T	C	7: 24,697,051 (GRCm39)	D217G	probably damaging	Het
Bcar3	A	G	3: 122,302,033 (GRCm39)	I123V	possibly damaging	Het
Bdp1	G	A	13: 100,180,321 (GRCm39)	L1833F	probably damaging	Het
Cdc14a	T	C	3: 116,122,355 (GRCm39)	Y155C	probably damaging	Het
Cdo1	C	A	18: 46,853,380 (GRCm39)	R126M	possibly damaging	Het
Cfap99	G	T	5: 34,484,604 (GRCm39)	R627L	probably damaging	Het
Efr3a	T	A	15: 65,720,030 (GRCm39)	L369*	probably null	Het
Erich6	A	C	3: 58,543,516 (GRCm39)	F185V	probably damaging	Het
Fam186a	T	C	15: 99,853,374 (GRCm39)	D122G	unknown	Het
Fank1	A	G	7: 133,478,627 (GRCm39)	I230M	possibly damaging	Het
Flg2	A	T	3: 93,109,977 (GRCm39)	E668D	unknown	Het
Flg2	A	C	3: 93,110,256 (GRCm39)	R761S	unknown	Het
Gabrr1	T	C	4: 33,158,157 (GRCm39)	L260P	probably damaging	Het
Gfm2	G	A	13: 97,285,868 (GRCm39)	R119K	probably damaging	Het
Gm14226	A	G	2: 154,866,357 (GRCm39)	T105A	probably benign	Het
Gm14496	A	G	2: 181,637,997 (GRCm39)	N357S	probably damaging	Het
Gm5916	G	A	9: 36,039,935 (GRCm39)	L18F	probably benign	Het
Golm1	A	T	13: 59,790,058 (GRCm39)	N247K	probably benign	Het
Gpatch2l	G	A	12: 86,290,958 (GRCm39)	R47H	probably damaging	Het
Greb1	C	T	12: 16,773,355 (GRCm39)	A240T	probably benign	Het
Gtf3c6	T	C	10: 40,125,774 (GRCm39)	M148V	probably benign	Het
Guca1a	T	C	17: 47,706,102 (GRCm39)	S126G	probably benign	Het
Hacl1	A	T	14: 31,337,380 (GRCm39)	I393N	possibly damaging	Het
Hddc3	A	G	7: 79,993,498 (GRCm39)	D68G	possibly damaging	Het
Hsfy2	T	C	1: 56,675,569 (GRCm39)	T323A	possibly damaging	Het
Kcng2	T	C	18: 80,366,358 (GRCm39)		probably benign	Het
Kdm2a	G	T	19: 4,395,669 (GRCm39)	P321T	probably benign	Het
Krt31	A	G	11: 99,938,558 (GRCm39)	V345A	probably benign	Het
Lrrc37	A	T	11: 103,509,583 (GRCm39)	L795*	probably null	Het
Mettl1	T	C	10: 126,880,887 (GRCm39)	S193P	probably benign	Het
Mme	G	A	3: 63,253,523 (GRCm39)	D456N	possibly damaging	Het
Mmrn1	A	G	6: 60,954,367 (GRCm39)	T883A	probably benign	Het
Mphosph10	C	G	7: 64,038,669 (GRCm39)	E293Q	probably benign	Het
Muc16	C	A	9: 18,557,193 (GRCm39)	K3033N	unknown	Het
Myo16	C	T	8: 10,619,496 (GRCm39)	T1349M	probably damaging	Het
Myo5c	T	C	9: 75,157,746 (GRCm39)	I233T	probably benign	Het
Or4p4b-ps1	A	G	2: 88,454,189 (GRCm39)	T181A	unknown	Het
Or52a33	T	G	7: 103,289,065 (GRCm39)	N94T	probably benign	Het
Or52ac1	A	T	7: 104,246,018 (GRCm39)	F123L	probably benign	Het
Or5b111	A	T	19: 13,291,036 (GRCm39)	S204R	probably benign	Het
Or5h22	A	G	16: 58,894,555 (GRCm39)	M296T	probably benign	Het
Or6c2	T	A	10: 129,362,732 (GRCm39)	V212E	probably damaging	Het
Oxct2b	A	G	4: 123,011,480 (GRCm39)	I467V	probably benign	Het
Parp1	A	T	1: 180,414,936 (GRCm39)	N425Y	possibly damaging	Het
Pcdhgc3	T	A	18: 37,939,656 (GRCm39)	V19D	possibly damaging	Het
Pfkl	T	A	10: 77,833,423 (GRCm39)	I260F	probably damaging	Het
Pkd1l1	C	T	11: 8,799,046 (GRCm39)	G1789R	probably damaging	Het
Pla1a	G	A	16: 38,217,830 (GRCm39)	A386V	probably benign	Het
Pml	A	G	9: 58,142,169 (GRCm39)	L221P	probably damaging	Het
Rcn2	C	T	9: 55,964,845 (GRCm39)	Q268*	probably null	Het
Reps1	T	A	10: 17,969,603 (GRCm39)	D235E	probably damaging	Het
Rsf1	CGGCGGCGG	CGGCGGCGGGGGCGGCGG	7: 97,229,118 (GRCm39)		probably benign	Het
Sap30bp	A	G	11: 115,824,314 (GRCm39)		probably benign	Het
Scn1a	A	T	2: 66,118,075 (GRCm39)	S1433T	probably damaging	Het
Sde2	T	C	1: 180,678,754 (GRCm39)	V6A	probably benign	Het
Sdk1	C	A	5: 142,197,769 (GRCm39)	R2141S	probably benign	Het
Setd2	T	C	9: 110,379,640 (GRCm39)	S1152P	probably damaging	Het
Slc26a2	C	T	18: 61,334,926 (GRCm39)	V176I	probably damaging	Het
Snx7	A	G	3: 117,640,281 (GRCm39)	I76T	possibly damaging	Het
Specc1l	C	A	10: 75,082,113 (GRCm39)	A520D	probably benign	Het
Spop	A	G	11: 95,362,136 (GRCm39)	T56A	possibly damaging	Het
Syne2	T	A	12: 76,074,786 (GRCm39)	D4576E	probably damaging	Het
Tas2r134	A	C	2: 51,517,601 (GRCm39)	M27L	probably benign	Het
Tecta	A	C	9: 42,278,082 (GRCm39)	I1142S	probably benign	Het
Timm44	T	C	8: 4,316,611 (GRCm39)	D311G	possibly damaging	Het
Tmem123	C	G	9: 7,791,071 (GRCm39)	T124R	possibly damaging	Het
Tmem184b	A	T	15: 79,246,959 (GRCm39)	L370Q	probably benign	Het
Trim25	T	A	11: 88,890,329 (GRCm39)	N5K	probably benign	Het
Vmn2r93	A	G	17: 18,524,903 (GRCm39)	Y187C	probably damaging	Het
Vpreb1a	A	G	16: 16,686,678 (GRCm39)	Y71H	probably damaging	Het
Vpreb1b	T	C	16: 17,798,441 (GRCm39)	S5P	probably benign	Het
Xpo7	A	T	14: 70,906,888 (GRCm39)	C939S	probably benign	Het
Zfp78	C	A	7: 6,381,764 (GRCm39)	S271R	probably benign	Het
Zic5	A	T	14: 122,702,080 (GRCm39)	M217K	probably benign	Het

Other mutations in Or7c70

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00904:Or7c70	APN	10	78,683,597 (GRCm39)	missense	probably damaging	1.00
IGL01343:Or7c70	APN	10	78,683,431 (GRCm39)	missense	probably damaging	0.97
IGL01576:Or7c70	APN	10	78,683,207 (GRCm39)	missense	possibly damaging	0.94
IGL02314:Or7c70	APN	10	78,683,099 (GRCm39)	missense	probably damaging	1.00
IGL02474:Or7c70	APN	10	78,682,897 (GRCm39)	missense	probably damaging	1.00
IGL02960:Or7c70	APN	10	78,683,371 (GRCm39)	missense	probably damaging	1.00
IGL03049:Or7c70	APN	10	78,683,356 (GRCm39)	missense	possibly damaging	0.81
IGL03328:Or7c70	APN	10	78,683,201 (GRCm39)	missense	probably benign	0.39
R1602:Or7c70	UTSW	10	78,682,802 (GRCm39)	missense	probably benign
R1722:Or7c70	UTSW	10	78,682,805 (GRCm39)	missense	probably benign
R2178:Or7c70	UTSW	10	78,683,612 (GRCm39)	missense	probably damaging	0.96
R3903:Or7c70	UTSW	10	78,683,132 (GRCm39)	missense	probably benign	0.00
R3904:Or7c70	UTSW	10	78,683,132 (GRCm39)	missense	probably benign	0.00
R4241:Or7c70	UTSW	10	78,683,739 (GRCm39)	missense	probably benign	0.00
R4833:Or7c70	UTSW	10	78,683,409 (GRCm39)	missense	probably damaging	1.00
R5465:Or7c70	UTSW	10	78,682,852 (GRCm39)	missense	probably benign	0.00
R5527:Or7c70	UTSW	10	78,683,609 (GRCm39)	missense	probably benign	0.02
R5606:Or7c70	UTSW	10	78,683,395 (GRCm39)	missense	probably benign	0.19
R5977:Or7c70	UTSW	10	78,683,572 (GRCm39)	missense	possibly damaging	0.95
R6219:Or7c70	UTSW	10	78,683,093 (GRCm39)	missense	possibly damaging	0.88
R7136:Or7c70	UTSW	10	78,683,615 (GRCm39)	missense	probably benign	0.43
R7782:Or7c70	UTSW	10	78,683,447 (GRCm39)	missense	probably benign	0.01
R7996:Or7c70	UTSW	10	78,683,155 (GRCm39)	missense	probably damaging	1.00
R8955:Or7c70	UTSW	10	78,683,576 (GRCm39)	missense	probably damaging	1.00
R9330:Or7c70	UTSW	10	78,683,153 (GRCm39)	missense	probably benign	0.00
R9427:Or7c70	UTSW	10	78,682,906 (GRCm39)	missense	probably damaging	0.99
R9474:Or7c70	UTSW	10	78,682,891 (GRCm39)	missense	probably damaging	0.99
Z1176:Or7c70	UTSW	10	78,682,855 (GRCm39)	missense	possibly damaging	0.73
Z1177:Or7c70	UTSW	10	78,683,290 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CAGGCAAGCTTCAGGACTTC -3'
(R):5'- TGTGGCCATCATATCTGACCC -3'

Sequencing Primer
(F):5'- CTTCAGGACTTCGGGAAGATCAC -3'
(R):5'- ACCTGTCCATAGCTGACATCGG -3'

Posted On

2019-05-13