Mutagenetix > Incidental Mutation

Incidental Mutation 'R1763:Or4c10b'

193166

Institutional Source

Beutler Lab

Gene Symbol

Or4c10b

Ensembl Gene

ENSMUSG00000049057

Gene Name

olfactory receptor family 4 subfamily C member 10B

Synonyms

MOR232-1, Olfr1257, GA_x6K02T2Q125-51319458-51320387

MMRRC Submission

039795-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.087) question?

Stock #

R1763 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

89878437-89883026 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 89881129 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Glutamic Acid at position 101 (G101E)

Ref Sequence

ENSEMBL: ENSMUSP00000107144 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000060795] [ENSMUST00000111519]

AlphaFold

Q8VGP0

Predicted Effect

probably damaging
Transcript: ENSMUST00000060795
AA Change: G101E

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000056439
Gene: ENSMUSG00000049057
AA Change: G101E

Domain	Start	End	E-Value	Type
Pfam:7tm_1	39	285	2.6e-31	PFAM
Pfam:7tm_4	137	278	8e-42	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000111519
AA Change: G101E

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000107144
Gene: ENSMUSG00000049057
AA Change: G101E

Domain	Start	End	E-Value	Type
Pfam:7tm_4	29	303	1.5e-49	PFAM
Pfam:7tm_1	39	285	3.9e-18	PFAM

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.1%
20x: 92.0%

Validation Efficiency

98% (85/87)

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: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4fm4	A	G	4: 144,669,959 (GRCm38)	V401A	probably benign	Het
Abca4	A	T	3: 122,163,830 (GRCm38)	T772S	probably damaging	Het
Abca4	G	A	3: 122,110,681 (GRCm38)	V794M	probably benign	Het
Acox3	G	A	5: 35,608,339 (GRCm38)		probably null	Het
Adamts17	A	G	7: 67,147,715 (GRCm38)	N1060S	probably damaging	Het
Akap8l	C	T	17: 32,332,483 (GRCm38)	R511H	probably damaging	Het
Als2	T	C	1: 59,174,991 (GRCm38)	Y1346C	probably benign	Het
Apol10b	A	T	15: 77,585,015 (GRCm38)	F321I	probably benign	Het
Atp5pb	A	G	3: 105,951,589 (GRCm38)		probably null	Het
Bloc1s5	A	G	13: 38,619,084 (GRCm38)		probably benign	Het
Btbd9	T	C	17: 30,334,297 (GRCm38)	N397S	possibly damaging	Het
Cacna1d	A	G	14: 30,099,196 (GRCm38)	V1121A	probably benign	Het
Cad	G	A	5: 31,060,951 (GRCm38)	V460I	probably damaging	Het
Caprin2	A	T	6: 148,843,121 (GRCm38)	D935E	probably damaging	Het
Ccdc150	A	T	1: 54,354,636 (GRCm38)	K686N	probably benign	Het
Ccnt2	T	C	1: 127,799,406 (GRCm38)	F186L	possibly damaging	Het
Cd5l	G	A	3: 87,367,880 (GRCm38)		probably null	Het
Chrna7	A	G	7: 63,099,252 (GRCm38)	V494A	probably benign	Het
Clec2i	T	G	6: 128,895,425 (GRCm38)	Y198*	probably null	Het
Col22a1	A	G	15: 72,007,176 (GRCm38)	V44A	probably damaging	Het
Cspg4	T	A	9: 56,886,979 (GRCm38)	I666N	probably damaging	Het
Cyp3a16	A	T	5: 145,465,031 (GRCm38)		probably null	Het
Dlk1	G	T	12: 109,458,119 (GRCm38)	C102F	probably damaging	Het
Dscc1	T	A	15: 55,084,139 (GRCm38)	H215L	probably damaging	Het
Dscc1	CTGAATGAAT	CTGAAT	15: 55,080,176 (GRCm38)		probably benign	Het
Dus1l	C	G	11: 120,795,671 (GRCm38)	G15R	probably benign	Het
Eps8l1	G	T	7: 4,471,823 (GRCm38)	V268L	probably benign	Het
F2	A	C	2: 91,634,906 (GRCm38)	C104W	probably damaging	Het
F5	C	A	1: 164,192,535 (GRCm38)	Q860K	probably benign	Het
Fmn2	T	C	1: 174,502,266 (GRCm38)	L74P	unknown	Het
Frmd6	G	A	12: 70,893,622 (GRCm38)	R347Q	possibly damaging	Het
Gabbr1	T	G	17: 37,054,767 (GRCm38)	S158A	probably damaging	Het
Galc	T	C	12: 98,234,266 (GRCm38)	N295S	probably damaging	Het
Gm6408	A	T	5: 146,482,322 (GRCm38)	N49I	probably damaging	Het
Grm1	T	A	10: 11,079,866 (GRCm38)	T225S	possibly damaging	Het
Grm8	C	T	6: 27,285,867 (GRCm38)	V849I	possibly damaging	Het
Hmcn2	A	G	2: 31,314,590 (GRCm38)	D59G	probably damaging	Het
Iars1	G	A	13: 49,723,077 (GRCm38)		probably null	Het
Ifi27	C	T	12: 103,437,682 (GRCm38)	A127V	possibly damaging	Het
Ikbip	A	G	10: 91,096,481 (GRCm38)	N329S	probably damaging	Het
Ikbke	T	C	1: 131,265,877 (GRCm38)	T479A	probably benign	Het
Krt12	T	A	11: 99,416,060 (GRCm38)	N472I	probably damaging	Het
Lmnb2	A	T	10: 80,907,191 (GRCm38)	L193Q	probably damaging	Het
Lrriq4	T	C	3: 30,650,252 (GRCm38)	V128A	probably benign	Het
Map4k4	C	A	1: 40,000,757 (GRCm38)		probably benign	Het
Mtmr7	T	C	8: 40,551,811 (GRCm38)	T575A	probably benign	Het
Myh13	G	A	11: 67,334,576 (GRCm38)	A256T	probably benign	Het
Napepld	A	G	5: 21,683,410 (GRCm38)	Y14H	probably benign	Het
Npr1	T	C	3: 90,459,337 (GRCm38)	T552A	probably damaging	Het
Nudt15	A	G	14: 73,521,647 (GRCm38)	F127S	probably benign	Het
Nwd2	T	A	5: 63,808,271 (GRCm38)	S1733T	probably benign	Het
Or11a4	T	C	17: 37,225,430 (GRCm38)	F102L	probably benign	Het
Or4c102	A	G	2: 88,592,436 (GRCm38)	I211V	probably benign	Het
Or6z1	T	G	7: 6,501,441 (GRCm38)	I262L	probably benign	Het
Or8b44	A	G	9: 38,499,038 (GRCm38)	Y123C	probably damaging	Het
Paqr7	A	T	4: 134,507,098 (GRCm38)	I89F	probably benign	Het
Pidd1	C	A	7: 141,439,630 (GRCm38)	V706L	probably benign	Het
Polr3c	A	T	3: 96,713,595 (GRCm38)	I469N	probably damaging	Het
Ppip5k1	A	G	2: 121,348,547 (GRCm38)	Y233H	probably damaging	Het
Psmc3	A	G	2: 91,055,995 (GRCm38)	T166A	possibly damaging	Het
Ptchd3	A	T	11: 121,842,542 (GRCm38)	I753L	probably benign	Het
Rad21	T	C	15: 51,978,170 (GRCm38)	K50R	probably damaging	Het
Rad54b	A	G	4: 11,604,989 (GRCm38)	E479G	possibly damaging	Het
Rfwd3	C	T	8: 111,288,242 (GRCm38)	R326Q	probably damaging	Het
Rgs20	C	T	1: 4,910,640 (GRCm38)	R154Q	probably damaging	Het
Sbf1	T	C	15: 89,294,425 (GRCm38)	D1449G	probably damaging	Het
Sema4g	C	T	19: 45,001,605 (GRCm38)	R708*	probably null	Het
Septin9	T	C	11: 117,290,428 (GRCm38)	I18T	probably benign	Het
Serpinb6b	A	G	13: 32,978,058 (GRCm38)	E280G	probably damaging	Het
Slamf6	T	C	1: 171,942,587 (GRCm38)		probably benign	Het
Slc6a21	G	A	7: 45,287,734 (GRCm38)	W554*	probably null	Het
Slco1a4	A	C	6: 141,812,731 (GRCm38)	I518R	probably benign	Het
Stab1	T	A	14: 31,168,416 (GRCm38)	Q26L	probably benign	Het
Stox1	A	G	10: 62,667,965 (GRCm38)	F104L	probably damaging	Het
Suco	T	C	1: 161,834,949 (GRCm38)	K638E	possibly damaging	Het
Synpo	T	C	18: 60,602,784 (GRCm38)	K458E	probably damaging	Het
Szt2	A	T	4: 118,372,368 (GRCm38)	W2820R	unknown	Het
Tmtc1	C	A	6: 148,294,618 (GRCm38)	G499W	probably damaging	Het
Tonsl	A	C	15: 76,638,066 (GRCm38)	S242R	probably damaging	Het
Trpc4	G	T	3: 54,194,822 (GRCm38)	S47I	possibly damaging	Het
Zfp106	G	A	2: 120,520,428 (GRCm38)	R1581C	probably benign	Het
Zfp27	A	G	7: 29,895,376 (GRCm38)	L388P	possibly damaging	Het

Other mutations in Or4c10b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01600:Or4c10b	APN	2	89,881,662 (GRCm38)	missense	probably benign	0.02
IGL01641:Or4c10b	APN	2	89,881,608 (GRCm38)	missense	probably benign	0.01
IGL01668:Or4c10b	APN	2	89,881,099 (GRCm38)	missense	probably benign	0.01
IGL01901:Or4c10b	APN	2	89,881,482 (GRCm38)	missense	probably damaging	1.00
IGL02401:Or4c10b	APN	2	89,881,453 (GRCm38)	missense	probably damaging	1.00
IGL02472:Or4c10b	APN	2	89,881,411 (GRCm38)	missense	probably benign	0.44
IGL02631:Or4c10b	APN	2	89,881,255 (GRCm38)	missense	possibly damaging	0.95
PIT4354001:Or4c10b	UTSW	2	89,881,508 (GRCm38)	missense	probably benign	0.04
R0552:Or4c10b	UTSW	2	89,880,891 (GRCm38)	nonsense	probably null
R0616:Or4c10b	UTSW	2	89,881,591 (GRCm38)	missense	probably benign	0.07
R0943:Or4c10b	UTSW	2	89,880,961 (GRCm38)	missense	probably benign	0.11
R1146:Or4c10b	UTSW	2	89,881,206 (GRCm38)	missense	probably damaging	1.00
R1146:Or4c10b	UTSW	2	89,881,206 (GRCm38)	missense	probably damaging	1.00
R1314:Or4c10b	UTSW	2	89,880,877 (GRCm38)	missense	probably benign	0.35
R1641:Or4c10b	UTSW	2	89,881,401 (GRCm38)	missense	probably benign	0.07
R1836:Or4c10b	UTSW	2	89,881,285 (GRCm38)	missense	probably damaging	1.00
R2125:Or4c10b	UTSW	2	89,881,638 (GRCm38)	missense	probably benign
R4322:Or4c10b	UTSW	2	89,881,734 (GRCm38)	missense	probably benign	0.07
R4897:Or4c10b	UTSW	2	89,881,132 (GRCm38)	missense	probably benign	0.39
R5446:Or4c10b	UTSW	2	89,881,549 (GRCm38)	missense	probably damaging	1.00
R5456:Or4c10b	UTSW	2	89,881,258 (GRCm38)	missense	probably damaging	0.97
R6415:Or4c10b	UTSW	2	89,880,862 (GRCm38)	missense	probably damaging	1.00
R6905:Or4c10b	UTSW	2	89,881,708 (GRCm38)	missense	probably benign	0.05
R7170:Or4c10b	UTSW	2	89,881,053 (GRCm38)	missense	possibly damaging	0.70
R7170:Or4c10b	UTSW	2	89,880,841 (GRCm38)	missense	probably benign	0.12
R7411:Or4c10b	UTSW	2	89,881,261 (GRCm38)	missense	probably damaging	0.98
R8171:Or4c10b	UTSW	2	89,881,065 (GRCm38)	missense	probably benign	0.05
R8490:Or4c10b	UTSW	2	89,881,167 (GRCm38)	missense	probably damaging	1.00
R9176:Or4c10b	UTSW	2	89,881,171 (GRCm38)	missense	probably benign	0.05
R9204:Or4c10b	UTSW	2	89,881,138 (GRCm38)	missense	probably damaging	1.00
R9751:Or4c10b	UTSW	2	89,881,612 (GRCm38)	missense	probably benign	0.02

Predicted Primers

PCR Primer
(F):5'- TCTGGGACTCACAGAGAACCCAAAG -3'
(R):5'- GGTGGCATGAAGAAAACCTCCTAGC -3'

Sequencing Primer
(F):5'- ACAGGAAATGTGCTCATTGTG -3'
(R):5'- TGAAGAAAACCTCCTAGCCATGAC -3'

Posted On

2014-05-23