Mutagenetix > Incidental Mutation

Incidental Mutation 'R4756:Or7a38'

358028

Institutional Source

Beutler Lab

Gene Symbol

Or7a38

Ensembl Gene

ENSMUSG00000094673

Gene Name

olfactory receptor family 7 subfamily A member 38

Synonyms

GA_x6K02T03FR9-4826-3919, Olfr1354, Olfr233-ps1, MOR185-8, EG257869, MOR139-7, MOR139-5, GA_x6K02T2QGN0-2895081-2894349

MMRRC Submission

041972-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.170) question?

Stock #

R4756 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

78752676-78753770 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 78753361 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 229 (I229N)

Ref Sequence

ENSEMBL: ENSMUSP00000150374 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000075859] [ENSMUST00000204587] [ENSMUST00000217073]

AlphaFold

E9Q5G9

Predicted Effect

probably damaging
Transcript: ENSMUST00000075859
AA Change: I229N

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000093126
Gene: ENSMUSG00000094673
AA Change: I229N

Domain	Start	End	E-Value	Type
Pfam:7tm_4	32	309	2.4e-49	PFAM
Pfam:7tm_1	42	291	3.8e-22	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000203132
AA Change: I229N

SMART Domains

Protein: ENSMUSP00000144897
Gene: ENSMUSG00000094673
AA Change: I229N

Domain	Start	End	E-Value	Type
Pfam:7tm_4	32	309	2.4e-49	PFAM
Pfam:7tm_1	42	291	3.8e-22	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000204587
AA Change: I229N

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000205040

SMART Domains

Protein: ENSMUSP00000144994
Gene: ENSMUSG00000094673

Domain	Start	End	E-Value	Type
Pfam:7tm_4	32	146	9.6e-24	PFAM
Pfam:7TM_GPCR_Srsx	36	147	1.8e-6	PFAM
Pfam:7tm_1	42	147	4e-20	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000217073
AA Change: I229N

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 94.9%

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
4930550C14Rik	A	T	9: 53,336,830 (GRCm39)	M45L	probably benign	Het
Acss2	T	C	2: 155,403,063 (GRCm39)	F627L	probably damaging	Het
Akap8	A	G	17: 32,535,184 (GRCm39)	S277P	probably damaging	Het
Akap9	T	A	5: 4,051,418 (GRCm39)	M1395K	probably damaging	Het
Ank1	A	G	8: 23,612,893 (GRCm39)	D1468G	probably benign	Het
Apoe	A	G	7: 19,430,846 (GRCm39)	V121A	probably benign	Het
Aqp9	A	T	9: 71,070,331 (GRCm39)	L12H	probably damaging	Het
Atp2b4	G	A	1: 133,639,529 (GRCm39)	A1115V	probably benign	Het
Atp2b4	G	A	1: 133,667,134 (GRCm39)	P139L	probably benign	Het
B430218F22Rik	T	C	13: 118,523,980 (GRCm39)		probably benign	Het
Bltp2	T	A	11: 78,154,854 (GRCm39)	L122H	probably damaging	Het
Brsk1	A	G	7: 4,711,866 (GRCm39)	E572G	possibly damaging	Het
C6	T	C	15: 4,811,394 (GRCm39)	I414T	probably benign	Het
C8b	T	A	4: 104,644,083 (GRCm39)	M250K	probably benign	Het
Camk1g	T	A	1: 193,044,393 (GRCm39)	E7V	probably benign	Het
Clcc1	A	G	3: 108,580,236 (GRCm39)		probably null	Het
Col4a3	G	T	1: 82,694,018 (GRCm39)		probably null	Het
Cox5b	T	A	1: 36,732,310 (GRCm39)	W104R	probably damaging	Het
Cyp2c55	A	C	19: 39,019,815 (GRCm39)	H251P	probably damaging	Het
Cyp2c67	G	A	19: 39,632,188 (GRCm39)	T60I	probably benign	Het
Defb42	T	A	14: 63,285,824 (GRCm39)	V68E	probably benign	Het
Ercc4	T	A	16: 12,941,287 (GRCm39)	I225N	probably damaging	Het
Fam120b	G	T	17: 15,622,658 (GRCm39)	C212F	probably damaging	Het
Fgf10	T	C	13: 118,918,045 (GRCm39)	V111A	probably benign	Het
Fn1	G	T	1: 71,629,967 (GRCm39)	T2186K	probably damaging	Het
Fras1	T	C	5: 96,929,518 (GRCm39)	V3974A	probably benign	Het
Galnt4	T	C	10: 98,944,362 (GRCm39)	V29A	probably benign	Het
Gpr26	T	C	7: 131,569,230 (GRCm39)	Y192H	probably damaging	Het
Heatr9	A	T	11: 83,407,475 (GRCm39)	L236Q	probably damaging	Het
Hivep3	C	A	4: 119,955,020 (GRCm39)	P1112H	probably damaging	Het
Hnf4g	A	G	3: 3,708,069 (GRCm39)	Y106C	possibly damaging	Het
Hnrnpdl	A	T	5: 100,185,783 (GRCm39)	Y69*	probably null	Het
Itgb1	G	A	8: 129,443,703 (GRCm39)	A320T	probably damaging	Het
Kcna2	T	C	3: 107,012,733 (GRCm39)	I438T	probably benign	Het
Kif24	A	G	4: 41,397,545 (GRCm39)		probably null	Het
Klhl1	G	A	14: 96,389,402 (GRCm39)	T584I	probably benign	Het
Ltbp1	A	G	17: 75,532,199 (GRCm39)	D91G	probably damaging	Het
Mdga2	T	C	12: 66,844,427 (GRCm39)	I190M	probably damaging	Het
Meis2	G	A	2: 115,830,686 (GRCm39)	R276C	probably damaging	Het
Mob4	C	T	1: 55,191,855 (GRCm39)	R190W	probably damaging	Het
Mrgpra2a	A	G	7: 47,077,114 (GRCm39)	I48T	possibly damaging	Het
Mst1	T	C	9: 107,960,826 (GRCm39)	V481A	probably benign	Het
Mttp	A	T	3: 137,821,832 (GRCm39)	V245E	possibly damaging	Het
Nbn	T	A	4: 15,981,470 (GRCm39)	S521T	probably benign	Het
Neb	G	T	2: 52,083,243 (GRCm39)	T5654N	probably damaging	Het
Nlrp9a	A	T	7: 26,256,866 (GRCm39)	K161N	probably damaging	Het
Nod2	T	G	8: 89,390,902 (GRCm39)	F388C	possibly damaging	Het
Or3a1	G	T	11: 74,225,402 (GRCm39)	F218L	probably benign	Het
Or4a75	G	T	2: 89,447,814 (GRCm39)	H241N	possibly damaging	Het
Or4f58	A	G	2: 111,851,332 (GRCm39)	F289S	possibly damaging	Het
Or52e2	A	T	7: 102,804,332 (GRCm39)	N207K	probably benign	Het
Or7g25	G	A	9: 19,160,153 (GRCm39)	L181F	possibly damaging	Het
P2ry1	A	G	3: 60,911,898 (GRCm39)	S346G	probably benign	Het
Polr1f	T	A	12: 33,487,679 (GRCm39)		probably null	Het
Prkcd	A	G	14: 30,321,623 (GRCm39)	F524L	probably benign	Het
Qrfprl	T	C	6: 65,429,898 (GRCm39)	I198T	probably benign	Het
Ramp3	A	T	11: 6,624,843 (GRCm39)	M46L	probably benign	Het
Rint1	T	C	5: 24,014,791 (GRCm39)	Y278H	probably damaging	Het
Skint11	C	T	4: 114,051,874 (GRCm39)	T74I	probably benign	Het
Slc10a7	T	C	8: 79,433,579 (GRCm39)		probably null	Het
Slc45a2	T	A	15: 11,028,016 (GRCm39)	Y528*	probably null	Het
Slit1	A	G	19: 41,637,452 (GRCm39)	F329L	probably damaging	Het
Sltm	A	T	9: 70,498,892 (GRCm39)	M989L	possibly damaging	Het
Smad9	A	T	3: 54,701,874 (GRCm39)	T372S	possibly damaging	Het
Snrpc	T	A	17: 28,061,306 (GRCm39)	Y38*	probably null	Het
Spag17	A	G	3: 100,010,701 (GRCm39)	K2065R	possibly damaging	Het
Stxbp4	T	A	11: 90,498,197 (GRCm39)	K87N	probably damaging	Het
Tbc1d23	AT	ATT	16: 57,019,258 (GRCm39)		probably null	Het
Tgfb1i1	A	T	7: 127,848,571 (GRCm39)	M96L	probably damaging	Het
Tnc	T	A	4: 63,885,580 (GRCm39)	I1841F	probably damaging	Het
Ubap2	G	T	4: 41,211,771 (GRCm39)	H63Q	probably damaging	Het
Vps13a	T	C	19: 16,632,580 (GRCm39)	N2592S	probably benign	Het
Xdh	G	A	17: 74,193,381 (GRCm39)	P1305L	probably benign	Het
Xrn1	G	A	9: 95,921,862 (GRCm39)	R1425K	probably benign	Het
Zfp418	G	A	7: 7,185,762 (GRCm39)	R575Q	possibly damaging	Het
Zfp608	T	A	18: 55,027,544 (GRCm39)	Q1424H	probably damaging	Het
Zfp839	C	A	12: 110,821,635 (GRCm39)	L150I	possibly damaging	Het

Other mutations in Or7a38

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02903:Or7a38	APN	10	78,753,250 (GRCm39)	missense	probably damaging	0.99
IGL02962:Or7a38	APN	10	78,752,773 (GRCm39)	missense	probably damaging	1.00
IGL03032:Or7a38	APN	10	78,753,471 (GRCm39)	missense	probably benign	0.21
PIT4495001:Or7a38	UTSW	10	78,752,821 (GRCm39)	missense	probably benign
R0268:Or7a38	UTSW	10	78,753,439 (GRCm39)	missense	probably damaging	0.99
R0359:Or7a38	UTSW	10	78,753,177 (GRCm39)	missense	probably benign	0.00
R0382:Or7a38	UTSW	10	78,752,960 (GRCm39)	nonsense	probably null
R1895:Or7a38	UTSW	10	78,752,758 (GRCm39)	missense	probably damaging	1.00
R1946:Or7a38	UTSW	10	78,752,758 (GRCm39)	missense	probably damaging	1.00
R2035:Or7a38	UTSW	10	78,753,421 (GRCm39)	missense	possibly damaging	0.86
R3853:Or7a38	UTSW	10	78,752,781 (GRCm39)	missense	probably damaging	1.00
R5326:Or7a38	UTSW	10	78,753,420 (GRCm39)	missense	possibly damaging	0.86
R5607:Or7a38	UTSW	10	78,752,933 (GRCm39)	missense	possibly damaging	0.93
R7070:Or7a38	UTSW	10	78,753,102 (GRCm39)	missense	probably benign
R7088:Or7a38	UTSW	10	78,753,593 (GRCm39)	missense	probably benign	0.00
R7212:Or7a38	UTSW	10	78,753,339 (GRCm39)	missense	possibly damaging	0.81
R7348:Or7a38	UTSW	10	78,753,396 (GRCm39)	missense	probably damaging	1.00
R7386:Or7a38	UTSW	10	78,752,677 (GRCm39)	start codon destroyed	probably null	0.98
R7847:Or7a38	UTSW	10	78,752,730 (GRCm39)	missense	probably benign	0.02
R8976:Or7a38	UTSW	10	78,753,418 (GRCm39)	missense	possibly damaging	0.79
R9267:Or7a38	UTSW	10	78,752,803 (GRCm39)	missense	probably damaging	1.00
R9502:Or7a38	UTSW	10	78,753,559 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCCTTCTTACAGAGCTCAATTGTG -3'
(R):5'- TAAAGGGGTTCAGCATCGG -3'

Sequencing Primer
(F):5'- GAGCTCAATTGTGCTACAGTTGACC -3'
(R):5'- ATCACAGAGGCTCTTGCA -3'

Posted On

2015-11-11