Mutagenetix > Incidental Mutation

Incidental Mutation 'R7327:Or5h27'

569021

Institutional Source

Beutler Lab

Gene Symbol

Or5h27

Ensembl Gene

ENSMUSG00000061501

Gene Name

olfactory receptor family 5 subfamily H member 27, pseudogene 1

Synonyms

Olfr197, GA_x54KRFPKG5P-55400292-55399363, MOR183-3

MMRRC Submission

045420-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.221) question?

Stock #

R7327 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

59005919-59006844 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 59006376 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Isoleucine at position 157 (F157I)

Ref Sequence

ENSEMBL: ENSMUSP00000146916 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080031] [ENSMUST00000207772]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000080031
AA Change: F157I

Predicted Effect

unknown
Transcript: ENSMUST00000207772
AA Change: F157I

Coding Region Coverage

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

Validation Efficiency

100% (63/63)

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcf3	C	T	16: 20,367,430 (GRCm39)	T3I	probably benign	Het
Ahi1	T	A	10: 20,862,976 (GRCm39)	V717E	probably damaging	Het
Anapc4	A	G	5: 53,002,672 (GRCm39)	T238A	probably damaging	Het
Arhgap27	A	T	11: 103,251,367 (GRCm39)	C120*	probably null	Het
Bdp1	A	T	13: 100,178,040 (GRCm39)	V1943D	probably damaging	Het
Cdc14b	A	G	13: 64,373,461 (GRCm39)	V141A	probably damaging	Het
Cfap46	G	T	7: 139,215,062 (GRCm39)		probably null	Het
Cgnl1	C	A	9: 71,633,165 (GRCm39)	R62L	possibly damaging	Het
Chaf1a	A	G	17: 56,369,573 (GRCm39)	S522G	probably benign	Het
Cox19	A	G	5: 139,328,402 (GRCm39)	F37S	probably damaging	Het
Csmd1	G	A	8: 16,108,721 (GRCm39)	S1894L	probably damaging	Het
Cyp4a12a	A	T	4: 115,184,756 (GRCm39)	R346W	probably damaging	Het
Dip2a	A	C	10: 76,108,396 (GRCm39)	C1315G	probably benign	Het
Dmxl2	A	C	9: 54,308,869 (GRCm39)	W1961G	probably damaging	Het
Dst	T	C	1: 34,240,486 (GRCm39)	L1945P	probably damaging	Het
Efr3a	A	G	15: 65,691,627 (GRCm39)	S92G	probably damaging	Het
Ep300	C	T	15: 81,511,515 (GRCm39)	T865I	unknown	Het
Ercc6	A	G	14: 32,248,361 (GRCm39)	E304G	probably benign	Het
Filip1l	A	C	16: 57,391,300 (GRCm39)	E629D	probably damaging	Het
Frem1	G	A	4: 82,938,992 (GRCm39)	T30I	possibly damaging	Het
Glb1	T	C	9: 114,246,126 (GRCm39)	F59S	probably benign	Het
Gli3	T	C	13: 15,900,144 (GRCm39)	L1177P	probably benign	Het
Gpatch2l	A	G	12: 86,303,646 (GRCm39)	T223A	probably damaging	Het
Gpt2	G	A	8: 86,244,681 (GRCm39)	E325K	probably benign	Het
Hmcn1	A	T	1: 150,479,565 (GRCm39)	M4633K	probably benign	Het
Hoxc8	T	A	15: 102,899,542 (GRCm39)	Y111N	probably damaging	Het
Ifi207	A	G	1: 173,556,581 (GRCm39)	L726P	probably benign	Het
Iqcn	T	A	8: 71,169,453 (GRCm39)	M1181K	possibly damaging	Het
Iqgap2	T	A	13: 95,772,163 (GRCm39)	M1339L	probably benign	Het
Kif21b	A	G	1: 136,087,387 (GRCm39)	Q901R	possibly damaging	Het
Krtap4-8	C	A	11: 99,671,234 (GRCm39)	C79F	unknown	Het
Ldb3	T	C	14: 34,293,759 (GRCm39)	N155S	probably damaging	Het
Mad2l1	T	A	6: 66,516,794 (GRCm39)	V162E	probably benign	Het
Map7	T	A	10: 20,109,208 (GRCm39)	V87E	unknown	Het
Mndal	A	T	1: 173,703,185 (GRCm39)	D73E	unknown	Het
Msantd1	T	C	5: 35,075,039 (GRCm39)	S34P	probably damaging	Het
Myh14	T	C	7: 44,260,977 (GRCm39)	Q1838R	possibly damaging	Het
Myh15	G	T	16: 48,993,369 (GRCm39)	R1668L	possibly damaging	Het
Ncoa7	A	G	10: 30,565,796 (GRCm39)	M666T	probably damaging	Het
Nol6	A	T	4: 41,116,686 (GRCm39)	L944Q	probably benign	Het
Orc1	A	G	4: 108,445,911 (GRCm39)	T10A	probably benign	Het
Pcp4l1	G	A	1: 171,002,034 (GRCm39)	A42V	possibly damaging	Het
Pglyrp2	C	T	17: 32,634,893 (GRCm39)	A490T	probably benign	Het
Pirb	A	T	7: 3,720,187 (GRCm39)	C395*	probably null	Het
Ppp1r11	T	C	17: 37,261,900 (GRCm39)	R12G	possibly damaging	Het
Prlr	A	G	15: 10,346,524 (GRCm39)	D290G	probably benign	Het
Ptpn21	G	T	12: 98,646,360 (GRCm39)	R1033S	probably damaging	Het
Rad54l2	A	G	9: 106,570,660 (GRCm39)	L1220P	possibly damaging	Het
Rufy3	G	A	5: 88,790,811 (GRCm39)	R504H	probably damaging	Het
Scgb2b21	C	T	7: 33,219,330 (GRCm39)	V25I	probably benign	Het
Sh3bgrl2	T	C	9: 83,430,542 (GRCm39)	S11P	possibly damaging	Het
Slain2	A	T	5: 73,132,002 (GRCm39)	T498S	probably benign	Het
Slc12a4	C	T	8: 106,682,347 (GRCm39)	G121S	probably damaging	Het
Slc30a9	A	T	5: 67,499,462 (GRCm39)	I307F	probably damaging	Het
Snap91	C	T	9: 86,655,598 (GRCm39)	G800R	unknown	Het
Tnc	G	T	4: 63,882,999 (GRCm39)		probably null	Het
Trav21-dv12	T	C	14: 54,113,514 (GRCm39)		probably benign	Het
Txk	A	T	5: 72,873,226 (GRCm39)	I228N	probably damaging	Het
Vac14	T	C	8: 111,438,252 (GRCm39)	Y622H	probably damaging	Het
Vmn2r111	T	C	17: 22,778,032 (GRCm39)	N549S	possibly damaging	Het
Wdr35	T	G	12: 9,037,312 (GRCm39)	M306R	probably benign	Het
Zan	A	T	5: 137,463,494 (GRCm39)	S562T	probably benign	Het

Other mutations in Or5h27

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R4612:Or5h27	UTSW	16	59,006,674 (GRCm39)	missense	probably damaging	1.00
R5777:Or5h27	UTSW	16	59,006,266 (GRCm39)	missense	unknown
R5945:Or5h27	UTSW	16	59,006,091 (GRCm39)	missense	unknown
R6045:Or5h27	UTSW	16	59,006,454 (GRCm39)	missense	probably benign	0.07
R6752:Or5h27	UTSW	16	59,006,694 (GRCm39)	missense	probably damaging	1.00
R7284:Or5h27	UTSW	16	59,006,331 (GRCm39)	makesense	probably null
R7387:Or5h27	UTSW	16	59,006,699 (GRCm39)	missense	probably damaging	1.00
R8089:Or5h27	UTSW	16	59,006,073 (GRCm39)	missense	unknown
R8420:Or5h27	UTSW	16	59,006,117 (GRCm39)	missense	unknown
R8489:Or5h27	UTSW	16	59,006,400 (GRCm39)	makesense	probably null
R8870:Or5h27	UTSW	16	59,006,130 (GRCm39)	missense	unknown
R9311:Or5h27	UTSW	16	59,006,106 (GRCm39)	missense	unknown
R9431:Or5h27	UTSW	16	59,006,090 (GRCm39)	missense	unknown
Z1176:Or5h27	UTSW	16	59,006,848 (GRCm39)	start gained	probably benign
Z1177:Or5h27	UTSW	16	59,006,363 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- TGTGTAAGAGCCTAGAATAGTTGAG -3'
(R):5'- GATGCTCCTCACCTTCACAG -3'

Sequencing Primer
(F):5'- AGATAGTGAAAACTTGAATTGAGCC -3'
(R):5'- GAGCAAACTGATCTCTCTGAATGC -3'

Posted On

2019-09-13