Mutagenetix > Incidental Mutation

Incidental Mutation 'R8471:Or10d5b'

657029

Institutional Source

Beutler Lab

Gene Symbol

Or10d5b

Ensembl Gene

Gene Name

olfactory receptor family 10 subfamily D member 5B, pseudogene 1

Synonyms

GA_x6K02T2PVTD-33675353-33674411, MOR224-11, Olfr977

MMRRC Submission

067915-MU

Accession Numbers

Essential gene?

Not available question?

Stock #

R8471 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

39885175-39886117 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 39885901 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 73 (S73P)

Ref Sequence

ENSEMBL: ENSMUSP00000149176 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000217438]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000217438
AA Change: S73P

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

100% (36/36)

Allele List at MGI

Other mutations in this stock

Total: 36 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700066M21Rik	T	A	1: 57,422,223 (GRCm39)	C200S	probably damaging	Het
Abca1	G	A	4: 53,044,187 (GRCm39)	H1812Y	probably damaging	Het
Adgrv1	T	A	13: 81,594,591 (GRCm39)	D4141V	probably benign	Het
Arhgef38	A	T	3: 132,940,472 (GRCm39)	V38E	probably damaging	Het
Arl15	T	A	13: 114,037,632 (GRCm39)		probably benign	Het
Cwh43	T	A	5: 73,591,644 (GRCm39)	L493Q	probably damaging	Het
Dnah7b	C	T	1: 46,138,650 (GRCm39)	H231Y	possibly damaging	Het
Eif2d	C	A	1: 131,092,155 (GRCm39)	Q309K	probably benign	Het
Epop	A	G	11: 97,520,073 (GRCm39)	V12A	possibly damaging	Het
Fkbp5	C	T	17: 28,634,943 (GRCm39)	V189I	probably benign	Het
Ikzf2	T	C	1: 69,578,499 (GRCm39)	M343V	probably benign	Het
Kdm5a	T	A	6: 120,407,192 (GRCm39)	L1469*	probably null	Het
Man2b2	A	T	5: 36,979,183 (GRCm39)	W286R	probably damaging	Het
Naip5	G	T	13: 100,358,153 (GRCm39)	Q1028K	probably damaging	Het
Nlrp1a	T	A	11: 71,013,885 (GRCm39)	D455V	possibly damaging	Het
Or10ag60	A	G	2: 87,437,989 (GRCm39)	R86G	probably damaging	Het
Or1e32	A	T	11: 73,705,309 (GRCm39)	F200I	probably benign	Het
Or5af1	A	G	11: 58,722,597 (GRCm39)	M206V	probably benign	Het
Pcdh12	G	A	18: 38,415,308 (GRCm39)	P606S	probably benign	Het
Plec	A	G	15: 76,070,620 (GRCm39)	V894A	probably damaging	Het
Ppp4r3a	T	C	12: 101,021,901 (GRCm39)	N333S	probably benign	Het
Ptger4	A	T	15: 5,271,800 (GRCm39)	M273K	probably damaging	Het
Pzp	T	C	6: 128,464,411 (GRCm39)	D1372G	probably benign	Het
Rai14	T	C	15: 10,575,245 (GRCm39)	K571R	probably benign	Het
Rarb	T	A	14: 16,548,456 (GRCm38)		probably benign	Het
Ros1	A	G	10: 51,997,078 (GRCm39)	V1198A	probably benign	Het
Ryr3	A	G	2: 112,484,125 (GRCm39)	V3879A	probably damaging	Het
Serpinb6d	A	T	13: 33,848,137 (GRCm39)	I34F	probably damaging	Het
Slc44a2	T	G	9: 21,253,265 (GRCm39)	I62S	probably null	Het
Snx9	T	A	17: 5,940,365 (GRCm39)	W39R	probably damaging	Het
Tbcb	A	T	7: 29,931,100 (GRCm39)	S7T	probably benign	Het
Ttc21a	C	A	9: 119,792,242 (GRCm39)		probably null	Het
Ttc7	G	A	17: 87,601,454 (GRCm39)	G63R	probably benign	Het
Zdhhc3	A	T	9: 122,929,440 (GRCm39)	V65D	probably damaging	Het
Zfp518b	T	C	5: 38,831,426 (GRCm39)	Y193C	probably damaging	Het
Zw10	T	A	9: 48,982,914 (GRCm39)	I515N	probably damaging	Het

Other mutations in Or10d5b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R6984:Or10d5b	UTSW	9	39,886,030 (GRCm39)	missense	unknown
R7643:Or10d5b	UTSW	9	39,886,117 (GRCm39)	start codon destroyed	unknown

Predicted Primers

Posted On

2021-01-18