Mutagenetix > Incidental Mutation

Incidental Mutation 'R5325:Noa1'

421881

Institutional Source

Beutler Lab

Gene Symbol

Noa1

Ensembl Gene

ENSMUSG00000036285

Gene Name

nitric oxide associated 1

Synonyms

2610024G14Rik, mAtNOS1

MMRRC Submission

042908-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R5325 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

77442029-77457931 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 77452042 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glutamic Acid at position 547 (D547E)

Ref Sequence

ENSEMBL: ENSMUSP00000045948 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000047860]

AlphaFold

Q9JJG9

Predicted Effect

probably damaging
Transcript: ENSMUST00000047860
AA Change: D547E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000045948
Gene: ENSMUSG00000036285
AA Change: D547E

Domain	Start	End	E-Value	Type
low complexity region	2	29	N/A	INTRINSIC
coiled coil region	83	125	N/A	INTRINSIC
low complexity region	224	238	N/A	INTRINSIC
Pfam:MMR_HSR1	342	526	6.5e-9	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139435

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150451

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150722

Meta Mutation Damage Score

0.2233

Coding Region Coverage

1x: 99.3%
3x: 98.8%
10x: 97.6%
20x: 96.0%

Validation Efficiency

98% (55/56)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a nuclear-encoded GTPase that functions in the mitochondrion. Upon translation, this protein is imported into the nucleus and then into the nucleolus before being exported to the mitochondrion. The encoded protein is required for oxygen-dependent regulation of mitochondrial respiratory complexes and for mitochondrial protein synthesis. [provided by RefSeq, Dec 2015]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit embryonic lethality during organogenesis associated with developmental retardation, decreased cell proliferation and apoptosis, increased cell necrosis, and abnormal mitochondrial morphology and physiology. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ace3	T	A	11: 105,896,079 (GRCm39)	M675K	probably benign	Het
Ccdc186	A	T	19: 56,801,613 (GRCm39)	I168N	probably damaging	Het
Ccnb1	C	G	13: 100,918,283 (GRCm39)	Q121H	possibly damaging	Het
Cep83	A	G	10: 94,573,768 (GRCm39)	E219G	probably damaging	Het
Ctsj	T	C	13: 61,151,839 (GRCm39)	T73A	possibly damaging	Het
Ddr2	T	A	1: 169,829,406 (GRCm39)	T283S	probably benign	Het
Ehbp1	T	A	11: 22,045,370 (GRCm39)	D768V	possibly damaging	Het
Evpl	T	C	11: 116,112,191 (GRCm39)	D1833G	probably damaging	Het
Exoc1	A	G	5: 76,685,549 (GRCm39)	N87S	probably benign	Het
Fam98b	A	C	2: 117,101,132 (GRCm39)	I315L	possibly damaging	Het
Fancg	A	G	4: 43,006,564 (GRCm39)	V330A	probably damaging	Het
Fbxo30	G	A	10: 11,166,846 (GRCm39)	V523I	possibly damaging	Het
Fbxw27	A	G	9: 109,599,161 (GRCm39)	C419R	probably damaging	Het
Flt3	C	A	5: 147,312,459 (GRCm39)	V161L	probably benign	Het
Fndc7	G	A	3: 108,790,765 (GRCm39)	T87I	probably damaging	Het
Gm4787	G	C	12: 81,424,604 (GRCm39)	T518S	probably benign	Het
Gm6457	A	T	18: 14,703,498 (GRCm39)		noncoding transcript	Het
Gpr63	T	C	4: 25,007,294 (GRCm39)	V6A	probably benign	Het
Grhl3	T	A	4: 135,286,415 (GRCm39)	K89*	probably null	Het
H2-M10.2	C	A	17: 36,596,471 (GRCm39)	V125L	probably benign	Het
Hrh4	C	T	18: 13,155,054 (GRCm39)	Q198*	probably null	Het
Lrch4	A	G	5: 137,636,168 (GRCm39)	E373G	probably damaging	Het
Mroh9	C	G	1: 162,888,329 (GRCm39)	G249R	probably damaging	Het
Nr2e1	G	A	10: 42,448,780 (GRCm39)	R153W	probably damaging	Het
Nudt9	A	C	5: 104,198,487 (GRCm39)	M1L	possibly damaging	Het
Odf2	T	A	2: 29,802,583 (GRCm39)	D282E	probably benign	Het
Olfr908	A	T	9: 38,427,454 (GRCm39)	N42I	probably damaging	Het
Or13a25	C	A	7: 140,247,705 (GRCm39)	H168Q	probably benign	Het
Or6ae1	T	A	7: 139,742,026 (GRCm39)	Y279F	probably damaging	Het
Osbpl5	C	G	7: 143,245,665 (GRCm39)	A816P	probably damaging	Het
Pan2	T	C	10: 128,153,503 (GRCm39)	I924T	possibly damaging	Het
Ppat	A	G	5: 77,076,269 (GRCm39)		probably benign	Het
Rad50	T	G	11: 53,583,690 (GRCm39)	I364L	probably benign	Het
Rnf7l	A	G	10: 63,257,458 (GRCm39)	S21P	probably benign	Het
Robo2	A	G	16: 73,770,673 (GRCm39)	I484T	possibly damaging	Het
Ryr2	A	T	13: 11,705,249 (GRCm39)	M2839K	probably damaging	Het
Sin3b	A	G	8: 73,477,154 (GRCm39)	D807G	probably damaging	Het
Sirpb1a	G	A	3: 15,476,503 (GRCm39)	T98I	possibly damaging	Het
Smim17	G	A	7: 6,432,321 (GRCm39)	V88M	probably damaging	Het
Spib	T	C	7: 44,177,505 (GRCm39)	T229A	probably damaging	Het
St14	A	T	9: 31,008,274 (GRCm39)		probably null	Het
Syne4	A	T	7: 30,018,401 (GRCm39)	Y381F	probably damaging	Het
Sytl1	T	C	4: 132,988,382 (GRCm39)		probably benign	Het
Tnpo3	A	C	6: 29,602,012 (GRCm39)		probably benign	Het
Trim12a	T	A	7: 103,953,413 (GRCm39)	I233F	probably damaging	Het
Tspan1	T	A	4: 116,021,536 (GRCm39)	N82Y	probably damaging	Het
Vmn1r60	T	A	7: 5,547,201 (GRCm39)	M300L	probably benign	Het
Wdr17	G	A	8: 55,112,716 (GRCm39)	A788V	possibly damaging	Het
Wwtr1	A	T	3: 57,482,658 (GRCm39)	V63E	probably benign	Het
Ylpm1	A	G	12: 85,060,735 (GRCm39)		probably benign	Het
Zfp956	T	C	6: 47,928,012 (GRCm39)		probably benign	Het

Other mutations in Noa1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02119:Noa1	APN	5	77,455,426 (GRCm39)	missense	probably benign
IGL02850:Noa1	APN	5	77,442,338 (GRCm39)	missense	probably benign	0.14
R0149:Noa1	UTSW	5	77,445,020 (GRCm39)	nonsense	probably null
R0361:Noa1	UTSW	5	77,445,020 (GRCm39)	nonsense	probably null
R0645:Noa1	UTSW	5	77,457,722 (GRCm39)	missense	probably benign	0.00
R1226:Noa1	UTSW	5	77,455,402 (GRCm39)	missense	possibly damaging	0.82
R1710:Noa1	UTSW	5	77,457,572 (GRCm39)	missense	possibly damaging	0.49
R1721:Noa1	UTSW	5	77,455,428 (GRCm39)	missense	probably benign	0.00
R1732:Noa1	UTSW	5	77,454,221 (GRCm39)	missense	probably benign	0.01
R2061:Noa1	UTSW	5	77,452,034 (GRCm39)	missense	possibly damaging	0.64
R2262:Noa1	UTSW	5	77,457,651 (GRCm39)	nonsense	probably null
R2965:Noa1	UTSW	5	77,454,191 (GRCm39)	missense	possibly damaging	0.79
R2966:Noa1	UTSW	5	77,454,191 (GRCm39)	missense	possibly damaging	0.79
R4405:Noa1	UTSW	5	77,454,219 (GRCm39)	missense	probably benign	0.00
R4664:Noa1	UTSW	5	77,447,600 (GRCm39)	missense	probably benign	0.31
R4849:Noa1	UTSW	5	77,454,179 (GRCm39)	missense	possibly damaging	0.61
R4920:Noa1	UTSW	5	77,454,334 (GRCm39)	splice site	probably null
R5005:Noa1	UTSW	5	77,456,873 (GRCm39)	missense	probably damaging	1.00
R6112:Noa1	UTSW	5	77,457,593 (GRCm39)	missense	probably benign	0.01
R6254:Noa1	UTSW	5	77,457,516 (GRCm39)	missense	probably benign	0.12
R7659:Noa1	UTSW	5	77,457,237 (GRCm39)	missense	not run
R7810:Noa1	UTSW	5	77,457,071 (GRCm39)	missense	probably damaging	0.99
R7879:Noa1	UTSW	5	77,445,044 (GRCm39)	missense	probably benign	0.01
R7911:Noa1	UTSW	5	77,457,677 (GRCm39)	missense	probably damaging	1.00
R9123:Noa1	UTSW	5	77,457,038 (GRCm39)	missense	possibly damaging	0.87

Predicted Primers

PCR Primer
(F):5'- TTCTCTGGTACCAACTTCACAG -3'
(R):5'- TCTGGCTTACTCTAAAGTCTGAAC -3'

Sequencing Primer
(F):5'- GGTACCAACTTCACAGATTTTAACAC -3'
(R):5'- GAAATAAATACTGTTTTGCCG -3'

Posted On

2016-08-04