Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00909:Naca'

28314

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Naca

Ensembl Gene

ENSMUSG00000061315

Gene Name

nascent polypeptide-associated complex alpha polypeptide

Synonyms

LOC380777, skNAC

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.734) question?

Stock #

IGL00909

Quality Score

Status

Chromosome

Chromosomal Location

127871444-127884506 bp(+) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

A to G at 127877551 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000073532 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073868] [ENSMUST00000092048]

AlphaFold

P70670

Predicted Effect

probably benign
Transcript: ENSMUST00000073868

SMART Domains

Protein: ENSMUSP00000073532
Gene: ENSMUSG00000061315

Domain	Start	End	E-Value	Type
low complexity region	44	57	N/A	INTRINSIC
Pfam:NAC	73	130	3.9e-27	PFAM
low complexity region	157	178	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000092048
AA Change: N861S

SMART Domains

Protein: ENSMUSP00000089680
Gene: ENSMUSG00000061315
AA Change: N861S

Domain	Start	End	E-Value	Type
low complexity region	61	72	N/A	INTRINSIC
low complexity region	105	117	N/A	INTRINSIC
low complexity region	128	142	N/A	INTRINSIC
low complexity region	516	533	N/A	INTRINSIC
low complexity region	704	718	N/A	INTRINSIC
low complexity region	937	954	N/A	INTRINSIC
low complexity region	976	998	N/A	INTRINSIC
low complexity region	1174	1195	N/A	INTRINSIC
low complexity region	1349	1370	N/A	INTRINSIC
low complexity region	1489	1504	N/A	INTRINSIC
low complexity region	1572	1593	N/A	INTRINSIC
low complexity region	1636	1670	N/A	INTRINSIC
low complexity region	1714	1727	N/A	INTRINSIC
low complexity region	1806	1827	N/A	INTRINSIC
low complexity region	1889	1926	N/A	INTRINSIC
low complexity region	1943	1957	N/A	INTRINSIC
low complexity region	1972	1986	N/A	INTRINSIC
low complexity region	2016	2029	N/A	INTRINSIC
Pfam:NAC	2045	2101	1.7e-25	PFAM
low complexity region	2129	2150	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that associates with basic transcription factor 3 (BTF3) to form the nascent polypeptide-associated complex (NAC). This complex binds to nascent proteins that lack a signal peptide motif as they emerge from the ribosome, blocking interaction with the signal recognition particle (SRP) and preventing mistranslocation to the endoplasmic reticulum. This protein is an IgE autoantigen in atopic dermatitis patients. Alternative splicing results in multiple transcript variants, but the full length nature of some of these variants, including those encoding very large proteins, has not been determined. There are multiple pseudogenes of this gene on different chromosomes. [provided by RefSeq, Feb 2016]
PHENOTYPE: Mice homozygous for a point mutation exhibit decreased bone volume and bone formation associated with accelerated mineralization and immature woven-bone formation. Mice null for the muscle specific isoform die during organogenesis with cardiac abnormalities. [provided by MGI curators]

Allele List at MGI

All alleles(156) : Targeted, other(1) Gene trapped(155)

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931429L15Rik	T	A	9: 46,220,250 (GRCm39)	D94V	possibly damaging	Het
Adamts20	T	C	15: 94,277,694 (GRCm39)	Y256C	probably damaging	Het
Ajm1	A	G	2: 25,469,419 (GRCm39)	L164P	probably damaging	Het
Ampd1	A	C	3: 102,995,744 (GRCm39)	D218A	probably benign	Het
Arcn1	T	C	9: 44,662,651 (GRCm39)	N332D	probably damaging	Het
Arpp21	T	A	9: 112,005,191 (GRCm39)	I219F	probably damaging	Het
Bicra	A	T	7: 15,730,502 (GRCm39)	D5E	possibly damaging	Het
Birc2	A	C	9: 7,833,666 (GRCm39)	W272G	probably damaging	Het
Cd2ap	A	T	17: 43,141,005 (GRCm39)		probably benign	Het
Celsr1	G	A	15: 85,806,436 (GRCm39)	R974W	probably damaging	Het
Col4a2	A	C	8: 11,498,167 (GRCm39)	T1659P	possibly damaging	Het
Coq9	C	T	8: 95,578,530 (GRCm39)	L215F	possibly damaging	Het
Cped1	A	G	6: 22,122,426 (GRCm39)		probably benign	Het
Elapor2	A	T	5: 9,430,282 (GRCm39)	D64V	probably damaging	Het
Gga3	T	A	11: 115,482,567 (GRCm39)	R105W	probably damaging	Het
Hmcn1	C	T	1: 150,514,620 (GRCm39)	R3584Q	probably benign	Het
Hs6st3	T	A	14: 119,376,446 (GRCm39)	L207Q	probably damaging	Het
Ift43	A	G	12: 86,208,807 (GRCm39)	E141G	probably damaging	Het
Mrps31	T	G	8: 22,917,841 (GRCm39)	F287V	probably damaging	Het
Nrf1	C	T	6: 30,098,477 (GRCm39)	T135M	probably damaging	Het
Or5p81	A	G	7: 108,266,907 (GRCm39)	I95V	possibly damaging	Het
Pfas	A	T	11: 68,894,640 (GRCm39)	Y8*	probably null	Het
Ppip5k1	G	A	2: 121,177,839 (GRCm39)	R323W	probably damaging	Het
Rasal1	A	G	5: 120,802,872 (GRCm39)	E376G	probably damaging	Het
Rfc1	A	G	5: 65,437,042 (GRCm39)	L546P	probably benign	Het
Rheb	A	T	5: 25,012,073 (GRCm39)	I129N	probably damaging	Het
Scpep1	A	T	11: 88,843,303 (GRCm39)	F52I	probably damaging	Het
Six2	A	T	17: 85,995,319 (GRCm39)	L21Q	probably damaging	Het
Slit1	G	T	19: 41,590,694 (GRCm39)	T1326K	possibly damaging	Het
Spata2l	T	C	8: 123,960,716 (GRCm39)	D191G	possibly damaging	Het
Susd4	C	A	1: 182,719,552 (GRCm39)	A389D	probably damaging	Het
Tcaf2	A	T	6: 42,601,510 (GRCm39)	F850I	probably damaging	Het
Teddm1b	T	C	1: 153,750,391 (GRCm39)	S67P	probably damaging	Het
Tiparp	T	A	3: 65,439,530 (GRCm39)	V100D	probably damaging	Het
Zdhhc14	A	G	17: 5,803,067 (GRCm39)	H390R	probably benign	Het

Other mutations in Naca

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00990:Naca	APN	10	127,879,669 (GRCm39)	intron	probably benign
IGL01093:Naca	APN	10	127,883,982 (GRCm39)	missense	probably damaging	0.99
IGL01356:Naca	APN	10	127,877,584 (GRCm39)	intron	probably benign
IGL01548:Naca	APN	10	127,876,773 (GRCm39)	intron	probably benign
IGL02089:Naca	APN	10	127,872,358 (GRCm39)	splice site	probably benign
IGL02148:Naca	APN	10	127,879,753 (GRCm39)	intron	probably benign
IGL02494:Naca	APN	10	127,877,179 (GRCm39)	intron	probably benign
IGL02672:Naca	APN	10	127,876,152 (GRCm39)	intron	probably benign
IGL02822:Naca	APN	10	127,875,214 (GRCm39)	intron	probably benign
IGL02904:Naca	APN	10	127,879,159 (GRCm39)	intron	probably benign
IGL02931:Naca	APN	10	127,883,551 (GRCm39)	missense	probably damaging	1.00
IGL02971:Naca	APN	10	127,877,437 (GRCm39)	intron	probably benign
IGL03104:Naca	APN	10	127,876,233 (GRCm39)	intron	probably benign
Sinewy	UTSW	10	127,884,227 (GRCm39)	missense	probably damaging	1.00
D4216:Naca	UTSW	10	127,880,109 (GRCm39)	missense	possibly damaging	0.73
P0042:Naca	UTSW	10	127,877,422 (GRCm39)	intron	probably benign
R0110:Naca	UTSW	10	127,880,659 (GRCm39)	missense	probably benign	0.13
R0220:Naca	UTSW	10	127,879,255 (GRCm39)	intron	probably benign
R0469:Naca	UTSW	10	127,880,659 (GRCm39)	missense	probably benign	0.13
R0528:Naca	UTSW	10	127,879,162 (GRCm39)	missense	probably benign	0.23
R0594:Naca	UTSW	10	127,876,224 (GRCm39)	intron	probably benign
R0626:Naca	UTSW	10	127,877,031 (GRCm39)	intron	probably benign
R0885:Naca	UTSW	10	127,876,048 (GRCm39)	nonsense	probably null
R1129:Naca	UTSW	10	127,876,071 (GRCm39)	intron	probably benign
R1437:Naca	UTSW	10	127,878,048 (GRCm39)	intron	probably benign
R1464:Naca	UTSW	10	127,884,157 (GRCm39)	missense	probably damaging	0.96
R1464:Naca	UTSW	10	127,884,157 (GRCm39)	missense	probably damaging	0.96
R1509:Naca	UTSW	10	127,879,266 (GRCm39)	intron	probably benign
R1561:Naca	UTSW	10	127,876,267 (GRCm39)	intron	probably benign
R1574:Naca	UTSW	10	127,876,267 (GRCm39)	intron	probably benign
R1678:Naca	UTSW	10	127,879,395 (GRCm39)	intron	probably benign
R1901:Naca	UTSW	10	127,879,590 (GRCm39)	intron	probably benign
R2884:Naca	UTSW	10	127,877,547 (GRCm39)	intron	probably benign
R2886:Naca	UTSW	10	127,877,547 (GRCm39)	intron	probably benign
R3176:Naca	UTSW	10	127,876,530 (GRCm39)	intron	probably benign
R3276:Naca	UTSW	10	127,876,530 (GRCm39)	intron	probably benign
R4227:Naca	UTSW	10	127,877,530 (GRCm39)	intron	probably benign
R4388:Naca	UTSW	10	127,880,661 (GRCm39)	missense	probably damaging	0.99
R4402:Naca	UTSW	10	127,879,341 (GRCm39)	intron	probably benign
R4798:Naca	UTSW	10	127,883,672 (GRCm39)	missense	probably null	0.99
R4955:Naca	UTSW	10	127,878,084 (GRCm39)	intron	probably benign
R4996:Naca	UTSW	10	127,878,298 (GRCm39)	intron	probably benign
R5027:Naca	UTSW	10	127,883,990 (GRCm39)	missense	possibly damaging	0.63
R5580:Naca	UTSW	10	127,876,462 (GRCm39)	intron	probably benign
R5752:Naca	UTSW	10	127,877,797 (GRCm39)	intron	probably benign
R5788:Naca	UTSW	10	127,876,011 (GRCm39)	intron	probably benign
R6156:Naca	UTSW	10	127,875,160 (GRCm39)	intron	probably benign
R6227:Naca	UTSW	10	127,879,785 (GRCm39)	intron	probably benign
R6317:Naca	UTSW	10	127,879,993 (GRCm39)	missense	probably benign	0.33
R6665:Naca	UTSW	10	127,884,227 (GRCm39)	missense	probably damaging	1.00
R7170:Naca	UTSW	10	127,875,990 (GRCm39)	missense	unknown
R7247:Naca	UTSW	10	127,878,467 (GRCm39)	missense	unknown
R7632:Naca	UTSW	10	127,876,375 (GRCm39)	missense	unknown
R7826:Naca	UTSW	10	127,879,479 (GRCm39)	intron	probably benign
R7921:Naca	UTSW	10	127,878,918 (GRCm39)	missense	unknown
R8059:Naca	UTSW	10	127,876,372 (GRCm39)	missense	unknown
R8084:Naca	UTSW	10	127,877,400 (GRCm39)	missense	unknown
R8385:Naca	UTSW	10	127,878,307 (GRCm39)	missense	unknown
R8515:Naca	UTSW	10	127,880,112 (GRCm39)	missense	possibly damaging	0.73
R8708:Naca	UTSW	10	127,883,943 (GRCm39)	missense	probably damaging	1.00
R9629:Naca	UTSW	10	127,878,226 (GRCm39)	missense	unknown
X0053:Naca	UTSW	10	127,884,124 (GRCm39)	missense	probably damaging	0.98

Posted On

2013-04-17