Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01969:Aire'

181636

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Aire

Ensembl Gene

ENSMUSG00000000731

Gene Name

autoimmune regulator

Synonyms

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL01969

Quality Score

Status

Chromosome

Chromosomal Location

77865856-77879444 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 77878816 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Valine at position 77 (D77V)

Ref Sequence

ENSEMBL: ENSMUSP00000121477 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000019257] [ENSMUST00000105395] [ENSMUST00000105396] [ENSMUST00000128241] [ENSMUST00000130972] [ENSMUST00000131028] [ENSMUST00000140636] [ENSMUST00000143735] [ENSMUST00000155021] [ENSMUST00000145975] [ENSMUST00000148469] [ENSMUST00000154374] [ENSMUST00000156417] [ENSMUST00000138785]

AlphaFold

Q9Z0E3

Predicted Effect

probably damaging
Transcript: ENSMUST00000019257
AA Change: D77V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000019257
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	8.9e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	299	342	6.75e-11	SMART
RING	300	341	3.63e0	SMART
low complexity region	398	419	N/A	INTRINSIC
PHD	432	475	7.82e-7	SMART
RING	433	474	2.49e0	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000105395
AA Change: D77V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000101034
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	1.6e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	300	343	6.75e-11	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000105396
AA Change: D77V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000101035
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	2.2e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	299	342	6.75e-11	SMART
RING	300	341	3.63e0	SMART
PHD	373	416	7.82e-7	SMART
RING	374	415	2.49e0	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000128241
AA Change: D77V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000114904
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	5	104	3.3e-27	PFAM
SAND	198	264	2.61e-26	SMART
PHD	300	343	6.75e-11	SMART
RING	301	342	3.63e0	SMART
low complexity region	399	420	N/A	INTRINSIC
PHD	433	476	7.82e-7	SMART
RING	434	475	2.49e0	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000130972
AA Change: D77V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000122659
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	2.6e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	295	338	6.75e-11	SMART
RING	296	337	3.63e0	SMART
low complexity region	394	415	N/A	INTRINSIC
PHD	428	471	7.82e-7	SMART
RING	429	470	2.49e0	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000131028

SMART Domains

Protein: ENSMUSP00000114808
Gene: ENSMUSG00000000731

Domain	Start	End	E-Value	Type
Pfam:Sp100	5	57	2.6e-13	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135316

Predicted Effect

probably damaging
Transcript: ENSMUST00000140636
AA Change: D77V

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000121477
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	1.6e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	295	338	6.75e-11	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000143735
AA Change: D77V

PolyPhen 2 Score 0.960 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000123678
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	1.1e-34	PFAM
SAND	198	264	2.61e-26	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000155021
AA Change: D77V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000122190
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	2.2e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	295	338	6.75e-11	SMART
RING	296	337	3.63e0	SMART
PHD	369	412	7.82e-7	SMART
RING	370	411	2.49e0	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000145975
AA Change: D77V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000120150
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	2.6e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	296	339	6.75e-11	SMART
RING	297	338	3.63e0	SMART
low complexity region	395	416	N/A	INTRINSIC
PHD	429	472	7.82e-7	SMART
RING	430	471	2.49e0	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000148469
AA Change: D77V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000118317
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	1.6e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	296	339	6.75e-11	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000154374
AA Change: D77V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000117094
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	7.4e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	300	343	6.75e-11	SMART
RING	301	342	3.63e0	SMART
PHD	374	417	7.82e-7	SMART
RING	375	416	2.49e0	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000156417
AA Change: D77V

PolyPhen 2 Score 0.940 (Sensitivity: 0.80; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000115162
Gene: ENSMUSG00000000731
AA Change: D77V

Domain	Start	End	E-Value	Type
Pfam:Sp100	1	107	1.6e-34	PFAM
SAND	198	264	2.61e-26	SMART
PHD	299	342	6.75e-11	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141255

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143548

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143452

Predicted Effect

probably benign
Transcript: ENSMUST00000138785

SMART Domains

Protein: ENSMUSP00000121562
Gene: ENSMUSG00000000730

Domain	Start	End	E-Value	Type
low complexity region	22	32	N/A	INTRINSIC
PDB:2PVC\|C	38	415	1e-163	PDB
SCOP:d1fp0a1	123	191	5e-3	SMART
Blast:RING	130	179	1e-18	BLAST

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 transcriptional regulator that forms nuclear bodies and interacts with the transcriptional coactivator CREB binding protein. The encoded protein plays an important role in immunity by regulating the expression of autoantigens and negative selection of autoreactive T-cells in the thymus. Mutations in this gene cause the rare autosomal-recessive systemic autoimmune disease termed autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy (APECED). [provided by RefSeq, Jun 2012]
PHENOTYPE: Targeted mutations that inactivate the gene result in immune system dysfunction characterized by multiorgan lymphocytic infiltration and circulating autoantibodies. Whereas one line is fertile, another exhibits male and female sterility. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Afg3l1	C	A	8: 124,207,170 (GRCm39)	P74H	probably damaging	Het
Ank2	T	A	3: 126,746,872 (GRCm39)	H571L	possibly damaging	Het
Apol10b	T	C	15: 77,472,885 (GRCm39)		probably null	Het
Cacna2d2	A	T	9: 107,386,415 (GRCm39)	M181L	probably benign	Het
Ccnl1	T	C	3: 65,855,908 (GRCm39)		probably benign	Het
Chd9	A	G	8: 91,760,138 (GRCm39)	E1961G	possibly damaging	Het
Dnajc12	C	A	10: 63,231,609 (GRCm39)	H42N	probably damaging	Het
Eml4	T	C	17: 83,753,409 (GRCm39)	V248A	possibly damaging	Het
Epha10	A	C	4: 124,779,670 (GRCm39)	K172T	probably damaging	Het
Fat1	T	C	8: 45,405,636 (GRCm39)	Y796H	probably damaging	Het
Gpr176	A	C	2: 118,110,118 (GRCm39)	F380L	probably damaging	Het
Guca1a	A	T	17: 47,711,268 (GRCm39)	M26K	probably damaging	Het
Gucy2g	T	G	19: 55,215,870 (GRCm39)	M501L	probably benign	Het
Herc2	T	C	7: 55,835,579 (GRCm39)		probably benign	Het
Itgav	A	G	2: 83,633,627 (GRCm39)	E1028G	probably damaging	Het
Itpr1	A	G	6: 108,354,652 (GRCm39)	T179A	probably damaging	Het
Lpin2	A	G	17: 71,538,502 (GRCm39)	T383A	probably benign	Het
Midn	A	G	10: 79,991,093 (GRCm39)	T325A	probably benign	Het
Mpdz	A	G	4: 81,276,961 (GRCm39)	Y788H	probably damaging	Het
Muc1	A	T	3: 89,139,313 (GRCm39)	D571V	probably damaging	Het
Myo3a	A	T	2: 22,302,499 (GRCm39)	H316L	probably benign	Het
Nagpa	T	C	16: 5,013,753 (GRCm39)	K362E	probably benign	Het
Ola1	G	A	2: 72,930,490 (GRCm39)	A266V	probably benign	Het
Or1e33	T	C	11: 73,738,435 (GRCm39)	N172S	possibly damaging	Het
Or4a47	A	G	2: 89,666,064 (GRCm39)	I75T	probably benign	Het
Or5b97	C	A	19: 12,878,416 (GRCm39)	A243S	possibly damaging	Het
Otof	A	G	5: 30,539,827 (GRCm39)		probably benign	Het
Pi4ka	A	C	16: 17,196,347 (GRCm39)	V105G	probably benign	Het
Plppr4	G	T	3: 117,122,008 (GRCm39)	T190K	probably damaging	Het
Pnpla3	G	A	15: 84,063,425 (GRCm39)	A268T	probably benign	Het
Ppp6r2	C	T	15: 89,159,713 (GRCm39)	H467Y	probably damaging	Het
Prkd2	C	T	7: 16,599,682 (GRCm39)	T715M	probably damaging	Het
Rusc2	A	G	4: 43,415,738 (GRCm39)	N348S	probably benign	Het
Ska3	A	G	14: 58,049,119 (GRCm39)	V284A	probably benign	Het
Slc23a1	A	T	18: 35,757,807 (GRCm39)	V199D	possibly damaging	Het
Slc6a13	T	C	6: 121,312,601 (GRCm39)	L445P	probably damaging	Het
Smo	A	T	6: 29,755,171 (GRCm39)		probably null	Het
Tmem131	A	G	1: 36,864,541 (GRCm39)	L564S	possibly damaging	Het
Ttc23l	G	A	15: 10,551,520 (GRCm39)	Q69*	probably null	Het

Other mutations in Aire

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01744:Aire	APN	10	77,872,557 (GRCm39)	nonsense	probably null
Million	UTSW	10	77,873,809 (GRCm39)	missense	probably damaging	1.00
BB008:Aire	UTSW	10	77,866,130 (GRCm39)	missense	probably damaging	1.00
BB018:Aire	UTSW	10	77,866,130 (GRCm39)	missense	probably damaging	1.00
E0370:Aire	UTSW	10	77,877,897 (GRCm39)	missense	probably damaging	1.00
IGL03055:Aire	UTSW	10	77,878,903 (GRCm39)	missense	probably damaging	1.00
R0326:Aire	UTSW	10	77,878,433 (GRCm39)	missense	probably damaging	1.00
R0675:Aire	UTSW	10	77,870,327 (GRCm39)	splice site	probably benign
R1748:Aire	UTSW	10	77,879,314 (GRCm39)	missense	probably damaging	0.99
R1754:Aire	UTSW	10	77,866,124 (GRCm39)	missense	probably damaging	1.00
R2014:Aire	UTSW	10	77,878,792 (GRCm39)	missense	probably damaging	1.00
R2015:Aire	UTSW	10	77,878,792 (GRCm39)	missense	probably damaging	1.00
R3800:Aire	UTSW	10	77,877,889 (GRCm39)	splice site	probably null
R5424:Aire	UTSW	10	77,872,553 (GRCm39)	missense	probably damaging	1.00
R5517:Aire	UTSW	10	77,875,525 (GRCm39)	missense	probably benign	0.14
R5983:Aire	UTSW	10	77,878,903 (GRCm39)	missense	probably damaging	1.00
R6135:Aire	UTSW	10	77,878,801 (GRCm39)	missense	probably damaging	1.00
R6856:Aire	UTSW	10	77,866,089 (GRCm39)	missense	probably damaging	1.00
R7405:Aire	UTSW	10	77,870,447 (GRCm39)	missense	probably benign	0.01
R7484:Aire	UTSW	10	77,878,404 (GRCm39)	missense	probably damaging	1.00
R7606:Aire	UTSW	10	77,873,767 (GRCm39)	missense	probably damaging	1.00
R7931:Aire	UTSW	10	77,866,130 (GRCm39)	missense	probably damaging	1.00
R8867:Aire	UTSW	10	77,873,809 (GRCm39)	missense	probably damaging	1.00
R8887:Aire	UTSW	10	77,870,298 (GRCm39)	missense	probably damaging	0.96
R9115:Aire	UTSW	10	77,879,309 (GRCm39)	missense
R9562:Aire	UTSW	10	77,871,579 (GRCm39)	missense	probably benign
R9623:Aire	UTSW	10	77,873,809 (GRCm39)	missense	probably damaging	1.00

Posted On

2014-05-07