Mutagenetix > Incidental Mutation

Incidental Mutation 'R5790:Irx3'

448279

Institutional Source

Beutler Lab

Gene Symbol

Irx3

Ensembl Gene

ENSMUSG00000031734

Gene Name

Iroquois related homeobox 3

Synonyms

MMRRC Submission

043384-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5790 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

92525139-92528282 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 92526304 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 467 (T467A)

Ref Sequence

ENSEMBL: ENSMUSP00000135488 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000093312] [ENSMUST00000175795]

AlphaFold

P81067

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000062522

Predicted Effect

probably benign
Transcript: ENSMUST00000093312
AA Change: T467A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000091002
Gene: ENSMUSG00000031734
AA Change: T467A

Domain	Start	End	E-Value	Type
low complexity region	19	52	N/A	INTRINSIC
low complexity region	59	78	N/A	INTRINSIC
low complexity region	106	123	N/A	INTRINSIC
HOX	131	195	3.47e-12	SMART
coiled coil region	210	244	N/A	INTRINSIC
low complexity region	294	300	N/A	INTRINSIC
IRO	345	362	2.66e-6	SMART
low complexity region	365	384	N/A	INTRINSIC
low complexity region	416	429	N/A	INTRINSIC
low complexity region	436	461	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133337

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133528

Predicted Effect

probably benign
Transcript: ENSMUST00000175795
AA Change: T467A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000135488
Gene: ENSMUSG00000031734
AA Change: T467A

Domain	Start	End	E-Value	Type
low complexity region	19	52	N/A	INTRINSIC
low complexity region	59	78	N/A	INTRINSIC
low complexity region	106	123	N/A	INTRINSIC
HOX	131	195	3.47e-12	SMART
coiled coil region	210	244	N/A	INTRINSIC
low complexity region	294	300	N/A	INTRINSIC
IRO	345	362	2.66e-6	SMART
low complexity region	365	384	N/A	INTRINSIC
low complexity region	416	429	N/A	INTRINSIC
low complexity region	436	461	N/A	INTRINSIC
low complexity region	495	507	N/A	INTRINSIC

Meta Mutation Damage Score

0.0625

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.5%

Validation Efficiency

99% (73/74)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] IRX3 is a member of the Iroquois homeobox gene family (see IRX1; MIM 606197) and plays a role in an early step of neural development (Bellefroid et al., 1998 [PubMed 9427753]). Members of this family appear to play multiple roles during pattern formation of vertebrate embryos (Lewis et al., 1999 [PubMed 10370142]).[supplied by OMIM, Aug 2009]
PHENOTYPE: Mice homozygous for a null allele display right bundle branch block, decreased body weight, increased energy expenditure, reduced adiposity and decreased susceptibility to diet induced obesity. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Agbl5	A	T	5: 31,051,702 (GRCm39)	R633*	probably null	Het
Ahnak	T	C	19: 8,992,612 (GRCm39)	V4632A	probably damaging	Het
Asap1	T	A	15: 63,966,114 (GRCm39)	D997V	probably damaging	Het
Atad2	T	C	15: 57,989,990 (GRCm39)	Y162C	probably damaging	Het
Atp2b2	G	T	6: 113,736,270 (GRCm39)	S936R	probably damaging	Het
Bcl11a	T	A	11: 24,113,650 (GRCm39)	L331Q	probably damaging	Het
C6	T	A	15: 4,792,968 (GRCm39)	F358I	probably damaging	Het
Capn15	C	T	17: 26,183,521 (GRCm39)	S386N	probably benign	Het
Ccdc66	G	A	14: 27,222,404 (GRCm39)	T113I	possibly damaging	Het
Cd200	G	T	16: 45,217,621 (GRCm39)	H23Q	possibly damaging	Het
Cdh17	A	G	4: 11,814,945 (GRCm39)		probably null	Het
Ces2b	C	T	8: 105,560,568 (GRCm39)	P128S	probably damaging	Het
Ces3b	A	T	8: 105,819,270 (GRCm39)	Q442L	probably damaging	Het
Chil4	T	C	3: 106,109,894 (GRCm39)	H373R	probably benign	Het
Ciapin1	C	A	8: 95,551,811 (GRCm39)		probably benign	Het
Cnot10	A	C	9: 114,454,985 (GRCm39)		probably null	Het
Cpq	A	G	15: 33,250,143 (GRCm39)	K167E	probably damaging	Het
Dennd4b	T	A	3: 90,184,757 (GRCm39)	D1118E	probably damaging	Het
Dnah8	T	A	17: 31,093,978 (GRCm39)	C4691S	probably damaging	Het
Dnajc1	A	G	2: 18,311,898 (GRCm39)		probably benign	Het
Dnhd1	G	A	7: 105,304,981 (GRCm39)	R341H	probably damaging	Het
Dock10	G	T	1: 80,482,887 (GRCm39)	T2145K	probably benign	Het
Eif3b	T	C	5: 140,427,886 (GRCm39)	V736A	probably benign	Het
Eno1	G	T	4: 150,329,710 (GRCm39)	V195L	probably benign	Het
Ewsr1	C	T	11: 5,032,263 (GRCm39)		probably benign	Het
Fbn2	T	C	18: 58,209,768 (GRCm39)	T1038A	probably benign	Het
Gabrb1	T	C	5: 72,293,827 (GRCm39)	I367T	possibly damaging	Het
Gigyf1	C	T	5: 137,522,517 (GRCm39)		probably benign	Het
Glp2r	T	A	11: 67,655,625 (GRCm39)	Y39F	probably damaging	Het
Gm10036	T	A	18: 15,966,243 (GRCm39)	Y131*	probably null	Het
Gm38706	T	C	6: 130,461,961 (GRCm39)		noncoding transcript	Het
Gna15	G	A	10: 81,345,218 (GRCm39)	R216C	probably damaging	Het
Grin3a	A	G	4: 49,792,717 (GRCm39)	F339L	probably damaging	Het
Grk3	T	G	5: 113,114,842 (GRCm39)	K126T	possibly damaging	Het
Hspa1l	T	C	17: 35,196,216 (GRCm39)	V85A	probably benign	Het
Iqsec1	A	T	6: 90,666,862 (GRCm39)	L525*	probably null	Het
Itga2	G	A	13: 115,004,742 (GRCm39)	T530I	probably benign	Het
Lonp2	T	C	8: 87,358,118 (GRCm39)	V113A	probably benign	Het
Msx3	C	T	7: 139,628,866 (GRCm39)	R16H	possibly damaging	Het
Nek3	C	A	8: 22,621,313 (GRCm39)	Q405H	probably damaging	Het
Nek3	T	A	8: 22,621,314 (GRCm39)	Q403L	probably damaging	Het
Or2b6	T	C	13: 21,823,046 (GRCm39)	T216A	probably benign	Het
Or6c66	A	G	10: 129,461,757 (GRCm39)	Y58H	probably damaging	Het
P4ha1	A	G	10: 59,190,184 (GRCm39)	N367S	probably benign	Het
Padi6	C	A	4: 140,459,569 (GRCm39)	G429C	probably damaging	Het
Pidd1	T	C	7: 141,021,305 (GRCm39)		probably benign	Het
Plekhg5	T	C	4: 152,198,392 (GRCm39)	V847A	probably benign	Het
Polr3e	A	G	7: 120,527,190 (GRCm39)	D56G	probably damaging	Het
Pomt2	T	G	12: 87,174,152 (GRCm39)	N347T	probably damaging	Het
Ppp1r9a	T	C	6: 5,134,363 (GRCm39)		probably benign	Het
Rbm33	A	T	5: 28,544,296 (GRCm39)	D184V	probably damaging	Het
Rims2	A	T	15: 39,544,441 (GRCm39)	T1431S	probably damaging	Het
Saal1	T	C	7: 46,351,352 (GRCm39)	D208G	probably damaging	Het
Sis	T	C	3: 72,835,507 (GRCm39)	I952V	probably benign	Het
Slc30a1	T	A	1: 191,640,997 (GRCm39)	D214E	probably benign	Het
Slc30a8	T	C	15: 52,197,043 (GRCm39)	V318A	possibly damaging	Het
Smarca2	A	G	19: 26,654,124 (GRCm39)	T770A	probably damaging	Het
Sptbn4	T	A	7: 27,065,853 (GRCm39)	H2031L	probably damaging	Het
Ssbp1	A	G	6: 40,457,804 (GRCm39)	S141G	probably benign	Het
Tgm4	A	G	9: 122,890,808 (GRCm39)	E45G	probably damaging	Het
Thra	T	A	11: 98,653,777 (GRCm39)	S203T	probably benign	Het
Tle2	T	C	10: 81,426,149 (GRCm39)	Y763H	probably damaging	Het
Tmem141	T	A	2: 25,511,087 (GRCm39)	I102L	probably benign	Het
Tmem63c	C	T	12: 87,104,410 (GRCm39)	T77I	probably benign	Het
Tspo2	C	A	17: 48,756,047 (GRCm39)		probably null	Het
Ttc19	T	A	11: 62,172,340 (GRCm39)	M1K	probably null	Het
Ucp1	A	G	8: 84,024,520 (GRCm39)	N282D	possibly damaging	Het
Vmn1r33	A	T	6: 66,589,198 (GRCm39)	F119I	probably benign	Het
Vmn2r24	A	T	6: 123,792,499 (GRCm39)	M609L	probably benign	Het
Vwc2l	A	T	1: 70,790,142 (GRCm39)	H146L	probably damaging	Het

Other mutations in Irx3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0058:Irx3	UTSW	8	92,527,168 (GRCm39)	missense	possibly damaging	0.88
R0080:Irx3	UTSW	8	92,526,954 (GRCm39)	missense	possibly damaging	0.94
R0402:Irx3	UTSW	8	92,527,296 (GRCm39)	missense	possibly damaging	0.77
R0418:Irx3	UTSW	8	92,526,708 (GRCm39)	missense	probably benign	0.00
R0609:Irx3	UTSW	8	92,527,721 (GRCm39)	missense	probably benign	0.18
R0709:Irx3	UTSW	8	92,526,048 (GRCm39)	missense	possibly damaging	0.94
R1753:Irx3	UTSW	8	92,527,362 (GRCm39)	missense	probably damaging	0.98
R3406:Irx3	UTSW	8	92,525,555 (GRCm39)	missense	unknown
R5472:Irx3	UTSW	8	92,526,108 (GRCm39)	splice site	probably null
R5896:Irx3	UTSW	8	92,527,763 (GRCm39)	missense	probably benign
R6611:Irx3	UTSW	8	92,526,631 (GRCm39)	missense	probably damaging	0.97
R6776:Irx3	UTSW	8	92,526,463 (GRCm39)	missense	probably benign	0.00
R6861:Irx3	UTSW	8	92,525,530 (GRCm39)	utr 3 prime	probably benign
R6978:Irx3	UTSW	8	92,527,356 (GRCm39)	missense	probably damaging	0.99
R7472:Irx3	UTSW	8	92,526,625 (GRCm39)	missense	probably benign	0.25
R8304:Irx3	UTSW	8	92,526,834 (GRCm39)	missense	probably damaging	1.00
R8412:Irx3	UTSW	8	92,527,028 (GRCm39)	missense	possibly damaging	0.92
R8906:Irx3	UTSW	8	92,526,915 (GRCm39)	missense	possibly damaging	0.94
R9157:Irx3	UTSW	8	92,527,694 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- ACTTCCAAGGCACTACAGCG -3'
(R):5'- CTTGGCAAATTCCCCGCTTG -3'

Sequencing Primer
(F):5'- TTCCAAGGCACTACAGCGATCTG -3'
(R):5'- TGGACCAACAGGCCTTTC -3'

Posted On

2016-12-15