Mutagenetix > Incidental Mutation

Incidental Mutation 'R5503:Mlxip'

430727

Institutional Source

Beutler Lab

Gene Symbol

Mlxip

Ensembl Gene

ENSMUSG00000038342

Gene Name

MLX interacting protein

Synonyms

Mir, bHLHe36, Mondoa

MMRRC Submission

043064-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.309) question?

Stock #

R5503 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

123532861-123595995 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 123533390 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 133 (M133K)

Ref Sequence

ENSEMBL: ENSMUSP00000064943 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000068237] [ENSMUST00000111596]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000068237
AA Change: M133K

PolyPhen 2 Score 0.977 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000064943
Gene: ENSMUSG00000038342
AA Change: M133K

Domain	Start	End	E-Value	Type
low complexity region	9	19	N/A	INTRINSIC
low complexity region	27	44	N/A	INTRINSIC
low complexity region	47	73	N/A	INTRINSIC
PDB:4GNT\|B	157	177	8e-7	PDB
low complexity region	347	363	N/A	INTRINSIC
low complexity region	436	467	N/A	INTRINSIC
low complexity region	514	539	N/A	INTRINSIC
low complexity region	557	570	N/A	INTRINSIC
low complexity region	632	643	N/A	INTRINSIC
low complexity region	686	704	N/A	INTRINSIC
HLH	723	773	2.81e-9	SMART
low complexity region	880	894	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000111596
AA Change: M133K

PolyPhen 2 Score 0.971 (Sensitivity: 0.77; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000107223
Gene: ENSMUSG00000038342
AA Change: M133K

Domain	Start	End	E-Value	Type
low complexity region	9	19	N/A	INTRINSIC
low complexity region	27	44	N/A	INTRINSIC
low complexity region	47	73	N/A	INTRINSIC
PDB:4GNT\|B	157	177	6e-7	PDB
low complexity region	347	363	N/A	INTRINSIC
low complexity region	436	467	N/A	INTRINSIC
low complexity region	514	539	N/A	INTRINSIC
low complexity region	557	570	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141216

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151096

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000199793

Meta Mutation Damage Score

0.6134

Coding Region Coverage

1x: 98.3%
3x: 97.4%
10x: 95.4%
20x: 91.5%

Validation Efficiency

96% (103/107)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that functions as part of a heterodimer to activate transcription. The encoded protein forms a heterodimer with Max-like protein X (MLX) and is involved in the regulation of genes in response to cellular glucose levels. [provided by RefSeq, Mar 2014]

Allele List at MGI

Other mutations in this stock

Total: 88 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700049A03Rik	A	T	12: 71,211,321 (GRCm39)	E685V	possibly damaging	Het
2700049A03Rik	G	T	12: 71,211,320 (GRCm39)	E685*	probably null	Het
Abca6	A	G	11: 110,109,083 (GRCm39)	S696P	probably damaging	Het
Abca9	G	A	11: 110,032,436 (GRCm39)	T727M	probably damaging	Het
Alpk2	T	C	18: 65,439,312 (GRCm39)	R1161G	probably benign	Het
Amy1	T	C	3: 113,349,709 (GRCm39)	D487G	probably benign	Het
Arap2	G	A	5: 62,787,529 (GRCm39)	A1409V	probably damaging	Het
B4galt6	C	A	18: 20,878,409 (GRCm39)		probably null	Het
Cacna1s	G	A	1: 136,014,480 (GRCm39)	G382D	probably damaging	Het
Camk2a	A	G	18: 61,111,072 (GRCm39)	D87G	probably damaging	Het
Cdh18	A	G	15: 23,436,620 (GRCm39)	Y492C	probably damaging	Het
Cert1	C	T	13: 96,679,747 (GRCm39)	R26C	possibly damaging	Het
Col18a1	C	T	10: 76,907,454 (GRCm39)	G861D	probably damaging	Het
Crybg1	C	A	10: 43,874,762 (GRCm39)	S782I	probably benign	Het
Csgalnact1	G	A	8: 68,914,125 (GRCm39)	L27F	probably damaging	Het
Dab1	T	A	4: 104,369,461 (GRCm39)	C3S	probably benign	Het
Dapk1	T	C	13: 60,873,126 (GRCm39)	F343L	probably benign	Het
Dgat1	A	T	15: 76,386,394 (GRCm39)		probably benign	Het
Dnah11	C	A	12: 117,844,186 (GRCm39)		probably null	Het
Dsg2	T	A	18: 20,713,708 (GRCm39)	Y226*	probably null	Het
Epg5	T	A	18: 77,994,422 (GRCm39)	M351K	possibly damaging	Het
F13b	A	G	1: 139,450,281 (GRCm39)	T648A	probably benign	Het
Fgf17	T	C	14: 70,874,408 (GRCm39)	Y127C	probably damaging	Het
Fkbp15	G	A	4: 62,246,124 (GRCm39)	P435S	probably benign	Het
Gfm1	G	A	3: 67,361,060 (GRCm39)		probably null	Het
Gigyf1	T	C	5: 137,521,729 (GRCm39)		probably benign	Het
Gm12830	A	T	4: 114,678,936 (GRCm39)	T6S	unknown	Het
Gm6465	A	T	5: 11,898,150 (GRCm39)	N88I	probably damaging	Het
Gpr18	C	T	14: 122,149,159 (GRCm39)	V289I	probably damaging	Het
Ipp	G	T	4: 116,395,135 (GRCm39)	E557*	probably null	Het
Klhl12	T	A	1: 134,413,653 (GRCm39)		probably null	Het
Klhl38	A	G	15: 58,185,745 (GRCm39)	V328A	possibly damaging	Het
Kndc1	A	G	7: 139,511,802 (GRCm39)	T1470A	probably damaging	Het
Kntc1	T	A	5: 123,957,939 (GRCm39)	D2173E	possibly damaging	Het
Lipi	T	C	16: 75,370,864 (GRCm39)	K118E	probably benign	Het
Marf1	A	C	16: 13,970,095 (GRCm39)	L208R	probably damaging	Het
Misp	G	A	10: 79,662,552 (GRCm39)	R323K	probably damaging	Het
Mon2	A	T	10: 122,868,550 (GRCm39)	M501K	possibly damaging	Het
Myh2	A	G	11: 67,064,275 (GRCm39)	I77V	probably benign	Het
Napa	C	A	7: 15,849,549 (GRCm39)	Q254K	probably benign	Het
Nckap5l	C	A	15: 99,323,503 (GRCm39)	G1000V	probably damaging	Het
Neo1	A	T	9: 58,892,933 (GRCm39)	S236R	possibly damaging	Het
Neurl4	T	A	11: 69,797,194 (GRCm39)	Y594N	probably damaging	Het
Nmral1	G	A	16: 4,533,493 (GRCm39)	P94L	probably benign	Het
Notch3	A	T	17: 32,366,029 (GRCm39)	I1024N	probably benign	Het
Nsd1	T	A	13: 55,393,752 (GRCm39)	I451K	probably damaging	Het
Nt5c3b	T	C	11: 100,323,883 (GRCm39)	D143G	probably benign	Het
Oplah	A	G	15: 76,189,646 (GRCm39)		probably null	Het
Or13a17	A	C	7: 140,271,309 (GRCm39)	M164L	probably benign	Het
Or2ak4	T	A	11: 58,649,154 (GRCm39)	V221E	probably damaging	Het
Or6b2b	C	A	1: 92,418,918 (GRCm39)	K186N	probably benign	Het
Or7d10	A	G	9: 19,831,675 (GRCm39)	T57A	probably benign	Het
Or8b48	T	C	9: 38,493,368 (GRCm39)	V265A	probably benign	Het
Or8g19	A	G	9: 39,055,780 (GRCm39)	N128S	probably benign	Het
Phb2	T	A	6: 124,689,985 (GRCm39)		probably benign	Het
Plcl2	A	G	17: 50,816,957 (GRCm39)	I108V	probably benign	Het
Plpp6	T	A	19: 28,942,146 (GRCm39)	M249K	probably damaging	Het
Pnpt1	G	A	11: 29,088,156 (GRCm39)	G189E	probably damaging	Het
Pramel17	A	T	4: 101,692,999 (GRCm39)	Y334N	probably benign	Het
Ptprn	C	T	1: 75,228,519 (GRCm39)	V853M	probably damaging	Het
Ptprq	T	C	10: 107,524,189 (GRCm39)		probably null	Het
Rai1	G	A	11: 60,077,279 (GRCm39)	V448I	probably benign	Het
Rbm20	T	A	19: 53,839,785 (GRCm39)	C925S	possibly damaging	Het
Rin3	C	A	12: 102,279,314 (GRCm39)	P41Q	probably benign	Het
Rpl31-ps21	T	C	5: 21,324,505 (GRCm39)		noncoding transcript	Het
Rpl39-ps	A	T	15: 102,543,561 (GRCm39)		noncoding transcript	Het
Rtn4ip1	T	A	10: 43,783,879 (GRCm39)	D133E	probably benign	Het
Ryr1	T	C	7: 28,768,453 (GRCm39)	K2839E	possibly damaging	Het
Septin5	T	C	16: 18,442,118 (GRCm39)	K268R	probably benign	Het
Serpinb6b	T	A	13: 33,161,642 (GRCm39)	D238E	possibly damaging	Het
Slc15a2	C	T	16: 36,582,747 (GRCm39)	V214M	probably damaging	Het
Smarca2	T	C	19: 26,601,336 (GRCm39)	M18T	probably damaging	Het
Smarca2	C	A	19: 26,659,446 (GRCm39)	T912K	possibly damaging	Het
Smdt1	A	T	15: 82,232,101 (GRCm39)	R46S	possibly damaging	Het
Spa17	A	C	9: 37,523,273 (GRCm39)	F5V	probably damaging	Het
Spag17	A	G	3: 99,934,560 (GRCm39)	E614G	possibly damaging	Het
Sstr4	CGAGGAGGAGGAGGA	CGAGGAGGAGGAGGAGGA	2: 148,237,471 (GRCm39)		probably benign	Het
Tlr1	A	T	5: 65,083,635 (GRCm39)	V314D	probably damaging	Het
Trappc8	A	T	18: 20,969,957 (GRCm39)	L1011Q	probably benign	Het
Tsga10	A	G	1: 37,800,028 (GRCm39)	*691Q	probably null	Het
Vav1	A	T	17: 57,610,079 (GRCm39)	K420*	probably null	Het
Vmn1r174	C	G	7: 23,453,562 (GRCm39)	T76R	probably benign	Het
Vmn2r116	A	G	17: 23,605,778 (GRCm39)	E230G	probably benign	Het
Vps13b	A	G	15: 35,452,312 (GRCm39)	T637A	probably damaging	Het
Zbtb7a	A	G	10: 80,980,631 (GRCm39)	E275G	probably damaging	Het
Zfp280b	A	G	10: 75,875,296 (GRCm39)		probably null	Het
Zfp763	A	G	17: 33,238,507 (GRCm39)	Y213H	possibly damaging	Het
Zfp78	T	A	7: 6,381,528 (GRCm39)	W161R	probably benign	Het

Other mutations in Mlxip

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00519:Mlxip	APN	5	123,585,268 (GRCm39)	missense	probably benign	0.35
IGL00922:Mlxip	APN	5	123,578,128 (GRCm39)	missense	probably damaging	1.00
IGL01138:Mlxip	APN	5	123,588,219 (GRCm39)	missense	probably damaging	1.00
IGL01624:Mlxip	APN	5	123,533,392 (GRCm39)	missense	probably benign	0.08
IGL02155:Mlxip	APN	5	123,591,455 (GRCm39)	missense	probably benign
IGL03011:Mlxip	APN	5	123,584,014 (GRCm39)	missense	probably benign	0.01
IGL03177:Mlxip	APN	5	123,584,044 (GRCm39)	missense	possibly damaging	0.86
IGL03242:Mlxip	APN	5	123,578,124 (GRCm39)	missense	probably damaging	1.00
confutatis	UTSW	5	123,580,512 (GRCm39)	splice site	probably null
BB008:Mlxip	UTSW	5	123,588,558 (GRCm39)	missense	probably damaging	1.00
BB018:Mlxip	UTSW	5	123,588,558 (GRCm39)	missense	probably damaging	1.00
PIT4366001:Mlxip	UTSW	5	123,533,173 (GRCm39)	missense	probably benign	0.00
R0136:Mlxip	UTSW	5	123,580,369 (GRCm39)	missense	probably damaging	1.00
R1583:Mlxip	UTSW	5	123,588,286 (GRCm39)	missense	possibly damaging	0.86
R2410:Mlxip	UTSW	5	123,581,132 (GRCm39)	missense	probably damaging	1.00
R2869:Mlxip	UTSW	5	123,590,730 (GRCm39)	missense	probably benign	0.04
R2869:Mlxip	UTSW	5	123,590,730 (GRCm39)	missense	probably benign	0.04
R2870:Mlxip	UTSW	5	123,590,730 (GRCm39)	missense	probably benign	0.04
R2870:Mlxip	UTSW	5	123,590,730 (GRCm39)	missense	probably benign	0.04
R2871:Mlxip	UTSW	5	123,590,730 (GRCm39)	missense	probably benign	0.04
R2871:Mlxip	UTSW	5	123,590,730 (GRCm39)	missense	probably benign	0.04
R2873:Mlxip	UTSW	5	123,590,730 (GRCm39)	missense	probably benign	0.04
R2962:Mlxip	UTSW	5	123,578,887 (GRCm39)	missense	probably damaging	0.99
R3709:Mlxip	UTSW	5	123,585,537 (GRCm39)	missense	probably benign	0.00
R4512:Mlxip	UTSW	5	123,533,128 (GRCm39)	missense	probably benign
R4536:Mlxip	UTSW	5	123,588,566 (GRCm39)	missense	probably damaging	0.97
R4722:Mlxip	UTSW	5	123,585,265 (GRCm39)	missense	probably benign	0.39
R4993:Mlxip	UTSW	5	123,533,357 (GRCm39)	missense	probably damaging	1.00
R5715:Mlxip	UTSW	5	123,578,121 (GRCm39)	missense	probably damaging	1.00
R6006:Mlxip	UTSW	5	123,583,721 (GRCm39)	missense	possibly damaging	0.93
R6330:Mlxip	UTSW	5	123,533,015 (GRCm39)	missense	probably benign
R6617:Mlxip	UTSW	5	123,580,512 (GRCm39)	splice site	probably null
R6709:Mlxip	UTSW	5	123,585,339 (GRCm39)	missense	possibly damaging	0.89
R6970:Mlxip	UTSW	5	123,583,735 (GRCm39)	missense	possibly damaging	0.52
R7718:Mlxip	UTSW	5	123,583,577 (GRCm39)	missense	probably benign	0.00
R7931:Mlxip	UTSW	5	123,588,558 (GRCm39)	missense	probably damaging	1.00
R8222:Mlxip	UTSW	5	123,585,596 (GRCm39)	missense	probably benign	0.01
R9188:Mlxip	UTSW	5	123,583,642 (GRCm39)	missense	probably benign	0.05

Predicted Primers

PCR Primer
(F):5'- CGACGTTTTCATGTGTTCGC -3'
(R):5'- TCTAAAACCGGTGACCACGG -3'

Sequencing Primer
(F):5'- TGCTCAAGCCTCAGGTGC -3'
(R):5'- TGACCACGGGCATTGGAG -3'

Posted On

2016-10-05