Mutagenetix > Incidental Mutation

Incidental Mutation 'R7047:Mixl1'

547351

Institutional Source

Beutler Lab

Gene Symbol

Mixl1

Ensembl Gene

ENSMUSG00000026497

Gene Name

Mix paired-like homeobox

Synonyms

Mml

MMRRC Submission

045145-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7047 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

180520608-180524599 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

A to G at 180524183 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000027778 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027778]

AlphaFold

Q9WUI0

Predicted Effect

probably null
Transcript: ENSMUST00000027778

SMART Domains

Protein: ENSMUSP00000027778
Gene: ENSMUSG00000026497

Domain	Start	End	E-Value	Type
low complexity region	72	85	N/A	INTRINSIC
HOX	86	148	1.58e-24	SMART

Meta Mutation Damage Score

0.9506

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

98% (53/54)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Homeodomain proteins, such as MIXL1, are transcription factors that regulate cell fate during development (Hart et al., 2005 [PubMed 15982639]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Homozygous null embryos are mostly arrested in development by E9 exhibiting abnormalities in primitive streak and node formation, disorganized head folds, foreshortened body axis, absence of heart tube and gut, deficient paraxial mesoderm, abnormal notochord morphology, and an enlarged allantois. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	A	T	14: 32,382,131 (GRCm39)	I1278N	possibly damaging	Het
Adcy5	T	A	16: 35,087,585 (GRCm39)	L482Q	probably damaging	Het
Adora2a	A	G	10: 75,162,145 (GRCm39)	I95V	probably damaging	Het
Anapc1	A	C	2: 128,457,350 (GRCm39)	C1887G	probably damaging	Het
Arfgef2	T	A	2: 166,693,865 (GRCm39)		probably null	Het
Capn11	G	T	17: 45,949,622 (GRCm39)	S448*	probably null	Het
Capn7	C	T	14: 31,058,642 (GRCm39)		probably benign	Het
Cep55	T	A	19: 38,048,539 (GRCm39)	V65D	possibly damaging	Het
Col5a1	A	G	2: 27,818,096 (GRCm39)	K107R	unknown	Het
Dbh	T	A	2: 27,055,622 (GRCm39)	I32N	possibly damaging	Het
Disp1	C	A	1: 182,869,030 (GRCm39)	R1130L	probably damaging	Het
Dzip3	A	T	16: 48,802,489 (GRCm39)	N13K	probably benign	Het
Emilin1	A	G	5: 31,074,422 (GRCm39)	N221S	probably benign	Het
Ext2	A	G	2: 93,570,002 (GRCm39)	F470L	probably damaging	Het
Filip1	T	A	9: 79,760,916 (GRCm39)	Q206L	probably damaging	Het
Garin1b	T	A	6: 29,323,809 (GRCm39)	L178H	probably damaging	Het
Gpr63	G	T	4: 25,007,320 (GRCm39)	A15S	probably benign	Het
Grhl3	T	C	4: 135,276,551 (GRCm39)		probably null	Het
Hspa5	C	T	2: 34,663,204 (GRCm39)	P127L	probably damaging	Het
Ift172	G	T	5: 31,433,238 (GRCm39)	Y193*	probably null	Het
Ints1	A	C	5: 139,744,226 (GRCm39)	L1512*	probably null	Het
Kat2b	A	G	17: 53,970,597 (GRCm39)	Q661R	probably benign	Het
Kat6a	A	G	8: 23,428,554 (GRCm39)	N1303S	possibly damaging	Het
L3mbtl4	G	T	17: 68,768,561 (GRCm39)	R223L	probably benign	Het
Maml2	T	C	9: 13,532,177 (GRCm39)		probably benign	Het
Mocs1	T	C	17: 49,759,887 (GRCm39)		probably null	Het
Ms4a15	T	G	19: 10,962,236 (GRCm39)	N36T	probably damaging	Het
Msr1	G	A	8: 40,095,657 (GRCm39)	T2I	possibly damaging	Het
Nlgn1	A	C	3: 25,490,199 (GRCm39)	Y509*	probably null	Het
Nsmce1	C	A	7: 125,090,606 (GRCm39)	G4C	probably benign	Het
Or4c113	A	T	2: 88,885,490 (GRCm39)	F93L	probably damaging	Het
Or51v15-ps1	A	G	7: 103,278,918 (GRCm39)	V83A	probably damaging	Het
Pan3	G	A	5: 147,483,175 (GRCm39)	G452D	probably damaging	Het
Pcyox1	G	T	6: 86,365,891 (GRCm39)	P441H	probably damaging	Het
Phf12	T	C	11: 77,904,099 (GRCm39)	V273A	probably damaging	Het
Plcd4	A	G	1: 74,591,148 (GRCm39)	E181G	possibly damaging	Het
Ptgfr	A	T	3: 151,541,178 (GRCm39)	I110N	possibly damaging	Het
Rab40c	A	C	17: 26,138,458 (GRCm39)	V8G	probably damaging	Het
Rasal3	T	A	17: 32,615,458 (GRCm39)	Y460F	probably damaging	Het
Rhbdf2	A	G	11: 116,494,477 (GRCm39)		probably null	Het
Ryr2	T	A	13: 11,839,286 (GRCm39)	N496Y	possibly damaging	Het
Sacs	A	T	14: 61,450,451 (GRCm39)	I4166F	probably damaging	Het
Sh2d3c	T	C	2: 32,611,172 (GRCm39)	M1T	probably null	Het
Smarca2	C	T	19: 26,646,555 (GRCm39)	S651L	possibly damaging	Het
Sned1	A	T	1: 93,213,540 (GRCm39)	R1204S	possibly damaging	Het
Spata31d1b	T	C	13: 59,860,249 (GRCm39)	Y41H	probably damaging	Het
Stab2	C	T	10: 86,694,016 (GRCm39)	C2075Y	probably damaging	Het
Tcte1	A	T	17: 45,844,294 (GRCm39)	Q90L	possibly damaging	Het
Tll2	C	T	19: 41,074,679 (GRCm39)	G945S	probably damaging	Het
Tmbim7	A	T	5: 3,720,112 (GRCm39)	T116S	probably benign	Het
Tnfrsf19	A	T	14: 61,242,667 (GRCm39)	C72*	probably null	Het
Usp17le	T	A	7: 104,417,640 (GRCm39)	T501S	probably benign	Het
Wnt5b	T	A	6: 119,425,217 (GRCm39)		probably benign	Het

Other mutations in Mixl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02548:Mixl1	APN	1	180,522,269 (GRCm39)	missense	probably benign	0.03
IGL03371:Mixl1	APN	1	180,522,191 (GRCm39)	missense	probably benign	0.00
R0453:Mixl1	UTSW	1	180,524,211 (GRCm39)	missense	probably damaging	1.00
R0838:Mixl1	UTSW	1	180,524,365 (GRCm39)	missense	probably benign	0.45
R1832:Mixl1	UTSW	1	180,522,296 (GRCm39)	missense	probably benign	0.11
R4870:Mixl1	UTSW	1	180,522,237 (GRCm39)	missense	probably benign	0.06
R6046:Mixl1	UTSW	1	180,524,336 (GRCm39)	missense	possibly damaging	0.94
R6918:Mixl1	UTSW	1	180,522,243 (GRCm39)	missense	probably benign	0.02
R6980:Mixl1	UTSW	1	180,524,453 (GRCm39)	missense	possibly damaging	0.51
R7296:Mixl1	UTSW	1	180,524,523 (GRCm39)	missense	probably benign
R8108:Mixl1	UTSW	1	180,524,267 (GRCm39)	missense	probably damaging	1.00
R8237:Mixl1	UTSW	1	180,524,322 (GRCm39)	nonsense	probably null
R9074:Mixl1	UTSW	1	180,522,245 (GRCm39)	missense	probably damaging	1.00
R9095:Mixl1	UTSW	1	180,524,402 (GRCm39)	missense	probably benign
R9254:Mixl1	UTSW	1	180,522,258 (GRCm39)	missense	probably benign	0.00
R9379:Mixl1	UTSW	1	180,522,258 (GRCm39)	missense	probably benign	0.00
R9749:Mixl1	UTSW	1	180,522,311 (GRCm39)	missense	probably benign	0.00
X0065:Mixl1	UTSW	1	180,522,266 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCTGCCCAGATCAATCACATG -3'
(R):5'- TGCTTTCCAAACCGCGACTC -3'

Sequencing Primer
(F):5'- ATGGTAACGCGGCCTTAACTG -3'
(R):5'- GCGACTCCAGTCCCACAG -3'

Posted On

2019-05-13