Mutagenetix > Incidental Mutation

Incidental Mutation 'R6358:Mia'

513336

Institutional Source

Beutler Lab

Gene Symbol

Mia

Ensembl Gene

ENSMUSG00000089661

Gene Name

melanoma inhibitory activity

Synonyms

Cdrap, Mia1

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6358 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

27179742-27181157 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 27180978 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 24 (D24G)

Ref Sequence

ENSEMBL: ENSMUSP00000122859 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000071986] [ENSMUST00000093040] [ENSMUST00000121848] [ENSMUST00000153511] [ENSMUST00000154724]

AlphaFold

Q61865

Predicted Effect

probably benign
Transcript: ENSMUST00000071986
AA Change: D23G

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

SMART Domains

Protein: ENSMUSP00000071876
Gene: ENSMUSG00000089661
AA Change: D23G

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
SH3	45	111	8.92e-5	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000093040

SMART Domains

Protein: ENSMUSP00000090727
Gene: ENSMUSG00000053291

Domain	Start	End	E-Value	Type
RAB	9	172	2.47e-101	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000121848
AA Change: D24G

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

SMART Domains

Protein: ENSMUSP00000114063
Gene: ENSMUSG00000089661
AA Change: D24G

Domain	Start	End	E-Value	Type
signal peptide	1	23	N/A	INTRINSIC
SH3	46	112	8.92e-5	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127491

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000128409

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134462

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141906

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152753

Predicted Effect

probably benign
Transcript: ENSMUST00000153511

SMART Domains

Protein: ENSMUSP00000138477
Gene: ENSMUSG00000053291

Domain	Start	End	E-Value	Type
Pfam:Arf	3	97	1.8e-11	PFAM
Pfam:Miro	10	95	9.5e-15	PFAM
Pfam:Ras	10	95	7.8e-35	PFAM
Pfam:Gtr1_RagA	10	98	4.8e-6	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000154724
AA Change: D24G

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

SMART Domains

Protein: ENSMUSP00000122859
Gene: ENSMUSG00000095538
AA Change: D24G

Domain	Start	End	E-Value	Type
signal peptide	1	23	N/A	INTRINSIC
SH3	46	112	8.92e-5	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000175607

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000205990

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.8%

Validation Efficiency

100% (61/61)

MGI Phenotype

PHENOTYPE: Mice homozygous for a targeted null mutation are viable and fertile but display alterations in the fibrillar ultrastructure of cartilage as well as minor changes in the number and morphology of chondrocytic microvilli. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam39	T	C	8: 40,826,681	V703A	probably benign	Het
Adgrv1	T	A	13: 81,414,583	Q5389L	probably damaging	Het
Aldh18a1	A	T	19: 40,577,678	I42N	possibly damaging	Het
Ankrd28	A	C	14: 31,710,864	C575W	probably damaging	Het
Car14	T	A	3: 95,898,175	T329S	possibly damaging	Het
Cdhr2	T	C	13: 54,736,546	F1298S	probably damaging	Het
Crhr2	A	G	6: 55,093,043	I341T	probably benign	Het
D5Ertd579e	T	A	5: 36,616,236		probably null	Het
Emilin1	A	G	5: 30,918,218	E601G	probably damaging	Het
Erbin	T	A	13: 103,845,565	Q456L	probably damaging	Het
Glp1r	T	C	17: 30,932,644	V405A	probably benign	Het
Gm10220	C	G	5: 26,120,305		probably null	Het
Gm2016	A	G	12: 87,877,000	E139G	unknown	Het
Gm527	A	T	12: 64,923,548	H219L	possibly damaging	Het
Gorasp2	T	A	2: 70,672,760	M1K	probably null	Het
H2-DMa	T	A	17: 34,137,984	L152H	probably damaging	Het
Hsd3b7	T	A	7: 127,801,537	H54Q	probably damaging	Het
Hspa12b	T	C	2: 131,137,066		probably benign	Het
Iars	C	A	13: 49,727,143	T1006K	possibly damaging	Het
Jmjd1c	T	C	10: 67,225,939	V1357A	probably benign	Het
Magi3	T	C	3: 104,050,952	M606V	probably damaging	Het
Mon2	A	T	10: 123,013,504	L1297Q	probably damaging	Het
Musk	T	A	4: 58,373,171	S691T	possibly damaging	Het
Myo5c	A	T	9: 75,296,012	E1463D	possibly damaging	Het
Ndufs6	C	T	13: 73,320,319	G87D	probably damaging	Het
Npnt	C	T	3: 132,904,718	V415I	probably benign	Het
Ntsr2	A	G	12: 16,656,768	I266V	probably benign	Het
Olfr259	T	C	2: 87,108,434		probably benign	Het
Olfr736	A	T	14: 50,393,388	I211F	possibly damaging	Het
Pkmyt1	T	A	17: 23,733,656		probably null	Het
Polr1e	T	C	4: 45,026,813	L166P	probably damaging	Het
Ppib	T	G	9: 66,061,474	F48C	probably damaging	Het
Ppl	C	A	16: 5,087,929	E1501*	probably null	Het
Prpf8	T	C	11: 75,491,495	V384A	probably benign	Het
Ptch1	T	G	13: 63,513,689	S1212R	probably damaging	Het
Ralb	C	A	1: 119,476,005	D131Y	probably damaging	Het
Rfx4	T	A	10: 84,844,235	M141K	probably damaging	Het
Rgl2	T	A	17: 33,937,131		probably null	Het
Rpl27	A	G	11: 101,443,956		probably benign	Het
Sdc1	A	C	12: 8,791,297	T213P	probably damaging	Het
Setx	T	A	2: 29,171,348	N2256K	possibly damaging	Het
Shank2	A	G	7: 144,031,297	M12V	probably benign	Het
Slc22a28	T	A	19: 8,071,888	K332M	probably damaging	Het
Slf2	A	T	19: 44,935,425	H226L	probably benign	Het
Tbc1d10b	T	C	7: 127,203,412	S362G	probably benign	Het
Tbxas1	G	A	6: 38,952,112		probably benign	Het
Tctn1	A	G	5: 122,261,512	V83A	probably damaging	Het
Tgm4	A	G	9: 123,056,518	E375G	probably damaging	Het
Tmeff2	T	A	1: 51,133,114	Y247*	probably null	Het
Tmem167b	C	T	3: 108,558,895	R79H	possibly damaging	Het
Tmprss7	T	G	16: 45,669,573	M429L	probably benign	Het
Tnfsf18	T	A	1: 161,503,579	D99E	probably benign	Het
Tnrc18	A	T	5: 142,727,981	S2534T	probably damaging	Het
Tnxb	A	G	17: 34,678,994	E872G	probably damaging	Het
Tomm40l	C	T	1: 171,219,637	V237I	possibly damaging	Het
Trbv2	A	G	6: 41,047,902	Q84R	probably benign	Het
Tspan18	T	C	2: 93,209,874	R179G	probably benign	Het
Tspan8	G	T	10: 115,833,227	V56L	probably benign	Het
Zbtb22	T	C	17: 33,918,737	S619P	probably damaging	Het
Zfp2	A	T	11: 50,900,601	I205N	probably damaging	Het
Zfpm1	A	G	8: 122,337,111		probably benign	Het

Other mutations in Mia

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0991:Mia	UTSW	7	27180720	missense	probably damaging	1.00
R7204:Mia	UTSW	7	27180933	missense	possibly damaging	0.68
R8903:Mia	UTSW	7	27180805	missense	probably damaging	1.00
R8903:Mia	UTSW	7	27180806	missense	possibly damaging	0.92

Predicted Primers

PCR Primer
(F):5'- GCCCTTCAACTTGGAGAAGAC -3'
(R):5'- TGGCTGGAGAACAACCTTGG -3'

Sequencing Primer
(F):5'- TGGCCCCTATATATAGTCAAGAAGCG -3'
(R):5'- ACAACCTTGGGGAGTGGGTG -3'

Posted On

2018-04-27