Mutagenetix > Incidental Mutation

Incidental Mutation 'R5451:Micall1'

434605

Institutional Source

Beutler Lab

Gene Symbol

Micall1

Ensembl Gene

ENSMUSG00000033039

Gene Name

microtubule associated monooxygenase, calponin and LIM domain containing -like 1

Synonyms

Mus EST 820961, D15Mit260, D15N2e

MMRRC Submission

043016-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.082) question?

Stock #

R5451 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

78993098-79021100 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to A at 79011104 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000042053 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040320] [ENSMUST00000229031]

AlphaFold

Q8BGT6

Predicted Effect

probably null
Transcript: ENSMUST00000040320

SMART Domains

Protein: ENSMUSP00000042053
Gene: ENSMUSG00000033039

Domain	Start	End	E-Value	Type
CH	4	103	5.64e-19	SMART
low complexity region	113	135	N/A	INTRINSIC
LIM	164	219	1.15e-5	SMART
low complexity region	241	250	N/A	INTRINSIC
low complexity region	375	394	N/A	INTRINSIC
low complexity region	414	467	N/A	INTRINSIC
low complexity region	477	497	N/A	INTRINSIC
low complexity region	515	530	N/A	INTRINSIC
low complexity region	571	586	N/A	INTRINSIC
DUF3585	685	825	5.07e-68	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185944

Predicted Effect

probably benign
Transcript: ENSMUST00000229004

Predicted Effect

probably benign
Transcript: ENSMUST00000229031

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000229113

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000229694

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000230202

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000230779

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.1%
20x: 94.6%

Validation Efficiency

96% (52/54)

Allele List at MGI

Other mutations in this stock

Total: 48 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca12	A	G	1: 71,334,076 (GRCm39)	F1142S	possibly damaging	Het
Abca5	G	A	11: 110,210,622 (GRCm39)	Q186*	probably null	Het
Calhm2	T	A	19: 47,121,314 (GRCm39)	Y285F	possibly damaging	Het
Casr	T	C	16: 36,330,270 (GRCm39)	T355A	probably damaging	Het
Ccnq	T	A	11: 78,642,115 (GRCm39)	Q125L	possibly damaging	Het
Clca3a1	T	C	3: 144,733,747 (GRCm39)	Y63C	probably damaging	Het
Cntnap5a	T	C	1: 115,612,873 (GRCm39)	S3P	probably benign	Het
Col27a1	G	A	4: 63,143,476 (GRCm39)	G388D	probably damaging	Het
Cwh43	T	C	5: 73,589,256 (GRCm39)	M447T	probably benign	Het
Dnah7b	G	A	1: 46,281,179 (GRCm39)	G2747S	possibly damaging	Het
Fbxo7	A	G	10: 85,864,901 (GRCm39)	S51G	probably benign	Het
Gabbr2	T	A	4: 46,684,294 (GRCm39)	Y660F	probably benign	Het
Galnt15	A	G	14: 31,751,868 (GRCm39)	E140G	probably benign	Het
Gemin6	T	G	17: 80,535,178 (GRCm39)	V46G	probably damaging	Het
Gsap	T	A	5: 21,422,445 (GRCm39)	L138Q	probably damaging	Het
Igflr1	A	G	7: 30,265,747 (GRCm39)	N57S	possibly damaging	Het
Ighv13-2	A	G	12: 114,321,473 (GRCm39)	F89L	probably damaging	Het
Irf2bpl	A	G	12: 86,928,846 (GRCm39)	V609A	probably benign	Het
Jkampl	A	G	6: 73,445,850 (GRCm39)	V233A	probably benign	Het
Lingo1	T	G	9: 56,527,711 (GRCm39)	I293L	probably damaging	Het
Lrrc14	A	G	15: 76,598,173 (GRCm39)	D301G	probably benign	Het
Lsm2	T	C	17: 35,201,185 (GRCm39)		probably benign	Het
Map4	C	T	9: 109,866,851 (GRCm39)		probably benign	Het
Mpp7	T	C	18: 7,442,855 (GRCm39)	D156G	probably null	Het
Mybbp1a	A	G	11: 72,338,939 (GRCm39)	D822G	probably damaging	Het
Naip2	A	G	13: 100,325,368 (GRCm39)	V180A	probably benign	Het
Nol10	T	A	12: 17,409,103 (GRCm39)	Y159*	probably null	Het
Nphp3	A	G	9: 103,919,221 (GRCm39)	T1290A	probably benign	Het
Or12e1	T	A	2: 87,022,796 (GRCm39)	V255E	probably damaging	Het
Or5aq1b	T	C	2: 86,902,341 (GRCm39)	I46V	probably damaging	Het
Or7g20	T	C	9: 18,946,787 (GRCm39)	Y123H	probably damaging	Het
Pcsk5	T	A	19: 17,440,720 (GRCm39)	Y1290F	possibly damaging	Het
Rab42	T	C	4: 132,029,827 (GRCm39)	N132D	probably benign	Het
Rfx3	T	G	19: 27,827,359 (GRCm39)	T76P	probably damaging	Het
Rps13-ps2	G	T	7: 88,180,036 (GRCm39)		noncoding transcript	Het
Slc12a3	A	G	8: 95,083,655 (GRCm39)	D894G	possibly damaging	Het
Slc25a15	G	A	8: 22,879,983 (GRCm39)	T54I	probably benign	Het
Slco1c1	A	T	6: 141,505,604 (GRCm39)	Q461L	probably benign	Het
Slfn5	T	G	11: 82,850,912 (GRCm39)	I403R	probably damaging	Het
Srxn1	G	A	2: 151,947,799 (GRCm39)	V66M	probably damaging	Het
Tbc1d32	T	A	10: 56,071,571 (GRCm39)	T318S	possibly damaging	Het
Tiam2	G	T	17: 3,479,271 (GRCm39)	R668M	probably damaging	Het
Tle7	A	T	8: 110,836,503 (GRCm39)	I160F	probably damaging	Het
Trgj4	G	T	13: 19,526,335 (GRCm39)		probably benign	Het
Trim9	A	G	12: 70,393,603 (GRCm39)	S114P	probably benign	Het
Trp53i11	T	C	2: 93,030,200 (GRCm39)	L169P	possibly damaging	Het
Ttn	T	A	2: 76,585,168 (GRCm39)	I22042F	probably damaging	Het
Vmn1r190-ps	A	G	13: 22,328,901 (GRCm39)		noncoding transcript	Het

Other mutations in Micall1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00493:Micall1	APN	15	78,999,221 (GRCm39)	splice site	probably benign
IGL00496:Micall1	APN	15	78,999,221 (GRCm39)	splice site	probably benign
IGL00508:Micall1	APN	15	79,014,768 (GRCm39)	missense	probably damaging	0.99
IGL01626:Micall1	APN	15	79,014,712 (GRCm39)	missense	possibly damaging	0.46
IGL01868:Micall1	APN	15	78,999,260 (GRCm39)	missense	probably benign	0.41
IGL03062:Micall1	APN	15	78,998,881 (GRCm39)	missense	probably damaging	1.00
R0086:Micall1	UTSW	15	79,009,689 (GRCm39)	utr 3 prime	probably benign
R0099:Micall1	UTSW	15	79,016,101 (GRCm39)	splice site	probably benign
R0282:Micall1	UTSW	15	79,016,101 (GRCm39)	splice site	probably benign
R0727:Micall1	UTSW	15	79,004,978 (GRCm39)	missense	probably benign	0.00
R1859:Micall1	UTSW	15	79,007,145 (GRCm39)	intron	probably benign
R2142:Micall1	UTSW	15	79,014,995 (GRCm39)	missense	probably damaging	0.98
R2228:Micall1	UTSW	15	79,014,036 (GRCm39)	missense	probably damaging	1.00
R3508:Micall1	UTSW	15	79,006,965 (GRCm39)	missense	probably damaging	1.00
R4858:Micall1	UTSW	15	79,007,146 (GRCm39)	intron	probably benign
R4888:Micall1	UTSW	15	79,016,048 (GRCm39)	nonsense	probably null
R5059:Micall1	UTSW	15	79,007,034 (GRCm39)	intron	probably benign
R5097:Micall1	UTSW	15	79,014,078 (GRCm39)	missense	probably benign	0.17
R5710:Micall1	UTSW	15	79,011,290 (GRCm39)	missense	probably damaging	1.00
R5727:Micall1	UTSW	15	79,014,678 (GRCm39)	missense	possibly damaging	0.64
R7135:Micall1	UTSW	15	78,993,624 (GRCm39)	missense	unknown
R7186:Micall1	UTSW	15	79,009,575 (GRCm39)	missense	unknown
R7297:Micall1	UTSW	15	79,005,097 (GRCm39)	missense	unknown
R7472:Micall1	UTSW	15	79,006,760 (GRCm39)	missense	unknown
R8494:Micall1	UTSW	15	79,005,080 (GRCm39)	missense	probably damaging	1.00
R8714:Micall1	UTSW	15	79,011,510 (GRCm39)	missense	probably benign	0.03
R8937:Micall1	UTSW	15	79,011,198 (GRCm39)	missense	probably damaging	1.00
R9440:Micall1	UTSW	15	79,011,159 (GRCm39)	missense
R9760:Micall1	UTSW	15	79,005,032 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- ATCGGGATACAAAGTGGGTCTG -3'
(R):5'- TGACAGAGTTCCCAGAGGTG -3'

Sequencing Primer
(F):5'- CTGAAGGTGGATTCATTTGTAACACG -3'
(R):5'- ACGTGCACAGCAGGATC -3'

Posted On

2016-10-06