Mutagenetix > Incidental Mutation

Incidental Mutation 'R9651:Mical1'

727110

Institutional Source

Beutler Lab

Gene Symbol

Mical1

Ensembl Gene

ENSMUSG00000019823

Gene Name

microtubule associated monooxygenase, calponin and LIM domain containing 1

Synonyms

Nical

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.121) question?

Stock #

R9651 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

41352310-41363028 bp(+) (GRCm39)

Type of Mutation

critical splice acceptor site

DNA Base Change (assembly)

A to T at 41362022 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000019967 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000019965] [ENSMUST00000019967] [ENSMUST00000099934] [ENSMUST00000105507] [ENSMUST00000119962] [ENSMUST00000126436] [ENSMUST00000155411]

AlphaFold

Q8VDP3

PDB Structure

STRUCTURE OF N-TERMINAL FAD BINDING MOTIF OF MOUSE MICAL [X-RAY DIFFRACTION]
CRYSTAL STRUCTURE OF THE NATIVE MONOOXYGENASE DOMAIN OF MICAL AT 1.45 A RESOLUTION [X-RAY DIFFRACTION]
CRYSTAL STRUCTURE OF THE NADPH-TREATED MONOOXYGENASE DOMAIN OF MICAL [X-RAY DIFFRACTION]

Predicted Effect

probably benign
Transcript: ENSMUST00000019965

SMART Domains

Protein: ENSMUSP00000019965
Gene: ENSMUSG00000019822

Domain	Start	End	E-Value	Type
Pfam:Exo_endo_phos	11	272	3.9e-24	PFAM
transmembrane domain	322	344	N/A	INTRINSIC
transmembrane domain	353	375	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000019967

SMART Domains

Protein: ENSMUSP00000019967
Gene: ENSMUSG00000019823

Domain	Start	End	E-Value	Type
Pfam:FAD_binding_3	84	140	5.5e-8	PFAM
Pfam:FAD_binding_2	86	125	6.1e-6	PFAM
low complexity region	160	171	N/A	INTRINSIC
CH	509	606	4.18e-13	SMART
low complexity region	649	666	N/A	INTRINSIC
LIM	682	736	2.07e-3	SMART
low complexity region	766	785	N/A	INTRINSIC
low complexity region	787	803	N/A	INTRINSIC
low complexity region	855	877	N/A	INTRINSIC
DUF3585	912	1048	3.07e-44	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000099934

SMART Domains

Protein: ENSMUSP00000097519
Gene: ENSMUSG00000019823

Domain	Start	End	E-Value	Type
PDB:2C4C\|B	1	86	5e-49	PDB
low complexity region	87	98	N/A	INTRINSIC
PDB:2C4C\|B	99	416	N/A	PDB
CH	436	533	4.18e-13	SMART
low complexity region	576	593	N/A	INTRINSIC
LIM	609	663	2.07e-3	SMART
low complexity region	693	712	N/A	INTRINSIC
low complexity region	714	730	N/A	INTRINSIC
low complexity region	782	804	N/A	INTRINSIC
DUF3585	839	975	3.07e-44	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000105507

SMART Domains

Protein: ENSMUSP00000101146
Gene: ENSMUSG00000078451

Domain	Start	End	E-Value	Type
low complexity region	20	33	N/A	INTRINSIC
Pfam:Pro_isomerase	147	310	1.3e-41	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000119962

SMART Domains

Protein: ENSMUSP00000113783
Gene: ENSMUSG00000019823

Domain	Start	End	E-Value	Type
Pfam:FAD_binding_3	84	140	7.2e-8	PFAM
Pfam:FAD_binding_2	86	125	3.8e-6	PFAM
low complexity region	160	171	N/A	INTRINSIC
CH	509	606	4.18e-13	SMART
low complexity region	649	666	N/A	INTRINSIC
LIM	682	736	2.07e-3	SMART
low complexity region	766	785	N/A	INTRINSIC
low complexity region	787	803	N/A	INTRINSIC
low complexity region	855	877	N/A	INTRINSIC
DUF3585	912	1048	3.07e-44	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000126436

SMART Domains

Protein: ENSMUSP00000114969
Gene: ENSMUSG00000019823

Domain	Start	End	E-Value	Type
Pfam:FAD_binding_3	84	140	1.1e-7	PFAM
Pfam:FAD_binding_2	86	125	3.2e-6	PFAM
low complexity region	160	171	N/A	INTRINSIC
CH	509	606	4.18e-13	SMART
low complexity region	649	666	N/A	INTRINSIC
LIM	682	736	2.07e-3	SMART
low complexity region	766	785	N/A	INTRINSIC
low complexity region	787	803	N/A	INTRINSIC
low complexity region	855	877	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000155411

SMART Domains

Protein: ENSMUSP00000115461
Gene: ENSMUSG00000019822

Domain	Start	End	E-Value	Type
SCOP:d2dnja_	9	81	2e-4	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an enzyme that oxidizes methionine residues on actin, thereby promoting depolymerization of actin filaments. This protein interacts with and regulates signalling by NEDD9/CAS-L (neural precursor cell expressed, developmentally down-regulated 9). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933405L10Rik	T	C	8: 106,436,604 (GRCm39)	S267P		Het
Abca13	C	T	11: 9,243,741 (GRCm39)	P1868L	probably benign	Het
Abca13	A	G	11: 9,535,484 (GRCm39)	S4703G	probably benign	Het
Abca9	A	T	11: 110,006,319 (GRCm39)	M1262K	probably benign	Het
Acta1	A	T	8: 124,619,431 (GRCm39)	Y220*	probably null	Het
Actr6	A	G	10: 89,564,877 (GRCm39)	V24A	probably damaging	Het
Adam30	T	C	3: 98,069,936 (GRCm39)	Y590H	possibly damaging	Het
Akap8l	T	C	17: 32,557,783 (GRCm39)	N35D	probably damaging	Het
Ankle2	A	G	5: 110,385,661 (GRCm39)	I337V	probably benign	Het
Arid2	T	C	15: 96,256,822 (GRCm39)	V220A	probably benign	Het
Atp8b2	T	C	3: 89,865,603 (GRCm39)	D99G	probably damaging	Het
Baz1b	A	T	5: 135,252,022 (GRCm39)	H940L	probably benign	Het
Cacna1d	C	T	14: 29,764,881 (GRCm39)	V2017I	probably benign	Het
Ccn1	G	T	3: 145,354,583 (GRCm39)	N109K	probably damaging	Het
Cd226	T	A	18: 89,265,395 (GRCm39)	C224*	probably null	Het
Cdrt4	T	A	11: 62,883,466 (GRCm39)	I56N	possibly damaging	Het
Ces3b	G	T	8: 105,812,257 (GRCm39)	A169S	probably damaging	Het
Cramp1	C	A	17: 25,201,783 (GRCm39)	K566N	probably damaging	Het
Cryz	A	G	3: 154,327,765 (GRCm39)	Q289R	probably benign	Het
Csn1s2b	T	A	5: 87,968,820 (GRCm39)	M94K	probably benign	Het
Ctnnd1	T	C	2: 84,439,899 (GRCm39)	K804E	possibly damaging	Het
Cwh43	T	C	5: 73,572,340 (GRCm39)	S193P	probably benign	Het
Dcstamp	A	T	15: 39,623,792 (GRCm39)	D469V	probably benign	Het
Dffa	A	G	4: 149,190,674 (GRCm39)	T68A	probably damaging	Het
Dnah2	C	T	11: 69,341,824 (GRCm39)		probably null	Het
Dst	T	A	1: 34,219,458 (GRCm39)	I1966N	probably benign	Het
Efcab5	G	A	11: 77,022,934 (GRCm39)	T593I	probably damaging	Het
Epn3	C	T	11: 94,383,687 (GRCm39)		probably null	Het
Fem1c	A	T	18: 46,657,674 (GRCm39)	D13E		Het
Foxo3	C	T	10: 42,073,021 (GRCm39)	V499M	probably damaging	Het
Fpr2	T	A	17: 18,113,484 (GRCm39)	I160N	probably benign	Het
Gabra1	A	G	11: 42,045,853 (GRCm39)	Y86H	probably damaging	Het
Gabrb3	T	C	7: 57,415,202 (GRCm39)	Y91H	probably damaging	Het
Gcn1	T	C	5: 115,747,665 (GRCm39)		probably null	Het
Gp5	A	C	16: 30,128,393 (GRCm39)	F94V	probably damaging	Het
Gpr152	T	G	19: 4,192,614 (GRCm39)	W52G	probably damaging	Het
Hsd17b12	A	G	2: 93,988,081 (GRCm39)	V45A	probably benign	Het
Htr5a	A	G	5: 28,047,838 (GRCm39)	N131S	possibly damaging	Het
Il16	T	A	7: 83,332,064 (GRCm39)	N172I	probably damaging	Het
Itga2	G	A	13: 115,020,991 (GRCm39)	P120L	probably benign	Het
Itpkb	G	T	1: 180,160,056 (GRCm39)	E61*	probably null	Het
Lama1	T	C	17: 68,101,215 (GRCm39)	S1903P		Het
Llgl2	A	T	11: 115,742,941 (GRCm39)		probably null	Het
Muc2	C	T	7: 141,288,014 (GRCm39)	P262S	probably damaging	Het
Myo9a	A	G	9: 59,778,764 (GRCm39)	R1507G	probably damaging	Het
Ndst1	G	A	18: 60,833,539 (GRCm39)	H491Y	probably damaging	Het
Nfasc	T	C	1: 132,527,791 (GRCm39)	T872A	probably benign	Het
Nipal3	A	T	4: 135,174,634 (GRCm39)	C372*	probably null	Het
Nmrk1	A	G	19: 18,616,929 (GRCm39)	H26R	probably benign	Het
Nubp2	G	A	17: 25,103,382 (GRCm39)	T165I	probably damaging	Het
Or2m12	C	T	16: 19,105,489 (GRCm39)	M1I	probably null	Het
Or51d1	T	A	7: 102,347,832 (GRCm39)	M129K	probably damaging	Het
Or5au1	T	C	14: 52,273,205 (GRCm39)	D121G	probably damaging	Het
Or5b102	T	G	19: 13,041,256 (GRCm39)	D160E	probably benign	Het
P2ry12	T	C	3: 59,134,931 (GRCm39)		probably benign	Het
Pax8	T	A	2: 24,331,173 (GRCm39)	D174V	probably damaging	Het
Pbxip1	A	G	3: 89,352,795 (GRCm39)	D147G	probably damaging	Het
Pnpla7	T	C	2: 24,892,931 (GRCm39)	S451P	probably benign	Het
Polm	A	G	11: 5,781,732 (GRCm39)	Y255H	probably damaging	Het
Polr1has	C	T	17: 37,276,353 (GRCm39)	Q242*	probably null	Het
Rdh14	T	A	12: 10,441,118 (GRCm39)	C93*	probably null	Het
Rnf213	C	A	11: 119,331,238 (GRCm39)	S2150Y		Het
Rpap1	G	A	2: 119,598,484 (GRCm39)	P1111L	probably damaging	Het
Rpl3l	T	A	17: 24,947,328 (GRCm39)	L14Q	probably damaging	Het
Sbp	A	G	17: 24,164,419 (GRCm39)	*200W	probably null	Het
Scn10a	A	G	9: 119,439,063 (GRCm39)	M1601T	probably benign	Het
Sertad4	C	T	1: 192,528,836 (GRCm39)	D327N	probably damaging	Het
Slc4a1	A	T	11: 102,242,256 (GRCm39)	I821N	probably damaging	Het
Spaca6	T	A	17: 18,057,829 (GRCm39)	D164E	probably benign	Het
Synj1	T	C	16: 90,735,412 (GRCm39)	T1514A	probably benign	Het
Synj1	C	T	16: 90,757,343 (GRCm39)	V902I	possibly damaging	Het
Tctn1	A	G	5: 122,384,576 (GRCm39)	Y443H	probably benign	Het
Thoc5	C	T	11: 4,849,883 (GRCm39)	R25W	possibly damaging	Het
Tmem200c	A	G	17: 69,149,181 (GRCm39)	H588R	probably benign	Het
Trim45	C	T	3: 100,832,705 (GRCm39)	Q313*	probably null	Het
Ubqlnl	T	C	7: 103,799,122 (GRCm39)	D125G	possibly damaging	Het
Ubr4	A	T	4: 139,206,859 (GRCm39)	E4926V	unknown	Het
Usp5	T	C	6: 124,799,501 (GRCm39)	D349G	possibly damaging	Het
Vmn1r25	T	A	6: 57,956,306 (GRCm39)		probably benign	Het
Xirp2	A	G	2: 67,344,167 (GRCm39)	Q2136R	possibly damaging	Het
Zfp28	G	A	7: 6,395,623 (GRCm39)	R134H		Het
Zfp712	A	G	13: 67,188,824 (GRCm39)	S568P	probably benign	Het

Other mutations in Mical1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01455:Mical1	APN	10	41,355,065 (GRCm39)	critical splice donor site	probably null
IGL01594:Mical1	APN	10	41,356,325 (GRCm39)	missense	probably damaging	1.00
IGL02065:Mical1	APN	10	41,360,407 (GRCm39)	missense	possibly damaging	0.55
IGL02321:Mical1	APN	10	41,362,660 (GRCm39)	missense	possibly damaging	0.52
IGL02323:Mical1	APN	10	41,362,660 (GRCm39)	missense	possibly damaging	0.52
IGL02324:Mical1	APN	10	41,362,660 (GRCm39)	missense	possibly damaging	0.52
IGL02327:Mical1	APN	10	41,362,660 (GRCm39)	missense	possibly damaging	0.52
IGL02416:Mical1	APN	10	41,360,806 (GRCm39)	critical splice donor site	probably null
IGL02419:Mical1	APN	10	41,358,273 (GRCm39)	missense	possibly damaging	0.73
IGL03027:Mical1	APN	10	41,355,501 (GRCm39)	unclassified	probably benign
IGL03087:Mical1	APN	10	41,358,686 (GRCm39)	missense	probably damaging	1.00
IGL03368:Mical1	APN	10	41,355,625 (GRCm39)	missense	probably damaging	0.96
IGL03387:Mical1	APN	10	41,354,195 (GRCm39)	missense	probably damaging	1.00
PIT1430001:Mical1	UTSW	10	41,359,492 (GRCm39)	missense	possibly damaging	0.55
R0433:Mical1	UTSW	10	41,355,486 (GRCm39)	missense	probably benign	0.15
R0617:Mical1	UTSW	10	41,357,311 (GRCm39)	missense	probably damaging	0.97
R0638:Mical1	UTSW	10	41,358,235 (GRCm39)	missense	probably benign	0.01
R1535:Mical1	UTSW	10	41,361,207 (GRCm39)	missense	possibly damaging	0.55
R1623:Mical1	UTSW	10	41,357,389 (GRCm39)	critical splice donor site	probably null
R1712:Mical1	UTSW	10	41,356,359 (GRCm39)	missense	probably damaging	1.00
R1806:Mical1	UTSW	10	41,354,210 (GRCm39)	missense	probably damaging	0.96
R1835:Mical1	UTSW	10	41,359,531 (GRCm39)	missense	probably benign	0.00
R1866:Mical1	UTSW	10	41,361,466 (GRCm39)	missense	probably benign	0.39
R2134:Mical1	UTSW	10	41,358,708 (GRCm39)	missense	probably damaging	1.00
R2352:Mical1	UTSW	10	41,358,229 (GRCm39)	missense	probably benign	0.21
R3740:Mical1	UTSW	10	41,355,067 (GRCm39)	missense	probably benign	0.01
R4033:Mical1	UTSW	10	41,357,172 (GRCm39)	missense	probably benign	0.40
R4093:Mical1	UTSW	10	41,362,933 (GRCm39)	unclassified	probably benign
R4184:Mical1	UTSW	10	41,357,866 (GRCm39)	unclassified	probably benign
R4194:Mical1	UTSW	10	41,357,624 (GRCm39)	missense	possibly damaging	0.88
R4659:Mical1	UTSW	10	41,362,932 (GRCm39)	unclassified	probably benign
R5139:Mical1	UTSW	10	41,354,411 (GRCm39)	splice site	probably null
R5173:Mical1	UTSW	10	41,360,985 (GRCm39)	missense	probably damaging	1.00
R5340:Mical1	UTSW	10	41,359,427 (GRCm39)	splice site	probably null
R5501:Mical1	UTSW	10	41,362,075 (GRCm39)	missense	probably benign	0.01
R5560:Mical1	UTSW	10	41,354,961 (GRCm39)	missense	probably damaging	1.00
R5726:Mical1	UTSW	10	41,359,692 (GRCm39)	unclassified	probably benign
R5864:Mical1	UTSW	10	41,362,064 (GRCm39)	missense	possibly damaging	0.88
R5905:Mical1	UTSW	10	41,362,873 (GRCm39)	missense	probably benign	0.00
R6028:Mical1	UTSW	10	41,362,873 (GRCm39)	missense	probably benign	0.00
R6047:Mical1	UTSW	10	41,357,703 (GRCm39)	critical splice donor site	probably null
R6074:Mical1	UTSW	10	41,362,061 (GRCm39)	missense	probably benign	0.27
R6458:Mical1	UTSW	10	41,360,731 (GRCm39)	missense	probably benign	0.44
R6879:Mical1	UTSW	10	41,360,515 (GRCm39)	missense	probably damaging	0.99
R6966:Mical1	UTSW	10	41,355,750 (GRCm39)	missense	probably damaging	0.98
R7049:Mical1	UTSW	10	41,358,246 (GRCm39)	missense	possibly damaging	0.63
R7095:Mical1	UTSW	10	41,355,206 (GRCm39)	splice site	probably null
R7156:Mical1	UTSW	10	41,361,253 (GRCm39)	critical splice donor site	probably null
R7312:Mical1	UTSW	10	41,355,772 (GRCm39)	critical splice donor site	probably null
R8021:Mical1	UTSW	10	41,358,720 (GRCm39)	missense	probably damaging	0.97
R8056:Mical1	UTSW	10	41,357,168 (GRCm39)	missense	probably damaging	1.00
R8427:Mical1	UTSW	10	41,354,591 (GRCm39)	missense	probably damaging	1.00
R8883:Mical1	UTSW	10	41,355,636 (GRCm39)	missense
R9021:Mical1	UTSW	10	41,361,141 (GRCm39)	missense	probably benign	0.43
R9368:Mical1	UTSW	10	41,357,302 (GRCm39)	missense	possibly damaging	0.76
R9526:Mical1	UTSW	10	41,358,602 (GRCm39)	missense	probably benign
X0020:Mical1	UTSW	10	41,354,992 (GRCm39)	missense	probably damaging	1.00
Z1177:Mical1	UTSW	10	41,357,701 (GRCm39)	missense	probably null	1.00

Predicted Primers

PCR Primer
(F):5'- ACTAAGTACCCAACGTGGCG -3'
(R):5'- ACTCCTGAACCAGAGAGATGG -3'

Sequencing Primer
(F):5'- TGGCGTCGAACCCTCATG -3'
(R):5'- GTATGTGCTAGCATGTCACAGAG -3'

Posted On

2022-10-06