Mutagenetix > Incidental Mutation

Incidental Mutation 'R0134:Map9'

21808

Institutional Source

Beutler Lab

Gene Symbol

Map9

Ensembl Gene

ENSMUSG00000033900

Gene Name

microtubule-associated protein 9

Synonyms

ASAP, 5330427D05Rik, Mtap9, 5033421J10Rik

MMRRC Submission

038419-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.255) question?

Stock #

R0134 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

82358044-82395268 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

G to A at 82359983 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000142206 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000091014] [ENSMUST00000192595] [ENSMUST00000193559] [ENSMUST00000195471] [ENSMUST00000195640]

AlphaFold

Q3TRR0

Predicted Effect

probably benign
Transcript: ENSMUST00000091014

SMART Domains

Protein: ENSMUSP00000088535
Gene: ENSMUSG00000033900

Domain	Start	End	E-Value	Type
low complexity region	41	52	N/A	INTRINSIC
Pfam:DUF4207	340	566	3.6e-10	PFAM
low complexity region	607	622	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000192595

SMART Domains

Protein: ENSMUSP00000141828
Gene: ENSMUSG00000033900

Domain	Start	End	E-Value	Type
low complexity region	41	52	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000193559

SMART Domains

Protein: ENSMUSP00000142014
Gene: ENSMUSG00000033900

Domain	Start	End	E-Value	Type
low complexity region	41	52	N/A	INTRINSIC
low complexity region	356	365	N/A	INTRINSIC
coiled coil region	476	513	N/A	INTRINSIC
low complexity region	516	537	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000195471

SMART Domains

Protein: ENSMUSP00000141282
Gene: ENSMUSG00000033900

Domain	Start	End	E-Value	Type
low complexity region	41	52	N/A	INTRINSIC
low complexity region	356	365	N/A	INTRINSIC
coiled coil region	476	513	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000195640

SMART Domains

Protein: ENSMUSP00000142206
Gene: ENSMUSG00000033900

Domain	Start	End	E-Value	Type
low complexity region	41	52	N/A	INTRINSIC
Pfam:DUF4207	332	562	4.4e-11	PFAM
low complexity region	564	596	N/A	INTRINSIC
low complexity region	607	622	N/A	INTRINSIC

Coding Region Coverage

1x: 99.0%
3x: 98.2%
10x: 96.4%
20x: 93.3%

Validation Efficiency

100% (59/59)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] ASAP is a microtubule-associated protein required for spindle function, mitotic progression, and cytokinesis (Saffin et al., 2005 [PubMed 16049101]).[supplied by OMIM, Mar 2008]

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610009O20Rik	G	A	18: 38,261,264	V505I	probably benign	Het
1110059E24Rik	T	C	19: 21,598,201		probably benign	Het
Abca16	T	A	7: 120,540,155	L1470Q	probably damaging	Het
Arhgap23	G	T	11: 97,444,328	V70L	probably benign	Het
AW549877	T	C	15: 3,986,294	K263E	probably damaging	Het
Bicd1	T	C	6: 149,512,950	I387T	probably benign	Het
Btbd9	C	T	17: 30,274,942	D492N	possibly damaging	Het
Cd59b	G	A	2: 104,078,941		probably null	Het
Ddx50	A	T	10: 62,621,377		probably benign	Het
Dnlz	T	C	2: 26,351,368	N116S	probably damaging	Het
Efcab14	T	C	4: 115,740,531	F108L	probably damaging	Het
Esyt2	A	G	12: 116,367,710	N736S	probably damaging	Het
Exoc4	A	G	6: 33,971,946	D908G	possibly damaging	Het
Garnl3	T	C	2: 33,006,804	T608A	possibly damaging	Het
Hdac2	T	A	10: 36,989,184	D131E	probably benign	Het
Hes1	T	C	16: 30,067,250	V224A	probably damaging	Het
Hps1	G	T	19: 42,766,180	Q277K	probably damaging	Het
Ighv15-2	T	G	12: 114,565,037		probably benign	Het
Il3	A	G	11: 54,265,680		probably null	Het
Itgae	A	C	11: 73,111,342	M91L	probably benign	Het
Kctd21	T	A	7: 97,348,091	I257N	probably benign	Het
Kif16b	A	T	2: 142,672,375	S1215T	probably benign	Het
Lhx9	A	T	1: 138,838,679	C124S	probably damaging	Het
Lipo4	A	G	19: 33,501,606	V278A	probably benign	Het
Lrp1b	T	C	2: 40,596,983	E142G	probably damaging	Het
Macf1	T	C	4: 123,432,843	M2835V	possibly damaging	Het
Miox	C	T	15: 89,334,454		probably benign	Het
Mndal	A	T	1: 173,857,513		probably benign	Het
Nanos3	C	T	8: 84,176,134	R133Q	probably damaging	Het
Nepn	A	T	10: 52,400,437	T29S	probably damaging	Het
Nlgn1	C	T	3: 25,435,925	C546Y	probably damaging	Het
Olfr1055	T	C	2: 86,347,728	I13V	possibly damaging	Het
Olfr307	A	G	7: 86,335,595	I267T	probably benign	Het
Pdgfra	A	G	5: 75,166,511	D123G	probably damaging	Het
Plekhn1	T	C	4: 156,228,243	R53G	probably benign	Het
Pnp2	T	C	14: 50,963,177	F100S	probably damaging	Het
Prickle1	A	G	15: 93,510,777	L47P	possibly damaging	Het
Ptar1	T	A	19: 23,718,095	C309S	probably benign	Het
Rxfp1	A	G	3: 79,657,476	S327P	probably damaging	Het
Siah2	A	G	3: 58,676,115	V250A	probably damaging	Het
Siglecg	G	A	7: 43,411,171	G325D	probably damaging	Het
Slc10a7	T	A	8: 78,697,158		probably null	Het
Slc9a1	A	G	4: 133,420,605	K645E	probably benign	Het
Smarca4	T	C	9: 21,637,324	L302P	probably damaging	Het
Smyd1	G	T	6: 71,216,765	T392N	probably damaging	Het
Snrnp40	C	G	4: 130,378,043		probably null	Het
Tenm3	A	T	8: 48,674,472	L57Q	probably damaging	Het
Tep1	C	T	14: 50,829,693	V2269I	possibly damaging	Het
Tpd52l1	A	G	10: 31,379,256	S32P	probably damaging	Het
Tsfm	A	G	10: 127,022,929		probably benign	Het
Ttn	T	A	2: 76,710,124	R34173W	probably damaging	Het
Ttn	C	A	2: 76,793,130	V15368L	possibly damaging	Het
Vmn2r13	C	A	5: 109,175,049	V125L	probably benign	Het
Vps13b	T	C	15: 35,887,261	I3272T	probably benign	Het
Zfp108	A	G	7: 24,260,467	H161R	probably benign	Het
Zfp518b	A	G	5: 38,674,659	M1T	probably null	Het

Other mutations in Map9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00742:Map9	APN	3	82363420	missense	probably benign	0.37
IGL01520:Map9	APN	3	82378965	missense	probably damaging	0.99
IGL02281:Map9	APN	3	82391146	missense	possibly damaging	0.53
IGL02931:Map9	APN	3	82377121	missense	possibly damaging	0.86
IGL02937:Map9	APN	3	82363512	missense	possibly damaging	0.95
IGL02985:Map9	APN	3	82359902	nonsense	probably null
IGL03113:Map9	APN	3	82359978	splice site	probably benign
R0225:Map9	UTSW	3	82359983	splice site	probably benign
R0468:Map9	UTSW	3	82374203	critical splice donor site	probably null
R1027:Map9	UTSW	3	82377094	missense	probably damaging	1.00
R1794:Map9	UTSW	3	82380221	missense	probably damaging	1.00
R4008:Map9	UTSW	3	82359083	missense	probably damaging	1.00
R5728:Map9	UTSW	3	82363335	missense	probably benign	0.00
R5905:Map9	UTSW	3	82380248	critical splice donor site	probably null
R6028:Map9	UTSW	3	82380248	critical splice donor site	probably null
R6334:Map9	UTSW	3	82383305	missense	probably damaging	1.00
R6798:Map9	UTSW	3	82380164	missense	probably damaging	1.00
R7135:Map9	UTSW	3	82363458	missense	probably benign	0.03
R7443:Map9	UTSW	3	82371356	missense	possibly damaging	0.72
R7694:Map9	UTSW	3	82358983	start gained	probably benign
R8224:Map9	UTSW	3	82359063	missense	probably benign	0.33
R8237:Map9	UTSW	3	82377160	missense	probably damaging	0.97
R8395:Map9	UTSW	3	82381969	missense	probably benign	0.06
R8504:Map9	UTSW	3	82377169	critical splice donor site	probably null
R8696:Map9	UTSW	3	82363361	missense	possibly damaging	0.53
R8818:Map9	UTSW	3	82383963	missense	possibly damaging	0.86
R8957:Map9	UTSW	3	82371380	missense	probably benign
R9044:Map9	UTSW	3	82380218	missense	possibly damaging	0.92
R9266:Map9	UTSW	3	82371287	missense	possibly damaging	0.48
R9695:Map9	UTSW	3	82376985	missense	probably benign	0.18

Predicted Primers

PCR Primer
(F):5'- GCTCAATTCTGCGCTGAGTCTGATG -3'
(R):5'- CACCACTGTTTAACCCTGTGAACCC -3'

Sequencing Primer
(F):5'- CGCTGAGTCTGATGACGTG -3'
(R):5'- GACAGCTTAGTCCTAAGGTAGC -3'

Posted On

2013-04-12