Mutagenetix > Incidental Mutation

Incidental Mutation 'R8826:Mapre2'

673503

Institutional Source

Beutler Lab

Gene Symbol

Mapre2

Ensembl Gene

ENSMUSG00000024277

Gene Name

microtubule-associated protein, RP/EB family, member 2

Synonyms

C820009F03Rik, D18Abb1e, RP1, EB2

MMRRC Submission

068729-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.192) question?

Stock #

R8826 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

23885390-24026918 bp(+) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

A to T at 23886888 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000128040 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000115830] [ENSMUST00000118826] [ENSMUST00000155708] [ENSMUST00000170802]

AlphaFold

Q8R001

Predicted Effect

probably benign
Transcript: ENSMUST00000115830

SMART Domains

Protein: ENSMUSP00000111496
Gene: ENSMUSG00000024277

Domain	Start	End	E-Value	Type
Pfam:CH	50	149	1.2e-12	PFAM
low complexity region	190	226	N/A	INTRINSIC
Pfam:EB1	250	289	5.4e-18	PFAM
low complexity region	291	316	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000118826

SMART Domains

Protein: ENSMUSP00000114113
Gene: ENSMUSG00000024277

Domain	Start	End	E-Value	Type
Pfam:CH	17	116	5.7e-13	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000155708

SMART Domains

Protein: ENSMUSP00000118807
Gene: ENSMUSG00000024277

Domain	Start	End	E-Value	Type
Pfam:CH	17	116	1.9e-12	PFAM
low complexity region	157	193	N/A	INTRINSIC
Pfam:EB1	217	256	5.4e-18	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000170802

SMART Domains

Protein: ENSMUSP00000128040
Gene: ENSMUSG00000024277

Domain	Start	End	E-Value	Type
Pfam:CH	17	116	2.3e-12	PFAM
low complexity region	157	193	N/A	INTRINSIC
Pfam:EB1	217	256	6.1e-18	PFAM
low complexity region	258	283	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

100% (91/91)

Allele List at MGI

Other mutations in this stock

Total: 90 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acta1	T	C	8: 124,619,978 (GRCm39)	M121V	probably damaging	Het
AI987944	A	T	7: 41,024,627 (GRCm39)	H120Q	possibly damaging	Het
Aldh9a1	C	G	1: 167,184,119 (GRCm39)	P205A	probably damaging	Het
Ank2	A	T	3: 126,740,951 (GRCm39)	N1644K	unknown	Het
Arfgef2	A	T	2: 166,677,386 (GRCm39)		probably benign	Het
Bpifb4	G	T	2: 153,783,817 (GRCm39)	V54L	probably benign	Het
Cacna1c	T	A	6: 118,711,836 (GRCm39)	M456L		Het
Cbln1	T	C	8: 88,198,420 (GRCm39)	N95S	probably benign	Het
Ccl11	G	T	11: 81,953,044 (GRCm39)	R67S	possibly damaging	Het
Cd200	G	A	16: 45,215,157 (GRCm39)	R165C	probably benign	Het
Cd2bp2	A	T	7: 126,793,257 (GRCm39)	M283K	probably damaging	Het
Cd86	G	T	16: 36,435,650 (GRCm39)	L256I	possibly damaging	Het
Ces2f	T	A	8: 105,679,734 (GRCm39)	F409Y	probably benign	Het
Cisd3	A	T	11: 97,579,158 (GRCm39)	Q100L	probably damaging	Het
Cntnap1	C	T	11: 101,077,655 (GRCm39)	R1106C	probably damaging	Het
Col6a2	A	T	10: 76,439,433 (GRCm39)	M777K	probably damaging	Het
Cp	A	G	3: 20,039,739 (GRCm39)	Y852C	probably damaging	Het
Ddx1	T	C	12: 13,277,332 (GRCm39)	E523G	probably damaging	Het
Ddx60	T	A	8: 62,398,990 (GRCm39)	D236E	probably benign	Het
Dnah9	A	T	11: 65,740,742 (GRCm39)	F4148Y	probably benign	Het
Dusp6	G	T	10: 99,099,469 (GRCm39)		probably benign	Het
Eif2a	C	A	3: 58,456,049 (GRCm39)	Y349*	probably null	Het
Enpep	G	A	3: 129,065,067 (GRCm39)	T874I	probably damaging	Het
Eps15	A	G	4: 109,169,505 (GRCm39)	D105G	possibly damaging	Het
Ess2	A	T	16: 17,722,954 (GRCm39)	M320K	probably damaging	Het
Exosc10	G	A	4: 148,653,159 (GRCm39)		probably null	Het
Fam13b	A	T	18: 34,631,070 (GRCm39)	N36K	probably damaging	Het
Fanca	T	C	8: 123,995,209 (GRCm39)	D1431G	probably benign	Het
Fgg	A	G	3: 82,921,625 (GRCm39)	D436G	probably benign	Het
Fip1l1	C	T	5: 74,725,188 (GRCm39)	T251I	probably benign	Het
Galnt2	A	G	8: 125,032,347 (GRCm39)	N104S	probably damaging	Het
Gmip	T	C	8: 70,268,748 (GRCm39)	S458P	possibly damaging	Het
Herc2	A	G	7: 55,756,144 (GRCm39)	D728G	probably benign	Het
Hif3a	A	G	7: 16,788,671 (GRCm39)	L100P	probably damaging	Het
Hmox2	C	G	16: 4,583,866 (GRCm39)	P282R	possibly damaging	Het
Hook1	A	T	4: 95,880,432 (GRCm39)	H90L	probably benign	Het
Igf2bp2	C	A	16: 21,883,866 (GRCm39)	G473C	probably damaging	Het
Ip6k2	T	C	9: 108,675,379 (GRCm39)		probably null	Het
Ipo5	G	T	14: 121,157,366 (GRCm39)	R68L	probably damaging	Het
Kif19b	A	G	5: 140,455,434 (GRCm39)	M347V	probably damaging	Het
Klhdc1	G	T	12: 69,305,392 (GRCm39)	W234L	probably damaging	Het
Krt8	A	G	15: 101,909,870 (GRCm39)	V178A	possibly damaging	Het
Lgi3	T	A	14: 70,768,712 (GRCm39)		probably null	Het
Litaf	T	G	16: 10,784,421 (GRCm39)	N30H	probably benign	Het
Lman2	C	A	13: 55,510,368 (GRCm39)	W12L	unknown	Het
Macf1	A	G	4: 123,276,022 (GRCm39)	L6182P	probably damaging	Het
Magi3	A	T	3: 103,992,662 (GRCm39)	M270K	probably benign	Het
Minar1	T	A	9: 89,483,234 (GRCm39)	E721V	probably damaging	Het
Mllt10	T	A	2: 18,167,353 (GRCm39)	V426D	probably benign	Het
Mrgprf	A	G	7: 144,862,046 (GRCm39)	I203V	probably benign	Het
Mrnip	G	A	11: 50,067,688 (GRCm39)	C27Y	probably damaging	Het
Mrpl24	C	T	3: 87,829,701 (GRCm39)	R96*	probably null	Het
Nbas	T	A	12: 13,402,875 (GRCm39)		probably benign	Het
Nipal4	G	A	11: 46,045,470 (GRCm39)	T131M	possibly damaging	Het
Nlrp12	T	C	7: 3,289,621 (GRCm39)	D297G	possibly damaging	Het
Nol6	A	C	4: 41,121,823 (GRCm39)	M237R	probably benign	Het
Olig1	A	G	16: 91,067,027 (GRCm39)	E88G	probably benign	Het
Or1j19	T	A	2: 36,676,855 (GRCm39)	L106*	probably null	Het
Parg	A	G	14: 31,931,175 (GRCm39)	D265G	possibly damaging	Het
Pcdhgb8	A	T	18: 37,895,301 (GRCm39)	I124L	probably damaging	Het
Pign	A	G	1: 105,481,827 (GRCm39)	F822L	probably damaging	Het
Plch2	T	C	4: 155,071,140 (GRCm39)	T1080A	probably benign	Het
Pld4	A	T	12: 112,733,210 (GRCm39)	Y262F	possibly damaging	Het
Ppp1r12b	A	G	1: 134,693,730 (GRCm39)	V977A	probably benign	Het
Ppp6r3	C	T	19: 3,521,984 (GRCm39)	E565K		Het
Psmg2	A	G	18: 67,787,158 (GRCm39)		probably benign	Het
Ptcd3	C	T	6: 71,885,645 (GRCm39)	G27D	probably benign	Het
Retreg2	G	T	1: 75,119,525 (GRCm39)	G7C	unknown	Het
Rlbp1	A	T	7: 79,027,114 (GRCm39)	F182Y	probably benign	Het
Rnf148	G	C	6: 23,654,378 (GRCm39)	S206C	probably benign	Het
Sash1	A	G	10: 8,637,869 (GRCm39)	M1T	probably null	Het
Shank3	A	T	15: 89,433,598 (GRCm39)	T1448S	probably damaging	Het
Sipa1l1	A	G	12: 82,389,207 (GRCm39)	K478E	probably damaging	Het
Slitrk6	A	G	14: 110,988,801 (GRCm39)	I302T	probably benign	Het
Smc1b	A	G	15: 84,950,529 (GRCm39)	V1165A	probably damaging	Het
Sncaip	A	T	18: 53,048,381 (GRCm39)	H939L	probably benign	Het
Stn1	T	C	19: 47,524,709 (GRCm39)	D27G	probably damaging	Het
Sugct	T	G	13: 17,427,180 (GRCm39)		probably null	Het
Tmem259	A	G	10: 79,814,983 (GRCm39)	S214P	probably damaging	Het
Trdv4	G	A	14: 54,312,946 (GRCm39)	G107S	probably damaging	Het
Ttc3	C	T	16: 94,232,829 (GRCm39)	L957F	possibly damaging	Het
Ttn	A	G	2: 76,711,471 (GRCm39)	Y8357H	unknown	Het
Twnk	T	C	19: 44,996,434 (GRCm39)	V289A	probably benign	Het
Umodl1	A	G	17: 31,202,958 (GRCm39)	D437G	possibly damaging	Het
Upf1	T	C	8: 70,790,930 (GRCm39)	T590A	probably benign	Het
Vmn2r63	A	T	7: 42,576,441 (GRCm39)	D457E	probably benign	Het
Wdr82	A	T	9: 106,061,975 (GRCm39)	T213S	probably benign	Het
Zfp267	T	C	3: 36,218,255 (GRCm39)	Y93H	possibly damaging	Het
Zfp672	A	T	11: 58,220,590 (GRCm39)	M3K	unknown	Het
Zfyve26	A	G	12: 79,285,742 (GRCm39)	V2345A	probably benign	Het

Other mutations in Mapre2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02557:Mapre2	APN	18	23,966,014 (GRCm39)	missense	probably damaging	0.99
IGL02632:Mapre2	APN	18	23,991,217 (GRCm39)	missense	probably benign
R0005:Mapre2	UTSW	18	23,986,750 (GRCm39)	missense	probably damaging	1.00
R0127:Mapre2	UTSW	18	23,937,232 (GRCm39)	missense	probably benign	0.41
R0892:Mapre2	UTSW	18	23,991,200 (GRCm39)	missense	probably benign	0.07
R1244:Mapre2	UTSW	18	23,986,774 (GRCm39)	missense	probably damaging	0.98
R1631:Mapre2	UTSW	18	23,966,011 (GRCm39)	missense	probably damaging	1.00
R1893:Mapre2	UTSW	18	23,986,774 (GRCm39)	missense	probably damaging	0.98
R4786:Mapre2	UTSW	18	24,011,016 (GRCm39)	missense	probably benign	0.05
R4912:Mapre2	UTSW	18	23,965,990 (GRCm39)	missense	probably damaging	1.00
R5133:Mapre2	UTSW	18	23,991,190 (GRCm39)	missense	possibly damaging	0.73
R5637:Mapre2	UTSW	18	23,886,919 (GRCm39)	intron	probably benign
R6620:Mapre2	UTSW	18	23,991,002 (GRCm39)	missense	probably benign	0.38
R7250:Mapre2	UTSW	18	23,991,119 (GRCm39)	missense	possibly damaging	0.64
R7736:Mapre2	UTSW	18	24,011,012 (GRCm39)	missense	probably benign
R8157:Mapre2	UTSW	18	23,991,218 (GRCm39)	missense	probably benign	0.00
R8698:Mapre2	UTSW	18	24,011,090 (GRCm39)	missense	probably benign	0.02
R8742:Mapre2	UTSW	18	24,016,688 (GRCm39)	missense	probably benign	0.00
R9150:Mapre2	UTSW	18	23,991,208 (GRCm39)	missense	probably benign	0.25
R9234:Mapre2	UTSW	18	23,937,236 (GRCm39)	missense	probably benign	0.01
R9490:Mapre2	UTSW	18	23,986,764 (GRCm39)	missense	possibly damaging	0.88
R9558:Mapre2	UTSW	18	23,991,195 (GRCm39)	missense	possibly damaging	0.92
R9563:Mapre2	UTSW	18	24,023,981 (GRCm39)	missense	unknown
R9574:Mapre2	UTSW	18	23,965,993 (GRCm39)	missense	probably benign	0.16
R9598:Mapre2	UTSW	18	24,016,707 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- GGAGTCGCAGGAACTTTCTTG -3'
(R):5'- TCGTCTGCTCATGTAAAGGAAG -3'

Sequencing Primer
(F):5'- GATTAGTATAAGTATCTGCCCCGG -3'
(R):5'- CTTGTGAAGTTTACCCAAAGACC -3'

Posted On

2021-07-15