Mutagenetix > Incidental Mutation

Incidental Mutation 'R6273:Ankrd31'

507488

Institutional Source

Beutler Lab

Gene Symbol

Ankrd31

Ensembl Gene

ENSMUSG00000109561

Gene Name

ankyrin repeat domain 31

Synonyms

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6273 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

96748272-96910039 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 96851673 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 1065 (I1065V)

Ref Sequence

ENSEMBL: ENSMUSP00000146720 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000207464] [ENSMUST00000208758]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000207464
AA Change: I915V

PolyPhen 2 Score 0.061 (Sensitivity: 0.94; Specificity: 0.84)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000208758
AA Change: I1065V

PolyPhen 2 Score 0.605 (Sensitivity: 0.87; Specificity: 0.91)

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.0%
20x: 94.2%

Validation Efficiency

98% (78/80)

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610040J01Rik	T	A	5: 63,898,218	I99N	probably damaging	Het
Ank3	G	A	10: 70,002,565	R1566K	possibly damaging	Het
Aox2	A	G	1: 58,339,672	T1027A	probably benign	Het
Atm	G	A	9: 53,487,922	P1593L	probably benign	Het
Atp13a5	T	G	16: 29,348,737	I132L	probably benign	Het
BC035044	A	G	6: 128,890,889		probably benign	Het
C530008M17Rik	A	T	5: 76,857,721	D643V	unknown	Het
Cadm3	CT	C	1: 173,349,124		probably benign	Homo
Car3	C	T	3: 14,871,617	P247S	probably benign	Het
Ccdc7a	T	C	8: 128,787,338	Y160C	probably damaging	Het
Cd1d1	A	G	3: 86,998,257	V143A	probably benign	Het
Cog6	A	T	3: 52,996,052	F142I	probably damaging	Het
Crhr1	T	G	11: 104,163,856	N98K	possibly damaging	Het
Csf1	A	G	3: 107,749,163	V72A	probably damaging	Het
Cwc15	T	A	9: 14,510,241	I201K	probably benign	Het
Dgka	T	C	10: 128,723,646	K482R	probably benign	Het
Dnah7b	T	C	1: 46,242,316	S2846P	possibly damaging	Het
Dst	T	A	1: 34,275,266	I4199N	probably damaging	Het
Dusp7	A	G	9: 106,373,896	T407A	possibly damaging	Het
Eml2	G	A	7: 19,201,163	V432I	probably damaging	Het
Fem1a	T	C	17: 56,257,083	Y59H	possibly damaging	Het
Fetub	C	T	16: 22,932,331	R143C	probably damaging	Het
Filip1	A	T	9: 79,815,886	D1150E	probably benign	Het
Gabra1	A	G	11: 42,140,311	V264A	probably damaging	Het
Gm4131	T	C	14: 62,464,850	E223G	probably damaging	Het
Gon4l	T	C	3: 88,855,849	V333A	probably damaging	Het
Gsk3b	A	G	16: 38,208,046	T289A	probably benign	Het
Hmcn2	T	C	2: 31,411,834	S2912P	probably damaging	Het
Htr7	A	T	19: 36,041,569		probably benign	Het
Ibsp	A	G	5: 104,310,301	T235A	probably benign	Het
Ints13	A	T	6: 146,565,681	D116E	probably damaging	Het
Kctd19	T	C	8: 105,385,485	N753S	probably benign	Het
Mdn1	A	G	4: 32,715,979	N2054D	probably benign	Het
Mink1	A	T	11: 70,611,435	K880*	probably null	Het
Mrvi1	G	T	7: 110,871,583	H848N	probably benign	Het
Myo15b	T	A	11: 115,862,799	L824Q	possibly damaging	Het
Napepld	T	C	5: 21,665,322	E366G	probably benign	Het
Obscn	T	A	11: 59,076,993	T2662S	possibly damaging	Het
Olfr130	T	G	17: 38,067,795	L208R	probably damaging	Het
Olfr1302	T	C	2: 111,781,222	F301L	probably benign	Het
Olfr133	T	A	17: 38,148,942	M118K	possibly damaging	Het
Olfr1448	A	G	19: 12,919,400	V303A	probably benign	Het
Olfr213	A	G	6: 116,541,316	T288A	possibly damaging	Het
Olfr656	A	G	7: 104,617,895	D72G	probably damaging	Het
Pah	T	C	10: 87,576,215		probably null	Het
Panx3	T	G	9: 37,667,429	I85L	probably benign	Het
Pate4	T	C	9: 35,607,790	N94D	probably benign	Het
Pde4d	A	G	13: 109,950,221	M610V	possibly damaging	Het
Pik3c2b	T	C	1: 133,066,711	S138P	probably benign	Het
Pkn1	T	C	8: 83,672,270	N696S	probably damaging	Het
Plppr2	A	G	9: 21,944,505	E258G	probably damaging	Het
Plxnd1	A	T	6: 115,978,492	M538K	probably damaging	Het
Prepl	G	T	17: 85,083,268	N87K	probably benign	Het
Prkag2	C	A	5: 24,947,536	R190L	probably damaging	Het
Rara	A	G	11: 98,970,222	T179A	probably benign	Het
Rfx7	A	G	9: 72,616,997	K490E	possibly damaging	Het
Rgsl1	C	T	1: 153,827,465	V147M	possibly damaging	Het
Rph3a	A	G	5: 120,945,422	I595T	possibly damaging	Het
Rsf1	CG	CGACGGCGGTG	7: 97,579,908		probably benign	Homo
Slc35e2	C	T	4: 155,610,026	P10L	probably benign	Het
Slc8a2	T	C	7: 16,145,334	F582L	possibly damaging	Het
Sprr2e	A	G	3: 92,352,864	M1V	probably null	Het
Steap1	T	A	5: 5,740,827	R40S	possibly damaging	Het
Tbc1d2	C	T	4: 46,629,912	G252R	probably benign	Het
Thsd7a	A	T	6: 12,408,836	V729E	probably damaging	Het
Tmem2	T	A	19: 21,802,005	V393E	probably damaging	Het
Tmprss13	A	G	9: 45,345,332	Y525C	probably damaging	Het
Tnik	A	T	3: 28,577,500	H383L	possibly damaging	Het
Vars	T	C	17: 35,013,743	L881S	probably damaging	Het
Vmn1r201	A	C	13: 22,475,215	S200R	probably damaging	Het
Vmn2r14	A	T	5: 109,221,267	W147R	probably benign	Het
Vmn2r-ps130	A	T	17: 23,076,785	H643L	probably benign	Het
Vps53	T	C	11: 76,102,018	E367G	probably benign	Het
Xab2	C	T	8: 3,611,822	G544S	probably damaging	Het
Ythdf3	T	A	3: 16,204,856	V400E	possibly damaging	Het
Zfand5	C	T	19: 21,279,696	P147S	probably benign	Het
Zfp768	A	T	7: 127,345,147		probably null	Het
Zswim8	A	G	14: 20,713,453	M423V	probably benign	Het

Other mutations in Ankrd31

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R6001:Ankrd31	UTSW	13	96826209	missense	probably damaging	1.00
R6035:Ankrd31	UTSW	13	96832213	missense	probably benign	0.00
R6035:Ankrd31	UTSW	13	96832213	missense	probably benign	0.00
R6291:Ankrd31	UTSW	13	96878238	missense	possibly damaging	0.72
R6387:Ankrd31	UTSW	13	96830573	missense	probably damaging	0.99
R6608:Ankrd31	UTSW	13	96832780	missense	probably damaging	0.99
R6680:Ankrd31	UTSW	13	96830609	critical splice donor site	probably null
R6738:Ankrd31	UTSW	13	96904127	missense	possibly damaging	0.79
R6860:Ankrd31	UTSW	13	96831586	missense	probably benign	0.01
R6988:Ankrd31	UTSW	13	96878249	missense	probably damaging	1.00
R7305:Ankrd31	UTSW	13	96878971	missense	probably damaging	0.99
R7586:Ankrd31	UTSW	13	96832054	missense	possibly damaging	0.92
R7631:Ankrd31	UTSW	13	96878954	missense	probably benign	0.04
R7842:Ankrd31	UTSW	13	96821458	critical splice donor site	probably null
R7890:Ankrd31	UTSW	13	96831871	missense	probably benign	0.27
R7911:Ankrd31	UTSW	13	96879100	missense	possibly damaging	0.47
R8052:Ankrd31	UTSW	13	96832528	missense	probably benign	0.07
R8133:Ankrd31	UTSW	13	96866495	critical splice donor site	probably null
R8430:Ankrd31	UTSW	13	96851691	missense	possibly damaging	0.78
R8752:Ankrd31	UTSW	13	96780371	missense	probably damaging	0.99
R8767:Ankrd31	UTSW	13	96832716	missense	probably damaging	1.00
R8793:Ankrd31	UTSW	13	96831713	missense	probably damaging	0.97
R8903:Ankrd31	UTSW	13	96832821	missense	probably damaging	1.00
R8917:Ankrd31	UTSW	13	96832704	missense	probably damaging	0.98
R8946:Ankrd31	UTSW	13	96909529	makesense	probably null
R9006:Ankrd31	UTSW	13	96830596	missense	probably benign	0.00
R9022:Ankrd31	UTSW	13	96826147	missense	probably benign	0.01
R9045:Ankrd31	UTSW	13	96831526	nonsense	probably null
R9098:Ankrd31	UTSW	13	96780371	missense	probably damaging	0.97
R9115:Ankrd31	UTSW	13	96804265	critical splice donor site	probably null
R9202:Ankrd31	UTSW	13	96878875	nonsense	probably null
R9211:Ankrd31	UTSW	13	96893043	missense	possibly damaging	0.93
R9297:Ankrd31	UTSW	13	96878577	missense	probably benign	0.04
R9318:Ankrd31	UTSW	13	96878577	missense	probably benign	0.04
R9377:Ankrd31	UTSW	13	96878225	missense	probably benign	0.10
R9454:Ankrd31	UTSW	13	96780334	missense	probably damaging	0.97
R9454:Ankrd31	UTSW	13	96780338	missense	possibly damaging	0.70
R9538:Ankrd31	UTSW	13	96872685	missense	probably benign	0.24

Predicted Primers

PCR Primer
(F):5'- CCAGTGTTTCCAGGAGTTTTATC -3'
(R):5'- TCACCCAGTATCAAAATTAGGGGC -3'

Sequencing Primer
(F):5'- GTGACTCCCTACATAGTGATGGTC -3'
(R):5'- CCCAGTATCAAAATTAGGGGCAAAGG -3'

Posted On

2018-03-15