Mutagenetix > Incidental Mutation

Incidental Mutation 'R5109:Anxa10'

393745

Institutional Source

Beutler Lab

Gene Symbol

Anxa10

Ensembl Gene

ENSMUSG00000031635

Gene Name

annexin A10

Synonyms

MMRRC Submission

042697-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.060) question?

Stock #

R5109 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

62510076-62576184 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 62516093 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 193 (E193G)

Ref Sequence

ENSEMBL: ENSMUSP00000034054 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000034052] [ENSMUST00000034054]

AlphaFold

Q9QZ10

Predicted Effect

possibly damaging
Transcript: ENSMUST00000034052
AA Change: E213G

PolyPhen 2 Score 0.790 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000034052
Gene: ENSMUSG00000031635
AA Change: E213G

Domain	Start	End	E-Value	Type
ANX	34	86	6.71e-16	SMART
ANX	106	158	8.13e-15	SMART
ANX	198	241	5.48e-2	SMART
ANX	264	316	6.51e-14	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000034054
AA Change: E193G

PolyPhen 2 Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000034054
Gene: ENSMUSG00000031635
AA Change: E193G

Domain	Start	End	E-Value	Type
ANX	34	86	6.71e-16	SMART
ANX	106	161	2.38e-1	SMART
ANX	178	221	5.48e-2	SMART
ANX	244	296	6.51e-14	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210799

Meta Mutation Damage Score

0.3247

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 95.9%
20x: 91.2%

Validation Efficiency

95% (78/82)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the annexin family. Members of this calcium-dependent phospholipid-binding protein family play a role in the regulation of cellular growth and in signal transduction pathways. The function of this gene has not yet been determined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Litter sizes from crosses of females that are either homozygous or heterozygous for a null allele contain fewer pups than wild-type females, indicating a dominant maternal effect on embryonic lethality. Embryos of homozygous null females die between E4.5 and E12.5. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ankrd17	T	C	5: 90,391,395 (GRCm39)	S1841G	possibly damaging	Het
Ap3d1	T	C	10: 80,545,284 (GRCm39)	S1056G	probably benign	Het
Apbb1	T	C	7: 105,214,242 (GRCm39)	N62D	probably damaging	Het
Apobec2	A	T	17: 48,730,022 (GRCm39)	Y215N	probably damaging	Het
Apobec2	T	A	17: 48,730,024 (GRCm39)	Y214F	probably damaging	Het
Appl2	A	T	10: 83,436,871 (GRCm39)	V630E	probably benign	Het
Bud23	T	C	5: 135,089,877 (GRCm39)		probably benign	Het
Cacna1b	A	T	2: 24,580,797 (GRCm39)	M683K	possibly damaging	Het
Cbfa2t2	T	A	2: 154,373,293 (GRCm39)	D187E	probably damaging	Het
Cfap54	G	T	10: 92,773,753 (GRCm39)	F96L	probably benign	Het
Cimap1a	A	T	7: 140,429,461 (GRCm39)	S197C	probably benign	Het
Crebbp	A	G	16: 3,906,295 (GRCm39)		probably benign	Het
Crocc	C	T	4: 140,755,722 (GRCm39)	R1102Q	probably damaging	Het
Dcaf12	T	C	4: 41,298,329 (GRCm39)	D273G	possibly damaging	Het
Dchs1	T	C	7: 105,414,221 (GRCm39)	T865A	probably benign	Het
Dhfr	A	T	13: 92,491,788 (GRCm39)	I8F	probably damaging	Het
Dnaja2	A	T	8: 86,279,887 (GRCm39)	F97L	possibly damaging	Het
Dnase1l1	C	T	X: 73,320,644 (GRCm39)		probably null	Het
Doc2b	T	C	11: 75,667,967 (GRCm39)	D261G	probably benign	Het
Ear1	A	G	14: 44,056,485 (GRCm39)	Y128H	probably benign	Het
Elac2	T	A	11: 64,883,142 (GRCm39)	I171N	probably damaging	Het
Entpd3	C	A	9: 120,395,380 (GRCm39)	N454K	possibly damaging	Het
Flrt3	A	G	2: 140,502,663 (GRCm39)	S322P	possibly damaging	Het
Fn1	C	T	1: 71,688,394 (GRCm39)	C170Y	probably damaging	Het
Gabbr1	T	A	17: 37,382,920 (GRCm39)		probably benign	Het
Gm7247	T	G	14: 51,602,774 (GRCm39)	S37A	probably damaging	Het
Gm8775	T	A	3: 4,277,008 (GRCm39)		noncoding transcript	Het
Gprc5c	G	T	11: 114,755,093 (GRCm39)	V257L	possibly damaging	Het
Gria4	A	C	9: 4,472,168 (GRCm39)	N440K	probably damaging	Het
H2-T22	T	A	17: 36,350,113 (GRCm39)	R334*	probably null	Het
Ift172	T	C	5: 31,423,330 (GRCm39)	D817G	probably benign	Het
Igkv9-124	T	A	6: 67,919,348 (GRCm39)	R21S	possibly damaging	Het
Itgam	G	A	7: 127,712,390 (GRCm39)	V846I	probably benign	Het
Kif11	T	A	19: 37,373,063 (GRCm39)	M94K	possibly damaging	Het
Krtcap2	T	C	3: 89,154,085 (GRCm39)	V2A	probably benign	Het
Lrrc47	A	G	4: 154,101,933 (GRCm39)	D400G	probably damaging	Het
Man2a1	T	A	17: 65,059,443 (GRCm39)	V1110E	probably benign	Het
Mfsd9	T	A	1: 40,813,365 (GRCm39)	I317F	probably damaging	Het
Mindy4	A	T	6: 55,193,730 (GRCm39)		probably null	Het
Mrpl53	A	G	6: 83,086,541 (GRCm39)	T82A	probably damaging	Het
Myo3b	A	G	2: 69,925,637 (GRCm39)	K35E	possibly damaging	Het
Nalcn	A	G	14: 123,515,650 (GRCm39)	V1717A	possibly damaging	Het
Ncoa2	A	G	1: 13,257,070 (GRCm39)	V143A	probably damaging	Het
Ndufa9	A	C	6: 126,809,520 (GRCm39)		probably null	Het
Or10ag60	G	A	2: 87,438,319 (GRCm39)	G196R	possibly damaging	Het
Or10ag60	G	A	2: 87,437,755 (GRCm39)	A8T	possibly damaging	Het
Or12e9	A	G	2: 87,201,878 (GRCm39)	M1V	probably null	Het
Or5k17	A	G	16: 58,746,422 (GRCm39)	S171P	probably benign	Het
Or5p55	T	C	7: 107,567,104 (GRCm39)	S167P	probably benign	Het
Or6c202	T	C	10: 128,996,106 (GRCm39)	Y249C	probably damaging	Het
Or7g28	A	T	9: 19,272,438 (GRCm39)	I71N	probably damaging	Het
Or9g8	G	A	2: 85,607,668 (GRCm39)	V247M	probably damaging	Het
Pde4b	G	T	4: 102,458,741 (GRCm39)	A466S	probably damaging	Het
Pfkfb3	A	T	2: 11,491,162 (GRCm39)		probably benign	Het
Ppp1r21	A	G	17: 88,866,268 (GRCm39)	K355E	probably damaging	Het
Psme4	T	A	11: 30,741,095 (GRCm39)	Y90*	probably null	Het
Rbms1	G	A	2: 60,612,284 (GRCm39)	L161F	probably damaging	Het
Rdh16f2	A	G	10: 127,702,672 (GRCm39)	D83G	probably damaging	Het
Sec16b	C	T	1: 157,392,361 (GRCm39)	R910*	probably null	Het
Sema4c	CTGGGCTT	C	1: 36,591,381 (GRCm39)		probably null	Het
Spata31e5	T	C	1: 28,816,636 (GRCm39)	I465M	possibly damaging	Het
Stambp	A	G	6: 83,540,803 (GRCm39)		probably null	Het
Tcf21	T	C	10: 22,695,558 (GRCm39)	N82S	probably damaging	Het
Tlr2	A	T	3: 83,745,030 (GRCm39)	V351D	probably damaging	Het
Tmem39a	G	A	16: 38,411,326 (GRCm39)	G359D	probably damaging	Het
Ttc23l	G	T	15: 10,551,636 (GRCm39)	T30K	possibly damaging	Het
Vmn2r17	C	A	5: 109,577,342 (GRCm39)	F464L	probably benign	Het
Vmn2r49	T	A	7: 9,710,204 (GRCm39)	T843S	probably benign	Het
Vmn2r7	T	C	3: 64,598,088 (GRCm39)	D823G	probably null	Het
Wrnip1	T	A	13: 33,000,319 (GRCm39)	L442Q	probably damaging	Het
Zbtb38	G	T	9: 96,569,062 (GRCm39)	S674Y	probably damaging	Het
Zfp639	T	G	3: 32,574,585 (GRCm39)		probably null	Het

Other mutations in Anxa10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01977:Anxa10	APN	8	62,529,348 (GRCm39)	missense	probably damaging	1.00
IGL03354:Anxa10	APN	8	62,549,778 (GRCm39)	missense	probably damaging	1.00
R0687:Anxa10	UTSW	8	62,545,606 (GRCm39)	missense	possibly damaging	0.69
R0826:Anxa10	UTSW	8	62,529,318 (GRCm39)	nonsense	probably null
R0883:Anxa10	UTSW	8	62,531,001 (GRCm39)	missense	probably benign	0.40
R0945:Anxa10	UTSW	8	62,513,279 (GRCm39)	splice site	probably benign
R1124:Anxa10	UTSW	8	62,514,038 (GRCm39)	splice site	probably null
R1647:Anxa10	UTSW	8	62,545,618 (GRCm39)	missense	probably damaging	1.00
R2877:Anxa10	UTSW	8	62,513,373 (GRCm39)	missense	probably damaging	1.00
R3706:Anxa10	UTSW	8	62,517,321 (GRCm39)	missense	probably damaging	1.00
R4677:Anxa10	UTSW	8	62,516,054 (GRCm39)	missense	probably damaging	1.00
R5554:Anxa10	UTSW	8	62,514,080 (GRCm39)	missense	possibly damaging	0.93
R5971:Anxa10	UTSW	8	62,530,960 (GRCm39)	missense	probably benign	0.00
R6079:Anxa10	UTSW	8	62,530,960 (GRCm39)	missense	probably benign	0.00
R6134:Anxa10	UTSW	8	62,530,977 (GRCm39)	missense	probably damaging	1.00
R6857:Anxa10	UTSW	8	62,514,051 (GRCm39)	missense	probably benign	0.19
R6901:Anxa10	UTSW	8	62,549,816 (GRCm39)	missense	probably damaging	1.00
R7428:Anxa10	UTSW	8	62,545,543 (GRCm39)	missense	probably benign	0.01
R8683:Anxa10	UTSW	8	62,510,825 (GRCm39)	missense	probably damaging	1.00
R8920:Anxa10	UTSW	8	62,527,580 (GRCm39)	missense	probably benign	0.00
R9276:Anxa10	UTSW	8	62,549,753 (GRCm39)	missense	probably damaging	1.00
R9500:Anxa10	UTSW	8	62,545,545 (GRCm39)	missense	probably benign	0.00
Z1088:Anxa10	UTSW	8	62,545,540 (GRCm39)	missense	probably damaging	0.97
Z1176:Anxa10	UTSW	8	62,516,104 (GRCm39)	critical splice acceptor site	probably null

Predicted Primers

PCR Primer
(F):5'- GATTCTACTCATGCACATGTTCAG -3'
(R):5'- CCAGCAACAGTAGTTCTTTGGAG -3'

Sequencing Primer
(F):5'- TGCACATGTTCAGTCAGAGC -3'
(R):5'- GCAACAGTAGTTCTTTGGAGTCCAAG -3'

Posted On

2016-06-15