Mutagenetix > Incidental Mutation

Incidental Mutation 'R6930:Spon2'

539931

Institutional Source

Beutler Lab

Gene Symbol

Spon2

Ensembl Gene

ENSMUSG00000037379

Gene Name

spondin 2, extracellular matrix protein

Synonyms

2310045I24Rik, Mindin, M-spondin

MMRRC Submission

045046-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.252) question?

Stock #

R6930 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

33370862-33375596 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 33373771 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 180 (V180A)

Ref Sequence

ENSEMBL: ENSMUSP00000042701 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000046186] [ENSMUST00000201475] [ENSMUST00000201475] [ENSMUST00000201475]

AlphaFold

Q8BMS2

Predicted Effect

probably benign
Transcript: ENSMUST00000046186
AA Change: V180A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000042701
Gene: ENSMUSG00000037379
AA Change: V180A

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Spond_N	40	234	2.3e-79	PFAM
TSP1	279	330	4.48e-7	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000201475

SMART Domains

Protein: ENSMUSP00000144416
Gene: ENSMUSG00000037379

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Spond_N	40	179	2.4e-50	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000201475

SMART Domains

Protein: ENSMUSP00000144416
Gene: ENSMUSG00000037379

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Spond_N	40	179	2.4e-50	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000201475

SMART Domains

Protein: ENSMUSP00000144416
Gene: ENSMUSG00000037379

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Spond_N	40	179	2.4e-50	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 100.0%
3x: 99.8%
10x: 99.0%
20x: 96.5%

Validation Efficiency

100% (63/63)

MGI Phenotype

PHENOTYPE: Mice homozygous for disruptions in this gene have an essentially normal phenotype. There is some alteration in succeptibility to bacterial infection however. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700093K21Rik	A	T	11: 23,466,563 (GRCm39)	D156E	probably benign	Het
Adam17	A	T	12: 21,403,949 (GRCm39)	V99E	probably damaging	Het
Akr1e1	T	C	13: 4,652,714 (GRCm39)	D41G	probably damaging	Het
Alcam	T	C	16: 52,126,018 (GRCm39)	I100V	probably benign	Het
Atr	T	C	9: 95,748,688 (GRCm39)	I411T	probably benign	Het
Bbs4	T	C	9: 59,230,764 (GRCm39)	S453G	probably benign	Het
Brdt	C	T	5: 107,507,081 (GRCm39)	L494F	probably benign	Het
Ccser1	T	C	6: 62,357,009 (GRCm39)	S816P	probably benign	Het
Cdk10	T	C	8: 123,957,347 (GRCm39)	I157T	probably damaging	Het
Ceacam5	G	A	7: 17,484,759 (GRCm39)		probably null	Het
Chst15	T	C	7: 131,870,759 (GRCm39)	I259V	possibly damaging	Het
Cracdl	A	T	1: 37,664,026 (GRCm39)	I624N	possibly damaging	Het
Csmd1	A	T	8: 16,142,409 (GRCm39)	M1498K	probably damaging	Het
D630045J12Rik	T	C	6: 38,135,151 (GRCm39)	D1343G	probably damaging	Het
Denr	T	C	5: 124,046,250 (GRCm39)	Y27H	probably benign	Het
Dop1a	T	C	9: 86,413,825 (GRCm39)		probably null	Het
Epg5	T	C	18: 78,057,378 (GRCm39)	F1819S	probably damaging	Het
Flg2	T	A	3: 93,108,642 (GRCm39)	Y223*	probably null	Het
Fry	T	C	5: 150,351,695 (GRCm39)	L1733P	probably benign	Het
Gabrb2	T	C	11: 42,488,440 (GRCm39)	V302A	probably damaging	Het
Gimap9	G	A	6: 48,654,601 (GRCm39)	D53N	probably damaging	Het
Gje1	G	T	10: 14,593,886 (GRCm39)	L3I	possibly damaging	Het
Gm49383	G	T	12: 69,239,586 (GRCm39)	A645E	probably damaging	Het
Gm8947	G	A	1: 151,068,347 (GRCm39)	G60D	probably damaging	Het
Gpatch2l	G	A	12: 86,290,958 (GRCm39)	R47H	probably damaging	Het
Gys2	A	G	6: 142,405,106 (GRCm39)		probably null	Het
Hace1	A	G	10: 45,494,598 (GRCm39)	H136R	probably damaging	Het
Herc3	T	G	6: 58,893,444 (GRCm39)	V902G	probably damaging	Het
Hspbp1	T	C	7: 4,687,606 (GRCm39)	R2G	probably benign	Het
Iqch	T	A	9: 63,387,856 (GRCm39)	K811N	possibly damaging	Het
Kmt2a	A	G	9: 44,753,962 (GRCm39)		probably benign	Het
Lonrf2	A	T	1: 38,843,417 (GRCm39)	V372D	probably benign	Het
Lpin2	T	C	17: 71,551,786 (GRCm39)	Y729H	probably damaging	Het
Lrrc32	A	G	7: 98,148,471 (GRCm39)	N417S	possibly damaging	Het
Malrd1	T	A	2: 15,802,478 (GRCm39)	C1064S	unknown	Het
Mast3	G	A	8: 71,252,115 (GRCm39)	R20*	probably null	Het
Mypn	A	C	10: 62,952,718 (GRCm39)	I174S	probably damaging	Het
Nrg1	G	A	8: 32,308,534 (GRCm39)	T505M	probably damaging	Het
Or13p8	A	G	4: 118,584,338 (GRCm39)	K298R	probably damaging	Het
Or6y1	A	G	1: 174,276,677 (GRCm39)	I163V	probably damaging	Het
Or7a42	A	G	10: 78,791,615 (GRCm39)	D192G	possibly damaging	Het
Or7e178	A	G	9: 20,225,395 (GRCm39)	Y266H	probably damaging	Het
Phf3	T	C	1: 30,850,958 (GRCm39)	E1132G	probably damaging	Het
Pla2g4d	A	T	2: 120,101,114 (GRCm39)	M521K	probably damaging	Het
Plekhg1	A	G	10: 3,913,770 (GRCm39)	H1164R	possibly damaging	Het
Plxnb2	A	G	15: 89,044,592 (GRCm39)	V1218A	probably benign	Het
Pold1	A	G	7: 44,191,630 (GRCm39)	S119P	probably benign	Het
Pole	T	A	5: 110,441,156 (GRCm39)	D203E	probably benign	Het
Rapgefl1	T	A	11: 98,737,947 (GRCm39)	L387Q	probably damaging	Het
Rbm33	T	C	5: 28,557,504 (GRCm39)	I199T	probably benign	Het
Rsrc1	C	T	3: 66,901,982 (GRCm39)	P44L	unknown	Het
Rufy1	C	A	11: 50,289,207 (GRCm39)	R545L	probably benign	Het
Ryr3	T	A	2: 112,690,699 (GRCm39)	D1117V	probably damaging	Het
Sap130	T	C	18: 31,815,141 (GRCm39)	V621A	possibly damaging	Het
Sparcl1	T	A	5: 104,234,940 (GRCm39)	Y525F	probably damaging	Het
Trav10n	G	A	14: 53,359,947 (GRCm39)	V75M	probably benign	Het
Ttc34	T	C	4: 154,923,543 (GRCm39)	L84P	probably damaging	Het
Vmn1r23	C	T	6: 57,903,130 (GRCm39)	R216K	probably benign	Het
Vmn2r61	A	G	7: 41,949,364 (GRCm39)	T595A	probably benign	Het
Vmn2r66	T	A	7: 84,661,216 (GRCm39)	I5F	possibly damaging	Het
Zfp879	C	T	11: 50,723,839 (GRCm39)	G406R	probably damaging	Het
Zic2	A	T	14: 122,713,869 (GRCm39)	D261V	probably damaging	Het

Other mutations in Spon2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01557:Spon2	APN	5	33,374,047 (GRCm39)	missense	probably damaging	1.00
IGL01781:Spon2	APN	5	33,372,904 (GRCm39)	missense	probably benign	0.09
IGL02533:Spon2	APN	5	33,371,942 (GRCm39)	missense	probably damaging	1.00
R1557:Spon2	UTSW	5	33,374,108 (GRCm39)	missense	probably damaging	1.00
R1711:Spon2	UTSW	5	33,373,729 (GRCm39)	missense	probably damaging	1.00
R4728:Spon2	UTSW	5	33,374,682 (GRCm39)	missense	probably benign	0.01
R4793:Spon2	UTSW	5	33,371,904 (GRCm39)	missense	probably damaging	0.99
R4961:Spon2	UTSW	5	33,371,896 (GRCm39)	nonsense	probably null
R7067:Spon2	UTSW	5	33,371,958 (GRCm39)	missense	probably damaging	1.00
R7643:Spon2	UTSW	5	33,374,800 (GRCm39)	missense	probably benign	0.00
R7727:Spon2	UTSW	5	33,373,019 (GRCm39)	missense	probably damaging	1.00
R8398:Spon2	UTSW	5	33,374,154 (GRCm39)	missense	probably damaging	1.00
R8847:Spon2	UTSW	5	33,371,841 (GRCm39)	missense	probably benign	0.00
R9076:Spon2	UTSW	5	33,374,054 (GRCm39)	nonsense	probably null
R9124:Spon2	UTSW	5	33,372,935 (GRCm39)	missense	possibly damaging	0.67
R9295:Spon2	UTSW	5	33,373,844 (GRCm39)	missense	probably damaging	1.00
R9665:Spon2	UTSW	5	33,374,702 (GRCm39)	missense	probably benign	0.03

Predicted Primers

PCR Primer
(F):5'- AGGCACCCTCTTTGTTGCAC -3'
(R):5'- GCAGACTTCCACAGAGTTAGAG -3'

Sequencing Primer
(F):5'- TGTTGCACCCACCTCAGAG -3'
(R):5'- CTTCCACAGAGTTAGAGGTGCAC -3'

Posted On

2018-11-06