Mutagenetix > Incidental Mutation

Incidental Mutation 'R4799:D130043K22Rik'

369369

Institutional Source

Beutler Lab

Gene Symbol

D130043K22Rik

Ensembl Gene

ENSMUSG00000006711

Gene Name

RIKEN cDNA D130043K22 gene

Synonyms

Kiaa0319

MMRRC Submission

041997-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4799 (G1)

Quality Score

135

Status

Validated

Chromosome

Chromosomal Location

25029118-25085253 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 25062023 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 664 (I664T)

Ref Sequence

ENSEMBL: ENSMUSP00000116004 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000006893] [ENSMUST00000141572]

AlphaFold

Q5SZV5

Predicted Effect

probably damaging
Transcript: ENSMUST00000006893
AA Change: I664T

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000006893
Gene: ENSMUSG00000006711
AA Change: I664T

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
Blast:MANEC	23	102	3e-44	BLAST
low complexity region	236	270	N/A	INTRINSIC
FN3	332	427	3.43e1	SMART
PKD	345	436	3.96e0	SMART
FN3	435	521	3.08e1	SMART
PKD	444	533	7.12e-10	SMART
PKD	539	629	1.46e-6	SMART
PKD	630	723	6.75e-11	SMART
FN3	634	711	5.1e1	SMART
FN3	728	808	9.15e1	SMART
PKD	729	820	4.38e-10	SMART
transmembrane domain	965	987	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000141572
AA Change: I664T

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000116004
Gene: ENSMUSG00000006711
AA Change: I664T

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
Blast:MANEC	23	102	2e-44	BLAST
low complexity region	236	270	N/A	INTRINSIC
FN3	332	427	3.43e1	SMART
PKD	345	436	3.96e0	SMART
FN3	435	521	3.08e1	SMART
PKD	444	533	7.12e-10	SMART
PKD	539	629	1.46e-6	SMART
PKD	630	723	6.75e-11	SMART
FN3	634	711	5.1e1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000169411

Meta Mutation Damage Score

0.6969

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.4%
20x: 92.6%

Validation Efficiency

97% (122/126)

MGI Phenotype

FUNCTION: This gene encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. The encoded protein may play a role in the development of the cerebral cortex by regulating neuronal migration and cell adhesion. Single nucleotide polymorphisms in a similar gene in human are associated with dyslexia. Alternatively spliced transcript variants have been identifed. [provided by RefSeq, May 2015]
PHENOTYPE: Homozygous knockout results in a mild behavioral phenotype: increased prepulse inhibition in males under certain conditions and decreased anxiety-related response. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 119 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abhd12b	C	G	12: 70,215,838 (GRCm39)	S170C	probably damaging	Het
Acads	T	A	5: 115,251,149 (GRCm39)	T112S	probably benign	Het
Adgrl1	A	G	8: 84,662,202 (GRCm39)	H1021R	probably benign	Het
Ago3	A	T	4: 126,241,665 (GRCm39)		probably null	Het
Ap5m1	A	G	14: 49,318,527 (GRCm39)	K412E	probably benign	Het
Arid1b	C	T	17: 5,389,496 (GRCm39)	P1681S	probably damaging	Het
Atxn10	T	C	15: 85,260,909 (GRCm39)		probably null	Het
AU040320	A	G	4: 126,733,462 (GRCm39)	T661A	probably benign	Het
Bhmt1b	C	A	18: 87,774,573 (GRCm39)	A32E	probably damaging	Het
Capn7	T	C	14: 31,082,514 (GRCm39)	I455M	probably benign	Het
Capzb	A	G	4: 138,920,310 (GRCm39)		probably benign	Het
Car10	G	A	11: 93,469,492 (GRCm39)	V156I	possibly damaging	Het
Cbs	T	A	17: 31,851,826 (GRCm39)	D59V	probably damaging	Het
Ccar2	T	C	14: 70,377,003 (GRCm39)	E819G	probably damaging	Het
Cdc73	T	A	1: 143,503,613 (GRCm39)	Q346L	probably benign	Het
Cdhr4	T	C	9: 107,875,898 (GRCm39)		probably benign	Het
Cfap251	C	T	5: 123,440,835 (GRCm39)	H1131Y	probably benign	Het
Chd2	A	T	7: 73,134,184 (GRCm39)	M721K	possibly damaging	Het
Cntnap5b	G	A	1: 100,286,450 (GRCm39)	G402R	probably benign	Het
Cps1	T	C	1: 67,182,145 (GRCm39)	Y120H	probably damaging	Het
Csf2	T	C	11: 54,140,306 (GRCm39)	D44G	probably benign	Het
Cubn	T	A	2: 13,291,835 (GRCm39)	Q3330L	possibly damaging	Het
Cubn	A	G	2: 13,355,869 (GRCm39)	S1788P	probably damaging	Het
Cul9	T	C	17: 46,811,770 (GRCm39)	D2486G	possibly damaging	Het
Cyp2c40	A	T	19: 39,762,293 (GRCm39)	S451R	probably damaging	Het
Cyp51	T	A	5: 4,133,256 (GRCm39)	T461S	probably damaging	Het
Cyth1	T	C	11: 118,074,768 (GRCm39)	M164V	probably damaging	Het
Ddc	T	C	11: 11,796,632 (GRCm39)		probably null	Het
Ddx21	A	T	10: 62,423,900 (GRCm39)	D589E	probably damaging	Het
Dgkb	C	T	12: 38,164,567 (GRCm39)	R113C	possibly damaging	Het
Dglucy	A	T	12: 100,816,602 (GRCm39)	M415L	probably benign	Het
Efnb2	A	T	8: 8,673,104 (GRCm39)		probably null	Het
Elp4	T	A	2: 105,639,612 (GRCm39)	Q189L	probably damaging	Het
Enpp2	T	C	15: 54,773,490 (GRCm39)	N77S	probably damaging	Het
Eps15	G	A	4: 109,223,727 (GRCm39)		probably benign	Het
F2rl1	G	A	13: 95,650,477 (GRCm39)	S135F	possibly damaging	Het
Fam133b	T	C	5: 3,607,815 (GRCm39)	M65T	probably damaging	Het
Fanca	A	G	8: 124,014,941 (GRCm39)	V689A	probably damaging	Het
Fbh1	C	T	2: 11,760,558 (GRCm39)	C79Y	probably damaging	Het
Fbxw7	C	T	3: 84,811,168 (GRCm39)	Q98*	probably null	Het
Flrt3	T	C	2: 140,502,086 (GRCm39)	N514S	probably damaging	Het
Foxj3	A	T	4: 119,478,857 (GRCm39)	S438C	unknown	Het
Gcm2	T	C	13: 41,256,970 (GRCm39)	K260E	possibly damaging	Het
Gm12863	C	T	4: 118,811,685 (GRCm39)		noncoding transcript	Het
Gpnmb	G	T	6: 49,022,417 (GRCm39)		probably null	Het
Gsap	C	A	5: 21,455,941 (GRCm39)	N379K	probably benign	Het
Hsd3b1	T	A	3: 98,760,181 (GRCm39)	Y270F	probably benign	Het
Ift70a2	T	A	2: 75,807,729 (GRCm39)	Y261F	probably benign	Het
Il22	C	A	10: 118,041,058 (GRCm39)	R55S	probably damaging	Het
Kcnd3	C	T	3: 105,566,082 (GRCm39)	A421V	probably damaging	Het
Klhdc3	T	C	17: 46,988,226 (GRCm39)	R180G	possibly damaging	Het
Lmbrd1	G	A	1: 24,784,056 (GRCm39)		probably null	Het
Lrrcc1	C	T	3: 14,601,156 (GRCm39)	R63*	probably null	Het
Lyar	A	G	5: 38,382,123 (GRCm39)	D35G	probably damaging	Het
Mbd4	C	T	6: 115,822,283 (GRCm39)	R442Q	probably benign	Het
Mib2	G	T	4: 155,744,229 (GRCm39)	S144R	probably benign	Het
Mms22l	A	T	4: 24,580,052 (GRCm39)		probably null	Het
Mtmr3	G	A	11: 4,437,764 (GRCm39)	H897Y	probably benign	Het
Muc5b	T	A	7: 141,401,453 (GRCm39)	C566*	probably null	Het
Nap1l4	A	T	7: 143,088,200 (GRCm39)		probably null	Het
Ncor2	A	T	5: 125,114,124 (GRCm39)		probably null	Het
Ndufa7	T	C	17: 34,057,187 (GRCm39)		probably benign	Het
Ndufs1	C	A	1: 63,200,108 (GRCm39)	G268V	probably damaging	Het
Nfs1	A	G	2: 155,976,369 (GRCm39)	V175A	possibly damaging	Het
Obsl1	C	A	1: 75,466,145 (GRCm39)	A1528S	possibly damaging	Het
Or2z8	A	G	8: 72,811,938 (GRCm39)	N138S	probably benign	Het
Or4a79	C	T	2: 89,551,706 (GRCm39)	V250I	probably benign	Het
Or52z1	A	T	7: 103,436,688 (GRCm39)	F265L	possibly damaging	Het
Or7a42	T	G	10: 78,791,931 (GRCm39)	D297E	probably null	Het
Or8k39	C	T	2: 86,563,018 (GRCm39)		probably null	Het
Pcdhb8	A	G	18: 37,488,706 (GRCm39)	D128G	probably damaging	Het
Pkp4	A	T	2: 59,172,449 (GRCm39)	I522F	probably damaging	Het
Plod3	G	A	5: 137,019,654 (GRCm39)	A398T	probably benign	Het
Pou4f3	A	G	18: 42,529,052 (GRCm39)	M332V	possibly damaging	Het
Prox1	A	G	1: 189,885,669 (GRCm39)	F593L	probably damaging	Het
Prrc2a	G	A	17: 35,369,018 (GRCm39)	P2006L	probably damaging	Het
Prss50	A	G	9: 110,692,864 (GRCm39)	D328G	probably damaging	Het
Psmd6	C	T	14: 14,120,126 (GRCm38)	S71N	probably benign	Het
Ptprd	A	G	4: 76,009,769 (GRCm39)	I764T	probably benign	Het
Ptprr	C	T	10: 115,884,123 (GRCm39)	A60V	probably benign	Het
Raet1e	T	A	10: 22,057,199 (GRCm39)	D174E	probably damaging	Het
Rbfox2	T	C	15: 76,976,018 (GRCm39)	I308M	probably benign	Het
Rnf20	G	C	4: 49,649,962 (GRCm39)		probably null	Het
Rpap2	A	T	5: 107,768,113 (GRCm39)	H317L	probably benign	Het
Rsph6a	T	A	7: 18,799,783 (GRCm39)	Y471*	probably null	Het
Sdhb	A	G	4: 140,704,777 (GRCm39)	H246R	possibly damaging	Het
Sh3bp5	C	A	14: 31,099,452 (GRCm39)	R265L	probably benign	Het
Sin3b	A	C	8: 73,452,271 (GRCm39)	I126L	probably benign	Het
Skint2	G	A	4: 112,509,305 (GRCm39)	A363T	probably benign	Het
Slc22a30	A	G	19: 8,321,768 (GRCm39)	I432T	probably benign	Het
Slc2a2	G	A	3: 28,771,681 (GRCm39)		probably null	Het
Slco1a5	T	C	6: 142,194,533 (GRCm39)	Y370C	possibly damaging	Het
Sltm	A	G	9: 70,496,339 (GRCm39)	H958R	probably damaging	Het
Smpdl3a	C	T	10: 57,684,111 (GRCm39)	H290Y	probably damaging	Het
Snrnp40	A	G	4: 130,256,549 (GRCm39)	I91M	probably damaging	Het
Spag9	T	A	11: 93,939,343 (GRCm39)	F91I	probably damaging	Het
Spag9	A	T	11: 93,939,342 (GRCm39)	K90N	possibly damaging	Het
Stox1	A	C	10: 62,501,516 (GRCm39)	I348S	probably damaging	Het
Sult1e1	A	G	5: 87,738,027 (GRCm39)	V18A	possibly damaging	Het
Syne2	A	G	12: 75,945,941 (GRCm39)	M338V	probably benign	Het
Tbc1d23	T	A	16: 57,012,991 (GRCm39)	Q327L	probably benign	Het
Terf2	G	T	8: 107,803,307 (GRCm39)	H425Q	probably benign	Het
Timd2	A	T	11: 46,568,094 (GRCm39)	Y233*	probably null	Het
Tmem39a	A	G	16: 38,411,524 (GRCm39)		probably benign	Het
Trappc10	T	C	10: 78,037,424 (GRCm39)	D793G	possibly damaging	Het
Ugt1a10	TAAAAAAAAA	TAAAAAAA	1: 88,143,650 (GRCm39)		probably benign	Het
Unc93a	T	C	17: 13,339,782 (GRCm39)		probably null	Het
Utrn	T	C	10: 12,625,813 (GRCm39)	T123A	probably damaging	Het
Vmn1r171	T	C	7: 23,332,369 (GRCm39)	I198T	probably benign	Het
Vmn1r213	T	A	13: 23,196,016 (GRCm39)	S200T	probably damaging	Het
Vmn2r108	T	A	17: 20,682,891 (GRCm39)	D771V	probably damaging	Het
Wls	C	T	3: 159,603,082 (GRCm39)	T165I	probably benign	Het
Zc3h13	G	A	14: 75,576,863 (GRCm39)	C1657Y	probably damaging	Het
Zdhhc5	T	C	2: 84,523,775 (GRCm39)	K224E	probably damaging	Het
Zfp54	T	A	17: 21,654,402 (GRCm39)	Y299N	probably damaging	Het
Zfp820	A	T	17: 22,037,966 (GRCm39)	L454Q	probably benign	Het
Zfp960	T	A	17: 17,308,698 (GRCm39)	F471I	probably damaging	Het
Zswim5	A	G	4: 116,830,169 (GRCm39)	I515V	probably benign	Het
Zzef1	G	T	11: 72,750,449 (GRCm39)	S919I	probably benign	Het

Other mutations in D130043K22Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00850:D130043K22Rik	APN	13	25,051,157 (GRCm39)	missense	probably damaging	1.00
IGL01114:D130043K22Rik	APN	13	25,041,139 (GRCm39)	missense	probably damaging	0.99
IGL01412:D130043K22Rik	APN	13	25,071,843 (GRCm39)	missense	probably damaging	1.00
IGL01542:D130043K22Rik	APN	13	25,060,020 (GRCm39)	splice site	probably null
IGL01615:D130043K22Rik	APN	13	25,083,779 (GRCm39)	missense	probably damaging	1.00
IGL01705:D130043K22Rik	APN	13	25,041,924 (GRCm39)	missense	probably benign	0.00
IGL02220:D130043K22Rik	APN	13	25,067,738 (GRCm39)	missense	possibly damaging	0.95
IGL02229:D130043K22Rik	APN	13	25,059,907 (GRCm39)	missense	probably damaging	1.00
IGL02576:D130043K22Rik	APN	13	25,040,853 (GRCm39)	missense	possibly damaging	0.74
IGL03038:D130043K22Rik	APN	13	25,063,602 (GRCm39)	missense	probably damaging	1.00
IGL03117:D130043K22Rik	APN	13	25,073,825 (GRCm39)	missense	probably damaging	1.00
IGL03014:D130043K22Rik	UTSW	13	25,042,075 (GRCm39)	missense	possibly damaging	0.88
R0019:D130043K22Rik	UTSW	13	25,064,795 (GRCm39)	missense	probably damaging	1.00
R0019:D130043K22Rik	UTSW	13	25,064,795 (GRCm39)	missense	probably damaging	1.00
R0020:D130043K22Rik	UTSW	13	25,038,475 (GRCm39)	utr 5 prime	probably benign
R0172:D130043K22Rik	UTSW	13	25,056,389 (GRCm39)	missense	probably benign	0.16
R0276:D130043K22Rik	UTSW	13	25,042,028 (GRCm39)	missense	possibly damaging	0.92
R0304:D130043K22Rik	UTSW	13	25,048,798 (GRCm39)	missense	probably benign	0.07
R0335:D130043K22Rik	UTSW	13	25,071,860 (GRCm39)	missense	probably damaging	0.98
R0744:D130043K22Rik	UTSW	13	25,047,563 (GRCm39)	splice site	probably benign
R0833:D130043K22Rik	UTSW	13	25,047,563 (GRCm39)	splice site	probably benign
R0836:D130043K22Rik	UTSW	13	25,047,563 (GRCm39)	splice site	probably benign
R1270:D130043K22Rik	UTSW	13	25,041,321 (GRCm39)	missense	probably benign	0.00
R1433:D130043K22Rik	UTSW	13	25,055,324 (GRCm39)	missense	probably damaging	1.00
R1682:D130043K22Rik	UTSW	13	25,066,539 (GRCm39)	missense	probably damaging	1.00
R1772:D130043K22Rik	UTSW	13	25,059,982 (GRCm39)	missense	probably damaging	1.00
R1773:D130043K22Rik	UTSW	13	25,066,585 (GRCm39)	missense	possibly damaging	0.80
R1800:D130043K22Rik	UTSW	13	25,067,877 (GRCm39)	missense	probably damaging	1.00
R1956:D130043K22Rik	UTSW	13	25,069,578 (GRCm39)	missense	probably damaging	1.00
R2255:D130043K22Rik	UTSW	13	25,040,894 (GRCm39)	missense	probably damaging	1.00
R2445:D130043K22Rik	UTSW	13	25,041,019 (GRCm39)	missense	probably benign	0.04
R2568:D130043K22Rik	UTSW	13	25,067,874 (GRCm39)	missense	probably damaging	0.97
R4160:D130043K22Rik	UTSW	13	25,046,679 (GRCm39)	missense	probably benign	0.02
R4494:D130043K22Rik	UTSW	13	25,055,339 (GRCm39)	missense	probably benign	0.16
R4732:D130043K22Rik	UTSW	13	25,083,648 (GRCm39)	missense	probably damaging	1.00
R4733:D130043K22Rik	UTSW	13	25,083,648 (GRCm39)	missense	probably damaging	1.00
R4782:D130043K22Rik	UTSW	13	25,062,023 (GRCm39)	missense	probably damaging	1.00
R4864:D130043K22Rik	UTSW	13	25,047,595 (GRCm39)	missense	probably damaging	1.00
R5155:D130043K22Rik	UTSW	13	25,056,273 (GRCm39)	missense	probably damaging	1.00
R5240:D130043K22Rik	UTSW	13	25,061,960 (GRCm39)	missense	probably damaging	1.00
R5383:D130043K22Rik	UTSW	13	25,041,397 (GRCm39)	missense	probably benign	0.02
R5493:D130043K22Rik	UTSW	13	25,047,586 (GRCm39)	missense	probably damaging	1.00
R6184:D130043K22Rik	UTSW	13	25,069,574 (GRCm39)	missense	probably damaging	1.00
R6305:D130043K22Rik	UTSW	13	25,069,668 (GRCm39)	missense	probably damaging	1.00
R6436:D130043K22Rik	UTSW	13	25,061,918 (GRCm39)	missense	probably damaging	1.00
R6980:D130043K22Rik	UTSW	13	25,048,764 (GRCm39)	missense	probably damaging	0.98
R7038:D130043K22Rik	UTSW	13	25,077,391 (GRCm39)	missense	probably damaging	1.00
R7085:D130043K22Rik	UTSW	13	25,056,285 (GRCm39)	missense	possibly damaging	0.95
R7147:D130043K22Rik	UTSW	13	25,066,546 (GRCm39)	missense	probably benign	0.31
R7384:D130043K22Rik	UTSW	13	25,066,588 (GRCm39)	missense	probably damaging	1.00
R7398:D130043K22Rik	UTSW	13	25,077,360 (GRCm39)	missense	probably damaging	0.97
R7584:D130043K22Rik	UTSW	13	25,056,353 (GRCm39)	missense	probably damaging	1.00
R7585:D130043K22Rik	UTSW	13	25,069,568 (GRCm39)	missense	probably benign	0.01
R7588:D130043K22Rik	UTSW	13	25,071,876 (GRCm39)	missense	probably damaging	0.99
R7610:D130043K22Rik	UTSW	13	25,059,985 (GRCm39)	missense	probably benign	0.30
R7903:D130043K22Rik	UTSW	13	25,059,995 (GRCm39)	missense	probably damaging	0.98
R7966:D130043K22Rik	UTSW	13	25,077,406 (GRCm39)	missense	probably damaging	1.00
R8014:D130043K22Rik	UTSW	13	25,040,685 (GRCm39)	missense	probably damaging	1.00
R8374:D130043K22Rik	UTSW	13	25,041,962 (GRCm39)	missense	probably benign	0.07
R8543:D130043K22Rik	UTSW	13	25,073,852 (GRCm39)	missense	probably benign	0.08
R8775:D130043K22Rik	UTSW	13	25,040,982 (GRCm39)	nonsense	probably null
R8775-TAIL:D130043K22Rik	UTSW	13	25,040,982 (GRCm39)	nonsense	probably null
R8806:D130043K22Rik	UTSW	13	25,083,618 (GRCm39)	missense	probably benign	0.11
R8916:D130043K22Rik	UTSW	13	25,056,254 (GRCm39)	missense	probably benign
R9209:D130043K22Rik	UTSW	13	25,041,090 (GRCm39)	missense	possibly damaging	0.96
R9524:D130043K22Rik	UTSW	13	25,071,876 (GRCm39)	missense	possibly damaging	0.89
R9743:D130043K22Rik	UTSW	13	25,056,299 (GRCm39)	missense	probably damaging	0.97
Z1177:D130043K22Rik	UTSW	13	25,056,231 (GRCm39)	missense	possibly damaging	0.79
Z1177:D130043K22Rik	UTSW	13	25,040,817 (GRCm39)	missense	probably benign	0.39
Z1177:D130043K22Rik	UTSW	13	25,040,692 (GRCm39)	missense	probably damaging	1.00
Z1177:D130043K22Rik	UTSW	13	25,064,830 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACACTGATTACGGTTCTCTCTTT -3'
(R):5'- ACTGCCAACCCATGTCCTTC -3'

Sequencing Primer
(F):5'- GATTACGGTTCTCTCTTTTCTCTCC -3'
(R):5'- GCTTAGGCTAGCCTTGAACTCAAG -3'

Posted On

2016-02-04