Mutagenetix > Incidental Mutation

Incidental Mutation 'R4690:Arhgef16'

354830

Institutional Source

Beutler Lab

Gene Symbol

Arhgef16

Ensembl Gene

ENSMUSG00000029032

Gene Name

Rho guanine nucleotide exchange factor 16

Synonyms

Neuroblastoma

MMRRC Submission

041941-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4690 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

154362926-154384535 bp(-) (GRCm39)

Type of Mutation

splice site (5 bp from exon)

DNA Base Change (assembly)

C to T at 154372420 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000126296 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000030898] [ENSMUST00000152947] [ENSMUST00000154895] [ENSMUST00000169623]

AlphaFold

Q3U5C8

Predicted Effect

probably null
Transcript: ENSMUST00000030898

SMART Domains

Protein: ENSMUSP00000030898
Gene: ENSMUSG00000029032

Domain	Start	End	E-Value	Type
low complexity region	51	72	N/A	INTRINSIC
RhoGEF	292	471	5.9e-52	SMART
PH	506	626	6.46e-8	SMART
SH3	636	692	2.31e-12	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129189

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144145

Predicted Effect

probably benign
Transcript: ENSMUST00000152947

SMART Domains

Protein: ENSMUSP00000119398
Gene: ENSMUSG00000029032

Domain	Start	End	E-Value	Type
low complexity region	51	72	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000154895

SMART Domains

Protein: ENSMUSP00000121273
Gene: ENSMUSG00000029032

Domain	Start	End	E-Value	Type
low complexity region	51	72	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000169623

SMART Domains

Protein: ENSMUSP00000126296
Gene: ENSMUSG00000029032

Domain	Start	End	E-Value	Type
low complexity region	51	72	N/A	INTRINSIC
RhoGEF	292	471	5.9e-52	SMART
PH	506	626	6.46e-8	SMART
SH3	636	692	2.31e-12	SMART

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.9%
20x: 94.5%

Validation Efficiency

98% (89/91)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Although the specific function of this protein is not known yet, it is thought to be involved in protein-protein and protein-lipid interactions. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 85 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca9	A	G	11: 110,039,706 (GRCm39)	F436L	probably damaging	Het
Adam28	G	T	14: 68,879,497 (GRCm39)	Q184K	probably benign	Het
Adh6a	A	G	3: 138,031,932 (GRCm39)	T275A	possibly damaging	Het
Agap2	A	G	10: 126,927,244 (GRCm39)	D1082G	possibly damaging	Het
Alox5	A	T	6: 116,400,150 (GRCm39)	V263E	probably damaging	Het
Bspry	G	A	4: 62,404,762 (GRCm39)	R186Q	probably damaging	Het
Ccdc188	T	A	16: 18,036,159 (GRCm39)	H111Q	probably damaging	Het
Cd40	T	C	2: 164,911,615 (GRCm39)	F209S	possibly damaging	Het
Cfap43	C	A	19: 47,736,298 (GRCm39)	V1398L	probably benign	Het
Cln3	A	T	7: 126,174,565 (GRCm39)	I286N	possibly damaging	Het
Col9a1	T	C	1: 24,263,787 (GRCm39)		probably null	Het
Cpne9	A	G	6: 113,279,016 (GRCm39)	E470G	probably damaging	Het
Cul5	A	T	9: 53,534,171 (GRCm39)	W654R	probably damaging	Het
Cyp2a22	T	A	7: 26,638,634 (GRCm39)	K51*	probably null	Het
Dcaf10	G	A	4: 45,372,769 (GRCm39)	R394Q	possibly damaging	Het
Dot1l	C	A	10: 80,622,016 (GRCm39)	S556*	probably null	Het
Eif3d	A	T	15: 77,851,516 (GRCm39)	M98K	probably benign	Het
Fiz1	A	G	7: 5,012,167 (GRCm39)	V117A	probably benign	Het
Fryl	A	G	5: 73,257,636 (GRCm39)	V722A	probably benign	Het
Ftdc1	G	A	16: 58,434,333 (GRCm39)	T128I	probably benign	Het
Gm3095	G	T	14: 3,964,471 (GRCm38)	R63I	probably benign	Het
Gm7133	A	T	1: 97,197,224 (GRCm39)		noncoding transcript	Het
Hoxb8	A	T	11: 96,175,286 (GRCm39)	D241V	probably benign	Het
Hrnr	A	G	3: 93,230,959 (GRCm39)	Q399R	unknown	Het
Itpk1	A	T	12: 102,572,434 (GRCm39)	V93D	probably damaging	Het
Kars1	C	T	8: 112,729,216 (GRCm39)	A164T	probably benign	Het
Kcnq4	A	T	4: 120,574,208 (GRCm39)	I150N	probably damaging	Het
Kcnrg	A	T	14: 61,849,176 (GRCm39)	L212F	probably damaging	Het
Kif5b	A	T	18: 6,216,759 (GRCm39)	D521E	probably benign	Het
Klf11	C	T	12: 24,705,071 (GRCm39)	T158M	probably damaging	Het
Klhl6	T	C	16: 19,776,034 (GRCm39)	I175V	probably benign	Het
Lsm1	A	G	8: 26,283,708 (GRCm39)	N40S	probably damaging	Het
Map1b	T	C	13: 99,567,576 (GRCm39)	E1715G	unknown	Het
Mecom	C	A	3: 30,292,459 (GRCm39)	A4S	probably benign	Het
Muc5b	G	A	7: 141,396,031 (GRCm39)	V96M	unknown	Het
Mug2	A	T	6: 122,013,255 (GRCm39)	I341L	probably benign	Het
Mxra7	A	T	11: 116,707,078 (GRCm39)		probably null	Het
Myo5a	T	C	9: 75,061,105 (GRCm39)	L537P	probably damaging	Het
Myo5b	A	T	18: 74,855,533 (GRCm39)	N1241Y	probably damaging	Het
Naa16	T	C	14: 79,582,497 (GRCm39)	R531G	probably damaging	Het
Neb	T	A	2: 52,134,087 (GRCm39)	M3299L	probably benign	Het
Nlrp4b	T	A	7: 10,453,130 (GRCm39)	Y76N	probably benign	Het
Nmral1	T	C	16: 4,534,205 (GRCm39)	T79A	probably damaging	Het
Noct	C	T	3: 51,155,300 (GRCm39)	Q23*	probably null	Het
Nrxn1	A	T	17: 90,344,509 (GRCm39)	V438D	probably damaging	Het
Or5b109	A	C	19: 13,212,132 (GRCm39)	N173H	possibly damaging	Het
Or5m9	T	A	2: 85,877,242 (GRCm39)	C139S	probably damaging	Het
Oxct2a	T	C	4: 123,216,836 (GRCm39)	T182A	probably benign	Het
Pank2	T	C	2: 131,115,945 (GRCm39)	I121T	probably damaging	Het
Pcdh1	T	A	18: 38,336,528 (GRCm39)	T36S	probably benign	Het
Pfdn1	A	T	18: 36,584,133 (GRCm39)	M67K	possibly damaging	Het
Plec	T	C	15: 76,058,456 (GRCm39)	E3849G	probably damaging	Het
Polr3a	A	T	14: 24,514,349 (GRCm39)	S817T	possibly damaging	Het
Pomgnt1	T	A	4: 116,012,707 (GRCm39)	D401E	probably damaging	Het
Ppp1r13b	T	A	12: 111,798,992 (GRCm39)	D891V	probably damaging	Het
Prr14l	A	G	5: 33,001,500 (GRCm39)		probably benign	Het
Ptk2b	A	G	14: 66,410,749 (GRCm39)		probably null	Het
Rab13	G	C	3: 90,128,330 (GRCm39)		probably null	Het
Rexo1	C	T	10: 80,382,255 (GRCm39)	A751T	probably benign	Het
Rfx1	T	C	8: 84,809,374 (GRCm39)	V233A	possibly damaging	Het
Rnf149	C	T	1: 39,616,295 (GRCm39)		probably benign	Het
Rrm1	A	G	7: 102,097,086 (GRCm39)	D122G	probably benign	Het
Serpina1b	A	G	12: 103,698,639 (GRCm39)	F70S	probably damaging	Het
Serpinb13	C	T	1: 106,910,574 (GRCm39)	S66L	probably damaging	Het
Sh3rf3	T	C	10: 58,649,526 (GRCm39)	S44P	possibly damaging	Het
Shroom1	A	G	11: 53,356,549 (GRCm39)	T471A	possibly damaging	Het
Slc6a1	A	G	6: 114,279,792 (GRCm39)	Y152C	probably damaging	Het
Spata31f3	T	A	4: 42,873,032 (GRCm39)		probably null	Het
Spata6	A	T	4: 111,632,023 (GRCm39)	T145S	probably damaging	Het
Srcap	G	A	7: 127,137,186 (GRCm39)	G956D	probably damaging	Het
Ssh2	A	T	11: 77,346,031 (GRCm39)	I1339F	possibly damaging	Het
Tardbp	A	T	4: 148,697,078 (GRCm39)	*99K	probably null	Het
Tbc1d22a	A	G	15: 86,196,037 (GRCm39)	Y336C	probably damaging	Het
Tmcc3	G	A	10: 94,381,419 (GRCm39)		probably benign	Het
Tmem178b	T	G	6: 40,222,547 (GRCm39)	D87E	probably benign	Het
Tmem184a	A	C	5: 139,791,377 (GRCm39)	S380A	probably benign	Het
Tnfaip2	A	G	12: 111,411,682 (GRCm39)	K84R	possibly damaging	Het
Tpgs1	A	G	10: 79,511,235 (GRCm39)	T126A	probably benign	Het
Traf3ip1	A	G	1: 91,447,834 (GRCm39)	E437G	possibly damaging	Het
Trpc4ap	C	T	2: 155,477,053 (GRCm39)	C755Y	probably damaging	Het
Tsfm	A	G	10: 126,866,547 (GRCm39)		probably benign	Het
Tulp1	A	C	17: 28,570,811 (GRCm39)		probably benign	Het
Vmn1r23	A	T	6: 57,903,010 (GRCm39)	M256K	probably benign	Het
Zdhhc8	T	C	16: 18,044,605 (GRCm39)	D305G	probably damaging	Het
Zfp326	G	A	5: 106,054,942 (GRCm39)	R282H	probably damaging	Het

Other mutations in Arhgef16

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01107:Arhgef16	APN	4	154,364,701 (GRCm39)	missense	probably benign	0.01
IGL02422:Arhgef16	APN	4	154,371,522 (GRCm39)	nonsense	probably null
IGL02801:Arhgef16	APN	4	154,375,964 (GRCm39)	missense	probably damaging	0.99
IGL02928:Arhgef16	APN	4	154,367,350 (GRCm39)	missense	probably benign	0.00
R0518:Arhgef16	UTSW	4	154,375,491 (GRCm39)	missense	probably damaging	0.99
R1148:Arhgef16	UTSW	4	154,365,346 (GRCm39)	missense	probably benign	0.05
R1148:Arhgef16	UTSW	4	154,365,346 (GRCm39)	missense	probably benign	0.05
R1576:Arhgef16	UTSW	4	154,375,769 (GRCm39)	missense	probably damaging	1.00
R1778:Arhgef16	UTSW	4	154,372,443 (GRCm39)	missense	probably benign	0.17
R1853:Arhgef16	UTSW	4	154,375,563 (GRCm39)	missense	probably benign	0.14
R1912:Arhgef16	UTSW	4	154,364,780 (GRCm39)	splice site	probably null
R2269:Arhgef16	UTSW	4	154,369,490 (GRCm39)	missense	probably damaging	0.98
R4437:Arhgef16	UTSW	4	154,364,153 (GRCm39)	critical splice donor site	probably null
R5174:Arhgef16	UTSW	4	154,366,504 (GRCm39)	missense	probably damaging	1.00
R5566:Arhgef16	UTSW	4	154,370,105 (GRCm39)	missense	probably benign	0.01
R6348:Arhgef16	UTSW	4	154,371,540 (GRCm39)	missense	probably benign	0.18
R7264:Arhgef16	UTSW	4	154,365,387 (GRCm39)	missense	probably damaging	1.00
R7469:Arhgef16	UTSW	4	154,375,763 (GRCm39)	missense	probably damaging	1.00
R7626:Arhgef16	UTSW	4	154,367,339 (GRCm39)	missense	possibly damaging	0.89
R7651:Arhgef16	UTSW	4	154,375,524 (GRCm39)	missense	probably damaging	1.00
R7684:Arhgef16	UTSW	4	154,366,285 (GRCm39)	missense	possibly damaging	0.62
R7759:Arhgef16	UTSW	4	154,371,432 (GRCm39)	missense	probably benign	0.00
R8334:Arhgef16	UTSW	4	154,367,224 (GRCm39)	nonsense	probably null
R8993:Arhgef16	UTSW	4	154,371,495 (GRCm39)	missense	probably damaging	1.00
R8995:Arhgef16	UTSW	4	154,371,495 (GRCm39)	missense	probably damaging	1.00
R9141:Arhgef16	UTSW	4	154,366,300 (GRCm39)	missense	probably damaging	1.00
R9256:Arhgef16	UTSW	4	154,363,502 (GRCm39)	nonsense	probably null
R9266:Arhgef16	UTSW	4	154,375,922 (GRCm39)	missense	probably benign	0.14
R9426:Arhgef16	UTSW	4	154,366,300 (GRCm39)	missense	probably damaging	1.00
R9515:Arhgef16	UTSW	4	154,365,432 (GRCm39)	missense	possibly damaging	0.65
R9516:Arhgef16	UTSW	4	154,365,432 (GRCm39)	missense	possibly damaging	0.65
R9784:Arhgef16	UTSW	4	154,371,422 (GRCm39)	missense	probably damaging	1.00
Z1177:Arhgef16	UTSW	4	154,365,910 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGGGTCTCATCGGATACTCAAG -3'
(R):5'- TATCTTCTCGAGTCAGCAAAGC -3'

Sequencing Primer
(F):5'- GTCTCATCGGATACTCAAGATAGTGG -3'
(R):5'- AAAGCCCCCTCCCATTGGG -3'

Posted On

2015-10-21