Mutagenetix > Incidental Mutation

Incidental Mutation 'R4721:Raph1'

354429

Institutional Source

Beutler Lab

Gene Symbol

Raph1

Ensembl Gene

ENSMUSG00000026014

Gene Name

Ras association (RalGDS/AF-6) and pleckstrin homology domains 1

Synonyms

C730009O10Rik, lamellipodin, 9430025M21Rik, Lpd

MMRRC Submission

041986-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.138) question?

Stock #

R4721 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

60521451-60606263 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

G to A at 60542160 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027168] [ENSMUST00000090293] [ENSMUST00000140485]

AlphaFold

F2Z3U3

Predicted Effect

probably benign
Transcript: ENSMUST00000027168

SMART Domains

Protein: ENSMUSP00000027168
Gene: ENSMUSG00000026014

Domain	Start	End	E-Value	Type
low complexity region	201	218	N/A	INTRINSIC
low complexity region	294	308	N/A	INTRINSIC
RA	322	408	1.63e-13	SMART
PH	450	560	3.38e-11	SMART
low complexity region	581	604	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000090293

SMART Domains

Protein: ENSMUSP00000087763
Gene: ENSMUSG00000026014

Domain	Start	End	E-Value	Type
low complexity region	201	218	N/A	INTRINSIC
low complexity region	294	308	N/A	INTRINSIC
RA	322	408	1.63e-13	SMART
PH	450	560	3.38e-11	SMART
low complexity region	581	604	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000140485

SMART Domains

Protein: ENSMUSP00000121023
Gene: ENSMUSG00000026014

Domain	Start	End	E-Value	Type
low complexity region	201	218	N/A	INTRINSIC
low complexity region	245	256	N/A	INTRINSIC
RA	270	356	1.63e-13	SMART
PH	398	508	3.38e-11	SMART
low complexity region	529	552	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000182085

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000189383

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.2%

Validation Efficiency

98% (90/92)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that belongs to the Mig10/Rap1-interacting adaptor molecule/Lamellipodin family of adapter proteins, which function in cell migration. Members of this family contain pleckstrin-homology domains, Ras-association domains, and proline-rich C-termini. The protein encoded by this gene regulates actin dynamics through interaction with Ena/Vasodilator proteins as well as direct binding to filamentous actin to regulate actin network assembly. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]
PHENOTYPE: Mice homozygous for a conditional allele activated in all cells exhibit background sensitive neonatal or postnatal lethality, decreased body size, belly spotting and decreased melanocyte numbers in the trunk. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	T	C	14: 32,385,107 (GRCm39)	D286G	probably benign	Het
Abca15	G	A	7: 119,949,998 (GRCm39)	E491K	probably benign	Het
Acsl5	A	G	19: 55,268,962 (GRCm39)	T208A	probably benign	Het
Adamts10	T	A	17: 33,764,511 (GRCm39)		probably null	Het
Ahcyl1	T	C	3: 107,577,233 (GRCm39)	Q313R	possibly damaging	Het
Ccdc71	C	T	9: 108,340,622 (GRCm39)	S145L	possibly damaging	Het
Cep250	A	G	2: 155,812,119 (GRCm39)	T472A	probably damaging	Het
Copa	T	C	1: 171,931,841 (GRCm39)		probably benign	Het
Crybg1	C	A	10: 43,873,883 (GRCm39)	R1075L	probably damaging	Het
Ddr2	T	A	1: 169,832,809 (GRCm39)	K84*	probably null	Het
Ddx59	C	T	1: 136,344,844 (GRCm39)	P172S	probably benign	Het
Dhx34	T	A	7: 15,931,307 (GRCm39)	Q1118L	possibly damaging	Het
Dkkl1	T	A	7: 44,857,232 (GRCm39)	I112F	probably damaging	Het
Dnah8	T	A	17: 30,944,140 (GRCm39)	C1786S	probably damaging	Het
Eml6	T	A	11: 29,788,525 (GRCm39)	D520V	possibly damaging	Het
Ergic1	T	A	17: 26,857,750 (GRCm39)	V192E	probably damaging	Het
Fat3	T	C	9: 15,941,262 (GRCm39)	E1343G	probably damaging	Het
Fxr1	T	C	3: 34,118,381 (GRCm39)	S535P	possibly damaging	Het
Gkn3	C	T	6: 87,360,507 (GRCm39)	A163T	probably damaging	Het
Gm15446	C	T	5: 110,090,866 (GRCm39)	H373Y	probably damaging	Het
Gpr157	A	T	4: 150,183,420 (GRCm39)	N197Y	probably benign	Het
Grid2	G	A	6: 64,643,185 (GRCm39)	M982I	probably benign	Het
Hey2	G	T	10: 30,710,304 (GRCm39)	R150S	possibly damaging	Het
Hmcn1	T	C	1: 150,648,322 (GRCm39)		probably null	Het
Ighv3-3	G	A	12: 114,160,156 (GRCm39)	R85*	probably null	Het
Ighv5-4	A	T	12: 113,561,060 (GRCm39)		probably benign	Het
Igsf21	A	G	4: 139,834,621 (GRCm39)	S84P	probably benign	Het
Kif20b	A	G	19: 34,915,773 (GRCm39)	T517A	probably benign	Het
Krt87	T	C	15: 101,385,863 (GRCm39)	E244G	probably damaging	Het
Lrp1	T	C	10: 127,390,928 (GRCm39)	T2990A	possibly damaging	Het
Lrp1b	T	A	2: 40,605,381 (GRCm39)		probably null	Het
Lrrc42	A	T	4: 107,091,050 (GRCm39)	S382T	probably benign	Het
Magi2	C	T	5: 20,739,467 (GRCm39)	R737W	probably damaging	Het
Mcc	A	G	18: 44,652,623 (GRCm39)	L267P	probably damaging	Het
Mzf1	T	A	7: 12,777,223 (GRCm39)	Q727L	possibly damaging	Het
Mzf1	C	T	7: 12,777,448 (GRCm39)	R652Q	possibly damaging	Het
Nkain3	C	T	4: 20,485,015 (GRCm39)	A21T	probably damaging	Het
Nlrp4e	T	A	7: 23,020,521 (GRCm39)	V336E	possibly damaging	Het
Nptn	C	T	9: 58,548,059 (GRCm39)	R155C	probably damaging	Het
Nr2c2	T	C	6: 92,116,828 (GRCm39)	I10T	possibly damaging	Het
Or12e13	T	A	2: 87,663,515 (GRCm39)	I44N	probably damaging	Het
Or1e26	C	T	11: 73,480,273 (GRCm39)	C97Y	probably damaging	Het
Or1j13	T	C	2: 36,369,836 (GRCm39)	Y102C	probably benign	Het
Pdzk1	G	T	3: 96,776,518 (GRCm39)	E493*	probably null	Het
Plekhh1	GTCAAA	G	12: 79,122,194 (GRCm39)		probably null	Het
Polr3b	T	C	10: 84,491,867 (GRCm39)	V342A	possibly damaging	Het
Prg3	T	C	2: 84,821,750 (GRCm39)	V125A	possibly damaging	Het
Rassf2	A	G	2: 131,846,358 (GRCm39)	V133A	probably benign	Het
Rbm22	G	A	18: 60,697,463 (GRCm39)	R56H	probably damaging	Het
Rbpjl	A	C	2: 164,246,447 (GRCm39)	S31R	probably benign	Het
Reln	A	G	5: 22,124,220 (GRCm39)	V2762A	probably damaging	Het
Rxrg	T	A	1: 167,452,621 (GRCm39)	I141N	probably damaging	Het
Scn7a	C	A	2: 66,514,529 (GRCm39)	G1082C	probably damaging	Het
Selenon	C	A	4: 134,270,387 (GRCm39)	E322*	probably null	Het
Sipa1	C	T	19: 5,710,413 (GRCm39)	R199Q	probably damaging	Het
Slc26a7	A	T	4: 14,510,261 (GRCm39)		probably null	Het
Slc37a4	T	C	9: 44,312,787 (GRCm39)	S314P	possibly damaging	Het
Smarce1	T	C	11: 99,111,543 (GRCm39)	I59V	probably benign	Het
Stk19	T	C	17: 35,042,120 (GRCm39)		probably null	Het
Susd2	C	T	10: 75,473,964 (GRCm39)	D544N	probably benign	Het
Tcf7l2	G	T	19: 55,919,886 (GRCm39)	R465L	possibly damaging	Het
Tfap2d	T	A	1: 19,174,984 (GRCm39)	S146T	possibly damaging	Het
Tmem156	A	G	5: 65,248,870 (GRCm39)	F10S	probably benign	Het
Tmem63c	G	T	12: 87,103,954 (GRCm39)	A68S	possibly damaging	Het
Tnfrsf21	T	C	17: 43,396,395 (GRCm39)	C560R	probably damaging	Het
Trav10n	C	T	14: 53,359,590 (GRCm39)	T7I	probably benign	Het
Ttc38	C	T	15: 85,722,947 (GRCm39)	R132W	probably benign	Het
Tvp23a	T	C	16: 10,245,275 (GRCm39)	K108R	probably benign	Het
Vmn1r233	T	C	17: 21,214,879 (GRCm39)	M24V	probably benign	Het
Vmn1r88	T	A	7: 12,912,451 (GRCm39)	L269*	probably null	Het
Vmn2r101	T	A	17: 19,832,287 (GRCm39)	M761K	probably damaging	Het
Vps13b	C	T	15: 35,910,864 (GRCm39)	Q3543*	probably null	Het
Wdr37	T	C	13: 8,904,065 (GRCm39)	E101G	possibly damaging	Het
Zc3hc1	A	G	6: 30,374,899 (GRCm39)	V214A	probably benign	Het
Zcchc9	A	T	13: 91,948,728 (GRCm39)		probably null	Het
Zdbf2	A	T	1: 63,347,951 (GRCm39)	Q2110L	possibly damaging	Het
Zfp516	T	G	18: 82,975,236 (GRCm39)	L478R	possibly damaging	Het

Other mutations in Raph1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02300:Raph1	APN	1	60,565,106 (GRCm39)	missense	possibly damaging	0.76
IGL02900:Raph1	APN	1	60,542,022 (GRCm39)	missense	probably damaging	1.00
FR4976:Raph1	UTSW	1	60,528,426 (GRCm39)	intron	probably benign
R0048:Raph1	UTSW	1	60,539,764 (GRCm39)	missense	probably benign	0.03
R0048:Raph1	UTSW	1	60,539,764 (GRCm39)	missense	probably benign	0.03
R0049:Raph1	UTSW	1	60,565,058 (GRCm39)	missense	probably benign	0.03
R0049:Raph1	UTSW	1	60,565,058 (GRCm39)	missense	probably benign	0.03
R0227:Raph1	UTSW	1	60,565,136 (GRCm39)	missense	probably benign	0.00
R0387:Raph1	UTSW	1	60,549,655 (GRCm39)	intron	probably benign
R0607:Raph1	UTSW	1	60,565,028 (GRCm39)	missense	probably damaging	1.00
R1740:Raph1	UTSW	1	60,558,183 (GRCm39)	nonsense	probably null
R2274:Raph1	UTSW	1	60,537,659 (GRCm39)	missense	probably damaging	1.00
R3108:Raph1	UTSW	1	60,532,545 (GRCm39)	missense	probably benign	0.01
R3977:Raph1	UTSW	1	60,537,682 (GRCm39)	missense	probably benign	0.39
R4260:Raph1	UTSW	1	60,542,124 (GRCm39)	missense	possibly damaging	0.94
R4487:Raph1	UTSW	1	60,542,028 (GRCm39)	missense	possibly damaging	0.68
R4782:Raph1	UTSW	1	60,528,273 (GRCm39)	missense	probably damaging	1.00
R5027:Raph1	UTSW	1	60,535,436 (GRCm39)	missense	probably damaging	1.00
R5037:Raph1	UTSW	1	60,535,381 (GRCm39)	splice site	probably null
R5106:Raph1	UTSW	1	60,572,459 (GRCm39)	missense	probably damaging	1.00
R5506:Raph1	UTSW	1	60,532,657 (GRCm39)	intron	probably benign
R5510:Raph1	UTSW	1	60,562,105 (GRCm39)	unclassified	probably benign
R5587:Raph1	UTSW	1	60,537,632 (GRCm39)	missense	probably damaging	1.00
R5591:Raph1	UTSW	1	60,540,905 (GRCm39)	unclassified	probably benign
R5619:Raph1	UTSW	1	60,529,414 (GRCm39)	intron	probably benign
R5776:Raph1	UTSW	1	60,529,315 (GRCm39)	intron	probably benign
R5802:Raph1	UTSW	1	60,527,832 (GRCm39)	missense	possibly damaging	0.81
R6742:Raph1	UTSW	1	60,564,879 (GRCm39)	missense	probably damaging	0.97
R7122:Raph1	UTSW	1	60,565,136 (GRCm39)	missense	probably benign	0.10
R7219:Raph1	UTSW	1	60,542,032 (GRCm39)	missense	unknown
R7251:Raph1	UTSW	1	60,529,027 (GRCm39)	missense	unknown
R7254:Raph1	UTSW	1	60,538,767 (GRCm39)	missense	unknown
R7732:Raph1	UTSW	1	60,572,447 (GRCm39)	missense	possibly damaging	0.82
R7979:Raph1	UTSW	1	60,565,148 (GRCm39)	missense	probably benign	0.00
R7986:Raph1	UTSW	1	60,535,445 (GRCm39)	missense
R8167:Raph1	UTSW	1	60,529,270 (GRCm39)	missense	unknown
R8168:Raph1	UTSW	1	60,538,779 (GRCm39)	missense	unknown
R8399:Raph1	UTSW	1	60,528,477 (GRCm39)	missense	unknown
R9036:Raph1	UTSW	1	60,542,124 (GRCm39)	missense	unknown
R9146:Raph1	UTSW	1	60,558,137 (GRCm39)	critical splice donor site	probably null
R9338:Raph1	UTSW	1	60,529,300 (GRCm39)	missense	unknown
R9381:Raph1	UTSW	1	60,540,959 (GRCm39)	missense	unknown
R9383:Raph1	UTSW	1	60,564,829 (GRCm39)	missense	unknown
R9399:Raph1	UTSW	1	60,565,154 (GRCm39)	missense	probably benign
R9454:Raph1	UTSW	1	60,528,753 (GRCm39)	missense	unknown
R9561:Raph1	UTSW	1	60,564,887 (GRCm39)	missense	possibly damaging	0.49
RF018:Raph1	UTSW	1	60,528,426 (GRCm39)	intron	probably benign
RF022:Raph1	UTSW	1	60,528,426 (GRCm39)	intron	probably benign

Predicted Primers

PCR Primer
(F):5'- ACTATGAAGGTTCAGGGTTACAC -3'
(R):5'- AGGGCTTAAAACTTACTTAGGTAGG -3'

Sequencing Primer
(F):5'- CGGAAGTGGCATTACTAACCCATTTG -3'
(R):5'- GTAGTAGTGTCAGAGTAGTCAT -3'

Posted On

2015-10-21