Mutagenetix > Incidental Mutations

Incidental Mutation 'R4833:Rab44'

373019

Institutional Source

Beutler Lab

Gene Symbol

Rab44

Ensembl Gene

ENSMUSG00000064147

Gene Name

RAB44, member RAS oncogene family

Synonyms

9830134C10Rik

MMRRC Submission

042449-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.063) question?

Stock #

R4833 (G1)

Quality Score

165

Status

Validated

Chromosome

Chromosomal Location

29135056-29148980 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 29136337 bp

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Proline at position 19 (Q19P)

Ref Sequence

ENSEMBL: ENSMUSP00000085253 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000087942]

Predicted Effect

probably damaging
Transcript: ENSMUST00000087942
AA Change: Q19P

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

SMART Domains

Protein: ENSMUSP00000085253
Gene: ENSMUSG00000064147
AA Change: Q19P

Domain	Start	End	E-Value	Type
coiled coil region	1	68	N/A	INTRINSIC
low complexity region	143	157	N/A	INTRINSIC
low complexity region	261	276	N/A	INTRINSIC
RAB	538	701	1.11e-53	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132262

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000138816

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139931

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141797

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000147311

Meta Mutation Damage Score

0.1758

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 93.8%

Validation Efficiency

99% (74/75)

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810055G02Rik	C	A	19: 3,716,872	T153K	possibly damaging	Het
4932438A13Rik	A	G	3: 36,964,968	I2007V	probably damaging	Het
Abca5	A	C	11: 110,279,316	Y1318D	probably benign	Het
Adam18	A	G	8: 24,674,101	I22T	probably benign	Het
Adgrv1	T	A	13: 81,560,844	H1147L	possibly damaging	Het
Ankrd2	T	C	19: 42,043,857		probably null	Het
Bdkrb2	T	C	12: 105,591,658	W53R	probably benign	Het
Blm	T	A	7: 80,466,826	I1111L	probably benign	Het
Bmp3	T	G	5: 98,855,207	L32R	probably damaging	Het
Cdh23	T	G	10: 60,385,038	E1312A	probably damaging	Het
Ceacam5	C	T	7: 17,752,258	T560M	probably benign	Het
Cmtm8	C	A	9: 114,796,165	R66I	probably benign	Het
Cnbd1	A	G	4: 18,862,120	Y357H	probably damaging	Het
Col4a4	A	T	1: 82,529,602	V252E	unknown	Het
Col6a4	A	T	9: 106,071,979	M819K	probably benign	Het
Cwf19l2	T	C	9: 3,430,783	S372P	probably benign	Het
Daam2	A	T	17: 49,490,145	I204N	possibly damaging	Het
Dock6	T	C	9: 21,844,280	D216G	probably damaging	Het
Epha5	C	T	5: 84,105,891	D548N	possibly damaging	Het
Erich2	T	C	2: 70,534,292	Y311H	possibly damaging	Het
Gm3985	A	G	8: 32,890,477		noncoding transcript	Het
Gnb1	A	G	4: 155,543,067	T102A	possibly damaging	Het
Hcfc2	C	T	10: 82,709,146	A204V	probably null	Het
Hnrnpu	T	C	1: 178,333,894		probably benign	Het
Htt	A	G	5: 34,852,225	T1517A	probably damaging	Het
Klhl6	T	A	16: 19,957,139	D223V	probably damaging	Het
Kpna6	A	G	4: 129,657,779	S71P	possibly damaging	Het
Lama3	A	G	18: 12,441,131	D590G	probably benign	Het
Lipt1	T	G	1: 37,875,529	L222R	probably damaging	Het
Lrrc41	A	G	4: 116,093,177		probably benign	Het
Lrrc59	T	C	11: 94,634,672	V98A	probably benign	Het
Mast4	A	G	13: 102,774,184		probably null	Het
Mdc1	C	T	17: 35,850,394	S733F	probably benign	Het
Mknk1	C	T	4: 115,878,186		probably benign	Het
Mtmr7	A	G	8: 40,590,462	F141S	probably damaging	Het
Myo15b	A	G	11: 115,887,602	D1G	possibly damaging	Het
Odf3	T	C	7: 140,848,278	M1T	probably null	Het
Olfr1356	T	G	10: 78,847,575	L113F	probably damaging	Het
Phkb	T	A	8: 85,901,911	V183E	probably damaging	Het
Pola2	T	C	19: 5,953,864	Y161C	probably damaging	Het
Psen1	G	A	12: 83,731,778	V412I	probably benign	Het
Psmc4	C	A	7: 28,047,512	G77V	probably damaging	Het
Psmd3	A	G	11: 98,687,760	Y207C	probably damaging	Het
Pxk	T	A	14: 8,130,653	M84K	probably damaging	Het
Rbks	A	G	5: 31,624,515	Y314H	probably benign	Het
Rftn2	T	C	1: 55,214,240	D68G	possibly damaging	Het
Rims2	T	A	15: 39,535,914	S838R	probably damaging	Het
Sdc4	A	T	2: 164,431,218	D57E	probably damaging	Het
Slfn14	A	G	11: 83,279,156	L554P	probably damaging	Het
Spink2	G	T	5: 77,205,392	D83E	possibly damaging	Het
Srsf4	C	T	4: 131,900,102		probably benign	Het
Taar8b	A	T	10: 24,092,132	S55T	possibly damaging	Het
Tbca	A	G	13: 94,832,410	E35G	probably benign	Het
Tmc5	C	A	7: 118,628,829	H307Q	probably benign	Het
Tmem169	A	G	1: 72,298,152	D82G	probably benign	Het
Tmem72	T	C	6: 116,698,358	T58A	probably benign	Het
Ttc7	C	T	17: 87,334,321	P449S	probably damaging	Het
Ttf2	T	C	3: 100,961,406	E449G	probably benign	Het
Ubr4	C	A	4: 139,402,546	T659K	probably damaging	Het
Wdr1	A	G	5: 38,547,029	Y98H	probably damaging	Het
Wfikkn2	A	G	11: 94,239,052	Y88H	probably benign	Het
Zfp384	A	T	6: 125,030,848	H247L	probably damaging	Het
Zfp526	C	T	7: 25,225,870	A518V	probably damaging	Het
Zfp788	T	A	7: 41,647,568	H47Q	probably benign	Het

Other mutations in Rab44

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00864:Rab44	APN	17	29139737	missense	probably benign
IGL01545:Rab44	APN	17	29147377	missense	unknown
IGL02314:Rab44	APN	17	29139353	missense	probably benign	0.04
IGL02402:Rab44	APN	17	29140516	missense	probably benign	0.01
IGL02492:Rab44	APN	17	29146049	splice site	probably benign
R0018:Rab44	UTSW	17	29139380	missense	probably benign	0.03
R0135:Rab44	UTSW	17	29138132	missense	probably benign	0.01
R0193:Rab44	UTSW	17	29140307	missense	probably benign
R0398:Rab44	UTSW	17	29145370	splice site	probably benign
R0403:Rab44	UTSW	17	29145261	missense	probably damaging	1.00
R0608:Rab44	UTSW	17	29147343	splice site	probably null
R0631:Rab44	UTSW	17	29139144	missense	possibly damaging	0.91
R0762:Rab44	UTSW	17	29145270	missense	unknown
R1128:Rab44	UTSW	17	29140461	missense	possibly damaging	0.90
R1681:Rab44	UTSW	17	29140124	missense	possibly damaging	0.47
R1706:Rab44	UTSW	17	29138106	missense	probably damaging	1.00
R2679:Rab44	UTSW	17	29144477	splice site	probably null
R3500:Rab44	UTSW	17	29138067	missense	probably benign	0.09
R3709:Rab44	UTSW	17	29139869	missense	probably benign	0.08
R4497:Rab44	UTSW	17	29139897	missense	probably benign	0.04
R4655:Rab44	UTSW	17	29139194	missense	probably benign
R4850:Rab44	UTSW	17	29140089	missense	possibly damaging	0.95
R4926:Rab44	UTSW	17	29139555	missense	probably benign	0.01
R5694:Rab44	UTSW	17	29140500	missense	probably damaging	1.00
R5694:Rab44	UTSW	17	29145966	missense	unknown
R5835:Rab44	UTSW	17	29148238	missense	probably benign	0.13
R6146:Rab44	UTSW	17	29135417	start gained	probably benign
R6629:Rab44	UTSW	17	29135780	start gained	probably benign
R6814:Rab44	UTSW	17	29139810	missense	probably benign	0.18
R6865:Rab44	UTSW	17	29139227	missense	probably benign
R6872:Rab44	UTSW	17	29139810	missense	probably benign	0.18
R7032:Rab44	UTSW	17	29140464	missense	unknown
R7058:Rab44	UTSW	17	29138176	splice site	probably null
R7207:Rab44	UTSW	17	29138039	nonsense	probably null
R7218:Rab44	UTSW	17	29139444	missense
R7418:Rab44	UTSW	17	29140496	missense	unknown
R7651:Rab44	UTSW	17	29148205	missense	unknown
R8336:Rab44	UTSW	17	29148275	makesense	probably null

Predicted Primers

PCR Primer
(F):5'- GAGAATCTAGGCCCAAGTGG -3'
(R):5'- TATGGCAGTGTTCCCAGGAC -3'

Sequencing Primer
(F):5'- AAAGTCCTCTTTGTGGGTACC -3'
(R):5'- CACTGGGAAGAGAGCCCTG -3'

Posted On

2016-03-01