Mutagenetix > Incidental Mutation

Incidental Mutation 'R7732:Ranbp10'

595913

Institutional Source

Beutler Lab

Gene Symbol

Ranbp10

Ensembl Gene

ENSMUSG00000037415

Gene Name

RAN binding protein 10

Synonyms

4432417N03Rik

MMRRC Submission

045788-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7732 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

106494940-106553982 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 106499723 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 502 (I502T)

Ref Sequence

ENSEMBL: ENSMUSP00000040045 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041400]

AlphaFold

Q6VN19

Predicted Effect

probably benign
Transcript: ENSMUST00000041400
AA Change: I502T

PolyPhen 2 Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)

SMART Domains

Protein: ENSMUSP00000040045
Gene: ENSMUSG00000037415
AA Change: I502T

Domain	Start	End	E-Value	Type
low complexity region	44	59	N/A	INTRINSIC
SPRY	128	249	5.47e-44	SMART
LisH	281	313	1.63e-2	SMART
CTLH	319	376	4.19e-14	SMART
low complexity region	437	464	N/A	INTRINSIC
CRA	534	636	2.04e-22	SMART

Meta Mutation Damage Score

0.1352

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

100% (73/73)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] RAN is a small GTPase involved in the assembly of microtubules to form mitotic spindles. The protein encoded by this gene is a cytoplasmic guanine nucleotide exchange factor (GEF) that binds beta-tubulin and has GEF activity toward RAN. The encoded protein plays a role in the formation of noncentrosomal microtubules. In addition, this protein may be involved in the regulation of D(1) receptor signaling by protein kinase C delta and protein kinase C gamma. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]
PHENOTYPE: Mice homozygous for a gene trap allele exhibit slight defects in erythrocyte number and volume, decreased platelet aggregattion and increased bleeding time associated with impaired platelet dense granule release. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcd2	A	T	15: 91,075,451 (GRCm39)	S121T	possibly damaging	Het
Alpk1	T	C	3: 127,478,041 (GRCm39)	M69V		Het
Ap3m2	G	T	8: 23,287,105 (GRCm39)	D192E	probably benign	Het
Arel1	A	G	12: 84,974,663 (GRCm39)	V493A	probably benign	Het
Arhgap27	T	C	11: 103,230,869 (GRCm39)	H140R	probably benign	Het
Bcat2	C	T	7: 45,234,617 (GRCm39)	T166M	possibly damaging	Het
Brd4	C	A	17: 32,440,386 (GRCm39)	A318S	unknown	Het
Cabp4	T	A	19: 4,185,994 (GRCm39)	T270S	probably benign	Het
Cd22	G	A	7: 30,569,482 (GRCm39)	R545C	probably damaging	Het
Cdc23	C	A	18: 34,769,755 (GRCm39)		probably null	Het
Chst4	G	A	8: 110,756,514 (GRCm39)	Q450*	probably null	Het
Ctsc	G	A	7: 87,946,367 (GRCm39)	R132Q	probably damaging	Het
Cyp2b19	A	G	7: 26,470,769 (GRCm39)	D470G	possibly damaging	Het
Dcc	C	T	18: 71,579,506 (GRCm39)	G689D	probably benign	Het
Disc1	G	T	8: 125,977,714 (GRCm39)	G779*	probably null	Het
Dock1	T	G	7: 134,346,699 (GRCm39)	D210E	probably benign	Het
Dynlt1a	A	G	17: 6,365,220 (GRCm39)	V14A	probably benign	Het
Dynlt2a3	A	G	17: 15,187,947 (GRCm39)	V109A	probably benign	Het
Epha10	A	G	4: 124,809,092 (GRCm39)	D779G		Het
Eprs1	A	G	1: 185,105,136 (GRCm39)	H137R	probably benign	Het
Eps15l1	A	C	8: 73,134,820 (GRCm39)	L447R	probably damaging	Het
Esyt1	A	G	10: 128,357,694 (GRCm39)		probably null	Het
Fam221a	A	G	6: 49,349,563 (GRCm39)	K43E	probably benign	Het
Fanci	A	G	7: 79,062,400 (GRCm39)	S309G	possibly damaging	Het
Fbxo48	T	A	11: 16,903,601 (GRCm39)	W76R	probably damaging	Het
Fgd4	A	G	16: 16,302,459 (GRCm39)	V32A	probably benign	Het
Foxe1	A	T	4: 46,345,287 (GRCm39)	D365V	unknown	Het
Gabrd	C	T	4: 155,470,075 (GRCm39)	R378H	probably benign	Het
Greb1	A	G	12: 16,723,864 (GRCm39)	S1862P	probably damaging	Het
H2al2b	T	C	Y: 2,720,436 (GRCm39)	H80R	possibly damaging	Het
Hectd4	T	C	5: 121,474,692 (GRCm39)	V2771A	probably benign	Het
Hoxa11	A	T	6: 52,220,415 (GRCm39)	F289L	probably damaging	Het
Hsp90aa1	A	G	12: 110,659,852 (GRCm39)	V412A	probably damaging	Het
Igsf11	A	G	16: 38,829,160 (GRCm39)	Q77R	probably damaging	Het
Lrig1	C	A	6: 94,603,358 (GRCm39)	M263I	probably benign	Het
Ms4a14	C	T	19: 11,279,047 (GRCm39)	M1170I	probably benign	Het
Ndufs7	G	A	10: 80,089,618 (GRCm39)		probably null	Het
Nectin4	A	T	1: 171,214,246 (GRCm39)	E467V	probably benign	Het
Or8d1b	A	G	9: 38,887,560 (GRCm39)	E196G	probably damaging	Het
Otogl	G	A	10: 107,642,525 (GRCm39)	H1302Y	probably benign	Het
Pigg	A	G	5: 108,466,841 (GRCm39)	S241G	probably benign	Het
Pip4p1	C	T	14: 51,168,090 (GRCm39)	G48D	possibly damaging	Het
Pom121l12	T	A	11: 14,549,843 (GRCm39)	V183D	probably damaging	Het
Prickle2	T	A	6: 92,388,205 (GRCm39)	E455V	probably damaging	Het
Ptpn4	A	C	1: 119,620,532 (GRCm39)	V488G	probably benign	Het
Raph1	T	A	1: 60,572,447 (GRCm39)	Q40L	possibly damaging	Het
Rgs22	A	T	15: 36,026,127 (GRCm39)	C1056S	probably damaging	Het
Serpinb6b	G	A	13: 33,152,590 (GRCm39)	S33N	probably damaging	Het
Serpinb6d	A	G	13: 33,853,082 (GRCm39)	N158S	probably benign	Het
Serping1	A	T	2: 84,600,448 (GRCm39)	V298D	probably damaging	Het
Sgsm1	T	A	5: 113,414,196 (GRCm39)	H637L	probably benign	Het
Sh3rf2	G	T	18: 42,234,753 (GRCm39)	V179L	probably damaging	Het
Slc1a3	T	C	15: 8,680,472 (GRCm39)	T129A	probably benign	Het
Slit1	T	A	19: 41,592,847 (GRCm39)	Y1202F	probably benign	Het
Spsb2	T	C	6: 124,786,656 (GRCm39)	S130P	probably damaging	Het
Sulf1	A	G	1: 12,913,013 (GRCm39)	D749G	probably benign	Het
Taok3	A	G	5: 117,331,813 (GRCm39)	E10G	possibly damaging	Het
Tbl3	G	T	17: 24,923,136 (GRCm39)	A368D	probably benign	Het
Tdh	T	A	14: 63,733,507 (GRCm39)	H127L	probably damaging	Het
Tmem205	C	A	9: 21,838,703 (GRCm39)		probably null	Het
Tmem30a	A	C	9: 79,687,826 (GRCm39)	F114L	possibly damaging	Het
Tmprss15	T	C	16: 78,800,308 (GRCm39)	K607E	probably benign	Het
Tnxb	A	T	17: 34,913,254 (GRCm39)	D1756V	probably damaging	Het
Trhde	A	G	10: 114,623,969 (GRCm39)	F312L	probably benign	Het
Ttn	G	A	2: 76,656,793 (GRCm39)	P12494L	probably null	Het
Vmn2r61	A	G	7: 41,916,097 (GRCm39)	R237G	probably benign	Het
Vps13c	A	T	9: 67,847,798 (GRCm39)	N2187Y	probably damaging	Het
Wdr64	A	G	1: 175,617,495 (GRCm39)	T692A	probably benign	Het
Whamm	A	G	7: 81,221,172 (GRCm39)	N35D	probably damaging	Het
Wnt2	T	C	6: 18,023,335 (GRCm39)	S105G	probably damaging	Het
Zfp108	T	A	7: 23,960,952 (GRCm39)	H514Q	probably benign	Het
Zftraf1	C	T	15: 76,532,386 (GRCm39)	D241N	probably benign	Het
Znfx1	T	C	2: 166,884,589 (GRCm39)	K888E	possibly damaging	Het
Zzz3	T	C	3: 152,154,479 (GRCm39)	Y577H	probably damaging	Het

Other mutations in Ranbp10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02015:Ranbp10	APN	8	106,506,622 (GRCm39)	missense	probably damaging	1.00
IGL02119:Ranbp10	APN	8	106,553,635 (GRCm39)	missense	probably damaging	1.00
IGL02120:Ranbp10	APN	8	106,532,214 (GRCm39)	missense	probably damaging	1.00
R1532:Ranbp10	UTSW	8	106,500,963 (GRCm39)	missense	probably benign	0.01
R1743:Ranbp10	UTSW	8	106,506,610 (GRCm39)	missense	probably damaging	1.00
R1970:Ranbp10	UTSW	8	106,513,340 (GRCm39)	missense	probably damaging	1.00
R3084:Ranbp10	UTSW	8	106,501,263 (GRCm39)	missense	probably damaging	1.00
R3605:Ranbp10	UTSW	8	106,502,667 (GRCm39)	missense	probably benign	0.40
R3606:Ranbp10	UTSW	8	106,502,667 (GRCm39)	missense	probably benign	0.40
R3607:Ranbp10	UTSW	8	106,502,667 (GRCm39)	missense	probably benign	0.40
R4815:Ranbp10	UTSW	8	106,552,757 (GRCm39)	nonsense	probably null
R5996:Ranbp10	UTSW	8	106,499,672 (GRCm39)	missense	probably benign	0.04
R6178:Ranbp10	UTSW	8	106,498,296 (GRCm39)	missense	possibly damaging	0.82
R6528:Ranbp10	UTSW	8	106,506,588 (GRCm39)	missense	probably damaging	1.00
R6718:Ranbp10	UTSW	8	106,501,260 (GRCm39)	missense	possibly damaging	0.62
R7082:Ranbp10	UTSW	8	106,500,578 (GRCm39)	missense	probably damaging	0.99
R8073:Ranbp10	UTSW	8	106,513,261 (GRCm39)	missense	probably damaging	1.00
R8103:Ranbp10	UTSW	8	106,499,179 (GRCm39)	missense	probably benign	0.20
R8796:Ranbp10	UTSW	8	106,499,665 (GRCm39)	splice site	probably benign
R9152:Ranbp10	UTSW	8	106,499,140 (GRCm39)	missense	probably benign	0.12
R9789:Ranbp10	UTSW	8	106,513,306 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATGCCATCCAGAAGTGACCAAG -3'
(R):5'- GCAGACCTTGAGTTTGATGC -3'

Sequencing Primer
(F):5'- CCAAGAACGTGGCAGACTTAGTG -3'
(R):5'- TTGATGCCATTATAGGACCCG -3'

Posted On

2019-11-12