Incidental Mutation 'IGL01907:Racgap1'
ID179706
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Racgap1
Ensembl Gene ENSMUSG00000023015
Gene NameRac GTPase-activating protein 1
SynonymsBand25, gtl11, GTPase, MgcRacGAP
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock #IGL01907
Quality Score
Status
Chromosome15
Chromosomal Location99620496-99651656 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 99626333 bp
ZygosityHeterozygous
Amino Acid Change Lysine to Stop codon at position 398 (K398*)
Ref Sequence ENSEMBL: ENSMUSP00000126417 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023756] [ENSMUST00000168065] [ENSMUST00000171702]
Predicted Effect probably null
Transcript: ENSMUST00000023756
AA Change: K398*
SMART Domains Protein: ENSMUSP00000023756
Gene: ENSMUSG00000023015
AA Change: K398*

DomainStartEndE-ValueType
coiled coil region 35 110 N/A INTRINSIC
C1 288 336 2.44e-5 SMART
RhoGAP 361 537 3.4e-51 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000165745
Predicted Effect probably benign
Transcript: ENSMUST00000168065
SMART Domains Protein: ENSMUSP00000132732
Gene: ENSMUSG00000023015

DomainStartEndE-ValueType
coiled coil region 6 81 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000169700
Predicted Effect noncoding transcript
Transcript: ENSMUST00000170369
Predicted Effect noncoding transcript
Transcript: ENSMUST00000171017
Predicted Effect probably null
Transcript: ENSMUST00000171702
AA Change: K398*
SMART Domains Protein: ENSMUSP00000126417
Gene: ENSMUSG00000023015
AA Change: K398*

DomainStartEndE-ValueType
coiled coil region 35 110 N/A INTRINSIC
C1 288 336 2.44e-5 SMART
RhoGAP 361 537 3.4e-51 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a GTPase-activating protein (GAP) that is a compoment of the centralspindlin complex. This protein binds activated forms of Rho GTPases and stimulates GTP hydrolysis, which results in negative regulation of Rho-mediated signals. This protein plays a regulatory role in cytokinesis, cell growth, and differentiation. Alternatively spliced transcript variants have been found for this gene. There is a pseudogene for this gene on chromosome 12. [provided by RefSeq, Feb 2016]
PHENOTYPE: Embryos homozygous for a gene-trapped allele exhibit pre-implantation lethality associated with the formation of multinucleated blastomeres and failure to complete cytokinesis. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ap1g1 T C 8: 109,843,343 probably benign Het
Asph A T 4: 9,514,643 D491E possibly damaging Het
D930020B18Rik A G 10: 121,642,010 N47D probably damaging Het
Fam49b A G 15: 63,931,686 probably benign Het
Gad1 T C 2: 70,574,126 V120A possibly damaging Het
Gm10717 C T 9: 3,025,616 S67L probably benign Het
Gm10717 A T 9: 3,026,287 Y195F probably damaging Het
Grin2b T G 6: 135,733,740 E936A probably damaging Het
Iars T C 13: 49,709,655 F528L probably damaging Het
Iyd C T 10: 3,540,407 P38S probably damaging Het
Krt24 A G 11: 99,285,204 F2L unknown Het
Mnat1 T A 12: 73,272,439 S279T probably benign Het
Mptx1 A T 1: 174,332,646 I173L probably benign Het
Olfr1016 T A 2: 85,799,602 T223S probably benign Het
Per1 T C 11: 69,105,599 S810P probably benign Het
Rnf133 T C 6: 23,649,304 N209D probably benign Het
Rp1 T C 1: 4,348,507 E794G possibly damaging Het
Ryr3 A T 2: 112,869,001 probably benign Het
Slc27a2 A G 2: 126,587,874 T465A probably benign Het
Smarca2 T C 19: 26,698,465 M1035T possibly damaging Het
Spink5 A G 18: 43,996,676 N445D probably damaging Het
Stard3nl G A 13: 19,372,589 A127V probably damaging Het
Trim69 C T 2: 122,167,661 T38M probably benign Het
Vmn2r-ps159 C T 4: 156,338,254 noncoding transcript Het
Zfp438 G A 18: 5,213,815 A381V probably damaging Het
Other mutations in Racgap1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00088:Racgap1 APN 15 99636122 unclassified probably benign
IGL01450:Racgap1 APN 15 99626363 missense probably benign 0.00
IGL02584:Racgap1 APN 15 99623634 missense probably benign 0.00
IGL02733:Racgap1 APN 15 99639704 missense probably damaging 1.00
IGL03137:Racgap1 APN 15 99628741 missense probably damaging 0.96
IGL03145:Racgap1 APN 15 99623640 missense probably benign 0.00
IGL02799:Racgap1 UTSW 15 99632747 missense probably benign 0.09
R0106:Racgap1 UTSW 15 99642958 missense possibly damaging 0.66
R0106:Racgap1 UTSW 15 99642958 missense possibly damaging 0.66
R0140:Racgap1 UTSW 15 99623651 missense probably benign 0.00
R0398:Racgap1 UTSW 15 99628627 splice site probably benign
R0496:Racgap1 UTSW 15 99639832 splice site probably benign
R0528:Racgap1 UTSW 15 99628706 missense probably damaging 1.00
R0893:Racgap1 UTSW 15 99626530 missense probably benign
R0947:Racgap1 UTSW 15 99624314 missense possibly damaging 0.83
R1348:Racgap1 UTSW 15 99626365 missense possibly damaging 0.54
R1470:Racgap1 UTSW 15 99639775 missense probably damaging 0.99
R1470:Racgap1 UTSW 15 99639775 missense probably damaging 0.99
R1720:Racgap1 UTSW 15 99628769 nonsense probably null
R2235:Racgap1 UTSW 15 99626536 missense probably benign
R3624:Racgap1 UTSW 15 99642891 missense probably damaging 0.97
R4621:Racgap1 UTSW 15 99626206 missense probably benign 0.10
R4622:Racgap1 UTSW 15 99626206 missense probably benign 0.10
R4623:Racgap1 UTSW 15 99626206 missense probably benign 0.10
R5046:Racgap1 UTSW 15 99628762 missense probably damaging 1.00
R5899:Racgap1 UTSW 15 99623628 missense possibly damaging 0.80
R6306:Racgap1 UTSW 15 99623953 missense probably benign
R6513:Racgap1 UTSW 15 99624275 missense probably damaging 1.00
R6618:Racgap1 UTSW 15 99623994 missense probably damaging 0.97
R6953:Racgap1 UTSW 15 99626329 missense probably damaging 1.00
Posted On2014-05-07