Incidental Mutation 'IGL01452:Tiparp'
ID84664
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tiparp
Ensembl Gene ENSMUSG00000034640
Gene NameTCDD-inducible poly(ADP-ribose) polymerase
SynonymsPARP7, PARP-7, DDF1
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.835) question?
Stock #IGL01452
Quality Score
Status
Chromosome3
Chromosomal Location65528410-65555518 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to T at 65552609 bp
ZygosityHeterozygous
Amino Acid Change Glycine to Stop codon at position 442 (G442*)
Ref Sequence ENSEMBL: ENSMUSP00000048051 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047906]
Predicted Effect probably null
Transcript: ENSMUST00000047906
AA Change: G442*
SMART Domains Protein: ENSMUSP00000048051
Gene: ENSMUSG00000034640
AA Change: G442*

DomainStartEndE-ValueType
Blast:ZnF_C3H1 238 264 2e-8 BLAST
Pfam:PARP 463 650 2e-37 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000154094
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 member of the poly(ADP-ribose) polymerase superfamily. Studies of the mouse ortholog have shown that the encoded protein catalyzes histone poly(ADP-ribosyl)ation and may be involved in T-cell function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit postnatal lethality, skeletal and craniofacial defects, kidney defects and embryonic hemorrhaging. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438A13Rik T A 3: 36,996,308 probably benign Het
AI314180 A G 4: 58,836,181 S720P probably damaging Het
Carmil3 A G 14: 55,496,058 N344D probably damaging Het
Cd300ld2 G A 11: 115,012,602 probably benign Het
Ddx19b A G 8: 111,020,988 S105P probably damaging Het
Dpf3 C A 12: 83,269,489 R336L probably benign Het
Foxj3 T C 4: 119,621,628 L427P unknown Het
Hdac11 A G 6: 91,167,861 D157G probably damaging Het
Klk13 G T 7: 43,726,636 R245L possibly damaging Het
Med25 C T 7: 44,882,831 M367I possibly damaging Het
Mindy3 G A 2: 12,355,272 probably benign Het
Mtf2 C T 5: 108,080,943 P42S probably damaging Het
Muc5ac A T 7: 141,817,555 L3269F probably benign Het
Olfr344 T A 2: 36,568,742 L48H probably damaging Het
Pcnx2 A G 8: 125,838,032 S1041P probably damaging Het
Pcnx4 G T 12: 72,574,400 G998V possibly damaging Het
Ptprk G A 10: 28,574,917 probably null Het
Scn9a A G 2: 66,527,072 F951L probably damaging Het
Sept11 A C 5: 93,161,204 K248Q possibly damaging Het
Src T A 2: 157,462,983 Y151N probably damaging Het
Tbc1d32 A T 10: 56,215,080 M119K possibly damaging Het
Ttn A G 2: 76,826,131 probably benign Het
Vmn2r4 A T 3: 64,406,395 N388K probably damaging Het
Other mutations in Tiparp
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00909:Tiparp APN 3 65532109 missense probably damaging 1.00
IGL01448:Tiparp APN 3 65552609 nonsense probably null
IGL01454:Tiparp APN 3 65552609 nonsense probably null
IGL01456:Tiparp APN 3 65552609 nonsense probably null
IGL01463:Tiparp APN 3 65552609 nonsense probably null
IGL01467:Tiparp APN 3 65552609 nonsense probably null
IGL01468:Tiparp APN 3 65552609 nonsense probably null
IGL01470:Tiparp APN 3 65552609 nonsense probably null
IGL01476:Tiparp APN 3 65552609 nonsense probably null
IGL01481:Tiparp APN 3 65552609 nonsense probably null
IGL01590:Tiparp APN 3 65531976 missense probably benign 0.14
IGL01684:Tiparp APN 3 65553333 missense probably damaging 0.99
IGL02322:Tiparp APN 3 65532020 nonsense probably null
IGL02572:Tiparp APN 3 65531889 missense probably benign 0.01
R0401:Tiparp UTSW 3 65531436 missense probably benign 0.06
R0674:Tiparp UTSW 3 65553165 missense probably benign 0.03
R1316:Tiparp UTSW 3 65553351 missense probably damaging 1.00
R1766:Tiparp UTSW 3 65532049 missense probably damaging 1.00
R2140:Tiparp UTSW 3 65529252 intron probably benign
R2568:Tiparp UTSW 3 65553130 nonsense probably null
R4533:Tiparp UTSW 3 65546347 missense probably benign 0.05
R4751:Tiparp UTSW 3 65552804 missense probably damaging 1.00
R4812:Tiparp UTSW 3 65552769 missense possibly damaging 0.94
R5268:Tiparp UTSW 3 65547565 missense possibly damaging 0.72
R5622:Tiparp UTSW 3 65547525 missense probably benign 0.00
R5693:Tiparp UTSW 3 65553492 missense possibly damaging 0.89
R5765:Tiparp UTSW 3 65531350 missense possibly damaging 0.69
R6061:Tiparp UTSW 3 65553243 missense probably damaging 0.98
R6875:Tiparp UTSW 3 65531642 missense probably benign 0.01
R7123:Tiparp UTSW 3 65553527 missense probably damaging 1.00
R8023:Tiparp UTSW 3 65531803 missense probably benign 0.01
Posted On2013-11-11