Incidental Mutation 'IGL03035:Crip2'
ID408614
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Crip2
Ensembl Gene ENSMUSG00000006356
Gene Namecysteine rich protein 2
SynonymsCrp, ESP1, Hlp, CRP4, 0610010I23Rik
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL03035
Quality Score
Status
Chromosome12
Chromosomal Location113140236-113145506 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to C at 113144125 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Proline at position 103 (T103P)
Ref Sequence ENSEMBL: ENSMUSP00000081943 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084882] [ENSMUST00000196015] [ENSMUST00000199089] [ENSMUST00000200380]
Predicted Effect probably benign
Transcript: ENSMUST00000084882
AA Change: T103P

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000081943
Gene: ENSMUSG00000006356
AA Change: T103P

DomainStartEndE-ValueType
LIM 4 56 2.08e-12 SMART
low complexity region 104 115 N/A INTRINSIC
LIM 125 177 6.05e-14 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000196015
SMART Domains Protein: ENSMUSP00000143009
Gene: ENSMUSG00000006356

DomainStartEndE-ValueType
LIM 1 53 3e-16 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000197396
Predicted Effect noncoding transcript
Transcript: ENSMUST00000198597
Predicted Effect probably benign
Transcript: ENSMUST00000199089
SMART Domains Protein: ENSMUSP00000142803
Gene: ENSMUSG00000006360

DomainStartEndE-ValueType
LIM 54 106 9.5e-17 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199976
Predicted Effect noncoding transcript
Transcript: ENSMUST00000200177
Predicted Effect probably benign
Transcript: ENSMUST00000200380
SMART Domains Protein: ENSMUSP00000143334
Gene: ENSMUSG00000006356

DomainStartEndE-ValueType
LIM 1 53 3e-16 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a null allele display abnormal inflammatory pain responses. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc9 A G 6: 142,627,593 L1004P probably damaging Het
Adgrf5 T C 17: 43,430,627 I385T possibly damaging Het
Alpk3 T C 7: 81,078,604 V494A probably benign Het
Camta2 C A 11: 70,671,509 E1021* probably null Het
Ccdc6 T A 10: 70,182,176 S334T probably benign Het
Cd84 T C 1: 171,852,034 V93A probably damaging Het
Ceacam20 T C 7: 19,977,908 probably null Het
Cyp4f14 T A 17: 32,914,634 T83S probably benign Het
Dapk1 T A 13: 60,716,773 V127D probably damaging Het
Dnah7c A G 1: 46,524,117 E609G probably benign Het
Dscam T A 16: 96,819,970 I513F possibly damaging Het
Ell2 T A 13: 75,763,648 L351* probably null Het
Emcn G T 3: 137,372,851 probably null Het
Fdft1 A T 14: 63,163,389 C98* probably null Het
Fer1l4 A G 2: 156,022,606 S1663P possibly damaging Het
Flt4 C A 11: 49,645,897 Y1231* probably null Het
Gatb A G 3: 85,601,947 K139E probably damaging Het
Gm13212 C A 4: 145,622,232 Q80K possibly damaging Het
Gtf2a1 C A 12: 91,572,637 probably benign Het
Gtf3c2 A C 5: 31,166,014 V574G possibly damaging Het
Heatr1 T C 13: 12,413,219 probably benign Het
Homer2 T A 7: 81,624,278 T57S possibly damaging Het
Ice2 C A 9: 69,425,688 F825L probably benign Het
Lepr C A 4: 101,764,980 L370I probably damaging Het
Nalcn G A 14: 123,278,218 Q1724* probably null Het
Nufip1 A G 14: 76,115,818 D222G probably damaging Het
Olfr1289 T C 2: 111,483,823 V159A probably benign Het
Prl3b1 A G 13: 27,249,533 probably benign Het
Ptbp3 A T 4: 59,477,218 M393K probably benign Het
Ptgds T C 2: 25,469,610 T22A probably benign Het
Rapgef2 T A 3: 79,094,424 H282L probably damaging Het
Rars2 T C 4: 34,656,865 probably null Het
Rnf213 G A 11: 119,445,626 probably benign Het
Ros1 C A 10: 52,075,984 probably benign Het
Slx4ip A G 2: 137,067,703 D206G possibly damaging Het
Sprr1a T A 3: 92,484,577 D39V probably benign Het
Stab1 A G 14: 31,147,769 V1442A probably benign Het
Tbx3 C A 5: 119,683,096 probably benign Het
Ubl3 A G 5: 148,506,137 *118Q probably null Het
Vmn2r55 G A 7: 12,670,816 S220L probably benign Het
Vps36 A G 8: 22,218,415 K362E probably benign Het
Other mutations in Crip2
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0732:Crip2 UTSW 12 113140558 unclassified probably benign
R1111:Crip2 UTSW 12 113144074 nonsense probably null
R1186:Crip2 UTSW 12 113144959 splice site probably benign
R1445:Crip2 UTSW 12 113143504 missense probably damaging 1.00
R1473:Crip2 UTSW 12 113143500 missense probably damaging 0.99
R1541:Crip2 UTSW 12 113144966 missense possibly damaging 0.65
R2270:Crip2 UTSW 12 113144866 missense probably damaging 0.99
R4852:Crip2 UTSW 12 113140584 missense probably damaging 1.00
R6935:Crip2 UTSW 12 113140593 missense probably damaging 1.00
R7461:Crip2 UTSW 12 113144157 critical splice donor site probably null
R7613:Crip2 UTSW 12 113144157 critical splice donor site probably null
Posted On2016-08-02