Incidental Mutation 'IGL03035:Crip2'
ID 408614
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Crip2
Ensembl Gene ENSMUSG00000006356
Gene Name cysteine rich protein 2
Synonyms Hlp, 0610010I23Rik, ESP1, Crp, CRP4
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03035
Quality Score
Status
Chromosome 12
Chromosomal Location 113103856-113109126 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 113107745 bp (GRCm39)
Zygosity Heterozygous
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]
AlphaFold Q9DCT8
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: 142,573,319 (GRCm39) L1004P probably damaging Het
Adgrf5 T C 17: 43,741,518 (GRCm39) I385T possibly damaging Het
Alpk3 T C 7: 80,728,352 (GRCm39) V494A probably benign Het
Camta2 C A 11: 70,562,335 (GRCm39) E1021* probably null Het
Ccdc6 T A 10: 70,018,006 (GRCm39) S334T probably benign Het
Cd84 T C 1: 171,679,601 (GRCm39) V93A probably damaging Het
Ceacam20 T C 7: 19,711,833 (GRCm39) probably null Het
Cyp4f14 T A 17: 33,133,608 (GRCm39) T83S probably benign Het
Dapk1 T A 13: 60,864,587 (GRCm39) V127D probably damaging Het
Dnah7c A G 1: 46,563,277 (GRCm39) E609G probably benign Het
Dscam T A 16: 96,621,170 (GRCm39) I513F possibly damaging Het
Ell2 T A 13: 75,911,767 (GRCm39) L351* probably null Het
Emcn G T 3: 137,078,612 (GRCm39) probably null Het
Fdft1 A T 14: 63,400,838 (GRCm39) C98* probably null Het
Fer1l4 A G 2: 155,864,526 (GRCm39) S1663P possibly damaging Het
Flt4 C A 11: 49,536,724 (GRCm39) Y1231* probably null Het
Gatb A G 3: 85,509,254 (GRCm39) K139E probably damaging Het
Gtf2a1 C A 12: 91,539,411 (GRCm39) probably benign Het
Gtf3c2 A C 5: 31,323,358 (GRCm39) V574G possibly damaging Het
Heatr1 T C 13: 12,428,100 (GRCm39) probably benign Het
Homer2 T A 7: 81,274,026 (GRCm39) T57S possibly damaging Het
Ice2 C A 9: 69,332,970 (GRCm39) F825L probably benign Het
Lepr C A 4: 101,622,177 (GRCm39) L370I probably damaging Het
Nalcn G A 14: 123,515,630 (GRCm39) Q1724* probably null Het
Nufip1 A G 14: 76,353,258 (GRCm39) D222G probably damaging Het
Or4f4b T C 2: 111,314,168 (GRCm39) V159A probably benign Het
Prl3b1 A G 13: 27,433,516 (GRCm39) probably benign Het
Ptbp3 A T 4: 59,477,218 (GRCm39) M393K probably benign Het
Ptgds T C 2: 25,359,622 (GRCm39) T22A probably benign Het
Rapgef2 T A 3: 79,001,731 (GRCm39) H282L probably damaging Het
Rars2 T C 4: 34,656,865 (GRCm39) probably null Het
Rnf213 G A 11: 119,336,452 (GRCm39) probably benign Het
Ros1 C A 10: 51,952,080 (GRCm39) probably benign Het
Slx4ip A G 2: 136,909,623 (GRCm39) D206G possibly damaging Het
Sprr1a T A 3: 92,391,884 (GRCm39) D39V probably benign Het
Stab1 A G 14: 30,869,726 (GRCm39) V1442A probably benign Het
Tbx3 C A 5: 119,821,161 (GRCm39) probably benign Het
Ubl3 A G 5: 148,442,947 (GRCm39) *118Q probably null Het
Vmn2r55 G A 7: 12,404,743 (GRCm39) S220L probably benign Het
Vps36 A G 8: 22,708,431 (GRCm39) K362E probably benign Het
Zfp268 C A 4: 145,348,802 (GRCm39) Q80K possibly damaging Het
Other mutations in Crip2
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0732:Crip2 UTSW 12 113,104,178 (GRCm39) unclassified probably benign
R1111:Crip2 UTSW 12 113,107,694 (GRCm39) nonsense probably null
R1186:Crip2 UTSW 12 113,108,579 (GRCm39) splice site probably benign
R1445:Crip2 UTSW 12 113,107,124 (GRCm39) missense probably damaging 1.00
R1473:Crip2 UTSW 12 113,107,120 (GRCm39) missense probably damaging 0.99
R1541:Crip2 UTSW 12 113,108,586 (GRCm39) missense possibly damaging 0.65
R2270:Crip2 UTSW 12 113,108,486 (GRCm39) missense probably damaging 0.99
R4852:Crip2 UTSW 12 113,104,204 (GRCm39) missense probably damaging 1.00
R6935:Crip2 UTSW 12 113,104,213 (GRCm39) missense probably damaging 1.00
R7461:Crip2 UTSW 12 113,107,777 (GRCm39) critical splice donor site probably null
R7613:Crip2 UTSW 12 113,107,777 (GRCm39) critical splice donor site probably null
R9036:Crip2 UTSW 12 113,108,030 (GRCm39) missense probably benign 0.29
Posted On 2016-08-02