Incidental Mutation 'IGL00708:Cela3b'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cela3b
Ensembl Gene ENSMUSG00000023433
Gene Namechymotrypsin-like elastase family, member 3B
Synonyms2310074F01Rik, Ela3b, Ela3, 0910001F22Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.075) question?
Stock #IGL00708
Quality Score
Chromosomal Location137420999-137430540 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 137421969 bp
Amino Acid Change Leucine to Phenylalanine at position 241 (L241F)
Ref Sequence ENSEMBL: ENSMUSP00000099581 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000102522]
Predicted Effect probably benign
Transcript: ENSMUST00000102522
AA Change: L241F

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000099581
Gene: ENSMUSG00000023433
AA Change: L241F

signal peptide 1 16 N/A INTRINSIC
Tryp_SPc 27 262 8.81e-94 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134565
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode the structurally similar proteins elastase 1, 2, 2A, 2B, 3A, and 3B. Unlike other elastases, elastase 3B has little elastolytic activity. Like most of the human elastases, elastase 3B is secreted from the pancreas as a zymogen and, like other serine proteases such as trypsin, chymotrypsin and kallikrein, it has a digestive function in the intestine. Elastase 3B preferentially cleaves proteins after alanine residues. Elastase 3B may also function in the intestinal transport and metabolism of cholesterol. Both elastase 3A and elastase 3B have been referred to as protease E and as elastase 1, and excretion of this protein in fecal material is frequently used as a measure of pancreatic function in clinical assays. [provided by RefSeq, May 2009]
Allele List at MGI
Other mutations in this stock
Total: 19 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts17 A G 7: 66,968,902 E388G probably damaging Het
Arid4a T C 12: 71,072,728 S374P probably benign Het
Ccdc186 A T 19: 56,813,447 S79R probably benign Het
Dsg4 T A 18: 20,461,326 V504D probably benign Het
Fam160a2 C T 7: 105,388,260 R372Q probably damaging Het
Meis2 C T 2: 115,864,244 D473N probably benign Het
Mri1 A T 8: 84,251,648 I338N probably damaging Het
Mroh8 A G 2: 157,220,170 S868P probably damaging Het
Mtus1 G A 8: 41,084,349 T110I probably damaging Het
Mug2 A G 6: 122,047,487 E506G possibly damaging Het
Napsa A G 7: 44,581,421 T71A probably benign Het
Prepl T C 17: 85,078,507 Y243C probably damaging Het
Prkdc A G 16: 15,779,426 I2817V probably damaging Het
Rbm26 C T 14: 105,159,960 V69I unknown Het
Tcerg1 T A 18: 42,571,125 N949K probably benign Het
Tgfbr1 C T 4: 47,383,992 T45I probably benign Het
Trim37 T A 11: 87,186,393 D516E probably damaging Het
Wdr7 C T 18: 63,778,033 T832M probably benign Het
Zfp280d T C 9: 72,312,135 V198A probably benign Het
Other mutations in Cela3b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00504:Cela3b APN 4 137423281 missense probably damaging 1.00
IGL01301:Cela3b APN 4 137423843 critical splice donor site probably null
IGL01613:Cela3b APN 4 137425071 missense possibly damaging 0.66
ANU18:Cela3b UTSW 4 137423843 critical splice donor site probably null
R0669:Cela3b UTSW 4 137428530 missense probably benign 0.06
R2937:Cela3b UTSW 4 137423263 missense probably benign 0.01
R2938:Cela3b UTSW 4 137423263 missense probably benign 0.01
R4327:Cela3b UTSW 4 137423931 missense probably benign 0.26
R4451:Cela3b UTSW 4 137421044 utr 3 prime probably benign
R5059:Cela3b UTSW 4 137424870 missense probably benign 0.00
R5707:Cela3b UTSW 4 137424856 missense probably damaging 1.00
R7952:Cela3b UTSW 4 137421908 missense probably benign 0.27
X0019:Cela3b UTSW 4 137423310 missense probably damaging 1.00
X0019:Cela3b UTSW 4 137423311 missense probably damaging 1.00
Z1177:Cela3b UTSW 4 137428484 missense probably damaging 0.99
Posted On2012-12-06