Incidental Mutation 'R4154:Nucb2'
ID315045
Institutional Source Beutler Lab
Gene Symbol Nucb2
Ensembl Gene ENSMUSG00000030659
Gene Namenucleobindin 2
SynonymsNEFA, Calnuc, nesfatin-1
MMRRC Submission 040998-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.193) question?
Stock #R4154 (G1)
Quality Score225
Status Validated
Chromosome7
Chromosomal Location116504369-116540584 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 116527667 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Alanine at position 172 (T172A)
Ref Sequence ENSEMBL: ENSMUSP00000032895 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032895] [ENSMUST00000183175]
Predicted Effect probably benign
Transcript: ENSMUST00000032895
AA Change: T172A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000032895
Gene: ENSMUSG00000030659
AA Change: T172A

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
low complexity region 196 213 N/A INTRINSIC
EFh 245 273 5.63e-1 SMART
EFh 297 325 6.56e0 SMART
coiled coil region 341 403 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000183175
AA Change: T172A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000138741
Gene: ENSMUSG00000030659
AA Change: T172A

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
low complexity region 196 213 N/A INTRINSIC
EFh 245 273 5.63e-1 SMART
EFh 297 325 6.56e0 SMART
coiled coil region 341 403 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000183335
Meta Mutation Damage Score 0.0581 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.5%
Validation Efficiency 98% (51/52)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein with a suggested role in calcium level maintenance, eating regulation in the hypothalamus, and release of tumor necrosis factor from vascular endothelial cells. This protein binds calcium and has EF-folding domains. [provided by RefSeq, Oct 2011]
PHENOTYPE: Homozygous mutation of this gene results in decreased heart rate and increased serum alkaline phosphatase levels. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
AI593442 A T 9: 52,677,904 H124Q probably benign Het
Asph C T 4: 9,639,250 W38* probably null Het
Bicdl2 A G 17: 23,666,092 probably null Het
Chd8 T C 14: 52,207,211 probably benign Het
Clcn4 T C 7: 7,294,834 N67D probably benign Het
Cptp A G 4: 155,867,200 V12A possibly damaging Het
Crim1 A G 17: 78,237,843 I145V probably benign Het
Ctsc G A 7: 88,299,547 M195I probably benign Het
Ddx41 G A 13: 55,534,480 R205W possibly damaging Het
Fas T G 19: 34,318,828 I180S possibly damaging Het
Fsip2 A C 2: 82,987,069 E4382A possibly damaging Het
Galnt5 T G 2: 57,998,493 L35R probably damaging Het
Gfpt2 G A 11: 49,835,778 probably null Het
Gjd4 G T 18: 9,280,811 S89* probably null Het
Gm14496 A T 2: 181,995,079 H110L probably benign Het
Golm1 A G 13: 59,642,353 V211A probably benign Het
Gsc2 TGCAGCAGCAGCAGCAG TGCAGCAGCAGCAG 16: 17,914,802 probably benign Het
Ighv1-72 A T 12: 115,758,397 M7K probably benign Het
Igkv12-44 C T 6: 69,814,655 C108Y possibly damaging Het
Lum T C 10: 97,568,953 S237P probably damaging Het
Macf1 T C 4: 123,471,813 K3052E probably damaging Het
Mdn1 A G 4: 32,707,475 E1588G probably damaging Het
Ndst3 T C 3: 123,672,227 Y32C probably damaging Het
Olfr690 T C 7: 105,329,385 N269S probably damaging Het
Pard3 G T 8: 127,474,396 R978L probably damaging Het
Pcdha4 A G 18: 36,953,586 probably null Het
Pgk2 A G 17: 40,208,258 V93A probably damaging Het
Pik3c3 G A 18: 30,311,283 M516I probably benign Het
Plxnb2 A G 15: 89,159,642 F1336L probably damaging Het
Shroom3 G T 5: 92,943,086 V1151F probably damaging Het
Sipa1l1 G C 12: 82,425,214 G1323R possibly damaging Het
Sntg1 A T 1: 8,583,345 probably null Het
Spef2 T C 15: 9,626,021 K1153R probably benign Het
Strn3 C T 12: 51,627,131 V566M probably damaging Het
Svep1 A G 4: 58,069,068 F2906S possibly damaging Het
Tbc1d8 C T 1: 39,386,135 V545M probably damaging Het
Tmem131 T C 1: 36,808,793 probably benign Het
Tnfsf8 A G 4: 63,834,358 S157P probably benign Het
Tubgcp5 G A 7: 55,805,329 V258M probably benign Het
Vat1l G C 8: 114,205,803 G30R possibly damaging Het
Vegfb T C 19: 6,986,078 Y106C probably damaging Het
Vmn2r100 AAAACAGGAGTATTGATTGGAAAC AAAAC 17: 19,523,419 probably null Het
Zc3h15 T C 2: 83,658,569 V161A probably benign Het
Other mutations in Nucb2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00423:Nucb2 APN 7 116521831 splice site probably benign
IGL02347:Nucb2 APN 7 116535878 missense probably benign 0.00
R0017:Nucb2 UTSW 7 116533151 missense probably benign 0.01
R0017:Nucb2 UTSW 7 116533151 missense probably benign 0.01
R0207:Nucb2 UTSW 7 116536010 missense probably damaging 1.00
R0690:Nucb2 UTSW 7 116535851 splice site probably benign
R1526:Nucb2 UTSW 7 116524407 critical splice donor site probably null
R3964:Nucb2 UTSW 7 116528875 missense probably damaging 1.00
R3966:Nucb2 UTSW 7 116528875 missense probably damaging 1.00
R4619:Nucb2 UTSW 7 116527824 critical splice donor site probably null
R4705:Nucb2 UTSW 7 116540027 critical splice donor site probably null
R4913:Nucb2 UTSW 7 116524305 nonsense probably null
R4934:Nucb2 UTSW 7 116539964 missense possibly damaging 0.93
R5210:Nucb2 UTSW 7 116528987 missense probably damaging 1.00
R7227:Nucb2 UTSW 7 116526076 missense probably damaging 1.00
R7776:Nucb2 UTSW 7 116529013 missense probably damaging 1.00
R7899:Nucb2 UTSW 7 116521970 missense probably benign 0.01
R8200:Nucb2 UTSW 7 116533163 critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- CGTCTGTTAGAGAGCTCAGG -3'
(R):5'- TCTATGAACCCCAGTCCTTACG -3'

Sequencing Primer
(F):5'- CTGCCTCAGTGACTAAGGTAG -3'
(R):5'- CCTTACGGGATGATTAACTTTGG -3'
Posted On2015-05-14