Incidental Mutation 'R6950:Nipsnap3b'
ID541202
Institutional Source Beutler Lab
Gene Symbol Nipsnap3b
Ensembl Gene ENSMUSG00000015247
Gene Namenipsnap homolog 3B
Synonyms
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.078) question?
Stock #R6950 (G1)
Quality Score225.009
Status Validated
Chromosome4
Chromosomal Location53011880-53022060 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 53015136 bp
ZygosityHeterozygous
Amino Acid Change Histidine to Leucine at position 61 (H61L)
Ref Sequence ENSEMBL: ENSMUSP00000103292 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000015391] [ENSMUST00000107665]
Predicted Effect possibly damaging
Transcript: ENSMUST00000015391
AA Change: H61L

PolyPhen 2 Score 0.503 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000015391
Gene: ENSMUSG00000015247
AA Change: H61L

DomainStartEndE-ValueType
Pfam:NIPSNAP 37 136 1.5e-32 PFAM
Pfam:NIPSNAP 146 245 5.5e-29 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000107665
AA Change: H61L

PolyPhen 2 Score 0.900 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000103292
Gene: ENSMUSG00000015247
AA Change: H61L

DomainStartEndE-ValueType
Pfam:NIPSNAP 37 136 2.2e-30 PFAM
Pfam:NIPSNAP 134 195 8.5e-16 PFAM
Meta Mutation Damage Score 0.3784 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.4%
Validation Efficiency 98% (59/60)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] NIPSNAP3A belongs to a family of proteins with putative roles in vesicular transport (Buechler et al., 2004 [PubMed 15177564]).[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc1 T A 16: 14,411,616 V404D probably damaging Het
Adcy2 A G 13: 68,888,065 M159T possibly damaging Het
Agtpbp1 T C 13: 59,450,266 K674R probably benign Het
Atxn7 C A 14: 14,095,511 P403H probably damaging Het
Cav3 C T 6: 112,472,210 T63I probably damaging Het
Ccr6 T C 17: 8,257,066 *368Q probably null Het
Cdh8 A T 8: 99,030,763 N734K probably benign Het
Ces5a G T 8: 93,530,774 N134K probably benign Het
Cisd3 T G 11: 97,686,160 probably null Het
Cyp4f39 T G 17: 32,492,306 C476G probably damaging Het
Dffb A T 4: 153,970,092 M180K probably benign Het
Dock4 A G 12: 40,733,314 E749G possibly damaging Het
Eogt A G 6: 97,134,382 F173L possibly damaging Het
Ephb1 T A 9: 102,194,909 T224S probably benign Het
Fam114a1 A T 5: 64,979,979 E88D possibly damaging Het
Fam84b T C 15: 60,823,714 D61G probably benign Het
Fbn2 A C 18: 58,035,921 M2262R probably null Het
Fsip2 A G 2: 82,985,988 I4022V probably benign Het
Gapvd1 A G 2: 34,684,245 V1301A probably benign Het
Gch1 A T 14: 47,189,266 M1K probably null Het
Hes1 T C 16: 30,067,271 F231S probably damaging Het
Hoxb2 A G 11: 96,351,901 T31A probably benign Het
Ifngr1 T A 10: 19,607,293 V265D probably damaging Het
Ifnl3 A T 7: 28,523,007 I58F probably benign Het
Igf2r T C 17: 12,718,718 T561A probably benign Het
Igfbpl1 T A 4: 45,815,494 H214L probably damaging Het
Irf8 A G 8: 120,755,125 T318A probably benign Het
Kmt2d T C 15: 98,840,020 probably benign Het
Lrrc36 G T 8: 105,425,389 probably null Het
Msl2 C T 9: 101,101,975 P516L possibly damaging Het
Naaladl1 A T 19: 6,105,981 I62F probably damaging Het
Neto2 G T 8: 85,670,443 P60Q probably damaging Het
Npb T C 11: 120,608,647 F47L probably benign Het
Nutm1 T A 2: 112,248,559 T1004S probably benign Het
Olfr1251 T A 2: 89,667,551 I112F probably benign Het
Olfr1427 A G 19: 12,099,390 V83A probably benign Het
Olfr895 A T 9: 38,268,546 N3I probably damaging Het
Oxr1 C A 15: 41,820,555 A439E probably benign Het
Phf14 A T 6: 12,006,855 K835N probably damaging Het
Prkdc T A 16: 15,815,986 V3518E probably damaging Het
Ptpru T A 4: 131,776,352 E1132D probably damaging Het
Rapgef6 T A 11: 54,676,380 M1129K probably benign Het
Rgmb T C 17: 15,807,786 K224E probably damaging Het
Ryr3 T C 2: 112,686,825 I3318V possibly damaging Het
Slc9a4 A G 1: 40,602,885 Y338C probably damaging Het
Smg5 T C 3: 88,349,269 probably null Het
Tenm3 A T 8: 48,240,479 Y1789* probably null Het
Tgm7 T C 2: 121,093,647 E598G probably damaging Het
Tiam1 C T 16: 89,860,204 probably null Het
Tmem175 A G 5: 108,643,082 N166S probably benign Het
Trp73 G T 4: 154,062,053 N368K probably benign Het
Trpc3 C T 3: 36,638,590 R751H probably damaging Het
Trpm4 C A 7: 45,319,280 A410S probably damaging Het
Ube2t T G 1: 134,971,357 probably null Het
Vmn2r114 C T 17: 23,310,163 A322T probably benign Het
Xylt2 C T 11: 94,667,629 R567H probably benign Het
Zfp119b T C 17: 55,939,137 K318E probably damaging Het
Zfp626 T G 7: 27,818,914 L440R probably damaging Het
Zfp850 A G 7: 27,990,514 S90P possibly damaging Het
Other mutations in Nipsnap3b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03032:Nipsnap3b APN 4 53015016 missense possibly damaging 0.80
R0008:Nipsnap3b UTSW 4 53015112 missense probably damaging 1.00
R0008:Nipsnap3b UTSW 4 53015112 missense probably damaging 1.00
R0148:Nipsnap3b UTSW 4 53017088 missense possibly damaging 0.56
R0518:Nipsnap3b UTSW 4 53021343 missense probably damaging 0.99
R1261:Nipsnap3b UTSW 4 53015166 missense probably damaging 1.00
R1262:Nipsnap3b UTSW 4 53015166 missense probably damaging 1.00
R1954:Nipsnap3b UTSW 4 53017213 splice site probably benign
R5861:Nipsnap3b UTSW 4 53021177 missense probably damaging 1.00
R6213:Nipsnap3b UTSW 4 53017066 missense probably benign 0.01
R7076:Nipsnap3b UTSW 4 53021095 intron probably null
Predicted Primers PCR Primer
(F):5'- AACTATGTATCGACTTTGTGTCCC -3'
(R):5'- CCATGTGTATGTACAGTAACACAGAC -3'

Sequencing Primer
(F):5'- CCTTGTTTCCAGGCTCAAATATATTG -3'
(R):5'- TGTATGTACAGTAACACAGACTGAAG -3'
Posted On2018-11-28