Incidental Mutation 'IGL02152:Nsg1'
ID282061
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Nsg1
Ensembl Gene ENSMUSG00000029126
Gene Nameneuron specific gene family member 1
SynonymsNEEP21, m234, p21
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL02152
Quality Score
Status
Chromosome5
Chromosomal Location38137192-38159907 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 38144801 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Leucine at position 50 (F50L)
Ref Sequence ENSEMBL: ENSMUSP00000143921 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031009] [ENSMUST00000201341] [ENSMUST00000201363] [ENSMUST00000201415]
Predicted Effect probably benign
Transcript: ENSMUST00000031009
AA Change: F89L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000031009
Gene: ENSMUSG00000029126
AA Change: F89L

DomainStartEndE-ValueType
Pfam:Calcyon 1 180 1.2e-88 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000201341
AA Change: F89L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000144641
Gene: ENSMUSG00000029126
AA Change: F89L

DomainStartEndE-ValueType
Pfam:Calcyon 1 117 5.4e-56 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000201363
AA Change: F89L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000144396
Gene: ENSMUSG00000029126
AA Change: F89L

DomainStartEndE-ValueType
Pfam:Calcyon 1 180 1.2e-88 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000201415
AA Change: F50L

PolyPhen 2 Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000143921
Gene: ENSMUSG00000029126
AA Change: F50L

DomainStartEndE-ValueType
Pfam:Calcyon 1 47 7.5e-19 PFAM
Pfam:Calcyon 43 141 1e-44 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700016K19Rik A G 11: 76,003,225 I143V probably benign Het
1700028K03Rik A G 5: 107,548,117 T140A probably benign Het
4933430I17Rik T C 4: 62,542,754 Y289H possibly damaging Het
Adamts17 T A 7: 67,125,000 S956T probably benign Het
Adamts6 A T 13: 104,313,660 S290C probably null Het
Apaf1 A T 10: 91,061,819 H267Q probably benign Het
Aplp2 G A 9: 31,211,651 P26L unknown Het
Arid1b C T 17: 5,313,968 S1019F probably damaging Het
Armc3 G A 2: 19,286,137 probably null Het
Ass1 T C 2: 31,492,324 I169T probably damaging Het
Ccser1 A G 6: 61,311,708 D285G possibly damaging Het
Cenpf A G 1: 189,649,012 V2737A probably benign Het
Chrm5 A G 2: 112,480,568 Y68H probably damaging Het
Cops4 A G 5: 100,533,590 T164A probably benign Het
Cox4i1 A G 8: 120,672,865 S72G probably benign Het
Cpox A G 16: 58,674,424 T275A possibly damaging Het
Cyb5a T C 18: 84,873,156 I68T probably benign Het
Efna5 T C 17: 62,651,060 D67G probably benign Het
Enpp3 T C 10: 24,774,002 E842G probably damaging Het
Fam208b C T 13: 3,585,371 E479K probably benign Het
Fam210b A G 2: 172,351,503 K79E probably benign Het
Gm17359 T C 3: 79,345,532 I18T possibly damaging Het
Gm4799 T C 10: 82,954,755 noncoding transcript Het
Gpr146 A T 5: 139,392,712 R90W probably damaging Het
Hal A G 10: 93,503,542 I498V possibly damaging Het
Hist1h2af A G 13: 23,534,281 H124R probably benign Het
Hnrnpm C T 17: 33,658,412 G365R probably damaging Het
Jakmip3 A G 7: 139,025,488 D407G probably damaging Het
Kank1 A G 19: 25,428,172 I1185V possibly damaging Het
Kcnj16 A T 11: 111,025,210 M233L probably benign Het
Klhl5 A T 5: 65,148,800 Q370L probably damaging Het
L3hypdh C T 12: 72,077,143 probably null Het
Las1l A G X: 95,953,302 V130A probably damaging Het
Lrp2bp A T 8: 46,023,044 Y274F probably damaging Het
Morc2b T A 17: 33,137,943 K285M probably damaging Het
Mpp3 A T 11: 102,025,390 Y45* probably null Het
Muc4 T A 16: 32,777,649 probably benign Het
Muc5ac T C 7: 141,800,177 C837R possibly damaging Het
Mum1 A G 10: 80,239,978 D466G probably damaging Het
Nr2f6 T A 8: 71,376,166 I155F probably damaging Het
Olfr304 T A 7: 86,386,043 M206L probably benign Het
Ostf1 C A 19: 18,590,458 G101C probably damaging Het
Pam C T 1: 97,840,749 R552Q probably damaging Het
Pkd1l3 A G 8: 109,669,292 N2108S probably damaging Het
Prkdc A T 16: 15,669,285 H484L probably benign Het
Rfx5 G A 3: 94,957,182 R213Q probably damaging Het
Ryr1 T C 7: 29,052,015 S3715G possibly damaging Het
Sall2 A G 14: 52,315,514 S73P probably damaging Het
Sec22c G A 9: 121,684,779 A264V probably benign Het
Sis A C 3: 72,888,986 probably benign Het
Spam1 T A 6: 24,800,803 probably benign Het
St13 T A 15: 81,366,382 I318F probably damaging Het
Syne1 T C 10: 5,424,382 I142V probably damaging Het
Trpm6 A T 19: 18,832,539 T1100S possibly damaging Het
Ttll6 G A 11: 96,135,540 W90* probably null Het
Txndc12 T A 4: 108,834,792 C9* probably null Het
Ubr7 C T 12: 102,768,276 Q270* probably null Het
Vps33b A G 7: 80,285,069 S302G probably benign Het
Xylt1 T A 7: 117,634,770 V508E probably damaging Het
Zbtb26 A T 2: 37,436,691 L111Q possibly damaging Het
Zfp410 T C 12: 84,332,928 probably benign Het
Zscan18 A T 7: 12,775,296 probably benign Het
Other mutations in Nsg1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00897:Nsg1 APN 5 38144716 missense probably damaging 0.99
IGL01646:Nsg1 APN 5 38155691 missense probably damaging 1.00
IGL02393:Nsg1 APN 5 38158911 missense probably damaging 1.00
IGL02994:Nsg1 APN 5 38155602 intron probably benign
R0089:Nsg1 UTSW 5 38155630 missense probably benign 0.45
R0102:Nsg1 UTSW 5 38158910 missense probably damaging 0.99
R0102:Nsg1 UTSW 5 38158910 missense probably damaging 0.99
R1443:Nsg1 UTSW 5 38155643 missense probably benign 0.00
R1611:Nsg1 UTSW 5 38138716 nonsense probably null
R4825:Nsg1 UTSW 5 38159047 unclassified probably benign
Posted On2015-04-16