Incidental Mutation 'IGL03301:Saal1'
ID416235
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Saal1
Ensembl Gene ENSMUSG00000006763
Gene Nameserum amyloid A-like 1
Synonyms5031425D22Rik
Accession Numbers

Genbank: NM_030233

Is this an essential gene? Probably non essential (E-score: 0.116) question?
Stock #IGL03301
Quality Score
Status
Chromosome7
Chromosomal Location46686108-46710680 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to G at 46702520 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000120658 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000143082]
Predicted Effect probably benign
Transcript: ENSMUST00000143082
SMART Domains Protein: ENSMUSP00000120658
Gene: ENSMUSG00000006763

DomainStartEndE-ValueType
low complexity region 15 24 N/A INTRINSIC
SCOP:d1gw5a_ 40 455 2e-5 SMART
low complexity region 456 465 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209780
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209797
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210628
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210791
Coding Region Coverage
Validation Efficiency
Allele List at MGI

All alleles(6) : Gene trapped(6)

Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts3 T C 5: 89,707,404 E418G probably damaging Het
Arl14 T C 3: 69,222,943 F141S probably damaging Het
C1s1 A T 6: 124,541,324 probably benign Het
Cilp T C 9: 65,280,217 V1198A probably benign Het
Cnbd1 A T 4: 19,055,039 I129K probably benign Het
Ctdp1 G A 18: 80,449,634 Q549* probably null Het
Cyp2ab1 T A 16: 20,313,799 I250F possibly damaging Het
Dmd G A X: 83,908,514 R1765Q probably damaging Het
Dnah1 C T 14: 31,292,692 G1739R probably damaging Het
Eml6 T C 11: 29,764,083 K1350E probably benign Het
Ephx4 C A 5: 107,426,864 T256K probably benign Het
Fnd3c2 G T X: 106,252,263 Q49K probably benign Het
Heatr1 G T 13: 12,434,205 G1889W probably damaging Het
Igkv19-93 A T 6: 68,736,481 W55R probably damaging Het
Jak1 T C 4: 101,175,173 Y412C probably damaging Het
Moxd1 A T 10: 24,279,484 N261I probably damaging Het
Mrgpra1 T C 7: 47,335,416 N172D probably benign Het
Papolg T C 11: 23,874,503 N293S probably benign Het
Piezo2 A G 18: 63,027,704 S2294P probably damaging Het
Ppp3cb A T 14: 20,523,984 V262D probably damaging Het
Rhox7a A G X: 37,840,011 T235A probably benign Het
Scrn1 G A 6: 54,548,337 R16* probably null Het
Slc22a2 A G 17: 12,606,039 R263G probably damaging Het
Speer3 T A 5: 13,795,433 L160H probably damaging Het
Tmcc2 T C 1: 132,360,819 M377V possibly damaging Het
Tsen2 T G 6: 115,568,771 Y341D probably damaging Het
Vmn2r13 A T 5: 109,158,089 V541D probably damaging Het
Vmn2r15 A G 5: 109,297,355 probably null Het
Zfp711 T C X: 112,633,401 Y710H probably damaging Het
Zmiz2 C T 11: 6,401,170 T566M probably damaging Het
Other mutations in Saal1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02727:Saal1 APN 7 46689799 splice site probably null
G5030:Saal1 UTSW 7 46692783 missense probably damaging 1.00
R0021:Saal1 UTSW 7 46692892 missense probably damaging 0.96
R0765:Saal1 UTSW 7 46699647 missense possibly damaging 0.76
R1086:Saal1 UTSW 7 46689459 splice site probably benign
R1273:Saal1 UTSW 7 46692942 missense probably damaging 0.99
R1466:Saal1 UTSW 7 46702545 intron probably null
R1466:Saal1 UTSW 7 46702545 intron probably null
R1661:Saal1 UTSW 7 46692800 missense possibly damaging 0.93
R1695:Saal1 UTSW 7 46692916 missense probably damaging 0.97
R2018:Saal1 UTSW 7 46699489 missense possibly damaging 0.93
R2058:Saal1 UTSW 7 46699456 missense probably damaging 1.00
R2059:Saal1 UTSW 7 46699456 missense probably damaging 1.00
R2326:Saal1 UTSW 7 46692811 missense probably benign 0.02
R4182:Saal1 UTSW 7 46710652 unclassified probably benign
R4704:Saal1 UTSW 7 46699740 intron probably benign
R4831:Saal1 UTSW 7 46699647 missense probably benign 0.22
R5270:Saal1 UTSW 7 46701733 intron probably benign
R5471:Saal1 UTSW 7 46699648 missense probably benign 0.06
R5790:Saal1 UTSW 7 46701928 missense probably damaging 1.00
R6699:Saal1 UTSW 7 46692817 missense probably damaging 1.00
R6804:Saal1 UTSW 7 46699640 frame shift probably null
R6934:Saal1 UTSW 7 46702664 missense probably benign 0.00
R7863:Saal1 UTSW 7 46692903 missense probably benign 0.08
R7946:Saal1 UTSW 7 46692903 missense probably benign 0.08
Posted On2016-08-02