Incidental Mutation 'IGL02216:Albfm1'
ID 284920
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Albfm1
Ensembl Gene ENSMUSG00000070690
Gene Name albumin superfamily member 1
Synonyms 5830473C10Rik, Gm17754, ARG
Accession Numbers
Essential gene? Probably non essential (E-score: 0.062) question?
Stock # IGL02216
Quality Score
Status
Chromosome 5
Chromosomal Location 90708966-90745730 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 90727438 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000144527 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094615] [ENSMUST00000200765]
AlphaFold F8VQ07
Predicted Effect probably benign
Transcript: ENSMUST00000094615
SMART Domains Protein: ENSMUSP00000092198
Gene: ENSMUSG00000070690

DomainStartEndE-ValueType
ALBUMIN 17 207 8.87e-26 SMART
ALBUMIN 214 399 1.45e-53 SMART
ALBUMIN 406 598 7.07e-43 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000200765
SMART Domains Protein: ENSMUSP00000144527
Gene: ENSMUSG00000070690

DomainStartEndE-ValueType
ALBUMIN 17 207 4.3e-28 SMART
ALBUMIN 214 355 3.3e-15 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000200783
Predicted Effect noncoding transcript
Transcript: ENSMUST00000200893
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930544D05Rik T C 11: 70,507,005 (GRCm39) F48L possibly damaging Het
Adamts12 A G 15: 11,241,571 (GRCm39) N381S possibly damaging Het
Akp3 A T 1: 87,055,372 (GRCm39) Q473L probably damaging Het
Ap5s1 T A 2: 131,054,887 (GRCm39) probably benign Het
Atp10b T A 11: 43,150,616 (GRCm39) L1438Q probably damaging Het
B3galt4 G A 17: 34,169,539 (GRCm39) P233L probably damaging Het
Brd8 C T 18: 34,735,780 (GRCm39) S899N probably damaging Het
Cc2d1a C A 8: 84,865,942 (GRCm39) E393* probably null Het
Cd209a G T 8: 3,795,576 (GRCm39) T165N probably damaging Het
Chid1 T C 7: 141,076,506 (GRCm39) probably benign Het
Cln3 A T 7: 126,174,514 (GRCm39) probably null Het
Cped1 A T 6: 22,059,944 (GRCm39) R203S probably damaging Het
Dele1 A T 18: 38,385,913 (GRCm39) I102F probably damaging Het
Dnttip2 G T 3: 122,069,910 (GRCm39) W375L probably benign Het
Dync1h1 T C 12: 110,629,436 (GRCm39) F4280S probably damaging Het
Ephb4 A G 5: 137,370,332 (GRCm39) D844G possibly damaging Het
Fhl2 T A 1: 43,170,879 (GRCm39) E145V probably null Het
Gne T C 4: 44,044,761 (GRCm39) K458E probably benign Het
Grid2 G T 6: 64,322,650 (GRCm39) R550L probably damaging Het
Klhl1 T A 14: 96,360,658 (GRCm39) T731S probably benign Het
Kng1 T A 16: 22,877,283 (GRCm39) D30E probably damaging Het
Kyat1 A G 2: 30,077,264 (GRCm39) V158A probably benign Het
Mcm8 G T 2: 132,681,449 (GRCm39) V642F probably damaging Het
Mdn1 C T 4: 32,739,092 (GRCm39) H3638Y probably benign Het
Neb T G 2: 52,116,502 (GRCm39) T4158P probably benign Het
Neo1 T C 9: 58,824,336 (GRCm39) I697M probably damaging Het
Nfkb1 A T 3: 135,300,724 (GRCm39) V614D probably damaging Het
Or7e169 G A 9: 19,757,861 (GRCm39) S18L probably damaging Het
Otog T C 7: 45,950,892 (GRCm39) S2555P probably damaging Het
Pkd1l1 T A 11: 8,784,897 (GRCm39) R1962S probably damaging Het
Plxnb1 A G 9: 108,929,918 (GRCm39) Y258C probably damaging Het
Pramel12 T A 4: 143,144,298 (GRCm39) probably null Het
Prl3a1 A G 13: 27,454,127 (GRCm39) D35G probably benign Het
Rag1 A T 2: 101,473,726 (GRCm39) V472D possibly damaging Het
Rbpj-ps3 G A 6: 46,506,641 (GRCm39) probably benign Het
Rnf112 C T 11: 61,340,804 (GRCm39) V472M probably damaging Het
Rps18 A G 17: 34,171,015 (GRCm39) probably benign Het
Rptn T C 3: 93,303,080 (GRCm39) S138P possibly damaging Het
Sbpl A C 17: 24,172,690 (GRCm39) N76K probably benign Het
Sh3bp1 A T 15: 78,789,364 (GRCm39) M241L probably benign Het
Slc22a17 T C 14: 55,145,433 (GRCm39) *198W probably null Het
Smc3 C T 19: 53,610,275 (GRCm39) R221C probably damaging Het
Snai1 A G 2: 167,380,768 (GRCm39) E87G probably benign Het
Snx22 C A 9: 65,976,470 (GRCm39) A49S probably benign Het
Tas2r143 A T 6: 42,377,268 (GRCm39) R33* probably null Het
Try4 A G 6: 41,281,965 (GRCm39) I184V probably benign Het
Ttn T A 2: 76,584,896 (GRCm39) K20355* probably null Het
Ttn A G 2: 76,622,069 (GRCm39) V15491A probably benign Het
Tut7 T C 13: 59,948,237 (GRCm39) T293A probably benign Het
Vmn1r170 A G 7: 23,305,915 (GRCm39) T106A probably damaging Het
Vmn2r59 A T 7: 41,661,817 (GRCm39) V666E probably damaging Het
Vsx1 T C 2: 150,526,495 (GRCm39) N221S possibly damaging Het
Zfp846 A G 9: 20,499,905 (GRCm39) E45G probably damaging Het
Other mutations in Albfm1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02343:Albfm1 APN 5 90,727,473 (GRCm39) missense probably damaging 0.99
IGL02749:Albfm1 APN 5 90,719,624 (GRCm39) missense possibly damaging 0.84
IGL02956:Albfm1 APN 5 90,727,497 (GRCm39) missense possibly damaging 0.46
R0097:Albfm1 UTSW 5 90,732,795 (GRCm39) missense probably benign 0.02
R0097:Albfm1 UTSW 5 90,732,795 (GRCm39) missense probably benign 0.02
R0513:Albfm1 UTSW 5 90,725,786 (GRCm39) missense probably benign 0.00
R0551:Albfm1 UTSW 5 90,720,578 (GRCm39) missense probably damaging 1.00
R1508:Albfm1 UTSW 5 90,729,780 (GRCm39) missense probably benign 0.00
R1797:Albfm1 UTSW 5 90,727,460 (GRCm39) missense probably damaging 0.99
R2205:Albfm1 UTSW 5 90,717,421 (GRCm39) missense possibly damaging 0.50
R2323:Albfm1 UTSW 5 90,732,711 (GRCm39) nonsense probably null
R2440:Albfm1 UTSW 5 90,720,548 (GRCm39) critical splice acceptor site probably null
R4074:Albfm1 UTSW 5 90,740,727 (GRCm39) splice site probably null
R4211:Albfm1 UTSW 5 90,712,096 (GRCm39) missense probably damaging 1.00
R4426:Albfm1 UTSW 5 90,720,642 (GRCm39) missense probably damaging 1.00
R4625:Albfm1 UTSW 5 90,719,611 (GRCm39) missense probably damaging 0.99
R4823:Albfm1 UTSW 5 90,714,362 (GRCm39) missense probably benign 0.01
R4922:Albfm1 UTSW 5 90,727,570 (GRCm39) missense possibly damaging 0.84
R4923:Albfm1 UTSW 5 90,709,158 (GRCm39) missense probably benign 0.07
R5218:Albfm1 UTSW 5 90,729,777 (GRCm39) missense probably benign 0.34
R5267:Albfm1 UTSW 5 90,732,716 (GRCm39) missense probably damaging 0.99
R5447:Albfm1 UTSW 5 90,732,169 (GRCm39) missense probably damaging 1.00
R5737:Albfm1 UTSW 5 90,720,642 (GRCm39) missense probably damaging 1.00
R5966:Albfm1 UTSW 5 90,719,546 (GRCm39) missense probably damaging 1.00
R6045:Albfm1 UTSW 5 90,732,848 (GRCm39) missense possibly damaging 0.86
R6290:Albfm1 UTSW 5 90,740,864 (GRCm39) critical splice donor site probably null
R6799:Albfm1 UTSW 5 90,727,474 (GRCm39) missense probably damaging 0.99
R6923:Albfm1 UTSW 5 90,725,652 (GRCm39) missense probably benign 0.32
R7088:Albfm1 UTSW 5 90,720,609 (GRCm39) nonsense probably null
R7238:Albfm1 UTSW 5 90,727,519 (GRCm39) missense probably damaging 1.00
R7319:Albfm1 UTSW 5 90,719,625 (GRCm39) critical splice donor site probably null
R7631:Albfm1 UTSW 5 90,727,531 (GRCm39) missense probably damaging 1.00
R7798:Albfm1 UTSW 5 90,745,370 (GRCm39) missense possibly damaging 0.72
R7821:Albfm1 UTSW 5 90,740,747 (GRCm39) missense possibly damaging 0.95
R8041:Albfm1 UTSW 5 90,740,864 (GRCm39) critical splice donor site probably null
R8353:Albfm1 UTSW 5 90,714,360 (GRCm39) missense possibly damaging 0.67
R8453:Albfm1 UTSW 5 90,714,360 (GRCm39) missense possibly damaging 0.67
R8762:Albfm1 UTSW 5 90,714,461 (GRCm39) missense probably benign 0.32
Posted On 2015-04-16