Incidental Mutation 'R1941:Steap1'
ID213997
Institutional Source Beutler Lab
Gene Symbol Steap1
Ensembl Gene ENSMUSG00000015652
Gene Namesix transmembrane epithelial antigen of the prostate 1
Synonyms2410007B19Rik, Prss24
MMRRC Submission 039959-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.193) question?
Stock #R1941 (G1)
Quality Score225
Status Not validated
Chromosome5
Chromosomal Location5736317-5749326 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 5740541 bp
ZygosityHeterozygous
Amino Acid Change Alanine to Serine at position 136 (A136S)
Ref Sequence ENSEMBL: ENSMUSP00000015796 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000015796]
Predicted Effect probably damaging
Transcript: ENSMUST00000015796
AA Change: A136S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000015796
Gene: ENSMUSG00000015652
AA Change: A136S

DomainStartEndE-ValueType
Pfam:Ferric_reduct 118 264 2e-17 PFAM
transmembrane domain 289 311 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000169542
SMART Domains Protein: ENSMUSP00000126005
Gene: ENSMUSG00000015652

DomainStartEndE-ValueType
Pfam:Ferric_reduct 10 77 2.7e-10 PFAM
Coding Region Coverage
  • 1x: 97.3%
  • 3x: 96.6%
  • 10x: 94.8%
  • 20x: 91.1%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is predominantly expressed in prostate tissue, and is found to be upregulated in multiple cancer cell lines. The gene product is predicted to be a six-transmembrane protein, and was shown to be a cell surface antigen significantly expressed at cell-cell junctions. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Art2b A C 7: 101,580,317 F125C probably damaging Het
BC027072 T G 17: 71,752,068 T205P probably damaging Het
Camta1 T C 4: 151,075,155 Y1616C probably damaging Het
Cep162 T G 9: 87,199,995 I1286L probably benign Het
Chd9 T A 8: 90,977,069 probably null Het
Col11a2 T A 17: 34,044,951 S247T probably benign Het
Col6a4 T G 9: 106,075,010 D563A probably benign Het
Crebbp C T 16: 4,179,691 M176I probably benign Het
Cyp4a12b A G 4: 115,438,059 N454S probably damaging Het
Dhx8 T C 11: 101,752,198 probably null Het
Dock7 G A 4: 98,984,715 L1165F probably benign Het
Fam117a A T 11: 95,380,798 N399Y probably damaging Het
Fmn1 A G 2: 113,365,143 K396R unknown Het
Foxk1 T A 5: 142,456,674 V693E possibly damaging Het
Gml A G 15: 74,817,171 L10P probably damaging Het
Gpx8 A G 13: 113,046,275 L34P probably damaging Het
Kank2 A G 9: 21,772,866 L689P possibly damaging Het
Mt4 G A 8: 94,138,246 C16Y possibly damaging Het
Naa15 C A 3: 51,455,934 Y346* probably null Het
Ntrk3 C T 7: 78,247,262 V676I probably damaging Het
Oasl2 G A 5: 114,911,362 probably benign Het
Olfr376 T A 11: 73,375,621 F294I probably damaging Het
Olfr767 T G 10: 129,079,954 N3T probably damaging Het
Olfr811 T A 10: 129,802,412 M38L probably benign Het
Olfr835 A C 9: 19,035,866 T248P possibly damaging Het
Olfr860 G A 9: 19,845,950 S223F probably damaging Het
Otud7a C T 7: 63,729,826 R273* probably null Het
Pde11a C T 2: 76,291,250 R329Q probably benign Het
Pga5 G T 19: 10,669,456 probably null Het
Ppp1r1a A G 15: 103,533,101 probably null Het
Pus10 A G 11: 23,711,198 Q262R possibly damaging Het
Rbm17 T C 2: 11,589,074 K241R possibly damaging Het
Rp1l1 T G 14: 64,022,252 D114E probably damaging Het
Safb T A 17: 56,598,992 probably benign Het
Sgpl1 T C 10: 61,103,307 Y371C probably damaging Het
Siglec1 C A 2: 131,078,131 A827S possibly damaging Het
Smg5 T A 3: 88,345,380 S158T possibly damaging Het
Sp2 C T 11: 96,955,936 C527Y probably damaging Het
Spaca6 A G 17: 17,838,402 I71V probably benign Het
Spaca6 A G 17: 17,838,430 E80G probably damaging Het
Supv3l1 G C 10: 62,449,612 P25R probably benign Het
Tex21 T C 12: 76,221,684 K108R possibly damaging Het
Tnc A G 4: 64,014,964 Y688H probably damaging Het
Tnr G A 1: 159,850,134 E30K possibly damaging Het
Tnrc18 G T 5: 142,815,150 P18T probably damaging Het
Ttk T G 9: 83,853,126 S422A probably benign Het
Ubap1 A G 4: 41,378,968 K61E probably damaging Het
Ubr2 C T 17: 46,974,026 R522H probably damaging Het
Vwf A T 6: 125,639,279 E1185D possibly damaging Het
Wwp2 A G 8: 107,517,915 T194A probably benign Het
Zfp36 A G 7: 28,377,646 V279A probably damaging Het
Zfp870 C A 17: 32,882,804 R517L possibly damaging Het
Other mutations in Steap1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02492:Steap1 APN 5 5740561 missense possibly damaging 0.87
E0370:Steap1 UTSW 5 5740673 missense probably damaging 1.00
PIT4468001:Steap1 UTSW 5 5736642 missense probably damaging 0.98
R0087:Steap1 UTSW 5 5736664 missense probably damaging 1.00
R0281:Steap1 UTSW 5 5736431 missense probably benign
R0525:Steap1 UTSW 5 5742903 missense possibly damaging 0.65
R0834:Steap1 UTSW 5 5740357 missense probably damaging 0.98
R1665:Steap1 UTSW 5 5736498 missense probably damaging 1.00
R4808:Steap1 UTSW 5 5738829 intron probably benign
R4860:Steap1 UTSW 5 5736589 missense probably damaging 1.00
R4860:Steap1 UTSW 5 5736589 missense probably damaging 1.00
R5004:Steap1 UTSW 5 5742829 nonsense probably null
R5138:Steap1 UTSW 5 5736486 missense probably damaging 0.99
R5330:Steap1 UTSW 5 5740422 missense probably damaging 1.00
R5583:Steap1 UTSW 5 5740579 missense possibly damaging 0.93
R6273:Steap1 UTSW 5 5740827 missense possibly damaging 0.65
Z1177:Steap1 UTSW 5 5739882 missense probably damaging 0.98
Z1177:Steap1 UTSW 5 5740580 missense possibly damaging 0.61
Predicted Primers PCR Primer
(F):5'- CTGTTTGTAAGCCCAGTTGAGTAG -3'
(R):5'- ATTCTTTCCAAACTGGCGCTTG -3'

Sequencing Primer
(F):5'- AAGCCCAGTTGAGTAGCTTGTATC -3'
(R):5'- GTGAAAGTCGCTGCCATCATATC -3'
Posted On2014-07-14