ZMP
LOC100334768
Ensembl ID:
Human Orthologue:
ARHGAP33
Human Description:
Rho GTPase activating protein 33 [Source:HGNC Symbol;Acc:23085]
Mouse Orthologue:
Arhgap33
Mouse Description:
Rho GTPase activating protein 33 Gene [Source:MGI Symbol;Acc:MGI:2673998]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36246 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9276 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36245 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42808 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17463 | Essential Splice Site | Available for shipment | Available now |
sa12075 | Nonsense | Available for shipment | Available now |
sa19150 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19149 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36244 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36246
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022270 | Nonsense | 50 | 1964 | 1 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 47713334)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44911530 |
GRCz11 | 16 | 44878246 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGCTCGTGTATCAACATCAACCTGTCTGACAAACAACTGAGAGAATA[C/A]ACACATCAACACCAGGAGAAAATGCAGCGAAGAGTCACATGTGAGTTTTT
Long Flanking Sequence:
CTGGCTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGAGAGACTTGCTTTGTTTACTGGATAATTTGATTTGCATTGTAAACATTAAATAAAGATTAAAAAGGTATTACTTTTATTTAATATACTAAGTTTTTAGTTATACTCCAAAAAAATCATCCTGCATATATCTGGAGGATTTTATTTCCAAAATTTTTAGCAGAAATGGCAAAAAATGTCCACAGATTCTGTGTGGCCCTAATATTAACACTGCAAATAGTCAGCAGTTTATTAATTGTGAAGTATAAGCTCTCATGTTTACTGATGGTTGCAAACCAAAAGGTTTTTTCTCTCTCACCACACGCCCACTTGCATGAGATTCTAAAAGACTCATTTCCTAAAGCGGCTGTGAAAAAAAGCAGAAATGGCTCGTGTATCAACATCAACCTGTCTGACAAACAACTGAGAGAATA[C/A]ACACATCAACACCAGGAGAAAATGCAGCGAAGAGTCACATGTGAGTTTTTAGCTCTTCATTGCAAGTTTATTGATGTGTGGTTGTGTTTAGATGCCATGGTCTTAAAAAAACATGTTTATAAGTTGTATCAGTGTTCATCTTAACATCTCATCAGTGGTTAGTTTCTCTTTTCACTAATTCATGTTGAGTTGGTTTACAGATAACTATGCAAGCTCCACATTTGCTTACTCTGATAATGGGATAGGCTGTTCAACAATAACATTGTGGTCTGGTCAACAATTAAAGTGTTCTTATGCTTATATATGATGGTATTCATAATGTATTATATAATATTTCATATATCACTATGGTACTGGTATTATATTTAAGTTCAGGGTTTTTTTAAAAACTACCAGGTAGCTGCTTGAGATGATCTTAATAATATCATACGATAGCGCTGTGCCACCGTTTTGCATATCCGTGACGTACTTTAAAAAAACTGATATCTCCCTTTGACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9276
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022270 | Nonsense | 186 | 1964 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 47654752)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44852948 |
GRCz11 | 16 | 44819664 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGACCTCGGGCAGTGCCAAAGATCTGGTTTTCCTCGTGCAGGTGTCCTGC[C/T]AGGTGAGTGGGCGCACATTCACCAGACGCCGCTAATTATAAACAMCCCCT
Long Flanking Sequence:
GTCCCTTTCATTGCTGCTTGCAGCTTTAATTCACTTTCATTATTGCTCTCTAATAATTATCTATGCATGCAACTTGTTTTACATGCAGTGCATTTTTTATGCACGACTCTCTCCCCTACGGAATCAAAACAAAAATGACTAAATTTGATCTTATTTTCTTAATGAATAAATTCATTCTAAATAGAGCTAGTTAAGCCATCTGGTGAAATCGTACTCGTATCACAATATAAATCAGAGAAAAAGAAAATATCGCAATGTTCGATTCTTTTCAATATTATGCAGCCCTACTGGAATGGATTTCTTTATGTGTAAAATATCAATGTAAAACCATGCCCAGTTCCCACTAAACGTGTGTTTGTGCTTGTTTGAACTTCTTCACACCTCCATAAATTAATGTCTGCTCTTTACACCTCCAGCTTCAGTTTGCCAACGAGCAGAGCGATGCCAGCTGGACCTCGGGCAGTGCCAAAGATCTGGTTTTCCTCGTGCAGGTGTCCTGC[C/T]AGGTGAGTGGGCGCACATTCACCAGACGCCGCTAATTATAAACAACCCCTCCTGCCACAGAAATAAAAGCACCACTGACCAAATCAAAACGACACCTCCTTTTGCATCTTCTTGTTTGTTGATTTCTCCCTCCCTTCATCCTCTCTCTCTTCTCTCTGCCCCTATTTCCCCATCTCTCCTTTCCTTCCTGTGAAATCTAGGGTAAGACGTGGATGGTGCGGCGTTCGTATGAAGAGTTTCGGACGCTGGATGCCCACCTGCATCAGTGCATTTATGACCGCCGCTACTCGCAGCTCTTAGCACTGCCTGCCCTTTGCGAGATCGGAGACCGGCTGGAGGTGAGGTCTAATACTCTGGAGATTATTGCTACTTTTATCAGTAGCTTGTGTTTTATTGCTAGCACCGTTAGCTGCTCTCTATTGAGGTCGTCGGGTGGTTATGTAGGTTGGTGTCCAGCTCCTTGGGGATGGACTATGCTGGGAAAGACGCCACTTAATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36245
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022270 | Essential Splice Site | 263 | 1964 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 47652471)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44850667 |
GRCz11 | 16 | 44817383 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTGTGGACAATAAGCTGAACTGTGGGCCGGTTCTCACTTGGATGGAG[G/A]TAAGAGACAAACAGGGGGCCGTAAACATGTATTAAAGCAGTAAAATATTG
Long Flanking Sequence:
CCACAGTCACCAGAACTCAATCCAATAGAGCACCATTGGGATGTGGTGAATTGGGAGATTCGCATCATGAATGTGCATATGACAAATCTGCAGCGACTGCGTGATGCTATCATGTCAATATGGACCAAAATCTCTAAGGAATATTTCTTGTACCTTGTTGAATCTATGCCACAAAGGATTAAGGCAGTTCTGAAGGCAAAAGGGGGTATAAGTAAGGTGTACCTTAAAAAGTAGCCAGTGAGTGCACAGGATATTCTAATAAATCAAACAAGTTTGAGTTTGTCATCTGAATATCTTAAATTGTGTTAAACCTGGAGCACTGTTTTAATGTATTATTCGCTAGTGATAACATTGAGAAGTCTTTAACTGCTTTAATGGTGTTTGAACTTGTATGTTTGTTCTTGTAGATCCTAACACCACTGTTGTCAGAGTATCTAAACCGTCTCACCATGATTGTGGACAATAAGCTGAACTGTGGGCCGGTTCTCACTTGGATGGAG[G/A]TAAGAGACAAACAGGGGGCCGTAAACATGTATTAAAGCAGTAAAATATTGACACATAGAGAAGTAAATGAAACTTACAGGCCAACCTTTTCTCAAAATAACTTCTTTTTGGAACAATAAAAATATTGTATTCATATGCATTGCAAGCAATTTGTATTTGAGTGCTGTCATGTCTCAGATCCCAATATAAACATAATAACATGGCAGTATCTGTTGTTTCAATAAGATAACTGTAATCTTGCTGTGAGATTTCAGCTGCACGAATTCATGCATAATTAGTTAAATGACTTTTTCTTCTCATTATAGATTGACAACCATGGCAACAGGTTCCTGCTGAAAGAGGAAGCATCTTTAAACGTCCCTGCCATCGCCGCAGCTCACGTCATCAAGCGCTACACTGCTCAGGCTAGCGATGAGATCTCCATTGAGGTGTGCAGACCACTTGTGGTTTATCTTGTGATCATGCATTTCATTTTATTTCCTCTGCTTGCACCGTTCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42808
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022270 | Essential Splice Site | 330 | 1964 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 47649807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44848003 |
GRCz11 | 16 | 44814719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGCCCAAAGAGGACACTACATGGTGGAGAGGAAAGCATGGATTTCAGG[T/A]ACTGTTCTTAATCTCAGATCCTCATTTCCCCCCCTTTTTAGTAAAACAGA
Long Flanking Sequence:
CGCTCACGACGTGTCATTGAAATAATGCCATAGGTAGTTCTGTGTAAAATAGGCCTACCACCACAGCTGGGAAAAATCTTAGAGAAAACACTGTAGAAACACCATGGCAATCTCTTATAGTATCCTTACAACTACTTTGTAATAGGAATGCTCCAATCAATCGGTCGGAGATCAGTAATGGCTGATAATCACATTTTATGACTCGATCGGTACTTACTAATCTGGCCGATCACATGAACCAAAGTGTTCATTTACAGGTTTGCAAGCAGAGGAAGATCGGTATTAAATTCTTATGCATCAAATATGCACTCCAAACTTTTTTTTGATTGAGACATCACACGTAAGCTGATAATTTTGACTTCAACTGTAAGTGTGTCTGTTTGCACACTGATTGCTTGAGTCTTTGTTCCTCTTTCTAAAGGTTGGTGATATTTTGTCAGTGATTGACATGCCGCCCAAAGAGGACACTACATGGTGGAGAGGAAAGCATGGATTTCAGG[T/A]ACTGTTCTTAATCTCAGATCCTCATTTCCCCCCCTTTTTAGTAAAACAGACAACTCTGAGTCCAGCTCTCCCATCTTTGTTCTTCAGGTTGGCTTCTTTCCCAGTGAATGTGTGGAGTTAATCAATGAGAAGATGCCGCAGTCGGTCAGCGCTCCTGTCAGTAAGCAAGGTATAACACACAGTCTTCACTGTATAGGGATCAAGAGTGGACTGGCAGTAGAAAGAGCTGTGATGTGTTTTGCGACCGGATTTTCTCTCTTCATTTTGTTGGAGGTTGCAATGGAGCCACTAAAATTGTGTGTTGCCTGTGTTTACATATGATAAACATTATACACCTAAACCAGAAACAAACACTTATTTGAAACGATCAGACTTTTAATCAGCTTGGCCCAAAAAATGTGTGTATCACTTGAGCATTATCAAACAGCACAGTTCTCTGATACAAACGACAAATGTCTTTGGGATTTAAAACTTATGTAGGAGTAATTTCAGAGCGATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17463
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022270 | Essential Splice Site | 512 | 1964 | 15 | 24 |
ENSDART00000022270 | Essential Splice Site | 512 | 1964 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 47636784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44834980 |
GRCz11 | 16 | 44801696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGCTGCCCAATCCATTGCTCACATACCAGCTTTACGACAAGTTTGCTG[T/C]AAGTCATTCTGTCTCTAGCAGATATAAGACCARGGGATGATGTACATTTC
Long Flanking Sequence:
GGGTAGCAGCTGGAAGGGCATCTGCTGTGTAAAACACATGCTGGATAAGTTGGCGGTTCATTCCACTCTGGCTACCCCAGATTAATAAAGGGACTAAGCCGAAAAGAAAATGAATAAATGAATGAATAACAGTGTACCACAGGACTTTTTATTAACTAGCATGAACACATACTGTCATAAATGTATTGTTCATGTTAGTTAATGCATGAACTAATAAAACCTTGTTGTAAAGTGTTACCCAAACATTTAAGGTACTGTACAAGTCATGTTTATAATGTAGTGTAGTGTAGTTGATGCTGTTTATATCTGACATATGACAGTGACTTCTGTTCTCTTGAATTTCATCCCGATCAGGCATGAGTTTGACAGTGAAAACGTTCCAGACCTGACAAAAGATGTGTACATGCAGGATATTCACTGCGTCGGCTCGCTCTGCAAACTCTACTTCCGAGAGCTGCCCAATCCATTGCTCACATACCAGCTTTACGACAAGTTTGCTG[T/C]AAGTCATTCTGTCTCTAGCAGATATAAGACCAAGGGATGATGTACATTTCACTTATGAAAACGCATTACAAGAGAAAAGTTTTTCTAAATTGCAATAATAATTCACTCTATTGCTTTTGCTGTATTAATTACTGATTAATATATGCAGCCTAGGCTATGTTTTAAAATGACTAAGCAAACTGTGTCCTTGTCTGTCCAGGAATGTATGGGAGAAATGACGGAGGAAGAGAGAATGGTGAAAGTGCATGATGTTATCCAGCAGCTTCCTCCTCCGCATTACCGGTAAACCCAACACTGGCACTGAGGTGAAACTGCAGAGTGACAGGAAGAGCAGTGTTTTCTGACCATAAGCTGTGTGTTTGTGTCTCTTTCAGCACTTTGGAGTACCTCATCAGACACCTGGCCCATTTGGCCACCTGCAGTGCAGAGACGAACATGCACATAAAGAATCTGGCCATTGTCTGGGCCCCCAATCTGCTCAGGTAACTCCTATGTCTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12075
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022270 | Nonsense | 626 | 1964 | 19 | 24 |
ENSDART00000022270 | Nonsense | 626 | 1964 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 47628728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44826924 |
GRCz11 | 16 | 44793640 |
KASP Assay ID:
2261-0258.1 (used for ordering genotyping assays)
KASP Sequence:
GGAYCWGAATCTAAATCTTTTTCTTGCATTYGTTTTCTRACTTGACAGCA[C/T]GACAGTCCCTGACCAGGCCCAAGTCGTTTGTATCCACCAGGCTCCTGTCT
Long Flanking Sequence:
CTAGCCATGCAACTTTAATTTCAGATGTTGCATTTGGAAGTGTGTCAAATCATAATGTAAATAGAATTATGTAATAAGTTTTCTTAATATTGCCACAAGAGGCTCTTTGAGTTGCATTACAGTACCTGAATTGACATGGTATTGAAGAATGCAGCTCTCACTAAGCCCTTGCAAACATATTAATGTACGATGGTGTACTTGTGTAGAGTTTTTGTTACCTTAAGATTTTGTGAACCTGTCATCTGTTGACCAGCAATTGAATTTCTTCAACGAGCTTGTTGCAAGTACGAGCTTGTATGTAGACGTCTAAAGCTTTAAAGGAGCAGATGTTGTTGTTTTTATGCTTGGGTGTCTTGTCAGTTGCCATGTGTCATGTTAAATTGATTATATTTGTTGATGATCGCTGTGCTCTTTGCTCTGCATTTACTCGCTTTTATCCTTTGGCTTCATGGATCTGAATCTAAATCTTTTTCTTGCATTTGTTTTCTGACTTGACAGCA[C/T]GACAGTCCCTGACCAGGCCCAAGTCGTTTGTATCCACCAGGCTCCTGTCTCTGGAGGAGGCGCAGGCTCGCACACAAGCTCCCCTTCTCCTTCAGGGATCTCCTCACCATGCTATTGGCCAGTTCCACACTGTACTGGACCTGCCTGTCGACAAGTGGGTCTATTGTTTGATTGGTCACGCTTTACAATAAGGTTTTATTAGTTAATTATTTACTAACATAATTAACAACATTTATGGATCATTTATTAATCAAGTTCAATATTTAGTGCATTATTAACATCCAAATTCAAGCTTGGTAACATTCTTTTGATTGATGATATGGTAAAAAAAACTTGTTTCTATTAGAAGGAAAAGAGGGATGAAGGTGCGGAAGTCAGCGGGTGGAAGCTGGAAGACATTTTTTGCCATTGGGAAACCTGGGGCTGTAGGTCGACGCAAACCCGCCAGGATCACCTCTCTATTTCAGCCCACTACCTCTCATGCAGGTAAACCAGACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19150
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022270 | Nonsense | 626 | 1964 | 19 | 24 |
ENSDART00000022270 | Nonsense | 626 | 1964 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 47628728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44826924 |
GRCz11 | 16 | 44793640 |
KASP Assay ID:
2261-0258.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCTGAATCTAAATCTTTTTCTTGCATTTGTTTTCTGACTTGACAGCA[C/T]GACAGTCCCTGACCAGGCCCAAGTCGTTTGTATCCACCAGGCTCCTGTCT
Long Flanking Sequence:
CTAGCCATGCAACTTTAATTTCAGATGTTGCATTTGGAAGTGTGTCAAATCATAATGTAAATAGAATTATGTAATAAGTTTTCTTAATATTGCCACAAGAGGCTCTTTGAGTTGCATTACAGTACCTGAATTGACATGGTATTGAAGAATGCAGCTCTCACTAAGCCCTTGCAAACATATTAATGTACGATGGTGTACTTGTGTAGAGTTTTTGTTACCTTAAGATTTTGTGAACCTGTCATCTGTTGACCAGCAATTGAATTTCTTCAACGAGCTTGTTGCAAGTACGAGCTTGTATGTAGACGTCTAAAGCTTTAAAGGAGCAGATGTTGTTGTTTTTATGCTTGGGTGTCTTGTCAGTTGCCATGTGTCATGTTAAATTGATTATATTTGTTGATGATCGCTGTGCTCTTTGCTCTGCATTTACTCGCTTTTATCCTTTGGCTTCATGGATCTGAATCTAAATCTTTTTCTTGCATTTGTTTTCTGACTTGACAGCA[C/T]GACAGTCCCTGACCAGGCCCAAGTCGTTTGTATCCACCAGGCTCCTGTCTCTGGAGGAGGCGCAGGCTCGCACACAAGCTCCCCTTCTCCTTCAGGGATCTCCTCACCATGCTATTGGCCAGTTCCACACTGTACTGGACCTGCCTGTCGACAAGTGGGTCTATTGTTTGATTGGTCACGCTTTACAATAAGGTTTTATTAGTTAATTATTTACTAACATAATTAACAACATTTATGGATCATTTATTAATCAAGTTCAATATTTAGTGCATTATTAACATCCAAATTCAAGCTTGGTAACATTCTTTTGATTGATGATATGGTAAAAAAAACTTGTTTCTATTAGAAGGAAAAGAGGGATGAAGGTGCGGAAGTCAGCGGGTGGAAGCTGGAAGACATTTTTTGCCATTGGGAAACCTGGGGCTGTAGGTCGACGCAAACCCGCCAGGATCACCTCTCTATTTCAGCCCACTACCTCTCATGCAGGTAAACCAGACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19149
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022270 | Nonsense | 692 | 1964 | 20 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 47628336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44826532 |
GRCz11 | 16 | 44793248 |
KASP Assay ID:
2261-0257.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAGAAGGAAAAGAGGGATGAAGGTGCGGAAGTCAGCGGGTGGAAGCTG[G/A]AAGACATTTTTTGCCATTGGGAAACCTGGGGCTGTAGGTCGACGCAAACC
Long Flanking Sequence:
GTTGATGATCGCTGTGCTCTTTGCTCTGCATTTACTCGCTTTTATCCTTTGGCTTCATGGATCTGAATCTAAATCTTTTTCTTGCATTTGTTTTCTGACTTGACAGCACGACAGTCCCTGACCAGGCCCAAGTCGTTTGTATCCACCAGGCTCCTGTCTCTGGAGGAGGCGCAGGCTCGCACACAAGCTCCCCTTCTCCTTCAGGGATCTCCTCACCATGCTATTGGCCAGTTCCACACTGTACTGGACCTGCCTGTCGACAAGTGGGTCTATTGTTTGATTGGTCACGCTTTACAATAAGGTTTTATTAGTTAATTATTTACTAACATAATTAACAACATTTATGGATCATTTATTAATCAAGTTCAATATTTAGTGCATTATTAACATCCAAATTCAAGCTTGGTAACATTCTTTTGATTGATGATATGGTAAAAAAAACTTGTTTCTATTAGAAGGAAAAGAGGGATGAAGGTGCGGAAGTCAGCGGGTGGAAGCTG[G/A]AAGACATTTTTTGCCATTGGGAAACCTGGGGCTGTAGGTCGACGCAAACCCGCCAGGATCACCTCTCTATTTCAGCCCACTACCTCTCATGCAGGTAAACCAGACATTTCACTCGTTATGTATATTCATAAATATATGTTTAAGTTATTGTACGATTTGCACGTCATATTGAAAGAAGATGATTTTTAGAGCTTTATGTGTACTTTAGGTTGCAGGGTGGACAGTGTGACGCTCAGGTCTGCGAAAAGTGAGGAGTCGCTGTCCTCTCAGCACAGTGGAGCAGGTTTGAAGGACATCTGGACACTTTAATGTCTTAGGGTGCTTTCACACCTACACTTTTGTTTCGGAACGTATCTCGTTTGCCCAGTTAGCGCGGTTCGTTTGGCATATGTGAACAGGGTAATCGCTCCGAGATCGCTTGAATGAGGTGGTCTCGGCTCGATTGAAACGAACCCTGGAGCGGATCGATTGCAGTGAGAAAGCGATCCGATCCGAGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36244
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022270 | Nonsense | 825 | 1964 | 22 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 47626215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44824411 |
GRCz11 | 16 | 44791127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAAGACGAAGAGGATGAGGAGGGTGTGTACATGCTGCCTGATTTCTCC[C/T]AGGAACCACCCTCTTCATGGATAACGGAGGATGTCATTGACTTTAGCCCA
Long Flanking Sequence:
GTTAGCATATACCTTCTCTGTGAATATATATTTTGGGTTTTAACTGCAAATGTCACATAACGCTGGATATATATATATATATATATATATATATATATATATATATATATATATAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGATTGGCTTAGACTGACAGTGTAAGAAGTACTTATTAAATGCAAACTTTTAAATGCCAGTAGATTTGTCGATGCAAAAATACTGGATATATATAATTAAGGTAAAACTAATGTGCATGTTTTCCCCTCAGGTCAAGGCAAGATTCAGCGGTTACGGAGACCTCGCTCCAGCAGTGACGGTCTCTCTCTGGCTGCCTCTGTGGATCCGCAGCTCCTTCCCCAAAACTCCCCATCCAAAATCCACCCGAGCCGCTCCTACGACAGCCTGCTGCCAGAGGAGACCCGTGATGCTGATGAGGAAGAGGAAAACGAAGACGAAGAGGATGAGGAGGGTGTGTACATGCTGCCTGATTTCTCC[C/T]AGGAACCACCCTCTTCATGGATAACGGAGGATGTCATTGACTTTAGCCCAACCTTTCTGGAAGATGGGCCAATAGGGTTGGGGGGCACAGGCGGAGCTCCAAGTGGTAGAGAGTCTCCTCCTGCGGCCGCACCCCCTCCATACCGCTGTCTGAGCCATCAGGGCCACCATGCCCGCTCTGGAAGCCAGCGCTCGATCACTGAAGATCCAGACTCTGTTCTTAACCAGTCTGAAGCCGCAGCCCGCAGGAGTTTGATCCTGGCTGCAGCAGCTCCGCCTCAGCAAGTGTTCTGCCAGCACAGGCCGTCTAATGCCCCTGCAAACACAACCCAGTCGGGCGAGTCAAATTTAAGCCCGTCCCATGCCCAGACGCCAGCTCCAGCAACCTCTGCACCCCCTTCTCAGCCCCCTCAGGAAAGGCGCTCCTTTACACGTAAAGTGGTTCATGCACTTTCACCAAAAGCGCCAAAATCTCCTCCTCTGGACATCTCGGATCCCATC
Associated Phenotype:
Not determined