ZMP
mgam
Ensembl ID:
Human Orthologues:
MGAM, RP11-1220K2.2, SI
Human Descriptions:
Putative maltase-glucoamylase-like protein FLJ16351 [Source:UniProtKB/Swiss-Prot;Acc:Q6ZN80]
maltase-glucoamylase (alpha-glucosidase) [Source:HGNC Symbol;Acc:7043]
sucrase-isomaltase (alpha-glucosidase) [Source:HGNC Symbol;Acc:10856]
maltase-glucoamylase (alpha-glucosidase) [Source:HGNC Symbol;Acc:7043]
sucrase-isomaltase (alpha-glucosidase) [Source:HGNC Symbol;Acc:10856]
Mouse Orthologues:
Mgam, Sis
Mouse Descriptions:
maltase-glucoamylase Gene [Source:MGI Symbol;Acc:MGI:1203495]
sucrase isomaltase (alpha-glucosidase) Gene [Source:MGI Symbol;Acc:MGI:1917233]
sucrase isomaltase (alpha-glucosidase) Gene [Source:MGI Symbol;Acc:MGI:1917233]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13756 | Essential Splice Site | Available for shipment | Available now |
sa32180 | Nonsense | Available for shipment | Available now |
sa23206 | Essential Splice Site | Available for shipment | Available now |
sa15292 | Nonsense | Available for shipment | Available now |
sa15546 | Essential Splice Site | Available for shipment | Available now |
sa28958 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32181 | Essential Splice Site | Available for shipment | Available now |
sa36557 | Essential Splice Site | Available for shipment | Available now |
sa11174 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13756
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110351 | Essential Splice Site | 71 | 1809 | 3 | 52 |
Genomic Location (Zv9):
Chromosome 18 (position 2822402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2212069 |
GRCz11 | 18 | 1769819 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACACAGACACCCAACATGCTTTTCTGAACATTCCTYGTGTCTCCTTACA[G/T]CAAAAATGTTTGGAAAGAGCCTGTTGCTGGAGCCCCCTGGATGAGACCAA
Long Flanking Sequence:
TTTGTCATTAGCCCTAAATAAGGGGGGACTTTTCAGATTTGCCTAAGCTCAAACTCCCCTCTCGCCCTGCAAATGGGAGGGAGCCCCAGACTCGAGGATCTTATGTGTGAGAACTCAGGGCTCTCACACGGGACAGCATGTCAAACACACTTTATAATCAATCATCAGCTAAGTGTAAACTCTTGAAACAAATAAAAGTAGCCTTGTCCAGAGTAAAACTTTGTTTGTTGTTGTTTGGAATTACTTATGAATCTTATAAGTCTTTATCAAAATGTCCATCTGCTAACTGTCCCCAAACTAAATGTTAATATAATGTAAATGTTTTTTAGATTCAGGATCCGATCCAGACATCGTCCCAGAATGTCCTGACATTCCTCTAACAGACAGAGTGGACTGTTTTCCCGACGGCGGTGCATCTCAGGTACACAGCGCTGAACATCTCCTACACTACACACAGACACCCAACATGCTTTTCTGAACATTCCTTGTGTCTCCTTACA[G/T]CAAAAATGTTTGGAAAGAGCCTGTTGCTGGAGCCCCCTGGATGAGACCAACGTCCCCTGGTGCTTCTTTTCCAAAAATCACGGCTACACCGCGGACCGCGTAAGCAATCCTGACAGCACACGTGAGTACTGCAATGAGACTTGCTGTAATAAAATAGTATGATGCAGTTTATATCACTGGGCTTCAGATAAGTCTCTCTTGTCATGAGCCAGTTATTGTGAGATTATTTTAATGTTGGCATATCAGATTTCACTAATCAGCAAGGTTAAATCAGCTAACACTCTCTCTTCTTCACTATTTCTGTCACTTTTACATGTGGTGTGAAACACATTCCAGAGCTTTTGGTAGTAAACAAAAGTACATTCATTTGCATAAACATGGCTTGCTGAAGCAGCAGTACTATTACTTATGCTCATGATAAATGTTATGGATGAAATAACCCTTATAAGCTCTTTATGAAATCTTATGTAAATGTTTGTGTTGCGGACATAAATGATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32180
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110351 | Nonsense | 164 | 1809 | 5 | 52 |
Genomic Location (Zv9):
Chromosome 18 (position 2825241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2214908 |
GRCz11 | 18 | 1772658 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCACTGATGCAAAGCAAGCCAGGTTTGAAGTTCCTCATGAAAACGTG[A/T]AAGCCCCTGCCAACCCTCCCACCGGACCCTTAAAATACAAAGTAGAGATC
Long Flanking Sequence:
ACTGTGGACATACTATACCTACACACAGTTCTGTCCAAACAGCTTACAAAAGATGAATTTCATCGTAGGTGCCCTTTAATAATGGGCAGGTAATAAGCCAGTAGTTGATTAAATGAACTGTGACTAAAGTGTTTCCAAGCTGTAGCTTTTTCACTTTAAACTTTTAATAAATGTACAGTACTCTATGGGAAGTACAGTAAAGCTGACAATTCACTAAAATGTTGTGAAAAAATGCTTGTTTTTGTTTAGATATCGAGGCCAAGCTGACAAGAATGAATGCTCCTTCTCTGTTTGGAGCTGATATTAAGGATTTGACCTTCCACGGTGAAATGCAGACAGAAAACCGCTTTCGATTTAAGGTCTGTTTACGAACTGACCCAATAGCCACGATGTCATGTATGTAATGGGTAAACATGTATATAATGGTGTGCGATGTATTTTTGGTTTACCAGATCACTGATGCAAAGCAAGCCAGGTTTGAAGTTCCTCATGAAAACGTG[A/T]AAGCCCCTGCCAACCCTCCCACCGGACCCTTAAAATACAAAGTAGAGATCGTCCAGAAGCCCTTTGGAGTGAAAATCTGGAGAACAACACCAGAAAAACTCCTGTGAGTGCCGAGTTTTTCGTCTCTCTCATTTCCTTTTCAAATGCAGATCATATGTTGACTCTTTGCGTATTGCTAACAATGCAGCACGGAATCATTTCAGAGGGTTTCTTTGACTAAATGAAAAATCACAACAACAGCGAGAAGACTAAAATTAAAGGCATGAAAGAATCCGGAGAGAGAGAAAGAGAGCCTGAAGCAATGCAAACAAGGTTTTTTTTGTAAAGTCTCGACGTCTACATGCTGTGGATGGAAATTGGTTTGTTTCCTTTAGTTGTTGTCTGCCTTTGTGCCCAGGTTTTTTGTGTACTTAGAAAATAGACAGGCAGGTATAAGGTTAGTTATAAGTCTTAGTTCTTACACATTGTATTTGATCTAGGCAGCCTGTATAAGATTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23206
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110351 | Essential Splice Site | 255 | 1809 | 6 | 52 |
Genomic Location (Zv9):
Chromosome 18 (position 2828868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2218535 |
GRCz11 | 18 | 1776285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAACTGGAGGACCTGGCCTATCTTCACAAGAGACTCTTTCCCCAACGGC[G/A]TGAGTCTTAACATTTAGATCATGTATATCAGAGTATTCCAAACCAACATA
Long Flanking Sequence:
CAATGAACAATACAGTATTTATTTAACTTTGTTAGCGTTAGATAATGGAAATAAAGTTGTTCATGGTTAATTCAAGATAACTCACAGTGCATTAACCATTGTTAACAAGCACAACTTTGGCATTGAATAACAAGTAATAAGATAAGTGAATGTTGAACTATGAGTAATTAATGCTGTGTAAGCTTTGTTCATTATTAGTTCATGTTAGTAAATACATTAACTAATGGACCATTACTTTAAAGTGTGAACATTTTCTTTAACATAAAATAATACCTGTCAGCTGAAATATATATAGGGACATTAAGATCTTCTTGTCTTGGTGCGTCAGGTTTGACACCACCATTGGGCCACTGGTTTTTGCTGATCAGTACCTTCAGCTCTCAGCTAAACTCCCCTCTCACAATATTTATGGCCTCGGAGAGCACGTCCATCAGACCTTCCGTCATGACACCAACTGGAGGACCTGGCCTATCTTCACAAGAGACTCTTTCCCCAACGGC[G/A]TGAGTCTTAACATTTAGATCATGTATATCAGAGTATTCCAAACCAACATACAAATCGCCAGTGAAATCTGGATCTCAAAAAAAAAAAAAAAACATTTGCAATCAGGGCAATCAGTCAATGTTTTTTTGTGGTCCAGATTTCACTGGTAATTTGTATATTGGTTTGGGATTCTAATCAATGAGTCAATCAGTCATCAGTTAATTAATTTTATATTATTATTATTATTATAATTATTATTATTATTATTAATATTATTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNACACACACATATATATATATATTTTTTTCTTTTATATATATATATATATATATACATGCCCTCTTTCTGTCACTATGCGAGATATATATATATATATATATATATATATATATATATATATATATATACCCCCCCCCCCTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15292
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110351 | Nonsense | 427 | 1809 | 11 | 52 |
Genomic Location (Zv9):
Chromosome 18 (position 2841689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2231356 |
GRCz11 | 18 | 1789106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATTACAGGATCCTGCCGTATCCACAGGGCGCAGGWTAAACGGACCGTA[T/G]GACACAGTYGACAGGGGACATGCAGCTAAAGTTTGGGTCACTGAATCAGA
Long Flanking Sequence:
TCAATCATAACTTTCTCTGTTTCAGCAAATGGGATGATATTTGGTGAACTTATTTTGACACATAATTTAGGAAAATGCTTTGAAAATTTTCAAAAATTCAACAATACACTCAAATTGACTACCCTTTCTTTGTGTTCGGGGCTGTTTTTGCCCCATTGACGTTCATTATAATGAGATTTTTTGATTACAATGCATGACATCTTATAATCATGCCTTCTTGATTGTAGCTGGTTCATGGCTCCGCAAACAAAAAATGTCATTTTAAGTCAATGGGGCTAAAACAGCCCTGAACATAATGTAAGAGTAGTCAATCTGAATAATACACAAGGTTTAATAGGTTGACCAGTCACTTCTTATTTTTGGACAGTTGCAAATGTTGAGTCATTTAGCTGAATATGATTTTATTTGAGGGTATTTAGCTGTTTTGTTGAGCATCTCTACATATTTTCTTCATTACAGGATCCTGCCGTATCCACAGGGCGCAGGTTAAACGGACCGTA[T/G]GACACAGTCGACAGGGGACATGCAGCTAAAGTTTGGGTCACTGAATCAGATGGTGAAACGCCTCTAGTGGGAGAGGTAAAAATCATCCTTTATATCTACTTCTGATCGTGACATTTTGTTGGATTTTATTTGTTTTTGTTGGTTAACTGACCCCAAAAAATACCTAAATGATTCACATGACCATTGGTTTCGATAGTTGTAGTAATGTGTTCTGTTGACATATCTTTGTATTGTGCGACAAGAAAAGTAGCTGAGCAGTCTGATCTGGATTCACATGGTTAATTTATTATTCTAAATTGGCAAAAATATATATTTCCTAATCAATACATATTAAATCAAACATTTTAAATGTTAAATTGATTTGAGACATTAAAAGTATTTATAATGCTACATTTGAGAATAATGGTTTACACAAAATGAATCAGTTTTGAAATAATGTAATAATAAAATAATAATAATAATAATAATAATAATTATTATTATTATTATTATTATTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15546
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110351 | Essential Splice Site | 615 | 1809 | 15 | 52 |
Genomic Location (Zv9):
Chromosome 18 (position 2847923)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2030679 |
GRCz11 | 18 | 1839611 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGGGCGATACCTGGCAWGCTGGAGTTTAACCTCTTTGGCATCCCTTAC[G/A]TAAGTGCTTTGACTTTNAATCCTTTACACTGCAYACGTAAAGAGACATTMG
Long Flanking Sequence:
GGCCGGATGTTTTCCTCAAAGGGGCTTGAATAGATCTCAATTGTATCATGCTTGCTCCTTCTTGCTGCTTTTATTTTCAGCAGGAAATCTGTTTTACTCATCTTGTAATTTCTACATCATTGATTTGTTCCACTCTCGTTTCTCTATACGCCCCCTTTCTCGTTCAGCTCAACTCCCACTTAACTCCAGCTTGTGTGTTTGTCATTTCTCTGTTTTTCTGGGCCACCCTACTTGGCATCGTGTCTTTCCAAAGCCTCCCTCGTGTGGATTTTATCATCGTGCCAGCAATGCAATTTTGTGATTATTATTTTTTTTTTTTTGCTTCTAGGGCATCGAAAGAAGTGTTTGGGACCAACCGATCCATGGTCTTCACCCGCTCTTCATTCCCCGGTGTGGGCAAATATTCTGGGCATTGGTTGGGAGACAACGGCGCCAACTGGAATGACATTAAGTGGGCGATACCTGGCATGCTGGAGTTTAACCTCTTTGGCATCCCTTAC[G/A]TAAGTGCTTTGACTTTAATCCTTTACACTGCACACGTAAAGAGACATTCGTTCAATTTGATTTAATTTAAATAGTGTTACCTATGCTAGGGCTGCATGATATTAGATAAATCTGACATTGTGCTATTTTATTTTGCTGCTATTTACATTGCGATATGAACACAATATTGGCAGATGACTTGAATAGCTCTATCTGGAATGAAATCATTAACTTAGATTGGAATAATCTTATAGACGAGTGAATCAAAGAAATCACAAGAATAAATAAGATAAAAATAAAAGTGATACAGCAACACGATACGATATTATCACGATATTTTGCCCCCGATAATAATAGATAACAATAACAGAGATATACACAAGAAAACCCTCCACAATATGCATCAAAAAGTTTTAAGATGTATTTATTTTATTAACAGCGCATATTTTTCGTAGAATTGCAACATTGATATATGTTTGATCCTCCATTACGAGAAGCGTCACCTCATGCATATCACTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28958
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110351 | Essential Splice Site | 896 | 1809 | 26 | 52 |
Genomic Location (Zv9):
Chromosome 18 (position 2878014)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2060770 |
GRCz11 | 18 | 1869702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTAACCCTTTGCCTCAGTCACAGATTCAATACGACTCTGTCAAGCAGG[T/C]AAAAGCATTTATTCACCACTAAAGTCAAAAGTAATACTATGTGTCCGGTT
Long Flanking Sequence:
AATGTGAGCAAAACATTTATTTTATCTTTATTGTTGAGCCACATAATAGGCCTCTGTAAACTTAATTATTTCATTTAAACAGGTTTCTAACATAAATTGTGTTACTCATGCTTAAATATGTCTTTTTCTTTTTCCTTTTAGATACTGTTTCATCTGGAAATCACATTCATTACCAGTTTTCAGTGACTGATGTATGTCATCCTAACATCACATTTATTTTTGTGATGACACATCATAAAAACCTATTACAATTGTAATATATGCATTTATCAAAATATCTTTATGTTATAATATAATATATAATATCTATATATTTTCTTTGCAGGGCTCCTTGACAATGCATGTCACAAAGAATGGATACTCAGATCCAAACAACCTGAAGTTTGAGAACATCACAATTTTGGGATTCAGCTCTGCTCCACCTTTTGTGCTGGTGTCAGACGGGACCACTAGTAACCCTTTGCCTCAGTCACAGATTCAATACGACTCTGTCAAGCAGG[T/C]AAAAGCATTTATTCACCACTAAAGTCAAAAGTAATACTATGTGTCCGGTTTTGCTTATAGCAATTGAAGTAGGAGATTCAATACTGTTAAGGTCAGAATTACTAGCCCACCTTTGAATTATTTTTTTCTTTTTTAAATATTTCCAAAATGATGAGTAAAACAGCAAGGAAATGTTCACAGTATGTTTGATAATATTTTTTTCTTCTGGAGAAAGTCTTATTTGGTTTATTTCGAGTAGAGTAAAAGCAGTTTTAAATTTTTTAAACACCATTTTAAGGACAAAATATTAGCTTCTTTAAGCTATTTCCGATAGTGTACAGAACAAACCATTGTTATACAATAACTTGCATTTAGGATGTGTGTAAACGTAACATTCTGTAGTGCATTTAGTGATTGCCCAGCAGGCACACAACGTTATAAAACATTAATATTAGGTTAGATTTAGGTCGAGATAATAAACAGGGGTCGAAAAATTTAGGGGGGCTAATAATTCTGACTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32181
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110351 | Essential Splice Site | 1406 | 1809 | 41 | 52 |
Genomic Location (Zv9):
Chromosome 18 (position 2911155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2093911 |
GRCz11 | 18 | 1902843 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGAGAATACCAAACAGCCATGTAATAATATTGAATATATTGTCATTTTC[A/T]GCACTGGAGTCCAAGGAAAAAGGTCTGAACCATAAGACTTTATGCATGAA
Long Flanking Sequence:
AAATGTAAAGCTGACAGAGATGAAAACAGCTGATGGAGTATACACTAACCTGCCCATTATTTGGACACTAGATTGCGTCAAACAGTCAAAGCGTAAAGTTGACAGAAACAAAAACAGCTGATCGAGTAAACACTAACCTGTGCATTATTCAGTCACAAGATGGCACCAAACAGCCAAAAACACAAAGCTGACAGAGACAAAAACAGCTGTTGTAGTATACACTAACCTGCGCAATATGCAGACACAAGATGGCGCCAAGCGGTCAAAAAGTACAGCTAATAGAGATGAAAACAGCTGATGGAGTATACACTAACCTGCACATTATTCAGTCAAAAACAGTTAAAAACTGCAGGGTCAAGGTGATTTGAAGTTCCTGGATGAACTTGTGTTATTTAGCGGTTGTTATCTCAGAATAACATACCTTGAGATGTCACAACTGACCAATCAGAATCGAGAATACCAAACAGCCATGTAATAATATTGAATATATTGTCATTTTC[A/T]GCACTGGAGTCCAAGGAAAAAGGTCTGAACCATAAGACTTTATGCATGAACAGCGAGCAGATCCTTGCTGATGGCACGCGCGTCAGACATTATGACGTTCACAACTTGTACGGCTTATCTCACACCAAACCCACCTACGAGTAAGTTCCTCCACATTTACTATGCATTTATATCCAGATTGTTCTGGAATGGGTTGTAATTGCTGTGTTTGTTTACGTGTTCGTCACAGTGCTTTGCATAGTACCACCGGAAAGAGAGGAGTTATAATTACCCGCTCAACATACCCAACGAGTGGACGCTGGGCTGGACATTGGCTGGGAGACAACTACTCTGCCTGGGACCAGCTCCTCAAGTCCATCATAGGTTTGTGGTTATTTATTATATGGAAAAAAATAAGCGCCACAAAGGCTCAGATTTTAGGTTAAAATTTACAATAATAAGAACCATAGTTTCAATACTAGAGATCAAAGCTCTATTAAATTAAATTAATCACAACTAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36557
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110351 | Essential Splice Site | 1452 | 1809 | 42 | 52 |
Genomic Location (Zv9):
Chromosome 18 (position 2911383)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2094139 |
GRCz11 | 18 | 1903071 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTTCTGGAATGGGTTGTAATTGCTGTGTTTGTTTACGTGTTCGTCAC[A/T]GTGCTTTGCATAGTACCACCGGAAAGAGAGGAGTTATAATTACCCGCTCA
Long Flanking Sequence:
GCGCAATATGCAGACACAAGATGGCGCCAAGCGGTCAAAAAGTACAGCTAATAGAGATGAAAACAGCTGATGGAGTATACACTAACCTGCACATTATTCAGTCAAAAACAGTTAAAAACTGCAGGGTCAAGGTGATTTGAAGTTCCTGGATGAACTTGTGTTATTTAGCGGTTGTTATCTCAGAATAACATACCTTGAGATGTCACAACTGACCAATCAGAATCGAGAATACCAAACAGCCATGTAATAATATTGAATATATTGTCATTTTCAGCACTGGAGTCCAAGGAAAAAGGTCTGAACCATAAGACTTTATGCATGAACAGCGAGCAGATCCTTGCTGATGGCACGCGCGTCAGACATTATGACGTTCACAACTTGTACGGCTTATCTCACACCAAACCCACCTACGAGTAAGTTCCTCCACATTTACTATGCATTTATATCCAGATTGTTCTGGAATGGGTTGTAATTGCTGTGTTTGTTTACGTGTTCGTCAC[A/T]GTGCTTTGCATAGTACCACCGGAAAGAGAGGAGTTATAATTACCCGCTCAACATACCCAACGAGTGGACGCTGGGCTGGACATTGGCTGGGAGACAACTACTCTGCCTGGGACCAGCTCCTCAAGTCCATCATAGGTTTGTGGTTATTTATTATATGGAAAAAAATAAGCGCCACAAAGGCTCAGATTTTAGGTTAAAATTTACAATAATAAGAACCATAGTTTCAATACTAGAGATCAAAGCTCTATTAAATTAAATTAATCACAACTAGGGCTGCACGATATTGGAAAAATCTCACTTTGCAATATTTGTTTTACTGAAATATATATTGCGATTTGAATATAATTTAAGCAGATAATTAGAATAGCTACAGTTGAAGTCATAATTATTAGCCCCCCTGAATTATTAGACCCCCTGTTTATTTTTTCCCCTATTTCTGTTTAACAGAGAGCATATTTTTTTTCAACACATTTCTAAATATAATAGTTTGAATAACTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11174
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110351 | Nonsense | 1577 | 1809 | 45 | 52 |
Genomic Location (Zv9):
Chromosome 18 (position 2924859)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2107615 |
GRCz11 | 18 | 1916547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTCTCGTGAYGTGCTGAATATCCGCTACMCCCTCYTGCCATACTTGTA[C/A]ACMCTGATGTRTGAAGCCMACACCAAGGGGACCACTGTGGTCAGACCAAT
Long Flanking Sequence:
TTATTGGTGTCCATGTAAACATACTCGCATCAGCGTACGTTAATCGCAACGAATGCCTTAAATGAAACTAATATTTGAAATTTGGAAAAAAAAAAATGTGATAATACTTTTATAGAAAAGAACGAATATTAAAAATTTACTGAAAGCCAAAAAACTCTTAATTTTTATATTTAAATTTAATTTAATATATTTTTTATTTAATATATTTACATTTTTTAATTTTTTATTTAAATCTTTATTTAATCTTAATTTAAATCCCAAGTATTCCTATATATTAAGTGCACTCGTAAAGAATCTTTTAGCAGTGCCCTTGCAATGCCCCAAACGCATGAGAATGTATTGAGATTATTTTCATAAATATTGCTGAATGATTTATATCTGATGAGTTTTTGTGATTTGTTTTTTCTACAGAGACAAGACCCAGTGGCCTGGGGACCAGAGTTTGCCAATATGTCTCGTGATGTGCTGAATATCCGCTACACCCTCCTGCCATACTTGTA[C/A]ACCCTGATGTATGAAGCCCACACCAAGGGGACCACTGTGGTCAGACCAATGCTGCACGAGTGAGTGTCAATACTCAATACTTATATACTTACAGCAAATTTACGCAGCAGATACCCTTCCAGCTGTAACCCATCACTGGGAAACACCCATACAGTCATTCACACACACACACACACACTACGAACAATTTAGCTTACCCAATTCCCCTATACCACATGTTTTTGGACTTTGGGGGAAACCGTAGCACCCGGAGGAAACCCACGCCAACACCAGGAGAACATGCAAACTCCACACAGAAATGCCAACAGACCAAGCCAGCAACCTTCTTGCTGTGAGGCAATTGTGCTACCCACTGTGCCACTGTGCTGCATTTTAATCAATAAACCTAGTTAAATTTGCATATAACAAACATTCTATTAACATTAGTTGAACAACATTTTGATTTTAGCTGAGCGAATGTTCGATTAGCCACCAAAATATAAACTAGAAGTAAACGATCT
Associated Phenotype:
Not determined