ZMP
ITGAE
Ensembl ID:
Description:
integrin, alpha E (antigen CD103, human mucosal lymphocyte antigen 1; alpha polypeptide) [Source:HGN
Human Orthologue:
ITGAE
Human Description:
integrin, alpha E (antigen CD103, human mucosal lymphocyte antigen 1; alpha polypeptide) [Source:HGN
Mouse Orthologue:
Itgae
Mouse Description:
integrin alpha E, epithelial-associated Gene [Source:MGI Symbol;Acc:MGI:1298377]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35847 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16148 | Nonsense | Available for shipment | Available now |
sa42515 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22611 | Nonsense | Available for shipment | Available now |
sa35846 | Essential Splice Site | Available for shipment | Available now |
sa35845 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30990 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12794 | Nonsense | Available for shipment | Available now |
sa22610 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35847
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080523 | Essential Splice Site | 10 | 1266 | 2 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 16232399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17277362 |
GRCz11 | 15 | 17213384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAATAACTTCGTTCTGAGTAGTGTTTCCACTCATTATTTGGTGTTTTAC[A/T]GTACTGTGTAATGCAGCTGGGTTTAACATTCAAATATCTCCAGTGAAACA
Long Flanking Sequence:
AATTACTTTTTACATTTGGGTGAACTATTCCCAGGGCTCCTATTTCAGAACTGATACAGTTTTTGAAAATAAAGATGTTTTAAAATTCAGAATAATAATCTACTTACTCTGGGTTCAGCTTTACACAAGAGAAAATATGCAGTGTCTGCAGTTTGTGAAGGGGGAGGGTTTGACAGTCAGCAGTAAATGAGTGCTGTTCTGCTTTCTCAAGACCAAAACAAGCTGCTTTGTATCTCGATGTGTCAATGTGTTTTCTTTAAAGAAAATTGATATTGATCAATCTACACAAAAATGTACAGAAAACTGCTATTTGTGATGGGTATGTATTGATTTACAGTGTTAAATATACTGTATATTTGTGTTTATAATATTGTTTGAAAACATGTTGCGCTTGTTTTAAACTCAAGCAAAAGATAAAAAAAATTAAAATCATAATGAATTCAATTTATCTTAATAACTTCGTTCTGAGTAGTGTTTCCACTCATTATTTGGTGTTTTAC[A/T]GTACTGTGTAATGCAGCTGGGTTTAACATTCAAATATCTCCAGTGAAACATTTCACAAATGAGGATCCACTCTTTGGCCAAACCATCATTCAGGCAAAAGATGGGTTGGTAATTCTAAACATATAATTTTTTATTTAATTTTATTTTAGATGTGTTCTGTAACATGTTACTGCTTTGTTCTGTTCTAGAATTTTTGTTCCCTCCCCAACATATGGAAGACTTTTCAAGTGCACTCTAGACAATGAATGCACCAAAGTAAACATTAACGGTAAGTTTATCTTTGCCTTTTTTTTTTATAACAGATCATTTGCAGAAATATAATGTTATTTTTTTAATATAATGTTATTACTTATTTACAGAATTAAAGAGATGTTTCAAAAAAAAAATTTAATTACCTCATCATTTACTCACACTCAGTTGGTTCTAAACAGTTTTCAATTCTTCTGCTGAACACAATTAAAGATATACTAAAGAATGTTGAAAAAACTGCTGTGGATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16148
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080523 | Nonsense | 189 | 1266 | 7 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 16229641)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17274604 |
GRCz11 | 15 | 17210626 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAYTTTCAGAAAGCGAAAGACTTCATCTACAATGTCATGTCCAATGTTT[G/A]GAAAACATGTTTCGATGCAAGTATAAAGAAAAAAAAANNNTCATGGCACAAAA
Long Flanking Sequence:
ATGTGTAATCAAGTTAGAACAGAGAACAGAGGAACTGAGTATTTGAATGGAATTTGCACACTTGTGAGTCCTTCTGGAAAAGTCAAACTATATCCTGCTGAATTAGGTATGTTTGGTGCATTTACTATGGGGTCTTCACATTCAACCAGATAAAATCTTATACCTGAAATTCCTAAATCTCTTTTTTCAAGACAACAACAAAAACAACAACAACAACAACAACAACAACAACAACAAATACCAAGGTGGAAGGATCAATCAAGGTGAGACTGTCTTAAGGAAAATGTAGATAGTGTTGAATTTATTTATAATGCATGATAATTAATAACGTATGGAGGGAAAAAACATAAAATGTGCCAGAATAAGCCAGGATGGCTAATTTACATCTTTCTTAGGTCCTGGGACAGAGATTGCTTTCGTTCTGGATGGTTCTGGCAGCATTCAAGATGATGACTTTCAGAAAGCGAAAGACTTCATCTACAATGTCATGTCCAATGTTT[G/A]GAAAACATGTTTCGATGCAAGTATAAAGAAAAAAAAATCATGGCACAAAATACAATTCAATTGATATTAACTTTACATTAACCCCTCTTCTCTCTGCAGTGTAATTTTGCAATAGTGCAATACGGTAGTTTGATCAGAACTGAGCTCTCGTTACTAGACAATGAGGATCGCGTGGGATCCTTGCTAAAGGTCAAACAAATAAAGCAAATTTACAATCTCACAAAGACGGCCTCTGCCATCAATCACGTCCTGTGAGTCTACAAACAATTTTTACAGCATTTGGAGATGACTTAATGGTGTGATTTTACAATGTTGTGGTTGATTACAGCACAGATATCTTCATCCCTGAGAATGGATCAAAAGATAACTCTGCAAAAATAATAATCGTCTTGTCTGATGGAAAGATTCTGGGAGACCCTATGACTCTTGATGAAGTTTTGAACAAGCCCCAAATGAAAGGTGTCACTCGCTACTCCATAGGGGTAAGTGTCCCATTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42515
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080523 | Nonsense | 254 | 1266 | 9 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 16229287)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17274250 |
GRCz11 | 15 | 17210272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACAATGTTGTGGTTGATTACAGCACAGATATCTTCATCCCTGAGAAT[G/T]GATCAAAAGATAACTCTGCAAAAATAATAATCGTCTTGTCTGATGGAAAG
Long Flanking Sequence:
TGCCAGAATAAGCCAGGATGGCTAATTTACATCTTTCTTAGGTCCTGGGACAGAGATTGCTTTCGTTCTGGATGGTTCTGGCAGCATTCAAGATGATGACTTTCAGAAAGCGAAAGACTTCATCTACAATGTCATGTCCAATGTTTGGAAAACATGTTTCGATGCAAGTATAAAGAAAAAAAAATCATGGCACAAAATACAATTCAATTGATATTAACTTTACATTAACCCCTCTTCTCTCTGCAGTGTAATTTTGCAATAGTGCAATACGGTAGTTTGATCAGAACTGAGCTCTCGTTACTAGACAATGAGGATCGCGTGGGATCCTTGCTAAAGGTCAAACAAATAAAGCAAATTTACAATCTCACAAAGACGGCCTCTGCCATCAATCACGTCCTGTGAGTCTACAAACAATTTTTACAGCATTTGGAGATGACTTAATGGTGTGATTTTACAATGTTGTGGTTGATTACAGCACAGATATCTTCATCCCTGAGAAT[G/T]GATCAAAAGATAACTCTGCAAAAATAATAATCGTCTTGTCTGATGGAAAGATTCTGGGAGACCCTATGACTCTTGATGAAGTTTTGAACAAGCCCCAAATGAAAGGTGTCACTCGCTACTCCATAGGGGTAAGTGTCCCATTTACTGCAAAGTTTAGATAATTTTAGATAATCCAGACTGATCTCAATGGAAAACATAACTGTTTTATAAAATATGAATATGAAAATGTATTATTTTTAAAAGAAGTCTTGACCCAAATTCTACACCCATATCAAACTGTCATTGGGAATGAGCAGTTTGTACTAAAATGTTATGAGATCATATGAACATCAAAAGTTATAAATTGCATTGAGATTGTATTGGATAATCCCAATTTTACATCATATGTTGGAGCAACAACTGCAAAAAAAGTAATCTGTAATCATAGATAACTCTGGTTCCCCTTCGGTTGGGGAACTTCAGTGCTATAAAGTGGATTTGATCTTGGAAAATCCACTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22611
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 |
---|---|---|---|---|---|
ENSDART00000080523 | Nonsense | 288 | 1266 | 9 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 16229185)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17274148 |
GRCz11 | 15 | 17210170 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGGGAGACCCTATGACTCTTGATGAAGTTTTGAACAAGCCCCAAATG[A/T]AAGGTGTCACTCGCTACTCCATAGGGGTAAGTGTCCCATTTACTGCAAAG
Long Flanking Sequence:
TCAGAAAGCGAAAGACTTCATCTACAATGTCATGTCCAATGTTTGGAAAACATGTTTCGATGCAAGTATAAAGAAAAAAAAATCATGGCACAAAATACAATTCAATTGATATTAACTTTACATTAACCCCTCTTCTCTCTGCAGTGTAATTTTGCAATAGTGCAATACGGTAGTTTGATCAGAACTGAGCTCTCGTTACTAGACAATGAGGATCGCGTGGGATCCTTGCTAAAGGTCAAACAAATAAAGCAAATTTACAATCTCACAAAGACGGCCTCTGCCATCAATCACGTCCTGTGAGTCTACAAACAATTTTTACAGCATTTGGAGATGACTTAATGGTGTGATTTTACAATGTTGTGGTTGATTACAGCACAGATATCTTCATCCCTGAGAATGGATCAAAAGATAACTCTGCAAAAATAATAATCGTCTTGTCTGATGGAAAGATTCTGGGAGACCCTATGACTCTTGATGAAGTTTTGAACAAGCCCCAAATG[A/T]AAGGTGTCACTCGCTACTCCATAGGGGTAAGTGTCCCATTTACTGCAAAGTTTAGATAATTTTAGATAATCCAGACTGATCTCAATGGAAAACATAACTGTTTTATAAAATATGAATATGAAAATGTATTATTTTTAAAAGAAGTCTTGACCCAAATTCTACACCCATATCAAACTGTCATTGGGAATGAGCAGTTTGTACTAAAATGTTATGAGATCATATGAACATCAAAAGTTATAAATTGCATTGAGATTGTATTGGATAATCCCAATTTTACATCATATGTTGGAGCAACAACTGCAAAAAAAGTAATCTGTAATCATAGATAACTCTGGTTCCCCTTCGGTTGGGGAACTTCAGTGCTATAAAGTGGATTTGATCTTGGAAAATCCACTTATGGGAGGATTCGGTTCAGAAGCCGCTTGTCTGAAAGAGTATTGAACAGGCCAATGAAAGCAATGAATTTGAAGCGTAAGCTTGCGCAGGTGCGCTTCAATGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35846
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 |
---|---|---|---|---|---|
ENSDART00000080523 | Essential Splice Site | 557 | 1266 | 15 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 16205981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17250944 |
GRCz11 | 15 | 17186966 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAATTACAGCTCGCTGAAGCTGGATTCAGCTCCCATCTCTTATACAAC[G/A]TAAGTATGATCGTTTCAAAAGACTTTCTGGTTTGTTTTCATCATGAACTT
Long Flanking Sequence:
ACACTCATAAGCTACTTTGTAGTTAATTGCAATTGTAATTAAAAATGTATAATAAGTTCCATACACTTACATCCTCATGTTACCTTTAGGTTGGCGATGGCATCCTGAAAAACAAGGATGCAATCAAAGAGATGACGCAAATAGCAGATCCTGGAAAGTATTATAGTGTTTCCAGTTATGGCGCATTAAATGATATTCTGTCCTCACTGGAAAGAGGGATAATTGGAACTGAAGGTATGAAATGTACAAATTACACTGAATAATAACCCTTATAGCCACGAAAAAAAAAATCCCAACAACTACAGTGCAAACTGAATACCTGTCTAGAGTGCACACATGGGCAATAGCCTCTCACATTTCACATGACTTGAGATGATATTTGTAATTGAATAGTCACTGTATCATTATTGTTTGTTAATAAACTTTGTGTGTCAGGCACTCAGCATGGATTTAAATTACAGCTCGCTGAAGCTGGATTCAGCTCCCATCTCTTATACAAC[G/A]TAAGTATGATCGTTTCAAAAGACTTTCTGGTTTGTTTTCATCATGAACTTGTACTCTTTCTTTCTGACACTGTATGTTAAATCTTGTGTTATATAGTATATTTATATCCGCAGCGTCTTTTCATGATGATTCACATACTGTTAACATTGTTTTGTTTTTGTACAGGAGCAGAAGGTTGAAGCACTATTTGGAGCTGTTGGAGCTTATGACTGGAGTGGTGGGGTCTTTTTGAAATCCGGCAACACGGTTAAATTCTTGAATGATTCTCACAATGAAACCAAATTTGGATATTTAGGTGAGTGATAATATACTATTCCCAAGTGATTGAGAGTAAAGATGTTCTCTTAATGTTCTCAAAAGTAAAGATGATGTGAAACACTGTTAAACATGCCTTTATCCCAATGTTTTTGTCGCCATTAAAATCTAAATGTATTCTTAACATTAGAAATCTTTTATTCCCAATTCTGTTCATTAAAATAAAAGTTAAAGGTCCTGTGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35845
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080523 | Nonsense | 645 | 1266 | 18 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 16204120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17249083 |
GRCz11 | 15 | 17185105 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCCAGTTTGCAAATGTAAATTTGATAATCAATAAATGATGTTTAGGTT[G/T]GATCTTACTTTGGATCGGTTCTTTGTGCCTTGGATATTAATAAGGATGAA
Long Flanking Sequence:
ATTTGATGGCTTAGAAAAGTATGTGCTTCACGGAGATCAGGTATTTGTAGTTAATTATTATTAACATATCCGACTACTTTCATTTTCAAATGGTTTTATTTTATATATACACAGTTAATGACAAAAACTTAATCCTCCAATGACATTTGAATTATTTGTCATTATTTTCCAACCTTAATGTCCAATGACCTATTAAATAAGCTTCTCTAGTAAATCTAAAAAGCCTGTTTAAGTCTTTAAACTGCACTACAGTGAATATCTTACTAAATTACTAGTACAATATTATATAACCGTAATATGTACTGTATCATGGCAAAGAGAAAACAAATTATTAGAAAATTTTGCAATATAATGATAATTGTGCTAATAATTTTGTCTTCAACTGTACATTTTGTCACTAAAATGAAATCTTTAAATGGCATTCACAGTACACATTCATAATAAAACCAAGCCCCAGTTTGCAAATGTAAATTTGATAATCAATAAATGATGTTTAGGTT[G/T]GATCTTACTTTGGATCGGTTCTTTGTGCCTTGGATATTAATAAGGATGAACACACAGATCATCTATTAGTTGGAGCTCCACATTTCCATCTGAATGGGGAAGAAGGCAAAGTGCTAGTGTACAAACTGAATCAAGTAAGACTATTGTTTTATGTGTGACTGCATTAGCATGAATAATAGCTAACGGTCTTGTTTTTCTCTAAGGAGGACAGGTTTGAACGTGCGCCCGTGGAGCTGCGGGGTGATGCAGGACAGACCTTTGCCAGGTTTGGTGCAGCCATTGGCTCTATTGGAGACATTGATAACAACAAGTTTAATGATGTAGCAGTAGGTGCTCCTCTGGAAACAGGCTCAGCTGGAAGCGTTTACATCTACAGTGGTTTCGAAGAAGGTCTTCGCTTTTCACAAGTGAGTTTAAGCATGTGTGAACTTGGACCGCAAAATTAATTAAATTAAGATTTATACACCTGAAAGCTGAGAGTATGGTTTGTTAAAACAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30990
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 |
---|---|---|---|---|---|
ENSDART00000080523 | Nonsense | 854 | 1266 | 22 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 16199623)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17244586 |
GRCz11 | 15 | 17180608 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATAACCACATTTCACTTCCTGTTGTTTTAGCTGAAAAATCTGAAACA[C/T]AGGCTGTTGACTATGAAATTGACTTGGATTCTGGTGCAAGCAAAAAGCGC
Long Flanking Sequence:
CATGTGGTCTCCCATCCAAGTACTGACCAGGCTCAGCCCTGCTTAGCTTCAGTGAGTAACCGGTCTTGGGCTGCAGGGTGATATGGCTGTGGAATTAGGGAAAATGGAAACAACTAAAAAAAAAAAAAAAATCACAGGGTTGACTTCAGCTGTACATTACTCTATTTTTCAATGTGACCGAATTTCTCATTATGTTTGAGTATACGTTCAGATTTACTATAGGATAGTTGAACCAGTTTTTTGACTGTATTATGTTTTACAGAACTATCCCAGTCTTGATTATCGAACCAACTATCAAAATTGATACAGAAGTCATTGCTCTCACTCACCAGATGAATAAAATATCCAGCGAGTTAAGCATGAAGATTACTGTTTGCTTTAACATAAAAAAAGGAAAGCTTAAGGGTAAGTGAGTTTAAGATCGCCGAAAATATTTGATGCTCATGTTCTATTATAACCACATTTCACTTCCTGTTGTTTTAGCTGAAAAATCTGAAACA[C/T]AGGCTGTTGACTATGAAATTGACTTGGATTCTGGTGCAAGCAAAAAGCGCCTCACTTGCGGCGCAGACAGCCTAATAAAAGACACTTTTACTCTGACACCAGATGAAGAGTGCACTAATAAGAAGCTAACATATTTGGTATGTTGGTTCATTTAATTATTTTTTTTTTCATGTAAAAAAACTATATAGCAATGTAAACCGACAATCAGCTTGAATTTACTGTTTCAAATTGTCAGTGATTATCACAGTGTTTTTGTCTGAGAGCTATGACTCTTATTTTGTCATATTAACTGAGACGAGCTGTGTTTTCCTTTCAGGGCTGCTTTGATTGTTTTTCACCTATTAAAATCAAGCTGAGTTTTTCATTGGCATCCAACAAAAATGAAGCACCTATTCGCATTCTTGATGCATTTACTCCAACAGAGGTTGTAAAAGAGGTAACCTTTTATTATTATTATTATTATTATTATTATTATTATTATTATTAATAAAATACAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12794
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080523 | Nonsense | 916 | 1266 | 23 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 16199257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17244220 |
GRCz11 | 15 | 17180242 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGCTGCTTTGATTGTTTTTCACCTATTAAAATCAAGCTGAGTTTTTCAT[T/A]GGCATCMWACAAAAATGAAGCACCTATTCGCATTCTTGATGCATTTACTC
Long Flanking Sequence:
TTACTGTTTGCTTTAACATAAAAAAAGGAAAGCTTAAGGGTAAGTGAGTTTAAGATCGCCGAAAATATTTGATGCTCATGTTCTATTATAACCACATTTCACTTCCTGTTGTTTTAGCTGAAAAATCTGAAACACAGGCTGTTGACTATGAAATTGACTTGGATTCTGGTGCAAGCAAAAAGCGCCTCACTTGCGGCGCAGACAGCCTAATAAAAGACACTTTTACTCTGACACCAGATGAAGAGTGCACTAATAAGAAGCTAACATATTTGGTATGTTGGTTCATTTAATTATTTTTTTTTTCATGTAAAAAAACTATATAGCAATGTAAACCGACAATCAGCTTGAATTTACTGTTTCAAATTGTCAGTGATTATCACAGTGTTTTTGTCTGAGAGCTATGACTCTTATTTTGTCATATTAACTGAGACGAGCTGTGTTTTCCTTTCAGGGCTGCTTTGATTGTTTTTCACCTATTAAAATCAAGCTGAGTTTTTCAT[T/A]GGCATCCAACAAAAATGAAGCACCTATTCGCATTCTTGATGCATTTACTCCAACAGAGGTTGTAAAAGAGGTAACCTTTTATTATTATTATTATTATTATTATTATTATTATTATTATTAATAAAATACAGTAAAAATAATCACCCATTACTACTAGTATGGATATAATGGATATACTGAAATTTTTATAATTTTTAATGATGAGAGAAATGCAACAAAATATTTCTAATTTACTTATGTAAAATGGAAAAATACTTTTATATAACAGTGACGTATGTTTTTTTTTTATTAAAGAGTTAAAAATCTTCAAAAATATTTTTGATACTTCATCATCAGGGCTGATTCTGATAAAGAAGTCTTTGAGAAAGCAGAAAATAAATGAATACAGTATATGATCATTTTTGACAGTTTTTGACAGACATTTTTGTTTTCTAAGGACTTACCACAAGGGTAAACATTATAAATGTCTTATTTTATAATCAGTAGTAATTGTGTCACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22610
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080523 | Essential Splice Site | 1005 | 1266 | 26 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 16197505)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17242468 |
GRCz11 | 15 | 17178490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCACAGTTGCATTTAACAGAGAGTCCTGACGAACTGTGCTCTGCAAAC[A/C]GAAAATTGAAGGAGCCGCCTGTCCTGTGAAGAATGACAATCAGATTCAGT
Long Flanking Sequence:
GTGTTTGTGTTAGTAAAAACAATAACTAACAGTAAATGTCCTGTATCATGAAGTGTTACCAATGACTTAGTAAATGATCAGAAATTTCAATTTGTTTTCATTAGATTCCATTTGAAAAGGACTGCCAGGCTGCAGATTGTAAACCTAGCATTACATTATCTGATTCAAAAATAAGGTACGTACTGATCAAATTCTAGTCTTTATCTAGTTAACTTCATTTCCGTTTTAGGAGTGTACGTATTTATAAGACATGTAAAAGTATATATTTTCTTGTAACTAAATGTATATTAATATTGCAGTGAAACCACTATCACAATGGGAGAAACGCAAAACCTGAATATCAATTTCAATTTCACCAACACTGGAGACCCTTCCTACAAGACCACCCTGACGTTGACGTACCCCAGCATACTCAGTGAGAGGGTAAAAAAAAAAAACACTCACAGCTCTTCTCACAGTTGCATTTAACAGAGAGTCCTGACGAACTGTGCTCTGCAAAC[A/C]GAAAATTGAAGGAGCCGCCTGTCCTGTGAAGAATGACAATCAGATTCAGTGTCATCTTCAACACCCGGTTTTCACAAGATCTGCACAGGTAAAAAATCTCACATCACATCTTTGAAATATTACCATTCTCATTTGTACCTTTTGTTTTATTTATTTTGTTAATTATTTTTCCAGACCAATCTCTTCATCTCCTGGCAACTTAATGACAAATCTGATCTCAAGAAGTCTGAGATTATAGCAAATCTTACCAGGTTTGAATGCTGGCTTGAACATTACTCTGGTTTTTGAACATCTGAATATAGTATTTCATCTGTTTTTATTGTTTATTTTTCTTTTTTTTAGTCAGAATAATGGCATTCAGCTTCTGGACTCTAGAATATATACGTTTAATGTGATGTATTTCCTACCAATTCTTATACGTGGGTGAGTAAACAAACAACCTGTGAATTATTTTACATAAAACCTATTGCTTTTGTAATATTGATTCATATATTATTATT
Associated Phenotype:
Not determined