ZMP
itga3a
Ensembl ID:
ZFIN ID:
Description:
LOC407685 protein [Source:UniProtKB/TrEMBL;Acc:Q6NW79]
Human Orthologues:
ITGA6, ITGA7
Human Descriptions:
integrin, alpha 6 [Source:HGNC Symbol;Acc:6142]
integrin, alpha 7 [Source:HGNC Symbol;Acc:6143]
integrin, alpha 7 [Source:HGNC Symbol;Acc:6143]
Mouse Orthologues:
Itga6, Itga7
Mouse Descriptions:
integrin alpha 6 Gene [Source:MGI Symbol;Acc:MGI:96605]
integrin alpha 7 Gene [Source:MGI Symbol;Acc:MGI:102700]
integrin alpha 7 Gene [Source:MGI Symbol;Acc:MGI:102700]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26106 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9528 | Nonsense | Available for shipment | Available now |
sa33228 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20069 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26106
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055263 | Nonsense | 87 | 1053 | 2 | 26 |
Genomic Location (Zv9):
Chromosome 3 (position 34959959)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34745155 |
GRCz11 | 3 | 34874663 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGCGGAGTCTGGACTGTCAGCCAATGAGACGGGAGATGTTTACGCCTG[T/A]CCGATCTCTGCAGACTCCAAAGACTGTGCAAGACTGAACCTCATCAGCTC
Long Flanking Sequence:
TGCTTTCTAGAGTTTTTTTATAATAATCTGCCACTTTTAACAGCAGGTTTCAGCAAATAGATAGACGCCAGGAGCTCCTTCAGTGGCGTTTTCTGTCCACAGTTCACTGTGTTCCGCAAGTAATACGTTCTGACAAGTCCTTCCAGTCAGAATCCGTTCACATATCCTGACAAGCTCAGACAGATAAGTGTTAGAAGTGCTGGTGTTTATCTGCAATGTGCACTCAATTGTAAGGGTACTCTGGAATACAAGCAATACCTGGCACACTGCCGAAGGTGAATTTCTGATTTATCCTTGAAAAGTGTTGTGTGAAAAATGTGCTTTGTTGTCTCAGATGACCATTACTGTGGTACTGCGGCAGATGTAATGTCTAATATTCTGCTTTGAGAGAGACTTGAGCTCAGTTGGGTTTATACATGTTTCAGGCTTCTGGTAGGAGCGCCAAAAGAGAAGGCGGAGTCTGGACTGTCAGCCAATGAGACGGGAGATGTTTACGCCTG[T/A]CCGATCTCTGCAGACTCCAAAGACTGTGCAAGACTGAACCTCATCAGCTCAAGTATGCCTTTCTTCTGCCATAGAAGTCTTAAATGTGCTTGTTCTTACATTCTTCCCATTTGCAATATTTAACCCTTGTGTGCTGTTGTGGATGTTTTCATCCACTCTGGGGTGATTTTGAGGCTTGATTAAGCCACAAATTTCTTTTTGTTTTTAACAAATGGAATGATTTTTGGTGATCTTATTTTGACACATTTTGGGAAAATGTTTGGGAATTTTTTAAAAACTCAACAATACACTTTGGGCAAATTTACTACTCTTTTGTTATGCTAGTGGCTGTTTTTGCCCCATTGACCTCATTATAGCAACATTTTATGATTGCAAAGACATGATACTTTTTTTGTTGTTGTTAGTGGTTTTCCCTGTTGGGAAGAGGTACAATTTGTGATTTTTACTGTTGAAAACAGGAAAACAACAGGGAAAACCGCACCAACAACCAAGAATGCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9528
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 |
---|---|---|---|---|---|
ENSDART00000055263 | Nonsense | 492 | 1053 | 11 | 26 |
Genomic Location (Zv9):
Chromosome 3 (position 34972545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34757741 |
GRCz11 | 3 | 34887249 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAAATCAGTACATTTTGTTTTCTCAAACAGCATTGAAGCAAAAGTCTG[T/A]TTCTCCTACACATACAGCACTGGCACTGCCAGTTCCCAGAAGGCCGTGAG
Long Flanking Sequence:
GGGCTTTTCTTTTTCTGGATTGCTTTTTAAAACTCGGTTGAGTTTAAGGAAGGATGGTTGGCAGGTCAGTAGGTGATTTTGAAAACACTATTGGTTGGGTTTAGGGAAGGGGGAGGGTGGAGGATGGGTCAGTTGGTCTGTCAGTTAGTCAACAACGGTCTCTTGTGGATTTACGTGAGAACAGCAGGTGCGAATGGCACTTACTAGAGACATTTGAGATCTGAAAAAGCATACACAGTGGTCTCTAGTGGATTCCTAAAAACAAAAACGGCAAAACGTTTCTCCAGAAATGTATATAGGGGTACGTAATCTGAATGAGCCTGGGTTGGATAAAAGCGTAAGAGTAATTGCAAATATATTGCTGTAATTTATAATTTGACCAATTATCTAATAGCAGCTGTAATGCTAGTATAATTTATCATCACTGTATAACTGAGCTGTTTAAATATGTTAAAATCAGTACATTTTGTTTTCTCAAACAGCATTGAAGCAAAAGTCTG[T/A]TTCTCCTACACATACAGCACTGGCACTGCCAGTTCCCAGAAGGCCGTGAGTAAGTCCCACATCGCAGTTTATTACCCTAAATACAACCATCTTAATGTTGTTGTCATGCAAAATGCATGATTCAGTATGATTCTGTTTCACTGTCCGAGTCCATATCTGACATGAAGTACCTACTGTATGAGAAAGACCTCTTCTTTTCACAGCTCTTCAATATACGGTGGAGGCCGATCAGCAGTCGTCTAGGAGCCCCCGTGTTAGTTTCCTTGACAACAATAAGGGCAAATACACTGGCAAAATGTCTGTTAATCCGTCTGGAGATTGTCATTCTCTAAAACTCGAGCTGGCGGTAAGACACAAGGCCATCCTTTCAACTGCCATCTGCTTGTTAAGTTGTGACGTATGGAATGTTGTTTCAGGGTCCAAACCTCCTCTTGTTTGAACTGAGAAATGTTTTATATATTAGTTTATAGTATGTTGAGTGAATCTTTTATAAAGTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33228
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055263 | Nonsense | 533 | 1053 | 12 | 26 |
Genomic Location (Zv9):
Chromosome 3 (position 34972820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34758016 |
GRCz11 | 3 | 34887524 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGATCAGCAGTCGTCTAGGAGCCCCCGTGTTAGTTTCCTTGACAACAAT[A/T]AGGGCAAATACACTGGCAAAATGTCTGTTAATCCGTCTGGAGATTGTCAT
Long Flanking Sequence:
ACGTTTCTCCAGAAATGTATATAGGGGTACGTAATCTGAATGAGCCTGGGTTGGATAAAAGCGTAAGAGTAATTGCAAATATATTGCTGTAATTTATAATTTGACCAATTATCTAATAGCAGCTGTAATGCTAGTATAATTTATCATCACTGTATAACTGAGCTGTTTAAATATGTTAAAATCAGTACATTTTGTTTTCTCAAACAGCATTGAAGCAAAAGTCTGTTTCTCCTACACATACAGCACTGGCACTGCCAGTTCCCAGAAGGCCGTGAGTAAGTCCCACATCGCAGTTTATTACCCTAAATACAACCATCTTAATGTTGTTGTCATGCAAAATGCATGATTCAGTATGATTCTGTTTCACTGTCCGAGTCCATATCTGACATGAAGTACCTACTGTATGAGAAAGACCTCTTCTTTTCACAGCTCTTCAATATACGGTGGAGGCCGATCAGCAGTCGTCTAGGAGCCCCCGTGTTAGTTTCCTTGACAACAAT[A/T]AGGGCAAATACACTGGCAAAATGTCTGTTAATCCGTCTGGAGATTGTCATTCTCTAAAACTCGAGCTGGCGGTAAGACACAAGGCCATCCTTTCAACTGCCATCTGCTTGTTAAGTTGTGACGTATGGAATGTTGTTTCAGGGTCCAAACCTCCTCTTGTTTGAACTGAGAAATGTTTTATATATTAGTTTATAGTATGTTGAGTGAATCTTTTATAAAGTCATGTTCAATATACAGTCCTTGGATTTGCTGCATCCTAGGCACCAATATTTCATGATGGACTGACACTTCCAGTCACTCTGCTCTGTAGGCAACTCGGACAAATGTGCTGCTGCAAACTTCTGTTTTTTAAGTGTGATTGGGATTACTGTGAGTGTGTGTTTTTGTTTTTGCTTGGTGCTATTCCTATTTCACTAAATCTCCGTTTTTTATTGTGTGTATATGAAATTCTGTGCATTCTTGTGTGTGAAAACCAATATTTCTTTATGTAAAAACACTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20069
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055263 | Essential Splice Site | 751 | 1053 | 17 | 26 |
Genomic Location (Zv9):
Chromosome 3 (position 34979211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34764407 |
GRCz11 | 3 | 34893915 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATTTCAATAGACATGCAGGAGATTGAGACAGAGCTGCAGCTCTCAACG[T/A]ATGAGAAATCACCCTGATTTACTTCAGATTCTCAAATAAGCTGCACATTT
Long Flanking Sequence:
TAAATGGTTTTGGGATCTCTTAACTGAAGACTGGAGTGATACATTGTATTAATCACAAGCTTTTAAACAGCAGTGTATAAAAATTTACAGGTAAACAATATTTTAATTATTTCTTGATTTGTTTTTTTGCAGACCCTGAATGGTGATCCATCTTCTGGGGGGTCTTATCTGTTGTGTACACTTGGTGACCCCTTCAAAAGCAATCAGAGGGTAAGTTCTCATTAGTATAAATGACCCTGAGATTTACTGTAATAGCAGATATCCTGCACAACCATATTAGACTTTAAGGTTACTGATTATACACTGGATGCAGTAATAGAATGTGAATTGAGCTAACAGTGTTGAAATAAAGAGCATTTCTAGAAGCATTAAGGTGATTCTTCTTTTTATTTTCTTGTGGCCACTTATGTATTTCACAGGTGGAGATCGAGATCACGTTTGAAACATCAGGAATTTCAATAGACATGCAGGAGATTGAGACAGAGCTGCAGCTCTCAACG[T/A]ATGAGAAATCACCCTGATTTACTTCAGATTCTCAAATAAGCTGCACATTTGGGGATGTTTTGCAGGAAATGAGGTTGAAAAAAAAAAAATCAATATCTCTACAGAGAGCACAGAATCCTGAAGAGAAACTGTGGCGCTCGTAGGTTTACATAACCCATGCTGAATCTCTTTGAAGTTTAGCGTTTAAATAAAAAGGAGAACAACAAAAAAAACAAGCCATAAAAACAATGTTGAAATAATTACTTGTATATGAAGAAGATGATTTTAAAAAATGCAGAGAATTGTTGTTGGATTATGCAGTATGTAATACTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTAACACAAGAGAGTGGAACGGTGGTTCAGTGTAATGTAATGTGTATTTATATAGCGCATTTATTGTGTATAGCCATACACCCAAA
Associated Phenotype:
Not determined