ZMP
si:dkey-27b3.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
ITGA1
Human Description:
integrin, alpha 1 [Source:HGNC Symbol;Acc:6134]
Mouse Orthologue:
Itga1
Mouse Description:
integrin alpha 1 Gene [Source:MGI Symbol;Acc:MGI:96599]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34849 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18063 | Nonsense | Available for shipment | Available now |
sa41595 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41596 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27560 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24864 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34849
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 |
---|---|---|---|---|---|
ENSDART00000112101 | Essential Splice Site | 482 | 1183 | 13 | 30 |
ENSDART00000145596 | Essential Splice Site | 482 | 1187 | 13 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 8897797)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 8973753 |
GRCz11 | 10 | 8807312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTCCATTTCCTTTTCTGGAGCATTAATAAGCATGTCATGTTGTTCTT[A/T]GATTGGCTCCTATTTCGGCAGCGTCCTTCAAACGCATGACATCGATGGTG
Long Flanking Sequence:
ATTCTTAACTGCAAATTCAGTAAAAATCTAAAAAATTATATATTTTATTTTATAAAATACAAAATGCAACAGTATAGTATTAGTATTTAGTTTTCTTTACATTAGAATCAATATTTTATGTATAAATAGTAATAATATATAAAAAATAATAAATACATAAAAACATTTTATAAATCGATTAGTTTTATGAAAAGTTATCTTTTTAAAGATGACAAGATTTTGTCCAAATTTTTGCCATTGTCTCATTGTCATTTTTATAATTTTGTAAGTGTACCCCCCCCCCCAAAAAAAAGCATAAATCAATGTAATGTAAAAAAAAATCCATATAATTCTTGCATATTCTAATATTTTTTACAAAGCACTGCTTTTAAATGTACTTTAATTAATTGTCATTTACTGTAAATTTTAATACATACTACAAATTTTAGTTTTGTCTTGTTTTTTTTTTTCATGTTCCATTTCCTTTTCTGGAGCATTAATAAGCATGTCATGTTGTTCTT[A/T]GATTGGCTCCTATTTCGGCAGCGTCCTTCAAACGCATGACATCGATGGTGACAATTACACCGACATCCTCCTGGTCGCAGCTCCCATGTTTATGGGTCCTGAGCGGGATGAACAAGGGCAGGTCTACGTCTACAAACTCAACGAGGTGTGTATGAGTGTTTAATCCACATACTGGAAACATGTGTAAGGGAGCAATGCACCTTCATTCCTCCACAAGAGCATGTGGGAGCAGTAAATCTGGGTCTGTCTTTAGGGAGTGAGTGTTGTGTTGTGTTGTGTTCAGCCTCAGATAAGTGCTCCCATAGCAGGGGAAGGGCTGCTGGAATGAGAGCTTGGCATCATGGGAATGGAAATCTAATGAAAGTCTAATATCTTCAGCCTCTGTTGAGCACCTTCTGTCAAGAGCTTATAAATAGAGGTTTAAATGAGGGGAATTTCCATTGGTTTAAGTTTTTTTTTTGTTCAGTTGTCAGGGTTTTTTGATATCTGTATTGATTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18063
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 |
---|---|---|---|---|---|
ENSDART00000112101 | Nonsense | 786 | 1183 | 18 | 30 |
ENSDART00000145596 | Nonsense | 785 | 1187 | 18 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 8915857)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 8991813 |
GRCz11 | 10 | 8825372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGGTGACGCTGGAATTCGGTCTAGCRGATGAAGACAAGGGTCYAGTTT[T/A]GGATGGAGAATTACCCACATCCCTCAACAAGACTGTAAGTTTTCCTCCTG
Long Flanking Sequence:
GCAGCGTCAGCAGTAATGCGGTTGATGTACCGATCCGTTGTGGTAAAGAAGGAGCTGTACTGAAAGGCAAAGCTCTCAATTTACCGGTCAATCTACGTTCCTACTCTCACCTATGTTCATGAGCTTTTGGTCATGACTGAAAGGACAAGATCTCGGATACAAGCAGCCAAAATGAGTTTCCTTCGCAGGGTGCCAGGGCGCACCTTTATAGGATGAGGAGCTCTGTCACCCGGGAGGAACTCAGCTTATGAGCTTATGTCTTATATTTATAACAGAAGGGCGAGTAAATGTTGGTAATGCAGTTAACCTTTAACAGAGTCTGCTGGGACAGAATGAACCTGATGCCATTTCTGGGATTTTCCAGTCTGTTTATGAGTTGCTATAAGCTGAAAAAATGTGCAACATCCTTTATTATCCCCCACAGGATAAACTGGATTTCAGAGACCCCATTATGGTGACGCTGGAATTCGGTCTAGCGGATGAAGACAAGGGTCCAGTTT[T/A]GGATGGAGAATTACCCACATCCCTCAACAAGACTGTAAGTTTTCCTCCTGCTAGAGGTTTATTAGTGTAACGTTGACTGCGCCAGTAACTGTGTCTGCTTATTAACAGAAGAGTGTGTGTGGGTGGCAGCTGCGAGTTTAATGAAGTCGCTCTAATTTTACAAGCACTGAGAGACTTTCTCCATGTTCAGCTGCTCTCTCACATGCAGTTGTATTGAGGTTTTAACTAGCAGAAACAGGGATGGGCTGGCATAGAGAATGGCATGACTTCCCCTAAATGAACCCAGTGGATTGTTGGCCAAATGTAGTTTCCTTTTTTATTTGATATTTTTGATGAATTAATTATGCGTGATTACAAAAACAGTGATTTTTTTGACGTTCAACATTTAAAGATGGTTCTGTTTTGCTTCTTAACAGTAAAATACAAATATTCGAATGTGAAGGAATCTGCACAACTTCATTTTGAGTAGCTTTTTGACAACTTACAAAGTTTAATTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41595
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 |
---|---|---|---|---|---|
ENSDART00000112101 | Nonsense | 857 | 1183 | 20 | 30 |
ENSDART00000145596 | Nonsense | 860 | 1187 | 20 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 8919510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 8995466 |
GRCz11 | 10 | 8829025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACACTGGAGACAACGCTTATAATACCAAAGTTACACTGAGCCACACT[G/T]AAAATATCAACTATGTCAAAGTGGAGGTAAGAAGAATTTAGAGAACATTT
Long Flanking Sequence:
TGGACTGTGGAAGTAATGAGAAGTGTGTTGCTAATCTACACCTACAAGCTTCTGCGAACATCTCAAGGTATTATTTAATGTTTAATCAATCTTTGATTTCCAATGAAAGAATGCCTTTAGGATTTTAATCAATATTTGATATAATTCTTAAAGATTCAATGACAATACAAATAATTATGGCCAGACTTTATCCTGGTGGCTGCTGTATTATTCATGAAGAAAATGTTTGATAATGTCTTCTAGTCATTTGTGTGATTTCCAGTGCTTTGCTGCCCCCTTCTGTCGAATTTTGTGTTCAAGTCGTTCTAGTCTGTATGTCATGAGAGAAATATAACAGAAGTGAACCAGAGAGCTAAATGTTAACTCATGTTCTCGATTTTATATTTTTGAATTGTTACAGTCTTCTCATAAAGAGTAACCAGGAGAAATTTTATGTCAATATCGACATCAAGAACACTGGAGACAACGCTTATAATACCAAAGTTACACTGAGCCACACT[G/T]AAAATATCAACTATGTCAAAGTGGAGGTAAGAAGAATTTAGAGAACATTTGAATCTTTTCTCTTTTTTTTCAGGGTCTAACAGTTTTTTAATTCCTGTTTTCACTTTTTTTCAGCCTAAAGATAAGGACTGTGAAACTAATCATACCAGAATAGTGTGTGCAGTTGGATATCCTTTCCTTAAAACTAAGGACAGGGTGAGATTAGCTTTGCTACTAAAAGGATTGTTCACACAAAAATGAATGTTTACTGTTAGTTTACTAACTCTCAGGCCATCAAAGTTGACTTTATTCTTCAGTTGAATATTAAAGAAGCGTTTTAGATAAAACCAATGTCCTTGGCAATTCAAAAAACATGGAAGTCATACTAGCCAGCAGGGACTTTAAGATTCAAAAAATATATAGAGAAAAAATGACTTAATATCTGTGACTACTGACAATACATTGAGTTTTTTTGAAGCAAAATGATCAGTCTGATGTTATTATTAACTTGCTATCAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41596
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 |
---|---|---|---|---|---|
ENSDART00000112101 | Nonsense | 1054 | 1183 | 26 | 30 |
ENSDART00000145596 | Nonsense | 1058 | 1187 | 26 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 8925781)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 9001737 |
GRCz11 | 10 | 8835296 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTAGCAAACCACATTCACTGAACACAAAAAAAGAGACCCTGAGCATCTA[T/A]CTTTTGGTGAGTAACCACTGCTTTTTTGATATGCGCATAGACATATGTTT
Long Flanking Sequence:
CCACAAACCAGACTGACAAAAATACTTAATAAAACCAGATTTTAATTAGATAGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATTGATTGATTGATTGATTGATTGATTGATTGATTGTGTTTAACAGATTGAGAAAGACCCTGACATGCCGAGTCCTCCAGTAAAGCTTACAATAATGTTTCCATATCAAACGTCTGCTAAAAACTTTCTGCTGTACCTGACAGATCTCAGCTACACAGCGGTAGGTGATTCCTCAAAACTATAACCACAATGACTGTATGACTGCTTTAGAAATATCTCAATTGTCCCATTTGGACACTTATAGGGCATTCGATGTTCCGCCGACTGGATTAACCCTTTGAAGATTCAACCTAGCAAACCACATTCACTGAACACAAAAAAAGAGACCCTGAGCATCTA[T/A]CTTTTGGTGAGTAACCACTGCTTTTTTGATATGCGCATAGACATATGTTTACCAGCTGTCCTGTATTGGCCCACATGTCCTATATATTGTGCCTAATTTATTCATCATCTTGCTTTCCCTGTTTACTTGCAGTAGTTCTTAACTGATCTAACCATAAAACATATCATACTTCCACAGATTGTACAGTACAGATTTTATTATGATAACTTGATCTCAGTTCTCTGTGCAATTAGCAGGATATACAGTATGTTCATTTGATTCTTGAAACAAATTTTATAATCTAAAGCTTAAGCAAACTAGACTATCATTATTTGGTTAAAAGAGAAAAATGCATGAACATGAAACATAAATTGGTGTCTATGACAAACTGAGCAGCTCAATGATGCTATATATACTGGAAGGAAATTCTAAATATTGATTTGGAGGGGAATTTTTAAGAACCTATAGTTTGAGGGAAACTAGCTGTCTTCGGTTTATATAGTATTTTATTTTTAGATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27560
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 |
---|---|---|---|---|---|
ENSDART00000112101 | Nonsense | 1129 | 1183 | 29 | 30 |
ENSDART00000145596 | Nonsense | 1133 | 1187 | 29 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 8930817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 9006773 |
GRCz11 | 10 | 8840332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTTTCACAATTGTGATGAGTGTTGCATTTATTATGCAGGTAAGGATT[C/T]AAGTCACCAAAGACATACGAACTGGAATCCCACTGTGGATTATTATCCTT
Long Flanking Sequence:
GTGTTAATATCTGAACTATAATCTGTAATTAGCCATTTTTCTCATCCTACATTTGTGATAATCATTTCTGTATCACAATACAGAAGACCTTGGTAGCTCTTTAGTATAGGGACCAATTCTGAATACTGGTTTATTACAGCACCTGCCTATTATTAAGATTGACTGTTTATTAGTACTTAAAAAGTACATATCCTGCTTAATTTTATTCTACATCCCTAATCTTACCCATTACCTAAACCGAACTACTACCTTATTAACTATTATTAAGCAGCAAAATAGGAGTTTACTGTACTAAAGTTTATAGTGAATGGTTTGTTAGTGGCGATATTTGTATCTTAAGATAAAGTTTGAACAAGATCTTAATTTTTCCAAATAAAAGTCAATAATAAAGGATTTATTTTGTCAGGTTGTACAGCAAAATAGTTTGAAATTACAACTTGGACTCCTTAGTAATTTTCACAATTGTGATGAGTGTTGCATTTATTATGCAGGTAAGGATT[C/T]AAGTCACCAAAGACATACGAACTGGAATCCCACTGTGGATTATTATCCTTAGTATTCTAATAGGACTTTTAATACTGGCACTTGTTATCTTCGCTTTATGGAAGGTAAGTAGTGATGTTTACCTTAAGCTTACTTGCTTTAACACACCAATGCCCTTTTTCACCTGGTATTATTAATGTTAACCTTGTTAAAAGGCTATCAACTGAGCAAGTGAATAAAAAAAACAATATGTAGGTGGTAATGATGTAATTCTACCAAATAAAACCTTAACTTAATTAAACTTCTCACAACATCTTTTATAACGATCATGTTTTCAGTCAATCAGTGTGGAGTACTGTAGATGATCTTTTGTCGGTTTGAACACATTTGACCACATGAACATTTACAATTCAAAACCAATTTGATCAAATGCCATTTTTAACTTCTGTACCTCTGAAAGTGGTCAAAAGTGGACAATTTCACCTGTAATTAAAGTGTCACCCACTTGTGATTAAAAACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24864
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 |
---|---|---|---|---|---|
ENSDART00000112101 | Nonsense | 1135 | 1183 | 29 | 30 |
ENSDART00000145596 | Nonsense | 1139 | 1187 | 29 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 8930835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 9006791 |
GRCz11 | 10 | 8840350 |
KASP Assay ID:
554-7712.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTGTTGCATTTATTATGCAGGTAAGGATTCAAGTCACCAAAGACATA[C/T]GAACTGGAATCCCACTGTGGATTATTATCCTTAGTATTCTAATAGGACTT
Long Flanking Sequence:
TAATCTGTAATTAGCCATTTTTCTCATCCTACATTTGTGATAATCATTTCTGTATCACAATACAGAAGACCTTGGTAGCTCTTTAGTATAGGGACCAATTCTGAATACTGGTTTATTACAGCACCTGCCTATTATTAAGATTGACTGTTTATTAGTACTTAAAAAGTACATATCCTGCTTAATTTTATTCTACATCCCTAATCTTACCCATTACCTAAACCGAACTACTACCTTATTAACTATTATTAAGCAGCAAAATAGGAGTTTACTGTACTAAAGTTTATAGTGAATGGTTTGTTAGTGGCGATATTTGTATCTTAAGATAAAGTTTGAACAAGATCTTAATTTTTCCAAATAAAAGTCAATAATAAAGGATTTATTTTGTCAGGTTGTACAGCAAAATAGTTTGAAATTACAACTTGGACTCCTTAGTAATTTTCACAATTGTGATGAGTGTTGCATTTATTATGCAGGTAAGGATTCAAGTCACCAAAGACATA[C/T]GAACTGGAATCCCACTGTGGATTATTATCCTTAGTATTCTAATAGGACTTTTAATACTGGCACTTGTTATCTTCGCTTTATGGAAGGTAAGTAGTGATGTTTACCTTAAGCTTACTTGCTTTAACACACCAATGCCCTTTTTCACCTGGTATTATTAATGTTAACCTTGTTAAAAGGCTATCAACTGAGCAAGTGAATAAAAAAAACAATATGTAGGTGGTAATGATGTAATTCTACCAAATAAAACCTTAACTTAATTAAACTTCTCACAACATCTTTTATAACGATCATGTTTTCAGTCAATCAGTGTGGAGTACTGTAGATGATCTTTTGTCGGTTTGAACACATTTGACCACATGAACATTTACAATTCAAAACCAATTTGATCAAATGCCATTTTTAACTTCTGTACCTCTGAAAGTGGTCAAAAGTGGACAATTTCACCTGTAATTAAAGTGTCACCCACTTGTGATTAAAAACTCAACACCAGGTGTAAACAG
Associated Phenotype:
Not determined