Busch Lab

ZMP

itga6b

Ensembl ID:
ENSDARG00000069946
ZFIN ID:
ZDB-GENE-050320-5
Description:
integrin, alpha 6b [Source:RefSeq peptide;Acc:NP_001013466]
Human Orthologue:
ITGA6
Human Description:
integrin, alpha 6 [Source:HGNC Symbol;Acc:6142]
Mouse Orthologue:
Itga6
Mouse Description:
integrin alpha 6 Gene [Source:MGI Symbol;Acc:MGI:96605]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa16239 Nonsense Available for shipment Available now
sa10618 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16239
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000102210 Nonsense 202 1085 4 25
Genomic Location (Zv9):
Chromosome 1 (position 30092997)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 30232809
GRCz11 1 31036740
KASP Assay ID:
2259-0705.1 (used for ordering genotyping assays)
KASP Sequence:
GGATCATGCCAGCAGGGCATGTCCGCCACRTTCACAAAGGACTATCACTA[T/G]CTGGTGTTTGGAGCACCAGGCGCTTACAACTGGAAAGGTATTAAAGGAAG
Long Flanking Sequence:
TATATGCATTTTTATCATAACAAAAGTATTCAACCTGTAGGTTCAATTGGGCTGAGGACAAGGACAGTGACAGAGTTTGTACAGTGTAAAGTGTTCCTTTACAGAACAACCGTAACAATCAGTCCATTTTAGAATATTTTGGGATGAAAACTTAAATCACTGTATTTATGTTTTTATTTCAGGGACAGATAATGAACATTGCTTGTAGATTGTCCCGTATGTTTAGTATTTATCAGTAAATGCTATTTAAACTTAACTCCCAATGTCTCAATCCAGGTCTGTGCACATCGATACCAGCGGCGCTTATTTGTTGGCTCAGTTCAGGAACTGCGTGACTTGACAGGTCGGTGCTATGTACTTAGTGAGGATGTGACGATTAATGAGATCTCAGATGAAGATGGAGGGGATTGGATGTTCTGCAATGGGAGAAACAGAGGGCACGAGCGGTTTGGATCATGCCAGCAGGGCATGTCCGCCACATTCACAAAGGACTATCACTA[T/G]CTGGTGTTTGGAGCACCAGGCGCTTACAACTGGAAAGGTATTAAAGGAAGAGCTTGTATTATTTAAACTTTTGTTAAAATTTGAATAGTATTTGATGCTTTTTTGCAAGGTCAAAAAATACTTTTATTGTCTTATGATGTGCATTTCTTTTACCGAATTATCCTAGCGACTCCCATATGATTCGTTCAGTGATTCATTTGTTCCCAAAACCCCTCCTTAGTGCGATGCCAGTCTGCGCTGATAGGTCCGATGACCCAGTCTGTTGCGATTGGTCGACTGCTTTCAGCGTGAGGCAGAGAGAAATGCCCACCATGGCTTATCAACAATTTTGAAGTAGAGTGCAGAGTGTATGTGTGAGCCCAATGTAGGAGTGCATTAAAACAATGCAGTAAACACCAGCATATTGCTATATTCTTAACCATAAGTAAAAACAGTGACACACATTTAGTATTAATCCACACAGCGGCAAAAGCTGAGCTATTTGGAAACTTGACTGCCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10618
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000102210 Nonsense 418 1085 8 25
Genomic Location (Zv9):
Chromosome 1 (position 30098702)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 30238514
GRCz11 1 31042445
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATATGACAGCAATGGAGCTGGAAACRTGATTATCTTCCACGGTTCACCA[C/T]AAGGACTGAAAAAATCCCAGGTGCAGCCATATATCCACTTTACTTTCTGT
Long Flanking Sequence:
AAAGTATTTCTGTGTTAATAACAAAACATTTAAGTTTTATTAACCTTTAGTTTTATAAATACACTATTCCAGAAGCATAATTATTTGAACTGATTCTTAAAACAGGTGGCAAGACATTGTAGTTGGAGCACCTCAGTACTTCATTAAAGATGGTGATATTGGTGGAGCAATCTATGTTTACCTTAACGAGGAAGGAGCTTGGGACAAGATTACTCCAAAGAGAATTGATGGACCTGCTTATTCCATGTTTGGTTTGGCTGTGGAAAACATGGGAGATGTGAATCTGGATGGATATCAAGGTATGTGTTCAGTATGTGTTATGAATACAACTAATGCAAACATATTAAAACATATCTTGCCACATGTTATTAAAGCAGAACCAATTGCACTCATTTAAATTATTTTTTAATGTGACCTATACTGTATCTTCAGATGTTGCTGTTAGCGCCCCATATGACAGCAATGGAGCTGGAAACGTGATTATCTTCCACGGTTCACCA[C/T]AAGGACTGAAAAAATCCCAGGTGCAGCCATATATCCACTTTACTTTCTGTTTACTTATTGACACATTTTCCATACACTTTTTTATGAATGGTTCTTTGATAATTTAAGGTTCTTGGAGGAAAAGATCACAATGTGAAACTCTTTGGATACTCTCTTGCTGGGAACATGGATCTGGACAGAAATAATTACCCTGATCTGGCCATTGGATCTCTTTCTGATTCAGTGTTTGTGTACAGGTATGATCCTACTGATGGACAGGACAATACCATATTGATAATACAGTTTATTTAATTTAATAATATCATCAATCATCTTTGATCATACGATTTTATATTTTATTGAATATTTAATAATATTTTATTTTAAGATTTATTTATTATTATTTTATAAAATTGCATAGAGCAGCCACACATTCTTTTATTCATTGAGCACTGTAAAACATAATTAGTTTTCAGTTTTTCCTATTTTTTACAATTCATTTTGAGGCTGATCTCTGCTCT
Associated Phenotype:
Not determined