ZMP

itga3b

Ensembl ID:

ENSDARG00000012824

ZFIN ID:

ZDB-GENE-050411-55

Description:

integrin, alpha 3b [Source:RefSeq peptide;Acc:NP_001177238]

Human Orthologues:

ITGA6, ITGA7

Human Descriptions:

integrin, alpha 6 [Source:HGNC Symbol;Acc:6142]
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]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22024	Nonsense	Available for shipment	Available now
sa35203	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa31854	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa22024

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

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105884	Nonsense	546	1041	12	26

Genomic Location (Zv9):

Chromosome 12 (position 6175251)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	5576074
GRCz11	12	5611031

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCACGTTTACAGGCCTTCTGTCTTTCTCTGCTTCTTCCTGTCAAGAGCTG[G/T]AGCTCAGTGTTAATGTGAGAGTCTATGATCACACTGTACACATTCTTTTT

Long Flanking Sequence:

CAAATTCTATAACAAATAAATAATTTTATATTAAATTTATTTATTTATTCATTTATTTATGTATATACATTTATATTAAAACTTTCAGGATGATTTTTTGGAGAAAAGACCTTATTATCAAAAGCATTTGATTTCACCTGTGTTGTATATTCTGTAAAAGGATGGTATTATTTCTTGGCGTTCATTTGAAAAGAGAAGAATGCTTTCAATGTGTGTTTCCAGCATAAAGGTGAAGGTGTGCTTCAGTTACACTCTCAGCAATGGAAACAGCAACTTCAGGAAGGAAATCAGTAAGTGAAGGCCTGATTCAGGAATGTTTGATGAGTGTTTTCATGGATTGATTGTGTGCTTCATTTTGTTTGTTTCTCTCTGCTTCAGCTGTGAAGTTTACGATAGATGCTGACCAGAATCGCAGAGGTGCTCGAGTACGCTTTATAGACAACAAGCAAAGCACGTTTACAGGCCTTCTGTCTTTCTCTGCTTCTTCCTGTCAAGAGCTG[G/T]AGCTCAGTGTTAATGTGAGAGTCTATGATCACACTGTACACATTCTTTTTCACACCGATATTAAAATTATATCTATATGTCAATAATCTATATGTCAATTTGTATTTACTGTCAGTGCATATAATGTTTCAGAAAAAGATTTATGGAAAAATAGATGAATGATTCATGAATATTTTTTGTTCAGTTAATTATAATATAAGGTTAATTATTAATAATTATTTTTTAAATGAATAATATTCATTTTTATGCATTTGTTATTTTATATATTATTTAATTGTTGAATTTAAGAATATTAATTAAAAAATATTCATAAACAATATGTTAATTTATTATGTATTATAGTGAGAAAATTATTATTTATTCTATATAATATTTATTACATTCATAATTTATTATATTAATATTTCATATTAAAATTTCAGCAATTTCTATAATAAAATACTCTATTATAAGAGAACATATTTAAATAATAAATAGATACTATATTATTTTTAGATGTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35203

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105884	Essential Splice Site	737	1041	18	26

Genomic Location (Zv9):

Chromosome 12 (position 6183532)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	5567793
GRCz11	12	5602750

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATCAATGCGCTATATGGTCACTGACAGTGATGATGTTTGTTTGTCTTCA[G/A]TATTAGTGAACAGGCGGATCTGTTTCCTGTTCTTGTCACCCTCAATGTGA

Long Flanking Sequence:

GCTTCAAAATGCAACTCTAAATACATCTGTCAGCCCCGTTTGAGAAGTCTATTTATAATTTTGCCTTTATTTTATCCACCACACACCGCAAAATAGTTTACTCTTTTGGATTAAAGATAGCCAACTCTCTCCTTCTAGCTAAAATAAACCTCTCCACCACTTTACATGAAACGATTGTTAACAAAGCATCTACTCAGTTTGTTCAAATATTTTTTAACAAATGAAGTGTAATTATTTTTCAAGTTTGTATTTTCAAGTGTGAGAGACAAGTACTGACATGAATTGCAGAGCGTCAGAGCAGAACTTATTAATATTCACAACCTTTCCAAATATGTTCAATATGGTCCTGTGGTTATAAATGAACATATTGAACCATTTGTGGAGATTTTTCTGAACTAAGCCACATATATTTCCTACTATGTAGATATCTGAGAACTATATAACATATTGAATCAATGCGCTATATGGTCACTGACAGTGATGATGTTTGTTTGTCTTCA[G/A]TATTAGTGAACAGGCGGATCTGTTTCCTGTTCTTGTCACCCTCAATGTGAAGAACACGATCCTCACTACATTTTCTTTGTACGTACTTTGATGTTATTAACAATAAAACAATCTGTGTGCATTTACATTTTACAAATAGTTCACCCAGAAATGAAAACTCTGTCATCATTTAGTCTGCACTTTATTTGTTTCAAACCTTTGAGTTTTTTTTCCTCTGTTAAAGACAAAAGAAGATATTTTAAAGAATGCTGGAAACCTGTAACCATTGCCTTCCATAGTATTTGTTTTTTTTTCTACTATGGAAGTCAGTGGTTATAGGTTTTGAGATATCTTCAAATTATTTTCTTTTATCTATATTTTGTGTTCAACAGTAGAAATAAACGGTAAGCCACATGAGGGTGAGTAAATAATGAGCAGATTTTCATTTTGGGGTGAACTATCCCTTTAAACAAACACAGTTGTGGTCTTGCTTAAAGCTTGATTTTCATTTTCTTCCTGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa31854

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

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105884	Essential Splice Site	763	1041	18	26

Genomic Location (Zv9):

Chromosome 12 (position 6183612)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	5567713
GRCz11	12	5602670

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCTTGTCACCCTCAATGTGAAGAACACGATCCTCACTACATTTTCTTTG[T/C]ACGTACTTTGATGTTATTAACAATAAAACAATCTGTGTGCATTTACATTT

Long Flanking Sequence:

ACACACCGCAAAATAGTTTACTCTTTTGGATTAAAGATAGCCAACTCTCTCCTTCTAGCTAAAATAAACCTCTCCACCACTTTACATGAAACGATTGTTAACAAAGCATCTACTCAGTTTGTTCAAATATTTTTTAACAAATGAAGTGTAATTATTTTTCAAGTTTGTATTTTCAAGTGTGAGAGACAAGTACTGACATGAATTGCAGAGCGTCAGAGCAGAACTTATTAATATTCACAACCTTTCCAAATATGTTCAATATGGTCCTGTGGTTATAAATGAACATATTGAACCATTTGTGGAGATTTTTCTGAACTAAGCCACATATATTTCCTACTATGTAGATATCTGAGAACTATATAACATATTGAATCAATGCGCTATATGGTCACTGACAGTGATGATGTTTGTTTGTCTTCAGTATTAGTGAACAGGCGGATCTGTTTCCTGTTCTTGTCACCCTCAATGTGAAGAACACGATCCTCACTACATTTTCTTTG[T/C]ACGTACTTTGATGTTATTAACAATAAAACAATCTGTGTGCATTTACATTTTACAAATAGTTCACCCAGAAATGAAAACTCTGTCATCATTTAGTCTGCACTTTATTTGTTTCAAACCTTTGAGTTTTTTTTCCTCTGTTAAAGACAAAAGAAGATATTTTAAAGAATGCTGGAAACCTGTAACCATTGCCTTCCATAGTATTTGTTTTTTTTTCTACTATGGAAGTCAGTGGTTATAGGTTTTGAGATATCTTCAAATTATTTTCTTTTATCTATATTTTGTGTTCAACAGTAGAAATAAACGGTAAGCCACATGAGGGTGAGTAAATAATGAGCAGATTTTCATTTTGGGGTGAACTATCCCTTTAAACAAACACAGTTGTGGTCTTGCTTAAAGCTTGATTTTCATTTTCTTCCTGTGGTCTGCAGGGAAAAGCTAATAATCGACACGTCGTTCAGCGGCAATGTGATCGGAGAATCTGCCATGAGCAGCACCAGTGA

Associated Phenotype:

Not determined