ENSDARG00000034836

Ensembl ID:

Human Orthologues:

KRT7, KRT81, KRT82, KRT83, KRT84, KRT85, KRT86

Human Descriptions:

keratin 7 [Source:HGNC Symbol;Acc:6445]
keratin 81 [Source:HGNC Symbol;Acc:6458]
keratin 82 [Source:HGNC Symbol;Acc:6459]
keratin 83 [Source:HGNC Symbol;Acc:6460]
keratin 84 [Source:HGNC Symbol;Acc:6461]
keratin 85 [Source:HGNC Symbol;Acc:6462]
keratin 86 [Source:HGNC Symbol;Acc:6463]

Mouse Orthologues:

4732456N10Rik, 5430421N21Rik, Krt7, Krt81, Krt82, Krt83, Krt84, Krt86

Mouse Descriptions:

RIKEN cDNA 4732456N10 gene Gene [Source:MGI Symbol;Acc:MGI:3045312]
RIKEN cDNA 5430421N21 gene Gene [Source:MGI Symbol;Acc:MGI:3690448]
keratin 7 Gene [Source:MGI Symbol;Acc:MGI:96704]
keratin 81 Gene [Source:MGI Symbol;Acc:MGI:1928858]
keratin 82 Gene [Source:MGI Symbol;Acc:MGI:2149248]
keratin 83 Gene [Source:MGI Symbol;Acc:MGI:3665486]
keratin 84 Gene [Source:MGI Symbol;Acc:MGI:96700]
keratin 86 Gene [Source:MGI Symbol;Acc:MGI:109362]

Allele Name	Consequence	Status	Availability
sa25387	Nonsense	Mutation detected in F1 DNA	Not yet available
sa9896	Essential Splice Site	Available for shipment	Available now
sa14026	Nonsense	Available for shipment	Available now

Allele Name:

sa25387

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000045669	Nonsense	91	376	2	8

Genomic Location (Zv9):

Chromosome 8 (position 7662774)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	7049577
GRCz11	8	7093125

KASP Assay ID:

554-7672.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCTCTGAAACACTGGCAGGTTCGCAAACTAGAGCAGGAGAACAAGCTTT[T/A]GGAGACCAAATGGCGACTACTACAGAAAGAGACTAAAGCGGAGTCTAAAC

Long Flanking Sequence:

GTGGATAACAGGTGGGCTGAACAGGTTTTTCAGACTGAGGAATGCTGGTTTATCTTCATTTATGCAGAAATACACACCCACCTGTCAGTATATAAGCATCAGGATTGTCAGGAGCAGCGTGTGTGTGTTTAGCCATGAGTTTCAGCAGCCGCTCTGTGGGCTCCAACGCCTCAATCCCCCGGCAGGGAAACTCTTATTTCGGCTTTGGGAACATGATGCCGGCATCTGGAGCCCCGATCAGACCTGTGTCTGTGAACAGCAGTCTGCTGGCGCCGGTGGATCTGCAGCTGGACCCAGAGCTGCAGACGGTGCGCATGCAGGAGACACAGCAGATGAAGACGCTCAACAACCGCTTCGCCTCCTTCATCGACAAGGTCTGTTAATCACACCAGACTGAAGTTGGAAATTAATTAGAATATTTTTCGACATCTGAATAAATGACAATAAACCTTCTCTGAAACACTGGCAGGTTCGCAAACTAGAGCAGGAGAACAAGCTTT[T/A]GGAGACCAAATGGCGACTACTACAGAAAGAGACTAAAGCGGAGTCTAAACTGGAGCCCATGCTGAAGAATTACAGCACTTCCTTACAGATGCAGCTGGAGAGAGTGAAGAAAGACAAAGAGCAGCTGGATAACGAGCTCAGAAAAGCCCACGCACAGGTCCAGGAGCAAAAGCAGAGGTATGTATAGTCGCATCTGCTGAAAACTACAGTTCAGTTTATCATCATCAGCAGAATAATAGTTTTAGTGTAAACGTTAAATTCAATATATCCTAATATAAATGCTAAATAATGTAAAACAACAACAATACTGTTTGCAGCTATTATCATGGTAATCAGAGCTTAAGGCATAATATTGTGCATAATTTTCAATATACAGTTGAAGTCATAATTATTAGCCCCCCTTTGAATTTTTTGTTCCTTTTTAAATATTTTACAAGTGATGTTTAACAGAGTGGGGCGAGGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAG

Associated Phenotype:

Not determined

Allele Name:

sa9896

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:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000045669	Essential Splice Site	150	376	2	8

Genomic Location (Zv9):

Chromosome 8 (position 7662596)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	7049399
GRCz11	8	7092947

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GATAACGAGCTCAGAAAAGCCCAYGCACAGGTCCAGGAGCAAAAGCAGAG[G/T]TATGTATAGTYGCATCTGCTGAAAACTACAGTTCAGTTTATCATCATCAG

Long Flanking Sequence:

CCGGCAGGGAAACTCTTATTTCGGCTTTGGGAACATGATGCCGGCATCTGGAGCCCCGATCAGACCTGTGTCTGTGAACAGCAGTCTGCTGGCGCCGGTGGATCTGCAGCTGGACCCAGAGCTGCAGACGGTGCGCATGCAGGAGACACAGCAGATGAAGACGCTCAACAACCGCTTCGCCTCCTTCATCGACAAGGTCTGTTAATCACACCAGACTGAAGTTGGAAATTAATTAGAATATTTTTCGACATCTGAATAAATGACAATAAACCTTCTCTGAAACACTGGCAGGTTCGCAAACTAGAGCAGGAGAACAAGCTTTTGGAGACCAAATGGCGACTACTACAGAAAGAGACTAAAGCGGAGTCTAAACTGGAGCCCATGCTGAAGAATTACAGCACTTCCTTACAGATGCAGCTGGAGAGAGTGAAGAAAGACAAAGAGCAGCTGGATAACGAGCTCAGAAAAGCCCACGCACAGGTCCAGGAGCAAAAGCAGAG[G/T]TATGTATAGTCGCATCTGCTGAAAACTACAGTTCAGTTTATCATCATCAGCAGAATAATAGTTTTAGTGTAAACGTTAAATTCAATATATCCTAATATAAATGCTAAATAATGTAAAACAACAACAATACTGTTTGCAGCTATTATCATGGTAATCAGAGCTTAAGGCATAATATTGTGCATAATTTTCAATATACAGTTGAAGTCATAATTATTAGCCCCCCTTTGAATTTTTTGTTCCTTTTTAAATATTTTACAAGTGATGTTTAACAGAGTGGGGCGAGGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCACTGGTTCGAACCTCGGCTCAGTTGGCGTTTCTGTGTGGAGTTTCCATGTTCTCCCTGCCTTCGTGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGTGGTACAGGTGAATTGGGTAGGCTAAATTGTCTGTAGTGTATGAGTGTGTGTGTGTGGA

Associated Phenotype:

Not determined

Allele Name:

sa14026

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000045669	Nonsense	334	376	7	8

Genomic Location (Zv9):

Chromosome 8 (position 7656281)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	7043084
GRCz11	8	7086632

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CRGTGCTTGATGCCACYGAGCAAATCCGCCTGCTGGAGGAAGCACTGCAG[A/T]AAGCCAAAAAGGAAATGGCCAGACAGCTTAGAGATTACCAGGAGCTGATG

Long Flanking Sequence:

CTTACTTCAACTGTATATATAGATATTATTAATTGTGTATTTCTATCTATGTATACCTCATAATTGTGCATATACCTGTTTTCCTCCACAGTTTGACTTGGTTTCATCTCAGGCTAACCAGTGCAGCACAGAGCTGAAAAACAACAAAGGTGCAATAGACGAGTTGAAAAGGAAAATACAGCGCCTGCAAAATGACATCACCTCAGCTAAATCACAGGTAAATTTCCAGATAACACTATTCATCGGCTCGTTTATTTACAATGAAACTGATTGTATCTGTCAGTAAAAGCATGGATGCCTTTCAATACTATCTCAGAGGCGATCTCTTAATGGGCCGGGCCTGTAGATGCATGTTAGCAGCTCGATCTGTGTGATTTACATTTCTGACACCATTACAGTGTGACAACGTGGAGGAGAAAATCAAGGAGGCGGAGCGTGACGGCGAGGAGGCGGTGCTTGATGCCACTGAGCAAATCCGCCTGCTGGAGGAAGCACTGCAG[A/T]AAGCCAAAAAGGAAATGGCCAGACAGCTTAGAGATTACCAGGAGCTGATGAACCTCAAACTGGCTCTGGATATCGAGATCGCCACATACAAGAAACTACTGGAAGGAGAAGAGGACAGGTGAGACCGTGAAGCCGGAGTGCCCCACTTATGATTTTAAGTACTGGATTAACTACTAATCTTTTAATATATCTATAGAGGGAAAATAAGTATTGAATAGGCCATCATTTTTCTCAGAAAACATATTTCTAAAGGTGCTGTTGACTTGAAATTTTCTCAAGATGTTGGTAACAACCAAAGAAATCTATATATGCAAAGAAAACTAAACTGATTAGATTATAAATTAAGTTATGTGTATTAAAATGAAATTACACCTGTAAAAAGTATTGAACACATGAAGAAAGGGAGGTGTAGAAAGGCAGTGAAAGCCCAGACAGCAGCTGAAATGTCTTGGTAGTTATTCAGCAACTCTCTGCTCTTCCTCAGTGTAAATGAATATTCG

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details