ZMP

krt4

Ensembl ID:

ENSDARG00000017624

ZFIN ID:

ZDB-GENE-000607-83

Description:

keratin 4 [Source:RefSeq peptide;Acc:NP_571584]

Human Orthologues:

KRT8, KRT8P11

Human Descriptions:

keratin 8 [Source:HGNC Symbol;Acc:6446]
keratin 8 pseudogene 11 [Source:HGNC Symbol;Acc:31058]

Mouse Orthologue:

Krt8

Mouse Description:

keratin 8 Gene [Source:MGI Symbol;Acc:MGI:96705]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38567	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa45260	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38567

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000012644	Essential Splice Site	222	497	4	9
ENSDART00000065351	Essential Splice Site	222	497	4	10

Genomic Location (Zv9):

Chromosome 6 (position 39241502)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	39313102
GRCz11	6	39310638

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCACTTCATTTTATTAGCAATAAGGTATTAATGTCCTCTCGTTTTTTTC[A/T]GGATGTTGATGCAGCCTACATGAACAAGGTTGAGCTTGAAGCCAAGGTTG

Long Flanking Sequence:

TCCCTAAGGTGCTTAAAAAACAAAAACCACAAATGTAATTGATTTTCCTCCCCTCAGGTGCGCTTCCTGGAACAGCAGAACAAGATGCTGGAGACCAAATGGAGTCTTCTCCAAGAACAGACAACCACACGTTCCAACATCGATGCCATGTTTGAGGCATACATCTCTAACCTGCGCAGACAGCTCGATGGACTGGGAAATGAGAAGATGAAGCTGGAGGGAGAGCTGAAGAACATGCAAGGCCTGGTTGAGGACTTCAAGAACAAGTGAGTGAAGCTGTATTCATGTAGTTGAATAATTTGACCAATAAACAACATTGACTCACTTGCTTTGTCTTATCTCTTAACAGGTACGAGGATGAGATCAACAAGCGTGCTTCCGTAGAGAATGAGTTTGTCCTTCTCAAGAAGGTAATGATTGCTTGCCTGTTTCTGTTCTGGTATCCTTTTTTGCACTTCATTTTATTAGCAATAAGGTATTAATGTCCTCTCGTTTTTTTC[A/T]GGATGTTGATGCAGCCTACATGAACAAGGTTGAGCTTGAAGCCAAGGTTGATGCTCTTCAGGATGAGATCAACTTCCTCAGGGCAGTCTATGAGGCTGTAAGTTAAACTCTGTTGTATTTTGGCACACGAAGAGTTCTGCTTCTTTGTAAGGGAGGATAATTAATTGGCTTTCATTTGCAGGAACTCCGGGAGCTCCAGTCTCAGATCAAGGACACATCAGTTGTTGTAGAAATGGACAACAGCAGAAACCTGGATATGGACTCCATCGTGGCTGAAGTTCGTGCTCAGTATGAAGACATCGCCAACCGCAGCCGTGCCGAGGCAGAGAGCTGGTACAAACAGAAGGTGGGTCAAACTCTAAAAGCTTCAACTCTTTGATCCCACCTCATCTGTCCATGCAAGTGCTTATTTGTGGCATTATTTCCAGTTTGAGGAGATGCAGAGCACCGCTGGTCAGTATGGTGATGACCTCCGCTCAACAAAGGCTGAGATTGCTGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45260

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000012644	Nonsense	313	497	6	9
ENSDART00000065351	Nonsense	313	497	6	10

Genomic Location (Zv9):

Chromosome 6 (position 39241061)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	39312661
GRCz11	6	39310197

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGTCCATGCAAGTGCTTATTTGTGGCATTATTTCCAGTTTGAGGAGATG[C/T]AGAGCACCGCTGGTCAGTATGGTGATGACCTCCGCTCAACAAAGGCTGAG

Long Flanking Sequence:

ATCCTTTTTTGCACTTCATTTTATTAGCAATAAGGTATTAATGTCCTCTCGTTTTTTTCAGGATGTTGATGCAGCCTACATGAACAAGGTTGAGCTTGAAGCCAAGGTTGATGCTCTTCAGGATGAGATCAACTTCCTCAGGGCAGTCTATGAGGCTGTAAGTTAAACTCTGTTGTATTTTGGCACACGAAGAGTTCTGCTTCTTTGTAAGGGAGGATAATTAATTGGCTTTCATTTGCAGGAACTCCGGGAGCTCCAGTCTCAGATCAAGGACACATCAGTTGTTGTAGAAATGGACAACAGCAGAAACCTGGATATGGACTCCATCGTGGCTGAAGTTCGTGCTCAGTATGAAGACATCGCCAACCGCAGCCGTGCCGAGGCAGAGAGCTGGTACAAACAGAAGGTGGGTCAAACTCTAAAAGCTTCAACTCTTTGATCCCACCTCATCTGTCCATGCAAGTGCTTATTTGTGGCATTATTTCCAGTTTGAGGAGATG[C/T]AGAGCACCGCTGGTCAGTATGGTGATGACCTCCGCTCAACAAAGGCTGAGATTGCTGAACTCAACCGCATGATCGCCCGCCTGCAGAACGAGATCGATGCTGTCAAGGCACAGGTAGAGTGGAGCAAGTGTAAATACACAAATAGTTTGCACTATTCATGAAAGACCCTGACTTCAATCAATATTGCTGTTTAGCGTGCCAACTTGGAGGCTCAGATTGCTGAGGCTGAGGAGCGTGGAGAGCTGGCAGTGAAGGATGCCAAGCTCCGCATCAGGGAGCTGGAGGAAGCTCTCCAGAGGGCCAAGCAAGACATGGCCCGCCAGGTCCGCGAGTACCAGGAGCTCATGAACGTCAAATTGGCTCTGGACATTGAGATCGCCACCTACAGGAAACTGTTGGAAGGAGAGGAGAGCAGGTAGGAAGTCTTGAACACTTCACTTACTGTCATAAAAAACATGGTGCTGAAAACCATGACTAAGCAAATCTATTGTCTACTTTAT

Associated Phenotype:

Not determined