ZMP

si:ch211-133j6.3

Ensembl ID:

ENSDARG00000058332

ZFIN ID:

ZDB-GENE-090312-205

Description:

LOC553479 protein [Source:UniProtKB/TrEMBL;Acc:Q502A4]

Human Orthologues:

AC090051.1, KRT18

Human Descriptions:

Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:C9JEA8]
keratin 18 [Source:HGNC Symbol;Acc:6430]

Mouse Orthologue:

Krt18

Mouse Description:

keratin 18 Gene [Source:MGI Symbol;Acc:MGI:96692]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa45788	Nonsense	Mutation detected in F1 DNA	Not yet available
sa11708	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa45788

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
ENSDART00000081193	Nonsense	196	410	3	7

Genomic Location (Zv9):

Chromosome 23 (position 10460482)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	10419284
GRCz11	23	10354254

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGCAGACATAAATGCACTGAGAAAAATGCTGGATGACACCAATGTGGCA[C/T]GACTCCATCTGGAAAATGATGTTGAAGGATTAAAGGTAGAGCTCATCGAG

Long Flanking Sequence:

ATAGGCTGTATTCTACTTGTCCACTTAGATCTTGGAGATGATTATGAGAAATGTAAATGTTAATCTTCAAATTGACAATGCCAAGTTGGCTGCTGAAGACTTCAAGATCAAGTACGTAATTACAAACACATTAAAACTAAGCTCTGTTTTTTTTTTGGGGGGGGGGGGGGGGGGGGTTATTGCTTTTCTGTTATTTAATTGATGGAGTTATATATATTTTAATTGTTGGAGTATTATATTTTTTATTTAATAAATGCATAGTCTTAACAATATAATTGTGTAGCAGATATGAACATGGGAACATACCGATAAATCATGTTGCGTCTAAATTTGTCTGATGAAACACAAAATTAAGAATGTCCCTCACCTTAATGTAATCCCATTAACAAAATATGTTTTTTTTTAAAATATGTAGGTTTGAAAATGAATTTCAGCAAAGACAGTGTGTTGAGGCAGACATAAATGCACTGAGAAAAATGCTGGATGACACCAATGTGGCA[C/T]GACTCCATCTGGAAAATGATGTTGAAGGATTAAAGGTAGAGCTCATCGAGATCAAGAAACAGCATCAACTGGTAAATACAACGATTATATAATATAGAAATATTGAATTTGCAGTCTGCTTACTGGCTCAGAAGGTGTAACAAACATATACATATAAAGGGGCCTAAGATATAACCCTGTGGAACATCAAATCACCTATTTTTCAGGAATTGTCAGCACTAAATGGTCAAATTACCCAATCAGGAGTGCAAGTGGACATAAATGCCCCTAAGGGACAGGACCTGGCTAAGATAATGGAGGAGATGAGAGCAAACTATGAAAAGATTGTGCTGAAAAACCAAGAAGAGCTCAAAGCCTGGCATGAATCAAAAGTGGGGCATCATTTCTCAATGCAAAGGTATTCATGTTTTAAAGAGAAATATTTAAATGTAATACACATTTATTTTGTATACGTAGATATCTGTGGTGCAGGTTCAAGTGACAGAAAACACTGCAGCATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11708

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081193	Essential Splice Site	220	410	4	7

Genomic Location (Zv9):

Chromosome 23 (position 10460687)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	10419489
GRCz11	23	10354459

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TAAAGGGGCCTAAGATATAACCCTGTGSAACATCAAATCACCTATTTTTC[A/T]GGAATTGTCAGCACTAWATGGTCAAATTACCCAATCAGGAGTGCAAGTGG

Long Flanking Sequence:

AGTTATATATATTTTAATTGTTGGAGTATTATATTTTTTATTTAATAAATGCATAGTCTTAACAATATAATTGTGTAGCAGATATGAACATGGGAACATACCGATAAATCATGTTGCGTCTAAATTTGTCTGATGAAACACAAAATTAAGAATGTCCCTCACCTTAATGTAATCCCATTAACAAAATATGTTTTTTTTTAAAATATGTAGGTTTGAAAATGAATTTCAGCAAAGACAGTGTGTTGAGGCAGACATAAATGCACTGAGAAAAATGCTGGATGACACCAATGTGGCACGACTCCATCTGGAAAATGATGTTGAAGGATTAAAGGTAGAGCTCATCGAGATCAAGAAACAGCATCAACTGGTAAATACAACGATTATATAATATAGAAATATTGAATTTGCAGTCTGCTTACTGGCTCAGAAGGTGTAACAAACATATACATATAAAGGGGCCTAAGATATAACCCTGTGGAACATCAAATCACCTATTTTTC[A/T]GGAATTGTCAGCACTAAATGGTCAAATTACCCAATCAGGAGTGCAAGTGGACATAAATGCCCCTAAGGGACAGGACCTGGCTAAGATAATGGAGGAGATGAGAGCAAACTATGAAAAGATTGTGCTGAAAAACCAAGAAGAGCTCAAAGCCTGGCATGAATCAAAAGTGGGGCATCATTTCTCAATGCAAAGGTATTCATGTTTTAAAGAGAAATATTTAAATGTAATACACATTTATTTTGTATACGTAGATATCTGTGGTGCAGGTTCAAGTGACAGAAAACACTGCAGCATTGAAGGAGGCCAGCACACAACTCAGCGTGAGCCGCAGGCGGATGCAGACTTTAGAAACTGACCTGCAGACTCTGACTGGAAGTGTAAGAGATTCTGAAACACCTCGATGGAGCTGCCTAAGTTTAAACATACTATTTACGCTCATGTTTTTTTGGCCTTTACTTGTAGAGAGCATCTCTGGAAGAAGCCCTTAATGAAACAAAGTT

Associated Phenotype:

Not determined