ZMP

kif19

Ensembl ID:

ENSDARG00000053026

ZFIN ID:

ZDB-GENE-080215-2

Description:

Kif19 protein [Source:UniProtKB/TrEMBL;Acc:A4IGD6]

Mouse Orthologue:

Kif19a

Mouse Description:

kinesin family member 19A Gene [Source:MGI Symbol;Acc:MGI:2447024]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22161	Essential Splice Site	Available for shipment	Available now
sa42087	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22161

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000130371	Essential Splice Site	194	1015	6	20

Genomic Location (Zv9):

Chromosome 12 (position 40325921)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	38607664
GRCz11	12	38782165

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGATACAAGTGGCGGGAATCACAGAGGTCTCCACCATTAATGCACGAGAG[G/A]TTAGAAACATTATTAATAGGCATTTCTTTTTCTTAAAACTCTAAAAGCAA

Long Flanking Sequence:

ATTCACTTTTAATGTTGAACACGTTTGTTAATGCCATTTTGAGGGTTCTCACCTGAAAAATGTCAAGAGATGAATGCATGTTCATGTGATAACTTTCACAATGCACCATGCTGCGCACTAATAGTCATGTTATCAAAAACCCCTCTCATATTTCACCAATTACACCAGTTGTCCTTGTGCTTGCCTTGTACTTTGCAATGGAAAGGTCACAGATTGCACTTTCTGATATTTATGCACAGCGAGTCCCCGCAGATAAAAGCATCTGTCAGATGCATGAATGTAAATGTCAAATGTGTAAATGTTCATACATAAACAATGATGCTAATCTTGAAATCTAAGCATGCTCTTTAATCTGTTGCATCCTTGTGTTGCAGATCTACAATGAGATGATAAGAGACTTGCTGAATCCGTCATCTGGGTTCCTGGACCTGAGAGAGGACTCAAAGGGAGAGATACAAGTGGCGGGAATCACAGAGGTCTCCACCATTAATGCACGAGAG[G/A]TTAGAAACATTATTAATAGGCATTTCTTTTTCTTAAAACTCTAAAAGCAAAAAAGTCAAAGCTGACTTTGACTTTGACTTTTGATGTCACAGTATCTATTTTTTGTTGTATGATATATTGTTTGTGGCTGGAAGGGCATCTACGGCGTAAAACATATCCTGGATAAGTTGGCAGTTCATTCCGCTGTGGTGACCCCAGATTAATAAAGGGACTTTATTATAAGGGGTTGTTCTTATTATATACATCATTGTTTAATGTATGATCTGTTGCTGTGGCTATCTTTGCACACAAGACGACATATTCATTGGCTTCAATTTATATTTAAATGTATTCATTTTGAGTATCCTTACTATTTACAACAATATTTTGTATGTTTTTTCTTAAATGATCAAATTAGACATTCTGTTCTGACTTATTTTTTTGTTCCTCGTTGTAAAAAATCTATGGGTAAAAGAGCTTTTATGTTTAAGGGTCCAACAGATTGGAATAATTTACCTGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42087

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
ENSDART00000130371	Nonsense	231	1015	7	20

Genomic Location (Zv9):

Chromosome 12 (position 40327648)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	38609391
GRCz11	12	38783892

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCAGACGTCTTCTCGCTCTCACGCTGTGCTGCAGGTGGTCGTGCGTCAA[C/T]AGAGTCGATGCCGAGACATCCTTCAGGAAGTGCGATTCGCACGACTCTTC

Long Flanking Sequence:

TTAATGTTTTACTGTATTTTATTGATATTACTTGTATAGTTTTTTCATTGTTTGCATTTTAGTTGTGTTGTATAATTTGTCCTTACTGGTGTAAAGCACTTTGGTCAACATTGGTTGTTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGGCCATAATTTGATTTAATAGGTAAACACAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTTTTACTTTTTTTTTATGTATGAAGTAAGTACATAATTTCTCAATATAAACGCACATGCATACACCTGGATGTTGACGTCTTTTCCGATCTGTTATTTCCTCATTCAGATCATGGAGTTGTTAATGAAGGGAAACAAACAGAGAACTCAAGAGCCGACTGCAGCCAATCAGACGTCTTCTCGCTCTCACGCTGTGCTGCAGGTGGTCGTGCGTCAA[C/T]AGAGTCGATGCCGAGACATCCTTCAGGAAGTGCGATTCGCACGACTCTTCATGATCGACCTGGCGGGGTCTGAACGGGCTTCGCAGGTATGATTTGCAGCTGTTAAACATAGCTATTTGTCTTTCAGAAGTTACATAAAAGCACAGTGGGTGAGTTTGGTGATGTGTGTGTTAATTTAAAATCACTAATATCCAAGCTATCAACCTTTCCAGTTACATAAAAGCTGGCACAGTCAGCGCCAAATATATTCAGAATCATAAATCAGCCAGTGATGTGGGAACAATTCCAAGAGTGATTTAGCTGAAGGGAAATGAAGCTTAAATGTAAATATGTATTGATTTATTCAGTGCATGAGACATCTCCATTTAAGTGTTTTTGATGAAAGACAAGAGAATCATGCTGTAAAATGTAATTTCCAGTCACTGCATGAGACTATGATACACCAGTGAACACATTTAGTACATGCCATGTATTTGCTATGGAAACGGTTAATAATGTGA

Associated Phenotype:

Not determined