ZMP

KIAA2026

Ensembl ID:

ENSDARG00000086023

Description:

KIAA2026 [Source:HGNC Symbol;Acc:23378]

Human Orthologue:

KIAA2026

Human Description:

KIAA2026 [Source:HGNC Symbol;Acc:23378]

Mouse Orthologue:

9930021J03Rik

Mouse Description:

RIKEN cDNA 9930021J03 gene Gene [Source:MGI Symbol;Acc:MGI:2444398]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23833	Nonsense	Available for shipment	Available now
sa37197	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23833

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000129678	Nonsense	846	1301	2	2

Genomic Location (Zv9):

Chromosome 21 (position 1296606)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	1001007
GRCz11	21	1026831

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTCATCCCACAGGACTGCAAGTCCCAAGTACTGTTCATCCTAAAGGAT[T/A]GCAAGTCACAAGTGTGGCTCCTTCTGTAGGATTGCAAGCCCCAAGTTCTG

Long Flanking Sequence:

TGCATCCCTTTGCACTTCACGCTCACCGGTTAAAACAACAGCCAATTCTTGTGCTTCTGGTGTATCTCATTCTGTTGCAATAAGCCCAAACTCTCCTTCAACTCTTCCAATTGTCATGACTTCTGGGATTCGACCTCCAGCCACAACTAACAAAAGTGTTCATGAAAGAGTCGTAATAAACACCACTGCCCCACTTGCTCCAGGAACTCAGCTGCTAATAAACAACACCAGATTTGTTGTCCCATCTCAAGGCCTTGGACCTGGCACCCATGTCTTGCTCATCAGCTCAGGATCTGGAGGACAGCAGGCCTCAAGTACGGTTCATCCCAAAGGATTACAAATTACAAGTTCAGTTCGTTCTAGAGGACTGCACGTCCAGAGTCCTGCTCATCCCACAGGACTGCAAGTCCAGAGTCTTGCTCATCCCACAGGACTGCAAGTCCAGAGTCCTGCTCATCCCACAGGACTGCAAGTCCCAAGTACTGTTCATCCTAAAGGAT[T/A]GCAAGTCACAAGTGTGGCTCCTTCTGTAGGATTGCAAGCCCCAAGTTCTGCTCATCCTGCAGAATTGCAAATCTCAAGTCCTGCTCGGCCTAAAGGATTGCAAGTTCCAAGTTCTGTTCATCTTTCAGGATTGCAAGTTCCAAGTTCTGCTCCTCCTGCAGTATTGCAAGTTCAAAGTCCTGTTTGTCCTGCAGGATTGCAAGTCTCAAGCCCTGTTCATTCGGCAGGATTGCACGTCCCAAGTCCTGCTTCTCCTGCTGTATTTCAAGTCACAAGTCCTGCTTGCCCCAAAGGATTGCAAGTTCCAAGTCCTGTTAATCCTGCAAGATTGCAAGTCTCAAGTACTGCTTCTCCTGTACAATTGCAACCCCCGAATCCTACTCATTCTGCGGGATTGCAAGTCCCAAGTCCTGTTAATCCTGCAGGATTGCAGGTTTCAAGACCTGTTCATCTTGCAGGTTTGCAAGTCTCAAGTCATGTTCATCCTGGGGGATTGCAGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37197

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
ENSDART00000129678	Nonsense	912	1301	2	2

Genomic Location (Zv9):

Chromosome 21 (position 1296804)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	1001205
GRCz11	21	1027029

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTCCTCCTGCAGTATTGCAAGTTCAAAGTCCTGTTTGTCCTGCAGGAT[T/A]GCAAGTCTCAAGCCCTGTTCATTCGGCAGGATTGCACGTCCCAAGTCCTG

Long Flanking Sequence:

TCCAGGAACTCAGCTGCTAATAAACAACACCAGATTTGTTGTCCCATCTCAAGGCCTTGGACCTGGCACCCATGTCTTGCTCATCAGCTCAGGATCTGGAGGACAGCAGGCCTCAAGTACGGTTCATCCCAAAGGATTACAAATTACAAGTTCAGTTCGTTCTAGAGGACTGCACGTCCAGAGTCCTGCTCATCCCACAGGACTGCAAGTCCAGAGTCTTGCTCATCCCACAGGACTGCAAGTCCAGAGTCCTGCTCATCCCACAGGACTGCAAGTCCCAAGTACTGTTCATCCTAAAGGATTGCAAGTCACAAGTGTGGCTCCTTCTGTAGGATTGCAAGCCCCAAGTTCTGCTCATCCTGCAGAATTGCAAATCTCAAGTCCTGCTCGGCCTAAAGGATTGCAAGTTCCAAGTTCTGTTCATCTTTCAGGATTGCAAGTTCCAAGTTCTGCTCCTCCTGCAGTATTGCAAGTTCAAAGTCCTGTTTGTCCTGCAGGAT[T/A]GCAAGTCTCAAGCCCTGTTCATTCGGCAGGATTGCACGTCCCAAGTCCTGCTTCTCCTGCTGTATTTCAAGTCACAAGTCCTGCTTGCCCCAAAGGATTGCAAGTTCCAAGTCCTGTTAATCCTGCAAGATTGCAAGTCTCAAGTACTGCTTCTCCTGTACAATTGCAACCCCCGAATCCTACTCATTCTGCGGGATTGCAAGTCCCAAGTCCTGTTAATCCTGCAGGATTGCAGGTTTCAAGACCTGTTCATCTTGCAGGTTTGCAAGTCTCAAGTCATGTTCATCCTGGGGGATTGCAGGCCCTTGGAGATTTACAAGCCCCAAGTTCTGCATCTACTGTTCTTAAAGGGCCAAAGAGTTTGGTCCCTTATACTGTTGCTTCAGTTGTACAAGGTGTAAGATTGGCAACTCCAGTCAGGCTTCCCTCGCCAATAACTGGGCCTTCCGGTCAAGTCCATCAGCAGCTAAACACCATAACTCCACTGAAGGTGGCTGGTC

Associated Phenotype:

Not determined