ZMP

LOC557896

Ensembl ID:

ENSDARG00000089320

Human Orthologue:

C14orf38

Human Description:

chromosome 14 open reading frame 38 [Source:HGNC Symbol;Acc:19847]

Mouse Orthologue:

4930403N07Rik

Mouse Description:

RIKEN cDNA 4930403N07 gene Gene [Source:MGI Symbol;Acc:MGI:1921186]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36353	Essential Splice Site	Available for shipment	Available now
sa44867	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36353

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
ENSDART00000125212	Essential Splice Site	16	631	2	16

Genomic Location (Zv9):

Chromosome 17 (position 14303455)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	14420555
GRCz11	17	14428488

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTTATAACATGACAAGTGATACAATGAAACCTATGTCTGTTATATTTCA[G/A]TCAGGGGAGAGAAAACATTACAAGAAACTATGAAGATGCTGTTGATCAGC

Long Flanking Sequence:

GTTTTATTTGCATTCAACTGGAGAGAAAAGAATGGTAGCCTGTTCCCCCCCCACTGAAAAAAAAAATATATAATAATACATTTTTTTACAATTATTAAGTCTGAATTCTGAGTTATTTAGTCAGAAATTCCGGGTTATAAAGTCAGAATTCTGAGTTATAAAGTCAGAATTTAAAGTTATAAATTCAGAATTCCAAGTTAATAAGTCAGAATTCCGAGTTAAAAAGTCAGAATTCCATGTAAGTCAGAATTCCGAGTTAAGTCAGAATTCTGAGCTGACAATACTGACTTTATAACTTTTTTTTTACATTGTATTTATTCATTTATTTATTTTTTATTCAGTGGTGGCAACGGGCTTTCATAGAAAATCTATCACACCAGGAAGTAAATTCTTCCACAACAGGGCCATGGCCCAAATCCTGATCATGGAGGAAACAAAATCATCAGCATATTTTATAACATGACAAGTGATACAATGAAACCTATGTCTGTTATATTTCA[G/A]TCAGGGGAGAGAAAACATTACAAGAAACTATGAAGATGCTGTTGATCAGCTGAACCAGATGCTGTCGAAGAAAGTTGATACACAGATGCTGCTCAAAGAAAAACAGAATGAGATCCAGTCATTAAAGGACAAAATCGCCCAGGTGGAAATGGCTCAACAGATCCTGAAAGAAAACAGGATTCAGAGAAACAAAATATTTACAGAAAGCAAACACTCTGTGCAAAAGGAGGTAATCTGAGCATATGTGTTTTATCTTGTTTGTTTTTAAAGGTAGATTTTCACATCAAGACTGTTGTTAAATTCACATTTTCCCTCTTTAGCTAGAGCAAATTGTTCTTAAGATAAAAGAACAAAGAAAAATCAATGCAGAAACACGGAGGGAAACAGACAGCATTACATCAGAGCTCCAAGACAAGGAGGACACAGTGACACAATGTGAAAACGTAAGCATCTACACACACTGCAAAATGTCAAACCAAACTGAAAATAATGTTGATATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44867

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000125212	Nonsense	26	631	2	16

Genomic Location (Zv9):

Chromosome 17 (position 14303486)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	14420586
GRCz11	17	14428519

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTATGTCTGTTATATTTCAGTCAGGGGAGAGAAAACATTACAAGAAACTA[T/G]GAAGATGCTGTTGATCAGCTGAACCAGATGCTGTCGAAGAAAGTTGATAC

Long Flanking Sequence:

ATGGTAGCCTGTTCCCCCCCCACTGAAAAAAAAAATATATAATAATACATTTTTTTACAATTATTAAGTCTGAATTCTGAGTTATTTAGTCAGAAATTCCGGGTTATAAAGTCAGAATTCTGAGTTATAAAGTCAGAATTTAAAGTTATAAATTCAGAATTCCAAGTTAATAAGTCAGAATTCCGAGTTAAAAAGTCAGAATTCCATGTAAGTCAGAATTCCGAGTTAAGTCAGAATTCTGAGCTGACAATACTGACTTTATAACTTTTTTTTTACATTGTATTTATTCATTTATTTATTTTTTATTCAGTGGTGGCAACGGGCTTTCATAGAAAATCTATCACACCAGGAAGTAAATTCTTCCACAACAGGGCCATGGCCCAAATCCTGATCATGGAGGAAACAAAATCATCAGCATATTTTATAACATGACAAGTGATACAATGAAACCTATGTCTGTTATATTTCAGTCAGGGGAGAGAAAACATTACAAGAAACTA[T/G]GAAGATGCTGTTGATCAGCTGAACCAGATGCTGTCGAAGAAAGTTGATACACAGATGCTGCTCAAAGAAAAACAGAATGAGATCCAGTCATTAAAGGACAAAATCGCCCAGGTGGAAATGGCTCAACAGATCCTGAAAGAAAACAGGATTCAGAGAAACAAAATATTTACAGAAAGCAAACACTCTGTGCAAAAGGAGGTAATCTGAGCATATGTGTTTTATCTTGTTTGTTTTTAAAGGTAGATTTTCACATCAAGACTGTTGTTAAATTCACATTTTCCCTCTTTAGCTAGAGCAAATTGTTCTTAAGATAAAAGAACAAAGAAAAATCAATGCAGAAACACGGAGGGAAACAGACAGCATTACATCAGAGCTCCAAGACAAGGAGGACACAGTGACACAATGTGAAAACGTAAGCATCTACACACACTGCAAAATGTCAAACCAAACTGAAAATAATGTTGATATGGGATGATTTGCATGGTGTGCATTCTTTTCAG

Associated Phenotype:

Not determined