ZMP

ENSDARG00000068085

Ensembl ID:

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa21127	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa21127

Status:

Available for shipment
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Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098268	Nonsense	21	510	1	6

Genomic Location (Zv9):

Chromosome 7 (position 68082752)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	10887352
GRCz10	15	43773229
GRCz10	21	42432061
GRCz10	3	57568799
GRCz10	5	26444770
GRCz10	7	65744610
GRCz10	9	23886633
GRCz11	15	10809747
GRCz11	21	42444827
GRCz11	3	57639323
GRCz11	5	27044923
GRCz11	7	65968258
GRCz11	9	23697502

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATTACTAATGTGTTACCAGACCTACCAACCTCAAATCTAAATATTGTAT[T/A]GGAGACATTACAATCTTTAGGTGTGGGAGCCACTGAAGATTTACAGTATA

Long Flanking Sequence:

GTCAGACAATATGGTTTCACTGATACCAACACAGCTGTCACAGTAGAAATGGTTTATAAAGGAACAGCCTACAAGAAAGGACAGTTCCTTGTCACAGGGTATACTGACTTGGTGGAATTTGGTGAACTTGTGCTCATTTTGGTAAAAAACAACACCGTTTATCTTTTGGTGTCAATGTACACAGCAGAATTCCTTCCTCAGTACCATGTGTACTCAGTGAGGAAAGACAATGAAATGATCCAGTGTTTTAACATCTGTGACATGATTGATTTCTATCCATTGGCTGCTTACATGAAAGATGGACAACGACTGGTTCCATTGAAACACAGTGTTTTGTCACACTAATTATGTCTTGTGCTGTCAAAATTGAAAGTTTTTTTTTTTCTTTTTGTCTTTTTACATTTTTTTACTCAGAATGGATGACGTAGAGCCAAGCAACATAAGCAGTGCCATTACTAATGTGTTACCAGACCTACCAACCTCAAATCTAAATATTGTAT[T/A]GGAGACATTACAATCTTTAGGTGTGGGAGCCACTGAAGATTTACAGTATATTAAGGAAGCTGATCTGCTCACAGTACTGAGACCAGTTCAAGCTAGAAAACTGTTGGCTGCATGGAAACAATCCAGTAAGTACATTATGCAGAAAGTTACATTTACTTGTAAGTTAAGATAAAAAAAAACAAATTTCATTCTGTACATTTAAATTTCAATTTATTTTACAGCAGAGACAACTGAATTCCATAGTCAGTCAACATTGACCTCTCCAGTGTCCTCAGCCTGCTCCTCAGTCTCACTGTCTTCCTCACCCTCACCCTCACCATCACCCAGACACATGATTGCTACTGCAGATTGGGTCGACAGCTTCCAGATTCCATGGGAGAAGCTCCCAGAAGCCTTAATGCAGAGTTTGGAGAGAGGGAAAAGGCCAAGCTCAAAGTTACGCAGAGAACTGATCCGAATTGTAGTTGCTGAAATGATGCATGCCTCTTCTTCTCCTGGTA

Associated Phenotype:

Not determined