ZMP

si:dkey-61f9.2

Ensembl ID:

ENSDARG00000045867

ZFIN ID:

ZDB-GENE-041210-12

Description:

Novel protein containing Lectin C-type domain [Source:UniProtKB/TrEMBL;Acc:Q5RIZ7]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20186	Essential Splice Site	Available for shipment	Available now
sa40207	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa20186

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
ENSDART00000067413	Essential Splice Site	134	365	3	5
ENSDART00000136225	Essential Splice Site	132	242	2	3

Genomic Location (Zv9):

Chromosome 4 (position 3676411)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	3795024
GRCz11	4	3803937

KASP Assay ID:

554-6372.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGAATCTGTCTTATGCAATGAGACAAAACACTTCATGTGCTATGAACAAG[G/A]TAATAAATACCAGTTTATAAATATTAAATGTAATTAAATGAAACAAAAAC

Long Flanking Sequence:

AACTATAAAAGACATTCATATGATACAATCTGATGATCAAAAGTGTCATTATAAGTCATTTCACTGTTTCAAGTCAAAGTGTCATTTCAGAGAAGATGTTGATGTTGTGTTTCTGAAATGTGGATTTTTCTCTTCAGCTTTTCCTCCTTCAGCTGCTGAAGGTCGACTGAGACAATTCTACATGCTGAACCAGAAGACTATCAATACATCTGCTGCTCAGAGTTTATGCAGAGTAAACTACACTGACCTCGTCACAGTTTATGACCAACAAGACAATATTAAACTACTGCAACTGATCAAGAACAGCAGCTCTTCAGTTGGCTGGATTGGTGCTTCTAGAGGAAACTACAGTCTGAAATGGTCAAATGGTGATGATGTTTCATACAGCAGATATTCTCCAAATTATTCTGATCAAACACACTGTGCTGCTATGAATGCTACTGGAGATTGGGAATCTGTCTTATGCAATGAGACAAAACACTTCATGTGCTATGAACAAG[G/A]TAATAAATACCAGTTTATAAATATTAAATGTAATTAAATGAAACAAAAACTCTTAATTCATCCACACAGAAGCTGGAGGATCATCATACATACACTCATTAATCCTTCAACCAAACAGCTGGTTTGATGCTCAGCTTTACTGCAGAGAGAATCACACTGATTTAGTCTCTATCAGAAATGAGGAGGAAAATACCCTGGTGATGAACAATGGAAATCAGAGTAATACTTCTTTCTGGATCGGCCTGCTGAATGACAGTGTGGACTGGAGAGATGGAGGACGATCTGCTTACAGAAACTGGCGTGAGAAGACTAATCACAGCATGAGTTATGTTGCCATACAGTCTGCTGATGGGCGATGGTTCAAAGCTAGCGCTGGGAACTTCTATCCTCTGTGCTACAGTAAGAAGACACACACAACAGCTGTAAAACTCAATTAATTTCCATTTTCTCTTCACATGTCATTATAATCTGCTGTATTTGACTAGTTTTGGATGTCTGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40207

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067413	Nonsense	204	365	4	5
ENSDART00000136225	Nonsense	202	242	3	3

Genomic Location (Zv9):

Chromosome 4 (position 3676135)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	3794748
GRCz11	4	3803661

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTCTTTCTGGATCGGCCTGCTGAATGACAGTGTGGACTGGAGAGATGGA[G/T]GACGATCTGCTTACAGAAACTGGCGTGAGAAGACTAATCACAGCATGAGT

Long Flanking Sequence:

TATTAAACTACTGCAACTGATCAAGAACAGCAGCTCTTCAGTTGGCTGGATTGGTGCTTCTAGAGGAAACTACAGTCTGAAATGGTCAAATGGTGATGATGTTTCATACAGCAGATATTCTCCAAATTATTCTGATCAAACACACTGTGCTGCTATGAATGCTACTGGAGATTGGGAATCTGTCTTATGCAATGAGACAAAACACTTCATGTGCTATGAACAAGGTAATAAATACCAGTTTATAAATATTAAATGTAATTAAATGAAACAAAAACTCTTAATTCATCCACACAGAAGCTGGAGGATCATCATACATACACTCATTAATCCTTCAACCAAACAGCTGGTTTGATGCTCAGCTTTACTGCAGAGAGAATCACACTGATTTAGTCTCTATCAGAAATGAGGAGGAAAATACCCTGGTGATGAACAATGGAAATCAGAGTAATACTTCTTTCTGGATCGGCCTGCTGAATGACAGTGTGGACTGGAGAGATGGA[G/T]GACGATCTGCTTACAGAAACTGGCGTGAGAAGACTAATCACAGCATGAGTTATGTTGCCATACAGTCTGCTGATGGGCGATGGTTCAAAGCTAGCGCTGGGAACTTCTATCCTCTGTGCTACAGTAAGAAGACACACACAACAGCTGTAAAACTCAATTAATTTCCATTTTCTCTTCACATGTCATTATAATCTGCTGTATTTGACTAGTTTTGGATGTCTGTTGTTGTCAGAGAGCTTCATTCATGTGAGTCTTGCTGAAATGTCCTGGGAAGATGCTATGAATTACTGCAGCTCTCAGTTTTCTGGAGCTCTGTGTCTGGAGTCTGAGAACGATCAGACAGAAACGCAGCGAGAGTTAAACAGAAATAATATCTCTGCTCCAGTTTGGGTGGGTCTCAGACAGAGCTGTCCTTTCGGATTCTGGATGTGGATCAATGGTCTTCAAGTGGGAAACTGGACAAACTGGAGAGGAGGAAAGGCTCCTGAAGCTGCGCTTTC

Associated Phenotype:

Not determined