ZMP

si:ch73-182i17.2

Ensembl ID:

ENSDARG00000079002

ZFIN IDs:

ZDB-GENE-040910-7, ZDB-GENE-100921-26

Human Orthologue:

DNAI1

Human Description:

dynein, axonemal, intermediate chain 1 [Source:HGNC Symbol;Acc:2954]

Mouse Orthologue:

Dnaic1

Mouse Description:

dynein, axonemal, intermediate chain 1 Gene [Source:MGI Symbol;Acc:MGI:1916172]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18389	Nonsense	Available for shipment	Available now
sa37271	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa18389

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
Order Allele From EZRC

Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000056647	Nonsense	209	556	9	17
ENSDART00000131444	None	None	225	None	8
ENSDART00000134914	Nonsense	236	583	10	18
ENSDART00000148114	None	None	169	None	8

The following transcripts of ENSDARG00000079002 do not overlap with this mutation:

ENSDART00000146523

Genomic Location (Zv9):

Chromosome 21 (position 16865896)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	18260059
GRCz11	21	18296695

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

WAAAAAAAANGTCTCTGCAGTGATTATTTGTGTCTGTTTGTTTCTAGGAAC[A/T]AAAAATACAATGATTTGTTTRCTRTTGGTCTTGGGTCACGTAAGTCACTA

Long Flanking Sequence:

GATTTGGTTTGTTAAGGTGCTGCTGAAGAGGAGATTTATATTATTATTAACACCTAACCTACATAAAGTGCCTGAAAAAAATCTCCTCGTTTGTTTATAGTCTGATCATGACCTGGCCATGTTATCTACAGCGGCCAAGCTTCTTGAATATGCGGTGAATGAAAATATAAATGGAGACATAATTGCAGGTAATTATAAAAATACAGTTTCTTTTCACCCCTACACCATTTATTTTTGATTACATTAAATGAATTTTCAAATTTAAACACTTTTTTTTTTAACCCAAACCTCAGATTTCAAGCACTTTGAAGACGAAGCGGATGAATTTCGAGGAGACAAGGGGACTCTTCTCCCACTGTGGGAGTTTCAGTATAATAAAGTCAAAAGTCTTCATGTGAGCGCCCTCTGCTGGTAAATCTCACACTAAATGATGTTAATTAGAGTTTAAGTAAAAAAAAAGTCTCTGCAGTGATTATTTGTGTCTGTTTGTTTCTAGGAAC[A/T]AAAAATACAATGATTTGTTTGCTGTTGGTCTTGGGTCACGTAAGTCACTATTTTTACAAATATGGCTGTGAAAAAAGTTTTAAATTTTTTACCTTTTATTCTTTTGCTCAAAATATGAACAAATGAATTAAGACACAAAAAAACTGCTCTGATTAAGAACCAACAATGTATTATTATAAATATAGGTAGGGTGACGCAGTGGCGCAGTTGGTAGTGCTGTCGCCTTACAGCAAGAAGGTCGCTGGGTTGCTGGTTTGAGCCTCGGCTGGGTCAGTTGGCATTTCTGTGAGGAGTTTGCATGTTCTCCCTGCGTTCGCGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTGGGAGTGTGTGTGTGTGAATAAGTGTGTTTGGATGTTTCCCAGAGATGGGTTGTAGCTGGAAGGGCATCCGCTGCATAAAAACGTGCTGGATAAGTTGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37271

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
ENSDART00000056647	Nonsense	335	556	12	17
ENSDART00000131444	None	None	225	None	8
ENSDART00000134914	Nonsense	362	583	13	18
ENSDART00000148114	None	None	169	None	8

The following transcripts of ENSDARG00000079002 do not overlap with this mutation:

ENSDART00000146523

Genomic Location (Zv9):

Chromosome 21 (position 16864027)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	18261928
GRCz11	21	18298564

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCAAATCATTACAGTAAGGTTAATTGATCCCAGTCATTTGGATTTCAGTA[T/A]GAGCTATTCTCCACCAATATCATCAAGCTCCCACCAATGGACAAAGTTCC

Long Flanking Sequence:

GTGGCGGTGGGTTTATTCAATGGCAATGTGTGTGTGTACAACCTGATGGCAAAGGATGATCAGCCCATTTATAACAGCATGGCCAGTTCTGGCAAACACTCAGGCACTGTATGGCAGGTATGGATAAGGATGAGATAATGGAGTTGTCATTAAAACTATATATATATATATATATATATATATATATATGTATGTATATATTTATATTATATATATTTTAAATATCTTTCCCCATCAGACTTTTGAATAGTTGTATATTTATTTGGATTTGACTTCTAGAAGTTCCGGAAGGATATAGATTTTGTGTTTCTTTTTCTTTGTTACAGGTGAAATGGTGGGAGGACGATTTATATGGCAATCACACTTTCTTCTCTGTGTCCGCTGATGGACGAGTGGTGTCTTGGACTCTGGGAAAGGTACACAAGTAAATATTTATGTTTTGAATGTAAAGCAAATCATTACAGTAAGGTTAATTGATCCCAGTCATTTGGATTTCAGTA[T/A]GAGCTATTCTCCACCAATATCATCAAGCTCCCACCAATGGACAAAGTTCCTGATGACCTTAACAATGTCATTGTCACAGGTATGAACCTCTTTAGCTTTGCCTTTCATAGTTTAGCAGTGACTTTACTCACAATATCAGGAAATGCATCAACAGATACAGAAATGTACAATAATTCAGTAATATTGAGAGAGTATCAGTGTTATTGCCACTATCCTGCACATCAGTCGTCAGCTTTTATATTTCTATTATTCAATTCTTCATTTCACCTGTACAGATTGAATAATACATACATTTCACCCTAACAAAATTAAAATTTTAAACTGTCTGAGATTGAATTTCAGACTGTAGTTCTCATCAGTTCCAATTGATCAACAAATCAACAGTTAAGGTTCATTCACACCAAGGTCGATAACTATAAATACAACAATAACTATATTTGTTCTATAAACCATATAATAACAATCTTTTTATTTTTAGCTTTTTTGCATAACATTTTTGC

Associated Phenotype:

Not determined