ZMP

tuba8l3

Ensembl ID:

ENSDARG00000070155

ZFIN ID:

ZDB-GENE-040801-77

Description:

tubulin, alpha 8 like 3 [Source:RefSeq peptide;Acc:NP_001003558]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21433	Nonsense	Available for shipment	Available now
sa27339	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa21433

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
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Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000102715	None	None	450	None	4
ENSDART00000125494	Nonsense	83	577	2	5

The following genes are also affected by this mutation:

ENSDARG00000094466

Genomic Location (Zv9):

Chromosome 9 (position 7720874)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	7700967
GRCz11	9	7679358

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAACAGACTGACACTTTCAGCTTTTTGTAAATGTAGATGAAGTGCGGACA[G/T]GAACCTACCGCCAGCTCTTCCACCCTGAACAACTGATTACTGGGAAAGAG

Long Flanking Sequence:

ATTGCTCTGCGCTGGACTTTAGACCGGGTTTGTTCTGGTCTAAAGAATAGACTATTACAGTTTCTCAAAATAGTTTGTTTCTGTTGTAGTTTCTGTTATCACTTTATTTTGATGGACTCTTTAACAAATTTTGTTGAATTTATGTTACATTGCATCTACAGGCCAACTAATTCTCATTAGATTATAAGTAGATTGTTAGCTTAGTGTAGGTTAGGGTTAGTGTAAGTTGAAATGTACTTGCAAAGTTGCTTATAGTCAGTTAAATATGTTGAAGCAGCAGTATCAAGAGATATTAAGCAGACTATCTATTAATACTCAAATGAGAAGTAATTGGCATGTAGGTGCAATGCAACTTTTAGTCAACAAAATGTGCAATAGGGACCATCAAAATAAAGTCTTACCTAGTTTTCATTTAATTTGAACTTTAAGTTCATTAAAATAAACAATAAAAAACAGACTGACACTTTCAGCTTTTTGTAAATGTAGATGAAGTGCGGACA[G/T]GAACCTACCGCCAGCTCTTCCACCCTGAACAACTGATTACTGGGAAAGAGGATGCTGCCAATAACTATGCCAGAGGACACTACACCATTGGCAAGGAGATTATTGATTCAGTTCTGGATCGTATACGCAAACTGGTAATATATTAATCTGATTATCTGCTTAGTTAATAAAATAAGTTCTGCTTCTTGGTCAAATTAGTGTGTTGTATTCTTATTTGAATGCTCTCTTTCTTATCTCTCCCAAAAGTCCGACCAATGCACTGGCCTTCAAGGTTTCTTAGTGTTCCACAGTTTCGGTGGAGGCACTGGCTCTGGCTTCACCTCTCTGCTGATGGAGCGTCTCTCTGTCGACTATGGCAAGAAGTCCAAGCTTGAGTTTGCCATCTATCCTGCTCCTCAAGTGTCCACAGCAGTGGTGGAGCCCTATAACTCCATCCTGACCACCCACACCACCCTGGAGCACTCCGATTGTGCCTTCATGGTGGACAATGAAGCCATCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa27339

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
ENSDART00000102715	Nonsense	220	450	4	4
ENSDART00000125494	Nonsense	347	577	5	5

Genomic Location (Zv9):

Chromosome 9 (position 7704997)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	7685090
GRCz11	9	7663481

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGTGGACAATGAAGCCATCTACGACATCTGCCGCAAAAACTTGGACATC[G/T]AGCGTCCAACCTACACCAACCTCAACAGGCTCATTGGGCAGATTGTGTCC

Long Flanking Sequence:

ACTGAATACAATCAATTCTAACTCTTATTATATTCATTTATCCAAATCTTAACTCTTTAACGTCAACACTTTACTCTGAAATGCTTCAACACCGAGAATTTAACTCAGATGAATTTGCTGTGTATATATATATATATATATATATATATATATATATATATTGTCATTTGTAAAATACAACTTCTAATAAAATAATGTACTTTACAAAAATCCAACAGGCTGACCAGTGCACTGGCCTTCAAGGATTTCTCATCTTTCACAGTTTTGGTGGAGGCACTGGGTCTGGCTTCACCTCTCTGCTGATGGAGCGTCTCTCCGTCGACTATGGCAAGAAGTCCAAGCTTGAGTTTGCCATCTATCCTGCTCCTCAAGTGTCCACAGCAGTGGTGGAGCCCTATAACTCCATCCTGACCACCCACACCACCCTGGAGCACTCCGATTGTGCCTTCATGGTGGACAATGAAGCCATCTACGACATCTGCCGCAAAAACTTGGACATC[G/T]AGCGTCCAACCTACACCAACCTCAACAGGCTCATTGGGCAGATTGTGTCCTCCATTACAGCCTCACTGAGATTCGATGGAGCTCTCAATGTGGATCTCACCGAGTTCCAAACCAATCTGGTGCCCTACCCCCGCATTCACTTCCCTCTGGCCACATATGCACCAGTGATTTCTGCTGAAAAGGCGTATCATGAGCAGCTCTCTGTGGCCGACATAACCAACGCCTGCTTTGAGCCGTCCAATCAGATGGTGAAGTGTGATCCTCGTCACGGTAAATACATGGCCTGCTGTCTTCTGTATCGCGGAGATGTGGTGCCCAAAGATGTCAACTCTGCCATCGCTGCCATTAAAACCAAACGCACCATCCAGTTTGTTGACTGGTGCCCCACTGGCTTCAAAGTAGGCATCAACTATCAGCCTCCAACAGTGGTTCCTGGTGGAGATCTGGCCAAAGTACAGAGAGCCGTGTGCATGTTGAGCAACACCACAGCTATCGCTGAG

Associated Phenotype:

Not determined