ZMP

si:ch73-199e17.1

Ensembl ID:

ENSDARG00000094466

ZFIN ID:

ZDB-GENE-100921-8

Description:

tubulin alpha 8-like 3b [Source:RefSeq peptide;Acc:NP_001161759]

Human Orthologue:

TUBA4A

Human Description:

tubulin, alpha 4a [Source:HGNC Symbol;Acc:12407]

Mouse Orthologue:

Tuba4a

Mouse Description:

tubulin, alpha 4A Gene [Source:MGI Symbol;Acc:MGI:1095410]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21433	Nonsense	Available for shipment	Available now
sa8481	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
ENSDART00000016360	Nonsense	109	477	4	5
ENSDART00000102713	Nonsense	81	449	3	4

The following genes are also affected by this mutation:

ENSDARG00000070155

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:

sa8481

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
ENSDART00000016360	Nonsense	248	477	5	5
ENSDART00000102713	Nonsense	220	449	4	4

Genomic Location (Zv9):

Chromosome 9 (position 7720345)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	7700438
GRCz11	9	7678829

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGGTGGACAATGAAGCCATCTACGACATCTGYCGCAAAAACCTGGACAWC[G/T]AGCGTCCGACCTACACCAACCTCAACAGGCTCATTGGGCAGATTGTGTCC

Long Flanking Sequence:

ACAACTGATTACTGGGAAAGAGGATGCTGCCAATAACTATGCCAGAGGACACTACACCATTGGCAAGGAGATTATTGATTCAGTTCTGGATCGTATACGCAAACTGGTAATATATTAATCTGATTATCTGCTTAGTTAATAAAATAAGTTCTGCTTCTTGGTCAAATTAGTGTGTTGTATTCTTATTTGAATGCTCTCTTTCTTATCTCTCCCAAAAGTCCGACCAATGCACTGGCCTTCAAGGTTTCTTAGTGTTCCACAGTTTCGGTGGAGGCACTGGCTCTGGCTTCACCTCTCTGCTGATGGAGCGTCTCTCTGTCGACTATGGCAAGAAGTCCAAGCTTGAGTTTGCCATCTATCCTGCTCCTCAAGTGTCCACAGCAGTGGTGGAGCCCTATAACTCCATCCTGACCACCCACACCACCCTGGAGCACTCCGATTGTGCCTTCATGGTGGACAATGAAGCCATCTACGACATCTGTCGCAAAAACCTGGACATC[G/T]AGCGTCCGACCTACACCAACCTCAACAGGCTCATTGGGCAGATTGTGTCCTCCATTACAGCTTCGCTGAGATTCGATGGAGCTCTCAATGTGGATCTCACCGAGTTCCAAACCAATCTGGTGCCCTATCCCCGCATTCACTTCCCTCTGGCCACATATGCACCAGTGATTTCTGCTGAAAAGGCATATCATGAGCAGCTCTCTGTGGCCGACATAACCAACGCCTGCTTTGAGCCGTCCAATCAGATGGTGAAGTGTGATCCTCGTCACGGTAAATACATGGCCTGCTGTCTTCTGTATCGTGGAGATGTGGTGCCCAAAGATGTCAACTCTGCCATCGCTGCCATTAAAACCAAACGCACCATCCAGTTTGTTGATTGGTGCCCCACTGGCTTCAAAGTAGGCATCAACTATCAGCCTCCAACAGTGGTTCCTGGTGGAGATCTGGCCAAAGTACAGAGAGCCGTGTGCATGTTGAGCAACACCACAGCTATCGCTGAG

Associated Phenotype:

Not determined