ZMP

tfe3b

Ensembl ID:

ENSDARG00000019457

ZFIN ID:

ZDB-GENE-010919-3

Description:

transcription factor binding to IGHM enhancer 3b [Source:RefSeq peptide;Acc:NP_001038531]

Human Orthologue:

TFE3

Human Description:

transcription factor binding to IGHM enhancer 3 [Source:HGNC Symbol;Acc:11752]

Mouse Orthologue:

Tcfe3

Mouse Description:

transcription factor E3 Gene [Source:MGI Symbol;Acc:MGI:98511]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14907	Essential Splice Site	Available for shipment	Available now
sa35090	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14907

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000011250	Essential Splice Site	230	447	5	8

Genomic Location (Zv9):

Chromosome 11 (position 26450216)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	25279041
GRCz11	11	25516657

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCCAGAGCTTTCATGAAGGAGAGACAGAAGAAAGATAATCACAATCTCAG[T/C]GARTTCAAAACACASAGACTTCAGTAGCGTATTATTGTCTGTTTGTGTGW

Long Flanking Sequence:

CTATATACAGAGCATACAGTCCTTCTGTTGCAGGTTGTTCAGGTGTCCAGAAATCTACATTTGATTTAATTTAGCGTTTTTTTGAAGTCATGTGCGTCAACAGTGCTAAACGTGGTGGTAAAGCAATATTCCTTCATAACATTGTGTTTTAGGCAGCTTTGATCATTATCTGTTTCTAGCAGAGTTTGATGTTTTTCAAAGTGTGTTTCTGTCATAGCTTCCAGGAAATCTTCTGGATGTCTACAACAGTCCTGGTATGACGACTCCAACCATCACCGTCAGCAACTCCTGTCCAGCAGATCTGCCCAACATCAAAAGGGAATATACTGGTAATGGTATTGTGATCGGTGTGTCTTCTATATTCCATTATTTTCTGTCGTGTTGTGTATCTGCTGTACAGTATAGGGTAGGCGGTGGTCATAATGGCTGTTGTGTTTTCCAGAAACAGAGGCCAGAGCTTTCATGAAGGAGAGACAGAAGAAAGATAATCACAATCTCAG[T/C]GAGTTCAAAACACACAGACTTCAGTAGCGTATTATTGTCTGTTTGTGTGACTGTGTGATTACATCTGTGCTTTGTTTTGTGAAGTTGAACGGCGGAGAAGATTCAACATAAATGACAGAATAAAGGAGTTAGGGGCTCTAATACCCAAATCCACTGATCCGTAAGTTTCTTTCCTTCAGGCTTTTGTGTTTTGAGAAACAATACAAAACTGACTGTAGCATTGTTTGAGCTTGAAATATTTTGATCCAAAACATCTCTCATGGTGAAAAGTTTCACATTTGTTGTGGAGACATTCTGGAAGTACCAAAACCAATTAATTCAAAGTTTGTGATGCTTTATTGTAATATAAATCTAAATCAGTATATTTATATAAACAACTTTTAAATAATAAAAAAAAGTTTTATTTGTTTTATTTCAGATAGTATAAAAGCAGTTTAAATTTTTTTAACCATTTTAAGGTAAATCATATTAAGCAATTTTTTTATTTACTACAGGATAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35090

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000011250	Nonsense	370	447	8	8

Genomic Location (Zv9):

Chromosome 11 (position 26452985)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	25281810
GRCz11	11	25519426

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTCAACATGGATGGAGCAATGGCACAGACTTCACCATCTCCTTTCCTCT[C/A]AGTACCTCCATCCGGCTCTCCGGCTGCTGTGGCTGTGAGCGGCCCGCTAC

Long Flanking Sequence:

TTTCAAAGTGTTACCTTAATCACATCCTTGACAACACCCAATACAAGAATCTTTGAAATCAGTGACGTAGAAATGTGCAGTTGATTTTAAAGGCAGGTGCTAACAGACACACACCAAATTCAACTATATCTTTGTCATGTAAACGCAGCCTTAGAATACCTAAATGTTTTGAGTAATCTAAATTTATCAGATTTGATGGTGTGTAACTGTTTTAGCTACTAATAGACTGCTTATTTTGCCAGTATATAATATATACACTGGCAAGATGACATGAATGTGACCTCCTGTTGTTTGTTGCATGCAGGAACTAGAAATACAAGCACGCCACCATGGCCTTAATGCTACCGTGTCTCCAGGCCTGAACACAGAGGCATCCTTCATCCAAAACCAGCTACTGCAGCCAAATGCGTCTATGCAGGCCGGCGTCGGAGATGGTCAGCCTCAGAGCCACCTCAACATGGATGGAGCAATGGCACAGACTTCACCATCTCCTTTCCTCT[C/A]AGTACCTCCATCCGGCTCTCCGGCTGCTGTGGCTGTGAGCGGCCCGCTACATCTGGAGACTTTTAGCTTCACAGAGCTGGACGAACATGCCTCTGATTTGTACCCTGACGTTGGTCTTAGTGACATTCTGATGGATGACGTCAGGGGTTCGGATGTGCTCTTCTCCCCGATGTCGCCCGGAGCCTCCAAAACCAGCAGCCAAGGGAGCAGCGTAAATATGGAGGATGACTTGTGACCCAACTGACCGCTAGATGTATGTTTCAGTGCTTTTTCCTAATGTGGGACGCTGTGAGGTTTTTTTTAAGGGAAAGTTCACCTAAAATTAATATTTTAAGTCCAAAGTACACTTTGTTGCCTTCTTTCTACTAGGATTGTCAATCAAGTTCAATAGCAATCAGTACTGAAATTTTCAAAACCTCCATTACTGCTAATATTTGAGCGTGTTCTTTAACACCCCTGATTGGCTATTGTGTTCACATGCTCAAAAGAAATGACTGTGA

Associated Phenotype:

Not determined