ZMP

tmod2

Ensembl ID:

ENSDARG00000002571

ZFIN ID:

ZDB-GENE-040912-185

Description:

tropomodulin-2 [Source:RefSeq peptide;Acc:NP_001004608]

Human Orthologues:

TMOD2, TMOD3

Human Descriptions:

tropomodulin 2 (neuronal) [Source:HGNC Symbol;Acc:11872]
tropomodulin 3 (ubiquitous) [Source:HGNC Symbol;Acc:11873]

Mouse Orthologues:

Tmod2, Tmod3

Mouse Descriptions:

tropomodulin 2 Gene [Source:MGI Symbol;Acc:MGI:1355335]
tropomodulin 3 Gene [Source:MGI Symbol;Acc:MGI:1355315]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa29074	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa17697	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa29074

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000012164	Essential Splice Site	202	344	6	10
ENSDART00000130473	Essential Splice Site	202	344	5	10

Genomic Location (Zv9):

Chromosome 18 (position 37805192)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	39386895
GRCz11	18	39367903

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAGGCCAATGATCCCACGTTGACTGAAGTCAATCTCAACAACATCAAGG[T/C]AATGAGACTTATCCACTAAATGTGTTCTAATGAGACATTAAAAACATAAA

Long Flanking Sequence:

AGTGACAAACTGCAAGCTTTAGACATTTATATAGGTTTTATACTTTCTAAACAGCAATTTTGGAACACACTAGCTCAGGGGTCACCAAACTTGTTCCTGGAGAGCCGGTGTCCTGCAGATTTTAGCTCCAACCCTAATCAAACACACCTGAACAAGCTAATCAAGGTCTTACTAGGTATAGTTGAAACATCTAAGCAGGTGTGTTGAGGCAAGTTGGAGCTAAACCCTGCTGGGACAACAGCCCTCCAGGACCGAGACTGGTGACCCCTGCACTAGCAAATAGATATCCTTAATTTTCATTTCACAGGACCTATAATGCACATGTTATTCAGTGGAAGCTCATTTGAGAATAAATCATTGTCTTGTAGATGTCATTAAAGGAGAAAAGGTAAAGCCTGTTTTTGATGAACCTCCAAACCCTACAAACGTTGAAGAAAGTCTGCAGAGGATAAAGGCCAATGATCCCACGTTGACTGAAGTCAATCTCAACAACATCAAGG[T/C]AATGAGACTTATCCACTAAATGTGTTCTAATGAGACATTAAAAACATAAACATACAAATTTCACTGAAATCCTATCATTATAAATGATGTTTATTAGTTTTATATTACTTAATGTGAAAAATGTGACTCTTGTGCAGACAAGTTTTTTTTTTTTTTTTGCAAAAGGTTACATGAACCATTTTAAATAATGCTGGGGAGCTTGATCATCAGGTTTTATGTTCATGTCAGCTAATTACATATAATGACGGACATTCTTAAATTATTCTTAAAATTTCACTCACTAGTGGTGCAACCAGTCACAGTTTATTTTATGATTCATACTGACCACAACTTACGATTTACATTTGATCCAGTGATAATCAGCTAAATGTAACCCAGACAGCCACATTTCAGATGATTTGTTAAATCCGAATAAGTTACAGTACATCCATGAGGACTTTTAAATAAGCCAGTTCTAGTTCTGGAGCTTCCAGTGAACTGTCCTGCTATAATAAACTCGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17697

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000012164	Essential Splice Site	286	344	8	10
ENSDART00000130473	Essential Splice Site	286	344	7	10

Genomic Location (Zv9):

Chromosome 18 (position 37810921)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	39392624
GRCz11	18	39373632

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGCTCTTCGAGACAACGACACGCTTTCAGAGATCAAGATCKACAACCAGG[T/A]AAGGTCACAAGCACATACTGACYGTCACAAACTGTTAATGGTCGTTTTTR

Long Flanking Sequence:

TGCATCTGCTTGTATTGCTCCTGAGTCATTTCTAATTAATTTAAGAGTAATGTAGTTTCATTCTTGCGTCATCGTGAAATAAGGTTTAATTAAAATTTTGGAGACTTGTAAAAACTTAACACATGTGGTGTCCAAGGTTATTCATAAAAGGTCATGTATGCATTTTAAATATTTTAAAAAAGCTTTCAAAAAGACTTTATATCAGGTTCCTGCAGAATCCCTGATCACAAATATGTTTGTCTTTTTTATCATTATTGTTTACATACAATGTTGGCTAATTTTAGCACTATAAACATTCATATAGTACATCTTAATGCCATGTAAAGCTTTGTTTGTTTCTTTGTGTTCGTTGCAGGCGTTCTCAGACATGCTGCGAGAAAATAAGACGCTAAGGAGTTTGAATTTGGAGTCTAATTTCATCACCGGTGCAGGAGTTCAGGCTCTTGTAGAAGCTCTTCGAGACAACGACACGCTTTCAGAGATCAAGATCGACAACCAGG[T/A]AAGGTCACAAGCACATACTGACCGTCACAAACTGTTAATGGTCGTTTTTGATTTATGGGTGTTTTCGATTGATTTTATCTTGCATGACATCAAACTGTGAGACATCAGTATCTTCTCAGACAACATTTGCTGTTGAAAAGTGTACCAACATGGCGCTTATTTCTATTTTTAGTTCTTTGAAACCATGAAATGTCCGGATTTTTAATAGAATTGCGGTAAAAATAAAGAAAGAATTGATGATTAGTCAAATTATTTTTATTATTATTATTAATGTTTAATGGATTATCAAAATAATTATTTGTTGCAGCCCTGTTTTTTTTTTTTTTTTAAAGTCTGATTTACCGTATTTGTTTGTAAATAACCAATATTTGTGAACTAAAACGAAAGATTTAAGTTATATTTTAAGGTGCATTTTACTATTTTTCTATTCTTCTTATTTTATTTACGCAGAACATTAAAATGTTTCAAATTTGAGCATTTTTAAGCTTATTAATAATATT

Associated Phenotype:

Not determined