ZMP

tti1

Ensembl ID:

ENSDARG00000004114

ZFIN ID:

ZDB-GENE-080819-3

Human Orthologue:

TTI1

Human Description:

Tel2 interacting protein 1 homolog (S. pombe) [Source:HGNC Symbol;Acc:29029]

Mouse Orthologue:

Tti1

Mouse Description:

Tel2 interacting protein 1 homolog (S. pombe) Gene [Source:MGI Symbol;Acc:MGI:1922675]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10103	Nonsense	Available for shipment	Available now
sa30002	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10103

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000022498	Nonsense	275	1112	2	8

Genomic Location (Zv9):

Chromosome 23 (position 43795889)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	43535627
GRCz11	23	43428231

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGAGATGTAAGACAAGGTCAGGCAGTTACGGTRAAGTCCATGAGATTTTG[G/A]TACAAGACTGTAGGTTTAGTTWTGGCCGATGAGCAGCTTGAGAAGACCGR

Long Flanking Sequence:

GTTATGGAAGCTATGACGTACATTCTAGAAAACACATGCGTACAGAGATGGGAATCTCTACGTGATCTTTTCTCCGAGTTGTGTCTTTGTCTCTGTTCGCCACAAGACCCTGGAAAGCCTGCTATGACCTCTGAGGAATTAAAAATATCCGTTCTTGGATGCTTGGACACTCTCTTGCACTCTGCCTACGGTGATATTGTTTTTAAACTCTACGAGCCAAGCATGTTGCCTGGACTTGGTGCTGCCGTGTCTTTACTTCTGGCACTGGCAGAACAAGAAAAAGCAAGAAGTGTACAAACAGCATCCCTCAAATGTCTGCTTTCGTTGTTTCTCCAATGCGATTGCAAGAAGGAGCACATTGAACCAAGACAACATGAGAGGTATTTGCTTGGAAGTGCCTTAGCTACATTTTTACCTGGCATTTCTCGTGCACTTAGTCTTGTAGTGAGTGGAGATGTAAGACAAGGTCAGGCAGTTACGGTAAAGTCCATGAGATTTTG[G/A]TACAAGACTGTAGGTTTAGTTATGGCCGATGAGCAGCTTGAGAAGACCGGGATTGACAAGGCAGCTGGAGATCTAGGAAGAGTTGGGGAACTTATTGTGAAGAGGACGCCATCATGGCGGAAATCCACATCCCAACGTCTTGCCATAGTCTTACAAAGGATAATTTCTTGCACTTCTGCTCACCCACATTGGAAGGTCAGACTTGAATTGGTCAATCTATCCCATCATCTTCTTTCTCAATGTAGCCAAGCAGTTGTCGAATGTGTTGGTCCTCTACTTGAAGCATTGGTAGGTGCAATCAATGATGAGGAACCAGAGGTTAAAAACAGATGCAATGCAGCATTGGATGATGTTGCGCAAAAAGGTCAAACTAATGGCAGACAGGACTTCACTGATGTACTATCCGAAAACCTCCACAGCCTGGCATCATCTTTACCTCGACTCATGAGAACGTCTGACGATCAACGCAAGCTCTTTGTTCTTAACGTGTTCCTTGGGTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30002

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
ENSDART00000022498	Nonsense	1060	1112	8	8

Genomic Location (Zv9):

Chromosome 23 (position 43815759)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	43555497
GRCz11	23	43448101

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGGATCTGGACTCGGATCTGTGCTGGTTTATTCTCAATCAGCTCTACTG[T/A]CCTGTAGTTTATGATCCTCCTCATCCATTACTGCTGCCTGTCAAGCTGAG

Long Flanking Sequence:

ACAGCAGATGCCCTACCAGCTGCAACCCAGTACTGAGAAACACCCATACACACTTATTCTCACACACACACACATACACTACGGCAAATTCAGTTTATTCAGTTCACCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCTGGAGGAAACCCACGGCAACACAGGAAGAACATGCAAACTCCACACAGAAATTGCCAACTGTCCCAGCCGGGACTCAAACCATCGACCTTCTTATTGTGAGGAGACAGTGCTAACCAATGAGCCACCGTGCCGCCTCATTCATTACATTAACGATGATAATCATCCTGGCAGATACAGATATTTTTACTGAAAGACATGTTTTATTATAATTATTATTTTTTTTAATAATCTTCTGCCTGCCCCTGACAGTAATATTGATGATGATGGTTTCTCATGTGTTTCAGTGTTTTCCGCTCTCTGATGGATCTGGACTCGGATCTGTGCTGGTTTATTCTCAATCAGCTCTACTG[T/A]CCTGTAGTTTATGATCCTCCTCATCCATTACTGCTGCCTGTCAAGCTGAGCGGAGCGAACAAACCCAGAAACCAGTTCACTGACAACATCCTCAAACTCCTGCAGGAGCTGGACGGAGAACCAGAGAAACCAGATATAGACGCTTCACATGACAGATAACCGGCCTTCAGGCAGTACTTCTCAATGCTATATTTAAAGGAGCAGTTCACTCAAAAATAAACATTTACTCACTATTTACTCTCCTTGTTGTGGTTATAAGTGGTTATAAACATTTATGAGATTTTTTTTGTTGTTGCACACAAAATAAGATATTTTGAAGAATGTTAGAAACCTCAAACCTTTGTTTTGTCTTACTATGGAAGTCAATGGTTACAGGTTTCTAACATCCTTCAAAAGTCAATGGTTAATGTTTTCCAACATTTTTCAAAATATCTTCTTTTGTGTTTAACAAGCTGGATGGAGAACCAGATGCTTCATATGACATATAACATTCCTTGCTA

Associated Phenotype:

Not determined