ZMP

si:ch211-268f14.2

Ensembl ID:

ENSDARG00000076113

ZFIN ID:

ZDB-GENE-070705-261

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:A5WW76]

Human Orthologue:

TRAPPC9

Human Description:

trafficking protein particle complex 9 [Source:HGNC Symbol;Acc:30832]

Mouse Orthologue:

Trappc9

Mouse Description:

trafficking protein particle complex 9 Gene [Source:MGI Symbol;Acc:MGI:1923760]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7465	Missense	Mutation detected in F1 DNA	Not yet available
sa4781	Nonsense	F2 line generated	Not yet available
sa43208	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7465

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 > A

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110213	Missense	12	164	1	3
ENSDART00000141079	None	None	133	None	2

Genomic Location (Zv9):

Chromosome 19 (position 5166858)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	4418204
GRCz11	19	4348452

KASP Assay ID:

554-4084.1 (used for ordering genotyping assays)

KASP Sequence:

TTCCTTGACCAGCGGTGCACTCGTCTCTTCAGCGCGGCGGGGAGGCCAGT[G/A]TGGAGGGCGTCCTYAACCAGCTGATCCTRGAGCATCTGCAGCTGGCTCCT

Long Flanking Sequence:

ATTTGTTATTTCATTTCAGTTTACGAACGTGCTTTTTGACTAACAGTTTTAGTCTTTTTCATTAGTTTGAGTTTTGATTTATGAAAATATCCTTAATCAGTAATTTCCTTGACCAGCAAAATGTCACTTATGAATTTTTAATTTTATTTCAGTCAACAAGCACATATATTGTAAATGCACTTAAAAAAAGAGATATGGGGTGATTGTAAAAAATTGTCTGGTGCAAATGTGCAAAAACTGGTGCAAGTGGTTTGTCAAGCCCACTCACCTGGTTGAGGCACACTCAGAAATGTCTTATAACTCATAATGTTTTGAGATTGTTGTGTCGTGTGGTGGAGGTACCCGTGTTATGACATTTCCCTTTTATTAAATGTCATATTTGTTTTAGACTACCCTTTACTTTATAGTCTTTTTCATCAGTTTGAGTTTTGGTTTCTGGGAATTTGTGTTTTCCTTGACCAGCGGTGCACTCGTCTCTTCAGCGCGGCGGGGAGGCCAGT[G/A]TGGAGGGCGTCCTTAACCAGCTGATCCTGGAGCATCTGCAGCTGGCTCCTCTTCAGTGGGGTAAGAAAAACACCTTTCGCTTTCCCTCAATTCAGATATTCAAATCTATTCACACTCAGAGGTGATCTGTCTCCAGGACCGGTCTCTGCTCATGTTTCTTATTTGCATTTGTAATGGAGGAGAACTGTCCCTCACCGTGTGTGATGGAGGCCGGAGACAAGGCTCTCGTGTCGTCCGTGCAGTTTTTATATTAGTGTTGTCGGTGTATGCAGGCATTTGGTTGAGAGACAATCTTGACTGCTTTCGTAAGAGCTGCGGTTGAAAGTCGGCTGTTTTCAAAAATTTACAACTGCACTGTAAATATGACGTGAATGCATTGGGACGCTTTTTTTTTTTTTACATTTCAGTGTTTACAAAGAGATTACTTCAAAAAGTACATGAGTAGTCTTGACAAATTATACATCAGTCTAAAGCTACAACCCTCAAGCAGCCATTGTAGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa4781

Status:

F2 line generated
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
ENSDART00000110213	Nonsense	81	164	2	3
ENSDART00000141079	Nonsense	50	133	1	2

Genomic Location (Zv9):

Chromosome 19 (position 5275681)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	4526937
GRCz11	19	4443433

KASP Assay ID:

554-3531.1 (used for ordering genotyping assays)

KASP Sequence:

AAGAGCGCCGTCGGGCCCTTYKCTCTGACCGTCGTCCCCTTCCAGGACTA[T/A]CAGAACGGGGTGCAAAACTAYGAGCTGCAGGACGCCGTCACCTTCATCGG

Long Flanking Sequence:

CGATCTCAATTTCTGACTAGTGTATAATTACGGGCACCGCTTGTGATGGATGTCTACTAAAATCAACAATAAGAGCTCTTAAGAGCAATCACTATCTGTTCATTAGCTACTACAGCAGGGGAGTTCTCGAGATCTACCTGAACTTAAACTCCCCTCTTGCCTTGCAAATGAAAGGGAGCCCCGGGCTCGAGGATCTTATGAGCTCAGGGATGCCAAACAAGCTTTATAATCAATCATCAGCTAATGTGAACTCTTGACATGTGATTCTGAAGGTGTTTAAACTGGCTTGTATTAAGGTTTAGTTCTAATGTGGAGACTTTGCTGTTACAGTGTTTTGTTTGCATGTGTGCAGATGTGCTGGTGAACGGGAAGCCGTGTGATTGTGACGTGGTTGCCGACTGTAATGTTGGAGATGCCGTGCCGTTAGAGGTGAAACTGACCAATCGCAGTAAGAGCGCCGTCGGGCCCTTTTCTCTGACCGTCGTCCCCTTCCAGGACTA[T/A]CAGAACGGGGTGCAAAACTACGAGCTGCAGGACGCCGTCACCTTCATCGGCTCCAACACCTTCTACATCAACTCGGTAAGCGAAGCGGAGGGACACTGACCCACATCATCATCGAGATTTCCTGAAAACCAATGATTTTTTTAGAGGGAAAAAGAATGCCGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTTTAAAATCTAAAATAATTACAAGCATTAAATCATAAACTCCTAAAAATGTGTAAATAAAGGTATTCAGCAAACAATGTATAGTACTAATATAATAATAATAATAATAACAATAATAATAATGTGTGTGCGCATGGGTGTGCATGAGTTTGCTTGTGCATGTTTGCATTTGTTTGTGTTTGCGTGCGTGCATGCATTTGTGTGTTTGTGTGTGCATGCGTGTGTGCATTTGCACATGCATGCATGTGAGTGTGTGCGCGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTGTGTGCATTTGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43208

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110213	Essential Splice Site	106	164	2	3
ENSDART00000141079	Essential Splice Site	75	133	1	2

Genomic Location (Zv9):

Chromosome 19 (position 5275757)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	4527013
GRCz11	19	4443509

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCAGGACGCCGTCACCTTCATCGGCTCCAACACCTTCTACATCAACTCG[G/A]TAAGCGAAGCGGAGGGACACTGACCCACATCATCATCGAGATTTCCTGAA

Long Flanking Sequence:

TCTTAAGAGCAATCACTATCTGTTCATTAGCTACTACAGCAGGGGAGTTCTCGAGATCTACCTGAACTTAAACTCCCCTCTTGCCTTGCAAATGAAAGGGAGCCCCGGGCTCGAGGATCTTATGAGCTCAGGGATGCCAAACAAGCTTTATAATCAATCATCAGCTAATGTGAACTCTTGACATGTGATTCTGAAGGTGTTTAAACTGGCTTGTATTAAGGTTTAGTTCTAATGTGGAGACTTTGCTGTTACAGTGTTTTGTTTGCATGTGTGCAGATGTGCTGGTGAACGGGAAGCCGTGTGATTGTGACGTGGTTGCCGACTGTAATGTTGGAGATGCCGTGCCGTTAGAGGTGAAACTGACCAATCGCAGTAAGAGCGCCGTCGGGCCCTTTTCTCTGACCGTCGTCCCCTTCCAGGACTATCAGAACGGGGTGCAAAACTACGAGCTGCAGGACGCCGTCACCTTCATCGGCTCCAACACCTTCTACATCAACTCG[G/A]TAAGCGAAGCGGAGGGACACTGACCCACATCATCATCGAGATTTCCTGAAAACCAATGATTTTTTTAGAGGGAAAAAGAATGCCGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTTTAAAATCTAAAATAATTACAAGCATTAAATCATAAACTCCTAAAAATGTGTAAATAAAGGTATTCAGCAAACAATGTATAGTACTAATATAATAATAATAATAATAACAATAATAATAATGTGTGTGCGCATGGGTGTGCATGAGTTTGCTTGTGCATGTTTGCATTTGTTTGTGTTTGCGTGCGTGCATGCATTTGTGTGTTTGTGTGTGCATGCGTGTGTGCATTTGCACATGCATGCATGTGAGTGTGTGCGCGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTGTGTGCATTTGCATGTTTGTGTGTGCTTGAATGTGTTTGTGTAAGTGCGTGTGTGTGTGCATTTGCACGTGCGTGTAATTGTCTGTGTG

Associated Phenotype:

Not determined