ZMP

si:ch211-278a6.1

Ensembl ID:

ENSDARG00000059773

ZFIN ID:

ZDB-GENE-060503-699

Description:

Novel protein similar to vertebrate SNAP25-interacting protein (SNIP) [Source:UniProtKB/TrEMBL;Acc:A

Human Orthologue:

SRCIN1

Human Description:

SRC kinase signaling inhibitor 1 [Source:HGNC Symbol;Acc:29506]

Mouse Orthologue:

Srcin1

Mouse Description:

SRC kinase signaling inhibitor 1 Gene [Source:MGI Symbol;Acc:MGI:1933179]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa40119	Nonsense	Mutation detected in F1 DNA	Not yet available
sa26123	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa18245	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa40119

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000083442	Nonsense	104	997	2	15
ENSDART00000148107	Nonsense	277	1052	5	13

Genomic Location (Zv9):

Chromosome 3 (position 37308590)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	37171950
GRCz11	3	37313808

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGATGAAGCCAGAAATGTCTTCTACGAGCTGGAGGATGTGAGGGACATA[C/T]AGGACCGCAGCATCATCAAAATCTATCGCAAAGAACCCATCTACGCCTCC

Long Flanking Sequence:

GCCAAGGATTGAACCAGCAACCCAGCAACCTTCTTGCTGTGAGGCGACAGCACTACCTAATGCGCCACTCCGTCACCTATGCTTTTTATTAATAAATAATAATCAATAATCAATCAGGAGCATAATGATAACTGTTACCTATTATTATTATTATTATTATTATTATCATTATTATTATTATTATCATCATCTCCTGCACAGTCTTGACTTCAGCCCTTAAAAGTTTTTTTAGTGTATGGTTAACCATTTCCATCTTGACCATGTGTTGTTTCTTTCCTGGCTTCTCGTCCTCAGGTGTGCTGTTCCTCCAGTTTGGAGATGAGACCCGGCGTGTTCACATCACCCATGAGCTTAACAGTCTGGAGACGCTGCACGCACTCATCGTGCACATGTTCCCTCAAAAACTGACTGCAGGAATGCTCAAGTCGCCTAACACAGCCATCCTGATCAAAGATGAAGCCAGAAATGTCTTCTACGAGCTGGAGGATGTGAGGGACATA[C/T]AGGACCGCAGCATCATCAAAATCTATCGCAAAGAACCCATCTACGCCTCCTATCCTGCAGCGCATCTGGCCAACGGAGATCTCAGGGTGAGATTTTTCATATTTGATTCAGTGATTCAGTTGGTTTTCCATCTTTCGTTGTCCCGCTGTGAGCTTATGTTGCGAAATAGATACCAGGCATGATCCATTTTTAAAGAACGCTTCTCTTCTAAGTCAAAATAAGAAATCACAAGGTTACGGAGGAAGATCAGAGGCAAGTCTAACCTTCAGACTGACGTCACGGTCCTCTTTGCATGTTAAATATTTTAAAGGGAAGTACCCTTCGTTTGATCCATTGAGCGCCGTCTTTCAGATTTGGATGTTCTTGAAGTCGGAGGTTTTTGAATTATGCACACTTTTTTGGTTTCACTTGGGATTGCGTTTCACTTTGTGAGCTGGCTGTGCTGCCACAGGAGTTTGATGTGGGTTGACTTTGAAATGCAATCATGTGGCGTCACTCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa26123

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000083442	Essential Splice Site	764	997	11	15
ENSDART00000148107	Essential Splice Site	912	1052	12	13

Genomic Location (Zv9):

Chromosome 3 (position 37262879)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	37126239
GRCz11	3	37268097

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGGAGGAAGAGGAGGGTCTGAGAAAGCCTCATCTGTGGAAGTCAGACTGG[T/G]GAGGATAGAGATTTCATTGTTTCCCTGTTTCAATGGAAATTACCAAGCAG

Long Flanking Sequence:

TGTTACACACTCAGAAGTATGTACACTTTCTTCACAATGAGAGTAAATGTTTTTAGGGCGTAGGTGTATTGGGAAAGAATCACAGAGTGCTGTAATTTAATCATTCTATGTCTATCCTTGTGATTTGACTGTCTCAAATGTATTTTAATCTCCATCACCTTGGGTGCATTGTGATGCTTGAATCAGGCAGGTGAATGAGGGAGTGTGGAAAAGCCAGGATGAGTTTTCCAGCCCCTCTGCTAAACTTGGAGGAGGGGACGAGTACAGAAAGAACACAGACTTTGACATTCCAACCAGCCCACCGCTGAGCCTCAATGAGAGCAGCTTGGCTAACTGGAGCCCTCACCCAGGGCAAGGTCATGGCCACTCTAACTCGTCCCATGCACAGCGAGAGAAGGACTCTCATGGGGTCATGGTGGGCTCACTGAAGACCCGGGGTCTGGAGGAGCTCGGAGGAAGAGGAGGGTCTGAGAAAGCCTCATCTGTGGAAGTCAGACTGG[T/G]GAGGATAGAGATTTCATTGTTTCCCTGTTTCAATGGAAATTACCAAGCAGAAATTACCAAGCAGCTACAATATGTTGTTTTCTAGTATCCATTGAATAAATATATATAATAGCATAACATCTTTTTTTAAATGAGTAATTTTGTTTGAAAGTGTGAAGGGCAAGTCTGATGATGACACTAATCATCATGTTATTAAGTATCTAAGGCATATGTCTCAAACTCAATTCCTGAAAAGCCGCAGCTCTGCAGAGTTTTGCTCTAACCCTCATCAAACACAGCTGATCCAACTAATGAAGGTCTTTATGTCTCTTTTGAACACCTCGATTATTTGGATCAGCTGTGTTTGATCAGGGTTGGAGCAAAACCGTGCAGAGCTTCCTATTCAATAGTAAGAGTTTTGTTATTCTGAATAAAGCAAAGCTGGCTTCAACATAACTTTAAAAATAATATTACATTTGCTGGATTTGTTTTTATTAATCCAGCCAACATTAGCCTTGCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa18245

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000083442	Nonsense	826	997	12	15
ENSDART00000148107	Nonsense	974	1052	13	13

Genomic Location (Zv9):

Chromosome 3 (position 37261144)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	37124504
GRCz11	3	37266362

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGATCAAACCTGCTCAGAACCAGAATCAGAAYCAGAACCAGAACCCAAAC[C/T]AAAACCAGAATCCAAGTCCATCCAGCACCAATGCCACACCTGAACACAGG

Long Flanking Sequence:

GTGGGCGGAGCTAAACAGACTGATGAAGGTGTAGCATCGGGTGATCGTCTGTGGAGGCGGAGTTTAACTATTACACAATTATAAGGCAGATTCACAACCTGTCGTTTTGGAAGATTGGCCAATGTAAATTTTTAGACCTACTGTATAAGAAAGTTTTGAACTCTGAATCTTACCAGATATTTACATAATACAGCAACAGTTTATAGGTAAAAACATCAGAGGAATTTAATTTCCCAGCTCATGACACCTTTAAATGGAATTCATAAAATGTATGTAACAAAATTGAAATAATGCCCCTGTAAATGGTGTCTTCTCAGGCAGCGGAGCGTGATTGGGAAGAGAAGAGGGCCAGTCTGACACAGTACAGCGCTCAGGACATCAATCGACTGTTGGAGGAGACTCAGGCAGAGCTCATGAAGGCCATTCCTGACTTGGACTTTGCCGCCAAGCAGATCAAACCTGCTCAGAACCAGAATCAGAACCAGAACCAGAACCCAAAC[C/T]AAAACCAGAATCCAAGTCCATCCAGCACCAATGCCACACCTGAACACAGGCCTAACAAACCTCAGCATAAACTCAACAGTAAAGATAGCGGATCTAGACGAGGCTCAGATGAACTGACGGTGGCAAGATATCGAACAGAGAAGCCTTCAAAATCACCTCCTCCTCCACCGCCCCGCCGTAGCTTCCCCTCCTCGCCGGGGCTGACTACACGTAGCGGAGAGATAATCATCCCTGGAAAGAGTATAAAGGTAACATTTCCAAACACTATGACCAAAGGTTGTGACTTAAGGTCTTTGCACACTGAAGTCTGAAATTTTATATGCGTTTTTTATTACGCATTTTGTATTAAGTCCGATCTGTATTAATTAATCCATTACGAAAAAACGCAAAACATTTCGGAGTCAATTTAAGTAGATTCTTTGATTCTTTGTTCTCCTCTCTTCTCCAAAGTAAAAAAAGAAAGAGGAATAGACTACATATTAATGTGTTTATCCAATACC

Associated Phenotype:

Not determined